一期手术治疗主动脉缩窄合并心内畸形86例

Yuhao Wu, Yuehang Zhou, X. Jin, Hongyu Kuang, Yonggang Li, Chun Wu
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摘要

目的总结婴幼儿主动脉缩窄合并心内异常的临床特点。方法收集2009年8月至2017年8月诊断为CoA合并心内异常的86例婴儿的资料。回顾性分析术前诊断、手术表现及术后随访情况。男56例,女30例,平均(95.1±78.0)天,体重(4.6±1.2)kg。解剖类型包括导管前CoA 37例,导管周围CoA 44例,导管后CoA 5例。该组还包括73名合并VSD的婴儿,59名合并ASD的婴儿,2名合并DORV的婴儿,1名合并TAPVC的婴儿。结果所有患者均行伴有心内异常的CoA单期修复。平均手术时间为(279.0±56.4)min,平均体外循环时间为(162.3±51.0)min,平均主动脉交叉夹持时间为(74.7±25.2)min,平均ICU住院时间为(7.4±4.7)d,平均通气时间为(101.1±75.4)h。出院前残留过缩梯度明显低于术前过缩梯度[(42.3±17.7)mmHg vs(22.1±9.4)mmHg, P<0.001],术后早期死亡7例。79例住院幸存者平均随访时间为(31.0±27.4)个月,无晚期死亡病例。医院幸存者最后一次随访时血管过缩梯度为(21.2±11.0)mmHg。29例经缩窄梯度大于20 mmHg,但仅有4例有明显下肢发育迟缓临床症状的患者被推荐为球囊血管成形术顾问。2年随访累计无再狭窄生存率为69.2%。结论单期修复CoA合并心内异常是安全有效的,可避免早期二次手术,早中期随访效果满意。关键词:先天性心脏病主动脉缩窄手术婴儿
本文章由计算机程序翻译,如有差异,请以英文原文为准。
One-stage surgical treatment of 86 cases of aortic coarctation combined with intracardiac malformation
Objective To summarize the clinical characteristics of coarctation of the aorta(CoA) associated with intracardiac anomalies in infants. Methods The data from August 2009 to August 2017 of 86 infants who were diagnosed with CoA associated with intracardiac anomalies. Preoperative diagnosis, surgical findings and post-operation follow-up were analyzed retrospectively. There were 56 boys an 30 girls, aqed(95.1±78.0) days, weight(4.6±1.2) kg. Anatomical types included 37 cases of pre-ductal CoA, 44 cases of peri-ducutal CoA, and 5 cases of post-ductal CoA. And this group also included 73 infants complicating VSD, 59 infants complicating ASD, 2 infants complicating DORV, and 1 infant complicating TAPVC. Results All of the included patients underwent single-stage repair of CoA associated with intracardiac anomalies. Mean operative time was(279.0±56.4) min, mean cardiopulmonary bypass time was(162.3±51.0) min, and mean aorta cross-clamp time was(74.7±25.2) min. Mean length of ICU stay and ventilation time were(7.4±4.7) days and(101.1±75.4) hours, respectively. The residual transcoarctation gradient before discharge was lower than pre-operative transcoarctation gradient significantly [(42.3±17.7) mmHg vs.(22.1±9.4)mmHg, P<0.001], and 7 early deaths were observed after surgery. The mean follow-up time of 79 hospital survivors was(31.0±27.4) months, and no late death was found. Transcoarctation gradient of hospital survivors in the last time follow-up was(21.2±11.0)mmHg. Transcoarctation gradient of 29 cases was higher than 20 mmHg, however, only 4 cases with significant clinical symptom of lower limbs retardation were recommended for ballon angioplasty consultant. The cumulative recoarctation-free survival in 2-year follow-up was 69.2%. Conclusion To avoid early second-stage operations, single-stage repair of CoA associated with intracardiac anomalies was effective and safe, and the outcomes of early to mid term follow-up were satisfactory. Key words: Congenital heart disease Coarctation of the aorta Surgery Infants
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