Lima Mario, D'Antonio Simone, Salvo Neil Di, Parente Giovanni, Randi Beatrice, Libri Michele, Gargano Tommaso, Ruggeri Giovanni, Catania Vincenzo Davide
Pediatric Surgery Unit, IRCCS Sant'Orsola-Malpighi Hospital, University of Bologna, Italy.
J Indian Assoc Pediatr Surg. 2021 May-Jun;26(3):170-176. doi: 10.4103/jiaps.JIAPS_70_20. Epub 2021 May 17.
Congenital lung malformation (CLM) is a rare developmental anomaly of the lower respiratory tract. The purposes are to define if the presence of respiratory symptoms, in CLM may affect surgical outcomes and to define optimal timing for surgery in asymptomatic patients.
Retrospective review of patients with CLM from 2004 to 2018. Asymptomatic and symptomatic patients were compared. Moreover, asymptomatic patients were stratified according to age at surgery (< or >6 months).
Demographic data, prenatal diagnosis, symptoms, CLM's characteristics, operative and postoperative data were collected. Patients were divided into two groups based on the presence or none of respiratory symptoms.
Data were compared using the Fisher's exact test for qualitative values and Mann-Whitney test for quantitative values < 0.05 was statistically significant.
One hundred and eighty-six patients were treated. Asymptomatic were 137 (74%), while symptomatic were 49 (26%). The most common presenting symptoms were respiratory distress ( = 30, 61%) followed by pneumonia ( = 18, 38%). Prenatal diagnosis of CLM was performed in 98% of asymptomatic patients compared to 30% of symptomatic ( = 0.001). Surgical excision was performed in all cases, and in 50% by thoracoscopy, without difference between the two groups. In 97% of all cases, a lung sparing surgery was performed without difference between the groups. Symptoms are significantly associated with older age, location in the upper lobe, and lobar emphysema. Length of stay in intensive care, postoperative complications, and reintervention rate were higher in the symptomatic group. Eighty-one asymptomatic patients underwent surgery <6 months of life; they had a lower rate of surgical complications (2%) compared with those >6 months (7%).
The present study describes a comprehensive picture of CLM. In addition, we emphasize the role of early postnatal management and thoracoscopic surgery, also before 6 months of life, to prevent the onset of symptoms that are associated with worse outcomes.
先天性肺发育异常(CLM)是下呼吸道一种罕见的发育异常。目的是确定CLM患者出现呼吸道症状是否会影响手术结果,并确定无症状患者的最佳手术时机。
对2004年至2018年的CLM患者进行回顾性研究。比较无症状和有症状的患者。此外,无症状患者根据手术年龄(<或>6个月)进行分层。
收集人口统计学数据、产前诊断、症状、CLM的特征、手术及术后数据。根据是否存在呼吸道症状将患者分为两组。
使用Fisher精确检验比较定性值,使用Mann-Whitney检验比较定量值,P<0.05具有统计学意义。
共治疗186例患者。无症状患者137例(74%),有症状患者49例(26%)。最常见的症状是呼吸窘迫(n=30,61%),其次是肺炎(n=18,38%)。98%的无症状患者进行了CLM的产前诊断,而有症状患者为30%(P=0.001)。所有病例均进行了手术切除,50%通过胸腔镜手术,两组之间无差异。97%的病例进行了肺保留手术,两组之间无差异。症状与年龄较大、上叶位置和大叶性肺气肿显著相关。有症状组的重症监护住院时间、术后并发症和再次干预率较高。81例无症状患者在6个月前接受了手术;他们的手术并发症发生率(2%)低于6个月以上患者(7%)。
本研究描述了CLM的全面情况。此外,我们强调出生后早期管理和胸腔镜手术的作用,即使在6个月前,以预防与较差预后相关的症状的发生。