PMID- 35617250 OWN - NLM STAT- MEDLINE DCOM- 20220530 LR - 20221207 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 17 IP - 5 DP - 2022 TI - Glycemic control in newly insulin-initiated patients with type 2 diabetes mellitus: A retrospective follow-up study at a university hospital in Ethiopia. PG - e0268639 LID - 10.1371/journal.pone.0268639 [doi] LID - e0268639 AB - BACKGROUND: Though many trials had examined the effectiveness of taking insulin with or without oral agents, there are limited real-world data, particularly among patients with type 2 diabetes mellitus (T2DM) in the resource limited settings. This study aimed to examine level of glycemic control among patients with T2DM after initiation of insulin and factors associated with poor glycemic control. METHODS: An analysis of retrospective medical records of patients with T2DM who initiated insulin due to uncontrolled hyperglycemia by oral agents was conducted from 2015-2020 in the University of Gondar Comprehensive Specialized Hospital. Difference in median fasting plasma glucose (FPG) before and after insulin initiations was examined by a Wilcoxon signed-rank test. Kruskal Wallis test was performed to explore difference in the median level of FPG among treatment groups. A logistic regression model was also used to identify associated factors of poor glycemic control after insulin initiation. Statistical significance was declared at p < 0.05. RESULTS: Of 424 enrolled patients with T2DM, 54.7% were males and the mean age was 59.3+/-9.3 years. A Wilcoxon signed-rank test showed that there was significant deference in FPG before and after insulin initiation (P < 0.001). A declining trend of blood glucose was observed during the 1-year follow-up period of post-initiation. However, majority of the participants did not achieve target glucose levels. Participants who had higher FPG and systolic blood pressure (SBP) before insulin initiation were found more likely to have poor glycemic control after insulin initiation. Similarly, patients who received atorvastatin compared with simvastatin were found to have poor glycemic control in the post-period of initiation (P = 0.04). Premixed insulin was associated with a lower likelihood of poor glycemic control than neutral protamine Hagedorn (NPH) insulin (P < 0.001). CONCLUSION: Following insulin initiation, a significant change in glycemic level and declining trend of FPG was observed during a 1-year follow-up period. However, the majority of patients still had a poorly controlled glycemic level. Appropriate management focusing on predictors of glycemic control would be of a great benefit to achieve glycemic control. FAU - Sendekie, Ashenafi Kibret AU - Sendekie AK AUID- ORCID: 0000-0001-5982-853X AD - Department of Clinical Pharmacy, School of Pharmacy, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia. FAU - Teshale, Achamyeleh Birhanu AU - Teshale AB AD - Department of Epidemiology and Biostatistics, Institute of Public health, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia. FAU - Tefera, Yonas Getaye AU - Tefera YG AD - Department of Clinical Pharmacy, School of Pharmacy, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20220526 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Blood Glucose) RN - 0 (Glycated Hemoglobin A) RN - 0 (Hypoglycemic Agents) RN - 0 (Insulin) RN - 0 (Insulin, Regular, Human) RN - 53027-39-7 (Insulin, Isophane) SB - IM MH - Aged MH - Blood Glucose/analysis MH - *Diabetes Mellitus, Type 2/drug therapy MH - Ethiopia MH - Female MH - Follow-Up Studies MH - Glycated Hemoglobin/analysis MH - Glycemic Control MH - Hospitals, University MH - Humans MH - *Hyperglycemia MH - Hypoglycemic Agents/therapeutic use MH - Insulin/therapeutic use MH - Insulin, Isophane MH - Insulin, Regular, Human MH - Male MH - Middle Aged MH - Retrospective Studies PMC - PMC9135271 COIS- The authors have declared that no competing interests exist. EDAT- 2022/05/27 06:00 MHDA- 2022/05/31 06:00 PMCR- 2022/05/26 CRDT- 2022/05/26 13:44 PHST- 2022/03/19 00:00 [received] PHST- 2022/05/04 00:00 [accepted] PHST- 2022/05/26 13:44 [entrez] PHST- 2022/05/27 06:00 [pubmed] PHST- 2022/05/31 06:00 [medline] PHST- 2022/05/26 00:00 [pmc-release] AID - PONE-D-22-08211 [pii] AID - 10.1371/journal.pone.0268639 [doi] PST - epublish SO - PLoS One. 2022 May 26;17(5):e0268639. doi: 10.1371/journal.pone.0268639. eCollection 2022.