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Wellness
Screening- Essential Periodic Laboratory Testing of Asymptomatic Patients
Dennis Hoyer, D.C., Associate Professor - Clinical
Sciences
Many
chiropractors, even [those that are] well trained, avoid ordering
laboratory tests. Sometimes this is because laboratory testing is
outside of their comfort zone; sometimes it is because of reimbursement
issues. However, a reluctance to order laboratory tests does not
preclude one from the responsibility of knowing which tests to order,
and when it is appropriate to order them.
An
aspect of laboratory diagnosis that is beginning to get more attention
in the world of preventive health care is that of wellness screening.
In wellness screening, we test asymptomatic patients who are basically
healthy. Tests are chosen that screen for the presence of prevalent
diseases that can be detected before clinical findings develop.
These diseases are treatable (not necessarily curable). Delay in
treatment results in harmful and sometimes preventable consequences1.
Timely detection and subsequent treatment will at the very least
delay eventual problems.
Many
medical associations, organizations and task forces have published
guidelines for prudent wellness screening. There is no total consensus
among these groups. However, the following chart summarizes my recommendations
based upon the varied groups whose guidelines I reviewed2.
(NOTE: You will find a more detailed explanation of these recommendations
following the chart below).
|
Test
|
Condition
|
Age
First Tested
|
Repeat
Testing
|
|
|
Coronary
Artery Disease
|
20
Years
|
Every
5 years
|
|
|
Diabetes
mellitus
|
45
years
|
Every
3 years
|
|
|
Colon
cancer
|
50
years
|
Annually
|
|
|
Cervical
cancer
|
18
years
|
Annually
|
|
|
Prostate
cancer
|
50
years
|
Annually
|
CHOLESTEROL
Most of the guidelines reviewed recommend serum total cholesterol
as a basic screening tool. The optimal level is <200 mg/dL (<5.2
mmol/L), although many holistic practitioners like myself advocate
a more rigid 180 mg/dL (4.65 mmol/L). The National Cholesterol Education
Program (NCEP) suggests also looking at both the LDL and HDL cholesterol
levels. The optimal levels for these lipoproteins are LDL <100
mg/dL (<2.59 mmol/L), HDL >40 mg/dL (>1.03 mmol/L) in men,
and HDL > 50 (1.3mmol.L) in women. Elevated LDL cholesterol is
considered a positive risk factor for coronary artery disease. Elevated
HDL cholesterol is considered a negative risk factor. I recommend
doing all three tests for the purpose of wellness screening. If
the levels are optimal the tests are repeated in five years. Test
should occur after a 12 hour fast. Abnormal tests should be confirmed
by at least one additional measurement within 8 weeks. I suggest
becoming familiar with NCEP's website which is www.nhlbi.nih.gov.
FASTING
PLASMA GLUCOSE (FPG)
Type 2 diabetes mellitus (formerly called non-insulin diabetes type
II) is a major public health concern. Its prevalence is increasing,
and it is appearing at earlier ages. The reason for this is obvious;
Americans eat unhealthy diets and they are overweight, including
our younger generations. The American Diabetes Association (ADA,
www.diabetes.org/main/application/commercewf)
recommends screening for diabetes commence at the age of 45 years
using a single fasting plasma glucose assay. A normal FPG level
is <110 mg/dL (<6.1 mmol/L). An individual is considered diabetic
if the FPG is ³126 mg/dL (³7.0 mmol/L). The ADA recommends
the test be confirmed on a separate day. If the test result is normal,
it is repeated in three years. If an individual is a member of a
high-risk ethnic population (African American, Native American,
Asian, or Hispanic) or is a first-degree relative of a diabetic,
screening should commence as early as age 30 years.
FECAL
OCCULT BLOOD TEST (FOBT)
Colorectal cancer is the third leading cause of cancer-related deaths
in both males and females in the USA. Most cancerous and some pre-cancerous
lesions bleed. Therefore, detection of these lesions by finding
hidden (occult) blood in the stool (termed melena) is the least
invasive and most cost-effective method of screening. A three-card
FOBT kit must be used. These kits require three specimens collected
on three consecutive days, thus increasing the probability of finding
blood if bleeding is occurring. Also, a specific diagnostic diet
must be followed for four days prior to and during testing. The
test kits always provide exact details about the diagnostic diet.
Screening via FOBT commences at the age of 50 years for average-risk
men and women. This initial screening should also be accompanied
by flexible sigmoidoscopy to 65 cm. The FOBT is repeated yearly.
