http://www.wfaa.com/wfaa/articledisplay/0,1002,20550,00.html
News 8 Investigates: Vaccine Safety
Reporter: Valeri Williams
Updated: Feb 23, 2001 at 12:57AM
DALLAS - Most parents trust the government to ensure that the vaccines we inject
into our children are safe. A News 8 Investigation focused on what some call the
questionable science behind getting vaccines licensed in this country. As we've
said before and we want to stress again: traditional childhood vaccinations have
been a good thing.
But what we've chosen to do with this is take a closer look at how some of the
newer vaccines are coming on to the market, and to ask why parents aren't being
told more. "I feel like I took him to the doctor's office and I paid them to
poison my son -- and I didn't know any better," said Melynda Slay. In June 1999,
Slay had her newborn son inoculated with the new RotoShield vaccine.
Vaccine ads from that time promised that RotoShield would help prevent childhood
diarrhea. But within days, Harrison's bowels were dangerously obstructed to the
point of possibly rupturing. "That probably was the worst week I've ever had in
my life because I wasn't sure if my son was going to live or die," Slay
recalled. Federal regulators from the Centers for Disease Control soon
discovered that more than 100 other infants had suffered the same problem.
RotoShield was pulled off the U.S. market in less than 15 months and some are
now questioning how the drug ever received government approval. "These
committees have become the rubber stamp committees for the drug companies to
push their product in the market," said Dr. Erdem Cantekin, a medical
researcher. Cantekin has long been concerned about the financial links between
the pharmaceutical industry and many doctors and scientists who sit on vaccine
approval committees.
He is not alone.
Last summer Rep. Dan Burton (R-Ind.) held Congressional hearings which revealed
that at least half the members of vaccine committees at both the Food and Drug
Administration and the Centers for Disease Control had financial ties to drug
companies developing different versions of the Rotovirus vaccine. "We have had
people who are head of advisory panels who own stock in pharmaceutical
companies," Burton said.
The report found others who received grants or contracts worth hundreds of
thousands of dollars, yet all were granted waivers which let them vote on the
vaccine's approval. "If you own stock in a pharmaceutical company, and you are
on an advisory panel that will be approving or disapproving a vaccine by that
pharmaceutical company and you know it could have an adverse impact on the stock
that you hold in that company, it just might taint your judgment," Burton said.
On the very same day that the CDC's Vaccine Advisory Committee pulled the plug
on RotoShield, it drafted a recommendation for another vaccine called Prevnar.
News 8's investigation found that out of 12 committee members, four had
financial ties to the drug company making Prevnar. At the FDA, three out of 12
committee members received waivers for conflicts of interest so they could vote
on Prevnar's license. Among them was Dr. Robert Daum, the newly-elected chairman
of the committee. He said his conflict amounted to research on another vaccine
for children at another company.
"You have to understand I still drive my 1989 Toyota, and the door on the right
side still doesn't open. Nothing good happened to me," Dr. Daum said. "They're
still selling God-knows how many million doses a year now for American Home
Products. I don't benefit from that. Nothing has changed in my life." Daum
admitted, however, that his role is "a very fine line." Daum and others argue
that there is a very limited list of experts within the world of vaccine
research. They say that in order to have the best professionals on the
committees, there must be acceptance of conflicts of interest.
"No man can serve two masters," Cantekin countered. "I could find 100 competent
scientists and doctors to put on these committees which are better than they
have. All of whom don't have any conflict of interest and have not taken a
single dollar from anybody." He and others claim all this chumminess has made
government committees unwilling to challenge poor testing procedures in studies
of a proposed vaccine's safety. For example, here are the results of a clinical
trial of Prevnar in 38,000 California children:
According to the drug company's own documentation, children receiving Prevnar
with other vaccines had more seizures, more rashes, higher fevers and other side
effects than children who received the control vaccine. And the real surprise?
The control vaccine in the testing was not a placebo, but another experimental
vaccine that was still being tested. Dr. Daum defended the testing procedure. "I
think it makes for better parent compliance and more willingness to participate
to have a control that would actually benefit from receiving something, and not
saline. I wouldn't want to submit my child to an experimental protocol where
there was a chance he just going to get a dummy shot."
Barbara Fisher is the only member of the FDA's Vaccine Committee who is not a
doctor or a scientist; she's a consumer advocate and the only committee member
to have voted against issuing a license for Prevnar. Fisher said the study
leading up to the license fails to measure up --
ethically, morally or scientifically.
