Harm from vaccines
Measuring the elimination of disease by
using vaccination programmes is one epidemiological problem. A harder one,
and where the heat is generated, comes from the epidemiological challenge of
showing that the vaccines themselves cause no serious harm. Common minor and
reversible harm (fever, malaise) is one facet of the problem. Rare major and
irreversible harm (autism, inflammatory bowel disease) is another.
In order to tackle both in an effective
way, the Finnish National Board of Health and Public Health started a
long-term country-wide surveillance system to detect serious adverse events
associated with MMR [3]. The system was designed to identify all events that
were too rare to have been identified in a blind crossover study on 1200
twins. A series of seminars was held for public health and other involved
professionals before the project started, and materials were made available
in both official languages (Finnish and Swedish). There was also public information.
In the event of a possible serious
adverse event (defined as any temporal association without limit of time
between MMR and a life-threatening disorder, triggering of a chronic disease
or hospital admission), then a form was completed forwarded to a central
office with a serum sample. A second form and second sample followed two
weeks later. Forms, envelopes and collection tubes were available at child
health centres and hospitals.
Results
The total number of reported
vaccine-associated events in 1.8 million people having 3 million vaccinations
was 437. Of these, potentially serious adverse events occurred in 169 people,
79 of whom went to hospital. These 169 people were subject to serious
scrutiny.
The details of the potentially serious
adverse events are shown in the Table. About half the reported adverse events
could be ascribed to other factors (like other vaccinations given with MMR)
on clinical, serological and epidemiological analyses. No event had an
incidence of more than 1 case per 100,000 doses of vaccine.
There were no cases of autism, and no
cases of ulcerative colitis, Crohn's disease or any chronic disorder
affecting the gastrointestinal tract.
Table: MMR vaccination in Finland - all potentially serious adverse
events in 1.8 ,illion people given 3 million doese of vaccine.
Event
|
Total number of events
|
Number with possible MMR
association
|
Incidence per 100,000 doses of
vaccine
|
|
Death
|
1
|
0
|
0.00
|
|
Allergic disorders
|
|
Anaphylaxis
|
30
|
14
|
0.50
|
|
Urticaria
|
30
|
25
|
0.80
|
|
Asthma
|
10
|
5
|
0.20
|
|
Henoch-Schenein
purpura
|
2
|
1
|
0.03
|
|
Stevens-Johnson
syndrome
|
1
|
1
|
0.03
|
|
Neurologic
disorders
|
|
Febrile seizure
|
52
|
28
|
0.90
|
|
Epilepsy
|
3
|
1
|
0.03
|
|
Undefined seizure
|
4
|
2
|
0.07
|
|
Encephalitis
|
4
|
3
|
0.10
|
|
Meningitis
|
4
|
0
|
0.00
|
|
Guillain-Barré
syndrome
|
2
|
2
|
0.07
|
|
Transient gait
disturbance
|
5
|
5
|
0.30
|
|
Confusion during
fever
|
3
|
2
|
0.07
|
|
Miscellaneous
|
|
Pneumonia
|
12
|
5
|
0.20
|
|
Orchitis
|
7
|
1
|
0.03
|
|
Diabetes
|
3
|
0
|
0.00
|
Other evidence
Other evidence rejecting a causal link
between MMR vaccine and autism comes from a retrospective study of about 500
cases of autism in North Thames [4]. Records of children with autistic
disorders born since 1979were identified, and their clinical details
examined. Immunisation data was obtained from a separate computerised
register.
The results showed that the incidence of
autism (core autism, atypical autism and Asperger's syndrome) rose from low
levels in 1979 to much higher levels by the early 1990s. This was a
continuous trend, with no evidence of a step-up after the introduction of MMR
in 1987. There were no differences in age at diagnosis between those
vaccinated with MMR and those not vaccinated. No other analysis showed any
association between autism and MMR vaccination. There was no temporal
clustering between MMR vaccination and diagnosis of autism.
Comment
Whenever we take a child to be
vaccinated, we are aware that there is a balance between benefit and harm,
just like any medical intervention. The potential for harm from infectious
disease like measles, mumps and rubella is significant. Unvaccinated children
contracting these diseases have a potential for serious and long-lasting
harm. The history of mumps and rubella in Finland [2] makes chilling reading
as the litany of harm from these infectious diseases unfolded.
The effects of measles can be seen from
a recent outbreak in Ireland. The Irish National Disease Surveillance Centre
reports more than 1220 cases of measles in 2000; two children in north Dublin
have died. There is also a report of an outbreak in the Netherlands. More
than 2300 cases arose in a community philosophically opposed to vaccination.
Three children have, 53 hospitalised, four developed encephalitis. That's one
death for every 700 children infected with measles in countries with some of
the best healthcare in the world.
By contrast, harm is much, much less
common. In the Finnish study [3] there was no more than three adverse effects
for every 100,000 doses of vaccines. While even these adverse effects were
best avoided, the balance between benefit and harm is very much on the side
of benefit. There were no cases of autism in 1.8 million people immunised.
There were no cases of inflammatory bowel disease. The rule of three (Bandolier 23)
tells us that we can be 95% confident that autism or inflammatory bowel
disease occur no more frequently than 1 in 600,000 cases of MMR vaccination.
And this is good, solid evidence. The
study was prospective. The study was comprehensive. The study had a long (14
year) follow up. The study had no artificial cut point for parent or
professional to link any childhood problem with MMR vaccination. And it was
big, and supported by other epidemiological studies [4].
The evidence taken to link MMR to autism
and inflammatory bowel disease [5] concerned 12 children referred because of
loss of skills plus gastrointestinal problems. This was associated with MMR
by the parents in eight cases. The authors themselves say that they did not
prove a link, which would be difficult, since anyway eight or nine out of
every 10 children is vaccinated with MMR.
Finland is a small enough county that it
is possible to be in touch with heroes (sharing Sibelius's drinking haunts,
or sniffing the tobacco in Mannerheim's study). Perhaps the lesson is that we
should take people's obvious concerns about adverse effects of healthcare
seriously. People would respect healthcare more if larger prospective studies
were done to collect rare but serious harm information. Bear in mind also
that there is more than one MMR vaccine. The Finnish study relates to only
one of them. One vaccine was withdrawn in the early 1990s [6], and the UK
epidemiological study [5] does not give the make of vaccines used.
References:
1 H Peltola et al. No measles in
Finland. Lancet 1997 350: 1364-5.
2 H Peltola et al. Mumps and rubella
eliminated from Finland. JAMA 2000 284: 2643-2647.
3 A Patja et al. Serious adverse events
after measles-mumps-rubella vaccination during a fourteen-year prospective
follow up. Pediatric Infectious Diseases Journal 2000 19: 1127-1134.
4 B Taylor et al. Autism and measles,
mumps, and rubella vaccine: no epidemiological evidence for a causal
association. Lancet 1999 353: 2026-2029.
5 AJ Wakefield et al.
Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive
developmental disorder in children. Lancet 351: 637-641.
6 MR Kiln. Autism, inflammatory bowel
disease, and MMR vaccine. Lancet 1998 351:1358.
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