Sexual and Reproductive Health Matters (Dec 2023)

Preferences for onward health data use in the electronic age among maternity patients and providers in South Africa: a qualitative study

  • Amnesty LeFevre,
  • Olivia Welte,
  • Kearabetswe Moopelo,
  • Nicki Tiffin,
  • Gaolatlhe Mothoagae,
  • Nobukhosi Ncube,
  • Nasiphi Gwiji,
  • Manape Shogole,
  • Amy L. Slogrove,
  • Nomakhawuta Moshani,
  • Andrew Boulle,
  • Jane Goudge,
  • Frances Griffiths,
  • Lee Fairlie,
  • Ushma Mehta,
  • Kerry Scott,
  • Nirvana Pillay

DOI
https://doi.org/10.1080/26410397.2023.2274667
Journal volume & issue
Vol. 31, no. 4

Abstract

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AbstractDespite the expanding digitisation of individual health data, informed consent for the collection and use of health data is seldom explicitly sought in public sector clinics in South Africa. This study aims to identify perceptions of informed consent practices for health data capture, access, and use in Gauteng and the Western Cape provinces of South Africa. Data collection from September to December 2021 included in-depth interviews with healthcare providers (n = 12) and women (n = 62) attending maternity services. Study findings suggest that most patients were not aware that their data were being used for purposes beyond the individualised provision of medical care. Understanding the concept of anonymised use of electronic health data was at times challenging for patients who understood their data in the limited context of paper-based folders and booklets. When asked about preferences for electronic data, patients overwhelmingly were in favour of digitisation. They viewed electronic access to their health data as facilitating rapid and continuous access to health information. Patients were additionally asked about preferences, including delivery of health information, onward health data use, and recontacting. Understanding of these use cases varied and was often challenging to convey to participants who understood their health data in the context of information inputted into their paper folders. Future systems need to be established to collect informed consent for onward health data use. In light of perceived ties to the care received, these systems need to ensure that patient preferences do not impede the content nor quality of care received.

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