ABSTRACT

Worldwide, hypertension remains one of the most significant causes of morbidity and mortality. Despite the substantial public burden of hypertension coupled with the sustained government efforts in controlling the disease among hypertensive patients, there is still slow progress in the prevention and control of the ailment. The majority of patients still have uncontrolled blood pressure levels, with a significant number having life-threatening complications. The malady continuously subjects patients to immense suffering as it affects their health, predisposing them to life-threatening complications such as heart failure and even stroke in their 50s. Most countries, especially in the global south, have reported uncontrolled blood pressure levels among hypertensive patients despite anti-hypertensive drugs. This study, therefore, aims to investigate the clinical management of hypertension in adult patients by healthcare providers in Kakamega County, Kenya. The Specific objectives will be threefold: To assess patients' factors that influence the clinical management of hypertension in Kakamega County. The second one will examine the health care provider's factors that influence the clinical management of hypertension in Kakamega county. The third specific objective is to determine health system factors influencing clinical management of hypertension in Kakamega county based on clinical guidelines of 2018. The researcher will employ a cross-sectional analytical study design in multiple study sites. The pilot study will be carried out in the Vihiga county referral hospital. The primary study will be carried out in both tier 2 and tier 3 public, together with private hospitals in Kakamega County. Data will be collected from both the patients and the health care providers. The study will employ the use of a questionnaire and an observation checklist. Analysis of the collected data will be by the Statistical Package for Social Science (SPSS) version 28. Logistic regression will be used to identify factors associated with uncontrolled blood pressure and prognosis. Research participants will be required to sign a written consent.

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