[sci.med] HICN233 News Part 2/2

ATW1H%ASUACAD.BITNET@oac.ucla.edu (Dr David Dodell) (09/12/89)

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3.  Melmon  KL.  Preventable  drug reactions:  causes and cures.  N Engl J Med
1971;284:1361-8.

4.  Moore SR,  Jones JK.  Adverse drug reaction surveillance in the  geriatric
population:  a pre liminary view.  In: Moore SR, Teal TW, eds.  Geriatric drug
use: clinical and social perspec tives. New York: Pergamon Press, 1985:70-7.

5. Tanner LA, Baum C, Prela MC, et al.  Spontaneous adverse reaction reporting
in the elderly for 1986. J Geriatr Drug Therapy 1989;3:31-54.

6.  Montamat  SC,  Cusack  BJ,  Vestal  RE.  Management of drug therapy in the
elderly. N Engl J Med 1989;321:303-9.

7.  German PS,  Klein LE.  Drug side effects and  doctor/patient  relationship
among elderly pa tients. J Soc Admin Pharm 1984;2:67-73.

8.  Hypertension Detection and Follow-Up Program Cooperative Group.  Five year
findings of the Hypertension Detection and Follow-up Program: I.  Reduction in
mortality of persons with high blood pressure,  including  mild  hypertension.
JAMA 1979;242:2562-71.

9.  Amery A,  Birkenhager W, Brixbo P, et al.  Mortality and morbidity results
from the European Working Party on High Blood Pressure in the  Elderly  trial.
Lancet 1985;1:1349-54.

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Volume  2, Number 33                                      September 11, 1989

                        Epidemiologic Notes and Reports
    Cadmium and Lead Exposure Associated with Pharmaceuticals Imported from
                                 Asia -- Texas

    In August 1988,  the Texas Department of Health (TDH) investigated illegal
sales in rural west Texas of pharmaceutical drugs manufactured in Asia.  These
drugs,  identified  by  TDH  and  Food and Drug Administration (FDA) agents as
"chuifong tokuwan" (a pharmaceutical compound manufactured  by  the  Nan  Ling
Pharmaceutical Company of Hong Kong), are sold in pill form.  Chuifong tokuwan
contains a  drug  combination  (diazepam,  indomethacin,  hydrochlorothiazide,
mefenamic acid,  dexamethasone, lead, and cadmium) that is not approved by FDA
and not legal for sale in or importation into the  United  States.  The  drugs
usually  were  repackaged  and relabeled as "The Miracle Herb--Mother Nature's
Finest."
    TDH tested 93  self-referred  persons  who  had  ingested  the  pills  for
exposure to lead and cadmium. Of these, 57 (61%) were female; greater than 90%
were white non-Hispanics; the mean age was 55 years.  Sixty-six (71%) reported
taking the pills to relieve symptoms of medical conditions such as arthralgias
(51%) and other pain (headache, stiff neck, back pain (26%)). Twenty-two (24%)
persons had elevated urine levels of cadmium; none had elevated levels of lead
(blood lead greater than or equal to 25 ug/mL).  However, 39 (42%) persons had
elevated  urine  values  for  retinol-binding protein (RBP),  a low-molecular-
weight protein indicative of renal tubular dysfunction (1-3).  The mean  urine
cadmium level for exposed persons was 1.8 ug/mL, compared with 0.5 ug/mL for a
nonrandom sampling of 14 unexposed persons. In exposed persons, 22 (24%) urine
samples  tested  for  cadmium were greater than 2.5 ug/mL,  the upper limit of
normal. None of the samples from unexposed persons had elevated values.
    The chuifong tokuwan seized  in  this  investigation  was  destroyed.  The
investigation is continuing.

Reported by:  D Baker,  MS,  Food and Drug Div,  J Brender, PhD, Environmental
Epidemiology,  KC Davis,  Texas Dept of Health.  Surveillance and Programs Br,
Div  of  Environmental  Hazards  and Health Effects,  Center for Environmental
Health and Injury Control, CDC.

