Lab Test Result Meaning

What Do My Lab Test Results Mean? Blood and Urine Tests

Interpret your lab results here.

  • LAB TEST RESULTS DISCUSSED:
    • ALT (Alanine)
    • Albumin/Globulin
    • Alkaline Phosphatase (Alk Phos)
    • AST (Aspartate aminotransferase)
    • Bilirubin
    • BUN (Blood Urea Nitrogen)
    • C-Peptide
    • Calcium
    • Cholesterol (Total, HDL, LDL, VLDL)
    • Creatinine (CK or CPK)
    • GGT (Gamma glutamyltransferase)
    • LDH (Lactate dehydrogenase)
    • Phosphorus
    • Potassium
    • Sodium
    • Total Protein
    • Triglycerides
    • Uric Acid
    • Bile Acids
    • CBC (Complete Blood Count)
    • WBC (White Blood Count)
    • Neutrophils
    • Lymphocytes (including T and B cells)
    • Monocytes
    • Eosinophils
    • Basophils
    • Platelet Count (Thrombocyte count)
    • RBC (Red Blood Cell Count)
    • Hgb (Hemoblobin)
    • HCT (Hematocrit or PCV or Pack Cell Volume)
    • MCH (Mean Corpuscular Hemoglobin)
    • MCHC (Mean Corpuscular Hemoglobin Content)
    • RDW (Red cell Distribution Width)
    • Blood Gasses (Oxygen, Carbon Dioxide, Bicarbonate)
    • Cardiac Risk Factors
    • Homocysteine
    • Lipoprotein
    • Thyroid Tests (TSH, Total and Free T3 & T4, Free Thyroxine
      Index, T3 Resin Uptake, Thyroid Antibody test, Reverse T3, Cortisol
      levels, Copper levels)
    • Diabetes and Blood Sugar tests (Glucose, Glycohemoglobin, IGF-1, Insulin, HOMA-IR)
    • Urinalysis (Volume, pH, Specific Gravity, Glucose, Protein, Blood, Bilirubin, Nitrate, Leukocytes and Sediment)
    • Sex Hormone Profile Tests (Estrogen, Estradiol, Estriol, Progesterone, Testosterone)
    • Tests for Sexually Transmitted Diseases (Herpes)
    • FAQ?s about Lab Work

Blood  Lab Test Results (Bloods for short):

Reference ?normal? ranges and unit measurements can vary from lab to
lab (sometimes up to 30% difference). Other factors influencing test
results include, dietetic preferences, sex, age, race, species,
menstrual cycles, amount of exercise, use of non-prescription drugs
(aspirin, cold medications, vitamins, etc.), prescription drugs, alcohol
consumption, collection and handling of the specimen. For best
comparisons of lab results, tests should be done in the same lab. Always use the normal ranges printed on the lab test result report of that particular sample.

Blood tests can have false positives and negatives. Interpretation of
blood tests takes knowledge of the underlying disease process and
experience. If your lab results are outside the normal range, we suggest
that you discuss them with your doctor. Often it is not the recent
result, but the change from a previous test that is most helpful in
trying to place a diagnosis on a condition.

Some tests cost more than others. If you can help the doctor
understand why a certain test may be important for you and they can
justify it in their mind, you may get to your diagnosis quicker and your
insurance may pay for the test saving time, money, and aggravation.

When a doctor evaluates the results of a  lab test, they try to figure out what all the causes could be then ?rule out?
the ones that don?t seem to fit after you add all the other signs and
symptoms into the picture. This is much like putting a jigsaw puzzle
together and searching for the exact placement of the pieces to the
puzzle. This Sherlock Holmes activity is one of my favorites because I
get to add in so many other tidbits of information that the medical
system doesn?t have time to ask in making a final ?jigsaw puzzle?
assessment.  Below are lists of ?Rule Outs? for
both high and low levels. You will see a veterinary flare to these as I
have put in the rule outs for animals as well. I have included the
medical term under each abnormality in parentheses. I have also tried to
explain in laymans terms the meaning of many of the scientific jargon.

To read more about Rule Out?s and what this term means, go to: http://naturalhealthtechniques.com/BasicsofHealth/what_is_a_rule_out.htm

The Basic Blood Chemistry Panel (Also called a Panel, Serum Chemistry Panel, Chemistry Screen, BMP or Basic Metabolic Panel):
For these lab tests, blood is drawn from the patient who has been
fasting 12 hours or more. Three tubes of blood are usually drawn from a
vein in the arm (human) or neck (animals).

________________________

Alanine (ALT, Alanine aminotransferase?formerly known as SGPT).

ALT is an enzyme contained inside the fluid part of each liver cell.
The larger the number of cells that are damaged, the higher the number.
This lab test is a good indicator of acute disease (disease coming on
quickly), but not for chronic liver diseases like cirrhosis where the
cells have died and been replaced by fibrous tissue. ALT stays in the
blood stream for about 60 hours. Because of this, sometimes your doctor
will want to repeat the blood lab test to track how the body is
responding.

ALT Too High (Liver enzymes elevated): Rule out
hepatocellular (liver cell) diseases such as cancer, fatty liver, cell
death due to bacteria/viruses/hepatitis or toxins, cirrhosis,
obstructive jaundice, and infectious mononucleosis.

ALT Too Low: Rule out pyridoxine (Vitamin B6) deficiency.

Albumin and Globulin

-This lab test measures the amount and type of
protein in your blood. Albumin and globulin are a general index of
overall health and nutrition. Globulin is the ?antibody? protein
important for fighting disease produced by white blood cells. Albumin
contains things like clotting factors, fibrin and binding proteins (much
like egg white) and it give the blood more substance.

Albumin/Globulin Too High: Rule out dehydration,
diabetes insipidus (low blood sugar diabetics that can?t get enough
water), antigenic responses, infection, and gammopathies such as
lymphosarcoma, multiple myeloma, and FIP?Feline Infectious Peritonitis

Albumin/Globulin Too Low: Rule out malnutrition,
overhydration, advanced liver disease, cancer, acute or chronic
hemorrhage, kidney disease (nephrosis), burns, multiple myeloma,
metastatic carcinomas, heart disease, loss of blood or protein into the
body cavity, malabsorption, parasites and pancreatic atrophy.

False Positives: False elevations in this lab test
can occur with red blood cell damage in the sample (hemolysis) and
lipemia (fat in the blood).

Alkaline Phosphatase (Alk. Phos.)

Alkaline phosphatase is an enzyme found primarily in bones and the
liver but can also be found in other tissues of the body as well such as
the intestine, kidney, placenta and in white blood cells. It is thought
that this enzyme is increased in the body only when there are actively
growing new cells being produced. Alkaline Phosphatase enzymes can be
further broken down to find out where they are specifically being
produced using a process called electrophoresis (a
special test not included in the regular blood panel). The alkaline
phosphatase enzyme circulates in the body for about three days before it
starts to break down, so if your blood tests are repeatedly high in
this area, there are actively growing cells.

Alkaline Phosphatase Too High: Rule outs include
gallstones, damage to bones, Paget?s disease (a chronic disorder of the
adult skeleton in which localized areas of hyperactive bone are replaced
by a softened and enlarged osseous structure), rickets, healing
fracture, hyperparathyroidism, pulmonary infarction, heart failure,
liver disease with too many cells growing (like cancer), obstruction
within the liver or the liver not getting what it needs because
something is obstructed outside the liver, pancreatitis, severe anemia,
lack of oxygen getting to the liver, Cushing?s disease, drugs such as
glucocorticoids (steroids), primidone, phenobarbital (anti-seizure
drugs). An elevated  alkaline phosphatase is normal in growing
children and in pregnant women.

Alkaline Phosphatase Too Low: Pernicious anemia,
hypoparathyroidism, hypophosphatasia and possibly the blood was taken
from a collection tube that had EDTA preservative in it.

AST (Aspartate aminotransferase?formerly known as SGOT):

AST is an enzyme contained in all cells of the body, but is used as a
diagnostic marker for liver and muscle damage. Its half-life is about
12 hours.

AST Too High: Rule out liver disease (death of cells
and cancer), skeletal muscle diseases, (myositis and muscular
dystrophy), trauma, pancreatitis, renal infarct, eclampsia (milk fever),
cancer, cerebral damage, seizures, alcohol, heart tissue disease (heart
attacks, pericarditis), infections in the bloodstream (septicemia),
intramuscular injections, drugs such as corticosteroids, primidone,
antibiotics and other drugs processed through the liver. Hemolysis
(ruptured red cells from improper handling of the blood) can also raise
AST levels.

AST Too Low: Rule out pyridoxine (Vitamin B6) deficiency, and terminal stages of liver disease.

Bilirubin (Bilirubinemia):

Most bilirubin (80%) is a breakdown component from dying red blood
cells. Bilirubin is also in macrophages of the spleen and in the liver,
bone marrow and non-heme porphyrins. Bilirubin travels via the blood
stream in the plasma part of the blood surrounded by albumin, globulin
and other proteins. As it gets to the liver via the blood system, it
disassociates from these proteins and the liver accepts it into it?s own
cells by binding (conjugating) it with glucuronic acid. This
conjugation makes it water-soluble. From here bilirubin gets into the
bile and then dumps into the small intestine, eventually leaving though
the feces after it changes form one more times. Some of this bilirubin
sneaks back into the bloodstream and is reabsorbed into the blood. This
happens repeatedly. Sometimes the bilirubin ends up being excreted via
the kidneys and dumps out into the urine. When this happens, it shows up
in abnormal levels within the blood and may also show up in the
urinalysis lab test on the dipstick test.

Urine Dipstick Lab Test Result Meaning

The urine dipstick for urinalysis lab test

Bilirubin lab test Too High (Hyperbilirubinemia):
Rule outs include hemolytic anemia, pulmonary infarct, Gilbert?s
syndrome (mild unconjugated hyperbilirubinemia), Dublin-Johnson syndrome
(a genetic symptomatic mild jaundice), neonatal jaundice, inadequate
liver uptake or defective conjugation, massive internal hemorrhage,
obstruction of bile within the liver or outside the liver, defective
secretion, acute or chronic hepatitis, fibrosis of the liver and liver
cancer. It can also be falsely elevated when there is too much fat in
the bloodstream. If only slightly elevated above the expected ranges,
but with all other enzymes (LDH, GOT, GPT, GGT) within expected values,
it is probably a condition known as Gilbert?s syndrome and is not
significant.

Bilirubin is also measured in the urine. Sometimes
the doctor?s will run a test to check both conjugated and unconjugated
bilirubin to help them determine where the extra is coming from.

They want to know if the liver is blocked or the blood cells have
broken (hemorrhage). When the liver is blocked totally the fecal
material will also be gray or whitish (acholic). When increased
bilirubin is caused from hemorrhage the stools will be almost orange in
color. You will want to tell your doctor this information because they
may not ask.

Bilirubin  lab test Too Low: Low values are of
no concern. Sunlight and fluorescent lights degrade the sample as the
bilirubin is very fragile when exposed to light.

BUN (Blood Urea Nitrogen, Urea Nitrogen):

High BUN values in the lab tests may mean that the
kidneys are not working as well as they should in clearing out the
breakdown products of digested protein. The major breakdown product of
protein you eat is urea, which is first formed in the liver. Urea
contains nitrogen and together, in excess quantity, they are both toxic
to the body and must be removed. Kidneys normally do an excellent job of
removing urea, but when they start to fail, the urine components get
all backed up in the system and the blood concentration of urea begins
to rise. If you smell the breath, it has a stale, sickly smell (see my
handout on the causes of Halitosis for other characteristics of bad breath: http://naturalhealthtechniques.com/specificdiseasesbad_breath_causes_%20and_%20remedies.htm ) The reference range (or range within which most normal people?s test values fall) for BUN is 10-20 mg/dl.

BUN  lab test Too High (Uremia, Azotemia or Uremic Acidosis):
Rule out dehydration (too little water in the tissues), too much
exercise, shock due to too much blood being lost (hemorrhagic shock),
pancreatitis, intestinal foreign body, adrenal cortical insufficiency
(adrenal glands not producing enough of the hormones it is suppose to be
producing), or any condition which decreases blood flow to the kidneys,
glomerulonephritis (the little tubules that make the urine in the
kidneys are swollen and not working right), amyloidosis (the kidney
tissue is being replaced with some kind of unnatural protein),
pyelonephritis (inflammation/infection of the kidney where the urine
pools before it dumps out into the ureters), nephrosis (a condition of
the kidneys), calcium nephropathy?also called lymphosarcoma (cancer of
the kidneys where the tissues are being replaced by calcium so the urine
can?t get out), kidney cancers, obstruction of the urine coming out of
the kidney, leukemia, heart failure, ruptures of the urine carrying
parts (kidney, ureters, bladder, urethra, kidney tubules), too much
protein in the diet, bleeding within the intestine, and drugs like
amphotericin B. Often, an additional test is done to measure creatinine.

BUN lab test Too Low: Severe liver disease, hepatic
venous shunts (portal-caval shunts), anorexia for several days
(starving, not eating, fasting), pregnancy.

BUN/Creatinine Ratio: This test is used to
differentiate kidney disease from dietary protein metabolism problems.
Considered together, the BUN, blood creatinine and their ratio give very
good evidence of the filtering function of the kidneys and a measure of
the degree of bodily hydration. The ratio of BUN: creatinine is
normally 10:1.

BUN/Creatinine Ratio Too High: Rule out dehydration
(if the ratio is 20:1 or even higher), certain types of kidney disease,
breakdown of blood in the intestinal tract, increased dietary protein,
and any clinical circumstance in which insufficient blood is flowing
through the blood vessels to the kidneys (such as heart failure or
kidney artery disease)..

BUN/Creatinine Ratio Too Low: Rule out certain types of kidney disease, liver disease, malnutrition and Sickle Cell Anemia.

C-Peptide (see under Glucose)

Calcium:

Calcium is controlled in the blood by the
parathyroid glands and the kidneys. Calcium is found mostly in bone and
is important for proper blood clotting, nerve, and cell activity.
Calcium is also found in the bloodstream.

Calcium lab test levels Too High (Hypercalcemia):
Rule out an elevation due to medications such as thiazide-type
diuretics, inherited disorders of calcium handling in the kidneys, diets
containing too much calcium, too many calcium supplements, too much
Vitamin D, multiple myeloma (cancer of the stem cells within the bone
that are responsible for producing all types of red and white cells),
bone cancer, sarcoid, too much protein in the blood, too much albumin in
the blood, fat in the blood (lipemia), excess parathyroid gland
activity such as primary hyperparathyroidism (the thyroid gland has some
kind of tumor or cancer causing the calcium levels to be to high), and
pseudohyperparathyroidism (cancer of the lymphatic system).

Calcium lab test levelsToo Low (Hypocalcemia):
Rule out certain drugs like Fosamax and furosemide-type diuretics, not
enough dietary calcium, not enough dietary Vitamin D, overhydration,
malabsorption, nutritional secondary hypoparathyroidism,
hypercalcitoninism, eclampsia (milk fever?the baby or muscle
contractions during birth have used up too much of the calcium),
pancreatitis with fat necrosis (an infection in the pancreas which has
affected all the extra fat in the body causing it to die from lack of
circulation and nutrition), and not enough protein or albumin in the
blood. Calcium is bound to a particular type of blood protein called
albumin in the blood, so a low albumin level will cause the total
calcium level in the blood to drop in proportion.

Cholesterol:

There are two types of cholesterol, those obtained
from the diet (exogenous) and that produced within the body
(endogenous). Most of the endogenous cholesterol is formed by the liver,
but each cell also produces a little bit as well which makes up part of
the cellular membrane. With just small modifications, cholesterol can
be used as the body needs it as steroids and cholic acid. Cholic acid
uses approximately 80% of the body?s cholesterol, which is converted
into bile?that substance that helps us digest fats. Cutting out
saturated fats from your diet can decrease your cholesterol levels from
15-25%. Eating more unsaturated fats (oils, nuts, seeds) can decrease
your cholesterol. The saturated and unsaturated fats fight for the same
receptor sites on cells. Saturated fats make the cell membranes sluggish
(so you get arthritis and other degenerative diseases) and unsaturated fats make the membranes more liquid so the body works better. (See the Eicosanoid handout: http://naturalhealthtechniques.com/Diet_Nutrition/eicosinoid_survey.htm ) Lack of insulin and thyroid hormones will also increase the cholesterol levels.

