Predictors of prognosis in neonates with congenital diaphragmatic hernia: experience of 12 years

C. Morais, G. Rocha, F. Flôr-de-Lima, P. Éden, A. Fragoso, H. Guimarães
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引用次数: 5

Abstract

Introduction: Congenital diaphragmatic hernia (CDH) is a severe malformation, displaying relevant mortality and morbidity rates in newborns. Aim: To characterize clinically and demographically all neonatal cases of CDH admitted to a level III Neonatal Intensive Care Unit during a 12-year period and to evaluate the predictive value of baseline characteristics on mortality and morbidity at discharge. Methods: Maternal/infant clinical and electronic records were ret- rospectively reviewed. All neonates with posterolateral CDH admitted between January 2003 and December 2014 were included. Results: Fifty-three newborns were included. Overall mortality during hospitalization was 22/53 (41.5%). Clinical characteristics associated with mortality were the presence of intrathoracic liver (p = 0.005), intrathoracic stomach (p = 0.015), elevated arterial pCO 2 or lower pH values at admission (respectively, p = 0.001 and p < 0.001), pre-ductal oxygen saturation < 85% at admission (p = 0.012) and surgical repair with prosthetic patch (p = 0.041). Morbidity at discharge was reported in 7 (22.6%) survivors. Stomach herniation and sepsis were associated with higher morbidity (respectively, p = 0.012 and p = 0.029). In a logistic regression, patch repair was the only variable with predictive value for death during hospitalization, with an odds ratio (OR) of 15 (95% CI 0.98-228.9), and intrathoracic stomach was a predictor of morbidity at discharge (OR = 15.7, 95% CI 1.4-174.2). Conclusion: Structural characteristics, namely defect size and presence of intrathoracic stomach, remain the primary determinants of neonatal prognosis in CDH. Although post-natal approaches have progressively proven their value in increasing survival and improving management of high-risk cases, future researches should continue focusing on the definition of foetal anatomical markers of severity and prenatal treatment of CDH.
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新生儿先天性膈疝预后的预测因素:12年的经验
引言:先天性膈疝(CDH)是一种严重的畸形,在新生儿中显示出相关的死亡率和发病率。目的:从临床和人口学角度描述12年内入住三级新生儿重症监护室的所有新生儿CDH病例,并评估基线特征对出院时死亡率和发病率的预测价值。方法:回顾性分析母婴临床及电子病历资料。纳入2003年1月至2014年12月期间入院的所有患有后外侧CDH的新生儿。结果:包括五十三名新生儿。住院期间的总死亡率为22/53(41.5%)。与死亡率相关的临床特征是存在胸腔内肝脏(p=0.005)、胸腔内胃(p=0.015)、入院时动脉pCO2升高或pH值降低(分别为p=0.001和p<0.001),入院时导管前氧饱和度<85%(p=0.012)和用假体补片进行手术修复(p=0.041)。据报道,出院时有7名(22.6%)幸存者患病。胃疝和败血症与较高的发病率相关(分别为p=0.012和p=0.029)。在逻辑回归中,补片修复是唯一对住院期间死亡有预测价值的变量,比值比(OR)为15(95%CI 0.98-228.9),胸内胃是出院时发病率的预测指标(OR=15.7,95%CI 1.4-174.2)。结论:结构特征,即缺损大小和胸内胃的存在,仍然是CDH新生儿预后的主要决定因素。尽管产后方法已逐渐证明其在提高生存率和改善高危病例管理方面的价值,但未来的研究应继续关注CDH严重程度的胎儿解剖标志物的定义和产前治疗。
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来源期刊
CiteScore
1.00
自引率
25.00%
发文量
0
审稿时长
12 weeks
期刊介绍: The Journal of Pediatric and Neonatal Individualized Medicine (JPNIM) is a peer-reviewed interdisciplinary journal which provides a forum on new perspectives in pediatric and neonatal medicine. The aim is to discuss and to bring readers up to date on the latest in research and clinical pediatrics and neonatology. Special emphasis is on developmental origin of health and disease or perinatal programming and on the so-called ‘-omic’ sciences. Systems medicine blazes a revolutionary trail from reductionist to holistic medicine, from descriptive medicine to predictive medicine, from an epidemiological perspective to a personalized approach. The journal will be relevance to clinicians and researchers concerned with personalized care for the newborn and child. Also medical humanities will be considered in a tailored way. Article submission (original research, review papers, invited editorials and clinical cases) will be considered in the following fields: fetal medicine, perinatology, neonatology, pediatrics, developmental programming, psychology and medical humanities.
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