The sigmoidoscopy is repeated in 3-5 years. Screening commences
no later than age 40 years for an individual who is a first-degree
relative of a patient with colorectal cancer. A good website for
FOBT is from the Cleveland Clinic in Ohio; ww.clevelandclinicmeded.com/ihpage/ihpage2/fecal.htm.
PAP
TEST
Cervical cancer can be detected via the Pap test which is part of
a yearly pelvic examination. Testing commences once the patient
becomes sexually active, but no later than age 18 years. Many women-healthcare
practitioners recommend yearly testing thereafter. However, some
current thinking is testing can be performed every 2 years if a
woman is monogamous for at least three years in which she has a
normal Pap in each of those years.
PROSTATE
SPECIFIC ANTIGEN (PSA)
Prostate cancer is the most common cancer of men. Transrectal ultrasound-
guided (TRUS) biopsy of the prostate is the "gold standard"
diagnostic test, but it is impractical as a screening test. Screening
via a combination of a digital-rectal examination (DRE) and serum
PSA seems to be the consensus recommendation. However, the use of
PSA in asymptomatic individuals is quite controversial. The following
website is just one illustration of this ongoing controversy. www.prostatepointers.org/ww/psamark.htm#acp)
The goal of screening via DRE and PSA is the early detection of
organ-confined (not spread beyond the gland) cancer. Once the cancer
spreads beyond the gland, the prognosis is poor. Currently, screening
commences at age 50 years, and is repeated yearly. Screening should
commence at the age of 40 years for an individual who is a member
of a high-risk ethnic population (African American) or is a first-degree
relative of a prostate cancer patient. A positive DRE regardless
of PSA level results in a biopsy. Depending upon which expert-opinion
one reads, the optimal PSA level is <2.5 ng/mL for men under
the age of 49 years3,
and <3.0 ng/mL for ages 50 years and beyond. No biopsy is required
at the optimal level, unless it is an increase of >0.75 ng/mL
from the previous year. A level of ³10.0 ng/mL is an absolute
indication for a biopsy. The screening PSA is a "total"
PSA. PSA circulates in two forms; complexed (primarily to protease
inhibitors) and free. When the screening PSA is between 2.5 (or
3.0)-10.0 ng/mL, a percent free PSA (% f-PSA) is reflexively performed.
A significant decrease in this fraction (malignant cells proportionately
produce less free PSA) aids in determining the need for a biopsy.
I recommend looking at the website of one of the experts on this
subject, William Catalona, MD who performed prostate surgery on
New York Yankees manager Joe Torre: www.drcatalona.com.
TRANSFERRIN
SATURATION (TSAT)
Also termed % saturation of transferrin (%sat), TSAT is used to
screen for a potentially life-threatening inherited disorder called
hemochromatosis, or iron overload. In this disease, an unusable
form of Iron called hemosiderin is deposited into multiple organs
causing irreversible damage. The most common complications include
hepatic, pancreatic, and cardiac insufficiency, and hypogonadism4.
The condition is rarely clinically evident until after the age of
50 years. Hence, it is recommended that all adults (>30 years)
be screened once for this condition no later than at age 50 years.
A fasting TSAT in excess of 60% is considered positive, and should
be repeated at least once. A serum ferritin is often used to confirm
these results. Tissue biopsy is then required to establish a definitive
diagnosis. There are many websites about this condition, but this
one is from the CDC; w.cdc.gov/nccdphp/dnpa/hemochromatosis/.
CONCLUSIONS
Chiropractors treat many patients who should be prudently and periodically
screened for certain diseases. Many of our patients are not receiving
such recommendations from their other health care providers. Sometimes
we are our patient's only doctors. As primary care providing, portal-of-entry
practitioners, chiropractors need to be certain our patients are
receiving the best preventive care possible. Wellness screening
should become a regular component to the care we provide.
*
This article was written by Dennis Hoyer, MT(ASCP), DC, Associate
Professor of Clinical Sciences Western States Chiropractic College.
1 Speicher, CE: The Right
Test, A Physician's Guide to Laboratory Medicine, 3rd edition, Saunders,
1998.
2 Guidelines from: American College
of Physicians; Canadian Task Force on the Periodic Health Examination;
College of American Pathologists; National Cholesterol Education
Program; Ohio State University Health Plan; US Preventive Services
Task Force; Washington State Clinical Laboratory Advisory Council.
3
Barry, MJ: Nonpalpable prostate cancer in Diagnostic Strategies
for Common Medical Problems, 1999, American College of Physicians,
Philadelphia, Pennsylvania.
4 Tierney, LM et al: Current
Medical Diagnosis and Treatment 2002, McGraw Hill, 2002.
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States Chiropractic College
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March 4, 2002
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