Cholesterol is further broken down as follows:

Total Cholesterol: High cholesterol in the blood lab
test is a major risk factor for heart and blood vessel disease.
Cholesterol in itself is not all bad. In fact, our bodies need a certain
amount of this substance to function properly. However, when the level
gets too high, vascular disease can result. Total cholesterol of less
than 200, and an LDL Cholesterol of 100 or less is considered optimal by
the National Heart, Lung, and Blood Institute. As the level of blood
cholesterol increases, so does the possibility of plugging the arteries
due to cholesterol plaque build-up. This is called ?hardening of the
arteries? or atherosclerosis. When the arteries feeding
the heart become plugged, a heart attack may occur. If the arteries
that go to the brain are affected, a stroke occurs.

There are three major kinds of cholesterol, High Density Lipoprotein (HDL) , Low Density Lipoprotein (LDL), and Very Low Density Lipoprotein (VLDL). The lower the density of cholesterol, the more cholesterol molecules there are.

HDL (High Density Lipoprotein)
cholesterol is a ?good cholesterol? as it protects against heart disease
by helping remove excess cholesterol deposited in the arteries. High
levels in the lab test seem to be associated with low incidence of
coronary heart disease.

LDL (Low Density Lipoprotein)
cholesterol is considered to be ?bad cholesterol? because cholesterol
deposits form in the arteries when LDL levels are high. LDL levels of
less than 130 are recommended. One hundred is optimal and values greater
than 160 are considered high risk. Those persons who have established
coronary or vascular disease may be instructed by their doctor to get
their LDL cholesterol well below 100. You should ask your doctor which
LDL target he or she wants for you-but do some of your own research as
well.

There are two ways to report LDL. The most common is simply an
estimate calculated from the Total Cholesterol, HDL, and triglycerides
results. This may read ?LDL Calc? on your lab test
results. A directly measured LDL cholesterol is usually more accurate,
but more expensive and may require that your doctor specify the Direct LDL test.

VLDL (Very Low Density Lipoprotein: This is the only
lipoprotein initially formed in the liver and contains mostly
triglycerides and very little phospholipids and cholesterol. As they
flow through the blood vessels they are quickly broken up and used as
energy or stored as fat.

Cholesterol lab test Too High: Rule out
hypothyroidism, obstructive jaundice, liver disease, nephrosis, diabetes
mellitus, familial, pancreatitis, hyperadrenocorticism, diet, retained
anger and resentment.

Cholesterol Too Low: Rule out hyperthyroidism,
infection, malnutrition, heart failure, malignancies, low fat diet,
intestinal malabsorption and hepatic insufficiency.

Creatinine. (Also known as Creatine phosphokinase, CK and CPK)

CPK is an enzyme which is very useful for diagnosing diseases of the
heart and skeletal muscle. This enzyme is the first to be elevated after
a heart attack. If CPK is high in the absence of heart muscle injury,
this is a strong indication of skeletal muscle disease. Most creatinine
is produced in the muscle, heart and brain. Creatinine is a
water-soluble waste product largely from muscle breakdown that is
excreted via the kidney tubules. Creatinine is not affected by the
amount of urine produced and excreted. When creatinine breaks down it
gives us energy because it acts as an enzyme important in the process of
forming ATP (that very basic process that gives us energy).

The rule outs for too high and too low creatinine levels in the lab test are the same as for BUN
(Blood Urea Nitrogen): If the kidneys are not functioning properly, the
concentrations of creatinine and blood urea nitrogen will rise in the
blood. The laboratory uses the blood urea nitrogen (BUN) and creatinine
levels to assess kidney function. In addition, a urinalysis is used to
measure kidney output function and health of the collecting system
(lower portion of kidney, ureters and bladder).

Creatinine lab test Too High: Rule out dehydration,
too much exercise, hemorrhagic shock (shock due to too much blood being
lost), pancreatitis, intestinal foreign body, too much protein in the
diet, bleeding within the intestine, drugs like amphotericin B,
hyperthyroidism (humans) and hypothyroidism (animals-sometimes), adrenal
cortical insufficiency (adrenal glands not producing enough of the
hormones it is suppose to be producing), any condition which decreases
blood flow to the kidneys such as, glomerulonephritis (the little
tubules that make the urine in the kidneys are swollen and not working
right), amyloidosis (the kidney tissue is being replaced with some kind
of unnatural protein), pyelonephritis (inflammation/infection of the
kidney where the urine pools before it dumps out into the ureters),
nephrosis (a condition of the kidneys), calcium nephropathy?also called
lymphosarcoma (cancer of the kidneys where the tissues are being
replaced by calcium so the urine can?t get out and so it builds up in
the body instead), kidney cancers, obstruction of the urine coming out
of the kidney, ruptures of the urine carrying parts (kidney, ureters,
bladder, urethra, kidney tubules.

Creatinine lab test Too Low: Rule out severe liver
disease, hepatic venous shunts (portal-caval shunts), anorexia for
several days (starving, not eating, fasting), and pregnancy.

GGT (Gamma glutamyltransferase or Gamma glutamyl transpeptidase)

GGT is an enzyme that is in high levels specifically
in kidney tubule cells and in bile producing cells of the liver. When
it shows up in high levels in the blood serum, it is of liver origin.
When it if from the kidneys, a special test needs to be run to see it,
so this one can be missed because it is not a part of routine blood
work.

GGT Too High: Rule out liver disease, particularly
with obstruction of the bile ducts (cholestasis) and in acute hepatic
necrosis (liver cells dying and rotting very quickly). Unlike alkaline
phosphatase it is not elevated with bone growth or damage.

C-peptide :

C-Peptide is a fragment cleaved off of the precursor of insulin
(pro-insulin) when insulin is manufactured in the pancreas. C-peptide
levels usually correlate with the insulin levels, except when people
take insulin injections. When a patient is hypoglycemic, this test may
be useful to determine whether high insulin levels are due to excessive
pancreatic release of insulin, or from an injection of insulin.

LDH (Lactate Dehydrogenase)

LDH is the enzyme present in all the cells of the
body. Anything that damages cells, including blood drawing itself, will
raise amounts in the blood. If blood is not processed promptly and
properly, high levels may occur.

Lactate Dehydrogenase Too High: Rule out heart
attack, pulmonary infarction, hemolytic anemia, pernicious anemia,
leukemia, lymphoma, malignancies, renal infarction, seizures, cerebral
damage, trauma, sprue (a chronic intestinal malabsorption disorder
caused by gluten intolerance), lymphosarcoma, lipemia (fat in the
bloodstream), improper sample handling (broken cells), necrosis (tissue
death) of the liver, skeletal muscle, kidney, pancreas and myocardium
and using old blood samples for running the test.

Note: If all values except LDH are within expected ranges, it is probably a processing error and does not require further evaluation.

Lactate Dehydrogenase Too Low: Not clinically significant.

Phosphorus:

Phosphorus is a mineral largely stored in the bone and is regulated by the kidneys.

Phosphorus Too High (Hyperphosphatemia): Rule out
kidney disease, normal in young animals, high protein diets, too much
Vitamin D, hypoparathyroidism, diabetic acidosis, acromegaly, Addison?s
disease, calcium nephropathy, lymphosarcoma (if BUN is also elevated),
and not allowing the blood tube to clot before separating the serum from
the sample before mailing.

Phosphorus Too Low (Hypophosphatemia): Rule out
inadequate diet, malabsorption, parathyroid conditions such as primary
hyperparathyroidism and pseudohyperparathyroidism, Vitamin D deficiency,
osteomalacia, rickets, Fanconi syndrome, cirrhosis, hypokalemia, excess
IV glucose, too much insulin in the system (either from injection or
cancer of the pancreas). When low levels of phosphorus are seen with
high levels of calcium it suggests parathyroid disease.

Potassium:

Potassium is an essential mineral controlled very
carefully by the kidneys. It is important for the proper functioning of
the nerves and muscles, particularly the heart. Any value outside the
expected range, high or low, requires medical evaluation. This is
especially important if you are taking a diuretic (water pill) or heart
pill (Digitalis, Lanoxin, etc.).

Potassium Too High (Hyperkalemia): Rule out
Addison?s disease (adrenal cortical insufficiency), dehydration, cardiac
arrhythmia, severe renal disease, hyperkalemic acidosis, diabetic
acidosis, hypoadrenalism, hereditary hyperkalemia, metabolic acidosis
(like in diabetes mellitus).

Note: Hemolyzed blood will also
cause a slight increase in potassium because 85% of all the potassium in
the body is stored within the cells. Hemolyzed blood can happen when
the sample is damaged and the blood cells have broken in the process of
either collecting the sample or in handling the vials during transport
to the lab. I have also seen it occur when the syringe is pulled back
too quickly or too far causing the vein to collapse (impatience). This
doesn?t happen often in humans because a needle is inserted into the arm
vein and the tube pushed onto the needle. In this way the blood does
not suck into the tubes too quickly and the sample stays intact (animals
are not that cooperative, so that?s another story).

Potassium Too Low (Hypokalemia): Rule out cirrhosis,
malnutrition, metabolic alkalosis, nephrosis, hyperadrenalism, familial
periodic paralysis (need DNA testing for this), overhydration with
potassium low fluids, diarrhea, vomiting, intestinal obstruction,
malabsorption, Cushing?s disease, insulin treatments driving potassium
into the cells, drugs such as mercurial diuretics and
hydrochlorothiazide (blood pressure medications).

Sodium:

Sodium is an essential mineral regulated by the kidneys and adrenal glands and present in every cell of our body.

Sodium Too High (Hypernatremia): Rule out
dehydration, heart disease, salt poisoning, eating too many salty foods,
faulty water softener dumping too much salt into the water, and
diabetes insipidus.

Sodium Too Low (Hyponatremia): Rule out Addison?s
disease (adrenal cortical insufficiency), diarrhea, overhydration with
fluids not containing salt, malabsorption, diabetic acidosis, severe
renal disease, ruptured or obstructed urinary system, overdose of
certain drugs such as diuretics and blood pressure medications (like
hydrochlorothiazide), excess antidiuretic hormone, nephrosis,
hypoadrenalism, myxedema, congestive heart failure, vomiting, diabetic
acidosis, and excessive water intake in patients with heart or liver
disease.

Total Protein (TP):

Total protein in the blood includes clotting
factors, enzymes, antibodies, transport substances, albumin and most of
the alpha and beta globulins. Total protein is measured in
grams/deciliter with an instrument called a refractometer. A
refractometer is a machine that can measure how much light passes
through a substance.

Protein Too High (Hyperproteinemia): Rule out
dehydration, too much albumin and fibrin,  globulin increases from
tissue injury, inflammation, active liver disease, strongylosis
(roundworm infestation), immune-mediated disease, lymphoid neoplasms,
and myelomas (bone cancer). Factors giving false elevations include
abnormally high concentrations of glucose, urea, sodium, chloride or
lipids. Hemolysis (but not icterus) also causes mild elevations.

Protein Too Low (Hypoproteinemia): Rule out decreased production, intestinal malabsorption, malnutrition, exocrine pancreatic insufficiency,
chronic liver disease, accelerated loss of protein, hemorrhage, renal
disease (proteinuria), protein-losing enteropathies, severe exudative
skin disease, burns, high-protein effusions, hepatic insufficiency,
colostrum deprivation, combined immunodeficiency (foals),
agammaglobulinemia, selective IgM deficiency, transient
hypogammaglobulinemia, and Disseminated Intravascular Coagulation (DIC).

Triglycerides (also called Neutral Fat):

Triglycerides (along with carbohydrates) are fats in the blood used
in the body mainly to provide energy for the different metabolic
processes. Those that are not used for energy are quickly stored as fat.

Triglycerides Too High: Rule out post-prandial (just
after eating they go up), heart disease (severe elevations), endocrine,
hepatic, pancreatic and renal disease, high-fat diets, low insulin,
hypothyroid, heparin injections, diabetes mellitus, and exogenous
corticosteroids.

Uric Acid:

Uric Acid is a breakdown product of nucleic acids
normally excreted in urine. Nucleic acids make up the components of DNA
and RNA in our bodies.

Uric Acid Too High: Rule out gout,
arthritis, kidney problems leukemia, lymphoma, polycythemia, acidosis,
psoriasis, hypothyroidism, eclampsia, multiple myeloma, pernicious
anemia, tissue necrosis, inflammation, and the use of some diuretics.

Uric Acid Too Low: Rule out uricosuric drugs (drugs
that break down uric acid and assist it to leave via the urine?as your
pharmacist on this), too much allopurinol (the drug used in the
treatment of gout), Wilson?s Disease (a genetic disease of the liver
which allows copper to build up to toxic levels), and large doses of
Vitamin C.

Bile Acids:

Bile acids produced by the liver cells. They are bound by the amino
acids glycine or taurine and then dumped into the bile. Bile acids help
us to digest our foods?especially the fatty ones. Sometimes I see people
(and cats) that have vision problems and enlarged hearts who test out
as having taurine deficiency so there may be an association. I don?t
know for sure.

Bile Acids Too High (Increased bile acids): Rule out
blocked bile ducts (gall stones?), acute toxic hepatic necrosis,
anicturic liver disease, alcoholic liver disease, biliary atresia,
chemical and drug induced liver injury, cirrhosis, cholestasis, cystic
fibrosis, generalized pruritus (itchy rash all over the body), hepatoma,
nausea and vomiting associated with pregnancy, neonatal hepatitis,
protracted diarrhea in infants, Reye?s syndrome, and viral hepatitis.

Bile Acids Too Low: Not clinically significant.

Complete Blood Count (CBC):

When all the cellular components of the blood are looked at and characterized as to their numbers this is called a Complete Blood Count or CBC. Within the CBC the white cells, red cells and platelets are counted. A white cell count is called a WBC (White Blood Cell count) and a red cell count is called an RBC (Red Blood Cell count). The CBC typically has several parameters that are created and evaluated using an automated cell counter. These are the most relevant:

WBC (White Blood Count)

White blood cells are responsible for detecting and destroying
diseases that come into our body. There are several ways to measure
white blood cells. White cells are also broken down into their
individual categories of types of cells that fight different things.
These include Neutrophils, Lymphocytes, Monocytes, Eosinophils, and Basophils.
Most times these cells are counted by automation (machine), but
sometimes the doctor would like to see the character of the cells to
detect any differences that the machine can?t detect with it?s
mechanism, so a hand count is done and abnormalities noted.

White Blood Count Too High: Rule out infection and leukemia.

White Blood Count Too Low: Rule out bone marrow
diseases or an enlarged spleen, pooling of the cells within the body
(like in pyometra), HIV (Note: The vast majority of low WBC counts in
our population is NOT HIV related.)

Neutrophils:

Neutrophils are a type of white blood cell that
circulate in both tissues and blood. They act like little ?Pac Men? in
the tissues finding bacteria and chomping them up. Once they move from
the circulation into the tissues, they don?t return. They are replaced
two times or more each day, so you can see that these cells can really
multiply when there is a problem.

Neutrophils Too High on the CBC lab test: Rule out
stress, pain, very high or very low body temperatures (which cause
cortisol to be released from the system), drugs such as cortisone,
strenuous exercise,  bacterial infections (cat bite abscesses are a
fabulous representation of this!), increased heart rate and increased
blood pressure. When neutrophils increase with stress (called a stress
leukogram), the neutrophil count goes up and the leukocyte count
decreases at the same time.

To Read about Gout go to: http://naturalhealthtechniques.com/SpecificDiseases/gout1.htm

Lymphocytes:

Lymphocytes live in the immune rich tissues like the
lymph nodes, spleen, tonsils, thymus, gastrointestinal lymphoid tissue,
bronchial lymphoid tissue, bone marrow and in the blood. There are lots
of lymph nodes in the breast, under the arm, behind the knees, in the
neck, and in the groin areas. Lymphocytes are specifically attracted to
viruses, pollens and cells that have anything wrong on them on the
outside of the cell (this is called cell-mediated immunity).
They live a lot longer (weeks) than neutrophils and DO recirculate from
the tissue to the blood and back. They go where they are needed.
Lymphocytes are further broken down into T-cells, and B-cells, but
special testing is needed to determine how much of each we have.

T-cells:

T-cells have the ability to never forgive and never
forget. When they detect something bad in the system they attack it. If a
particular T cell was programmed to attack the cancer virus, it will
always attack cancer virus (and not much else). Sometimes these
particular cancer-attacking white cells are called ?Killer cells?.
We stimulate our immune system to train the T-cells by using vaccines,
homeopathic nosodes, and exposing ourselves to infectious agents. This
makes our immune system strong.

B-cells:

B-cells wait around for orders. They will turn into T
cells if necessary, but most times their job is to produce antibodies.
Antibodies glom onto foreign substances that get into the body and they
remove it. When antibodies get the wrong orders (like when a person is
highly allergic to bee stings), the B cells sometimes overreact or react
too quickly causing anaphylactic shock.

