Drug-drug interactions and inappropriate medicines impact on glycemic control and kidney function in older adults with diabetes-attending specialty care institution

被引:6
作者
Al-Musawe, Labib [1 ]
Torre, Carla [1 ]
Guerreiro, Jose Pedro [2 ]
Rodrigues, Antonio Teixeira [2 ]
Raposo, Joao Filipe [3 ,4 ]
Mota-Filipe, Helder [1 ]
Martins, Ana Paula [1 ]
机构
[1] Univ Lisbon, Fac Pharm, Lisbon, Portugal
[2] Ctr Hlth Evaluat & Res CEFAR, Lisbon, Portugal
[3] Univ Nova Lisboa, Nova Med Sch, Lisbon, Portugal
[4] Portuguese Diabet Assoc APDP, Lisbon, Portugal
关键词
Drug-drug interactions; Potentially inappropriate medicines; Glycemic control; Kidney function; Elderly; Type; 2; diabetes; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; CALCIUM-CHANNEL BLOCKERS; RENAL-FAILURE; CLINICAL-PRACTICE; GLUCOSE CONTROL; FOLLOW-UP; RISK; CLOPIDOGREL; OUTCOMES; POLYPHARMACY;
D O I
10.1007/s00228-021-03107-y
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose To describe and assess the impact of polypharmacy, and its potential adverse reactions; serious clinically relevant drug-drug interactions (DDIs) and inappropriate medicines (PIMs) on glycemic target, and kidney function in a sample of older adults with type 2 diabetes (T2D). Methods Cross-sectional study was performed in a real-world database including 444 elderly people with T2D from the Portuguese Diabetes Association, aged >= 65 years, and registered in 2018. DDIs were analyzed using Micromedex drug-interaction platform and PIMs identified using STOPP criteria version-2. Results Polypharmacy was identified in 43.6% of patients. This group of patients has shown to be more females (50 vs. 39.6%, P=0.0208), higher HbA1c targets (P=0.0275), longer diabetes duration (66.4 vs. 54.4%, P=0.0019), more hypertensive (87 vs. 62.9%, P<0.0001), using more insulin (38.1 vs. 26%, P=0.0062), sulfonylureas (37.1 vs. 15.6%, P<0.0001), GLP-1 receptor-agonists (9.7 vs. 3.6%, P=0.0077), metformin-DPP-4 inhibitors (41.2 vs. 29.2%, P=0.0081), and SGLT2 inhibitors (19 vs. 9.6%, P=0.0040). A total of 8.7% of patients had potentially serious clinically relevant DDIs, mainly due to interacting medicine pairs dexamethasone and fluoroquinolones. Furthermore, 23.4% had PIMs, and cardiovascular medicines accounted for largest therapeutic group associated. Polypharmacy found to be associated with twofold greater odds of having HbA1c <= 8%, whereas PIMs associated with 2.5-fold greater odds of having HbA1c <= 9%, and 5.5-folds greater odds of having severe kidney function. Conclusions These findings suggested that there is a potential association between polypharmacy and PIMs and altered glycemic control, and PIMs with the deterioration of kidney function.
引用
收藏
页码:1397 / 1407
页数:11
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