Central venous pressure as a method of optimising atrio-ventricular delay after cardiac surgery

被引:0
|
作者
Tindale, Alexander [1 ,2 ]
Cretu, Ioana [3 ]
Gomez, Naomi [1 ]
Haynes, Ross [1 ]
Meng, Hongying [3 ]
Mason, Mark J. [1 ,3 ]
Francis, Darrel P. [2 ]
机构
[1] Guys & St Thomas Fdn Trust, Harefield Hosp, Dept Cardiol, London, England
[2] Imperial Coll London, Natl Heart & Lung Inst, London, England
[3] Brunel Univ London, Uxbridge, England
来源
PLOS ONE | 2025年 / 20卷 / 01期
关键词
RESYNCHRONIZATION THERAPY; AV DELAY; OPTIMIZATION;
D O I
10.1371/journal.pone.0310905
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction Haemodynamic atrioventricular delay (AVD) optimisation has primarily focussed on signals that are not easy to acquire from a pacing system itself, such as invasive left ventricular catheterisation or arterial blood pressure (ABP). In this study, standard clinical central venous pressure (CVP) signals are tested as a potential alternative. Methods Sixteen patients with a temporary pacemaker after cardiac surgery were studied. AV delay optimisation was performed by alternating between a reference AVD of 120ms and tested settings ranging from 40 to 280ms, with 8 replicates for each setting. Alongside (a) the raw data, three methods of correcting for respiration were tested: (b) limiting analysis to a respiratory cycle, (c) asymmetric least squares (ALS) and (d) discrete wavelet transform (DWT). The utility of a quality control step was tested. Results CVP signals were a mirror image of the systolic ABP signals: The four R values were -0.674, -0.692, -0.631, -0.671 respectively (all p<0.001). With quality control, the mirror image was best for DWT (R = -0.76, p<0.001), with the CVP and ABP optima agreeing well (R = 0.78, p<0.001). The automated quality control signal correctly predicted the gap between the AVD optima calculated from ABP and CVP (R = 0.8, p<0.001). Conclusions Central venous pressure signals could be used to optimise AVD, because they have a reliable inverse relationship with ABP when pacemaker settings undergo protocolised testing. However, protocols need careful design to circumvent spontaneous biological variability.
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