POST 00428E : PROTECTION OF MORE COLD-SENSITIVE VACCINES
Follow-up on Posts 00391E, 00400E, 00412E and 00419E
19 February 2002
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Carib Nelson from PATH is sharing with us quite an
interesting idea about the cold chain. Here is his integral contribution.
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Given the increasing awareness of the possible vaccine damage due to
freezing and the fact that some vaccines are freeze tolerant while others
are fairly heat tolerant, why don't we consider a 2-track cold chain?
One track, the existing cold chain, could handle the freeze-tolerant
vaccines OPV, measles, and BCG). The other track, a cool chain, could handle
the heat-tolerant, but freeze-sensitive vaccines (HepB, TT, DTP). The cool
chain could use a variety of non-freezing options to get the vaccine from
the central stores to the child. These cool chain options could include
transport at ambient temperature; air-conditioned room storage, cool
refrigerators (domestic refrigerators set at 15C), ambient temperature
outreach, evaporative coolers, or other cooling approaches. What makes this
possible are VVMs on these heat tolerant vaccines. They provide instant
feedback about whether vaccines have been exposed to too much heat . We no
longer need to be so conservative about he 2-8C cold chain for vaccines that
don't require 2-8C environments (and that are harmed by the sub-zero
environments that frequently accompany a 2-8C edict).
Different countries and regions could easily experiment with some of these
different options by running VVM-labeled vaccines through some different
scenarios. This is what PATH and the Indonesian MOH are doing in Indonesia
where hepatitis B vaccines are being transported from the national to
province level at ambient temperatures, stored at district level in air
conditioned offices, transported to health centers in cold boxes without
ice, stored out of the cold chain at the health center, and then stored at
midwives homes and taken for birth-dose outreach at ambient temperatures. So
far this experiment is working well without any vaccine spoilage due to heat
exposure AND reduced costs for vaccine transport and storage.
Again, VVMs provide the ultimate in easy-to-access information about the
vaccines' heat exposure at any point in this cool chain.
Taking these heat-tolerant vaccines partially or completely out of the
current cold chain would increase cold chain capacity, reduce distribution
costs, and reduce freeze damage. Significant potential advantages!
Carib Nelson
Technical Officer
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