Operative and nonoperative outcomes in patients with trisomy 13 and 18 with congenital heart disease

Christina L. Greene MD , Antonia Schulz MD , Mariana Chávez MD , Steven J. Staffa MS , David Zurakowski MS, PhD , Kevin G. Friedman MD , Sitaram M. Emani MD , Christopher W. Baird MD
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Abstract

Objective

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.

Methods

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.

Results

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 (P < .003). Nonoperative treatment had an increased risk of mortality (hazard ratio, 3.28; 95% CI, 1.46-7.4; P = .004).

Conclusions

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.

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13 和 18 三体综合征合并先天性心脏病患者的手术和非手术治疗效果
方法通过机构审查委员会批准的回顾性审查,确定所有入院的 13/18 三体综合征和先天性心脏病患者。结果1985年至2023年间,共发现62例13/18三体综合征患者(34例手术和28例非手术)(9例)和18/18三体综合征患者(53例)。手术组中 74% 为女孩,主要接受胸外科医师协会-欧洲心胸外科协会死亡率 1 类手术(n = 24 [71%]),中位年龄为 2.5 个月(四分位距 [IQR],1.3-4.5 个月)。与之相比,如果选择手术,64%(n = 18)的非手术队列将接受胸外科医师协会-欧洲心胸外科协会死亡率 1 类手术。最常见的诊断是室间隔缺损。术后重症监护室中位住院时间为6.5天(IQR,3.7-15天),总住院时间为15天(IQR,11-49天)。术后30天存活率为94%。手术组有 5 例院内死亡,非手术组有 7 例院内死亡。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)。手术组的一年存活率为 79%,而非手术组为 51.5%(P < .003)。不进行手术治疗会增加死亡风险(危险比,3.28;95% CI,1.46-7.4;P = .004)。结论:对于 13/18 三体综合征和先天性心脏病患者进行初级心脏修补术的作用存在争议。在我们的队列中,心脏修补术可以安全进行,早期死亡率较低,手术患者的长期存活率高于非手术患者。
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