Medical Forum / Diseases and Disorders / AIDS / December 2004
Woman Died During Nevirapine Study - AP
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PaulKing - 25 Dec 2004 00:25 GMT >http://story.news.yahoo.com/news?tmpl=story&cid=541&ncid=716&e=7&u=/ap/2004 1216/ap_on_he_me/aids_drug_death
AP Exclusive: Woman Died During AIDS Study
10 minutes ago Health - AP
By JOHN SOLOMON and RANDY HERSCHAFT, Associated Press Writers
A pregnant Tennessee woman who enrolled in federally funded research in hopes of saving her soon-to-be-born son from getting AIDS (news - web sites) died last year when doctors continued to give her an experimental drug regimen despite signs of liver failure, government memos say.
Family members of Joyce Ann Hafford say the 33-year-old HIV (news - web sites)-positive woman died without ever holding her newborn boy. They also said they never were told the National Institutes of Health (news - web sites) concluded the drug therapy likely caused her death.
The family first learned of NIH's conclusions when The Associated Press obtained copies of the case file this month. For the past year, they say they were left to believe Hafford, of Memphis, Tenn., died from AIDS complications but began pursuing litigation to learn more.
"They tried to make it sound like she was just sick. They never connected it to the drug," said Rubbie King, Hafford's sister.
"If it were the disease, solely the disease, and the complications associated with the disease, that would be more readily acceptable than her being administered medication that came with warnings that the medical community failed to get ... to her."
Documents show Hafford's case reverberated among the government's top scientists in Washington, who were monitoring reports of her declining health in late July 2003 as she lay on a respirator.
NIH officials quickly suspected the drug regimen because it included nevirapine, a drug known to cause liver problems, and the case eventually reached the nation's chief AIDS researcher.
"Ouch! Not much wwe (we) can do about dumd (dumb) docs," Dr. Edmund Tramont, NIH's AIDS Division chief, responded in an e-mail after his staff reported that doctors continued to administer the drugs nevirapine and Combivir to Hafford despite signs of liver failure.
Nevirapine is an antiretroviral AIDS drug used since the mid-1990s, and the government has warned since at least 2000 that it could cause lethal liver problems or rashes when taken in multiple doses over time.
NIH officials acknowledge that experimental drugs, most likely nevirapine, caused her death, and that keeping the family in the dark was inappropriate. But NIH usually leaves disclosures like that to the doctors who treated her, officials said.
"We feel horrible that something like this would happen to anyone in any circumstance," said Dr. H. Clifford Lane, NIH's No. 2 infectious disease specialist. "There are risks in research and we try to minimize them."
Jim Kyle, a lawyer representing Regional Medical Center in Memphis where Hafford died, declined comment because of the family's pending litigation. The doctors there referred a call seeking comment to NIH.
The study during which Hafford died recently led researchers to conclude that nevirapine poses risks when taken over time by certain pregnant women.
"Continuous nevirapine may be associated with increased toxicity among HIV-1 infected pregnant women" with certain liver cell counts, the study concluded.
Lane said Hafford should have signed a 15-page, NIH-approved consent form at the start of the experiment specifically warning her of the risks of liver failure. The family says Hafford seemed unaware of the liver risks. They even kept the bottle of nevirapine showing it had no safety warnings.
"My daughter didn't know any of the warning signs," said Rubbie Malone, Hafford's mother and now caretaker of Hafford's new baby and older son. "She never got to hold her baby."
Lane confirmed the nevirapine bottle Hafford received likely wouldn't have had safety warnings because the experiment's rules called for the patient to be unaware of the exact drug effects to avoid patient influence on the test results. That means the consent form would have been her lone warning about potential liver problems, he said.
That 15-page, single-spaced consent form is chock full of complex medical terms like "hypersensitivity reactions" and "pharmacokinetic test." The warning about potential liver problems shows up on the sixth page, where it said liver inflammation was possible and "rarely may lead to severe and life threatening liver damage and death."
