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Resources, indicators, data management, dissemination and use in health information systems in sub-Saharan Africa: results of a questionnaire-based survey
Objective To describe the status of health information systems in 14 sub-Saharan African countries of the World Health Organization African Region. Design A questionnaire-based survey. Setting Fourteen sub-Saharan African countries of the African Region. Participants Key informants in the ministries...
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Published in: | Journal of the Royal Society of Medicine 2014-05, Vol.107 (1_suppl), p.28-33 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Objective
To describe the status of health information systems in 14 sub-Saharan African countries of the World Health Organization African Region.
Design
A questionnaire-based survey.
Setting
Fourteen sub-Saharan African countries of the African Region.
Participants
Key informants in the ministries of health, national statistics offices, health programmes, donors and technical agencies.
Main outcome measures
State of resources, indicators, data sources, data management, information products, dissemination and use of health information.
Results
The highest average score was in the identification and harmonisation of indicators (73%), reflecting successful efforts to identify priority indicators and reach international consensus on indicators for several diseases. This was followed by information products (63%), which indicated the availability of accurate and reliable data. The lowest score (41%) was in data management, the ability to collect, store, analyse and distribute data, followed by resources – policy and planning, human and financial resources, and infrastructure (53%). Data sources (e.g. censuses, surveys) were on average inadequate with a score of 56%. The average score for dissemination and use of health information was 57%, which indicated limited or inadequate use of data for advocacy, planning and decision-making.
Conclusions
National health information systems are weak in the surveyed countries and much more needs to be done to improve the quality and relevance of data, and their management, sharing and use for policy-making and decision-making. |
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ISSN: | 0141-0768 1758-1095 |
DOI: | 10.1177/0141076814528690 |