Lymphocytes:

Lymphocytes Too Low (Lymphopenia): Rule out
corticosteroids, stress, pain, acute systemic infections (viral and
bacterial), acquired T lymphocyte deficiency (neonatal infections),
immunosuppressive drugs, irradiation, loss of lymph, chylous thoracic
effusion (ruptured thoracic duct), lymphosarcoma, enteric neoplasms,
granulomatous enteritis, Johne?s disease (cattle), protein-losing
enteropathies, ulcerative enteritis, lymphatic cancer destroying lymph
nodes, and hereditary T-cell deficiency.

Monocytes:

Monocytes can be elevated (monocytosis)
in response to corticosteroids, with pus conditions (abscesses),
necrosis, malignancy, hemolysis, hemorrhage, mononucleosis, immune
injury, pyogranulomatous diseases, and in acute and chronic stages of
disease.

Eosinophils:

Eosinophils are elevated (eosinophilia)
with parasite infestation, allergies, myositis, canine and feline
eosinophilic granuloma complex, eosinophilic gastroenteritis,
panosteitis, milk sensitivity (cattle), feline staphylococcal or
streptococcal infections and mast cell neoplasia.

Basophils:

Basophils are the least numerous of the white blood cells. Observing even a few cells on the blood smear usually attracts attention.

Basophils Too High (Basophilia): Rule out parasites,
hypersensitivities, heartworm (without microfilaria in the blood),
altered plasma lipoprotein metabolism causing endocrine diseases,
nephrotic syndrome, chronic liver disease, genetic
hyperlipoproteinemias, and mastocytomas (Mast cells look much like
basophils).

Platelet Count (PLT or Thrombocyte count):

Platelets are cells that plug up holes in blood vessels and prevent
bleeding. This test measures the number of platelets in a drop
(microliter) of blood. Normal values range from 150,000 to 400,000
platelets per microliter. A count below 50,000 can result in spontaneous
bleeding; below 5,000, patients are at risk of severe life-threatening
bleeding.

Platelet Count Too High (Thrombosis): Rule out
bleeding, cigarette smoking, excess production by the bone marrow,
strenuous activity, myeloproliferative disorders, infections,
inflammation, cancers, and when the spleen has been removed.

Platelet Count Too Low (Thrombocytopenia): Rule out
premature destruction states such as immune-mediated thrombocytopenia,
acute blood loss, drug effects (such as heparin), infections with
sepsis, entrapment of platelets in an enlarged spleen, or bone marrow
failure from diseases such as myelofibrosis or leukemia. Platelet counts
decrease just before menstruation. If there are not enough platelets in
your blood, you may notice signs of bleeding such as nosebleeds, easy
bruising, prolonged bleeding from a cut, black or bloody stools, brown
or red urine, or tiny pinpoint sized red or purple spots on your skin,
under your nails or in your gums (petechial hemorrhage). Low platelets
also can occur from clumping of the platelets in a lavender-top tube.
You may need to repeat the lab test with a green top tube in this case.

RBC (Red Blood Count)

Hemoglobin (Hgb):

Hemoglobin is the amount of oxygen carrying protein contained within the red blood cells.

Hemoglobin Too High: Rule out lung disease, living
at high altitude, excessive bone marrow production of blood cells,
kidney tumors, hepatomas (liver tumors), uterine leiomyomas, cerebellar
hemangioblastomas, and sickle cell anemia.

Hemoglobin Too Low: Rule out anemia due to
nutritional deficiencies, blood loss, destruction of blood cells
internally, or failure to produce blood in the bone marrow.

Hematocrit (HCT, Packed Cell Volume or PCV):

The hematocrit is the percentage of the blood volume occupied by red
blood cells. Men have a slightly higher hematocrit percentages than
women because women lose a bit of blood each month during their
menstrual cycle.

Hematocrit Too High: Rule out smoking (due to too much carbon dioxide exposure), high altitude, chronic lung disease, and newborn syndrome.

Hematocrit Too Low: Rule out anemia due to
nutritional deficiencies, blood loss, and destruction of blood cells
internally, or failure to produce blood in the bone marrow.

MCH (Mean Corpuscular Hemoglobin or Mean Corpuscular Volume (MCV):

MCH test helps diagnose the type of anemia.

MCH Too High: Rule out B12 deficiency, folate deficiency,
ineffective production in the bone marrow, or recent blood loss with
replacement by newer (and larger) reticulocytic cells from the bone
marrow, and in vitro or in vivo hemolysis.

MCH Too Low in the lab test: Rule out iron deficiency.

MCHC (Mean Corpuscular Hemoglobin Content or concentration):

MCHC denotes the volume and character of the hemoglobin and is the most accurate of the red cell indices.

MCHC Too High: Rule out spherocytosis (the cells are old and not being replaced as often), and in vitro or in vivo hemolysis.

MCHC Too Low: Rule out reticulocytes (too many young red cells), and iron deficiency.

RDW (Red cell Distribution Width):

RDW test measures the different sizes and shapes of
the red cell. RDW is important because the more surface area the red
cell has, the better it can hook onto and transport oxygen through the
system.

RDW and MCV both Too High: Rule out liver disease, hemolytic anemia, Vitamin B12 deficiency, folic acid deficiency.

RDW Too High, but MCV Too Low: Rule out iron deficiency anemia, thalassemia intermedia (defective hemoglobin), fragmented cells.

RDW Too High, but MCV Normal: Rule out low Vitamin B12 or folic acid, iron deficiency anemia (early stages)

RDW Too Low: Rule out macrocytic
anemia (red cells are too large), microcytic anemia (red cells too
small). When the cells are all the same size, the RDW level will be low.

Note: One simple way to tell if you are anemic is to
look at your cheeks and chin in the mirror. If they look like they have
a blotchy tan, you are anemic and it will show up on a test within two
weeks. My recommendation is to take about 3/4 tea. blackstrap molasses
every day for a couple of months. When the anemia is gone, the tan will
be too. Read this article if you have this symptom: http://naturalhealthtechniques.com/SpecificDiseases/anemiatanchin.htm

Blood Gasses:

Blood gasses measure how much influence oxygen,
carbon dioxide and hydrogen ion concentration (pH) has on our body. This
lab test sample has to be taken from an artery to accurately measure the oxygen content. The other blood samples are taken from veins and both pH and CO2 can be measured using venous blood.  Blood gas labtest results should be evaluated immediately.

Oxygen (PO2):

PO2 -The total oxygen concentration depends on total hemoglobin,
oxygen-carrying capability of hemoglobin, body temperature, blood pH,
certain blood enzymes and PO2 itself.

Oxygen lab test result Too High: Rule out gasses with high oxygen content (oxygen cages and anesthetic machines).

Oxygen Too Low (Hypoxia): Rule out respiratory disorders, heart shunts, or brain damage.

Carbon Dioxide (CO2):

CO2 level reflects the acid status of the blood and is a measure of the exchange of oxygen between the alveoli of the lungs.

Carbon Dioxide lab test result Too High: Rule out increased ventilation.

Carbon Dioxide Too Low: Rule out decreased
ventilation, increased acidity from uncontrolled diabetes, kidney
disease, heart shunts, and metabolic disorders.

Bicarbonate (HCO3):

Bicarbonate is maintained in health by conservation and production by
the renal tubules, so if there is kidney disease of some kind, the
values may be abnormal.

Cardiac Risk Factors

C Reactive Protein (CRP):

C Reactive Protein is a marker for inflammation.

C Reactive Protein lab test result Too High: Rule out inflammation in response to infection, vascular disease, heart attacks or strokes.

Homocysteine: Homocysteine is an amino acid that is
normally found in small amounts in the blood. Higher levels are
associated with increased risk of heart attack and other vascular
diseases. Men tend to have higher levels.

Homocysteine Too High:

Homocysteine levels rule out folic acid deficiency, Vitamin B12
deficiency, heredity, aging, kidney disease, and certain medications.

Lipoprotein or Lp:

Lipoproteins are a combination of water-soluble proteins containing
cholesterol and triglycerides and are present in the blood. The
lipoproteins in this test break the lipoprotein down into its alpha or
beta forms and determines the volumes of each. (Also see Cholesterol above).

Lipoproteins are also contained in the cholesterols high-density (HDL), low density (LDL), and very low density (VLDL)
lipoproteins which are all factors in heart disease and cholesterol
levels. These have been discussed under their individual cholesterol
categories above.

Lipoprotein lab test result Too High: Rule out
premature coronary heart disease (CHD) and the genetic link to heart
disease. Persons with diabetes and a high Lp level appear to have
increased risk of asymptomatic coronary disease.

Thyroid Lab Tests:

To evaluate the thyroid your doctor will take blood to run a Thyroid
Function Blood Panel, which will include many of the tests below
depending on the doctor?s education and the tests available at the
laboratory. It is important to understand each test because there is a
lot of confusion among doctors, nurses, lab
technicians, and patients as to which test is which. In particular, the
?Total T3″, ?Free T3″ and ?T3 Uptake tests? are very confusing, and are
not the same test.

You will want to have several thyroid factors evaluated from the following:

TSH (Thyroid Stimulating Hormone, sTSH):

The TSH test determines if your brain is producing the instructions for the body to respond by producing T4. Thyroid Stimulating Hormone is secreted by the pituitary gland and regulates the thyroid gland.

TSH Lab test results Too High: Rule out hypothyroidism.

TSH Lab test resultsToo Low: Rule out hyperthyroidism.

Total T4:

Total T4 measures the Free T4 and T4 bound to carrier proteins circulating within the blood.

Free T4 (Thyroxine, FT4):

Free T4 test is the basic thyroid molecule that circulates around the body before being activated to T3. The Free T4 directly
measures the free T4 in the blood. It is a more reliable, but a little
more expensive than Total T4. Some labs now do the Free T4 routinely
rather than the Total T4.

Free T4 Lab Test Too High: Rule out hyperthyroidism,
however technical artifact occurs when estrogen levels are higher from
pregnancy, birth control pills or estrogen replacement therapy.

Free Thyroxine Index (Free T4 Index, FTI or T7) :

Free Thyroxine Index is a mathematical computation
allows the lab to estimate the free thyroxine index from the T4 and T3
Uptake tests. The results tell us how much thyroid hormone is free in
the blood stream to work on the body. Unlike the T4 alone, it is not
affected by estrogen levels.

Total T3 (Triiodothyronine):

The Total T3 lab test is usually not ordered as a screening test, but
rather when thyroid disease is being evaluated. T3 is the more potent,
active, and shorter lived version of thyroid hormone. Some people with
high thyroid levels secrete more T3 than T4. In these hyperthyroid cases
the T4 can be normal, the T3 high, and the TSH low. The Total T3 reports the total amount of T3 in the bloodstream, including T3 bound to carrier proteins plus freely circulating T3.

Free T3 (Triiodothyronine):

The Free T3 lab test determines if the T4 is being
converted to its active form by the liver. This test measures the
free-floating T3 in the body.

T3 Resin Uptake or Thyroid Uptake.

The T3 Resin Uptake lab test confuses doctors, nurses, and patients. First, this is not
a thyroid test, but a test on the proteins that carry thyroid around in
your blood stream. Not only that, a high test number may indicate a low
level of the protein! The method of reporting varies from lab to lab.

The Resin T3 Uptake is used to assess the binding
capacity of the serum for thyroid hormone. The T3 Resin test is only
useful in conjunction with Total T4 or Total T3. If a patient has a high
total T4, it may be due to overproduction of thyroid hormone
(hyperthyroidism) or to an excess of one of the thyroid binding
proteins, usually Thyroid Binding Globulin (TBG). If the high Total T4
is secondary to high TBG, the Resin T3 will be low; otherwise it will be
normal or elevated. So, if the Total T4 or Total T3 deviates from
normal in one direction and the Resin T3 Uptake deviates in the opposite
direction, then the abnormality is due to changes in binding capacity.
If not, then it can be attributed to a true change in thyroid function
(i.e. hyperthyroidism or hypothyroidism). Estrogens increase the binding
capacity and decrease both the free labeled hormone and the Resin T3
uptake.

(Gee, I can see why it is so confusing!)

Thyroid Antibody test:

The thyroid antibody lab test is used to rule out autoimmune
hyperthyroidism diseases including Hashimoto?s disease (autoimmune
thyroiditis) and Graves? disease (toxic diffuse goiter).

Reverse T3 (the isomer of T3:

Reverse T3 (RT3) lab test is formed when T4 is deiodinated at the 5
position (T3 is formed from deiodination of the 5? position). RT3 has
little or no biological activity and serves as a disposal path for T4.
During periods of starvation or severe physical stress, the level of RT3
increases while the level of T3 decreases. In hypothyroidism both RT3
and T3 levels decrease. Thus RT3 can be used to help distinguish between
hypothyroidism and the changes in thyroid function associated with
acute illness (Euthyroid Sick Syndrome).

Cortisol:

Cortisol levels are tested to see how you are handling stress. Stress suppresses the thyroid.

Copper Levels:

Copper levels are run to rule out Wilson?s Disease and heavy metal interference. Copper
inhibits TRH (Thyroid Releasing Hormone) at the hypothalamus and in the
case of Wilson?s Syndrome, builds up in the liver preventing conversion
of T4 to T3. TRH is the messenger that keeps track of how much and
which thyroid hormones are needed.

Note: To read more about thyroid function, the role of iodine, and how to establish health using natural methods go to: http://naturalhealthtechniques.com/SpecificDiseases/thyroid_disease.htm

LAB TESTS FOR DIABETES AND BLOOD SUGAR MANAGEMENT:

Blood Glucose curve:

The blood glucose curve is created by a series of blood glucose lab
tests taken by either drawing blood out of a pre-inserted catheter or by
sticking the finger with a lancet at many different time intervals,
usually within a 1-3 day period. The goal is to figure out how many
units of insulin are needed to maintain the proper blood glucose levels
in the patient.

Glucose:

Glucose is a measure of the sugar level in the blood. The normal
range for a fasting glucose is 60 -109 mg/dl. According the 1999
American Dietetic Association criteria, diabetes is diagnosed with
fasting plasma glucose levels of 126 or more. A precursor, Impaired Fasting Glucose (IFG) is defined as a fasting glucose of 110 ? 125 mg/dl. Sometimes a glucose tolerance test,
which involves giving you a sugary drink followed by several blood
glucose tests, is necessary to properly sort out normal from IFG from
diabetes. Variations in lab normals exist.

Europeans tend to use a 2-hour after eating definition of diabetes
rather than a fasting glucose. Using the European standards tends to
increase the number of people who are classified as having diabetes. To
differentiate persistent problems from transient ones, a second blood
glucose sample should be taken within 24 hours.

Glucose Lab test Too High (Hyperglycemia): Rule out
eating before the test, IV glucose, diabetes, glucocorticoids,
thiazides, pheochromocytoma, Cushing?s syndrome, acromegaly, brain
damage, liver disease, nephrosis, hyperadrenocorticism,
hyperglucagonemia, ammonia toxicosis (cattle), milk fever (cattle),
insulin dosage too small, hyperthyroidism, pain induced catecholamine
and glucocorticoid release, listeriosis (sheep), transport tetany
(sheep), and pancreatitis.

Glucose Too Low (Hypoglycemia): Rule out Addison?s
disease (adrenocortical insufficiency), myxedema, aflatoxicosis (a
disease in horses where they eat too much grain infected with molds),
too much exercise, glycogen storage diseases, gram-negative septicemia,
liver insufficiency or failure, hyperinsulinism from insulin overdose or
insulinoma, hypopituitarism, juvenile hypoglycemia (toy and miniature
dog breeds), ketosis (cattle), malabsorption, neonatal hypoglycemia,
cancers, pregnancy toxemia (sheep), starvation, and malabsorption.

Glycohemoglobin (Hemoglobin A1 or A1C, HbA1C):

Glycohemoglobin measures the amount of glucose chemically attached to
your red blood cells. Since blood cells live about 3 months, it tells
us your average glucose for the last 6 ? 8 weeks. A high level suggests
poor diabetes control.

Insulin-Like Growth Factor I (IGF-1):

The IGF-1 lab test is used to determine acromegaly,
in which somatomedin-C (Sm-C) and growth factor (GH) are increased. It
is also used to evaluate hypopituitarism. Sm-C is a polypeptide hormone
produced by the liver and other tissues, with effects on growth
promoting activity and glucose metabolism (insulin-like activity). Sm-C
is carried in blood bound to a carrier protein, which prolongs its
half-life. Its level is therefore more constant than that of growth
hormone.

IGF-1 Too Low: Rule out ageing, hypopituitarism,
malnutrition, diabetes mellitus, Laron dwarfism, hypothyroidism,
maternal deprivation syndrome, pubertal delay, cirrhosis,
hepatoma,  nonfunctioning pituitary tumors with constitutional
delay of growth, and anorexia nervosa.

