Liu Ying-long, Hu Sheng-shou, Shen Xiang-dong, Li Shou-jun, Wang Xu, Yan Jun, Cui Bin
Pediatric Center of Cardiac Surgery, Cardiovascular Institute and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100037, China.
Zhonghua Yi Xue Za Zhi. 2006 Jan 3;86(1):23-5.
To summarize the experience in arterial switch operation (ASO) for complex congenital heart defect (CHD) with severe pulmonary hypertension (PH) and ventriculoarterial discordant connection in children older than 6 months.
Twenty-three consecutive pediatric patients suffering from severe CHD, such as transposition of great arteries (TGA), Taussing-Bing anomaly, etc, with moderate to severe PH, 15 male and 8 female, aged 7-84 months, with the body weight of 4.5-20.0 kg, pulmonary pressure of 24.0-80.0 mm Hg, and pulmonary resistance of 49.2-1261.9 dyn.s.cm(-5), and with different complication such as left ventricular outflow tract obstruction (3 cases), subpulmonary membrane (1 case), and subaortic membrane (1 case), underwent ASO under general anesthesia and extracorporeal circulation with low temperature (18 degrees C-22 degrees C) and low volume blood flow (50 ml.kg(-1).min(-1)). The complicated anomalies were corrected simultaneously. Nitric oxide and alpha-blocker were used to the children with PH during the peri-operational period.
Twenty children survived, and were cured and discharged with an obvious improvement of heart function, only one of which had sequel of coma due to cerebral anoxia. After operation the pulmonary pressure decreased to 23 mm Hg +/- 9 mm Hg, significantly lower than that before operation (P = 0.000). Physical activities increased obviously. Three children died post-operatively of the reasons un-related to the pre-operative PH and pulmonary arterial resistance, with a mortality of 13.04%. Follow-up of 14 +/- 8 months showed no death and complication.
ASO can still realize satisfactory early results for the children older than 6 months suffering from complex CHD with moderate to severe PH and ventriculoarterial discordant connection provided they are in a rather good condition without severe cyanosis (SaO(2) > 60%) and with the pulmonary arterial resistance being acceptable (pressure of right atrium < 1000 dyn.s.cm(-5)).
总结6个月以上儿童复杂先天性心脏病(CHD)合并重度肺动脉高压(PH)及心室动脉连接不一致时行动脉调转术(ASO)的经验。
连续23例患有严重CHD的儿科患者,如大动脉转位(TGA)、陶西格-宾畸形等,伴有中度至重度PH,男15例,女8例,年龄7-84个月,体重4.5-20.0 kg,肺动脉压24.0-80.0 mmHg,肺血管阻力49.2-1261.9 dyn.s.cm⁻⁵,伴有不同并发症,如左心室流出道梗阻(3例)、肺动脉瓣下隔膜(1例)和主动脉瓣下隔膜(1例),在全身麻醉和体外循环下,采用低温(18℃-22℃)和低流量血流(50 ml.kg⁻¹.min⁻¹)行ASO。同时矫正复杂畸形。围手术期对合并PH的患儿使用一氧化氮和α受体阻滞剂。
20例患儿存活,治愈出院,心功能明显改善,仅1例因脑缺氧留有昏迷后遗症。术后肺动脉压降至23 mmHg±9 mmHg,明显低于术前(P = 0.000)。体力活动明显增加。3例患儿术后因与术前PH和肺动脉阻力无关的原因死亡,死亡率为13.04%。随访14±8个月无死亡及并发症。
对于6个月以上患有复杂CHD合并中度至重度PH及心室动脉连接不一致的患儿,只要病情较好,无严重紫绀(SaO₂>60%)且肺动脉阻力可接受(右心房压力<1000 dyn.s.cm⁻⁵),ASO仍可取得满意的早期效果。