Department of Veterans Affairs Medical Center, Cardiovascular Section, Oklahoma City, Oklahoma.
Heart Rhythm Institute, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Heart Rhythm. 2018 Feb;15(2):240-247. doi: 10.1016/j.hrthm.2017.10.004. Epub 2017 Oct 7.
Inappropriate sinus tachycardia (IST) is debilitating despite available treatment. Off-label use of ivabradine for IST prompted this systematic analysis of existing data quality and sample size estimates for adequately powered studies.
To determine clinical efficacy of ivabradine in IST from pooled prospective studies.
Analysis included ivabradine studies for IST participants without structural heart disease and with follow-up of ≥2 weeks. Heart rate and symptom reduction with ivabradine were estimated based on results of subjective change in symptoms assessed by various data instruments used in each study. Studies were assessed for quality using validated checklists. Sample sizes were calculated based on the magnitude of symptom reduction encountered after treatment with ivabradine.
Nine studies met criteria, culminating in 145 patients pooled. Most patients were women (≥70%). Studies were small and not adequately powered, and all reported a decrease in maximum or mean resting heart rate or both, with complete or considerable amelioration of symptoms with ivabradine. Most studies had moderate quality with excellent consistency of study quality and narrow limits of agreement between the quality checklists. Sample size estimates for adequately powered studies with various placebo effects and comparisons with β-blockade are reported.
Ivabradine effectively reduces heart rate and symptoms in IST, but no study was adequately powered to account for the expected placebo effect on symptoms. A multicenter, randomized, placebo-controlled, active, comparative study with a β-blocker is needed for confirmation. This is especially relevant given the ivabradine's potential teratogenic effect, as many IST patients are females of childbearing potential.
尽管有治疗方法,但不适当的窦性心动过速(IST)仍然令人虚弱。伊伐布雷定在 IST 的标签外使用促使我们对现有数据质量和充分有力研究的样本量估计进行了系统分析。
从汇集的前瞻性研究中确定伊伐布雷定治疗 IST 的临床疗效。
分析包括无结构性心脏病且随访时间≥2 周的 IST 参与者的伊伐布雷定研究。根据每个研究中使用的各种数据仪器评估的症状主观变化的结果,估计伊伐布雷定对心率和症状的改善。使用经过验证的清单评估研究质量。根据治疗后伊伐布雷定引起的症状缓解程度计算样本量。
符合标准的 9 项研究最终纳入了 145 名患者。大多数患者为女性(≥70%)。这些研究规模较小且没有充分的效力,所有研究均报告最大或平均静息心率或两者均降低,并且伊伐布雷定完全或显著改善了症状。大多数研究的质量中等,研究质量的一致性极好,质量检查表之间的差异很小。报告了各种安慰剂效应和与β受体阻滞剂比较的充分有力研究的样本量估计值。
伊伐布雷定可有效降低 IST 的心率和症状,但没有研究充分有力地考虑到症状的预期安慰剂效应。需要进行一项多中心、随机、安慰剂对照、阳性、对照研究,以β受体阻滞剂作为比较药物进行确认。鉴于伊伐布雷定可能具有致畸作用,而许多 IST 患者是有生育能力的女性,因此这一点尤其重要。