Çetinarslan Özge, Yazıcı Sinan Efe, Atasever Ahmet
Department of Cardiology, TC Demiroğlu Science University, Istanbul Florence Nightingale Hospital, İstanbul, Turkey.
Liver Transplantation Center, TC Demiroğlu Science University, Istanbul Florence Nightingale Hospital, Istanbul, Turkey.
Ann Transplant. 2025 Aug 12;30:e950166. doi: 10.12659/AOT.950166.
BACKGROUND Chronotropic incompetence often prolongs dobutamine stress echocardiography (DSE) and provokes adverse events in liver-transplant (LT) candidates. We evaluated whether administering atropine 1 stage earlier than conventionally recommended improves test efficiency and tolerability. MATERIAL AND METHODS In this retrospective single-center study, 69 end-stage liver disease patients were assigned to 3 cohorts according to the protocol used: Group 1 - high-dose dobutamine alone (n=24); Group 2 - "late" atropine (1 mg at 40 µg/kg/min; n=22); Group 3 - "early" atropine (at 30 µg/kg/min; n=23). Primary endpoints were target heart rate (HR) achievement, procedure time, hypotension, and ventricular extrasystole (VES). RESULTS Target HR was reached in 83%, 86%, and 95% of Groups 1-3, respectively (P<0.001). Mean procedure duration fell from 27.82±2.06 min with late atropine to 18.48±0.95 min with early atropine (-33.6%). Hypotension dropped from 50.0% to 8.7% (relative reduction≈83%) and VES decreased from 59.1% to 13.0% (≈78%). Cumulative dobutamine exposure was halved (≈1 113→≈554 µg/kg). No early-atropine patients experienced test-terminating complications. CONCLUSIONS Introducing atropine at the preceding dobutamine stage offers a simple, cost-neutral modification that accelerates DSE, halves drug exposure, and substantially improves hemodynamic and arrhythmic safety in LT candidates. Prospective trials should confirm whether this streamlined protocol can be adopted as the new standard for chronotropically challenging patients.
变时性功能不全常使多巴酚丁胺负荷超声心动图(DSE)时间延长,并在肝移植(LT)候选者中引发不良事件。我们评估了比传统建议提前1个阶段给予阿托品是否能提高检测效率和耐受性。
在这项回顾性单中心研究中,69例终末期肝病患者根据使用的方案分为3组:第1组——仅使用高剂量多巴酚丁胺(n = 24);第2组——“晚期”给予阿托品(40μg/kg/min时给予1mg;n = 22);第3组——“早期”给予阿托品(30μg/kg/min时给予;n = 23)。主要终点为目标心率(HR)达标情况、检查时间、低血压和室性期前收缩(VES)。
第1 - 3组分别有83%、86%和95%的患者达到目标HR(P<0.001)。平均检查持续时间从晚期给予阿托品时的27.82±2.06分钟降至早期给予阿托品时的18.48±0.95分钟(-33.6%)。低血压发生率从50.0%降至8.7%(相对降低约83%),VES从59.1%降至13.0%(约78%)。多巴酚丁胺累积暴露量减半(约1113→约554μg/kg)。没有早期给予阿托品的患者出现检查终止并发症。
在前一个多巴酚丁胺阶段给予阿托品是一种简单、成本中性的改进措施,可加速DSE,使药物暴露量减半,并显著提高LT候选者的血流动力学和心律失常安全性。前瞻性试验应确认这种简化方案是否可作为变时性功能不全患者的新标准采用。