Kim Soo-Hong, Cho Yong-Hoon, Kim Hae-Young
Department of Surgery, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan 50612, South Korea.
Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, South Korea.
World J Clin Cases. 2022 Aug 16;10(23):8124-8132. doi: 10.12998/wjcc.v10.i23.8124.
Spontaneous pneumoperitoneum (SP) without gastrointestinal perforation rarely occurs in neonates, with most SP cases being idiopathic. Although SP usually follows a benign clinical course with favorable prognosis, it can become life-threatening in certain situations. In these cases, urgent surgical intervention may be required. Therefore, it may be difficult to decide when or how to perform prompt interventions.
To demonstrate the distinct clinical features of SP to guide appropriate management by comparing characteristics between SP and typical pneumoperitoneum secondary to gastrointestinal perforation.
We retrospectively reviewed electronic medical records and identified 37 neonates with radiological evidence of pneumoperitoneum who were treated at our institution. Clinical variables were compared between neonates with SP without gastrointestinal perforation (Group A) and those with pneumoperitoneum secondary to gastrointestinal perforation (Group B). Clinical variables between groups were compared using Student's t-test and the chi-square test. The risk factors related to mortality were examined using multi-logistic regression analysis.
Group A comprised 35.1% (13/37) of the patients. The frequency of persistent pulmonary hypertension (53.8%) and pneumothorax (46.2%) before the development of pneumoperitoneum was significantly higher in group A than in group B ( = 0.004). Platelet count and partial pressure of arterial oxygen (PaO2) were significantly lower in group A ( = 0.015 and 0.025, respectively). Overall mortality was significantly higher in group A than in group B (76.9% 16.7%, 0.001). Only preterm infants were significantly associated with high mortality ( 0.041; odds ratio = 18.0). Accompaniment with persistent pulmonary hypertension and pneumothorax were also significantly high ( = 0.004) in group A, but these were not strongly associated with high mortality.
This study identified a higher mortality rate in patients with SP than that described in previous reports. Neonates with SP were more likely to have thrombocytopenia, pneumothorax, and persistent pulmonary hypertension. Prematurity was the most significant factor affecting mortality.
无胃肠道穿孔的新生儿自发性气腹(SP)很少见,大多数SP病例为特发性。虽然SP通常临床过程良性,预后良好,但在某些情况下可能危及生命。在这些病例中,可能需要紧急手术干预。因此,很难决定何时或如何进行及时干预。
通过比较SP与典型胃肠道穿孔继发气腹的特征,阐明SP的独特临床特征,以指导适当的管理。
我们回顾性分析电子病历,确定了在我院接受治疗的37例有气腹影像学证据的新生儿。比较无胃肠道穿孔的SP新生儿(A组)和胃肠道穿孔继发气腹的新生儿(B组)的临床变量。组间临床变量采用Student t检验和卡方检验进行比较。使用多因素逻辑回归分析检查与死亡率相关的危险因素。
A组占患者的35.1%(13/37)。A组气腹发生前持续性肺动脉高压(53.8%)和气胸(46.2%)的发生率显著高于B组(P = 0.004)。A组血小板计数和动脉血氧分压(PaO2)显著更低(分别为P = 0.015和0.025)。A组总体死亡率显著高于B组(76.9%比16.7%,P = 0.001)。只有早产儿与高死亡率显著相关(P = 0.041;比值比 = 18.0)。A组中伴有持续性肺动脉高压和气胸的情况也显著更高(P = 0.004),但这些与高死亡率的相关性不强。
本研究发现SP患者的死亡率高于既往报道。患有SP的新生儿更易出现血小板减少、气胸和持续性肺动脉高压。早产是影响死亡率的最重要因素。