Editorial Note:  Chuifong tokuwan first appeared in the United States in 1974.
Although  it  was banned by FDA in 1978,  the drug is distributed illegally in
certain parts of the United States and is sometimes sold by mail.  The primary
users  of  chuifong  tokuwan  in this study were long-time residents of Texas;
however,  use of unapproved imported drug combinations is common among  recent
immigrants  to  the  United  States,  particularly  those  from Asia and Latin
America (4-7).  Although these products are frequently perceived as relatively
harmless  herbal  "folk  remedies,"  they  often  contain cortico- or anabolic
steroids;   nonsteroidal  anti-inflammatory   drugs   (NSAIDs);   prescription
antibiotics,   such  as  tetracycline  and  chloramphenicol;   and  controlled
substances,  such as diazepam or narcotics,  and have potentially  serious  or
fatal health effects.
    Use  of  chuifong  tokuwan may increase the body burden of cadmium and may
have contributed to renal tubular dysfunction in persons using this  compound.
Through   chronic   exposure,   cadmium  can  accumulate  in  certain  organs,
particularly the  kidneys.  Both  cadmium  and  several  of  the  prescription
analgesics  in  chuifong  tokuwan  can cause renal tubular cell damage (8-11).
Cadmium can adversely affect function of the proximal renal tubules  (3,8-10);
increased  urinary  protein  excretion of low-molecular-weight proteins (e.g.,
RBP) is an early consequence of  proximal  renal  tubular  damage  by  cadmium

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Volume  2, Number 33                                      September 11, 1989

(2,3,9,10).
    In  persons  who  were  also  taking  other  medications,   the  analgesic
nephropathy associated with chronic use of many NSAIDs may have contributed to
renal tubular dysfunction (9,11).  Alternatively, increased urinary RBP values
could  reflect  renal  dysfunction  related  to  the underlying illness (e.g.,
arthritis) for which many of  the  patients  took  this  medication.  However,
adverse  effects  on  renal function have not been reported with use of either
indomethacin or mefenamic acid (the NSAIDs present  in  the  pills  analyzed),
even with prolonged use (11).
    Cadmium  is a cumulative toxicant,  with a biological half-life of greater
than 10 years in humans (12).  Medical evaluation, including urine cadmium and
urinary RBP values, is recommended for persons who have used chuifong tokuwan.
Additional renal-function evaluation should be included in the medical follow-
up of persons whose urinary RBP or urine cadmium values are abnormal.
    Complex  cultural  and  linguistic  barriers  necessitate cooperation with
traditional healers (e.g.,  acupuncturists,  herbalists) and local leaders  of
immigrant communities to inform these groups about the hazards associated with
use of specific products.

References

1. Kowal NE, Zirkes M. Urinary cadmium and beta 2-microglobulin: normal values
and con centration adjustment. J Toxicol Environ Health 1983;11:607-24.

2.  Ormos G,  Cseh J,  Groszmann M, Timar M.  Urinary beta 2-microglobulin and
retinol binding protein:  individual fluctuations in cadmium-exposed  workers.
Toxicol Lett 1985;27:59-64.

3.  Kowal NE,  Johnson DE, Kraemer DF, Pahren HR.  Normal levels of cadmium in
diet,  urine,  blood,  and tissues of inhabitants  of  the  United  States.  J
Toxicol Environ Health 1979;5:995-1014.

4. Chan H, Billmeier GJ Jr, Evans WE, Chan H. Lead poisoning from ingestion of
Chinese herbal medicine. Clin Toxicol 1977;10:273-81.

5.  Brearley  RL,  Forsythe  AM.  Lead poisoning from aphrodisiacs:  potential
hazard in immigrants. Br Med J 1978;2:1748-9.

6.  CDC.  Folk remedy-associated lead poisoning in Hmong  children--Minnesota.
MMWR 1983;32:555-6.

7.  Lightfoote J, Blair HJ, Cohen JR.  Lead intoxication in an adult caused by
Chinese herbal medication. JAMA 1977;238:1539.

8.  Adams  RG.  Environmental  cadmium  and  renal  disease  (Letter).  Lancet
1981;1:845.

9.  Boelaert J, Daneels R, Schurgers M. Cadmium, kidneys, and Belgian industry
(Letter). Lancet 1981;1:672.

10.  Baker EL Jr, Peterson WA,  Holtz JL,  Coleman C,  Landrigan PJ.  Subacute
cadmium   intoxication  in  jewelry  workers:   an  evaluation  of  diagnostic
procedures. Arch Environ Health 1979;34:173-7.