Hafford, who was HIV-positive but otherwise healthy, agreed to participate in the NIH-funded research project that provided her multiple doses of nevirapine, also known as Viramune, to protect her soon-to-be-born son, Sterling, from getting HIV at birth.
The project was an outgrowth of earlier research in Africa that concluded the drug could be taken in single doses safely to protect newborns half the time.
"She didn't want her baby to be born with HIV infection if it could be prevented at any cost," said King, her sister.
Hafford died Aug. 1, 2003, less than 72 hours after giving birth. Sterling was delivered prematurely by Caesarean section as his mother was dying. Though premature, he was spared from HIV and is healthy.
NIH's documents suggest Hafford's life might also have been spared if the drug had been stopped when the first liver problems showed up in her blood work two weeks before death.
"This case was particularly unfortunate b/c (because) the PI (principle investigative doctor) didn't stop drug when grade 3 liver enzymes were reported," Dr. Jonathan Fishbein, NIH's chief of good research practices, told Tramont in an August 2003 e-mail.
Fishbein, who is seeking federal whistleblower protection after raising concerns about NIH's practices, told AP that Hafford's death is attributable to a bigger problem in government research.
"This is not just a clinical trial issue this is a healthcare issue. The public expects that diagnostic test results are promptly evaluated and acted on, if need be," Fishbein said. "Sadly, this is but one example where an assessment was not done quickly and it cost this young mother her life."
NIH's official review determined the Memphis hospital failed to react to lab results that showed her liver failure was starting well before she died. "The site had identified that there was a delay in reviewing laboratory evaluations from the clinic visit the week before she presented with clinical hepatitis," an Aug. 15, 2003, report concluded.
The official investigative files cited "drug-induced hepatitis" of the liver as the cause of death.
As is routine after a research-related death, NIH ordered changes to the rules its researchers followed in the nevirapine studies to ensure the early detection of liver problems, the memos show.
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On the Net:
Documents gathered by AP for this story are available at: http://wid.ap.org/documents/nevirapine3.html
National Institutes of Health: http://www.nih.gov
Fishbein's whistleblower Web site: http://www.honestdoctor.org/
Gary Stein - 25 Dec 2004 17:17 GMT Nevirapine Misinformation: Will It Kill?
by John S. James
December 23, 2004: For a few days last week an Associated Press
"exclusive" story touched off a firestorm of media by charging that
side effects of single-dose nevirapine (to prevent mothers with HIV
from infecting their babies during childbirth) had been covered up.
Later the AP quoted responses -- one comparing nevirapine's
distribution in Africa to the notorious Tuskegee Experiment, another
charging that Africans were treated like guinea pigs. In fact there
never was any evidence of a significant risk of side effects from only
a single dose of nevirapine. There is a risk of HIV drug resistance
from using even a single dose of the drug alone, but this is well known
to all AIDS doctors and experts and has never been covered up.
Every day about 1,800 babies are born with HIV, mostly to women who
have no treatment options either for themselves or to prevent the
infection of their child. There is no reason to doubt that single-dose
nevirapine works, and could prevent about half of these infections.
The brief media storm that still threatens the lives of thousands of
unborn children grew out of a bitter dispute between two officials of
the U.S. National Institutes of Health -- one of whom selectively
released "thousands" of documents (according to news reports) to
reporters and/or members of Congress. The danger now is that misleading
stories published around the world will cause patients, doctors, or
even some governments to reject single-dose nevirapine to prevent
mother-to-child HIV transmission, even when no other treatment choice
is possible.
Background
Nevirapine was approved in the U.S. in June 1996, for use in
combination with other antiretrovirals for treating HIV. For this use
it is taken twice a day for as long as the virus is under control.
Later, a study in Uganda from 1997 to 1999 (the HIVNET 012 clinical
trial) found that a single dose of nevirapine given to the mother and a
single dose to the infant reduced HIV transmission to about half of
what it was with a very short course of AZT. This study, conducted as a
collaboration between researchers from Johns Hopkins University and
Uganda and funded by the U.S. National Institutes of Health (NIH), was
published in September 1999. It showed that HIV transmission at
childbirth could be greatly reduced by a very inexpensive and easy
regimen, even when the mother had little or no prenatal care. It is
rightly considered one of the great successes in HIV prevention.