IGF-1 Too High: Rule out adolescence, true
precocious puberty, pregnancy, obesity, pituitary gigantism, acromegaly
and diabetic retinopathy. Since Sm-C is decreased with malnutrition, its
concentration provides an index with which to monitor therapy for food
deprivation.

Insulin:

Insulin is secreted by the pancreas in response to eating or elevated
blood sugar. Insulin levels vary widely from person to person depending
upon an individual?s insulin sensitivity (or conversely, their insulin
resistance) and when the last meal occurred. Insulin, when measured by
itself, at random times, is rarely useful.

Insulin Lab Test Too Low: Rule out diabetes. Insulin is deficient in persons with Type 1 diabetes (insulin-dependent diabetes), and borderline deficient in persons with Type 2 diabetes. The natural evolution of Type 2 diabetes causes insulin levels to fall from high levels to low levels over a course of years.

Insulin Too much: Rule out hypoglycemia.

HOMA-IR (the Homeostasis Model of Insulin Resistance):

HOMA-IR is a measure of insulin. Insulin resistance
is a risk factor for coronary disease so assessing an individual?s
insulin resistance may have some value. Other diseases associated with
an increased HOMA-IR test are AIDS and polycystic ovary syndrome (PCOS).
Polycystic ovary women have insulin resistance independent of obesity.

THE URINALYSIS:

The urinalysis lab test measures the presence and
amount of a number of chemicals in the urine, which reflect much about
the health of the kidneys, along with cells that may be present in the
urine (for example, red blood cells, white blood cells, or groups of
these called ?casts?). Also, the lab looks for crystals, bacteria, and
other organisms in the urinary sediment. Each of these elements give
hints as to function of the kidneys, kidney tubules, ureters (small
tubes that connect the kidneys with the urinary bladder), and the
urinary bladder.

Urine lab tests are typically evaluated with a reagent strip that is
briefly dipped into the urine sample. The technician reads the colors of
each test and compares them with a reference chart. The urine is then
spun down and the sediment checked for cells, yeast, bacteria, crystals,
and casts (groups of dead cells that indicate kidney tubule damage).
For a more in depth interpretation with pictures go to: http://naturalhealthtechniques.com/urinalysis-interpretation.htm

Here are some tips on collecting the urine sample for lab tests:

If you are doing a free-catch sample, it is nice to
have some urine caught in the beginning, middle and end of the urination
process. Why? The first fraction coming out flushes cells, yeast and
bacteria from the vulva or prepuce areas and the urethra (the tube that
connects the bladder to the outside world). The middle fraction is a
better picture of what has been stored in the bladder. The tail-end of
the sample gives a better idea of how the kidneys look.

My personal choice as a veterinarian is to stick a long needle
directly into the bladder so I don?t have to guess if the bacteria,
yeast and dead cells are from the urethra or the bladder. It doesn?t
hurt much and helps alleviate contamination of the sample. That way I
can treat the core cause instead of a secondary infection of some type.
Medical doctors sometimes insert a catheter into the bladder for this
reason.

If you are trying to get a sample from your pet at home, one easy way
to do it is to tape a small cup to the bottom of the ruler. As the pet
urinates, you can slip the cup underneath them without leaning over and
startling them. Label the sample with the date and time it was collected
then get the sample to your vet right away for lab testing.

Urine Volume:

Increased (Polyuria): Rule out acute renal disease,
chronic renal disease, diabetes mellitus hepatic failure,
hyperadrenocorticism, hypercalcemia, hyperparathyroidism (cats and
humans), nephrogenic diabetes insipidus, pituitary diabetes insipidus,
postobstructive diuresis, primary renal glycosuria, psychogenic
polydipsia, pyelonephritis, and pyometra.

Decreased (Oliguria): Rule out acute renal failure, dehydration, shock, terminal chronic renal disease, and urinary tract obstruction.

pH :

pH is a measure of hydrogen ion concentration
(acidity or alkalinity) of the urine. Fresh samples are necessary for
an accurate lab test reading because urine becomes alkaline when it is
older because the carbon dioxide escapes and the bacteria in the urine
convert urea to ammonia which is very alkaline. The healthy, normal pH
of human urine is less than 7.

Too High (Alkaline): Rule out diets high in vegetables and urinary tract infections (the bacteria convert the urine to ammonia). Note: This is the only instance where I tell people to eat lots of protein and junk food for 2-3 days!

Too Low (Acid): Rule out diets high in protein and refined carbohydrates, anorexia, and starvation.

Specific Gravity (SG):

Specific Gravity measures how dilute your urine is.
Specific gravity takes into account the weight of the urine and particle
size. Water would have a specific gravity of 1.000 Most human urine is
around 1.010, but it can vary greatly depending on when you drank fluids
last, or if you are dehydrated.

Glucose in the urine:

Normally there is no glucose in urine.

Detectable Glucose (Glucosuria): Rule out diabetes,
kidney disease (decreased tubular reabsorption), acromegaly,
hyperpituitarism, bovine milk fever, bovine neurologic disease,
excessive insulin dosage, fear or exertional catacholamine release,
Fanconi-like syndrome, moribund animals, sheep endotoxemia, and drugs
such as ACTH, glucocorticoids, fluids, ketamine, morphine,
phenothiazine, and xylazine. A small number of people have glucose in
their urine with normal blood glucose levels, however any glucose in the
urine would raise the possibility of diabetes or glucose intolerance.

Protein in the Urine:

Protein (Proteinuria): When you urinate and see foam
in the toilet bowl, this can indicate either sugar or protein and is
not normal. A urinalysis and blood work are used to determine what the
problem is. Talk with your doctor if you see this. Normally there is no
protein detectable on a urinalysis strip.

Detectable Protein: Rule out kidney damage,
increased glomerular permeability (from fever, cardiac disease, central
nervous system disease, shock, muscular exertion), blood in the urine,
inflammation, cancers, infection. High concentrations of very small
proteins can also show up in the urine such as Bence Jones protein,
hemoglobin monomers, and myoglobin. Up to 10% of children can have
protein in their urine. Sometimes this is due to colostral antibodies.

Certain diseases require the use of a special, more sensitive (and more expensive) test for protein called a microalbumin test. A microalbumin test is very useful in screening for early damage to the kidneys from diabetes.

False Positive causes: Rule out urine too alkaline.

Blood in the Urine:

Blood (Hematuria): Normally there is no blood in the urine lab test.

Detectable Blood: Rule out infection, kidney stones,
trauma, and bleeding from bladder or kidney tumors. The technician may
indicate whether the blood is hemolyzed (dissolved blood) or
non-hemolyzed (intact red blood cells). Note that blood also occurs when
a woman is having her period or in the dog when she is in heat so it
can be normal. Ask more questions if you see blood in the urine.

False Positive causes: Rarely, muscle injury can
cause myoglobin to appear in the urine which also causes the reagent pad
to falsely indicate blood. Mensus in humans or animals in
heat will also have blood in their urine as a normal occurrence.

Bilirubin in the Urine:

Bilirubin (Bilirubinuria): Normally there is no bilirubin or urobilinogen in the urine. These are pigments that are cleared by the liver.

Detectable Bilirubin: Rule out liver or gallbladder
disease, obstruction of bile flow, intravascular hemolysis,
hemoglobinuria, and tubular cell conjugation of free bilirubin.

False positives: Urine color may interfere with the reading of this lab test.

Nitrate:

Normally negative, the presence of nitrates usually indicates a
urinary tract infection caused from nitrate reducing bacteria including
veillonellae, haemophili, staphylococci, corynebacteria, lactobacilli,
flavobacteria and fusobacteria.

Leukocytes (Leukocyte esterase):

Normally negative. Leukocytes are the white blood cells (or pus cells).

Detectable Leukocytes: Rule out urinary tract infection.

Sediment in the Urine:

Sediment: Here the doctor, nurse, or lab technician
looks under a microscope at a portion of your urine that has been spun
in a centrifuge. Items such as mucous and squamous cells are commonly
seen. Abnormal findings would include more than 0-2 red blood cells,
more than 0-2 white blood cells, crystals, casts, renal tubular cells,
yeast or bacteria. (Bacteria and yeast can be present if there was
contamination at the time of collection.). The pH of the urine
determines what types of crystals will be formed.

For LOTS more info on urine sediments see the following handout: http://naturalhealthtechniques.com/SpecificDiseases/bladder_kidney_stones.htm

Sex Hormone Profile Lab Tests:

Sex hormone tests are popular these days and can be done at home via a
saliva or urine test or done in a doctor?s office using blood.

Estrogen:

Estrogen is tested to evaluate menstrual status and
sexual maturity. Estrogens are responsible for proliferation and growth
of specific cells and are responsible for development of most secondary
sexual characteristics in the female. Three types of estrogens are present in significant quantities in the blood lab test, estradiol, estrone, and estriol.

Estrogens Too High: Rule out gynecomastia (feminization syndrome) and estrogen-influenced ovarian tumors.

Estradiol:

Estradiol is the most common type of estrogen and the most important
estrogen in evaluating the fertility of the female because it is
produced almost solely by the ovary. In women estradiol varies according
to age, normal menstrual cycles, taking birth control pills or estrogen
replacement.

Estriol (E3):

Estriol is the major estrogen in the pregnant female produced by the
placenta. Excretion of estriol increases around the eighth week of
gestation and continues to rise until shortly before delivery. Serial
urine and blood studies of this hormone are used to assess placental
function and fetal normality in high-risk pregnancies. Falling values
during pregnancy suggest fetoplacental deterioration and require prompt
reassessment of the pregnancy, including the possibility of early
delivery.

Progesterone:

Progesterone is produced in the ovaries during the
second half of the menstrual cycle, by the placenta during pregnancy,
and in small amounts from the adrenal glands and testes. Progesterone
prepares the uterus for implantation of the fetus and is responsible for
increasing  breast milk in preparation for lactation. This is
another important hormone to evaluate for evaluating fertility in the
female.

After ovulation, an increase of progesterone causes the uterine
lining to thicken in preparation for the implantation of a fertilized
egg. If this event does not take place, progesterone and estrogen levels
fall, resulting in shedding of the uterine lining. Progesterone is
essential during pregnancy, not only ensuring normal functioning of the
placenta, but passing into the developing baby?s circulation, where it
is converted in the adrenal glands to corticosteroid hormones.

Testosterone:

Testosterone is the most important of the male sex
hormones. It is responsible for stimulating bone and muscle growth, and
sexual development. It is produced by the testes and in very small
amounts by the ovaries in women. Most testosterone tests measure total
testosterone. Testosterone stimulates sperm production
(spermatogenesis), and influences the development of male secondary sex
characteristics.

Testosterone Too High: Overproduction of
testosterone caused by testicular, adrenal, or pituitary tumors in the
young male may result in precocious (early) puberty. Overproduction of
testosterone in females, caused by ovarian and adrenal tumors, can
result in masculinization, the symptoms of which include cessation of
the menstrual cycle (amenorrhea) and excessive growth of body hair
(hirsutism).

Testosterone Too Low: When reduced levels of
testosterone in the male indicate under activity of the testes
(hypogonadism), testosterone stimulation tests may be ordered.

Tests for Sexually Transmitted Diseases:

Herpes Serology

(Herpes simplex viruses, HSV): A blood lab test for
herpes is now available. A blood test only tells whether you have been
infected with the herpes virus. Herpes serology cannot tell when you
became infected, what body parts will be affected, whether you will
develop symptoms of herpes or if your symptoms are due to herpes. A swab
of an active lesion is the only way to detect the virus itself. It may
take between six and eight weeks to detect antibodies in a herpes blood
test after first becoming infected with HSV. Also, antibodies may
disappear with time, especially if the person has infrequent recurrences
of herpes breakouts.

Genital Herpes is caused by either Herpes Simplex Virus type I (HSV-1) or Herpes Simplex Virus type II (HSV-2).
Herpes Simplex Virus II (HSV-2) is the usual cause of repeated attacks
of genital herpes and HSV-1 is usually the type that is responsible for
cold sores (oral herpes).

False positives and negatives: All lab tests
occasionally give incorrect results. The herpes test can be falsely
positive 5% of the time and a false negative result 15% of the time?so
before a marital blow-out happens?repeat the test using a different lab.

Note: I don?t know about the vaginal herpes, but the oral herpes usually goes away when you stop ?holding your tongue?.
So speak your truth and those cold sores should disappear in 1-3 days. I
have seen this as an effective treatment MANY times. Oh, and many more
people than you could imagine are infected with the vaginal herpes, so
if you are single, don?t let that keep you single for life. The truth
shall set you free. Forgive yourself and move on. Just be discerning
about whom you talk to about it and don?t have sex with those that are
unaware you have it. There are drugs and homeopathic drops that help
control active outbreaks.

Frequently Asked Questions about Lab Test Results:

Why do I have to have an empty stomach for at least 12 hours before they draw my blood for the lab tests? When
we eat, fat gets into our bloodstream and can affect the tests giving
false positive or false negative results. Fat in the bloodstream gives
cloudy serum and the scientific instruments they use to test different
blood levels can?t see through the cloudiness.

Why do they put the blood in several tubes each with a different color at the top of the tube? Each
tube your sample is put in does something different to the sample. Some
have preservatives in them, some have anticoagulants, and some don?t
have anything. Preservatives can prevent the breakdown of certain
enzymes so that the blood can be stored until it gets to the lab to be
tested. Anticoagulants prevent the blood from clotting so cells can be
counted and looked at with lab equipment. When the tube doesn?t have
anything in it (the red top tubes) we want the blood to clot so we can
gather the serum and not the red or white cells. This way we can run
different blood tests to see all aspects of how your body is functioning
or not functioning.

Helpful Links and References for Lab Test Results:

  • Veterinary Laboratory Medicine Clinical Pathology, 2nd Edition by J. Robert Duncan, DVM, Ph.D. and Keither W. Prasse, DVM, Ph.D.
  • What is a Rule Out? http://naturalhealthtechniques.com/whats-a-rule-out.htm
  • The Urinalysis Lab Test:

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    http://naturalhealthtechniques.com/basicsofhealthlab_result_meaning1.htm  Blood and Urine

    Best Medical Intuitive Online

Dormancy Period: 2 months up to several years.

An estimated 6 to 7 million people worldwide are infected with T. cruzi Chagas disease. Chagas disease is caused by infection with the protozoan parasite T. cruzi, which is typically introduced into humans through the bite of triatomine bugs, also called “kissing bugs”. When the insect defecates at the bite site, motile T. cruzi forms called trypomastigotes enter the bloodstream and invade various host cells. Over many years, cycles of parasite replication and immune response can severely damage these tissues, particularly the heart and digestive tract.

After the parasite enters through an open wound or mucous membrane, the infectious trypomastigote is found in the bloodstream plasma. The amastigote stage of the parasites is found inside pseudocysts located in muscle or nerve cells. There is a predilection for the myocardium or myenteric plexus of the gastrointestinal tract, where it replicates by binary fission. There are three phases of the disease: acute, indeterminate and chronic. 

Dormancy Period: Unknown.

T. brucei is transmitted between mammal hosts by an insect vector belonging to different species of tsetse fly (Glossina). Transmission occurs by biting during the insect’s blood meal. Trypanosoma brucei is a species of parasitic kinetoplastid belonging to the genus Trypanosoma that is present in sub-Saharan Africa. Unlike other protozoan parasites that normally infect blood and tissue cells, it is exclusively extracellular and inhabits the blood plasma and body fluids. It causes deadly vector-borne diseases: African trypanosomiasis or sleeping sickness in humans, and animal trypanosomiasis or nagana in cattle and horses.

In later stages of a T. brucei infection of a mammalian host the parasite may migrate from the bloodstream to also infect the lymph and cerebrospinal fluids. It is under this tissue invasion that the parasites produce the sleeping sickness.

Dormancy Period: Up to 60 days. Many are asymptomatic.

If symptoms develop, they typically occur 20–40 days after ingestion of sporocysts and during the subsequent migration of sporozoites through the body vessels. Acute lesions (edema, hemorrhages, and necrosis) develop in the affected tissues. The parasite has a predilection for skeletal muscle (myositis), cardiac muscle (petechial hemorrhages of cardiac muscle and serosae), and lymph nodes (edema, necrosis, and hemorrhage).

Humans can experience nausea, vomiting, acute and severe enteritis, or chronic enteritis, but many infections appear to be mild or asymptomatic. Differences depend on the number, and perhaps the species, of sarcocysts ingested. Several cases of sarcocystosis have been detected in patients with various types of cancer. Related to cardiomyopathy, intramuscular sarcocystosis, intestinal sarcocystosis.

Dormancy Period: Days to weeks.

Balamuthia mandrillaris is a free-living amoeba that causes the rare but deadly neurological condition granulomatous amoebic encephalitis (GAE).  B. mandrillaris can infect the body through open wounds or possibly by inhalation. It is distributed throughout the temperate regions of the world.

