New challenges for verbal autopsy: Considering the ethical and social implications of verbal autopsy methods in routine health information systems.

作者: Hebe N Gouda , Abraham D Flaxman , Claire E Brolan , Rohina Joshi , Ian D Riley

DOI: 10.1016/J.SOCSCIMED.2017.05.002

关键词:

摘要: Verbal autopsy (VA) methods are designed to collect cause-of-death information from populations where many deaths occur outside of health facilities and death certification is weak or absent. A VA consists an interview with a relative carer recently deceased individual in order gather on the signs symptoms decedent presented prior death. These details then used determine assign likely cause-of-death. At population level this can be invaluable help guide prioritisation direct policy services. To date VAs have largely been restricted research contexts but countries now venturing incorporate into routine civil registration vital statistics (CRVS) systems. Given sensitive nature death, however, there number ethical, legal social issues that should considered when scaling-up VAs, particularly cross-cultural socio-economically disadvantaged environments which they typically applied. Considering each step process paper provides narrative review context methods. Harnessing experiences applying rolling out as part CRVS systems low middle income countries, we identify potential implementing institutions need consider incorporating point areas could benefit further deliberation.

参考文章(84)
CE Brolan, C Rao, HT Nguyen, QT Chi Nguyen, HH Le Thi, Z Dawkins, PS Hill, AD Nao, None, A Time to Mourn: Cultural Considerations and Community Preferences for Verbal Autopsy in Vietnam Vietnam Journal of Public Health. ,vol. 2, pp. 4- 12 ,(2014)
, Healing the health system after civil unrest Global Health Action. ,vol. 8, pp. 1- 4 ,(2015) , 10.3402/GHA.V8.27381
Pascale A. Allotey, Daniel D. Reidpath, Natalie C. Evans, Nirmala Devarajan, Kanason Rajagobal, Ruhaida Bachok, Kridaraan Komahan, , Let's talk about death: Data collection for verbal autopsies in a demographic and health surveillance site in Malaysia Global Health Action. ,vol. 8, pp. 28219- 28219 ,(2015) , 10.3402/GHA.V8.28219
PAULINE E. OSAMOR, NANCY KASS, Decision-making and motivation to participate in biomedical research in southwest Nigeria. Developing World Bioethics. ,vol. 12, pp. 87- 95 ,(2012) , 10.1111/J.1471-8847.2012.00326.X
Kimberlyn M. McGrail, Charlyn Black, Access to data in health information systems. Bulletin of The World Health Organization. ,vol. 83, pp. 563- 563 ,(2005) , 10.1590/S0042-96862005000800003
Zulfiqar A. Bhutta, Beyond informed consent. Bulletin of The World Health Organization. ,vol. 82, pp. 771- 777 ,(2004) , 10.1590/S0042-96862004001000013
Cooper Rs, Kaufman Js, Asuzu Mc, Rotimi Cn, Johnson Oo, Owoaje Ee, Questions on adult mortality. WORLD HEALTH FORUM. ,vol. 17, pp. 373- ,(1996)
Bwire Chirangi, Gail C. Webber, Understanding Maternal Deaths from the Family’s Perspective: Verbal Autopsies in Rural Tanzania African Journal of Reproductive Health. ,vol. 18, pp. 128- 132 ,(2014)