"What's scientific about that? That every time something bad happens after
vaccination it's 'coincidence'? That's not science, that's politics," said
Fisher. Prevnar was licensed to vaccinate infants against certain strains of
meningitis, pneumonia and bacteremia -- horrible diseases which combined affect
fewer than 150,000 children each year.
Weighing the risks of vaccination versus the risks of disease is a tough
decision for any parent, but what many parents have told us upsets them is that
they were surprised -- and scared -- by how much information they did not know.
Rep. Burton said he is calling for another Congressional hearing on the approval
of Prevnar this spring.
Rotavirus Vaccine Urged for Babies
RotaTeq Recently Won FDA Approval
By Justin Gillis
Washington Post Staff Writer
Wednesday, February 22, 2006; A08
Every healthy newborn in the United States should receive a new vaccine designed
to protect against an intestinal germ called rotavirus, a federal advisory panel
decided yesterday as it set aside theoretical concerns about the vaccine's
safety.
The decision means that pediatricians are likely to recommend three doses of the
oral vaccine for nearly every child at age 2 months, 4 months and 6 months,
beginning almost immediately. The vaccine won approval from the Food and Drug
Administration on Feb. 3, and some doctors have received supplies of it.
The recommendation for universal use of the vaccine was approved at a meeting of
the Advisory Committee on Immunization Practices, the federal panel that sets
vaccination policy in the United States. It comes nearly seven years after an
earlier rotavirus vaccine was withdrawn from the market for causing a
potentially life-threatening form of intestinal blockage in some babies.
Vaccine-safety advocates are urging parents to be wary of the new vaccine
because of that history. The federal Centers for Disease Control and Prevention
and the manufacturer, Merck & Co. Inc. of Whitehouse Station, N.J., have
promised elaborate studies to catch any safety problems. Merck is selling the
vaccine under the brand name RotaTeq.
Merck has tested the vaccine in about 70,000 babies in 11 countries, one of the
biggest vaccine trials ever conducted. That test ruled out a safety problem
similar to the one that felled RotaShield, an earlier rotavirus vaccine
developed by Wyeth, a drugmaker in Madison, N.J. But doctors said it is
impossible to design a test big enough to catch all possible side effects that
might show up once the product is used in millions of children.
RotaTeq "generally appears to have a better safety profile than the earlier
vaccine," said Umesh D. Parashar, a medical epidemiologist at the CDC. "But at
the same time it's something we'll continue to look at, and hopefully confirm
absence of risk."
RotaTeq is expected to be one of the most expensive vaccines ever marketed, with
Merck listing it at $187.50 wholesale for the three-dose series. That means many
doctors are likely to charge more than $300 retail, putting the Merck product in
league with Prevnar, an expensive Wyeth vaccine that has been widely used in the
United States for five years. Prevnar, which protects children against certain
types of pneumonia, became the first vaccine to meet the pharmaceutical
industry's standard for a blockbuster product, with sales exceeding $1 billion a
year.
The development of such high-priced vaccines is causing strains, particularly in
state-sponsored vaccination programs for certain low-income children. But it is
also drawing new manufacturers into the vaccine market, which many drug
companies had abandoned in the 1980s and 1990s, citing too little profit.
RotaShield appeared on the market in late 1998 but was pulled less than a year
later after a handful of babies that received it developed a serious intestinal
problem called intussusception, a type of bowel obstruction that occurs when the
intestine folds in on itself, like a collapsing telescope.
The problem occurs naturally, albeit rarely; it showed up at a sharply elevated
rate in babies who received RotaShield. Intussusception is life-threatening for
some babies, though doctors can usually treat it.
Many people have never heard of rotavirus, but it is one of the most common
causes of childhood illness -- many ailments that parents or pediatricians
describe as "stomach flu" are caused by rotavirus infection. Virtually every
child in the world contracts the virus repeatedly by age 5, gradually building
immunity.
Most children get over rotavirus at home, but at least 55,000 American children
are hospitalized every year after becoming dehydrated from vomiting and diarrhea
associated with the infection. Fifty to 60 of them die, but it is a different
story overseas, where babies often do not receive good medical care and hundreds
of thousands die every year.
