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      Using verbal autopsy to measure causes of death: the comparative performance of existing methods

      research-article
      1 , , 1 , 2 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 3 , 4 , 3 , 1 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 2 , 1 , 13 , 3 , 14 , 14 , 15 , 16 , 13 , 17 , 18 , 2 , 15 , 19 , 2 , 18 , 15 , 9 , 10 , 15 , 20
      BMC Medicine
      BioMed Central
      Verbal autopsy, VA, Validation, Cause of death, Symptom pattern, Random forests, InterVA, King-Lu, Tariff

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          Abstract

          Background

          Monitoring progress with disease and injury reduction in many populations will require widespread use of verbal autopsy (VA). Multiple methods have been developed for assigning cause of death from a VA but their application is restricted by uncertainty about their reliability.

          Methods

          We investigated the validity of five automated VA methods for assigning cause of death: InterVA-4, Random Forest (RF), Simplified Symptom Pattern (SSP), Tariff method (Tariff), and King-Lu (KL), in addition to physician review of VA forms (PCVA), based on 12,535 cases from diverse populations for which the true cause of death had been reliably established. For adults, children, neonates and stillbirths, performance was assessed separately for individuals using sensitivity, specificity, Kappa, and chance-corrected concordance (CCC) and for populations using cause specific mortality fraction (CSMF) accuracy, with and without additional diagnostic information from prior contact with health services. A total of 500 train-test splits were used to ensure that results are robust to variation in the underlying cause of death distribution.

          Results

          Three automated diagnostic methods, Tariff, SSP, and RF, but not InterVA-4, performed better than physician review in all age groups, study sites, and for the majority of causes of death studied. For adults, CSMF accuracy ranged from 0.764 to 0.770, compared with 0.680 for PCVA and 0.625 for InterVA; CCC varied from 49.2% to 54.1%, compared with 42.2% for PCVA, and 23.8% for InterVA. For children, CSMF accuracy was 0.783 for Tariff, 0.678 for PCVA, and 0.520 for InterVA; CCC was 52.5% for Tariff, 44.5% for PCVA, and 30.3% for InterVA. For neonates, CSMF accuracy was 0.817 for Tariff, 0.719 for PCVA, and 0.629 for InterVA; CCC varied from 47.3% to 50.3% for the three automated methods, 29.3% for PCVA, and 19.4% for InterVA. The method with the highest sensitivity for a specific cause varied by cause.

          Conclusions

          Physician review of verbal autopsy questionnaires is less accurate than automated methods in determining both individual and population causes of death. Overall, Tariff performs as well or better than other methods and should be widely applied in routine mortality surveillance systems with poor cause of death certification practices.

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          Most cited references37

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              Causes of neonatal and child mortality in India: a nationally representative mortality survey.