11.   Flower  RJ,  Moncada  S,  Vane  JR.   Analgesic-antipyretics  and  anti-

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Volume  2, Number 33                                      September 11, 1989

inflammatory agents;  drugs employed in the treatment of gout.  In: Gilman AG,
Goodman LS, Gilman A,  eds.  Goodman and Gilman's the pharmacological basis of
therapeutics. 6th ed. New York: MacMillan Publishing, 1980:682-728.

12.  Lauwerys  RR.  Industrial  chemical  exposure:  guidelines for biological
monitoring. Davis, California: Biomedical Publications, 1983:17.

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Volume  2, Number 33                                      September 11, 1989

                               Notice to Readers
    Publication of Guide for Developing Policies for HIV-Infected Students
                               and School Staff

    The National Association of State Boards of Education (NASBE) is one of 20
national organizations that  receive  assistance  from  CDC  to  help  schools
provide  effective  health  education  programs to prevent the spread of human
immunodeficiency virus (HIV). NASBE has published a guide that CDC commends to
its readers:  Someone at School Has AIDS:  A Guide to Developing Policies  for
Students and School Staff Members Who Are Infected with HIV.
    To develop the guide,  NASBE convened experts in medicine,  public health,
education,  and law* and has  recommended  scientifically  and  legally  based
policy  statements  that  local  and state departments of education can use in
developing policies for HIV-infected students and staff.  The guide  addresses
infection  control,  HIV-infected students and school staff,  confidentiality,
and HIV-antibody testing.  The  guide  also  includes  resources  for  further
information   about   HIV   education,   discrimination,   disease  reporting,
policymaking, and crisis management.
    Copies of the guide are available  from  NASBE,  Publications  Department,
1012 Cameron Street, Alexandria, VA 22314; telephone (703) 684-4000.

*Representatives  of  the  following  organizations participated in developing
and/or  reviewing  the  guide:   American  Academy  of  Pediatrics,   American
Association  of  School  Administrators,  American  Bar Association,  American
Federation of Teachers, American Medical Association, Association of State and
Territorial Health Officials, CDC,  Council for Exceptional Children,  Council
of  Chief  State  School  Officers,  Intergovernmental  Health Policy Project,
Michigan Department of Education,  National Association of  Elementary  School
Principals,  National  Association  of School Nurses,  National Association of
Secondary School  Principals,  National  Congress  of  Parents  and  Teachers,
National  Education  Association,  National  School  Boards Association,  U.S.
Department of Education, and U.S. Department of Justice.

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Volume  2, Number 33                                      September 11, 1989

===============================================================================
                                  Dental News
===============================================================================

                ADA Voices Concern Over "Whitening" Toothpastes

The  American Dental Association is voicing its concern over several new tooth
whitening/bleaching products which have recently entered the market.  The  ADA
Council on Dental Therapeutics is aware of the existence of four brands:  Epi-
Smile, White and Brite, Whiter Teeth and Smith White.

"We have very little information on the ingredients as used in these  products
and  no  information  on  their  safey,"  said  Dr.  Kenneth Burrell,  council
secretary.   The  council  has  made  inquires  to  the  US  Food   and   Drug
Administration and to the manufacturers on product content and safety, but has
not received significant information to date.

"We  are  concerned  about  products  that  use  oxygenating  agents as active
ingredients.  There is some  evidence  that  indicates  that  regular  use  of
oxygenating agents in the mouth can cause irritation of the soft tissues," Dr.
Burrell said.

According  to Dr.  Burrell,  these products may really work and be safe to use
but at this point there is not enough evidence to  make  that  conclusion.  To
date,  no  such  products  have been submitted for inclusion in the Council on
Dental Therapeutics  Seal  of  Acceptance  Program,  which  requires  clinical
studies of product safety and effectiveness.

The  American  Dental  Association  has  received  more  than  300  calls from
consumers and dentists inquiring about these particular  products,  which  are
being marketed both to dentists and over the counter to consumers.

Some  of  the  manufacturers  are  contending that their product is considered
purely cosmetic and does not require FDA Approval.  A spokesperson for the FDA
said  its  compliance division is investigating whether these products will be
considered cosmetics, drugs or devices under the FDA rules.  Cosmetic products
have fewer premarket requirements than do therapeutic products.

The ADA is advising  consumers  to  confer  with  their  dentist  about  tooth
discoloration  concerns.  Professional  cleanings  and  tooth  bleaching  by a
dentist are safe and commonly used  procedures  that  can  remove  stains  and
whiten teeth.  In more difficult cases,  tooth bonding with plastic resins and
veneers much  like  artificial  fingernails  can  be  used  to  improve  tooth
appearance.

