PMID- 31179336 OWN - NLM STAT- MEDLINE DCOM- 20191125 LR - 20220408 IS - 2314-6141 (Electronic) IS - 2314-6133 (Print) VI - 2019 DP - 2019 TI - Utilization and Dose Optimization of Angiotensin-Converting Enzyme Inhibitors among Heart Failure Patients in Southwest Ethiopia. PG - 9463872 LID - 10.1155/2019/9463872 [doi] LID - 9463872 AB - BACKGROUND: Optimal use of angiotensin-converting enzyme inhibitors (ACEIs) is crucial to improve the treatment outcome in heart failure patients. However, little is known about the optimal use of ACEIs among heart failure patients in our setting. Therefore, our study aimed to investigate the utilization and optimal dosing of ACEIs and associated factors in heart failure patients. METHOD: A cross-sectional study was conducted on randomly selected patients with heart failure between February 2016 and June 2016 at ambulatory care clinic of Jimma University Medical Center, Ethiopia. Data were collected through patient interview and review of medical records. Binary logistic regression analysis was done to identify factors associated with utilization and optimal dosing of ACEIs. RESULTS: A total of 308 patients were included in the final analysis of this study. The mean (+/-standard deviation) age of the patients was 52.3 +/-15.5 years. Out of the total, 74.7% of the patients were receiving ACEIs. Among the patients who were receiving ACEIs, only 35.7% were taking optimal dose. New York Heart Association (NYHA) class III (Adjusted odds ratio (AOR):0.12, 95% confidence interval (CI):0.02-0.98), valvular heart disease (AOR: 0.27, 95% CI: 0.13-0.56), hypertension (AOR: 5.82, 95% CI: 2.16-15.71), and diabetes mellitus (AOR: 3.84, 95% CI: 1.07-13.86) were significantly associated with the use of ACEIs, whereas age >/=65 (AOR: 2.61, 95%CI: 1.20-5.64), previous hospitalization for heart failure (AOR: 2.08, 95%CI: 1.11-3.92), diuretic use (AOR: 5.60, 95%CI: 2.75-11.40), and dose of furosemide >40mg (AOR: 9.80, 95%CI: 3.00-31.98) were predictors of suboptimal dosing of ACEIs. CONCLUSION: Although majority of patients were receiving ACEIs, only about one-third were using optimal dosage. Valvular heart disease and NYHA class III were negatively associated with the use of ACEIs while previous hospitalization for heart failure, old age, diuretic use, and diuretic dose were predictors of suboptimal dosing of ACEIs. Therefore, more effort needs to be done to minimize the potentially modifiable risk factors of suboptimal use of ACEIs therapy in heart failure patients. FAU - Niriayo, Yirga Legesse AU - Niriayo YL AUID- ORCID: 0000-0002-6943-753X AD - Department of Clinical Pharmacy, School of Pharmacy, College of Health Sciences, Mekelle University, Mekelle, Tigray, Ethiopia. FAU - Kumela, Kabaye AU - Kumela K AUID- ORCID: 0000-0001-6453-9118 AD - Department of Clinical Pharmacy, School of Pharmacy, Faculty of Health Sciences, Jimma University, Jimma, Oromyia, Ethiopia. FAU - Gidey, Kidu AU - Gidey K AUID- ORCID: 0000-0002-7363-1327 AD - Department of Clinical Pharmacy, School of Pharmacy, College of Health Sciences, Mekelle University, Mekelle, Tigray, Ethiopia. FAU - Angamo, Mulugeta Tarekegn AU - Angamo MT AD - Department of Clinical Pharmacy, School of Pharmacy, Faculty of Health Sciences, Jimma University, Jimma, Oromyia, Ethiopia. AD - Division of Pharmacy, School of Medicine, University of Tasmania, Australia. LA - eng PT - Journal Article DEP - 20190424 PL - United States TA - Biomed Res Int JT - BioMed research international JID - 101600173 RN - 0 (Angiotensin-Converting Enzyme Inhibitors) SB - IM MH - Adult MH - Aged MH - Angiotensin-Converting Enzyme Inhibitors/*administration & dosage MH - Cross-Sectional Studies MH - Diabetes Mellitus/drug therapy MH - *Drug Utilization MH - Ethiopia MH - Female MH - Heart Failure/*drug therapy MH - Heart Valve Diseases/drug therapy MH - Hospitalization MH - Humans MH - Hypertension/drug therapy MH - Male MH - Middle Aged MH - Odds Ratio MH - Outpatient Clinics, Hospital MH - Risk Factors MH - Treatment Outcome PMC - PMC6507240 EDAT- 2019/06/11 06:00 MHDA- 2019/11/26 06:00 PMCR- 2019/04/24 CRDT- 2019/06/11 06:00 PHST- 2018/11/29 00:00 [received] PHST- 2019/04/17 00:00 [accepted] PHST- 2019/06/11 06:00 [entrez] PHST- 2019/06/11 06:00 [pubmed] PHST- 2019/11/26 06:00 [medline] PHST- 2019/04/24 00:00 [pmc-release] AID - 10.1155/2019/9463872 [doi] PST - epublish SO - Biomed Res Int. 2019 Apr 24;2019:9463872. doi: 10.1155/2019/9463872. eCollection 2019.