1. Again, we should not confuse with the committee’s
recommendations which are mainly for office practice.
Considering the current state of polio eradication in the
country, the committee believes that persisting with OPV
poses significant risks both at the individual and public
segment, vaccine associated paralytic polio (VAPP) at the
former and circulating vaccine derived poliomyelitis (cVDPVs)
at the latter. The move will also provide a timely policy
‘signal’ to Indian policymakers to expedite consultations on
endgame and post-eradication vaccine policy. The recent SAGE
April 2012 Working Group meeting confirmed early universal
IPV introduction (as early as October 2013) integrated into
routine immunization program (before planned April 2014 tOPV
to bOPV switch) of the country [1]. So, even at the public
sector, there is great pressure to introduce IPV to
facilitate gradual albeit staggered OPV removal from routine
immunization.
2. It is indeed a daunting task of how to
strike a balance between individual and public sector use
while formulating any recommendation on polio vaccines
considering the sensitive nature of the polio eradication
program in the country. Since OPV is still in use in the
country and SIAs are still organized, we have decided to
move gradually, hence the sequential schedule. This schedule
will meet our objectives of providing immunity against VAPP
and cVDPV, and at the same time permits the benefits of OPV.
Even WHO has instructed to move from sequential than to all
IPV schedule for countries using OPV during pre-eradication
era [2]. The new IAP Immunization timetable has slots for
Hepatitis-B and Measles vaccines at 6 and 9 months,
respectively. Hence, the new polio schedule will not entail
extra visits.
3. It is true that there is no efficacy
trial of available rotavirus vaccines in the country and
efficacy low in other developing countries. But considering
the huge burden of rotavirus disease in India, even a low
efficacy should translate in to significant number of lives
saved. Higher vaccine efficacy is desirable but should not
delay use of an effective public health tool. Regarding
proper strain match, it should be noted that there is
significant amount of cross-protection offered by the
rotavirus vaccines, and even RV1 provided comparable
protection against non-vaccine strains in the African trial
[3].
4. There is lack of epidemiological data
on the incidence of mumps and rubella in different ages in
the country but it is a common knowledge that all these
diseases are more common amongst school age group of
children. According to most recent unpublished data of the
last 18 months (till August 16th 2012) acquired through
IAP’s IDSurv passive reporting system from pediatricians,
school age group has now emerged as the commonest affected
group for varicella and mumps in the country. Fifty-five
percent of all varicella cases and 65% of all mumps cases
are in the age-group of 5-12 years.
The second dose of MMR vaccine is not a
"booster"; it is intended to produce immunity in the small
number of persons who failed to respond to the first dose.
If we delay these ‘boosters’ to 10 years of age, a
significant number of children will be exposed to these
diseases, will experience breakthrough diseases (varicella
and mumps), and vaccine efficacy especially against
varicella will be compromised. Besides, it is more
convenient to ‘catch’ susceptible children before school
entry than at later age.
1. Meeting of the Strategic Advisory
Group of Experts on immunization, Geneva, April 2012 -
conclusions and recommendations. Available from:
http://www.polioeradication.org/Portals/0/Document/Aboutus/Governance/IMB/6IMBMe
eting/2.11_6IMB.pdf Accessed on September 2, 2012.
2. WHO. Polio vaccines and polio
immunization in the pre-eradication era:WHO position paper.
Wkly Epidemiol Rec. 2010;85:213-28.
3. Madhi SA, Cunliffe NA, Steele D, Witte D, Kirsten M,
Louw C, et al. Effect of human rotavirus vaccine on
severe diarrhea in African infants. N Engl J Med. 2010;362:
289-98.