Faculty of Medicine, Universitas Pelita Harapan, Tangerang, Indonesia.
Faculty of Medicine, Universitas YARSI, Jakarta, Indonesia.
Indian Heart J. 2020 May-Jun;72(3):151-159. doi: 10.1016/j.ihj.2020.05.012. Epub 2020 May 29.
This systematic review and meta-analysis aimed to synthesize the latest evidence on the efficacy and safety of oral acetaminophen compared to oral ibuprofen for patent ductus arteriosus (PDA) in preterm infants.
We performed a systematic literature search on topics that assesses the use of oral paracetamol compared to oral ibuprofen in preterm neonates diagnosed with PDA from PubMed, EuropePMC, Cochrane Central Database, ScienceDirect, ProQuest, ClinicalTrials.gov, and hand-sampling from potential articles.
There were 1547 subjects from 10 selected studies. Primary closure rate was similar in both groups. Subgroup analysis on studies enrolling neonates with ≤30 weeks gestational age showed that ibuprofen was superior (OR 0.52 [0.31, 0.90], I: 0%). On the other hand, paracetamol was superior neonates with ≤34 weeks gestational age (OR 1.73 [1.01, 2.94], I: 30%). Reopening rate, surgical closure rate, mortality, intraventricular hemorrhage, and necrotizing enterocolitis were similar in both groups. Rate of renal dysfunction (OR 0.27 [0.10, 0.77], I: 0%) and gastrointestinal bleeding (OR 0.31 [0.11, 0.88], I: 0%) were lower in paracetamol group. Subgroup analysis of randomized controlled studies (RCTs) showed similar results. Meta-regression analysis showed that the primary closure rate was not influenced by gestational age, birth weight, and gender. GRADE demonstrates a low level of certainty for primary closure and mortality. Renal dysfunction and gastrointestinal bleeding havea moderate level of certainty.
There was no significant difference between the efficacy of oral paracetamol and oral ibuprofen. However, the rate of renal dysfunction and gastrointestinal bleeding were higher in oral ibuprofen.
本系统评价和荟萃分析旨在综合最新证据,评估口服扑热息痛与口服布洛芬治疗早产儿动脉导管未闭(PDA)的疗效和安全性。
我们在 PubMed、EuropePMC、Cochrane 中央数据库、ScienceDirect、ProQuest、ClinicalTrials.gov 上针对评估口服扑热息痛与口服布洛芬治疗早产儿 PDA 的文献进行系统检索,并从潜在文章中进行手工抽样。
共有 10 项研究的 1547 名受试者纳入分析。两组的动脉导管未闭结扎率相似。纳入≤30 周早产儿的亚组分析显示,布洛芬更优(OR 0.52 [0.31, 0.90],I²=0%);而对于≤34 周的早产儿,扑热息痛更优(OR 1.73 [1.01, 2.94],I²=30%)。两组再闭率、手术结扎率、死亡率、颅内出血和坏死性小肠结肠炎发生率相似。肾功能不全(OR 0.27 [0.10, 0.77],I²=0%)和胃肠道出血(OR 0.31 [0.11, 0.88],I²=0%)发生率较低。随机对照研究(RCT)的亚组分析结果相似。Meta 回归分析显示,出生胎龄、出生体重和性别均不影响动脉导管未闭结扎率。GRADE 对动脉导管未闭结扎率和死亡率的证据质量评价为低水平,对肾功能不全和胃肠道出血的证据质量评价为中等级。
口服扑热息痛与口服布洛芬的疗效无显著差异,但口服布洛芬的肾功能不全和胃肠道出血发生率较高。