Division of Pediatric Critical Care Medicine, Department of Pediatrics, University of Rochester, Rochester, NY, USA.
Division of Pediatric Cardiology, Department of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, USA.
World J Pediatr Congenit Heart Surg. 2024 Sep;15(5):604-613. doi: 10.1177/21501351241247501. Epub 2024 Aug 8.
Hybrid stage I palliation (HS1P) has been utilized for patients with single ventricle (SV) congenital heart disease (CHD). To date, reports on the use of HS1P for other indications including biventricular (BiV) CHD have been limited. We performed a single-center retrospective cohort study of patients who underwent HS1P with an anticipated physiologic outcome of BiV repair, or with an undetermined SV versus BiV outcome. Patient characteristics and outcomes from birth through definitive repair or palliation were collected and reported with descriptive statistics. Nineteen patients underwent HS1P with anticipated BiV repair. Extracardiac and intracardiac risk factors (ICRF) were common. Ultimately, 13 (68%) patients underwent BiV repair, 1 (5%) underwent SV palliation, and 5 (26%) died prior to further palliation or repair. Resolution of ICRF tracked with BiV outcome (6/6, 100%), persistence of ICRF tracked with SV outcome or death (3/3, 100%). Twenty patients underwent HS1P with an undetermined outcome. Ultimately, 13 (65%) underwent BiV repair, 6 (30%) underwent SV palliation, and 1 (5%) underwent transplant. There were no deaths. Intracardiac risk factors were present in 15 of 20 patients (75%); BiV repair only occurred when all ICRF resolved (67%). Post-HS1P complications and reinterventions occurred frequently in both groups, through all phases of care. Hybrid stage 1 palliation can be used to defer BiV repair and to delay decision between SV palliation and BiV repair. Resolution of ICRF was associated with ultimate outcome. In this high-risk group, complications are common, and mortality especially in the marginal BiV patient is high.
杂交一期姑息治疗(HS1P)已用于患有单心室(SV)先天性心脏病(CHD)的患者。迄今为止,关于将 HS1P 用于其他适应症(包括双心室(BiV)CHD)的报告有限。我们对在预期生理结果为 BiV 修复的情况下或在不确定 SV 与 BiV 结果的情况下接受 HS1P 的患者进行了单中心回顾性队列研究。收集并报告了从出生到确定性修复或姑息治疗的患者特征和结局,并进行了描述性统计分析。19 名患者接受了 HS1P 治疗,预期进行 BiV 修复。心脏外和心脏内危险因素(ICRF)很常见。最终,13 名(68%)患者进行了 BiV 修复,1 名(5%)进行了 SV 姑息治疗,5 名(26%)在进一步姑息治疗或修复前死亡。ICRF 的解决与 BiV 结局相关(6/6,100%),ICRF 的持续存在与 SV 结局或死亡相关(3/3,100%)。20 名患者接受了 HS1P 治疗,结果不确定。最终,13 名(65%)患者进行了 BiV 修复,6 名(30%)患者进行了 SV 姑息治疗,1 名(5%)患者进行了移植。没有死亡。20 名患者中有 15 名(75%)存在 ICRF;只有当所有 ICRF 解决时才进行 BiV 修复(67%)。两组患者在整个治疗过程中都经常出现 HS1P 后并发症和再次干预。HS1P 可用于延迟 BiV 修复,并延迟 SV 姑息治疗和 BiV 修复之间的决策。ICRF 的解决与最终结局相关。在这个高危人群中,并发症很常见,尤其是边缘 BiV 患者的死亡率很高。