Upon introduction, the amoeba may form a skin lesion, or in some cases, may migrate to the brain, causing a condition known as granulomatous amoebic encephalitis (GAE), which is usually fatal. This granulomatous feature is mostly seen in immunocompetent patients; immunocompromised individuals exhibit a “perivascular cuffing”. Balamuthia-induced GAE can cause focal paralysis, seizures, and brainstem symptoms such as facial paralysis, difficulty swallowing, and double vision.

Dormancy Period: 1 week to months.

Acanthamoeba spp. are among the most prevalent protozoa found in the environment. They are distributed worldwide, and have been isolated from soil, air, sewage, seawater, chlorinated swimming pools, domestic tap water, bottled water, dental treatment units, hospitals, air-conditioning units, and contact lens cases. Additionally, they have been isolated from human skin, nasal cavities, throats, and intestines, as well as plants and other mammals.

They are opportunistic pathogens able to cause serious and sometimes fatal infections in humans and other animals. Diseases caused by Acanthamoeba include keratitis and granulomatous amoebic encephalitis (GAE). The latter is often but not always seen in immunosuppressed patients. GAE is caused by the amoebae entering the body through an open wound and then spreading to the brain. The combination of host immune responses and secreted amoebal proteases causes massive brain swelling resulting in death in about 95% of those infected, within one week to several months.

Dormancy Period: Up to 9 weeks, or the life of the patient if asymptomatic.

People can get infected with Babesia parasites by the bite of an infected tick, by getting a blood transfusion from an infected donor of blood products, or by congenital transmission (an infected mother to her baby). Ticks transmit the human strain of babesiosis, so it often presents with other tick-borne illnesses such as Lyme disease.

After trypanosomes, Babesia is thought to be the second-most common blood parasite of mammals. Half of all children and a quarter of previously healthy adults with Babesia infection are asymptomatic. People with symptoms usually become ill 1 to 4 weeks after the bite, or 1 to 9 weeks after transfusion of contaminated blood products.

Dormancy Period: Can remain a dormant fungus or years.

This organism infects the mucosa of the nasal cavity, producing a mass-like lesion. This mass appears to be polypoidal in nature with a granular surface speckled with whitish spores. The rhinosporidial mass has been classically described as a strawberry-like mulberry mass. This mass may extend from the nasal cavity into the nasopharynx and present itself in the oral cavity. These lesions commonly cause bleeding from the nasal cavity. R. seeberi can also affect the lacrimal gland and also rarely the skin and genitalia. 

Infection in humans with this organism has been reported from about 70 countries, with the majority of cases (95%) reported from India and Sri Lanka; per capita, Sri Lanka has the highest incidence in the world. The common factor found in these areas was the practice of bathing in common ponds.

Dormancy Period: Up to 12 days, death up to two weeks after exposure. Early and accurate diagnosis is essential.

Naegleria fowleri, also known as the brain-eating amoeba. This free-living microorganism primarily feeds on bacteria but can become pathogenic in humans, causing an extremely rare, sudden, severe, and usually fatal brain infection known as naegleriasis or primary amoebic meningoencephalitis (PAM). A large proportion of reported cases of infection had a history of water exposure, 58% from swimming or diving, 16% from bathing, 10% from water sports such as jet skiing, water-skiing and wakeboarding and 9% from nasal irrigation. Swimmers should also avoid digging or stirring up sediment at the bottom of lakes, ponds and rivers as this is where amebae are most likely to live.

Dormancy Period: Days.

Isosporiasis, also known as cystoisosporiasis, is a human intestinal disease caused by the parasite. Infection often occurs in immuno-compromised individuals, notably AIDS patients. It is usually spread indirectly, normally through contaminated food or water. The infected host then produces an immature form of the parasite in their feces, and when the parasite matures, it is capable of infecting its next host, via food or water containing the parasite.

Infection causes acute, non-bloody diarrhea with crampy abdominal pain, which can last for weeks and result in malabsorption and weight loss. In immunodepressed patients, and in infants and children, the diarrhea can be severe.

Dormancy Period: Up to three weeks, non-symptomatic for weeks.

Giardiasis is a parasitic disease caused by Giardia duodenalis (also known as G. lamblia and G. intestinalis). Infected individuals who experience symptoms (about 10% have no symptoms) may have diarrhea, abdominal pain, and weight loss. Less common symptoms include vomiting and blood in the stool. Symptoms usually begin one to three weeks after exposure and, without treatment, may last two to six weeks or longer.

Giardiasis is one of the most common parasitic human diseases. Infection rates are as high as 7% in the developed world and 30% in the developing world. Symptoms usually begin one to three weeks after exposure and, without treatment, may last two to six weeks or longer. Symptoms typically develop 9–15 days after exposure, but may occur as early as one day. Many people with Giardia infections have no or few symptoms. They may, however, still spread the disease.

Incubation Period: Days.

Dientamoebiasis is a medical condition caused by infection with Dientamoeba fragilis, a single-cell parasite that infects the lower gastrointestinal tract of humans. It is an important cause of traveler’s diarrhea, chronic abdominal pain, chronic fatigue, and failure to thrive in children.

Many individuals are asymptomatic carriers of Dientamoebiasis fragilis. Pathogenic and non-pathogenic variants are proposed to exist. Generally considered not harmful if in balanced population.The most commonly reported symptoms in conjunction with infection with D. fragilis include abdominal pain (69%) and diarrhea (61%). Diarrhea may be intermittent and may not be present in all cases. It is often chronic, lasting over two weeks. The degree of symptoms may vary from asymptomatic to severe, and can include weight loss, vomiting, fever, and involvement of other digestive organs. D. fragilis is not considered to be invasive nor cause cell or tissue damage.

Incubation Period: 1 week

Cyclosporiasis primarily affects humans and other primates. When an oocyst of Cyclospora cayetanensis enters the small intestine, it invades the mucosa, where it incubates for about one week. After incubation, the infected person begins to experience severe watery diarrhea, bloating, fever, stomach cramps, and muscle aches.

Cyclosporiasis is a disease caused by infection with Cyclospora cayetanensis, a pathogenic apicomplexan protozoan transmitted by feces or feces-contaminated food and water. Outbreaks have been reported due to contaminated fruits and vegetables. It is not spread from person to person, but can be a hazard for travelers as a cause of diarrhea.

The parasite sporulation for Cyclosporiasisis is from 8–11 days, making the illness difficult to diagnose. It invades the mucosa, where it incubates for about one week. When examining feces, the unsporulated oocysts can easily be mistaken for fungal spores, and thus can be easily overlooked.

Dormancy Period: 2- 28 days.

Cryptosporidiosis, sometimes informally called crypto, is a parasitic disease caused by Cryptosporidium, a genus of protozoan parasites in the phylum Apicomplexa. It affects the distal small intestine and can affect the respiratory tract in both immunocompetent (i.e., individuals with a normal functioning immune system) and immunocompromised (e.g., persons with HIV/AIDS or autoimmune disorders) individuals, resulting in watery diarrhea with or without an unexplained cough. In immunosuppressed individuals, the symptoms are particularly severe and can be fatal. It is primarily spread through the fecal-oral route, often through contaminated water; recent evidence suggests that it can also be transmitted via fomites contaminated with respiratory secretions.

Dormancy Period: weeks to years.

Blastocystis is a protozoal, single-celled parasite that inhabits the gastrointestinal tracts of humans and other animals. Many different types of Blastocystis exist, and they can infect humans, farm animals, birds, rodents, amphibians, reptiles, fish, and even cockroaches. Blastocystosis has been found to be a possible risk factor for development of irritable bowel syndrome.

Common occurrences of Blastocystosis are both asymptomatic and symptomatic. Most cases of the infection appear to become diagnosed as irritable bowel syndrome. The timescale of infection with the parasite can range from weeks to years. Non-symptomatic humans and animals can act as reservoirs.

Dormancy Period: a few days to the lifetime of the patient.

Balantidiasis is a zoonotic disease and is acquired by humans via the feco-oral route from the normal host, the pig, where it is asymptomatic. Fecally contaminated food and water are the common sources of infection in humans.

Some people infected with Balantidiasis may have no symptoms or only mild diarrhea and abdominal discomfort but others may experience more severe symptoms reminiscent of an acute inflammation of the intestines. Balantidium mostly causes asymptomatic and self-limiting infections. Asymptomatic hosts serve as reservoirs of infection in the community.

Dormancy Period: a few days to a few weeks, but usually it is about two to four weeks.

Most infected people, about 90%, are asymptomatic, but this disease has the potential to become serious. It is estimated that about 40,000 to 100,000 people worldwide die annually due to amoebiasis

Since amoebiasis is transmitted through contaminated food and water, it is often endemic in regions of the world with limited modern sanitation systems, including México, Central America, western South America, South and Southeast Asia, and western and southern Africa.

Amoebiasis / Entamoeba species exist in 2 forms: A dormant parasite (cyst),and an active parasite (trophozoite). They can cause brain problems. Symptoms usually develop within 2 to 4 weeks but can show up later.

Dormancy Period: 3 months, up to 1 year or longer.

For about four weeks, the whipworms feed on blood vessels located within the cecum of the large intestine. Eventually, the whipworms leave the cecum and begin to lay thousands of eggs. These unembryonated eggs are then released from the host through feces. The process from egg ingestion to release takes around 12 weeks. The released eggs become embryonated in approximately nine to twenty-one days and are eventually ingested by another host. Eggs that are passed in the feces, can remain alive in soil for years.

The life cycle from the time of ingestion of eggs to the development of mature worms takes approximately three months. During this time, there may be limited signs of infection in stool samples, due to a lack of egg production and shedding. The female T. trichiura begin to lay eggs after three months of maturity. Worms commonly live for about one year, during which time females can lay up to 20,000 eggs per day.

Dormancy Period: Up to 7 days.

About 11 million humans are infected with Trichinella. The great majority of trichinosis infections have either minor or no symptoms and no complications. Trichinosis. During the initial infection, invasion of the intestines can result in diarrhea, abdominal pain, and vomiting. Migration of larvae to muscle, which occurs about a week after being infected, can cause swelling of the face, inflammation of the whites of the eyes, fever, muscle pains, and a rash. Complications may include inflammation of heart muscle, central nervous system involvement, and inflammation of the lungs.

They may very rarely cause enough damage to produce serious neurological deficits (such as ataxia or respiratory paralysis) from worms entering the central nervous system, which is compromised by trichinosis in 10–24% of reported cases of cerebral venous sinus thrombosis, a very rare form of stroke (three or four cases per million annual incidence in adults). 

Dormancy Period: 2 weeks to several years.

Toxocariasis is an illness of humans caused by the dog roundworm (Toxocara canis) and, less frequently, the cat roundworm (Toxocara cati). These are the most common intestinal roundworms of dogs, coyotes, wolves and foxes and domestic cats. Humans are among the many “accidental” or paratenic hosts of these roundworms.

While this zoonotic infection is usually asymptomatic, it may cause severe disease. There are three distinct syndromes of toxocariasis:

Covert toxocariasis is a relatively mild illness very similar to Löffler’s syndrome. It is characterized by fever, eosinophilia, urticaria, enlarged lymph nodes, cough, bronchospasm, wheezing, abdominal pain, headaches, and/or hepatosplenomegaly.

Dormancy Period: Days to 1 year.

Thelaziasis is the term for infestation with parasitic nematodes of the genus Thelazia. The adults of all Thelazia species discovered so far inhabit the eyes and associated tissues (such as eyelids, tear ducts, etc.) of various mammal and bird hosts, including humans. Thelazia nematodes are often referred to as “eyeworms”. In animal and human hosts, infestation by Thelazia may be asymptomatic, though it frequently causes watery eyes (epiphora), conjunctivitis, corneal opacity, or corneal ulcers (ulcerative keratitis). Infested humans have also reported “foreign body sensation” – the feeling that something is in the eye.

The larvae develop into adults in the eye or surrounding tissues of the host, where they may live for over one year.

Thelazia have been found in various tissues of the orbit (or socket) of the eye, including within the eyelids, in the tear glands, tear ducts, or the so-called “third eyelid” (nictitating membrane) or in the eyeball itself.

Dormancy Period: Lifetime of the patient.

The adult parasitic stage lives in tunnels in the mucosa of the small intestine. Many people infected are asymptomatic at first. Symptoms include dermatitis: swelling, itching, larva currens, and mild hemorrhage at the site where the skin has been penetrated. Spontaneous scratch-like lesions may be seen on the face or elsewhere. If the parasite reaches the lungs, the chest may feel as if it is burning, and wheezing and coughing may result, along with pneumonia-like symptoms (Löffler’s syndrome). The intestines could eventually be invaded, leading to burning pain, tissue damage, sepsis, and ulcers. Stools may have yellow mucus with a recognizable smell. Chronic diarrhea can be a symptom. In severe cases, edema may result in obstruction of the intestinal tract, as well as loss of peristaltic contractions.

Dormancy Period: 12 months to 15 years.

The average adult worm lifespan is 15 years, and mature females can produce between 500 and 1,500 microfilariae per day. The normal microfilarial lifespan is 1.0 to 1.5 years; however, their presence in the bloodstream causes little to no immune response until death or degradation of the microfilariae or adult worms. It is spread from person to person via female biting blackflies of the genus Simulium, and humans are the only known definitive host.

O. volvulus causes onchocerciasis, which causes severe itching. Long-term infection can cause keratitis, an inflammation of the cornea in the eye, and ultimately leads to blindness. Symptoms are caused by the microfilariae and the immune response to infection, rather than the adults themselves.

Dormancy Period: Days to weeks

The infection of these roundworms typically causes no overt symptoms but may sometimes cause a mild dermatitis of the thorax and shoulders. M. streptocerca infections fortunately do not cause any nodules, skin disease, or ocular infections like that of Onchocerca volvulus. However they may become visible just under the skin surface, and perhaps decrease skin health and immunity.

During a blood meal, an infected midge (genus Culicoides) or blackfly (genus Simulium) introduces third-stage filarial larvae onto the skin of the human host, where they penetrate into the bite wound. They develop into adults that reside in body cavities, most commonly the peritoneal cavity or pleural cavity, but also occasionally in the pericardium (M. perstans), subcutaneous tissue (M. ozzardi) or dermis (M. steptocerca).

Dormancy Period: Up to 1 year.

Loa loa filariasis, (Loiasis) is a skin and eye disease caused by the nematode worm Loa loa. Humans contract this disease through the bite of a deer fly (Chrysops spp.) or mango fly. These carriers are blood-sucking and day-biting, and they are found in rainforest-like environments in western and central Africa.

A filariasis such as loiasis most often consists of asymptomatic microfilaremia. Some patients can develop lymphatic dysfunction causing lymphedema. Episodic angioedema (Calabar swellings) in the arms and legs, caused by immune reactions, are common. Loa loa is also called the “African eye worm”. The passage over the eyeball can be sensed, but it usually takes less than 15 minutes. Eyeworms affect men and women equally, but advanced age is a risk factor. Eosinophilia is often prominent in filarial infections. Dead worms may cause chronic abscesses, which may lead to the formation of granulomatous reactions and fibrosis.

Dormancy Period: Possibly days to weeks.

Halicephalobus gingivalis is a free-living saprophagous nematode species. It is a facultative parasite of horses, invading the nasal cavity, and sometimes numerous other areas, where it produces granulomatous masses. On rare occasion, it can infect humans as well, causes a universally lethal meningoencephalitis. Infection of the brain is common, followed by the kidneys, oral and nasal cavities, lymph nodes, lungs, spinal cord, and adrenal gland, and also reports of infection of heart, liver, stomach and bone.

The site of entry for the parasite is thought to be through breaks in the skin or through mucous membranes. This nematode is now distributed worldwide, in all climates. It dwells actively in soil, around plants and other organically rich environments including manure and compost. 

Dormancy Period: Up to 4 weeks.

Gnathostomiasis is transmitted by the ingestion of third-stage larvae from raw or insufficiently cooked second intermediate or paratenic hosts such as freshwater fish, snakes, poultry, or frogs. The incubation period for gnathostomiasis is 3–4 weeks when the larvae begin to migrate through the subcutaneous tissue of the body.

A few days after ingestion epigastric pain, fever, vomiting, and loss of appetite resulting from migration of larvae through intestinal wall to the abdominal cavity will appear in the patient. Migration of parasites in the subcutaneous tissues causing intermittent, migratory, painful, pruritic swellings is known as cutaneous larva migrans. Patches of edema appear after initial symptoms clear and are usually found on the abdomen.

