Responding to emergencies is the vital stuff of television and film. Persons are in distress, injured, diseased: there is a natural disaster, an epidemic outbreak, a civil war, a nuclear event. Professionals of all stripes come to their aid, sometimes taking on substantial risks to their own well-being. Both heroic success and tragic failure in this domain rarely fail to generate human interest. Whereas data sharing … is the sharing of data. It just doesn’t generate that kind of excitement. Researchers or research agencies collect data. After they collect it, they may share datasets with others (other research institutions, governments, and so on) in order to spread scientific knowledge, stimulate further research, and perhaps improve the lot of humanity somewhere down the line. What happens when the excitement of emergency response meets the mundaneness of data sharing?
Apparently, Medecins Sans Frontieres (MSF) is what happens. MSF — a Nobel prizewinning humanitarian organization — collects data on the people they are assisting in the many emergencies they are engaged in. Not that this is a bad thing: some of the data collection (on routine medical procedures, adherence to treatments, etc.) are primarily for quality control purposes, and MSF also conducts operational research among groups affected by neglected diseases in impoverished countries. But data collecting in times of crisis leads to an ethical challenge: on the one hand, if the data collected could be used in beneficial ways by other researchers or agencies, it ought to be shared. On the other hand, the kinds of data collected in extreme circumstances (think sexual violence in the Democratic Republic of Congo or injection drug use in Thailand) is sensitive and could harm already vulnerable populations if it is not handled appropriately.
The views, opinions and positions expressed by these authors and blogs are theirs and do not necessarily represent that of the Bioethics Research Library and Kennedy Institute of Ethics or Georgetown University.