Consumers  should  also  generally  look  for  the ADA Seal of Acceptance when
purchasing dental hygiene products.  "The Seal of Acceptance is the consumer's
assurance  that  the products has been thoroughly evaluated by the ADA Council
on Dental Therapeutics and has been found to be both safe and effective," said
Dr.  Burrell.

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Volume  2, Number 33                                      September 11, 1989

===============================================================================
                                   Articles
===============================================================================

            HEART TRANSPLANT PROGRAMS INCREASE TEN-FOLD SINCE 1983;
    BUT LACK OF DONORS LEAVES 929 ON WAITING LIST, ACCORDING TO NEW SURVEY
                    from the American Council on Transplantation

     The  number  of  heart  transplant programs has increased by more than 10
times since 1983,  and yet,  the estimated number of patients  waiting  for  a
transplant  today  is  three  times  what  it was in 1986,  according to a new
government  survey.  A  report  by  the  Government  Accounting  Office  (GAO)
prepared  for  Representative  Fortney  H.  Stark (D-Calif.),  Chairman of the
House Subcommittee on Health,  reported there were 131 hospitals with approved
heart  transplant  programs  at  the  end  of  1988,  up from just 12 in 1983.

However,  while there were l,529 heart transplants performed in 1988  compared
to 172 in 1983,  an estimated 929 patients remained on waiting lists,  the GAO
found.  The report also revealed 91 of the programs did not perform  at  least
12 heart transplants, the minimum number recommended by the 1986 Task Force on
Transplantation  based  on  its  conclusion  there is a "positive relationship
between the number of  heart  transplants  performed  and  patient  outcomes."
However,  the task force, recognizing there is a "lack of conclusive evidence"
relating to the number of transplants  performed,  added  "that  as  data  are
collected  and  analyzed,  the  appropriateness  of  this requirement could be
reassessed."

A total of 69 hospitals performed from 1 to 11 transplants while  22  did  not
perform  any in 1988,  the GAO said.  The principle reason cited in the report
for the low number of transplants at many hospitals and the long waiting  list
is a lack of donors.

Of  the  929  patients  waiting,  20  percent had been on the waiting list six
months to a year;  10 percent were waiting a year or  more;  and  another  5l5
patients died before a donor could be found, the GAO said.  Hospitals surveyed
expressed   optimism  that  recently  enacted  "required  request  laws"  will
eventually help increase the organ supply.

The average cost of a heart transplant was about $ll5,000 in  1987,  according
to the report, and most recipients were found to have private health insurance
that paid for most of the costs.  For example,  the Blue Cross and Blue Shield
Association reported that as of January 1989 "all but 1 of its 76 member plans
reimbursed for heart transplants"  including  the  cost  of  immunosuppressive
medications.

Heart  transplant patients covered under Medicare presently receive medication
reimbursement for only one-year,  but  that  will  change  in  1990  when  the
recently  enacted  Medicare Catastrophic Coverage Act of 1988 goes into effect
providing  continual  reimbursement,   according  to  the  report.   Hospitals
surveyed  estimated the cost of these medications averaged about $6,200 during
the second year after transplantation.

     A demographic breakdown of those receiving heart  transplants  in  fiscal
1988,  conducted by the United Network for Organ Sharing (UNOS), revealed that
84 percent of transplant recipients were white;  8 percent  black;  2  percent

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Volume  2, Number 33                                      September 11, 1989

Hispanic;  and  6  percent  other  groups  or their race was unknown,  the GAO
reported.  Seventy-seven percent of the recipients were male  and  61  percent
were over 45 years of age.

     (To  obtain  a  complete  copy  of  the  report  which  is entitled Heart
Transplants:  Concerns About Cost,  Access,  and Availability of Donor  Organs
(GAO/HRD-89-61) write:  U.S.  General Accounting Office, Post Office Box 6015,
Gaithersburg,  MD 20877.  The first  five  copies  of  the  report  are  free.
Additional  copies  are  $2.00 each.  There is a 25 percent discount on orders
for 100 or more copies mailed to a single address.  Orders must be prepaid  by
cash  or by check or money order made out to the Superintendent of Documents.)

