期刊论文详细信息
Frontiers in Pediatrics
Selective Treatment of PDA in High-Risk VLBW Infants With Birth Weight ≤800 g or <27 Weeks and Short-Term Outcome: A Cohort Study
article
Thowfique Ibrahim1  Abdul Alim Abdul Haium1  Sarah Jane Tapawan1  Rowena Dela Puerta1  John C. Allen, Jr.2  Suresh Chandran1  Mei Chien Chua1  Victor Samuel Rajadurai1 
[1] Department of Neonatology, KK Women's and Children's Hospital;Duke-NUS Medical School;Department of Neonatology, National University of Singapore;Lee Kong Chian School of Medicine
关键词: PDA;    VLBW;    prematurity;    ductal diameter;    Indomethacin;   
DOI  :  10.3389/fped.2020.607772
学科分类:社会科学、人文和艺术(综合)
来源: Frontiers
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【 摘 要 】

Background: Patent ductus arteriosus (PDA) causing significant left to right shunt can increase key morbidities in preterm infants. Yet, treatment does not improve outcomes and spontaneous closure is the natural course of PDA. The Impact of PDA on 23–26-week gestation infants is uncertain. Selective treatment of such infants would likely balance outcomes. Objective: To test the hypothesis that treatment of PDA in high-risk VLBW infants [birth weight ≤800 g or gestation <27 weeks, hemodynamically significant, ductal diameter (DD, ≥1.6 mm), and mechanical ventilation] and expectant management in low-risk infants will reduce the need for treatment and surgical ligation, without altering short term morbidities. Methods: This prospective observational study was initiated subsequent to the introduction of a new treatment protocol in 2016. The 12-months before and after protocol introduction were, respectively, defined as standard and early selective treatment periods. In the early selective treatment cohort, PDA was treated with indomethacin, maximum of two courses, 1 week apart. Surgical ligation was considered after 30 days of age if indicated (DD ≥2 mm, mechanical ventilation). Primary outcomes were need for treatment and rate of ligation. Protocol compliance and secondary outcomes were documented. Results: 415 infants were studied, 202 and 213 in the standard treatment and early selective treatment cohorts, respectively. Numbers treated (per protocol) in the standard treatment and early selective treatment cohorts were 27.7 and 19.3% (56/202 and 41/213) ( p = 0.049), and the respective ligation rates were 7.54 and 2.96% ( P = 0.045). Secondary outcomes were comparable. Conclusion: The early selective treatment protocol reduced the rates of treatment and surgical ligation of PDA, without altering key morbidities. Further studies under a randomized control trial setting is warranted.

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