              More than 2·3 million children died in India in 2005; however, the major causes of death have not been measured in the country. We investigated the causes of neonatal and child mortality in India and their differences by sex and region. The Registrar General of India surveyed all deaths occurring in 2001-03 in 1·1 million nationally representative homes. Field staff interviewed household members and completed standard questions about events that preceded the death. Two of 130 physicians then independently assigned a cause to each death. Cause-specific mortality rates for 2005 were calculated nationally and for the six regions by combining the recorded proportions for each cause in the neonatal deaths and deaths at ages 1-59 months in the study with population and death totals from the United Nations. There were 10,892 deaths in neonates and 12,260 in children aged 1-59 months in the study. When these details were projected nationally, three causes accounted for 78% (0·79 million of 1·01 million) of all neonatal deaths: prematurity and low birthweight (0·33 million, 99% CI 0·31 million to 0·35 million), neonatal infections (0·27 million, 0·25 million to 0·29 million), and birth asphyxia and birth trauma (0·19 million, 0·18 million to 0·21 million). Two causes accounted for 50% (0·67 million of 1·34 million) of all deaths at 1-59 months: pneumonia (0·37 million, 0·35 million to 0·39 million) and diarrhoeal diseases (0·30 million, 0·28 million to 0·32 million). In children aged 1-59 months, girls in central India had a five-times higher mortality rate (per 1000 livebirths) from pneumonia (20·9, 19·4-22·6) than did boys in south India (4·1, 3·0-5·6) and four-times higher mortality rate from diarrhoeal disease (17·7, 16·2-19·3) than did boys in west India (4·1, 3·0-5·5). Five avoidable causes accounted for nearly 1·5 million child deaths in India in 2005, with substantial differences between regions and sexes. Expanded neonatal and intrapartum care, case management of diarrhoea and pneumonia, and addition of new vaccines to immunisation programmes could substantially reduce child deaths in India. US National Institutes of Health, International Development Research Centre, Canadian Institutes of Health Research, Li Ka Shing Knowledge Institute, and US Fund for UNICEF. Copyright © 2010 Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                BMC Med
                BMC Med
                BMC Medicine
                BioMed Central
                1741-7015
                2014
                9 January 2014
                : 12
                : 5
                Affiliations
                [1 ]Institute for Health Metrics and Evaluation, University of Washington, 2301 5th Avenue Suite 600, Seattle, WA 98121, USA
                [2 ]National Institute of Public Health, Universidad 655, 62100 Cuernavaca, Morelos, Mexico
                [3 ]Johns Hopkins University, Bloomberg School of Public Health, 615 N Wolfe St #5041, Baltimore, MD 21205, USA
                [4 ]Public Health Laboratory-IdC, P.O. BOX 122 Wawi Chake Chake Pemba, Zanzibar, Tanzania
                [5 ]Public Health Foundation of India, ISID Campus, 4 Institutional Area, Vasant Kunj, New Delhi 110070, India
                [6 ]Brigham and Women's Hospital, 75 Francis St, Boston, MA 02215, USA
                [7 ]Global Development, Bill and Melinda Gates Foundation, PO Box 23350, Seattle, WA 98012, USA
                [8 ]CSM Medical University, Shah Mina Road, Chowk, Lucknow, Uttar Pradesh 226003, India
                [9 ]Dept of International Health, Johns Hopkins Bloomberg School of Public Health, E5521, 615 N. Wolfe Street, Baltimore, MD 21205, USA
                [10 ]Public Health Laboratory-Ivo de Carneri, Wawi, Chake-Chake, Pemba, Zanzibar, Tanzania
                [11 ]Johns Hopkins University, 214A Basement, Vinobapuri Lajpat Nagar-II, New Delhi 110024, India
                [12 ]Harvard School of Public Health, 677 Huntington Avenue, Boston, MA 02115-6018, USA
                [13 ]The George Institute for Global Health, The University of Sydney, 83/117 Missenden Rd, Camperdown, NSW 2050, Australia
                [14 ]Community Empowerment Lab, Shivgarh, India
                [15 ]Research Institute for Tropical Medicine, Corporate Ave, Muntinlupa City 1781, Philippines
                [16 ]Division of Nutritional Sciences, Cornell University, 314 Savage Hall, Ithaca, NY 14853, USA
                [17 ]The George Institute for Global Health, 839C, Road No. 44A, Jubilee Hills, Hyderabad 500033, India
                [18 ]Muhimbili University of Health and Allied Sciences, United Nations Rd, Dar es Salaam, Tanzania
                [19 ]School of Population Health, University of Queensland, Level 2 Public Health Building School of Population Health, Herston Road, Herston, QLD 4006, Australia
                [20 ]University of Melbourne School of Population and Global Health, Building 379, 207 Bouverie St., Parkville 3010, VIC, Australia
                Article
                1741-7015-12-5
                10.1186/1741-7015-12-5
                3891983
                24405531
                a1a412cf-d265-478b-98f2-8cfeefde3e11
                Copyright © 2014 Murray et al.; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 28 September 2013
                : 10 December 2013
                Categories
                Research Article

                Medicine
                random forests,tariff,validation,king-lu,interva,cause of death,va,verbal autopsy,symptom pattern
                Medicine
                random forests, tariff, validation, king-lu, interva, cause of death, va, verbal autopsy, symptom pattern

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