Nevirapine alone is not the best regimen, however. Later it was learned
from the same study that even the single dose sometimes selects for
resistance mutations in the mother's HIV -- a serious problem because
it could make her treatment more difficult in the future. This can be
prevented by treating the mother's HIV if she needs antiretroviral
treatment, which of course should be done anyway -- or by using a much
more difficult regimen of AZT to prevent transmission -- or by adding
other drugs (usually AZT plus 3TC) to suppress the virus while the
nevirapine is slowly eliminated from the body. But still today the
great majority of women with HIV do not have access to any
antiretroviral treatment. Single-dose nevirapine is inexpensive and
easy to deliver -- and many women will not use a longer course of
medication, because they are afraid of the consequences if people
around them learn or suspect that they have HIV.
The recent controversy developed because after the Uganda study had
been published, an NIH audit found that data on possible side effects
had not been reported correctly by the Ugandan staff. This problem in
one trial did not change the known safety of single-dose nevirapine --
which has been tested in many other clinical trials and widely used to
prevent maternal transmission, without side effects. In continuous,
long-term use in HIV treatment, serious or fatal side effects can
occur, as with any antiretroviral. But these are rare, and they can be
prevented with proper medical care, and they do not happen with one
dose. Aside from the HIV resistance problem, there is no evidence of
any significant safety risk from a single dose of nevirapine.
The current dispute arose after NIAID/NIH hired a physician with
clinical-trials monitoring experience, Jonathan M. Fishbein, M.D., in
July, 2003, to help it correct the kinds of deficiencies that had been
found in the study conducted several years earlier in Uganda. The key
issue seems to be whether the reporting problems found in that study
should invalidate the conclusion that single-dose nevirapine is safe
and effective for preventing maternal-infant transmission. Recently Dr.
Fishbein, still a Federal employee, claimed whistleblower status and
used his Web site, http://www.honestdoctor.org, to release selected
documents about problems with the nevirapine study.
Comment
We looked through all the documents on Honestdoctor.org as of December
22, 2004, and found nothing there that raised any new doubt on
single-dose nevirapine -- now established by much more than the one
trial in Uganda. Instead, the documents on that site show the extensive
work that NIH and others were doing, both before and after Dr. Fishbein
was hired, to correct universally acknowledged technical reporting
problems. The goal was and is to re-analyze the Uganda trial in the
light of all available information, both to re-check the conclusions,
and also to improve clinical research in the future, particularly in
developing countries, which often have a steep learning curve in
applying standards created for pharmaceutical-company research in the
West. I have no idea why Dr. Fishbein alleged "widespread scientific
and professional misconduct at the NIH Division of AIDS (DAIDS)" (quote
from Honestdoctor.org).
There is no reason to doubt that single-dose nevirapine works and
reduces HIV transmission to about half of what it would be without
treatment. (It may do better than that, since the comparison group was
not a placebo but a very short course of AZT, which may have had fewer
HIV transmissions than a placebo would have.) The NIH Division of AIDS,
like almost all other experts, wants to focus on public-health efforts
to make preventive and other treatment available, and not derail these
efforts because of technical problems in a trial that ended five years
ago. This is not "scientific and professional misconduct."
AIDS organizations did well last week in answering the misinformation
about nevirapine. But the damage had already been done. The story went
out on December 13, and was totally unexpected because it was tied to
no medical or scientific development; it went around the world
immediately and no answer could catch up. It is possible that children
have already been born with HIV as a result, and that many more will be
infected unnecessarily.
What Can We Learn for the Future?
This is not the last time the AIDS world will face mass-media storms
that carry serious misinformation throughout the world. What can we do
about it?