RotaTeq contains live, but weakened, strains of rotavirus designed to build
immunity without causing illness.
© 2006 The Washington Post Company
http://www.redflagsweekly.com/conferences/vaccines/2004_jan12.html
HYPING VACCINES: AN INVESTIGATION
Chickenpox, Lyme, Rotavirus, And A Highly Revealing Analysis Of Flu
Statistics
By RFD Columnist, Dr. F. Edward Yazbak
TL Autism Research
Falmouth, Massachusetts
E-mail: tlautstudy@aol.com
Years ago, the description of diseases used to be accurate. Smallpox was a
very dreaded, serious, and often fatal illness. Certainly, no parent wished
smallpox on his children. Chickenpox on the other hand was a relatively
benign illness: a low-grade fever, an itchy rash and a week out of school.
Like all childhood illnesses, it was worse in adults and parents were
actually hoping that their children could “catch chickenpox” and be finished
with it for the future.
In 1995, chickenpox suddenly became a major health problem. Six children were
reported to have died from chickenpox; frequent and repeated TV coverage
lasted for weeks without anyone mentioning that two of the six children had
leukemia and the others were on cortico-steroids. Concurrently, chickenpox
became a major economical disaster that was gravely impacting the United
States economy, as working mothers stayed home to give their children Aveeno
baths and syrup to relieve itching. A short time later, the chickenpox
vaccine was cheerfully and successfully launched.
Historically, epidemics have occurred in cycles. Experts in infectious
diseases could often predict them. The number of unvaccinated children
increased during several successive years of low spread and when the
reservoir was full, an outbreak, an epidemic or a pandemic occurred. Children
then developed a solid immunity that was boosted successfully during
subsequent outbreaks. Recently, in the United States, a new epidemiological
trend has become very evident: MBAs and Marketing Directors predict epidemics
that are then orchestrated to occur, on cue, when a new vaccine is due to be
launched.
A flurry of interest about Lyme disease started in the Northeast and Upper
Midwest in 1996-97. It promptly snowballed into a major news campaign in the
targeted areas, where indeed there were increasing numbers of cases, many
with serious long-term complications. In 1998, the LYMErix vaccine received
conditional approval by the FDA and was welcome in the geographical locations
where the disease was common and often devastating. Unfortunately, it was
soon discovered that the vaccine itself had major side effects and doctors
became disenchanted with its use. Since the
manufacturer discontinued production of the vaccine, the newspaper articles,
experts’ interviews and television “health minutes” on Lyme disease have
completely stopped. It is almost as if the disease has totally disappeared,
when it obviously has not.
Years ago, we did not talk much about the rotavirus. Most people did not even
know the name and some thought that it was “RotoVirus”, because it kept
spreading “around and around” nursery schools. We were happy to tell the
parents the baby had “some kind of a virus”, that penicillin was not going to
help, that we were seeing many children with the same symptoms, and that they
improved after a few days. We then suggested liquids and a limited diet and
the reassured parents left with their little ones, to stop at their
neighborhood drugstore for Pampers and Pedialyte. We obviously were immensely
more alarmed when a child had salmonella, shigella, cholera, pathogenic E.
Coli and staphylococcus gastro-enteritis.
Rarely, the babies with rotavirus infections became dehydrated. They were
then brought to a holding unit at the hospital, given intravenous fluids and
discharged before 23 hours. Officially, they had not been actually “admitted”
to the hospital.
Suddenly, in 1998, every newspaper and every TV news program started
continuous reporting on the rotavirus. Overnight, the rotavirus became a
household name and the most common cause of diarrhea. It also killed
thousands of babies. The fact that the deaths occurred in Third World
countries was rarely, if ever, mentioned. In addition, the news programs
warned that the economy of the United States was once more in dire danger,
that HMOs were almost bankrupt trying to keep up with the rising costs of
hospitalizations and that millions of hours were lost in the workplace during
the rotavirus season; after all, mothers of affected children had to stay out
of work to care for them and could not drop them off, as usual, at schools
and day-care centers. In the midst of that intense “information” campaign,
the rotavirus vaccine “Rotashield” was released to the joy and relief of The
Centers for Disease Control and Prevention (CDC), pediatricians and parents.
Because three doses were needed, the delight of the manufacturer and
stockholders was tripled. One could almost imagine them visualizing a set of
gorgeous blond triplets singing “Triple the Doses, Triple the Dough” using
the old and proven tune of “Double the Mint, Double the Fun”.
