Deeney Scott, Howley Lisa W, Hodges Maggie, Liechty Kenneth W, Marwan Ahmed I, Gien Jason, Kinsella John P, Crombleholme Timothy M
The Colorado Fetal Care Center, Divisions of Pediatric General, Thoracic and Fetal Surgery, Pediatric Cardiology, Neonatology, and Multidisciplinary Congenital Diaphragmatic Hernia Management Team, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO.
The Colorado Fetal Care Center, Divisions of Pediatric General, Thoracic and Fetal Surgery, Pediatric Cardiology, Neonatology, and Multidisciplinary Congenital Diaphragmatic Hernia Management Team, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO.
J Pediatr. 2018 Jan;192:99-104.e4. doi: 10.1016/j.jpeds.2017.09.004. Epub 2017 Nov 6.
To assess the impact of specific echocardiographic criteria for timing of congenital diaphragmatic hernia repair on the incidence of acute postoperative clinical decompensation from pulmonary hypertensive crisis and/or acute respiratory decompensation, with secondary outcomes including survival to discharge, duration of ventilator support, and length of hospitalization.
The multidisciplinary congenital diaphragmatic hernia management team instituted a protocol in 2012 requiring the specific criterion of echocardiogram-estimated pulmonary artery pressure ≤80% systemic blood pressure before repairing congenital diaphragmatic hernias. A retrospective review of 77 neonatal patients with Bochdalek hernias repaired between 2008 and 2015 were reviewed: group 1 included patients repaired before protocol implementation (n = 25) and group 2 included patients repaired after implementation (n = 52).
The groups had similar baseline characteristics. Postoperative decompensation occurred less often in group 2 compared with group 1 (17% vs 48%, P = .01). Adjusted analysis accounting for repair type, liver herniation, and prematurity yielded similar results (15% vs 37%, P = .04). Group 2 displayed a trend toward improved survival to 30 days postoperatively, though this did not reach statistical significance (94% vs 80%, P = .06). Patient survival to discharge, duration of ventilator support, and length of hospitalization were not different between groups.
The implementation of a protocol requiring echocardiogram-estimated pulmonary arterial pressure ≤80% of systemic pressure before congenital diaphragmatic hernia repair may reduce the incidence of acute postoperative decompensation, although there was no difference in longer-term secondary outcomes, including survival to discharge.
评估先天性膈疝修补时机的特定超声心动图标准对术后因肺动脉高压危象和/或急性呼吸功能不全导致的急性临床失代偿发生率的影响,次要结局包括出院生存率、呼吸机支持时间和住院时间。
多学科先天性膈疝管理团队在2012年制定了一项方案,要求在修复先天性膈疝前,超声心动图估计的肺动脉压力≤体循环血压的80%这一特定标准。回顾性分析了2008年至2015年间接受Bochdalek疝修补术的77例新生儿患者:第1组包括方案实施前接受修补的患者(n = 25),第2组包括方案实施后接受修补的患者(n = 52)。
两组具有相似的基线特征。与第1组相比,第2组术后失代偿的发生率更低(17%对48%,P = .01)。对修复类型、肝脏疝出和早产进行校正分析后得出了相似的结果(15%对37%,P = .04)。第2组术后30天生存率有改善趋势,但未达到统计学意义(94%对80%,P = .06)。两组患者出院生存率、呼吸机支持时间和住院时间无差异。
先天性膈疝修补前实施要求超声心动图估计肺动脉压力≤体循环压力80%的方案,可能会降低术后急性失代偿的发生率,尽管在包括出院生存率在内的长期次要结局方面没有差异。