AIDS needs a major organization dedicated to consensus development, and
able to offer reporters a single entry point to learn what credible
consensus exists on almost any AIDS issue. No position will speak for
everybody, but the process should be open to hearing and understanding
all dissenting views. Two or more incompatible consensus clusters could
emerge, and they would have to be represented by different
organizations. But reporters could immediately find broadly credible
consensus statements, and talk with experts who have worked on an issue
for years. They may still publish misinformation, but at least an
answer could go out with it -- or be clearly missing from their story.
Years ago AIDS had well-known broad policy organizations, like the AIDS
Action Council in Washington DC. But they represented insiders with
their own interests more than a national or world community. For
example, treatment, research, and international issues were mostly
locked out for years -- and usually the only way to have a voice was to
be part of the scene in Washington. Still these organizations served an
important purpose in providing a common policy base for reporters and
others, and we miss that today.
But now we need a new kind of organization that prides itself on
listening and learning from different people (almost like social
scientists exploring what is out there instead of imposing their own
view) -- but then finds and suggests practical, creative ways these
views and movements can work together in a larger whole.
__________________________________________
Communication Note
Ten days into this controversy Dr. Fishbein has a better Web site than
most AIDS organizations do after many years -- immediately raising the
communication standard. AIDS will face new media storms in the future,
and must get its house in order.
Honestdoctor.org is very well organized, allowing readers to see
immediately what is available and navigate to what they want. The site
has a extensive collection of the recent press articles, consistently
and attractively laid out. Under "Definitions" it has a list of
acronyms and a list of people with their titles -- and will have a
glossary and organizational diagrams. When documents are photographed
and displayed as images, they are processed correctly, so that they are
entirely readable and yet download rapidly on any Internet connection.
And last but not least this site has clearly legible type on its main
pages, when most sites have text that is too small, too light, or
without enough contrast between text and background.
In the future, AIDS organizations should ask for volunteer or
professional Web help that can do at least as well. Remember that our
visitors have millions of other pages a few clicks away, and if a site
is hard to read or hard to use, many will leave.
____________________________________________
For More Information
Here are sources for more information on the recent nevirapine
controversy. Except for the last one, they are December 2004 statements
or articles in chronological order.
* December 14, 2004, "Elizabeth Glaser Pediatric AIDS Foundation on
issue of prevention of mother-to-child transmission of HIV/AIDS and
single-dose nevirapine,"
http://www.pedaids.org/press_release_nevirapine_december_14_2004.htm
* December 15, "Project Inform statement regarding the use of
single-dose nevirapine to prevent mother-to-child transmission of HIV,"
http://www.projectinform.org/news/04_12nvppr.html
* December 15, Treatment Action Campaign, South Africa, "Single-dose
nevirapine is safe and effective: But public health facilities must
switch to more effective regimens wherever possible."
http://www.tac.org.za/newsletter/2004/ns15_12_2004a.html
* December 17, the U.S. National Institute of Allergy and Infectious
Diseases, "Questions and answers: The HIVNET 012 study and the safety
and effectiveness of nevirapine in preventing mother-to-infant
transmission of HIV,"
http://www2.niaid.nih.gov/newsroom/Releases/HIVNET012QA.htm
* December 21 The New York Times, "Furor in Africa Over Drug for Women
with HIV,"
http://www.nytimes.com/2004/12/21/international/africa/21aids.html
* December 22, Nature, "Activists and Researchers Rally Behind AIDS
Drug for Mothers,"Nature.December 23, 2004; volume 432, page 935.
* December 25, Science, "Allegations Raise Fears of Backlash Against
AIDS Prevention Strategy,"Science. December 25, 2004; volume 306, pages
2168-2169.
* You can find more background on nevirapine for prevention of mother
to child transmission at
http://womenchildrenhiv.org/
--
John S James
AIDS Treatment News
www.aidsnews.org
> >http://story.news.yahoo.com/news?tmpl=story&cid=541&ncid=716&e=7&u=/ap/2004 > 1216/ap_on_he_me/aids_drug_death [quoted text clipped - 163 lines] > > Fishbein's whistleblower Web site: http://www.honestdoctor.org/
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