And then, something went wrong, very wrong. It became quickly evident that
some infants who received the vaccine developed intussusception, a form of
intestinal obstruction and that a few died. The CDC, to its credit, acted
promptly and suspended the administration of the Rotashield in July 1999,
just a few months after it was released. In October 1999, it issued a
detailed statement that started with the following two paragraphs: “The
Advisory Committee on Immunization Practices (ACIP) decided that Rotashield,
the only U.S.-licensed rotavirus vaccine, should no longer be recommended for
infants in the United States. This action was based on the results of an
expedited review of scientific data presented to the ACIP by CDC in
cooperation with the FDA, NIH, and Public Health Service officials, along
with Wyeth-Lederle. Data from the review indicated a strong association
between Rotashield and intussusception (bowel obstruction) among some infants
during the first 1-2 weeks following vaccination. Use of the vaccine was
suspended in July pending the data review by the ACIP. Parents should be
reassured that their children who received rotavirus vaccine before July and
remain well are not at increased risk for intussusception now.
Rotavirus is a severe diarrheal illness in childhood that accounts for more
than 500,000 physician visits and approximately 50,000 hospitalizations each
year among children less than 5 years of age. Symptoms include fever, an
upset stomach and vomiting followed by diarrhea, which may lead to
dehydration. This results in $264 million in direct medical costs and $1
billion in total costs to society.
The rotavirus media blitz came to a screeching halt and for four years,
interest in the “designer diarrhea” has ranged between nil and minimal.
Children with the disease had once again “some kind of a virus.”
However, this is due to change AGAIN. Yes indeed, very soon, we will be
undoubtedly bombarded once more with a barrage of relentless rotavirus
propaganda, diarrhea will become extremely serious in the United States and
the cost to the National economy will become even more staggering as the
launching of the “new, safe, effective and improved” rotavirus vaccine is
carefully orchestrated. This second vaccine has been developed for years and
has been ready to go. If rotavirus disease is so serious, the new formulation
should have been released already “to save lives”. But it was probably felt
that releasing it too soon after the first fiasco would not have been a good
business move and as it happens sometimes, when it comes to the care of
children, MBAs may overrule MDs. So everyone involved had to wait patiently
for the opportune time. Indications are that 2004 will be the year.
For years, the inactivated flu vaccine has been recommended for the elderly.
It was also recommended for children and adults at risk, mainly those with
chronic debilitating conditions. Recently, annual vaccination of all children
aged 6 to 23 months and older children and adolescents in their household was
recommended. Because of parental concerns over thimerosal, a
“preservative-free” pediatric flu vaccine was expressly produced for the
2003-2004 season. Marketing experts decided that the description of the
product as “preservative-free” was less controversial than “mercury-free”.
A live intranasal flu vaccine, FluMist, was also recently licensed. As per
the manufacturer: “Before you get the flu, ask your health care professional
about new FluMist — the first nasal flu vaccine that helps prevent the flu
where the flu virus typically enters your body — your nose. FluMist helps
prevent the flu for the entire season. FluMist is indicated for active
immunization for the prevention of disease caused by influenza A and B
viruses in healthy children and adolescents, 5 to 17 years of age, and
healthy adults, 18 to 49 years of age. FluMist is not indicated for
immunization of individuals less than 5 years of age, or 50 years of age and
older.”
It is not exactly clear why suddenly healthy infants, children and adults
under the age of 50 needed to be vaccinated. As expected, an outbreak of flu
occurred in the fall of 2003. A massive barrage of “information” was
orchestrated and news programs were saturated except for two days after the
capture of Saddam Hussein. There was special emphasis on pediatric cases and
particularly pediatric deaths.
