National health information systems for achieving the Sustainable Development Goals

Autor: Legre Roger Lobognon, Mphatso Mudenda, Aleya Khalifa, Michael de Klerk, Aime Nicoue, George S Mgomella, Mireille Cheyip, Mahesh Swaminathan, Daniel H. Rosen, Ibrahim Jahun, Victor Sebastian, Achara Teeraratkul, Nicholus Mutenda, Leonel Lerebours, Luis Bonilla, Eric–Jan Manders, Frank Amoyaw, Yassa Ndjakani, Wolfgang Hladik, Charles Echezona Nzelu, Rogers Galaxy Ngalamulume, Stanley Kamocha, Olga Joos, Douangchanh Xaymounvong, Ha Thai Son, Danielle T. Barradas, Getahun Aynalem, Vo Hai Son, Edwin Ramírez, Ray L. Ransom, Judith Hedje, Abel Yamba, Camara Aoua, Supiya Jantaramanee, Léopold Lubala, Christine West, Rennatus Mdodo, Bouathong Simanovong, Tuan Anh Nguyen, Suilanji Sivile, Alain Magazani, Denis Yoka, Abu S. Abdul-Quader, Christopher S. Murrill, Ibrahim Dalhatu, Amitabh B. Suthar, Anthony Ofosu, Jacob Dee, Hao Zhu, Erin Nichols, George Bello, Poruan Temu, Namarola Lote, Zukiswa Pinini, Lattah Asseka Monique, Jeremiah Mushi
Rok vydání: 2019
Předmět:
Zdroj: BMJ Open
ISSN: 2044-6055
Popis: ObjectivesAchieving the Sustainable Development Goals will require data-driven public health action. There are limited publications on national health information systems that continuously generate health data. Given the need to develop these systems, we summarised their current status in low-income and middle-income countries.SettingThe survey team jointly developed a questionnaire covering policy, planning, legislation and organisation of case reporting, patient monitoring and civil registration and vital statistics (CRVS) systems. From January until May 2017, we administered the questionnaire to key informants in 51 Centers for Disease Control country offices. Countries were aggregated for descriptive analyses in Microsoft Excel.ResultsKey informants in 15 countries responded to the questionnaire. Several key informants did not answer all questions, leading to different denominators across questions. The Ministry of Health coordinated case reporting, patient monitoring and CRVS systems in 93% (14/15), 93% (13/14) and 53% (8/15) of responding countries, respectively. Domestic financing supported case reporting, patient monitoring and CRVS systems in 86% (12/14), 75% (9/12) and 92% (11/12) of responding countries, respectively. The most common uses for system-generated data were to guide programme response in 100% (15/15) of countries for case reporting, to calculate service coverage in 92% (12/13) of countries for patient monitoring and to estimate the national burden of disease in 83% (10/12) of countries for CRVS. Systems with an electronic component were being used for case reporting, patient monitoring, birth registration and death registration in 87% (13/15), 92% (11/12), 77% (10/13) and 64% (7/11) of responding countries, respectively.ConclusionsMost responding countries have a solid foundation for policy, planning, legislation and organisation of health information systems. Further evaluation is needed to assess the quality of data generated from systems. Periodic evaluations may be useful in monitoring progress in strengthening and harmonising these systems over time.
Databáze: OpenAIRE