The burden of recording and reporting health data in primary health care facilities in five low- and lower-middle income countries

• Published in: BMC health services research 2021-09, Vol.21 (Suppl 1), p.691-691, Article 691
• Main Authors: Siyam, Amani, Ir, Por, York, Dararith, Antwi, James, Amponsah, Freddie, Rambique, Ofelia, Funzamo, Carlos, Azeez, Aderemi, Mboera, Leonard, Kumalija, Claud John, Rumisha, Susan Fred, Mremi, Irene, Boerma, Ties, O'Neill, Kathryn
• Format: Article
• Language: English
• Subjects: Acquired immune deficiency syndrome; AIDS; Ambulatory care; Ambulatory Care Facilities; Data Collection; Developing Countries; Female; Health Facilities; Health Personnel; Health services; Health worker; Humans; Information systems; Laboratories; Management; Management information systems; Medical personnel; Methods; Practice; Pregnancy; Primary Health Care; Public health; Public PHC facilities; Registers; Report writing; Reporting forms; Review; Time motion; Workers
• ISSN: 1472-6963; 1472-6963
• DOI: 10.1186/s12913-021-06652-5

Recording and reporting health data in facilities is the backbone of routine health information systems which provide data collected by health facility workers during service provision. Data is firstly collected in a register, to record patient health data and care process, and tallied into nationally designed reporting forms. While there is anecdotal evidence of large numbers of registers and reporting forms for primary health care (PHC) facilities, there are few systematic studies to document this potential burden on health workers. This multi-country study aimed to document the numbers of registers and reporting forms use at the PHC level and to estimate the time it requires for health workers to meet data demands. In Cambodia, Ghana, Mozambique, Nigeria and Tanzania, a desk review was conducted to document registers and reporting forms mandated at the PHC level. In each country, visits to 16 randomly selected public PHC facilities followed to assess the time spent on paper-based recording and reporting. Information was collected through self-reports of estimated time use by health workers, and observation of 1360 provider-patient interactions. Data was primarily collected in outpatient care (OPD), antenatal care (ANC), immunization (EPI), family planning (FP), HIV and Tuberculosis (TB) services. Cross-countries, the average number of registers was 34 (ranging between 16 and 48). Of those, 77% were verified in use and each register line had at least 20 cells to be completed per patient. The mean time spent on recording was about one-third the total consultation time for OPD, FP, ANC and EPI services combined. Cross-countries, the average number of monthly reporting forms was 35 (ranging between 19 and 52) of which 78% were verified in use. The estimated time to complete monthly reporting forms was 9 h (ranging between 4 to 15 h) per month per health worker. PHC facilities are mandated to use many registers and reporting forms pausing a considerable burden to health workers. Service delivery systems are expected to vary, however an imperative need remains to invest in international standards of facility-based registers and reporting forms, to ensure regular, comparable, quality-driven facility data collection and use.