Martens Pieter, Dupont Matthias, Mullens Wilfried
Department of Cardiology, Ziekenhuis Oost-Limburg, Genk, Belgium.
Doctoral School for Medicine and Life Sciences, Hasselt University, Diepenbeek, Belgium.
Acta Cardiol. 2020 Feb;75(1):49-53. doi: 10.1080/00015385.2018.1547469. Epub 2019 Jan 16.
Absence of beta-blocker use independently predicts appropriate therapy. Following cardiac resynchronisation therapy (CRT) implant, reverse remodelling and protection against bradycardia allows for beta-blocker dose uptitration. The differential dosing effects on the occurrence of a first episode of appropriate therapy in primary prevention CRT-defibrillator (CRT-D) patients remains unstudied. Changes in beta-blocker dose following CRT-D in consecutive primary prevention patients implanted between 2008 and 2015 were retrospectively studied. Beta-blocker dose was expressed as percent of target dose. Uptitration of beta-blocker dose following implant was calculated as the change in percent of target dose between implant and 6-months follow-up. Results from a prospectively maintained database of all device analysis were used to determine the occurrence of appropriate therapy. A total of 162 patients (68 ± 8 years) were studied. One hundred and ten (68%) patients underwent uptitration (mean 47 ± 19% in target dose) and 52 (32%) remained on a stable beta-blocker dose. During 37 ± 22 months follow-up, the cumulative percent of appropriate therapy was 31% in patient receiving no-uptitration versus 10% in the uptitrated patients (p < 0.001). After correction for known predictors of appropriate therapy, uptitration was independently associated with an OR = 0.263 (CI = 0.103-0.675; = 0.001) for the occurrence of appropriate therapy. Every 1%-increase in target dose for beta-blocker associated with a significant lower risk for appropriate therapy, OR = 0.982 (CI = 0.965-0.999; = 0.042). Following implantation of a primary prevention CRT-D, uptitration of beta-blockers associated with a reduced occurrence of a first episode of appropriate therapy for ventricular arrhythmias. An inverse dose-response effect was seen between beta-blocker dose and appropriate therapy.
未使用β受体阻滞剂可独立预测适当治疗。在植入心脏再同步治疗(CRT)后,逆向重构和预防心动过缓使得β受体阻滞剂剂量能够上调。在一级预防CRT除颤器(CRT-D)患者中,不同剂量的β受体阻滞剂对首次出现适当治疗的影响仍未得到研究。对2008年至2015年间连续植入的一级预防患者CRT-D后β受体阻滞剂剂量的变化进行了回顾性研究。β受体阻滞剂剂量以目标剂量的百分比表示。植入后β受体阻滞剂剂量的上调计算为植入时与6个月随访时目标剂量百分比的变化。使用前瞻性维护的所有设备分析数据库的结果来确定适当治疗的发生情况。共研究了162例患者(68±8岁)。110例(68%)患者进行了剂量上调(目标剂量平均为47±19%),52例(32%)患者的β受体阻滞剂剂量保持稳定。在37±22个月的随访期间,未上调剂量的患者中适当治疗的累积百分比为31%,而上调剂量的患者中为10%(p<0.001)。在校正了适当治疗的已知预测因素后,剂量上调与适当治疗发生的OR=0.263(CI=0.103-0.675;p=0.001)独立相关。β受体阻滞剂目标剂量每增加1%,适当治疗的风险显著降低,OR=0.982(CI=0.965-0.999;p=0.042)。在植入一级预防CRT-D后,β受体阻滞剂剂量上调与室性心律失常首次出现适当治疗的发生率降低相关。在β受体阻滞剂剂量与适当治疗之间观察到反向剂量反应效应。