Migration to other tissues causes visceral larva migrans and can result in cough, hematuria, ocular involvement, meningitis, encephalitis and eosinophilia. Eosinophilic myeloencephalitis may also result from invasion of the central nervous system by the larvae.

Dormancy Period: Up to 8 weeks, often asymtomatic.

The disease is spread between people by pinworm eggs. The eggs initially occur around the anus. The period of time from swallowing eggs to the appearance of new eggs around the anus is 4 to 8 weeks. The main symptoms are itching in and around the anus and perineum. One-third of individuals with pinworm infection are totally asymptomatic. The eggs are hardy and can remain infectious, outside the body, in a moist environment for up to three weeks.

They may move onto the vulva and into the vagina, from there moving to the external orifice of the uterus, and onwards to the uterine cavity, fallopian tubes, ovaries, and peritoneal cavity. This can cause inflammation of the vulva and vagina. This causes vaginal discharge and itchiness of the vulva. Pinworms can also enter the urethra, and presumably, they carry intestinal bacteria with them.

Dormancy Period: One year or longer. The first signs of dracunculiasis occur around a year after infection, as the full-grown female worm prepares to leave the infected person’s body.

About a year after the initial infection, the female migrates to the skin, forms an ulcer, and emerges. When the wound touches fresh water, the female spews a milky-white substance containing hundreds of thousands of larvae into the water. Over the next several days as the female emerges from the wound, she can continue to discharge larvae into surrounding water. The larvae are eaten by copepods (small aquatic crustaceans), and after two to three weeks of development, they are infectious to humans again. Infected people commonly harbor multiple worms – on average 1.8 worms per person, but as many as 40 – which will emerge from separate blisters at the same time. 90% of worms emerge from the legs or feet. However, worms can emerge from anywhere on the body.

Humans typically get infected when they unintentionally ingest copepods while drinking water or exposure while swimming. 

Dormancy Period: Possibly days to years.

Ophidascaris robertsi is a nematode (also known as roundworm) usually parasitic in the carpet python (Morelia spilota). It is found in Australia and Papua New Guinea,and possibly Indonesia. Pythons serve as the typical hosts for Ophidascaris robertsi.  Humans and mammals that live near carpet python habitat and forage for native vegetation to cook can be exposed by consuming the roundworm’s eggs.These eggs, which are commonly shed in snake droppings due to the snakes’ diet of infected animals, likely contaminates the grass and soil eaten by small mammals. Other vectors, such as domestic and wild animals, are yet to be investigated.

Doctors theorize that the various symptoms (diarrhea and abdominal pain, along with night sweats and dry cough, lung infection) result from the migration of the parasitic eggs and larva from the bowel, through various other organs, before arriving in the brain.

Dormancy Period: Up to 50 days.

After maturing for approximately 50 days, the juveniles then migrate to the kidneys (typically the right kidney). Upon maturation, D. renale can survive for five years. D. renale is distributed worldwide, but is less common in Africa and Oceania. It affects fish-eating mammals, particularly mink, wolves, coyotes, foxes, dogs, raccoons, and weasels. Human infestation is rare, but results in kidney destruction.

The only means of obtaining a definitive diagnosis is through the identification of D. renale eggs in a patient’s urine. However, obtaining patient history (i.e., if the patient has consumed under-cooked or raw freshwater fish) is an important first step that can be coupled with radiological exams to search for enlarged or calcified kidneys. Urinalysis will likely show hematuria, blood tests may reveal eosinophilia.

D. renale is the largest nematode to parasitize humans. Adult male worms are 20–40 cm long and 5–6 mm wide; females can grow to 103 cm in length with a width of 10–12 mm.

Dormancy Period: 1 month to 2 years.

The incubation period for infection ranges from 1 month to 2 years and typically microfilariae appear before overt symptoms.The accumulation of many infective mosquito bites – several hundreds to thousands – is required to establish infection.   Lymphedema can develop within six months and development of elephantiasis has been reported within a year of infection. Men tend to develop worse symptoms than women. The Brugia mosquito injects larvae into human blood stream. Adult worms can survive in the lymphatic system for 5–15 years. The accumulation of many mosquito bites is required to establish infection.

Dormancy Period: Several years asymptomatic.

Most people are asymptomatic unless heavily infected. Human infection with Baylisascaris procyonis has been relatively rare. However, disease caused by this parasite can be extremely dangerous, causing death or severe symptoms. The parasite has been known to infect more than 90 kinds of wild and domestic animals. Reported disease has primarily afflicted children and almost all cases were a result of the ingestion of contaminated soil or feces, via the oral fecal route. the infection results in the penetration of the gut wall by the larvae and subsequent invasion of tissue, resulting in severe disease. 

This parasite’s eggs are able to live for years, extremely resistant to many disinfectants, and cause serious infections in humans with poor treatment options. Community water supplies are easily susceptible to contamination due to the lack of filtration and treatment methods to get rid of the eggs.

Dormancy Period: Up to 3 years.

Often, people show no overt symptoms but may suffer from intestinal problems. When symptoms do occur, the person is usually infected with a large number of worms. Ascaris lumbricoides is one of the most difficult pathogens to kill (second only to prions), and the eggs commonly survive 1–3 years before hatching.

The A. lumbricoides roundworm lives in the intestine where it lays eggs. Infection occurs when the eggs, too small to be seen by the unaided eye, are eaten. The eggs may get onto vegetables when improperly washed. Ascaris lumbricoides infect and estimated 819 million people worldwide. A lumbricoides is the largest intestinal roundworm and is the most common helminth infection of humans worldwide. The worms lack teeth. However, they can rarely cause bowel perforations by inducing volvulus and closed-loop obstruction. Infestation can be deadly if not treated. Occasionally, a worm can travel through the biliary tree and even into the gallbladder, causing acute cholangitis or acute cholecystitis.

Dormancy Period: If no immediate allergic reaction, more severe digestive reactions may be experienced within a few days.

Anisakiasis is a human parasitic infection of the gastrointestinal tract caused by the consumption of raw or undercooked seafood containing larvae of the nematode Anisakis simplex. Reactions, mostly seen as fish allergies, tend to occur soon after consumption.

Within a few hours of ingestion, the parasitic worm tries to burrow though the intestinal wall, but since it cannot penetrate it, it gets stuck and dies. The presence of the parasite triggers an immune response; immune cells surround the worms, forming a ball-like structure that can block the digestive system, causing severe abdominal pain, malnutrition, and vomiting. Occasionally, the larvae are regurgitated. If the larvae pass into the bowel or large intestine, a severe eosinophilic granulomatous response may also occur one to two weeks following infection, causing symptoms mimicking Crohn’s disease.

Dormancy Period: The incubation period in humans is usually from 1 week to 47 days after infection. Most cases are asymptomatic.

In humans, A. cantonensis is the most common cause of eosinophilic meningitis or meningoencephalitis. Frequently the infection will resolve without treatment or serious consequences, but in cases with a heavy load of parasites the infection can be so severe it can cause permanent damage to the central nervous system or death.

Humans and rats acquire the infection when they ingest contaminated snails or paratenic (transport) hosts including prawns, crabs, and frogs, or raw vegetables containing material from these intermediate and paratenic hosts. After passing through the gastrointestinal tract, the worms enter circulation. The larvae then migrate to the meninges and develop for about a month before migrating to the pulmonary arteries, where they fully develop into adults. The larvae cannot reproduce in humans.

Dormancy Period: May remain undetected for many years, however anemia may be an indicator of long term infection..

Hookworms account for a high proportion of debilitating disease in the tropics and 50–60,000 deaths per year These worms produce an iron deficiency anemia by sucking blood from the host’s intestinal walls.

The infection is usually contracted by people walking barefoot over contaminated soil. In penetrating the skin, the larvae may cause an allergic reaction. It is due to the itchy patch at the site of entry that the early infection gets its nickname “ground itch”. Once larvae have broken through the skin, they enter the bloodstream and are carried to the lungs (however, unlike ascarids, hookworms do not usually cause pneumonia).

Dormancy Period: Up to several years, depending on the vector.

Ticks are external parasites, living by feeding on the blood of mammals, birds, and sometimes reptiles and amphibians. Ticks have up to seven nymphal stages (instars), each one requiring blood ingestion, and as such, Ticks undergo a multihost life cycle. Because of their hematophagous (blood-ingesting) diets, ticks act as vectors of many serious diseases that affect humans and other animals. 

Ticks are extremely resilient animals. They can survive in a near vacuum for as long as half an hour. Their slow metabolism during their dormant periods enables them to go prolonged durations between meals. Even after 18 weeks of starvation, they can endure repeated two-day bouts of dehydration followed by rehydration, but their survivability against dehydration drops rapidly after 36 weeks of starvation.

Dormancy Period: Up to six weeks.

Scabies, also sometimes known as the seven-year itch, is a contagious human skin infestation by the tiny (0.2–0.45 mm) mite Sarcoptes scabiei, In a first-ever infection, the infected person usually develops symptoms within two to six weeks. During a second infection, symptoms may begin within 24 hours. The mites burrow into the skin to live and deposit eggs.The symptoms of scabies are due to an allergic reaction to the mites. Scabies is most often spread during a relatively long period of direct skin contact with an infected person (at least 10 minutes) such as that which may occur during sexual activity or living together. Spread of the disease may occur even if the person has not developed symptoms yet.

Dormancy Period: Up to many years depending on the related vector.

Diagnosis can be challenging as the small size of avian mites make them “barely visible to the unaided eye”. Dermanyssus gallinae can also infest various body parts, including the ear canal and scalp. commonly found in the bedroom or where the patient sleeps, as they prefer to stay close to their host for optimal feeding. D. gallinae generally visit their host for up to 1–2 hours, leave after completing their blood meal, and typically feed every 2–4 days. They are able to move extremely quickly, and can take less than 1 second to bite; enough time to inject their saliva and to induce rash and itching.They locate potential hosts through temperature changes, vibrations, chemical signals and CO2.

They primarily infect egg laying chickens, canaries, sparrows, starlings, pigeons, and poultry and also cats, dogs, hamsters, gerbils. This blood-feeding parasite is broadly distributed, and has been reported on 72 host species of North American birds in 26 families.

Dormancy Period: Up to several years with vectored diseases.

Mosquito-borne diseases or illnesses are caused by bacteria, viruses, or parasites transmitted by mosquitoes. Nearly 700 million people contract mosquito-borne illnesses each year, resulting in more than a million deaths.

Diseases transmitted by mosquitoes include malaria, dengue, West Nile virus, chikungunya, yellow fever, filariasis, tularemia, dirofilariasis, Japanese encephalitis, Saint Louis encephalitis, Western equine encephalitis, Eastern equine encephalitis, Venezuelan equine encephalitis, Ross River fever, Barmah Forest fever, La Crosse encephalitis, and Zika fever, as well as newly detected Keystone virus and Rift Valley fever.

When a mosquito bites a human, it injects saliva and anti-coagulants. With the initial bite to an individual, there is no reaction, but with subsequent bites, the body’s immune system develops antibodies. The bites become inflamed and itchy within 24 hours. Avoid all mosquito bites, but especially those from larger black-and-white mosquitos.

Dormancy Period: Rickettsial pox is generally mild and resolves within 2–3 weeks if untreated. There are no known deaths resulting from the disease. Other vectors have been lab tested but not proven outside the lab.

It can transmit human disease, is associated with causing rodent mite dermatitis in humans and is noted for carrying Rickettsia akari, which causes rickettsialpox. Rodent mites are capable of surviving for long periods without feeding and traveling long distances when seeking hosts. Cases have been reported in homes, libraries, hospitals and care homes. A similar condition, known as gamasoidosis, is caused by avian mites.

No human disease has been definitively found to be naturally vectored by these mites. Lab demonstrations have proved that they are at least capable of vectoring murine typhus, rickettsial pox, tularemia, plague, coxsackievirus, and Q fever, although it has not been known to do so outside the lab. The mite was reported as capable of vectoring human typhus, but these reports are not generally accepted.

Dormancy Period: Adult lice will die within 2 days without a blood meal. Rare vectors in Africa with up to 20 days incubation.

Head lice feed only on human blood and are only able to survive on human head hair. They only spread by human to human contact. When adults, they are about 2 to 3 mm long. When not attached to a human, they are unable to live beyond three days. In Ethiopia, head lice appear to be able to spread louse-born epidemic typhus and Bartonella quintana. Elsewhere head lice do not appear to carry these infections.

During its lifespan of 4 weeks a female louse lays 50-150 eggs. Eggs hatch within 6–9 days, each nymphal stage last for 4–5 days and accordingly the period from egg to adults lasts for 18–24 days. Adult lice live for an additional 3–4 weeks. Although any part of the scalp may be colonized, lice favor the nape of the neck and the area behind the ears, where the eggs are usually laid. Head lice are repelled by light and move towards shadows or dark-colored objects in their vicinity.

Dormancy Period: Several months without food. Numerous dangerous vectors can emerge up to years later.

Fleas feed on a wide variety of warm-blooded vertebrates including dogs, cats, rabbits, squirrels, ferrets, rats, mice, birds, and sometimes humans. Female fleas can lay 5000 or more eggs over their life, an adult flea only lives for 2 or 3 months. Without a host to provide a blood meal. A flea’s life can be as short as a few days, or can live for up to a year and a half, can live for several months without eating, so long as they do not emerge from their puparia.

Fleas are vectors for viral, bacterial and rickettsial diseases of humans and other animals, as well as of protozoan and helminth parasites. Bacterial diseases carried by fleas include murine or endemic typhus and bubonic plague. Fleas can transmit Rickettsia typhi, Rickettsia felis, Bartonella henselae, and the myxomatosis virus. They can carry Hymenolepiasis tapeworms and Trypanosome protozoans. 

Dormancy Period: The total lifespan of a Demodex mite is several weeks, with skin diseases evolving over days or months.

Demodex canis lives on the domestic dog, can become mange, and are easily transferred from them. Demodicosis is most often seen in folliculitis (inflammation of the hair follicles of the skin). It may result in small pustules (pimples) at the base of a hair shaft on inflamed, congested skin.

Demodicosis may also cause itching, swelling, and erythema of the eyelid margins. Scales at the base of the eyelashes may develop. Typically, patients complain of eyestrain. Older people are much more likely to carry face mites; about a third of children and young adults, half of adults, and two-thirds of elderly people carry them. The lower rate in children may be because children produce less sebum, or simply have had less time to acquire the mite. The six-legged larvae hatch after 3–4 days, and the larvae develop into adults in about 7 days. The total lifespan of a Demodex mite is several weeks.

Dormancy Period: Adult louse live for up to 30 days. No vectored diseases are known.

Feeding exclusively on blood, the crab louse usually is found in the person’s pubic hair. Although the louse cannot jump, it can also live in other areas of the body that are covered with coarse hair, such as the peri-anal area, the entire body (in men), and the eyelashes (in children).

The total life cycle from egg to adult is 16–25 days. Adults live for up to 30 days. Crab lice feed exclusively on blood, and take a blood meal 4–5 times daily. Outside the host they can survive for 24–48 hours. Crab lice are transmitted from person to person most commonly via sexual contact, although fomites (bedding, clothing) may play a minor role in their transmission. Crab lice are not known to transmit disease; however, secondary bacterial infection can occur from scratching of the skin. Symptoms of crab louse infestation in the pubic area include itching, redness and inflammation.

Dormancy Period: From vectored pathogens up to 20 days.

Body lice may lay eggs on the host hairs and clothing, but clothing is where the majority of eggs are usually secured. The most important pathogens which are transmitted by them are Rickettsia prowazekii (causes epidemic typhus), Borrelia recurrentis (causes relapsing fever), and Bartonella quintana (causes trench fever). Adult lice can live for about thirty days, but if they are separated from their host they will die within two days.

Dormancy Period: Bug can be dormant up to 12 months. No vectored diseases are known.

Although they move away from the host after feeding, they remain within the confines of their host’s roost, nest or dwelling. They may be considered to be micro-predatory bloodsuckers. Adult bedbugs have been reported to live three to twelve months if in an untreated household situation. The effects of cimicid feeding on the host include causing an immune response that results in discomfort, the transmission of pathogens, secondary infections at the wound site, physiological changes such as iron deficiency, and reduced fitness. Although viruses and other pathogens can be acquired by cimicids, they rarely transmit them to their hosts, unless the host is immune compromised.

Dormancy Period: If progressed to Scrub Typhus, 21 days

Leptotrombidium deliense is considered a dangerous pest in East Asia and the South Pacific because it often carries Orientia tsutsugamushi, the tiny bacterium that causes scrub typhus, which is known alternatively as the Japanese river disease, scrub disease, or tsutsugamushi. The mites are infected by the Rickettsia passed down from parent to offspring before eggs are laid in a process called transovarial transmission. Symptoms of scrub typhus in humans include fever, headache, muscle pain, cough, and gastrointestinal symptoms.