According to the 2003 “Red Book” of the American Academy of Pediatrics (AAP),
the Report of the Committee on Infectious Diseases and the pediatrician's
reference on the subject, par excellence: “Influenza classically is
characterized by sudden onset of fever, often with chills or rigors,
headache, malaise, diffuse myalgia, and a nonproductive cough. Subsequently,
the respiratory tract signs of sore throat, nasal congestion, rhinitis, and
cough become more prominent. Conjunctival injection, abdominal pain, nausea
and vomiting can occur. In some children, influenza can appear as an upper
respiratory tract infection or as a febrile illness with few respiratory
tract signs. In young infants, influenza can produce a sepsis-like picture
and occasionally can cause croup, bronchiolitis or pneumonia. Acute myositis
characterized by calf tenderness and refusal to walk may develop after
several days of influenza illness…” (p. 382)
Epidemiology and Prevention of Vaccine-Preventable Diseases is an important
CDC publication that is often used as a resource. The following is from page
249 of the 5th Edition: “The severity of influenza illness depends on the
prior immunologic experience with antigenically related virus variants. In
general, only around 50% of infected persons will develop the classic
clinical symptoms of influenza.
‘Classic' influenza disease is characterized by the abrupt onset of fever,
myalgia, sore throat, and non-productive cough. The fever is usually
101-102°F, and accompanied by prostration. The onset of fever is so abrupt
that the exact hour is recalled by the patient. Myalgias mainly affect the
back muscles. Cough is believed to be the result of tracheal epithelial
destruction. Additional symptoms may include rhinorrhea (runny nose),
headache, substernal chest burning and ocular symptoms (e.g. eye pain and
sensitivity to light.)”
All of us who have had the flu remember the aches and pains, and how much our
eyes hurt when we moved them. We remember the cough and the fever and the
sick stomach. We remember how we felt tired and fatigued for a long while. We
actually remember our flu encounters so well that we feel sick all over again
watching that great commercial with the poor actor looking so miserable and
enumerating all his symptoms.
MMWR
For years, the Mortality and Morbidity Weekly Report published by the CDC has
been the most reliable source of accurate information on diseases. The CDC
was so careful about every statement and figure that it included the
following disclaimer in every report on the Internet: All MMWR HTML versions
of articles are electronic conversions from ASCII text into HTML. This
conversion may have resulted in character translation or format errors in the
HTML version. Users should not rely on this HTML document, but are referred
to the electronic PDF version and/or the original MMWR paper copy for the
official text, figures, and tables. An original paper copy of this issue can
be obtained from the Superintendent of Documents, U.S. Government Printing
Office (GPO), Washington, DC 20402-9371; telephone: (202) 512-1800. Contact
GPO for current prices
The MMWR of December 19, 2003 [/ 52(50);1232-1234] covers the period between
December 7 and 13. It can be accessed here
Important portions will be copied verbatim and footnotes will be
insertedbetween brackets, immediately after the corresponding statements
forclarity (italics). My comments will appear in bold.
Influenza activity in the United States continued to increase during December
7--13, 2003*. [* Provisional data reported as of December 17] The proportion
of patient visits to sentinel providers for influenza-like illness (ILI)†
overall was 7.4%, which is above the national baseline§ of 2.5%. [†
Temperature of >100.0º F (>37.8º C) and cough and/or sore throat in the
absence of a known cause other than influenza] [§ Calculated as the mean
percentage of visits for ILI during non-influenza weeks, plus two standard
deviations. Wide variability in regional data precludes calculating
region-specific baselines and makes it inappropriate to apply the national
baseline to regional data.] The above symptoms are not flu symptoms. They are
certainly not those listed in the Red Book and the quoted CDC publication and
they are certainly not those that the average person attributes to the flu. A
child or an adult with just such a low-grade fever and a cough or a sore
throat can hardly be said to have Influenza. The bar has been substantially
lowered if the CDC includes such cases in the national flu statistics,
whatever the intention. Similarly, one must wonder why and how the 2.5%
baseline for low-grade fever, sore throat or cough was decided on. Certainly
every primary physician and nurse practitioner will easily assert that
year-round, patients with such symptoms amount to a greater percentage of
visits. The unrealistic 2.5% figure lowers the bar further.
During the reporting week of December 7--13, World Health Organization (WHO)
and National Respiratory and Enteric Virus Surveillance System (NREVSS)
laboratories reported testing 3,814 specimens for influenza viruses; 1,365
(35.8%) were positive. Of these, 262 were influenza A (H3N2) viruses, 1,080
were influenza A viruses that were not subtyped, and 23 were influenza B
viruses.
