Left-Sided Atrioventricular Valve Regurgitation After the Repair of Complete Atrioventricular Septal Defect.

IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Takaya Hoashi, Akinori Hirano, Ryusuke Hosoda, Haruhiro Nagase, Yuji Fuchigami, Yukino Iijima, Takaaki Suzuki
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Abstract

This study aimed to investigate left-sided atrioventricular valve outcome after the repair of complete atrioventricular septal defect from single-institutional retrospective chart review. From 1998 to 2022, 55 patients with complete atrioventricular septal defect and balanced 2 ventricles underwent biventricular repair. Median age and weight at repair were 5.5 months old [interquartile range, 3.4-9.1] and 4.6 kg [3.9-5.9]. Analyzed possible risk factors were Rastelli classification, low birth weight < 2.5 kg, preterm < 37 weeks, proceeding pulmonary artery banding, Down syndrome, persistent left superior vena cava, tetralogy of Fallot, early surgical era < 2010, preoperative left-sided atrioventricular valve regurgitation > mild, modified single-patch repair, small left mural leaflet, and complete left-sided atrioventricular valve cleft closure. No patients underwent left-sided atrioventricular valve replacement at the timing of repair. No patient required subsequent single ventricular conversion. The median follow-up period in survivors was 11.0 years. The survival rate at 15 years from repair was 96.4%. Freedom from moderate or greater left-sided atrioventricular valve regurgitation rate at 10 years was 58.4%. After elimination of 3 patients undergone complete closure then experienced tone of closed cleft, complete cleft closure was significant inhibitor for moderate or greater left-sided atrioventricular valve regurgitation (p = 0.034, Odds ratio: 0.36, 95% Confidence intervals: 0.14-0.93). Twelve patients underwent 15 reoperations for left-sided atrioventricular valve. All 4 patients who developed left-sided atrioventricular valve stenosis and backward pulmonary hypertension required prosthetic valve replacement. Incomplete cleft closure was the only risk factor for significant postoperative left-sided atrioventricular valve regurgitation. Already small left-sided atrioventricular valve by previous repair developed significant regurgitation, it is no longer repairable therefore required to be replaced.

修复完全性房室隔缺损后的左侧房室瓣反流
本研究旨在通过单个机构的回顾性病历审查,研究完全性房室间隔缺损修复术后左侧房室瓣的预后。从1998年到2022年,55名患有完全性房室间隔缺损且两个心室平衡的患者接受了双心室修补术。修复时的中位年龄和体重分别为5.5个月大[四分位间范围为3.4-9.1]和4.6公斤[3.9-5.9]。分析的可能风险因素包括拉斯特利分类、出生体重轻、改良的单补片修复、左室壁小叶和左侧房室瓣裂完全闭合。没有患者在修复时接受左侧房室瓣置换术。没有患者需要随后进行单心室转换。幸存者的中位随访时间为 11.0 年。修复后15年的存活率为96.4%。10年后无中度或更严重左侧房室瓣返流的比例为58.4%。在剔除了3名接受完全闭合手术后出现闭合裂隙音的患者后,完全闭合裂隙对中度或更严重的左侧房室瓣反流有显著抑制作用(P = 0.034,Odds ratio:0.36,95% 置信区间:0.14-0.93)。12 名患者因左侧房室瓣接受了 15 次再手术。4名出现左侧房室瓣狭窄和后向肺动脉高压的患者都需要进行人工瓣膜置换术。裂隙关闭不全是术后左侧房室瓣明显反流的唯一风险因素。先前修复的左侧房室小瓣膜已经出现了明显的反流,无法再进行修复,因此需要进行人工瓣膜置换。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatric Cardiology
Pediatric Cardiology 医学-小儿科
CiteScore
3.30
自引率
6.20%
发文量
258
审稿时长
12 months
期刊介绍: The editor of Pediatric Cardiology welcomes original manuscripts concerning all aspects of heart disease in infants, children, and adolescents, including embryology and anatomy, physiology and pharmacology, biochemistry, pathology, genetics, radiology, clinical aspects, investigative cardiology, electrophysiology and echocardiography, and cardiac surgery. Articles which may include original articles, review articles, letters to the editor etc., must be written in English and must be submitted solely to Pediatric Cardiology.
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