Pediatric Heart Center, Justus-Liebig University, Feulgenstrasse 12, 35385, Giessen, Germany.
Pediatric Cardiology, University Clinic, Frankfurt, Germany.
Paediatr Drugs. 2021 Mar;23(2):195-202. doi: 10.1007/s40272-021-00438-2. Epub 2021 Mar 13.
Newborns with hypoplastic left heart (HLH) are usually palliated with the Norwood procedure or a hybrid stage I procedure. Hybrid is our preferred approach. Given the critical relationship between stage I, interstage, and comprehensive stage II or advanced biventricular repair, we hypothesized that appropriate drug treatment is a significant therapeutic cornerstone, especially for the management of the high-risk interstage.
We report a single-center observational study addressing the cardiovascular effects of, in particular, oral β-blockers and the additional use of angiotensin-converting enzyme (ACE) and mineralocorticoid inhibitors.
In total, 51 newborns-30 with HLH syndrome (HLHS) and 21 with HLH complex (HLHC)-with a median bodyweight of 3.0 kg (range 1.9-4.4; nine with bodyweight ≤ 2500 g) underwent an uneventful "Giessen hybrid approach" using a newly approved duct stent. All patients were discharged home with a single, double or triple therapy consisting of ß-blockers, ACE and mineralocorticoid inhibitors; 90% of the patients received bisoprolol, 10% received propranolol, 72% received lisinopril, and 78% received spironolactone. Resting heart rate decreased from 138 bpm (range 112-172; n = 51) at admission to 123 bpm (range 99-139; n = 51) at discharge and 110 bpm before stage II/biventricular repair/heart transplantation (range 90-140; n = 37) accompanied by favorable bodyweight gain. No side effects were evident.
In view of drug risk/benefit profiles, as well as the variable morphology and hemodynamics, the highly selective β1-adrenoceptor blocker bisoprolol is our preferred drug for treatment of HLHS/HLHC in the interstage. We avoid using ACE inhibitor monotherapy and exclude potential risks for coronary and cerebral perfusion pressure beforehand.
患有左心发育不良(HLH)的新生儿通常通过 Norwood 手术或杂交一期手术进行姑息治疗。我们更倾向于采用杂交手术。鉴于一期、过渡和全面二期或高级双心室修复之间的关键关系,我们假设适当的药物治疗是一个重要的治疗基石,特别是对高危过渡阶段的管理。
我们报告了一项单中心观察性研究,重点关注特别是口服β受体阻滞剂的心血管作用,以及血管紧张素转换酶(ACE)和盐皮质激素抑制剂的额外使用。
共有 51 名新生儿-30 名患有 HLH 综合征(HLHS)和 21 名患有 HLH 复合征(HLHC)-体重中位数为 3.0 公斤(范围 1.9-4.4;9 名体重≤2500 克)接受了一项使用新批准的导管支架的“吉森杂交手术”。所有患者均在家中出院,接受单一、双重或三重治疗,包括β受体阻滞剂、ACE 和盐皮质激素抑制剂;90%的患者使用比索洛尔,10%的患者使用普萘洛尔,72%的患者使用赖诺普利,78%的患者使用螺内酯。静息心率从入院时的 138bpm(范围 112-172;n=51)降至出院时的 123bpm(范围 99-139;n=51),在二期/双心室修复/心脏移植前降至 110bpm(范围 90-140;n=37),同时体重增加良好。没有明显的副作用。
鉴于药物风险/获益情况,以及形态和血液动力学的变化,高度选择性β1 肾上腺素能受体阻滞剂比索洛尔是我们在过渡阶段治疗 HLHS/HLHC 的首选药物。我们避免使用 ACE 抑制剂单药治疗,并预先排除对冠状动脉和脑灌注压的潜在风险。