Since September 28, WHO and NREVSS laboratories have tested 32,854specimens
for influenza viruses; 9,464 (28.8%) were positive. Of these, 9,395 (99.3%)
were influenza A viruses, and 69 (0.7%) were influenza B viruses. Of the
9,395 influenza A viruses, 2,113 (22.5%) have been subtyped; 2,112 (>99.9%)
were influenza A (H3N2) viruses, and one (<0.1%) was an influenza A (H1)
virus. All 50 states have reported laboratory-confirmed influenza this
season. The fact that only 1/3 of the submitted specimens were positive is of
some concern and may suggest that most of the patients tested may not have
had the flu. A more careful clinical diagnosis, based on more appropriate
criteria, would have yielded reasonable incidence figures and higher
confirmation rates. One can only imagine the uproar if surgeons performed
appendectomies on patients who vomited once, had a low-grade fever and a
vague tummy ache.
Of 269 influenza viruses collected by U.S. laboratories since October 1 and
characterized antigenically by CDC, 265 were influenza A (H3N2) viruses, two
were influenza A (H1) viruses, and two were influenza B viruses. The
hemagglutinin proteins of the influenza A (H1) viruses were similar
antigenically to the hemagglutinin of the vaccine strain A/New
Caledonia/20/99. Of the 265 influenza A (H3N2) isolates that have been
characterized, 62 (23%) were similar antigenically to the vaccine strain
A/Panama/2007/99 (H3N2), and 203 (77%) were similar to a drift variant, A/Fujian/411/2002
(H3N2)**. Both influenza B viruses characterized were similar
antigenically to B/Sichuan/379/99. [** Although vaccine effectiveness against
A/Fujian/411/2002-like viruses might be less than that against
A/Panama/2007/99-like viruses, the current U.S. vaccine probably will offer
some cross-protective immunity against the A/Fujian/411/2002-like viruses and
reduce the severity of disease.] It is imperative to point out that 77% of
the cultures antigenically identified by the CDC did not match the strain in
the flu vaccine this year. In addition, one must question the first statement
in the footnote “Although vaccine effectiveness against A/Fujian/411/2002-like
viruses might be less than that against A/Panama/2007/99-like viruses”. The
use of the word “might” seems inappropriate. The vaccine effectiveness
against A/Fujian/411/2002-like viruses is definitely less than that against
A/Panama/2007/99. The bar has been lowered further. The authors were wise to
use the word “probably” in the following sentence: the current U.S. vaccine
probably will offer some cross-protective immunity against the A/Fujian/411/2002-like
viruses and reduce the severity of disease. Commenting on that possibility,
an infectious disease specialist said in an interview: “The available flu
vaccine will prevent death”.
* * *
On December 19, 2003, a MMWR Dispatch was also published by the CDC
(52:1-2). Reported by J Wright, DVM, A Likos, MD, N
Bhat, MD [EIS officers, CDC], it was entitled Update: Influenza-Associated
Deaths Reported Among Children Aged <18 Years --- United States, 2003--04
Influenza Season.
Since October, 42 influenza-associated deaths among children aged <18 years
have been reported to CDC. All patients had influenza virus infection
detected by rapid antigen testing or other laboratory testing methods. The
fact that all 42 deaths, according to the authors, were
“influenza-associated” does not mean that the cause of death was the
influenza, of course. The second sentence serves to “reinforce” the first and
to convince anyone with doubts. But it cannot change the fact that detection
of influenza viral infection in the laboratory does not prove that “The Flu”
was the cause of death.
Among the 42 reported deaths, 20 (48%) patients were male, and 21 (50%) were
female; the sex of one patient was not reported. Twenty-three (55%) of the
children were aged <5 years, and 13 (31%) were aged 6--23 months. The median
age was 4 years (range: 9 weeks--17 years). Seventeen (40%) of the children
had underlying chronic medical conditions; the previous medical status for
four (10%) children was unknown. Among the 21 patients who had no underlying
chronic medical condition, five had invasive bacterial co-infections,
including three caused by methicillin-resistant Staphylococcus aureus (MRSA),
one by Streptococcus pneumoniae, and one by Group A streptococcus. Three
children with underlying chronic medical conditions had invasive bacterial
co-infections, including one caused by MRSA, one caused by Streptococcus
pneumoniae, and one caused by Neisseria menigitidis. One must wonder why in
a review of national importance, an
effort was not made to identify the sex of one child and the past history of
four others. The underlying chronic conditions (some children had more than
one) were: Lupus 1, cerebral palsy 2, chromosomal abnormality 1,
hypothyroidism 1, gastroesophageal reflux 1 and biliary atresia 1. Two
children were developmentally delayed and 2 had mental retardation. Three
children had asthma, one had received a heart transplant, 3 had seizure
disorders, one had Pierre Robin Syndrome and the last one had the syndrome of
Cornelia de Lange. The available information is not enough to determine the
role of the influenza infection in the demise of these children. Eight (19%)
of the 42 children had fulminating systemic infections. At least in these,
influenza was not the primary cause of death. [The immediate cause of
death is listed first on a death certificate. To its right, the physician
must enter the interval between onset and death. In the following three
lines, underlying and associated causes are listed in order of significance
with the intervals between onset and death.]