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Volume  2, Number 33                                      September 11, 1989

                         TISSUE TRANSPLANTS UP IN 1988
               DESPITE INCREASED SCREENING FOR INFECTIOUS AGENTS
                        TO ASSURE SAFE TISSUE PROCURRED
                 from the American Council on Transplantation

     The number of tissues transplanted in 1988 showed small increases in most
categories  even  though  nearly  half  of  the  tissues  donated   were   not
transplanted  because of increased attention to donor selection criteria which
includes more stringent screening tests  for  known  infectious  agents  being
implemented around the country,  according to Jeanne Mowe,  executive director
of the American Association of Tissue Banks (AATB).

     The cautious screening takes place because tissue transplantation  is  an
elective procedure, and there is a responsibility to provide safe tissue, Mowe
explained.  Tissue  banks  consider the tests vitally important to keeping the
public's trust.  The new statistics reveal there were 5,200  skin  transplants
in  1988 compared to 5,000 in 1987;  300,000 bone deposits in 1988 compared to
250,000 in 1987;  36,900 corneal transplants in 1988  compared  to  35,427  in
1987;   and  27,000  adult  heart  valve  and  5,000  pediatric  heart  valves
transplanted in 1988 (1987 figures for heart valves were not available).

     The reason the number of transplants did not decrease is due to increased
efficiency  during  the  procurement process,  Mowe said.  The screening tests
eliminate the poor donor tissue and enhances the quality  of  tissue  that  is
obtained.  "Tissue  referrals  are reported up all over the country but we are
constantly adding parameters that eliminate potential donors,"  Helen  Leslie,
RN, director of Organ and Tissue Recovery Services at the Virginia Tissue Bank
(VTB)  which  is  part of LifeNet,  added.  "For example,  we ask 22 questions
regarding the medical and social history of each potential donor and then test
for AIDS,  Hepatitis B,  Hepatitis Core Antibody  and  HTLV  1.  All  must  be
negative  or  the  tissue  will  not be acceptable for us.  We also require an
autopsy on all tissue donors."

     Leslie noted that the VTB had 20% more donors in  1986  when  they  would
procure  bone tissue from donors as old as 70 years of age.  Now they will not
consider a bone donor older than 60 and the result,  said Leslie,  is  greater
quality which in turn enhances the success of the tissue transplant.

     Other tissues may be procurred from older donors and have  good  results,
depending on the overall health the donor, Leslie added. "The ideal donor is a
30-year-old male who was in excellent health and drank lots of milk as a kid,"
Scott  Bottenfield,  director  of  Laboratory Services at the VTB,  explained.
Depending upon what type of grafts created, that one donor can provide as many
as 40 grafts in addition to the procurement of the solid organs.

     In addition,  new techniques in peridontal dentistry have created a  need
for  ground  bone  which,  when  transplanted,  stimulates  new  bone  growth.
Bottenfield said that one donor can provide as many as 150  to  200  vials  of
ground bone weighing 1/4 to 1/2 gram each.  Therefore,  in reality,  one ideal
donor may provide life saving organ transplants,  and  life  enhancing  tissue
transplants to as many as 250 different people.

     The  need  for  more  and more testing to assure safe tissues has made it
increasingly important to properly train the individuals doing the evaluation,
Leslie pointed out.  "We must ask the right questions and be assured  that  no

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Volume  2, Number 33                                      September 11, 1989

marginal donor slips through."

     The  improvement  in  graft survival and the technological breakthroughs,
coupled with increasingly stringent testing guidelines have created a  rapidly
growing number of people who could benefit from a tissue transplant.

     Writing  in  Foresight,  the  newsletter  of  the Eye Bank Association of
America,  Tom Moore,  EBAA president,  summed up the issues surrounding recent
gains in organ and tissue transplantation:  "Transplantation, like exploration
in outer space,  is relatively new and dramatic.  But with each passing  year,
each  exciting  new  development  in  organ and tissue preservation,  surgical
procedure, and chemical control of rejection,  public awe is replaced by quiet
and  confident  acceptance of transplantation as a medical therapy that works,
and will work even better in years to come as  medical  science  continues  to
perfect  its  tools  and  techniques...The critical need is for more organ and
tissue donors."

     (To receive a copy of the testing guidelines recommended by the  American
Association  of  Tissue  Banks contact:  American Association of Tissue Banks,
1350 Beverly Road, Suite 220A, McLean, VA 22101)

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