Outcomes of apixaban versus warfarin in patients with atrial fibrillation and multi-morbidity: Insights from the ARISTOTLE trial

被引:51
|
作者
Alexander, Karen P. [1 ]
Brouwer, Marc A. [2 ]
Mulder, Hillary [1 ]
Vinereanu, Dragos [3 ]
Lopes, Renato D. [1 ]
Proietti, Marco [4 ]
Al-Khatib, Sana M. [1 ]
Hijazi, Ziad [5 ,6 ]
Halvorsen, Sigrun [7 ]
Hylek, Elaine M. [8 ]
Verheugt, Freek W. A. [9 ]
Alexander, John H. [1 ]
Wallentin, Lars [5 ,6 ]
Granger, Christopher B. [1 ]
机构
[1] Duke Univ, Sch Med, Duke Clin Res Inst, Durham, NC USA
[2] Radboud Univ Nijmegen, Med Ctr, Nijmegen, Netherlands
[3] Univ & Emergency Hosp, Univ Med & Pharm Card Davila, Bucharest, Romania
[4] Sapienza Univ Rome, Dept Internal Med & Med Specialties, Rome, Italy
[5] Uppsala Univ, Dept Med Sci Cardiol, Uppsala, Sweden
[6] Uppsala Univ, Uppsala Clin Res Ctr, Uppsala, Sweden
[7] Oslo Univ Hosp, Oslo, Norway
[8] Boston Univ Med Ctr, Boston, MA USA
[9] Univ Med Ctr Nijmegen, Nijmegen, Netherlands
关键词
ORAL ANTICOAGULATION; INFORMED TREATMENT; STROKE PREVENTION; CLINICAL-OUTCOMES; ELDERLY-PATIENTS; FRAILTY; MULTIMORBIDITY; DISEASES; REGISTRY; RISK;
D O I
10.1016/j.ahj.2018.09.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Patients with atrial fibrillation (AF) often have multi-morbidity, defined as >= 3 comorbid conditions. Multi-morbidity is associated with polypharmacy, adverse events, and frailty potentially altering response to anticoagulation. We sought to describe the prevalence of multi-morbidity among older patients with AF and determine the association between multi-morbidity, clinical outcomes, and the efficacy and safety of apixaban compared with warfarin. Methods In this post-hoc subgroup analysis of the ARISTOTLE trial, we studied enrolled patients age >= 55 years (n = 16,800). Patients were categorized by the number of comorbid conditions at baseline: no multi-morbidity (0-2 comorbid conditions), moderate multi-morbidity (3-5 comorbid conditions), and high multi-morbidity (>= 6 comorbid conditions). Association between multi-morbidity and clinical outcomes were analyzed by treatment with a median follow-up of 1.8 (1.3-2.3) years. Results Multi-morbidity was present in 64% (n = 10,713) of patients; 51% (n = 8491) had moderate multi-morbidity, 13% (n = 2222) had high multi-morbidity, and 36% (n = 6087) had no multi-morbidity. Compared with the no multi-morbidity group, the high multi-morbidity group was older (74 vs 69 years), took twice as many medications (10 vs 5), and had higher CHA2DS2-VASc scores (4.9 vs 2.7) (all P < .001). Adjusted rates per 100 patient-years for stroke/systemic embolism, death, and major bleeding increased with multi-morbidity (Reference no multi-morbidity; moderate multi-morbidity 1.42 [1.24-1.64] and high multi-morbidity 1.92 [1.59-2.31]), with no interaction in relation to efficacy or safety of apixaban. Conclusions Multi-morbidity is prevalent among the population with AF; efficacy and safety of apixaban is preserved in this subgroup supporting extension of trial results to the most complex AF patients.
引用
收藏
页码:123 / 131
页数:9
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