Greene Christina L, Schulz Antonia, Chávez Mariana, Staffa Steven J, Zurakowski David, Friedman Kevin G, Emani Sitaram M, Baird Christopher W
Department of Cardiac Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Mass.
Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Mass.
JTCVS Open. 2024 Jun 22;20:123-131. doi: 10.1016/j.xjon.2024.06.007. eCollection 2024 Aug.
To evaluate the short- and long-term outcomes of cardiac repair versus nonoperative management in patients with trisomy 13 and trisomy 18 with congenital heart disease.
An institutional review board-approved, retrospective review was undertaken to identify all patients admitted with trisomy 13/18 and congenital heart disease. Patients were divided into 2 cohorts (operated vs nonoperated) and compared.
Between 1985 and 2023, 62 patients (34 operated and 28 nonoperated) with trisomy 13 (n = 9) and trisomy 18 (n = 53) were identified. The operated cohort was 74% girls, underwent mainly The Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery mortality category 1 procedures (n = 24 [71%]) at a median age of 2.5 months (interquartile range [IQR], 1.3-4.5 months). This compares with the nonoperative cohort where 64% (n = 18) would have undergone The Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery mortality category 1 procedures if surgery would have been elected. The most common diagnosis was ventricular septal defect. Postoperative median intensive care unit stay was 6.5 days (IQR, 3.7-15 days) with a total hospital length of stay of 15 days (IQR, 11-49 days). Thirty-day postoperative survival was 94%. There were 5 in-hospital deaths in the operated and 7 in the nonoperated cohort. Median follow-up was 15.4 months (IQR, 4.3-48.7 months) for the operated and 11.2 months (IQR, 1.2-48.3 months) for the nonoperated cohorts. One-year survival was 79% operated versus 51.5% nonoperated ( < .003). Nonoperative treatment had an increased risk of mortality (hazard ratio, 3.28; 95% CI, 1.46-7.4; = .004).
Controversy exists regarding the role of primary cardiac repair in patients with trisomy 13/18 and congenital heart disease. Cardiac repair can be performed safely with low early mortality and operated patients had higher long-term survival compared with nonoperated in our cohort.
评估13三体和18三体合并先天性心脏病患者心脏修复术与非手术治疗的短期和长期疗效。
进行一项经机构审查委员会批准的回顾性研究,以确定所有因13/18三体和先天性心脏病入院的患者。将患者分为两组(手术组与非手术组)并进行比较。
1985年至2023年期间,共确定了62例患有13三体(n = 9)和18三体(n = 53)的患者(34例接受手术,28例未接受手术)。手术组中74%为女孩,主要接受了胸外科医师协会-欧洲心胸外科学会死亡率分类1级手术(n = 24 [71%]),中位年龄为2.5个月(四分位间距[IQR],1.3 - 4.5个月)。相比之下,非手术组中若选择手术,64%(n = 18)本可接受胸外科医师协会-欧洲心胸外科学会死亡率分类1级手术。最常见的诊断是室间隔缺损。术后重症监护病房中位住院时间为6.5天(IQR,3.7 - 15天),总住院时间为15天(IQR,11 - 49天)。术后30天生存率为94%。手术组有5例住院死亡,非手术组有7例。手术组的中位随访时间为15.4个月(IQR,4.3 - 48.7个月),非手术组为11.2个月(IQR,1.2 - 48.3个月)。手术组1年生存率为79%;非手术组为51.5%(P <.003);非手术治疗的死亡风险增加(风险比为3.28;95%置信区间为1.46 - 7.4;P = 0.004)。
对于13/18三体合并先天性心脏病患者行一期心脏修复术的作用存在争议。在我们的队列中,心脏修复术可安全进行,早期死亡率低且手术患者的长期生存率高于非手术患者。