Department of Pediatric Surgery, Erasmus MC Sophia Children's Hospital, Rotterdam, the Netherlands.
Division of Gastroenterology, Department of Pediatrics, Erasmus MC Sophia Children's Hospital, Rotterdam, the Netherlands.
Eur J Pediatr Surg. 2022 Feb;32(1):111-119. doi: 10.1055/s-0041-1741544. Epub 2022 Jan 10.
To improve counseling of parents and to guide care strategies, we studied the disease course and outcomes of necrotizing enterocolitis (NEC) up to 2 years of corrected age (CA) from a multidisciplinary perspective.
This was a retrospective cohort study in preterm infants (birth weight < 1,500 g, gestational age < 32 weeks), diagnosed with NEC (Bell's stage ≥ II) from 2008 through 2020. Data on prevalence, mortality, surgery, intestinal failure (IF), growth, and neurodevelopment at 2-year follow-up were separately analyzed for medically and surgically treated children.
Of 3,456 preterm infants, 200 (6%) were diagnosed with NEC, of whom 135 developed an indication for surgery within 7 days after the diagnosis; 28/135 died before surgery, and 37/107 died after an open-and-close procedure. An enterostomy was constructed in 62 patients and an end-to-end anastomosis in 15. The postoperative course was described for 77 patients, of whom 23 developed surgical complications (12/23 incisional hernias, 9/23 anastomotic strictures), 13/77 a short bowel, and 25/77 IF. Sixty-day survival after birth for medical NEC patients was 88% (hazard ratio [HR]: 0.698; = 0.318), and for surgically treated NEC patients was 40% (HR: 3.729; < 0.001). At 2-year follow-up, one patient received parenteral nutrition. Severe delay in weight for age, motor, and cognitive development was seen in 3, 6, and 2%, respectively.
In this cohort, the mortality rate was high, especially in surgically treated NEC patients. The surgical complication rate is comparable to previous studies, but in surviving patients, persisting IF and severe delay in growth and neurodevelopment at 2 years CA were relatively rare.
为了改善家长咨询,并指导护理策略,我们从多学科角度研究了坏死性小肠结肠炎(NEC)的疾病进程和结局,直至纠正年龄(CA)2 年。
这是一项回顾性队列研究,纳入了 2008 年至 2020 年间出生体重<1500g、胎龄<32 周的早产儿,这些早产儿被诊断为 NEC(Bell 分期≥Ⅱ期)。分别对接受药物和手术治疗的患儿进行了 2 年随访时的患病率、死亡率、手术、肠衰竭(IF)、生长和神经发育方面的数据进行分析。
在 3456 名早产儿中,有 200 名(6%)被诊断为 NEC,其中 135 名在确诊后 7 天内出现手术指征;28/135 名患儿在手术前死亡,37/107 名患儿在接受剖腹-关腹手术后死亡。62 名患儿行造口术,15 名患儿行端端吻合术。对 77 名患儿的术后过程进行了描述,其中 23 名患儿发生手术并发症(12/23 例切口疝,9/23 例吻合口狭窄),13/77 名患儿发生短肠,25/77 名患儿发生 IF。药物治疗 NEC 患儿的出生后 60 天存活率为 88%(危险比[HR]:0.698; = 0.318),而手术治疗 NEC 患儿的存活率为 40%(HR:3.729; < 0.001)。在 2 年随访时,有 1 名患儿接受了肠外营养。分别有 3%、6%和 2%的患儿出现严重的体重迟缓、运动迟缓、认知迟缓。
在本队列中,死亡率较高,尤其是手术治疗的 NEC 患儿。手术并发症发生率与既往研究相似,但在幸存患儿中,2 年 CA 时持续存在 IF 以及生长和神经发育严重迟缓相对少见。