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The Rwanda Health Information Exchange (HIE) system focuses on patient identity management to uniquely identify individuals seeking healthcare across the country. By maintaining a set of identifiers in the client registry and avoiding duplication of patient records, the system ensures efficient and

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Clinical registries play a crucial role in tracking real-world data and outcomes for various medical conditions. They are observational databases that collect data systematically for specific purposes. Distinct from clinical trials, registries provide insights into broader patient populations and re

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Reporting bias poses a significant threat to the accuracy of systematic reviews, with publication bias affecting up to 50% of trials. This bias distorts treatment effect estimates, leading to exaggerated outcomes. Strategies to mitigate reporting bias include searching bibliographical databases, exp

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