靶向表面活性剂置换的多变量模型的外部验证。

Neonatology Pub Date : 2024-01-01 Epub Date: 2023-10-26 DOI:10.1159/000532083
Francesco Raimondi, Pasquale Dolce, Claudio Veropalumbo, Enrico Sierchio, Rebeca Gregorio Hernandez, Javier Rodriguez Fanjul, Fabio Meneghin, Roberto Raschetti, Luca Bonadies, Iuri Corsini, Almudena Alonso Ojembarrena, Serena Salomè, Lorena Rodeño Fernandez, Manuel Sanchez Luna, Gianluca Lista, Fabio Mosca, Carlo Dani, Eugenio Baraldi, Lucio Giordano, Peter G Davis, Letizia Capasso
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引用次数: 0

摘要

引言:建议对早产儿进行早期靶向表面活性剂治疗,但个性化治疗的最佳标准尚不明确。我们使用独立数据集验证了先前发表的基于胎龄(GA)、肺部超声评分(LUS)和血氧饱和度的多变量预后模型。方法:对10个意大利和西班牙新生儿重症监护室进行务实的观察性研究,包括有呼吸窘迫综合征临床症状并在CPAP上稳定的早产儿(250周和336周,分为3个GA间隔)。在稳定后不久收集LUS和SatO2/FiO2。由严格蒙面的医生在随后的表面活性剂给药中评估其预后准确性。结果:175名婴儿被纳入研究。74%的婴儿在25-27周出生,38.5%的婴儿在28-30周出生,26.5%的婴儿在31-33周出生。比较验证和发育群体的校准曲线显示出显著的重叠,截距=0.08,95%置信区间(-0.34;0.5),斜率=1.53,95%可信区间(1.07-1.98)。验证队列具有较高的预测准确性。其ROC曲线显示AUC=0.95,95%CI(0.91-0.99),灵敏度=0.93,95%可信区间(0.83-0.98),特异度=0.81,95%置信区间(0.73-0.88),PPV=0.76,95%置信度(0.65-0.84),NPV=0.95,95%可信度(0.88-0.98)。LUS和SatO2/FiO2的预后表现随GA的不同而不同。结论:我们验证了一个基于LUS和Sat/FiO2的预后模型,以促进早期定制的表面活性物质给药,从而改善早产儿的呼吸管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
External Validation of a Multivariate Model for Targeted Surfactant Replacement.

Introduction: Early targeted surfactant therapy for preterm infants is recommended but the best criteria to personalize treatment are unclear. We validate a previously published multivariate prognostic model based on gestational age (GA), lung ultrasound score (LUS), and oxygen saturation to inspire oxygen fraction ratio (SatO2/FiO2) using an independent data set.

Methods: Pragmatic, observational study in 10 Italian and Spanish NICUs, including preterm babies (250 and 336 weeks divided into 3 GA intervals) with clinical signs of respiratory distress syndrome and stabilized on CPAP. LUS and SatO2/FiO2 were collected soon after stabilization. Their prognostic accuracy was evaluated on the subsequent surfactant administration by a rigorously masked physician.

Results: One hundred seventy-five infants were included in the study. Surfactant was given to 74% infants born at 25-27 weeks, 38.5% at 28-30 weeks, and 26.5% at 31-33 weeks. The calibration curve comparing the validation and the development populations showed significant overlap with an intercept = 0.08, 95% CI (-0.34; 0.5) and a slope = 1.53, 95% CI (1.07-1.98). The validation cohort had a high predictive accuracy. Its ROC curve showed an AUC = 0.95, 95% CI (0.91-0.99) with sensitivity = 0.93, 95% CI (0.83-0.98), specificity = 0.81, 95% CI (0.73-0.88), PPV = 0.76, 95% CI (0.65-0.84), NPV = 0.95, 95% CI (0.88-0.98). LUS ≥9 demonstrated the highest sensitivity (0.91, 95% CI [0.82-0.97]) and specificity = 0.81, 95% CI (0.72-0.88) as individual predictor. LUS and SatO2/FiO2 prognostic performances varied with GA.

Conclusion: We validated a prognostic model based on LUS and Sat/FiO2 to facilitate early, customized surfactant administration that may improve respiratory management of preterm neonates.

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