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首页> 外文期刊>Journal of Korean medical science. >Survival Rate Changes in Neonates with Congenital Diaphragmatic Hernia and its Contributing Factors
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Survival Rate Changes in Neonates with Congenital Diaphragmatic Hernia and its Contributing Factors

机译:先天性Dia肌疝的成活率变化及其影响因素

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摘要

The purpose of this study was to demonstrate survival rate changes after the introduction of inhaled nitric oxide (iNO) therapy, and to identify the factors that influence these changes in neonates with a congenital diaphragmatic hernia (CDH) at a single center. A total of 48 neonates were divided into two groups based on the time of admission, i.e., into period I (P1; n=17; before the introduction of iNO therapy) and period II (P2; n=31; after the introduction of iNO therapy). Survival rates of the 48 neonates showed a tendency to increase from 53% during P1 to 77% during P2, but without a statistical significance, but a significant difference was found between survival rates during the two periods after adjusting for initial clinical characteristics, when the postoperative survival rate increased significantly from 69% for P1 to 100% for P2. The mean duration of preoperative respiratory management was significantly longer for P2 than for P1. Seven of 12 patients who received preoperative iNO therapy due to persistent pulmonary hypertension or refractory preductal hypoxemia in P2 survived after operation. We speculate that a management strategy based on iNO therapy and delayed operation, rather than differences between the initial clinical characteristics of the two study groups, might partially contribute to the observed improvements in postoperative and overall survival rates in neonates with CDH.
机译:这项研究的目的是证明采用吸入一氧化氮(iNO)治疗后的存活率变化,并确定影响单个中心先天性diaphragm肌疝(CDH)的新生儿中这些变化的因素。根据入院时间将总共48例新生儿分为两组,即分为I期(P1; n = 17;引入iNO治疗之前)和II期(P2; n = 31;引入iNO治疗之后)。 iNO治疗)。 48例新生儿的存活率显示从P1期间的53%增加到P2期间的77%,但无统计学意义,但是在调整初始临床特征后,这两个时期的存活率之间存在显着差异。术后生存率从P1的69%显着提高到P2的100%。 P2的术前呼吸管理的平均持续时间明显长于P1。因持续性肺动脉高压或顽固性P2血氧不足而接受术前iNO治疗的12例患者中有7例在手术后存活。我们推测基于iNO治疗和延迟手术的治疗策略,而不是两个研究组的初始临床特征之间的差异,可能部分有助于观察到的CDH新生儿术后和总体生存率的改善。

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