Evidence map›Paper›PMID 38832377›Full record

ArticleAfrican journal of primary health care & family medicine2024

Determinants of sub-optimal glycemic control among patients enrolled in a medicine dispensing programme in KwaZulu-Natal: A cohort study, 2018-2021.

Leigh C Johnston, Patrick Ngassa Piotie, Innocent Maposa, Sandhya Singh, Lazarus Kuonza, Alex De Voux

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Article in African journal of primary health care & family medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Leigh C JohnstonSouth African Field Epidemiology Training Program, National Institute for Communicable Disease, A Division of the National Health Laboratory Service, Johannesburg Division of Epidemiology and Biostatistics, School of Public Health, University of the Witwatersrand, Johannesburg Non-Communicable Disease Directorate, National Department of Health, Pretoria. leighj@nicd.ac.za.
Patrick Ngassa Piotie
Innocent Maposa
Sandhya Singh
Lazarus Kuonza
Alex De Voux

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Central Chronic Medicines Dispensing and Distribution (CCMDD) programme facilitates clinically stable patients to collect their chronic medication from community-based pick-up points.

aimWe determined baseline glycaemic control and rates and predictors of becoming sub-optimally controlled for type 2 diabetes mellitus (T2DM) CCMDD-enrolled patients.

settingThe setting of the study was eThekwini, KwaZulu-Natal, South Africa.

methodsWe performed a cohort study (April 2018- December 2021). We linked T2DM CCMDD-enrolled patients to glycated haemoglobin (HbA1c) data from the National Health Laboratory Service. We selected patients optimally controlled at their baseline HbA1c, with ≥ 1 repeat-test available. We used Kaplan-Meier analysis to assess survival rates and extended Cox regression to determine associations between time to sub-optimal control (HbA1c 7%) and predictors. Adjusted hazard ratios (aHRs), 95% confidence interval (CI), and p-values are reported.

resultsOf the 41145 T2DM patients enrolled in the CCMDD programme, 7960 (19%) had a HbA1c result available. Twenty-seven percent (2147/7960) were optimally controlled at their baseline HbA1c. Of those controlled at baseline, 695 (32%) patients had a repeat test available, with 35% (242/695) changing to sub-optimal status. The HbA1c testing frequency as per national guidelines was associated with a lower hazard of sub-optimal glycaemic control (aHR: 0.46; 95% CI: 0.24-0.91; p-value = 0.024). Patients prescribed dual-therapy had a higher hazard of sub-optimal glycaemic control (aHR: 1.50; 95% CI: 1.16-1.95; p-value = 0.002) versus monotherapy.

conclusionsThe HbA1c monitoring, in-line with testing frequency guidelines, is needed to alert the CCMDD programme of patients who become ineligible for enrolment. Patients receiving dual-therapy require special consideration.Contribution: Addressing identified shortfalls can assist programme implementation.

Indexed as

Diabetes Mellitus, Type 2Glycated HemoglobinGlycemic ControlHypoglycemic AgentsAdultAgedBlood GlucoseCohort StudiesFemaleHumansMaleMiddle AgedSouth AfricaBlood GlucoseGlycated HemoglobinHypoglycemic AgentsCCMDD programmeeThekwiniglucose controlglycaemic controlsurvival analysistype 2 diabetes

Identifiers

PMID38832377
PMCPMC11151363

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