POST 00480E : PROTECTION OF MORE COLD-SENSITIVE VACCINES
Follow-up on posts 00391E, 00400E, 00412E, 00419E, 00428E and 00475E
29 July 2002
________________________________________________________________
Carib Nelson (mailto:[log in to unmask]) from PATH is responding to Elly
(Post 00475E) and Anil Varshney (mailto:[log in to unmask]) from Health
Care Consultancy Services, New Delhi,
is also sharing some thoughts and suggestions.
________________________________________________________________
I don't see any problem in transporting vaccines on outreach without ice or
ice packs. While it is unfortunate that VVMs are not yet on all vaccines,
it seems fortuitous that OPV is the vaccine that got VVMs. Since it is the
least stable vaccine, it would seem reasonable to assume that in an
outreach box with a mix of vaccines, if the OVP VVM is still OK then the
others vaccines should be OK as well. Uganda seems relatively cool and the
OPV VVM reaches endpoint after 9 days at 25°C so a few hours or even days
of no-ice outreach shouldn't be a problem, even if the vaccines have had
some prior heat exposure.
One finding from Indonesia, where we transported vaccines without ice, was
the importance of keeping the vaccines and VVMs out of light. We found that
the VVMs reach endpoint more quickly when exposed to light, even indirect
light inside a building. Transporting vaccines in cold boxes or vaccine
carriers, though without ice, protects them from light and helps make sure
people recognize them as vaccines.
The only potential problem with no-ice outreach would seem to be the
practice of keeping the reconstituted measles and BCG chilled at the
outreach session. Without ice this would not be possible. Is it really
necessary to keep them cool after reconstitution or would a couple of hours
at 25°C be OK?
Carib Nelson
Technical Officer
Program for Appropriate Technology in Health (PATH)
_______________________________________
The points raised by Elly are very important from harsh field conditions.
Outreach usually would be 2- 3 hours from the static cold chain and the ice
packs would melt by that time. But the temperatures in the carrier would be
still below 12°C and more than adequate for vaccine preservation.
Even after 8-10 hours if vaccine carriers are properly closed and not
exposed to direct sunlight, vaccines would still be at favourable
temperatures, within which time it is expected that immunization session
would be complete. As regards steps to stop freezing, use any paper (news
paper, old papers) or thick cotton and even local grass to wrap the vaccine
vials after putting them in a plastic sheet, so that labels are not lost.
The suggestion to use racks similar to labs is interesting but the volumes
occupied by them would be 120% more than the vials volume thus straining
the cold chain capacity; that means more than doubling the cold chain
capacity and its consequences. Instead use a thermocool box to keep the T
series and the Hep B vaccines in that box kept in the ILR. The time taken
for it to reach 0° temperature would be far greater than it would be with
direct exposure. Ensure that each vial is in a plastic.
Dr Anil Varshney
New Delhi, India
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