新生儿期导管依赖性全身循环病变的处理:十年经验。

IF 1.9
Dilek Dilli, Hasan Akduman, Rumeysa Çitli, Utku Arman Örun, Vehbi Doğan, Mehmet Taşar, Tamer Yoldaş, Nurdan Dinlen Fettah, Ahmet Özyazıcı, Ayşegül Zenciroğlu
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引用次数: 0

摘要

背景:在导管依赖的左侧心脏病变中,体循环依赖于通过动脉导管从右到左的血流。这些病变可能是孤立的缺陷或复杂的疾病。目的:在本研究中,我们旨在探讨导管依赖性全身循环病变,特别是主动脉缩窄(CoA)和主动脉弓中断(IAA)的新生儿结局。方法:对2012 - 2022年我院心脏NICU收治的159例导管依赖性全身病变患者进行随访。我们回顾性地回顾了医院数据库中所有患者的病历。分析他们的临床和手术结果。结果的p值:159例患者中,120例(75.4%)检测到CoA, 39例(24.5%)检测到IAA。74例(61.6%)新生儿期CoA患者行心导管插入术;49例(40.8%)接受治疗,25例(20.8%)接受诊断。101例CoA患者(84.1%)在中位年龄14天(9-23天)时接受了手术。39例IAA患者中有34例(87.1%)接受了手术;单期修复13例(38.2%),两期修复21例(61.7%)。新生儿总死亡率为19.5% (n=31)。在多变量分析中,较高的STAT分类(OR:2.3, CI:95%, 1.1-5.1, p=0.03)和主要术后并发症的存在(OR:9.8, CI:95%, 2.1-35.1, p=0.003)增加了新生儿死亡的风险。结论:先天性导管依赖性主动脉异常新生儿由于其发病率和死亡率增高,围手术期护理十分必要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of Ductus-Dependent Systemic Circulatory Lesions in the Neonatal Period: A Ten-Year Experience.

Background: In ductus-dependent left-sided heart lesions, systemic circulation depends on right-to-left flow via the ductus arteriosus. These lesions may occur as an isolated defect or complex disease.

Objective: In this study, we aimed to investigate the neonatal outcomes of duct-dependent systemic circulatory lesions, especially aortic coarctation (CoA) and interrupted aortic arch (IAA).

Methods: A total of 159 patients with duct-dependent systemic lesions were followed up in the Cardiac NICU of our institution from 2012 to 2022. We retrospectively reviewed the medical charts of all patients from the hospital database. They were analyzed for clinical and surgical outcomes. A p-value of <0.05 was considered statistically significant.

Results: Of 159 patients, CoA was detected in 120 (75.4%) and IAA in 39 (24.5%) patients. Cardiac catheterization was performed in 74 (61.6%) patients with CoA in the neonatal period; 49 (40.8%) underwent therapeutic and 25 (20.8%) diagnostic procedures. One hundred one patients with CoA (84.1%) underwent surgery at a median age of 14 days (9-23). Thirty-four of 39 patients with IAA (87.1%) underwent surgery; single-stage repair was performed on 13 patients (38.2%), while two-stage repair was applied to 21 (61.7%) patients. The overall neonatal mortality rate was 19.5% (n=31). In multivariate analysis, the higher STAT categories (OR:2.3, CI:95%, 1.1-5.1, p=0.03) and the presence of major postoperative complications (OR:9.8, CI:95%, 2.1-35.1, p=0.003) have increased the risk of neonatal mortality.

Conclusion: Newborns with congenital duct-dependent aortic anomalies necessitate meticulous perioperative care due to their heightened risk of morbidity and mortality.

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