Autonomic Regulation Therapy via Left or Right Cervical Vagus Nerve Stimulation in Patients With Chronic Heart Failure: Results of the ANTHEM-HF Trial

被引:280
作者
Premchand, Rajendra K. [1 ]
Sharma, Kamal [2 ]
Mittal, Sanjay [3 ]
Monteiro, Rufino [4 ]
Dixit, Satyajit [2 ]
Libbus, Imad [5 ]
Dicarlo, Lorenzo A. [6 ]
Ardell, Jeffrey L. [7 ]
Rector, Thomas S. [8 ]
Amurthur, Badri [5 ]
Kenknight, Bruce H. [5 ]
Anand, Inder S. [8 ]
机构
[1] Krishna Inst Med Sci, Dept Cardiol, Secunderabad, India
[2] Sanjivani Super Specialty Hosp, Dept Cardiol, Ahmadabad, Gujarat, India
[3] Medanta, Dept Cardiol, Medicity, Haryana, India
[4] Vintage Hosp, Dept Cardiol, Panaji, Goa, India
[5] Cyberonics, Emerging Therapies, Houston, TX USA
[6] Biodev, San Francisco, CA USA
[7] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90024 USA
[8] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
关键词
Heart failure; autonomic regulation therapy; vagus nerve stimulation; nonpharmacologic therapy; HEALED MYOCARDIAL-INFARCTION; ISCHEMIA-REPERFUSION INJURY; LEFT-VENTRICULAR FUNCTION; VAGAL-STIMULATION; RATE-VARIABILITY; SUDDEN-DEATH; MORTALITY; ATRIAL; DOGS; ARRHYTHMIAS;
D O I
10.1016/j.cardfail.2014.08.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: ANTHEM-HF evaluated a novel autonomic regulation therapy (ART) via either left or right vagus nerve stimulation (VNS) in patients with heart failure (HF) and reduced ejection fraction (HFrEF). Methods and Results: Sixty subjects (New York Heart Association [NYHA] functional class left ventricular ejection fraction (LVEF) <= 40%, left ventricular end-diastolic diameter >= 50 mm to <80 mm) receiving optimal pharmacologic therapy were randomized at 10 sites. VNS systems were randomly implanted on the left (n = 31) or right (n = 29) side. All patients were successfully implanted and 59 were titrated over 10 weeks to a well tolerated stimulation intensity. One patient died 3 days after an embolic stroke that occurred during implantation. Common device-related adverse events after VNS titration were transient mild dysphonia, cough, and oropharyngeal pain, which were similar for left- and right-side VNS. After 6 months of ART, the adjusted left-right differences in LVEF, left ventricular end-systolic volume (LVESV), and left ventricular end-systolic diameter (LVESD) were 0.2% (95% CI -4.4 to 4.7), 3.7 mL (95% CI -7.0 to 14.4), and 1.3 mm (95% CI -0.9 to 3.6), respectively. In the combined population, absolute LVEF improved by 4.5% (95% CI 2.4-6.6), LVESV improved by -4.1 mL (95% CI -9.0 to 0.8), and LVESD improved by -1.7 mm (95% CI -2.8 to -0.7). Heart rate variability improved by 17 ms (95% CI 6.5-28) with minimal left-right difference. Six-minute walk distance improved an average of 56 m (95% CI 37-75); however, improvement was greater for right-side ART (77 m [95% CI 49-105]). NYHA functional class improved in 77% of patients (baseline to 6 months). Conclusions: Chronic open-loop ART via left- or right-side VNS is feasible and well tolerated in HFrEF patients. Safety and efficacy measures are encouraging and warrant further study.
引用
收藏
页码:808 / 816
页数:9
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