Chinese Journal of Modern Operative Surgery 2017, Vol. 21 Issue (5): 357-360 DOI: 10.16260/j.cnki.1009-2188.2017.05.009 |
Clinical Research |
|
|
|
|
|
Singlestage 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 |
|
|
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 casecontrol 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 followup 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 singlestage. 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.
|
Published: 25 May 2018
|
|
|
|
[1] |
Callahan C, Saudek D, Shillingford A, et al. Singlestage repair of coarctation of the aorta and ventricular septal defect: a comparison of surgical strategies and resource utilization[J]. World J Pediatr Congenit Heart Surg, 2017,8(5):559563. doi: 10.1177/2150135117727256.
|
[2] |
中华医学会心血管病学分会. 肺动脉高压筛查诊断与治疗专家共识[J]. 中华心血管病杂志, 2007, 35(11): 979987.
|
[3] |
武开宏, 孙剑, 莫绪明, 等. 儿童先天性主动脉缩窄的解剖特点及外科治疗策略[J]. 中华解剖与临床杂志, 2016, 21(6):548551.
|
[4] |
葛同开, 陈寄梅, 庄建, 等. 117例主动脉缩窄合并室间隔缺损一期矫治手术的疗效[J]. 中华胸心血管外科杂志, 2015, 31(3):138141.
|
[5] |
孙培吾. 瓣膜置换手术若干问题探讨[J]. 中国现代手术学杂志, 1998(2):8386.
|
[6] |
黄鹏, 罗金文, 刘剑, 等. 手术治疗新生儿主动脉缩窄合并室间隔缺损的安全性[J]. 中南大学学报(医学版), 2016, 41(7):696699.
|
[7] |
Luo K, Zheng J, Wang S, et al. Singlestage correction for taussigbing anomaly associated with aortic arch obstruction[J]. Pediatr Cardiol, 2017,38(8):15481555. doi: 10.1007/s0024601716946.
|
|
|
|