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阿联酋艾因市塔瓦姆医院贝拉克坦(珂立苏®)与固尔苏®治疗早产新生儿呼吸窘迫综合征的疗效比较:一项回顾性研究

Comparison of Efficacy of Beractant (SURVANTA®) and Poractant Alfa (CUROSURF®) in Preterm Infants With Respiratory Distress Syndrome in Tawam Hospital, Al Ain, UAE: A Retrospective Study.

作者信息

Butt Fahad, Mohamad Huda, Abusallout Nour, Zaineh Alaa, El Khatib Feryal, Abdulrahman Sarah, Hamwi Sara, Rahmani Mohamed, Alabdullatif Mustafa

机构信息

Neonatology, Tawam Hospital, Al Ain, ARE.

Pediatrics, Tawam Hospital, Al Ain, ARE.

出版信息

Cureus. 2024 Nov 29;16(11):e74790. doi: 10.7759/cureus.74790. eCollection 2024 Nov.

DOI:10.7759/cureus.74790
PMID:39737314
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11683160/
Abstract

Introduction Respiratory distress syndrome (RDS) is a leading cause of morbidity and mortality among preterm infants, necessitating effective treatment strategies. This study compared the efficacy of Beractant (SURVANTA®) to Poractant alfa (CUROSURF®) in treating RDS in preterm infants admitted to Tawam Hospital in the UAE. Methodology This retrospective study included preterm infants from 23+0 to 36+6 weeks of gestation with a diagnosis of RDS and treatment by Beractant or Poractant alfa within 48 hours of life between January 2020 and March 2023. Data collected from electronic medical records of Tawam Hospital include infant and maternal demographics, primary outcome parameters, such as bronchopulmonary dysplasia (BPD) and/or mortality, and secondary outcome parameters, such as surfactant redosing, air leak syndrome, and other complications. Results A total of 258 infants met the inclusion criteria: 178 were treated with Beractant, and 80 were treated with Poractant alfa. After adjusting the confounding factors, the occurrence of bronchopulmonary dysplasia (BPD) was not statistically significant, showing rates of 68.7% (n=46) in the Poractant group and 47.5% (n=75) in the Beractant group (p=0.71). Likewise, there was no significant difference in mortality rates between the two groups, with 22.5% (n=18) in the Poractant group and 11.8% (n=21) in the Beractant group (p=0.33). Furthermore, the combined incidence of BPD or mortality was also not statistically significant, recorded at 53.4% (n=95) for the Beractant group compared to 73.8% (n=59) for the Poractant group (p=0.93). However, the need for surfactant redosing and air leak syndrome was significantly lower in the Poractant group compared to the Beractant group, 26.2% (n=21) vs 45.5% (n=81), p < 0.00001 and 8.8% (n=7) vs 14.6% (n=26), p = 0.05, respectively. There was no difference in the incidence of other outcomes such as pulmonary hemorrhage, periventricular leukomalacia (PVL), intraventricular hemorrhage (IVH), necrotizing enterocolitis (NEC), significant patent ductus arteriosus (PDA), and retinopathy of prematurity (ROP) that required treatment. Conclusion There was no significant difference in the rates of bronchopulmonary dysplasia or mortality between Poractant alfa (CUROSURF®) and Beractant (SURVANTA®) in preterm infants suffering from respiratory distress syndrome. Poractant alfa (CUROSURF®) showed a reduced need for surfactant redosing and a lower incidence of air leak syndrome. However, the rates of other outcomes, including significant patent ductus arteriosus (PDA), intraventricular hemorrhage (IVH), retinopathy of prematurity (ROP), periventricular leukomalacia (PVL), and necrotizing enterocolitis (NEC), were comparable in both treatment groups. Further randomized prospective studies are necessary to evaluate these types of surfactants and investigate their efficacy as well as both short- and long-term outcomes.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f165/11683160/ce3b00c9a4d7/cureus-0016-00000074790-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f165/11683160/49e31a76a3e9/cureus-0016-00000074790-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f165/11683160/9aed61981169/cureus-0016-00000074790-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f165/11683160/ce3b00c9a4d7/cureus-0016-00000074790-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f165/11683160/49e31a76a3e9/cureus-0016-00000074790-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f165/11683160/9aed61981169/cureus-0016-00000074790-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f165/11683160/ce3b00c9a4d7/cureus-0016-00000074790-i03.jpg
摘要

引言

呼吸窘迫综合征(RDS)是早产婴儿发病和死亡的主要原因,因此需要有效的治疗策略。本研究比较了贝拉克坦(SURVANTA®)和猪肺磷脂(CUROSURF®)在阿联酋塔瓦姆医院收治的早产婴儿中治疗RDS的疗效。

方法

这项回顾性研究纳入了妊娠23+0至36+6周、诊断为RDS且在出生后48小时内接受贝拉克坦或猪肺磷脂治疗的早产婴儿,研究时间为2020年1月至2023年3月。从塔瓦姆医院的电子病历中收集的数据包括婴儿和母亲的人口统计学信息、主要结局参数(如支气管肺发育不良(BPD)和/或死亡率)以及次要结局参数(如表面活性剂重复给药、气漏综合征和其他并发症)。

结果

共有258名婴儿符合纳入标准:178名接受了贝拉克坦治疗,80名接受了猪肺磷脂治疗。在调整混杂因素后,支气管肺发育不良(BPD)的发生率无统计学意义,猪肺磷脂组为68.7%(n = 46),贝拉克坦组为47.5%(n = 75)(p = 0.71)。同样,两组的死亡率也无显著差异,猪肺磷脂组为22.5%(n = 18),贝拉克坦组为11.8%(n = 21)(p = 0.33)。此外,BPD或死亡率的合并发生率也无统计学意义,贝拉克坦组为53.4%(n = 95),猪肺磷脂组为73.8%(n = 59)(p = 0.93)。然而,与贝拉克坦组相比,猪肺磷脂组表面活性剂重复给药的需求和气漏综合征的发生率显著更低,分别为26.2%(n = 21)对45.5%(n = 81),p < 0.00001和8.8%(n = 7)对14.6%(n = 26),p = 0.05。在其他需要治疗的结局发生率上,如肺出血、脑室周围白质软化(PVL)、脑室内出血(IVH)、坏死性小肠结肠炎(NEC)、显著动脉导管未闭(PDA)和早产儿视网膜病变(ROP),两组之间没有差异。

结论

在患有呼吸窘迫综合征的早产婴儿中,猪肺磷脂(CUROSURF®)和贝拉克坦(SURVANTA®)在支气管肺发育不良或死亡率方面没有显著差异。猪肺磷脂(CUROSURF®)显示出表面活性剂重复给药需求降低和气漏综合征发生率较低。然而,在两个治疗组中,包括显著动脉导管未闭(PDA)、脑室内出血(IVH)、早产儿视网膜病变(ROP)、脑室周围白质软化(PVL)和坏死性小肠结肠炎(NEC)在内的其他结局发生率相当。需要进一步进行随机前瞻性研究来评估这类表面活性剂,并研究它们的疗效以及短期和长期结局。

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