The chiggers’ digestive enzymes in the saliva cause “the intensely itchy welts”. Humans are possible hosts. The length of the mite’s cycle normally lasts two to 12 months. After about six days, the prelarvae grow into their larval stage. the mite may still be attached for up to 3 days. The itching can be alleviated through use of over-the-counter topical corticosteroids and antihistamines. According to Mayo Clinic, the chiggers “fall off after a few days, leaving behind red, itchy welts”, which normally heal on their own within one to two weeks. Hot showers or baths also help reduce itching. 

Dormancy Period: Up to 20 years.

Schistosoma (Schistosomatidae) are responsible for human schistosomosis affecting more than 200 million people in tropical and subtropical countries. Pathology is frequently associated with inflammatory reactions to eggs trapped in various tissues/organs. They can live for 20 years and continue to cause damage. In the initial phase of the infection, early transformed schistosomula are localized in the skin. Most of schistosomula stay localized in the thoracic and cervical spinal cord and only exceptionally migrate to the brain.

Dormancy Period: Up to 5 months.

Echinostoma eggs can survive for about 5 months and still have the ability to hatch and develop into the next life cycle stage. Infection can lead to a disease called echinostomiasis. The flukes by the names of E. revolutum, E. echinatum, E. malaynum and E. hortense are particularly common causes of Echinostoma infections in humans.

Humans can become infected with Echinostoma by eating infected raw or undercooked food, particularly fish, clams and snails. A mild infection may not have any symptoms. If symptoms are present they can include abdominal pain, diarrhoea, tiredness and weight loss.

Dormancy Period: Up to 8 weeks.

The estimated annual mortality and risk of infection are 280,000 and 732 million cases, respectively, worldwide. The schistosomulae circulate in the host blood and turn into adults. Adult worms release eggs into the bloodstream that lodge in the small capillaries of the intestine or bladder, penetrate the wall, and are released in feces or urine, respectively. The cycle then repeats itself.

Schistosoma mekongi is much like Schistosoma japonicum in that adults more frequently in the superior mesenteric veins, but can be found in the central nervous system. The reservoir hosts for Schistosoma mekongi are dogs and pigs. It is believed that S. mekongi is unable to use cattle, such as water buffalo, as an effective reservoir host, unlike its close cousin S. japonicum.

Dormancy Period: 30 years or longer, with a large host of related diseases.

Each pair of flukes deposits around 1500–3500 eggs per day in the vessels of the intestinal wall. The eggs infiltrate through the tissues and are passed in the feces. The severity of S. japonicum arises in 60% of all neurological diseases in schistosomes due to the migration of schistosome eggs to the brain.

Individuals at risk to infection from S. japonicum are farmers who often wade in their irrigation water, fishermen who wade in streams and lakes, children who play in water, and people who wash clothes in streams. Once the parasite has entered the body and begun to produce eggs, it uses the hosts’ immune system (granulomas) for transportation of eggs into the gut. The eggs stimulate formation of granuloma around them. The granulomas, consisting of motile cells, carry the eggs to the intestinal lumen. When in the lumen, granuloma cells disperse leaving the eggs to be excreted within feces. Unfortunately, about two-thirds of eggs are not excreted, instead they build up in the gut. 

Dormancy Period: 4 years or more.

Sexual maturation is attained after 4–6 weeks of initial infection. A female generally lays 500–1,000 eggs in a day. The fluke continuously lays eggs throughout their life. An average lifespan is 3–4 years. Adults are found in the venous plexuses around the urinary bladder and the released eggs travels to the wall of the urine bladder causing haematuria and fibrosis of the bladder. The bladder becomes calcified, and there is increased pressure on ureters and kidneys otherwise known as hydronephrosis. Inflammation of the genitals due to S. haematobium may contribute to the propagation of HIV.

Along with other helminth parasites Clonorchis sinensis and Opisthorchis viverrini, S. haematobium was declared as Group 1 (extensively proven) carcinogens by the WHO International Agency for Research on Cancer (IARC) Working Group on the Evaluation of Carcinogenic Risks to Humans in 2009.

Dormancy Period: Up to 4 weeks.

As of 2021, the World Health Organization reports that 251.4 million people have schistosomiasis. As the leading cause of schistosomiasis in the world, it is the most prevalent parasite in humans. Snails are intermediate hosts. Each female lays approximately 300 eggs a day. It is classified as a neglected tropical disease.

Each schistosomule spends a few days in the skin and then enters the circulation starting at the dermal lymphatics and venules. Here, they feed on blood, regurgitating the haem as hemozoin.The schistosomule migrates to the lungs (5–7 days post-penetration) and then moves via circulation through the left side of the heart to the hepatoportal circulation (>15 days) where, if it meets a partner of the opposite sex, it develops into a sexually mature adult and the pair migrate to the mesenteric veins.The adult female worm resides within the adult male worm’s gynaecophoric canal, which is a modification of the ventral surface of the male, forming a groove. 

Dormancy Period: 30 years or longer, with a large host of related diseases.

Many individuals do not experience symptoms. If symptoms do appear, they usually take 4–6 weeks from the time of infection. Schistosomes can live an average of 3–5 years, and the eggs can survive for more than 30 years after infection. S. haematobium completes it life cycle in humans, as definitive hosts, and freshwater snails, as intermediate hosts, just like other schistosomes. But unlike other schistosomes that release eggs in the intestine, it releases its eggs in the urinary tract and excrete along with the urine.

Adults are found in the venous plexuses around the urinary bladder and the released eggs travels to the wall of the urine bladder causing haematuria and fibrosis of the bladder. The bladder becomes calcified, and there is increased pressure on ureters and kidneys otherwise known as hydronephrosis. Inflammation of the genitals due to S. haematobium may contribute to the propagation of HIV.

Dormancy Period: Infections can persist for 20 years or more, with few obvious symptoms, while related diseases progress.

About 22 million people are estimated to be affected yearly worldwide. It is particularly common in East Asia. Paragonimiasis is easily mistaken for other diseases with which it shares clinical symptoms, such as tuberculosis and lung cancer. As hermaphrodites, they produce and fertilise their own eggs that are released through the respiratory tract. The eggs are excreted to the environment either through the sputum or by being swallowed and passed out along with the faeces. Time from infection to laying of eggs is 65 to 90 days. Infections may persist for 20 years in humans.

Dormancy Period: Infection can last the lifetime of the patient.

The free metacercariae penetrate the intestinal mucosa and enter the bile ducts. Migration into the bile ducts takes 1–2 days. They start feeding on the bile secreted from the liver, and gradually grow. They become adults in about a month, and start laying eggs. The average lifespan of an adult fluke is 30 years. An individual fluke can produce 4,000 eggs in a day.

O. viverrini is a hermaphroditic liver fluke. Similar to C. sinensis and O. felineus, it requires three different hosts to complete its lifecycle. Freshwater snails are the first intermediate hosts, and freshwater fishes belonging to the family Cyprinidae are second intermediate hosts in which larval development occurs. Fish–eating (piscivorous) mammals, including humans, dogs, and cats, act as definitive hosts, in which sexual reproduction occurs. As a result of poor sanitation practices and inadequate sewerage infrastructure, O. viverrini-infected people pass the trematode’s eggs in their feces into bodies of fresh water from where snails become infected.

Dormancy Period: The incubation period is around 14 days and infestation may persist for more than one year.

After ingestion of fish infected with M. conjunctus, about 1–15 days are needed for symptoms to occur, namely for eggs to be detected in the stool. When untreated, symptoms may last from 3 days to 4 weeks.

The first intermediate host of M. conjunctus is a freshwater snail, Amnicola limosus.The second intermediate host is a freshwater fish.

The definitive hosts are fish-eating mammals such as domestic dogs, domestic cats, wolves, red foxes, gray foxes, coyotes, raccoons, muskrats, American minks, fishers, or bears. It can also infect humans, where it lives in the bile duct and in the gallbladder.

Dormancy Period: Up to 2 months.

Symptoms typically begin 30 to 60 days after exposure. Most infections are light, almost asymptomatic. In heavy infections, symptoms can include abdominal pain, chronic diarrhea, anemia, ascites, toxemia, allergic responses, sensitization caused by the absorption of the worms’ allergenic metabolites can lead to intestinal obstruction and may eventually cause death of the patient. The largest intestinal fluke of humans, growing up to 7.5 cm (3.0 in) long. 

The parasite infects an amphibic snail (Segmentina nitidella, Segmentina hemisphaerula, Hippeutis schmackerie, Gyraulus, Lymnaea, Pila, Planorbis (Indoplanorbis)) after being released by infected mammalian feces; metacercaria released from this intermediate host encyst on aquatic plants like water spinach, which are eaten raw by pigs and humans. Water itself can also be infective when drunk unboiled (“Encysted cercariae exist not only on aquatic plants, but also on the surface of the water.”)

Dormancy Period: Up to 14 days.

Flukes attach to the wall of the small intestine, but are often asymptomatic unless in large numbers. Infection can occur from eating a single infected fish source. The incubation period is around 14 days and infestation may persist for more than one year. In acute metagonimiasis, clinical manifestations are developed only 5–7 days after infection. 

Transmission requires two intermediate hosts, the first of which is snails, most commonly of species Semisucospira libertina, Semiculcospira coreana, and Thiara granifera.

Infection is acquired through the secondary intermediate host, fish, that have not been thoroughly cooked. Metacercariae encyst under the scales or in the flesh of fish from fresh or brackish water. Sweetfish (Pecoglossus altevelis) is one of the most common fish species infected, but others include the golden carp (Carassius auratus), common carp (Cyprinus carpio), Zacco temminckii, Protimus steindachneri, Acheilognathus lancedata, and Pseudorashora parva.

Dormancy Period: Up to 3 months.

The disease progresses through four distinct phases; an initial incubation phase of between a few days up to three months with little or no symptoms; an invasive or acute phase which may manifest with: fever, malaise, abdominal pain, gastrointestinal symptoms, urticaria, anemia, jaundice, and respiratory symptoms. The disease later progresses to a latent phase with less symptoms and ultimately into a chronic or obstructive phase months to years later. Humans are infected by eating water-grown plants, primarily wild-grown watercress in Europe or morning glory in Asia. Infection may also occur by drinking contaminated water with floating young fasciola or when using utensils washed with contaminated water. Cultivated plants do not spread the disease in the same capacity. Human infection is rare, even if the infection rate is high among animals. Especially high rates of human infection have been found in Bolivia, Peru and Egypt.

Dormancy Period: Up to 2 years.

The main reservoirs for Dicrocoelium dendriticum are sheep, cows, land snails and ants. However, Dicrocoelium dendriticum has also been found in goats, pigs and even llamas and alpacas. Infection is often asymptomatic. Most Dicrocoelium dendriticum infections of the biliary tree produce only mild symptoms. The incubation period is 1 day to 2 weeks. In this environment, D. dendriticum eggs are highly resistant and remain infectious for up to 20 months. Due to the highly specific nature of this parasite’s life cycle, human infections are generally rare.

Dormancy Period: Up to 25 years.

Clonorchiasis is endemic in the Far East, especially in Korea, Japan, Taiwan, and Southern China. The infection follows the ingestion of undercooked or pickled freshwater fish imported from one of the endemic areas and containing metacercariae. Humans become infected by eating infected fish that has been undercooked, smoked, pickled, or salted. Adult C. sinensis worms can inhabit the bile ducts of humans for 20–25 years without any clear clinical symptoms. This, in addition to the nonspecific symptoms infected persons may develop, can lead to missed diagnoses.

Dormancy period: Up  to six months – check before pregnancy.

Zika is a mosquito-borne flavivirus that can cause congenital defects, including microcephaly. Zika causes symptoms similar to other viral diseases spread through mosquito bites, like dengue and chikungunya. Many people infected with Zika virus will not have symptoms or will only have mild symptoms. Rarely, Zika infection can cause Guillain-Barré syndrome (GBS) or severe disease affecting the brain. Most Zika virus infections are asymptomatic.

Symptoms may include fever, red eyes, joint pain, headache, and a maculopapular rash. Symptoms generally last less than seven days. Most people who are infected have no or few symptoms. Otherwise the most common signs and symptoms of Zika fever are fever, rash, conjunctivitis (red eyes), muscle and joint pain, and headache, which are similar to signs and symptoms of dengue and chikungunya fever. The disease spreads from mother to child in the womb and can cause multiple problems, most notably microcephaly, in the baby.

Dormancy period: 3-6 days

The disease is caused by the yellow fever virus and is spread by the bite of an infected mosquito. It infects humans, other primates, and several types of mosquitoes.Iit is spread primarily by Aedes aegypti, a type of mosquito found throughout the tropics and subtropics.

Yellow fever is a viral disease of typically short duration. In most cases, symptoms include fever, chills, loss of appetite, nausea, muscle pains—particularly in the back—and headaches. Symptoms typically improve within five days. In about 15% of people, within a day of improving the fever comes back, abdominal pain occurs, and liver damage begins causing yellow skin. If this occurs, the risk of bleeding and kidney problems is increased.

In 15% of cases, people enter a second, toxic phase of the disease characterized by recurring fever, this time accompanied by jaundice due to liver damage, as well as abdominal pain. Bleeding in the mouth, nose, eyes, and the gastrointestinal tract cause vomit containing blood, hence one of the names in Spanish for yellow fever, vómito negro (“black vomit”). 

Dormancy period: Up to 30 days

Co-test with Salmonella Rapid Test.

Typhoid fever, or typhoid, is caused by Salmonella enterica serotype Typhi bacteria, also called Salmonella typhi. Typhoid is usually spread through the ingestion of contaminated food or water. Symptoms vary from mild to severe, and usually begin six to 30 days after exposure.

Often there is a gradual onset of a high fever over several days. This is commonly accompanied by weakness, abdominal pain, constipation, headaches, and mild vomiting. Some people develop a skin rash with rose colored spots. In severe cases, people may experience confusion. Without treatment, symptoms may last weeks or months. Diarrhea may be severe, but is uncommon. Other people may carry it without being affected, but are still contagious. Typhoid fever is a type of enteric fever, along with paratyphoid fever. Salmonella enterica Typhi is believed to infect and replicate only within humans.

Dormancy Period: 7-10 days, or in dormancy the lifetime of the patient.

Found worldwide, T. gondii is capable of infecting virtually all warm-blooded animals. In humans, particularly infants and those with weakened immunity, T. gondii infection is generally asymptomatic but may lead to a serious case of toxoplasmosis. T. gondii can initially cause mild, flu-like symptoms in the first few weeks following exposure, but otherwise, healthy human adults are asymptomatic.

This asymptomatic state of infection is referred to as a latent infection, and it has been associated with numerous subtle behavioral, psychiatric, and personality alterations in humans. Behavioral changes observed between infected and non-infected humans include a decreased aversion to cat urine (but with divergent trajectories by gender) and an increased risk of schizophrenia. Preliminary evidence has suggested that T. gondii infection may induce some of the same alterations in the human brain as those observed in rodents. Tissue cysts can be maintained in host tissue for the lifetime of the animal or human.

Dormancy Period: Several years in asymptomatic patients.

Trichomonas is a genus of anaerobic excavate parasites, and is estimated to be the most prevalent non-viral STI worldwide. Infection rates in men and women are similar but women are usually symptomatic, while infections in men are usually asymptomatic. Transmission usually occurs via direct, skin-to-skin contact with an infected individual, most often through vaginal intercourse. 160 million cases of infection are acquired annually worldwide.

Some of the complications of T. vaginalis in women include: Preterm delivery, low birth weight, and increased mortality as well as predisposing to HIV infection, AIDS, and cervical cancer. T. vaginalis has also been reported in the urinary tract, fallopian tubes, and pelvis and can cause pneumonia, bronchitis, and oral lesions. Condoms are effective at reducing, but not wholly preventing, transmission. Medication should be prescribed to any sexual partner(s) as well because they may be asymptomatic carriers.

Dormancy Period: Up to 7 days.

About 11 million humans are infected with Trichinella. The great majority of trichinosis infections have either minor or no symptoms and no complications. Trichinosis. During the initial infection, invasion of the intestines can result in diarrhea, abdominal pain, and vomiting. Migration of larvae to muscle, which occurs about a week after being infected, can cause swelling of the face, inflammation of the whites of the eyes, fever, muscle pains, and a rash. Complications may include inflammation of heart muscle, central nervous system involvement, and inflammation of the lungs.

They may very rarely cause enough damage to produce serious neurological deficits (such as ataxia or respiratory paralysis) from worms entering the central nervous system, which is compromised by trichinosis in 10–24% of reported cases of cerebral venous sinus thrombosis, a very rare form of stroke (three or four cases per million annual incidences in adults). Trichinosis can be fatal depending on the severity of the infection; death can occur 4–6 weeks after the infection, and is usually caused by myocarditis, encephalitis, or pneumonia.