What may be tragic is the fact that, because of the continuous bombardment
with reports of the “epidemic”, some parents, believing that their children
just had the flu, may have waited too long to seek medical advice for
meningitis, septicemia or pneumonia. Similarly, a busy ER physician seeing
a multitude of children brought by parents concerned about the “major flu
epidemic” going on, may have thought that the child he was sending home,
simply had the flu, like all the others. Symptoms of early bacterial
meningitis are easily mistaken for the flu. This was evident in New Hampshire
around Christmas when an 18-year old co-ed was seen in an Emergency Room,
diagnosed with the flu and discharged without further testing only to die of
meningococcal meningitis a short time later. The cases of the 5 children in
the MMWR report, who died of invasive bacterial illnesses, and who had no
underlying condition, should be thoroughly investigated. The fact that they
“tested positive for the flu” may be etiologically irrelevant.
Influenza vaccination status was available for only seven patients; five
(aged 1 year, 14 months, 20 months, 3 years, and 8 years) were not
vaccinated; two (aged 21 months and 5 years) received 1 dose of influenza
vaccine; however, their previous vaccination history was unknown. Influenza A
viruses were isolated from 11 (26%) patients; 29 (69%) infections were
detected by rapid diagnostic testing or by direct fluorescent antibody
testing of respiratory specimens. In two (5%) patients, evidence of influenza
A virus infection was solely by immunohistochemical staining (IHC) of
postmortem tissue specimens at CDC. Five cases that were positive by rapid
antigen testing of respiratory specimens also were tested by IHC; all five
also had influenza A viral antigens detected in bronchial epithelium tissues
obtained at autopsy. CDC continues to work with state health departments to
collect additional information on all cases. The lack of information on the
vaccination status of 83% of the deceased children is disturbing and
indicates a further lowering of the bar. Positive viral cultures are more
definitive proofs of viral presence. The fact that viral cultures were
positive in only 26% of cases is important. On the other hand, a positive
viral culture is not absolute proof that influenza is the cause of death;
without more details, its significance is hard to determine.
Lastly, the fact that the events that followed vaccination of seven children
were not made available for review is also of concern.
Before December 2002, there were 12 reports to the Vaccine Adverse Events
Reporting System (VAERS) of children under 10, who expired shortly after
receiving the inactivated flu vaccine. It is accepted that only a small
percentage of actual reactions are ever reported to VAERS. In 11 cases, the
flu vaccine was the only vaccine administered. All children had serious
underlying chronic illnesses. Five children died within 24 hours of
vaccination and 2 within 72 hours.
* * *
Influenza outbreaks are usually widespread and of uniform intensity. So, was
the flu a global emergency this past fall, as it seemed to be in the United
States? Specifically, what was the situation worldwide during the week of
December 7 to 13?
According to a December 23, 2003 report of the World Health Organization
(WHO) entitled “Widespread influenza activity persists in northern hemisphere
- update 5” Disease Outbreak Reported that covered Week 50, 7 December – 13
December 2003: “ Influenza activity associated with influenza A(H3N2)
viruses continues to increase in Africa (Tunisia), Europe (Czech Republic,
Denmark, Finland, Italy, Norway, Russia, Switzerland, Russia Federation and
Ukraine) and North America (the United States), and persists in France and
some parts of Canada. In other European countries (Portugal, Spain and the
United Kingdom) and most parts of Canada, activity has declined.
