Electronic death registration is a win-win for SA — let's make it happen
Several studies have flagged problems with South Africa's death registration processes. To address it, a critical first step is to replace our paper-based process with an electronic one.
A recent report by the South African Medical Research Council (SAMRC) highlights the underreporting of HIV in official mortality statistics.
Official cause of death statistics are based on what doctors write on death notification forms. As part of the process of death registration, medical practitioners are required by law to provide information about the medical conditions resulting in each death. Multiple studies have identified concerns about the quality of the information provided by doctors and the Department of Health has been urged in a policy brief to address them as it clearly undermines the quality of data used by our government for health planning and resource allocation.
The recently reported study found extensive underreporting of HIV as a cause of death. Only 28% of deaths that occurred in a national sample of public sector hospitals where the medical record had clear clinical indications of HIV, had HIV specified on their death notification form.
Aside from ensuring that medical certification of the cause of death is part of the medical training curriculum, and that additional training is provided during internship periods, another key issue to address is that many doctors are reluctant to record HIV/Aids as a cause of death due to concerns about maintaining patient confidentiality. In 2014, a self-sealing section was added to protect information about cause of death on the death notification form, but this has clearly not had the desired effect.
Following the deaths of at least 22 children from contaminated food in 2024, President Cyril Ramaphosa announced that the Department of Health would develop an electronic system for recording causes of death as one of several responses to the emergency. The move to an electronic system offers a strategic opportunity to address the challenge around confidentiality and promises a lot more. It allows for secure, institution-based data management that protects confidentiality, encourages accurate reporting and strengthens the integrity of vital statistics.
Benefits of this digital transition will include:
Improved data quality and confidentiality, encouraging accurate reporting of sensitive conditions like HIV/Aids;
Automated validation checks, reducing certification errors at the point of data entry;
Real-time access to mortality data, enabling rapid public health responses; and
A platform for quality assurance and feedback, currently not possible in the paper-based system.
Ultimately, moving away from a paper-based process of death registration will reduce the administrative burden and improve efficiency across the system. This presents a timely and valuable opportunity to collaborate across departments, including health, home affairs and Statistics South Africa, to modernise the country's civil registration and vital statistics system.
We are at a pivotal moment for such coordinated policy action. Investing in a robust electronic system for cause-of-death certification will strengthen South Africa's public health planning, improve disease surveillance and increase accountability. The long-term returns – through faster, more reliable data – are substantial for both governance and health outcomes. It is a win-win. DM
Dr Pam Groenewald and Professor Debbie Bradshaw are with the South African Medical Research Council's Burden of Disease Research Unit.
Note: Spotlight previously reported on the issues discussed in this opinion piece. That reporting included the sentence: 'In the meantime, routine mortality data from Stats SA should clearly be taken with a pinch of salt.' That sentence may have been construed as reflecting Groenewald and the SAMRC's views. Groenewald has asked us to clarify that it does not. She points out that Stats SA is obligated to process the data it receives and the quality issues stem from what doctors report.
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Beginning of dialog window. Escape will cancel and close the window. Text Color White Black Red Green Blue Yellow Magenta Cyan Transparency Opaque Semi-Transparent Background Color Black White Red Green Blue Yellow Magenta Cyan Transparency Opaque Semi-Transparent Transparent Window Color Black White Red Green Blue Yellow Magenta Cyan Transparency Transparent Semi-Transparent Opaque Font Size 50% 75% 100% 125% 150% 175% 200% 300% 400% Text Edge Style None Raised Depressed Uniform Dropshadow Font Family Proportional Sans-Serif Monospace Sans-Serif Proportional Serif Monospace Serif Casual Script Small Caps Reset restore all settings to the default values Done Close Modal Dialog End of dialog window. Advertisement Next Stay Close ✕ Ad Loading Indian South Africans are descendants of indentured labourers and free migrants who came to work in the sugar cane fields of Natal, later becoming traders, workers, and professionals despite the systematic discrimination of colonialism and apartheid. From forced removals under the Group Areas Act to limited political representation under white rule, their history is one of struggle and resilience. Post-apartheid freedom offered formal equality, but the legacy of exclusion persists. Indian South Africans remain a small minority navigating between integration and the preservation of cultural identity. This balancing act is complicated by rising economic inequality, political fragmentation, and at times, resurgent xenophobia and racial scapegoating. Economically, the Indian community often occupies a middle-tier status, better off than many, but still vulnerable. 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