Singh Sunita, Wakhlu Ashish, Pandey Anand, Singh Anita, Kureel Shiv N, Rawat Jiledar, Srivastava Payal Mishra
Department of Pediatric Surgery, CSM Medical University (Erstwhile King George Medical University), Lucknow, Uttar Pradesh, India.
J Indian Assoc Pediatr Surg. 2012 Jul;17(3):107-10. doi: 10.4103/0971-9261.98123.
To analyze whether outcome of neonates having esophageal atresia with or without tracheoesophageal fistula (EA±TEF) associated with anorectal malformation (ARM) can be improved by doing surgery in 2 stages.
A prospective study of neonates having both EA±TEF and ARM from 2004 to 2011. The patients with favorable parameters were operated in a single stage, whereas others underwent first-stage decompression surgery for ARM. Thereafter, once septicemia was under control and ventilator care available, second-stage surgery for EA±TEF was performed.
Total 70 neonates (single stage = 20, 2 stages = 30, expired after colostomy = 9, only EA±TEF repair needed = 11) were enrolled. The admission rate for this association was 1 per 290. Forty-one percent (24/70) neonates had VACTERL association and 8.6% (6/70) neonates had multiple gastrointestinal atresias. Sepsis screen was positive in 71.4% (50/70). The survival was 45% (9/20) in neonates operated in a single stage and 53.3% (16/30) when operated in 2 stages (P = 0.04). Data analysis of 50 patients revealed that the survived neonates had significantly better birth weight, better gestational age, negative sepsis screen, no cardiac diseases, no pneumonia, and 2-stage surgery (P value 0.002, 0.003, 0.02, 0.02, 0.04, and 0.04, respectively). The day of presentation and abdominal distension had no significant effect (P value 0.06 and 0.06, respectively). This was further supported by stepwise logistic regression analysis.
In a limited resources scenario, the survival rate of babies with this association can be improved by treating ARM first and then for EA±TEF in second stage, once mechanical ventilator care became available and sepsis was under control.
分析对于患有食管闭锁伴或不伴气管食管瘘(EA±TEF)且合并肛门直肠畸形(ARM)的新生儿,分两阶段进行手术是否能改善其预后。
对2004年至2011年期间患有EA±TEF和ARM的新生儿进行前瞻性研究。参数良好的患者进行一期手术,而其他患者则先接受ARM的一期减压手术。此后,一旦败血症得到控制且有呼吸机护理条件,便进行EA±TEF的二期手术。
共纳入70例新生儿(一期手术 = 20例,两期手术 = 30例,结肠造口术后死亡 = 9例,仅需进行EA±TEF修复 = 11例)。这种关联的发病率为每290例中有1例。41%(24/70)的新生儿患有VACTERL综合征,8.6%(6/70)的新生儿患有多处胃肠道闭锁。71.4%(50/70)的败血症筛查呈阳性。一期手术的新生儿存活率为45%(9/20),两期手术时为53.3%(16/30)(P = 0.04)。对50例患者的数据分析显示,存活的新生儿出生体重明显更高、孕周更好、败血症筛查阴性、无心脏病、无肺炎且接受两期手术(P值分别为0.002、0.003、0.02、0.02、0.04和0.04)。就诊时间和腹胀无显著影响(P值分别为0.06和0.06)。逐步逻辑回归分析进一步支持了这一点。
在资源有限的情况下,对于患有这种关联疾病的婴儿,先治疗ARM然后在有机械通气护理且败血症得到控制后进行二期EA±TEF手术,可提高存活率。