Most influenza infections this season have been attributed to influenza
A(H3N2) viruses. The majority of viruses antigenically characterized so far
have been shown to be A/Fujian/411/2002-like; the rest have been
A/Panama/2007/99-like. There have been few reports of influenza A/Fujian/411/2002-like
virus detections from Asia …
An avian influenza A(H5N1) outbreak in poultry in a chicken farm in the
Republic of Korea was reported on Tuesday 16 December. The outbreak was
recognized by the death of about 19 000 chickens. Surviving chickens in the
affected farm were slaughtered. As of Monday 22 December 2003, nine poultry
farms in 4 provinces were found to be infected by avian influenza. About one
million chickens and ducks are to be culled. The A(H5N1) strain isolated is
being examined to determine its relation to other influenza A(H5N1) viruses,
which emerged in Asia recently. So far no human A(H5N1) cases have been
reported. [http://www.who.int/csr/don/2003_12_23/en/]
It is not unusual for flu outbreaks to be increasing in the second week of
December. It is unusual that this outbreak was already decreasing in Spain,
Portugal, the United Kingdom and most of Canada. In fact, the British vaccine
authorities were so sure the flu season was over that they were
happy to sell their leftover stock of flu vaccines to the CDC. Over all, it
should be reassuring to note that a shorter paragraph was needed to summarize
the influenza activity globally in the week in question (December 7 to13)
than to describe what happened in chicken farms in Korea.
Over here, the CDC was publishing on December 11, a long and detailed report
entitled Flu Vaccine Supply—2003-04 Season [http://www.cdc.gov/flu/fluupdate.htm]
which started with the following statement: “The strong consumer demand for
influenza vaccine this year will likely exceed the consumer demand seen in
previous flu seasons. Some healthcare providers have used — or may use —- all
of their supplies of influenza vaccine. In past years, supply has generally
been sufficient to meet demand. This year, however, a strong demand has
continued for longer than usual into the month of December. At a time when
flu vaccination clinics are typically winding down, people are still seeking
vaccination.
That certainly says it all.
The early reports of vaccine shortage resulted in sustained greater demand.
People who had never been interested in previous flu vaccination programs,
when the vaccine supply was plentiful, were lining up this past fall before
the “vaccine ran out”. To its credit, the CDC was able to provide
vaccines for anyone who wanted to be vaccinated. Vaccine supplies were
redistributed to areas with increased demands and more stock was imported
from abroad. People lined up in clinics on a first come first serve basis and
in certain sites, had to pick up little pink numbered tickets like those used
at delicatessen counters. The vaccine was also administered in drugstores and
senior centers.
The owners of a retail chain considered distributing FluMist in their stores
but changed their mind when they realized that Christmas shoppers may not be
too thrilled if they were sneezed upon and showered with live viruses from
vaccinated folks. Computer-literate folks searched on eBay.
In New York, two entrepreneurs without medical or nursing training, rented
space in an apartment building and started administering the flu vaccine to
anyone who could afford it. [They were arrested]. In Florida, thousands of
doses of an unapproved vaccine almost found their way to the people.
Some HMO's became convinced that the flu was a National Emergency and decided
that distribution of the vaccine was the patriotic duty of all healthcare
providers. This resulted in payments that were less than the cost of the
product and its administration forcing some physicians to refer their private
patients to clinics.
Earlier in the season, the makers of FluMist were concerned about the limited
popular interest and offered $25 refunds to stimulate sales. Recovery was
quick when the shortage of the inactivated vaccine was publicized. The
perfect example of a win-win situation was the recent offer by the CDC to
purchase a substantial number of doses of FluMist at $20 a dose.
Over all, the sales of flu vaccines exceeded everyone's expectations. Large
bonuses must have certainly been distributed and everyone in flu vaccine
companies must have had wonderful holidays. That was indeed a very good year
and it would not be surprising if textbooks for Business 101 were rewritten
to include a chapter entitled: “The Marketing of an Epidemic: The Flu of
2003”.
Some of the following questions have been asked. Many more should be.
How effective is the inactivated flu vaccine? Is it safe? Does it still have
serious side effects? Does it cause long-term problems? Do the benefits
outweigh the risks for everyone including debilitated children and adults?
Should preservative–free products be developed for adults and particularly
the elderly? How are the strains for the upcoming season vaccine really
chosen? Do MDs get vaccinated yearly? How about the owners of the company
that manufactures the vaccines?
How good is the live flu vaccine? Will it be considered “safe and effective”
after a few years? Do we really need to vaccinate every one?
How serious was this Flu Epidemic?
Why is Medicine changing so much?
Back to page
