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  • Oral ibuprofen versus intravenous ibuprofen or intravenous indomethacin for the treatment of patent ductus arteriosus in preterm infants: a systematic review and meta-analysis.

Oral ibuprofen versus intravenous ibuprofen or intravenous indomethacin for the treatment of patent ductus arteriosus in preterm infants: a systematic review and meta-analysis.

Neonatology (2012-03-15)
Roland Neumann, Sven M Schulzke, Christoph Bührer
摘要

Pharmacological closure of patent ductus arteriosus (PDA) is commonly achieved by intravenous (IV) administration of ibuprofen or indomethacin. Occasionally, oral ibuprofen is used for PDA treatment although its efficacy and safety are unclear. To systematically review randomized and quasi-randomized trials comparing oral ibuprofen with IV ibuprofen or IV indomethacin for closure of PDA in preterm infants. The standard search methods of the Cochrane Neonatal Review Group were used. We identified two studies (n = 166) of good methodological quality comparing oral ibuprofen with IV ibuprofen and three small trials (n = 92) of moderate methodological quality comparing oral ibuprofen to IV indomethacin. Meta-analysis showed higher PDA closure rate of oral ibuprofen versus IV ibuprofen but no difference between oral ibuprofen and IV indomethacin. Meta-analysis did not indicate a significant difference in adverse effects. Oral ibuprofen for PDA closure appears to be as effective as IV ibuprofen and IV indomethacin. Due to small sample size, lack of data in extremely preterm neonates, and methodological limitations of reviewed trials, definitive conclusions cannot be drawn. Randomized trials with a low risk of bias and adequate sample size in extremely preterm infants are urgently needed.

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Sigma-Aldrich
布洛芬, ≥98% (GC)
Sigma-Aldrich
吲哚美辛, 98.5-100.5% (in accordance with EP)
USP
布洛芬, United States Pharmacopeia (USP) Reference Standard
Supelco
布洛芬, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
布洛芬
Sigma-Aldrich
吲哚美辛, meets USP testing specifications
Supelco
Ibuprofen 溶液, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
Supelco
吲哚美辛, Pharmaceutical Secondary Standard; Certified Reference Material
USP
吲哚美辛, United States Pharmacopeia (USP) Reference Standard
布洛芬, European Pharmacopoeia (EP) Reference Standard
布洛芬, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
布洛芬, meets USP testing specifications
吲哚美辛, European Pharmacopoeia (EP) Reference Standard