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5 Afternoon Discussion: Reaction to Rapporteurs, Day 1
Pages 99-102

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From page 99...
... And that might really throw things out of kilter. PARTICIPANT: I was also in Group 1, another point that I would make is that I think we all agreed on is that any sequencing data and attempts to correlate sequence with virulence need to be accompanied by very careful and detailed clinical histories of the individuals from whom these samples were obtained.
From page 100...
... The answer has tremendous implications for how we deal with it, because one is probably more of a secondary bacterial pneumonia type picture and the other not. I think that this area needs a lot more research because we have artificially lumped all pandemics under one category, when in fact they may be of a common origin, but not of common outcome or cause.
From page 101...
... Economically, this can be very cost effective to do this, because instead of having to go to complicated and very costly and dangerous clinical trials, it means that you could develop at least attenuated strains of contemporary viruses to have those available. I say this with feeling, because I have recently been through an experience with a clinical trial where an up-todate strain was not available.
From page 102...
... There are other possible approaches that presumably in the next year or two could be undertaken with regard to looking at resistance emergence strategies to reduce the combination therapies with antivirals. Another point of discussion within our group was the need to start studies of the available drugs to determine their impact, and their dose-related impact on some of the important outcomes in H5 disease in South Asia.


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