Association between early pulmonary arterial pressure measurements and bronchopulmonary dysplasia or mortality in very preterm infants: a prospective cohort study.

Mustafa Senol Akin, Gökce Kas, Emre Aydin, Aslıhan Kose Cetinkaya, Ibrahim Ece, Fatma Nur Sari, Evrim Alyamac Dizdar
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Abstract

Background: Prematurity is a significant risk for bronchopulmonary dysplasia related pulmonary artery pressure.

Objective: To determine the association between pulmonary artery pressure in the early days of life and the development of bronchopulmonary dysplasia or mortality.

Methods: This prospective observational cohort study included infants born at <32 weeks and weighing <1500 g. Pulmonary artery pressure was measured between postnatal days 3 and 7. Pulmonary hypertension was defined as systolic pulmonary artery pressure ≥40 mm Hg or systolic pulmonary artery pressure/systolic blood pressure >0.5 (pulmonary hypertension criterion-1). Infants were categorised into pulmonary hypertension and non-pulmonary hypertension groups. The primary endpoint was bronchopulmonary dysplasia or mortality. Receiver operating characteristic analysis established a new threshold value for predicting bronchopulmonary dysplasia or mortality (pulmonary hypertension criterion-2). Infants were reanalysed according to new criteria.

Results: A total of 329 infants were included in this study. Moderate-to-severe pulmonary hypertension was identified in 24% (n=79) of the infants. The pulmonary hypertension group exhibited a significantly lower gestational age, lower birth weight and a higher incidence of small for gestational age. Systolic pulmonary artery pressure >25 mm Hg or systolic pulmonary artery pressure/systolic blood pressure >0.35 was defined as the pulmonary hypertension criterion-2. Logistic regression analysis identified pulmonary hypertension criterion-2 as an independent risk factor for moderate-to-severe bronchopulmonary dysplasia or mortality (OR 2.67, 95% CI 1.3 to 5.51, p<0.01).

Conclusion: Pulmonary artery pressure exceeding 25 mm Hg in the early days of life may be considered a potential risk factor for bronchopulmonary dysplasia or mortality.

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早产儿早期肺动脉压测量与支气管肺发育不良或死亡率之间的关系:一项前瞻性队列研究。
背景:早产儿是支气管肺发育不良与肺动脉压力相关的重要风险因素:确定生命早期肺动脉压力与支气管肺发育不良或死亡率之间的关系:这项前瞻性观察队列研究包括出生时肺动脉压力为0.5(肺动脉高压标准-1)的婴儿。婴儿被分为肺动脉高压组和非肺动脉高压组。主要终点是支气管肺发育不良或死亡。接收者操作特征分析确定了预测支气管肺发育不良或死亡率的新阈值(肺动脉高压标准-2)。根据新标准对婴儿进行了重新分析:本研究共纳入 329 名婴儿。24%的婴儿(n=79)患有中度至重度肺动脉高压。肺动脉高压组的胎龄明显较小、出生体重较轻,胎龄小的发生率较高。收缩肺动脉压>25毫米汞柱或收缩肺动脉压/收缩压>0.35被定义为肺动脉高压标准-2。逻辑回归分析表明,肺动脉高压标准-2 是中重度支气管肺发育不良或死亡的独立风险因素(OR 2.67,95% CI 1.3 至 5.51,pConclusion):生命早期肺动脉压超过25毫米汞柱可被视为支气管肺发育不良或死亡的潜在风险因素。
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来源期刊
CiteScore
9.00
自引率
4.50%
发文量
90
审稿时长
6-12 weeks
期刊介绍: Archives of Disease in Childhood is an international peer review journal that aims to keep paediatricians and others up to date with advances in the diagnosis and treatment of childhood diseases as well as advocacy issues such as child protection. It focuses on all aspects of child health and disease from the perinatal period (in the Fetal and Neonatal edition) through to adolescence. ADC includes original research reports, commentaries, reviews of clinical and policy issues, and evidence reports. Areas covered include: community child health, public health, epidemiology, acute paediatrics, advocacy, and ethics.
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