Dollat Camille, Vergnat Mathieu, Laux Daniela, Stos Bertrand, Baruteau Alban, Capderou André, Demontoux Serge, Hamann Michel, Mokhfi Emir, Van Aerschot Isabelle, Roussin Régine, Le Bret Emmanuel, Ly Mohamed, Belli Emre, Lambert Virginie
Pôle des Cardiopathies Congénitales, Centre Chirurgical Marie Lannelongue, 133, avenue de la Résistance, 92350, Le Plessis-Robinson, France,
Pediatr Cardiol. 2015 Aug;36(6):1279-86. doi: 10.1007/s00246-015-1158-9. Epub 2015 Apr 9.
Prematurity is a recognized risk factor for morbidity and mortality following cardiac surgery. Postoperative and long-term outcomes after cardiac surgery performed in the preterm period are poorly described. The aim of this study was to analyze a population of preterm neonates operated on for critical congenital heart disease (CHD) before 37 weeks of gestational age (wGA) with special attention given to early and late mortality and morbidity. Between 2000 and 2013, 28 preterm neonates (median gestational age (GA) 34.3 weeks) underwent cardiopulmonary bypass (CPB) surgery for critical CHD before 37 wGA; records were retrospectively reviewed. All patients except three with single ventricle physiology had a single-stage anatomic repair. Overall mortality was 43 % (95 % CI 25-62). Risk factors for death were birth weight (p = 0.032) and weight at surgery (p = 0.037), independently of GA, preoperative status, CPB and aortic clamp time. Seven patients, including those with univentricular hearts, died during the postoperative period, and five in the first year after surgery. Median follow-up was 5.9 years (range 1 month-12.8 years). Kaplan-Meier survival rate was 75 % (95 % CI 59-91) at 1 month, and 57 % (95 % CI 39-75) at 1 and 5 years. Eight patients required reoperations after a delay of 2.8 ± 1.3 months; eight had bronchopulmonary dysplasia. At the end of follow-up, nine patients were asymptomatic. One-stage biventricular repair for critical CHD on preterm neonates was feasible. Mortality remained high but acceptable, mainly confined to the first postoperative year and related to small weight. Despite reoperations, long-term clinical status was good in most survivors. Further long-term prospective investigations are necessary to evaluate neurodevelopmental outcomes.
早产是心脏手术后发病和死亡的一个公认风险因素。关于早产期心脏手术后的术后及长期结局描述甚少。本研究的目的是分析一群孕龄(GA)小于37周时接受重症先天性心脏病(CHD)手术的早产新生儿,特别关注早期和晚期死亡率及发病率。2000年至2013年期间,28例早产新生儿(中位孕龄(GA)34.3周)在孕龄小于37周时接受了体外循环(CPB)下的重症CHD手术;对病历进行了回顾性分析。除3例单心室生理状态的患者外,所有患者均接受了一期解剖修复。总体死亡率为43%(95%可信区间25 - 62)。死亡的风险因素是出生体重(p = 0.032)和手术时体重(p = 0.037),与孕龄、术前状态、CPB及主动脉阻断时间无关。7例患者,包括单心室心脏患者,在术后期间死亡,5例在术后第一年死亡。中位随访时间为5.9年(范围1个月 - 12.8年)。1个月时的Kaplan - Meier生存率为75%(95%可信区间59 - 91),1年和5年时为57%(95%可信区间39 - 75)。8例患者在延迟2.8±1.3个月后需要再次手术;8例有支气管肺发育不良。随访结束时,9例患者无症状。对早产新生儿的重症CHD进行一期双心室修复是可行的。死亡率仍然很高但可接受,主要局限于术后第一年且与体重小有关。尽管进行了再次手术,但大多数幸存者的长期临床状况良好。需要进一步进行长期前瞻性研究以评估神经发育结局。