医学
心律
四分位间距
血管闭合器
外科
心脏病学
股动脉
作者
Mark T Mills,Dhiraj Gupta,Vishal Luther,Maura M. Zylla,Piotr Futyma,Laura Perrotta,Michał Mazurek,Christian‐Hendrik Heeger,Lina Marcantoni,Andreas Metzner,K.R. Julian Chun
出处
期刊:Europace
[Oxford University Press]
日期:2025-06-16
标识
DOI:10.1093/europace/euaf117
摘要
Abstract Aims Reliable vascular access and haemostasis techniques are important to the safety of electrophysiology (EP) procedures. This European Heart Rhythm Association (EHRA) survey aimed to evaluate contemporary vascular access site management practices across international EP centres. Methods and results A 30-question survey was disseminated via the EHRA between March and April 2025, with 401 responses from professionals across 51 countries. Most respondents were cardiology consultants/attendings (82.0%), with 57.3% performing over 150 EP procedures annually. Ultrasound guidance for vascular access was usually or always used by 71.7%, though 21.4% used it rarely or never, and only 17.3% had received formal ultrasound training. Institutional protocols for haemostasis were lacking in around half (46.8%) of centres. Suture-mediated closure was the most common method for haemostasis (60.4%), followed by manual compression (33.0%) and vascular closure devices (VCDs, 5.8%). The figure-of-eight suture with a hand-tied knot was the most frequently used suture technique (79.7%). Just over a third (36.0%) had experience with VCDs, typically reserved for high-risk cases. For procedures requiring transeptal access, 38.1% administered heparin before transeptal puncture, while protamine was rarely or never used by 62.1%. Anticoagulation was partially interrupted in 52.1% and continued uninterrupted in 41.1% of routine AF ablations. Median bed rest duration post-procedure ranged from 4 hours (right-sided EP procedures) to 6 hours (AF or left-sided EP procedures). The average quoted vascular complication risk during consent was 3% [interquartile range 1–5%]. Conclusion This survey highlights marked variation in vascular access site management during and following EP procedures, emphasising the need for further clinical trials to inform best practice and guide future standardisation efforts.
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