首页> 外文期刊>European journal of heart failure: journal of the Working Group on Heart Failure of the European Society of Cardiology >Effect of atrioventricular optimization on circulating N-terminal pro brain natriuretic peptide following cardiac resynchronization therapy
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Effect of atrioventricular optimization on circulating N-terminal pro brain natriuretic peptide following cardiac resynchronization therapy

机译:心脏再同步治疗后房室优化对循环性N末端脑钠肽前体的影响

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AimsFollowing CRT, atrioventricular (AV) optimization is not routinely practised. To evaluate its clinical utility, we examined the effect of AV delay optimization on the prognostic biomarker NT-proBNP.Methods and resultsWe prospectively studied 72 patients (mean age 73 ± 12.5 years, 70.8% male, 55.6% ischaemic) undergoing iterative AV optimization. Patients were divided into those whose nominal setting appeared ideal and not changed (Group 1, n = 22) and those whose AV delay was optimized (Group 2, n = 50). All patients underwent NT-proBNP assessment prior to CRT, and pre- and a median 5 days post-optimization. Compared with Group 1, NT-proBNP fell significantly in Group 2 patients (median 474 pg/mL) following optimization (P = 0.00001). A significant change in filling pattern (defined as a change in AV delay >50 ms) was required in 30% of patients, and it was this subgroup that derived the greater reduction in NT-proBNP levels [-1407 pg/mL, interquartile range (IQR) -3042 to -346 pg/mL] compared with those requiring <50 ms AV delay change (-125 pg/mL, IQR -1038 to 6 pg/mL), P = 0.0011. The benefit of AV optimization was principally observed in reverse remodelling non-responders (median -2167 pg/mL, IQR -3042 to -305 pg/mL) and in patients with a pseudonormal or restrictive filling pattern (median -1407 pg/mL, IQR -2809 to -342 pg/mL), compared with those with more benign diastolic filling (median - 264 pg/mL, IQR -1038 to -21 pg/mL), P = 0.033.ConclusionsIn one-third of patients, major filling pattern changes are achieved with AV optimization, associated with subsequent rapid falls in NT-proBNP. The greater the AV delay change, the larger the NT-proBNP fall, and non-responders and those with restrictive or pseudonormal filling despite CRT are most likely to benefit. All rights reserved.
机译:目的在CRT之后,通常不进行房室(AV)优化。为了评估其临床效用,我们检查了AV延迟优化对预后生物标志物NT-proBNP的影响。方法和结果我们前瞻性研究了72例进行迭代AV优化的患者(平均年龄73±12.5岁,男性70.8%,局部缺血55.6%)。将患者分为标称设置理想且未改变的患者(第1组,n = 22)和最佳AV延迟患者(第2组,n = 50)。所有患者均在CRT之前以及优化前后5天进行NT-proBNP评估。与第1组相比,优化后第2组患者的NT-proBNP显着下降(中位数474 pg / mL)(P = 0.00001)。 30%的患者需要显着改变充盈模式(定义为AV延迟变化> 50 ms),正是这一亚组导致NT-proBNP水平的更大降低[-1407 pg / mL,四分位间距(IQR)-3042至-346 pg / mL]与要求<50 ms AV延迟改变的那些(-125 pg / mL,IQR -1038至6 pg / mL)相比,P = 0.0011。 AV优化的好处主要体现在反向重塑无反应者(中值-2167 pg / mL,IQR -3042到-305 pg / mL)和假正常或限制性填充模式(中值-1407 pg / mL, IQR -2809至-342 pg / mL),而舒张压充盈程度更高(中位数-264 pg / mL,IQR -1038至-21 pg / mL),P = 0.033。结论在三分之一的患者中,严重填充模式的变化是通过AV优化实现的,与随后NT-proBNP的快速下降有关。 AV延迟变化越大,NT-proBNP下降幅度越大,无应答者和尽管使用CRT仍具有限制性或伪正常填充的应答者最有可能受益。版权所有。

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