Cardiovascular Outcomes According to Polypharmacy and Drug Adherence in Patients with Atrial Fibrillation on Long-Term Anticoagulation (from the RE-LY Trial)

被引:14
作者
Millenaar, Dominic [1 ]
Schumacher, Helmut [2 ]
Brueckmann, Martina [3 ,4 ]
Eikelboom, John W. [5 ,6 ]
Ezekowitz, Michael [7 ,8 ,9 ]
Slawik, Jonathan [1 ]
Ewen, Sebastian [1 ]
Ukena, Christian [1 ]
Wallentin, Lars [10 ,11 ]
Connolly, Stuart [5 ,6 ]
Yusuf, Salim [5 ,6 ]
Bohm, Michael [1 ]
机构
[1] Klin Innere Med III Kardiol Angiol Internist Inte, Homburg, Germany
[2] Ingelheim Rhein, Rhineland Palatinate, Germany
[3] Boehringer Ingelheim Int GmbH, Med CardioMetab & Resp, Binger Str 173, Ingelheim, Rhineland Palat, Germany
[4] Univ Klinikum Mannheim, Med Fak Mannheim, Theodor Kutzer Ufer 1-3, Mannheim, Baden Wurttembe, Germany
[5] McMaster Univ, Populat Hlth Res Inst, Hamilton, ON, Canada
[6] Hamilton Hlth Sci, Hamilton, ON, Canada
[7] Jefferson Univ, Sidney Kimmel Med Coll, Philadelphia, PA USA
[8] Lankenau Inst Med Res, Wynnewood, PA USA
[9] Heart Ctr, Wynnewood, PA USA
[10] Uppsala Univ, Uppsala Clin Res Ctr, Uppsala, Sweden
[11] Uppsala Univ, Dept Med Sci, Cardiol, Uppsala, Sweden
关键词
ORAL ANTICOAGULANTS; ELDERLY-PATIENTS; DABIGATRAN; NONADHERENCE; MORTALITY; WARFARIN; THERAPY; ADULTS; RISK;
D O I
10.1016/j.amjcard.2021.03.024
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Prevalence of atrial fibrillation (AF) increases with age, along with comorbidities and, thus, polypharmacy. Non-adherence is associated with polypharmacy. This study aimed to identify patients at risk for cardiovascular events according to their pharmacological treatment intensity and adherence. Patients (n = 18,113) with a mean age of 71.5 +/- 8.7 years, at high cardiovascular risk were followed between December 2005 until December 2007 for a median time of 2 years. The association between polypharmacy and adherence and their impact on cardiovascular and bleeding events were explored. Adherence was defined as a study drug intake of >= 80%. Patients with more co-medications had a higher body mass index, higher prevalence of hypertension, coronary heart disease, heart failure, and diabetes mellitus (all p < 0.0001) compared to <= 4 or 5-8 co-medications, but no differences in history of stroke (p = 0.68) or transient ischemic attack (p = 0.065). Across all treatments, the adjusted hazard ratios (HRs) increased in patients with more co-medications (>= 9 vs <= 4) for all-cause death (HR 1.30; 1.06-1.59), major bleeding (HR 1.65; 1.33-2.05), and all bleeding events (HR 1.44; 1.31-1.59). Yearly event rates were higher in non-adherent than adherent patients for stroke and systemic embolism (SSE) (3.14 vs 1.00), all-cause death (7.76 vs 2.66), major bleeding (6.21 vs 2.65), and all bleeding (28.71 vs 19.05; all p < 0.0001). After an event the patients were more likely to become non-adherent (adherence after SSE 30.3%, after major bleeding 33.4%, after all bleeding 66.7%; all p < 0.0001). The treatment effects were consistent to the overall group in the different polypharmacy groups. In conclusion, polypharmacy and non-adherence are risk indicators for increased adverse cardiovascular and bleeding events. Dabigatran is safe to use across the full spectrum of AF patients, independent of the number of co-medications and adherence. Patients with co-medications and comorbidities require special attention and encouragement to adhere to oral anticoagulation. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:27 / 35
页数:9
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