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中国现代手术学杂志  2017, Vol. 21 Issue (5): 357-360    DOI: 10.16260/j.cnki.1009-2188.2017.05.009
  临床论著 |
婴幼儿主动脉缩窄合并心内畸形及肺动脉高压的外科治疗
周文武,伍明,陈飞,侯安新,周庆,张志功,杨劲松
湖南省人民医院心胸外科,长沙 410005
Singlestage Correction of Coarctation of Aorta with Intracardiac Anomalies and Pulmonary Arterial Hypertension in Infants
ZHOU Wen-wu, WU Ming, CHEN Fei, HOU An-xin, ZHOU Qing, ZHANG Zhi-gong, YANG Jing-song
Department of Cardiovascular Surgery, Hunan Provincial People's Hospital, Changsha410005, Hunan, China
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摘要 目的总结分析婴幼儿主动脉缩窄(coarctation of aorta, COA)合并心内畸形及肺动脉高压(pulmonary arterial hypertension, PAH) 行外科手术治疗的经验体会。方法采用回顾性病例对照研究, 以2012年2月至2017年2月在我科行手术治疗的16例COA合并心内畸形婴幼儿为研究组(A组),术中均直接肺动脉测压确诊合并PAH, 另取同期室间隔缺损合并同等PAH的婴幼儿20例为对照组(B组),比较两组患儿的围术期临床资料及随访结果。结果两组均为胸骨正中切口体外循环下手术,两组转流前肺动脉平均压无明显差异(P>0.05),A组停机后肺动脉平均压为(28.4±8.8) mmHg(1 mmHg=0.133 kPa),高于B组的(21.2±5.0)mmHg,A组体外循环转流时间、主动脉阻断时间及术后呼吸机通气时间均长于B组(P<0.05);全组无手术死亡,无术后截瘫等并发症,A组术后上、下肢动脉压压差小于10 mmHg,术后3月超声复查无PAH。结论COA合并左向右分流型心内畸形者继发PAH进展更快,及时矫正心内畸形并解除主动脉缩窄可取得满意外科疗效。
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ZHOU Wen-wu
WU Ming
CHEN Fei
HOU An-xin
ZHOU Qing
ZHANG Zhi-gong
YANG Jing-song
关键词:  主动脉缩窄  肺动脉高压  体外循环    
Abstract: ObjectiveTo explore the clinical experiences of surgical treatments for coarctation of aorta(COA) with intracardiac anomalies and pulmonary arterial hypertension (PAH) in infants.MethodsA retrospective casecontrol study was carried out in 36 infants operated in our hospital during February 2012 to February 2017. There were 16 cases with COA and PAH in group A, and 20 cases with ventricular septal defect(VSD) and PAH in group B. The perioperative clinical data and followup data of the two groups were compared.ResultsAll the patients were operated by both arch repair and intracardiac anomalies repair completed via sternotomy under extracorporeal circulation in singlestage. There was no significant difference of the mean pulmonary arterial pressure preoperatively between the two groups(P>0.05). By the end of extracorporeal circulation, the mean pulmonary arterial pressure of group A was (28.4±8.8) mmHg(1mmHg=0.133 kPa), which was higher than (21.2±5.0 )mmHg of group B(P<0.05). It was longer in extracorporeal circulation time, aortic block time and postoperative ventilator aeration time of group A(P<0.05). There was no mortality, nor paraplegia after operation. The postoperative arterial pressure gradient between the upper and the lower extremities was less than 10 mmHg, and no PAH was found under ultrasound detection 3 months after operation.ConclusionsIt would turn a rapider deteriorate in infants of COA and left to right shunt combined with PAH. It may get satisfactory effect if correction of the heart malformation and relief of COA could achieve in time.
Key words:  aortic coarctation    pulmonary arterial hypertension    extracorporeal circulation
               出版日期:  2017-10-26      发布日期:  2018-05-25      期的出版日期:  2017-10-26
ZTFLH:  R654.2  
基金资助: 湖南省卫生和计划生育委员会湖南省高层次人才“225”工程项目 (编号:225人才计划201313)
作者简介:  周文武,48岁,男,湖南省人民医院心胸外科心胸外科主任医师,医学博士。
引用本文:    
周文武,伍明,陈飞,侯安新,周庆,张志功,杨劲松. 婴幼儿主动脉缩窄合并心内畸形及肺动脉高压的外科治疗[J]. 中国现代手术学杂志, 2017, 21(5): 357-360.
ZHOU Wen-wu, WU Ming, CHEN Fei, HOU An-xin, ZHOU Qing, ZHANG Zhi-gong, YANG Jing-song. Singlestage Correction of Coarctation of Aorta with Intracardiac Anomalies and Pulmonary Arterial Hypertension in Infants. Chinese Journal of Modern Operative Surgery, 2017, 21(5): 357-360.
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http://www.surgerychina.com/CN/10.16260/j.cnki.1009-2188.2017.05.009  或          http://www.surgerychina.com/CN/Y2017/V21/I5/357
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