Duration-to-Attain Target Blood Pressure Level and Its Predictors among Newly Diagnosed Hypertensive Adults Treated in a Comprehensive Hospital in Central Ethiopia

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Background: Timely blood pressure (BP) control is essential for preventing hypertension-related complications. However, longitudinal evidence on the time required to achieve target BP and its predictors among newly diagnosed hypertensive patients remains limited in Ethiopia. This study assessed the time to BP control and its predictors among newly diagnosed hypertensive adults receiving care at a comprehensive hospital in Central Ethiopia.

Methods: A five-year retrospective cohort study was conducted among 522 newly diagnosed hypertensive adults enrolled between 2021 and 2025. The primary outcome was time to BP control, defined as achieving a BP <140/90 mmHg at two consecutive follow-up visits. Participants were selected using systematic random sampling, and data were extracted from medical records by trained personnel. Missing data were handled using hot-deck imputation. Kaplan–Meier survival analysis and the log-rank test were used to compare time to BP control across groups. Variables meeting the proportional hazards assumption and a bivariate screening criterion of P < 0.25 were included in a multivariable Cox proportional hazards model to identify independent predictors. Statistical significance was declared at P < 0.05.

Results: Of the 522 patients included, 377 (72.2%) achieved BP control during 191,056 person-days of follow-up, corresponding to an incidence rate of 1.97 BP control events per 1,000 person-days (72 events per 100 person-years). The overall median time to BP control was 375 days (12.5 months; 95% CI: 338–410). Males required a longer median time than females (400 vs. 352 days). Urban residence (adjusted hazard ratio [AHR] = 1.36; 95% CI: 1.05–1.74), initiation with dual antihypertensive therapy (AHR = 1.52; 95% CI: 1.12–2.06), and normal total cholesterol levels (AHR = 2.09; 95% CI: 1.48–2.96) were independently associated with a shorter time to BP control. In contrast, the presence of comorbidities (AHR = 0.23; 95% CI: 0.16–0.33) and advanced baseline blood pressure severity independently prolonged the time required to achieve target levels. Compared to those who had baseline SBP of 140-159 mmHg, patients who had systolic blood pressure (SBP) of 160-179 mmHg and ≥180 mmHg showed significantly reduced rates of achieving timely blood pressure control (AHR = 0.61; 95% CI: 0.47–0.80 and AHR = 0.36; 95% CI: 0.24–0.54, respectively). Similarly, patients who had diastolic blood pressure (DBP) of 99-109 mmHg and ≥110 mmHg had strongly delayed treatment success (AHR = 0.53; 95% CI: 0.41–0.71 and AHR = 0.36; 95% CI: 0.23–0.56, respectively) compared with patients with DBP of 90-99 mmHg.

Conclusion: Newly diagnosed hypertensive patients experienced substantial delays in achieving target BP, with a median time to control exceeding one year. Early initiation of dual antihypertensive therapy and urban residence were associated with faster BP control, whereas higher baseline systolic and/or diastolic BP levels and comorbidities significantly prolonged the time to achieving target BP. Targeted management strategies for high-risk patients may help accelerate BP control and improve clinical outcomes.

Keywords

Authors

Kumlachew Mergiaw

School of Medicine, PhD

Habtemaryam Tedla

 Officer

Awraris Hailu

Epidemiology, PhD, Associate Professor

Zenebe Abebe

Department of Epidemiology, Lecturer 

Zenawi Hagos

Arnold School of Public Health, University of South Carolina, PhD 

How to Cite

Kumlachew Mergiaw, Habtemaryam Tedla, Awraris Hailu, Zenebe Abebe, Zenawi Hagos (2026-06-29). Duration-to-Attain Target Blood Pressure Level and Its Predictors among Newly Diagnosed Hypertensive Adults Treated in a Comprehensive Hospital in Central Ethiopia. Ethiopian Journal of Health and Biomedical Sciences, Vol. 16 No. 1 (2026), 3-15. https://doi.org/10.20372/ejhbs.1191

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Copyright & Licensing © Year The Author(s). This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0) , which permits unrestricted use; sharing (copying and redistributing the material in any medium or format); and adaptation (remixing, transforming, and building upon the material for any purpose), provided the original author(s) and the source are properly cited/credited and a link to the license is provided. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

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