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dc.contributor.authorKufakunesu, Ropafadzo-
dc.date.accessioned2026-10-24T08:15:38Z-
dc.date.available2026-10-24T08:15:38Z-
dc.date.issued2025-
dc.identifier.citationKufakunesu, R. (2025). Correlation between anaemia and renal dysfunction in HIV-positive patients receiving tenofovir-based antiretroviral therapy at Marondera Provincial Hospital from 2020 to 2025 (Research project). Africa University, Mutare, Zimbabwe.en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/5337-
dc.description.abstractTenofovir Disoproxil Fumarate (TDF), a key component of antiretroviral therapy (ART) in Zimbabwe, has been associated with nephrotoxicity, but its specific, concurrent impact on anaemia and the role of treatment duration are not well-quantified locally. The main objective of this study was to investigate the correlation between anaemia and renal dysfunction in HIV-positive patients receiving TDF-based ART at Marondera Provincial Hospital, considering data from 2020-2025. A retrospective cross-sectional analysis was conducted on 600 patient records. The variables of interest were ART duration, haemoglobin (Hb), serum creatinine, and estimated glomerular filtration rate (eGFR); the outcomes were the prevalence and severity of anaemia and renal dysfunction. The prevalence of any renal impairment (eGFR < 90) was 42.3%, with 6.8% of patients exhibiting moderate-to-severe dysfunction (eGFR < 60). The prevalence of anaemia (any stage) was 27.2%. A statistically significant, moderate positive correlation was found between haemoglobin and eGFR (r = 0.420, p < .001), while a weaker negative correlation was observed with serum creatinine (r = -0.245, p < .001). Critically, the duration of TDF-based ART was significantly associated with the severity of both renal impairment (F(4, 595) = 5.93, p = .0001) and anaemia (F(3, 596) = 4.87, p = .0024). A review of group means demonstrated a clear trend, with mean ART duration progressively increasing from 38.4 months in the normal renal function group to 52.1 months in the end-stage group, and similarly from 39.1 months in the normal haemoglobin group to 48.7 months in the severe anaemia group. These findings suggest a cumulative, duration-dependent toxicity from TDF, which likely causes anaemia via impaired erythropoietin production secondary to renal damage. The data confirms eGFR is a more sensitive marker for this systemic complication than creatinine alone. The study recommends the implementation of integrated monitoring protocols, including regular eGFR and Hb screening, particularly for patients on TDF-based ART for over three years.en_US
dc.language.isoenen_US
dc.publisherAfrica Universityen_US
dc.subjectTenofoviren_US
dc.subjectHIVen_US
dc.subjectAnaemiaen_US
dc.subjectRenal Dysfunctionen_US
dc.subjecteGFRen_US
dc.subjectCorrelationen_US
dc.subjectART Durationen_US
dc.titleCorrelation Between Anaemia and Renal Dysfunction in HIV-Positive Patients Receiving Tenofovir-Based Antiretroviral Therapy at Marondera Provincial Hospital from 2020 to 2025en_US
dc.typeOtheren_US
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