Dormancy period: Up to 12 days.

Scrub typhus is a mite-borne disease caused by a bacteria known as Orientia tsutsugamushi and transmitted by chiggers – larvae that grow into mites, in rural and forested areas of the Asia-Pacific region. Chiggers often pick up the bacteria when they feed on the skin cells of infected rats or mice. It can cause fever, breathing difficulty, heart palpitations, or sudden cardiac death. The bacteria’s incubation period inside the body is about 6-10 days. Symptoms may start suddenly at around 10-12 days after the bite.

Signs and symptoms include fever, headache, muscle pain, cough, and gastrointestinal symptoms. More virulent strains of O. tsutsugamushi can cause hemorrhaging and intravascular coagulation. Morbilliform rash, eschar, splenomegaly, and lymphadenopathies are typical signs. Leukopenia and abnormal liver function tests are commonly seen in the early phase of the illness. Pneumonitis, encephalitis, and myocarditis occur in the late phase of illness. It has particularly been shown to be the most common cause of acute encephalitis syndrome. Untreated cases are often fatal.

Dormancy period: From 6 hours to 6 days, and up to several weeks.

Salmonella is a bacterial pathogen that causes Salmonellosis. Salmonella bacteria typically live in animal and human intestines and are shed through feces. Humans become infected most frequently through contaminated water or food. Salmonella is notorious for its ability to survive desiccation and can persist for years in dry environments and foods. Symptoms usually begin six hours to six days after infection and last four to seven days. However, some people do not develop symptoms for several weeks after infection and others experience symptoms for several weeks. Multidrug-tolerant mutant Salmonella enter a near-dormant state protected from immune-mediated genotoxic damages.

Most infections are due to the ingestion of food contaminated by feces. Typhoidal Salmonella serotypes can only be transferred between humans and can cause foodborne illness as well as typhoid and paratyphoid fever. Typhoid fever is caused by typhoidal Salmonella invading the bloodstream, as well as spreading throughout the body, invading organs, and secreting endotoxins (the septic form). 

Dormancy period: Up to 23 days.

Rubella, or German measles or scarlet fever, is a mild viral infection that typically occurs in children and non-immune young adults. Rubella is highly contagious from person to person, transmitted primarily through direct or droplet contact from nasopharyngeal secretions. Humans are the only natural hosts.

The average incubation period of rubella virus is 12 to 23 days. People infected with rubella are most contagious when the rash is erupting. But they can be contagious from 7 days before to 7 days after the rash appears. About 25% to 50% of infections are asymptomatic.

Rubella is usually spread from one person to the next through the air via coughs of people who are infected. People are infectious during the week before and after the appearance of the rash. Babies with CRS may spread the virus for more than a year. Only humans are infected. Insects do not spread the disease. Once recovered, people are immune to future infections. Rubella infection of children and adults is usually mild, self-limiting, and often asymptomatic. 

Dormancy period: Typically up to 3 months. This period may be as short as four days or longer than six years, depending on the location and severity of the wound and the amount of virus introduced.

Rabies is a zoonotic disease (jumps from animal to human) that is caused by infection with viruses of the Lyssavirus genus, which are transmitted via the saliva of an infected animal. Dogs are the most important reservoir for rabies viruses, and dog bites account for >99% of human cases. When an individual with rabies develops symptoms, the disease is nearly always fatal. Two classical forms of rabies are generally recognized: furious (also called encephalitic) and paralytic.

Incubation periods can vary considerably, although most patients develop symptoms 20–90 days after exposure. Rabies can lay dormant in the body up to 6 years. Rabies causes about 59,000 deaths worldwide per year, about 40% of which are in children under the age of 15. More than 95% of human deaths from rabies occur in Africa and Asia. Its100% fatal after onset of symptoms.

Dormancy period: Up to 4 weeks.

The following information is biased by the CDC. Monkeypox is a zoonotic virus belonging to the Orthopoxvirus genus, making it closely related to the variola, cowpox, and vaccinia viruses. Symptoms of mpox in humans include a rash that forms blisters and then crusts over, fever, and swollen lymph nodes. The virus is transmissible between animals and humans by direct contact to the lesions or bodily fluids. Monkeypox virus can be transmitted from one person to another through contact with infectious lesion material or fluid on the skin, in the mouth or on the genitals; this includes touching, close contact and during sex. It may also spread by means of respiratory droplets from talking, coughing or sneezing. The virus then enters the body through broken skin, or mucosal surfaces such as the mouth, respiratory tract, or genitals. The disease has also been reported in a wide range of other animals, including monkeys, anteaters, hedgehogs, prairie dogs, squirrels, and shrews.

Dormancy Period: Up to 24 weeks after initial symptoms.

Human malaria is caused by single-celled microorganisms of the Plasmodium group. It is spread exclusively through bites of infected female Anopheles mosquitoes. The mosquito bite introduces the parasites from the mosquito’s saliva into a person’s blood. The parasites travel to the liver, where they mature and reproduce.

Some malaria parasite species can remain dormant (inactive) in the liver for months or years after the initial infection. Later, after returning from an area with malaria, these parasites can then leave the liver and infect red blood cells and cause another episode of illness.

Symptoms of malaria can recur after varying symptom-free periods. Depending upon the cause, recurrence can be classified as either recrudescence, relapse, or reinfection. Recrudescence is when symptoms return after a symptom-free period due to failure to remove blood-stage parasites by adequate treatment. Relapse is when symptoms reappear after the parasites have been eliminated from the blood but have persisted as dormant hypnozoites in liver cells. 

Dormancy Period: 1 to 8 years,

The larvae develop into adult worms over the course of a year, during which time the patient  can be asymptomatic, and reach sexual maturity in the afferent lymphatic vessels. The worms can live for approximately 6–8 years and, during their lifetime, produce millions of microfilariae (immature larvae) that circulate in the blood. After mating, the adult female worm can produce thousands of microfilariae that migrate into the bloodstream. A mosquito vector can bite the infected human host, ingest the microfilariae, and thus repeat the lifecycle. They migrate between the deep and the peripheral, circulation exhibiting unique diurnal periodicity. During the day, they are present in the deep veins, and during the night, they migrate to the peripheral circulation.

Affects over 120 million people, primarily in Central Africa and the Nile delta, South and Central America, the tropical regions of Asia including southern China, and the Pacific islands and Indonesia.

Dormancy period: 2-4 weeks.

Leptospirosis is a blood infection caused by the bacteria Leptospira that can infect humans, dogs, rodents and many other wild and domesticated animals. Signs and symptoms can range from none to mild (headaches, muscle pains, and fevers) to severe (bleeding in the lungs or meningitis). Weil’s disease, the acute, severe form of leptospirosis, causes the infected individual to become jaundiced (skin and eyes become yellow), develop kidney failure, and bleed. Bleeding from the lungs associated with leptospirosis is known as severe pulmonary haemorrhage syndrome.

Leptospirosis is one of the most important worldwide zoonosis (jumps from animal to human) and is a major public health issue in many countries. The disease is caused by spirochetes from the genus Leptospira and is transmitted by contact of abraded skin or mucous membranes with contaminated rodent urine, water, or soil. Leptospirosis can cause severe multiple organ failure with a mortality rate as high as 50%. 

Dormancy Period: Weeks to months.

Leishmaniasis is a wide array of clinical manifestations caused by protozoal parasites of the Trypanosomatida genus Leishmania. It is generally spread through the bite of phlebotomine sandflies, Phlebotomus and Lutzomyia, and occurs most frequently in the tropics and sub-tropics of Africa, Asia, the Americas, and southern Europe. The disease can present in three main ways: cutaneous, mucocutaneous, or visceral. The cutaneous form presents with skin ulcers, while the mucocutaneous form presents with ulcers of the skin, mouth, and nose. The visceral form starts with skin ulcers and later presents with fever, low red blood cell count, and enlarged spleen and liver.

Some infected persons are asymptomatic, particularly in settings where cyclosporiasis is endemic. Among symptomatic persons, the incubation period averages one week (ranging as soon as 2 days – 2 weeks or more)

Dormancy period: Up to the lifetime of the patient.

Gastric disorders due to infection begin with gastritis, inflammation of the stomach lining. When infection is persistent the prolonged inflammation will become chronic gastritis. Initially this will be non-atrophic gastritis, but damage caused to the stomach lining can bring about the change to atrophic gastritis, and the development of ulcers both within the stomach itself or in the duodenum, the nearest part of the intestine.

Helicobacter pylori is a class 1 carcinogen, and potential cancers include gastric mucosa-associated lymphoid tissue (MALT) lymphomas and gastric cancer. Infection with H. pylori is responsible for around 89 per cent of all gastric cancers and is linked to the development of 5.5 per cent of all cases of cancer worldwide. H. pylori is the only bacterium known to cause cancer. Most people infected with H. pylori never experience any symptoms or complications, but will have a 10% to 20% risk of developing peptic ulcers or a 0.5% to 2% risk of stomach cancer. It was estimated that about two-thirds of the world’s population were infected with H. pylori, being more common in developing countries.

Dormancy period: Up to 8 weeks

Hantaviruses are a family of viruses spread mainly by rodents by inhalation. They can cause serious illness or death in people. Most hantaviruses are not transmitted from person to person. The spectrum of disease associated with hantavirus infection include hemorrhagic fever with renal syndrome (HFRS) and hantavirus pulmonary syndrome (HPS) also known as hantavirus cardiopulmonary syndrome (HCPS). The virus can cause severe infections of the lungs (with cough and shortness of breath) or kidneys (with abdominal pain, and sometimes kidney failure). Symptoms of hantavirus typically develop 1-8 weeks after exposure to rodents or rodent droppings and may be non-specific, including fever, fatigue, muscle aches, nausea, and cough.

Dormancy period: 2 days, however some people are asymptomatic and can shed virus for weeks.

Avian influenza, also known as avian flu or bird flu, is a disease caused by the influenza A virus (IAV) which primarily affects birds but can sometimes affect mammals including humans. Rarely, humans can become infected by the avian flu if they are in close contact with infected birds. An avian influenza virus can acquire characteristics, such as the ability to infect humans, from a different virus strain. Influenza A virus, that has been modified with mRNA, can infect humans. Many people remain asymptomatic but can shed virus for weeks.

Dormancy period: Up to 10 days for poisonous strains. Beneficial strains persist for life.

Most E. coli strains are harmless, but some serotypes such as EPEC, and ETEC are pathogenic and can cause serious food poisoning in their hosts, and are occasionally responsible for food contamination incidents that prompt product recalls.

E. coli belongs to a group of bacteria informally known as coliforms that are found in the gastrointestinal tract of warm-blooded animals. E. coli normally colonizes an infant’s gastrointestinal tract within 40 hours of birth, arriving with food or water or from the individuals handling the child. In the bowel, E. coli adheres to the mucus of the large intestine. It is the primary facultative anaerobe of the human gastrointestinal tract. (Facultative anaerobes are organisms that can grow in either the presence or absence of oxygen.) As long as these bacteria do not acquire genetic elements encoding for virulence factors, they remain benign commensals.

The incubation period is usually 3–4 days after the exposure, but may be as short as 1 day or as long as 10 days.

Dormancy period: 2 days to 3 weeks. The patient can continue to be contagious for several months after recovery.

Ebola, also known as Ebola virus disease (EVD) and Ebola hemorrhagic fever (EHF), is a viral hemorrhagic fever in humans and other primates, caused by ebolaviruses. Symptoms typically start anywhere between two days and three weeks after infection. The first symptoms are usually fever, sore throat, muscle pain, and headaches. These are usually followed by vomiting, diarrhea, rash and decreased liver and kidney function, at which point some people begin to bleed both internally and externally. It kills between 25% and 90% of those infected – about 50% on average. Death is often due to shock from fluid loss, and typically occurs between six and 16 days after the first symptoms appear. Early treatment of symptoms increases the survival rate considerably compared to late start.

Dormancy period: Up to 14 days. Up to 80% are asymptomatic

Dengue fever is an illness you can get from the bite of a mosquito carrying one of four types of Dengue. Dengue isn’t contagious from person to person except when passed from a pregnant person to their child. Symptoms are usually mild with first infection, but repeated infections with a different version of dengue, the risk of severe complications increases. Dengue fever symptoms start to appear four to 10 days after a mosquito bite and can last three to seven days. About 1 in 20 people sick with dengue will develop severe dengue after their initial symptoms begin to fade. Do not take aspirin or ibuprofen. Some people remain asymptomatic but can still carry the parasite.

Typically, people infected with dengue virus are asymptomatic (80%) or have only mild symptoms such as an uncomplicated fever. Others have more severe illness (5%), and in a small proportion it is life-threatening. The incubation period (time between exposure and onset of symptoms) ranges from 3 to 14 days, but most often it is 4 to 7 days.

Dormancy period: Symptoms start 12 hours to 5 days after exposure

Cholera is a severe infection of the small intestine by some strains of the bacterium Vibrio cholerae, transmitted through the ingestion of contaminated food or water. It takes between 12 hours and 5 days for a person to show symptoms. Cholera can cause very bad diarrhea and dehydration that can kill within hours if left untreated. Raw fish and foods area common source of this disease. Most of those infected have no or mild symptoms.

The primary symptoms of cholera are profuse diarrhea and vomiting of clear fluid. These symptoms usually start suddenly, half a day to five days after ingestion of the bacteria. The diarrhea is frequently described as “rice water” in nature and may have a fishy odor. An untreated person with cholera may produce 10 to 20 litres (3 to 5 US gal) of diarrhea a day. Severe cholera, without treatment, kills about half of affected individuals. If the severe diarrhea is not treated, it can result in life-threatening dehydration and electrolyte imbalances. Estimates of the ratio of asymptomatic to symptomatic infections have ranged from 3 to 100. 

Dormancy period: Up to 12 days, some people are asymptomatic but can remain infected for a a year or longer.

Chikungunya is a disease transmitted to humans by mosquitoes in Africa, Asia, and the Americas. You can’t get it from another person, but mosquitoes do get it from biting a person who is infected. Most people don’t die from it. Chikungunya fever typically lasts from five to seven days and frequently causes severe and often incapacitating joint pain which sometimes persists for much longer periods.These typically occur two to twelve days after exposure. There is no modern medicine treatment however traditional cures are abundant. Approximately 3%-28% of people infected with chikungunya virus will remain asymptomatic.

Other symptoms may include headache, muscle pain, joint swelling, and a rash. Symptoms usually improve within a week; however, occasionally the joint pain may last for months or years. The risk of death is around 1 in 1,000. The very young, old, and those with other health problems are at risk of more severe disease. 

Dormancy period: Up to 6 weeks, plus lifetime negative damages.

After exposure to Brucella bacteria, humans generally have a two- to four-week latency period before exhibiting symptoms, which include acute undulating fever (>90% of all cases), headache, arthralgia (>50%), night sweats, fatigue, and anorexia. Later complications may include arthritis or epididymo-orchitis, spondylitis, neurobrucellosis, liver abscess formation, and endocarditis, the latter potentially fatal. The skeletal system is affected in 20–60% of cases, including arthritis (hip, knee, and ankle), spondylitis, osteomyelitis, and sacroiliitis (most common). Lumbar vertebrae can be affected showing the classical radiological sign of vertebral erosion.

Neurological symptoms include meningitis, encephalitis, radiculopathy, peripheral neuropathy, intracerebral abscesses, and acute or chronic neck rigidity (<50%), and the cerebrospinal fluid can show lymphocytic pleocytosis, low sugar, increased protein, positive bacterial culture (<50%), and agglutination (positive in >95%). Pulmonary infection can be from inhalation or hematogenous sources, and can cause any chest syndrome. Rarely is Brucella isolated from sputum.

Dormancy period: 2 days, however some people are asymptomatic and can shed virus for weeks.

Avian influenza, also known as avian flu or bird flu, is a disease caused by the influenza A virus (IAV) which primarily affects birds but can sometimes affect mammals including humans. Rarely, humans can become infected by the avian flu if they are in close contact with infected birds. An avian influenza virus can acquire characteristics, such as the ability to infect humans, from a different virus strain. Influenza A virus, that has been modified with mRNA, can infect humans. Many people remain asymptomatic but can shed virus for weeks.

Dormancy period: Up to the lifetime of the patient, depending on type of inoculation received.

Naturally-occurring spike proteins are normally produced by the body. The artificial spike protein, as contained in CV-19 inoculations, is known to be highly toxic – generally affecting any weakened function in the body. Also consider combing with the D-Dimer blood clotting test and Spike Protein Synthesis testing, extra charge.

High prevalence in Bali and Indonesia