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布洛芬与吲哚美辛用于动脉导管未闭封堵术的荟萃分析。

A meta-analysis of ibuprofen versus indomethacin for closure of patent ductus arteriosus.

作者信息

Thomas Ronald L, Parker Graham C, Van Overmeire Bart, Aranda Jacob V

机构信息

Children's Research Center of Michigan, Children's Hospital of Michigan, 3901 Beaubien Blvd, 48201 Detroit, Michigan, USA.

出版信息

Eur J Pediatr. 2005 Mar;164(3):135-40. doi: 10.1007/s00431-004-1596-5. Epub 2004 Dec 10.

DOI:10.1007/s00431-004-1596-5
PMID:15717178
Abstract

UNLABELLED

Ibuprofen (IBU) has previously been shown to be as effective as indomethacin (INDO) in closing the patent ductus arteriosus (PDA) of preterm infants, without severely affecting renal hemodynamics or basal cerebral blood flow. We conducted a meta-analysis of randomized trials to compare the efficacy and safety of IBU and INDO for treatment of PDA. Data from the nine relevant trials ( n =566), showed no significant difference in the efficacy of IBU and INDO in PDA closure ( P =0.70). However, five trials ( n =443) provided serum creatinine concentration data that revealed a significantly lower increase favoring IBU ( P < 0.001), and urine output data that showed a significantly lower decrease favoring IBU ( P < 0.001). In two trials ( n =188) the proportion of infants who required postnatal oxygen therapy at 28 days (defined as chronic lung disease) was significantly higher with IBU (52/94; 55.3%) than with INDO (38/94; 40.4%, P < 0.05). No statistically significant differences were found in mortality, intraventricular hemorrhage, necrotizing enterocolitis, surgical ligation, sepsis, retinopathy of prematurity, periventricular leukomalacia, length of hospital stay, gastrointestinal bleeding, re-opening of PDA, back-up treatment, surfactant therapy, or days on a ventilator.

CONCLUSION

ibuprofen and indomethacin have similar efficacy in patent ductus arteriosus closure, but preterm infants treated with ibuprofen experience lower serum creatinine values, higher urine output, and less undesirable decreased organ blood flow and vasoconstrictive adverse effects.

摘要

未标注

此前已表明,布洛芬(IBU)在闭合早产儿动脉导管未闭(PDA)方面与吲哚美辛(INDO)效果相当,且不会严重影响肾血流动力学或基础脑血流量。我们进行了一项随机试验的荟萃分析,以比较IBU和INDO治疗PDA的疗效和安全性。来自9项相关试验(n = 566)的数据显示,IBU和INDO在闭合PDA的疗效上无显著差异(P = 0.70)。然而,5项试验(n = 443)提供的血清肌酐浓度数据显示,有利于IBU的升高显著更低(P < 0.001),尿量数据显示,有利于IBU的降低显著更低(P < 0.001)。在2项试验(n = 188)中,使用IBU的婴儿在28天时需要产后氧疗(定义为慢性肺病)的比例显著高于使用INDO的婴儿(52/94;55.3% 对比38/94;40.4%,P < 0.05)。在死亡率、脑室内出血、坏死性小肠结肠炎、手术结扎、败血症、早产儿视网膜病变、脑室周围白质软化、住院时间、胃肠道出血、PDA重新开放、备用治疗、表面活性剂治疗或使用呼吸机天数方面未发现统计学显著差异。

结论

布洛芬和吲哚美辛在闭合动脉导管未闭方面疗效相似,但使用布洛芬治疗的早产儿血清肌酐值更低、尿量更高,且器官血流量减少和血管收缩不良反应等不良情况更少。

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J Pediatr. 2004 Mar;144(3):386-8. doi: 10.1016/j.jpeds.2003.11.027.
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Comparison of ibuprofen and indomethacin therapy for patent ductus arteriosus in preterm infants.布洛芬与吲哚美辛治疗早产儿动脉导管未闭的比较。
Pediatr Int. 2003 Dec;45(6):665-70. doi: 10.1111/j.1442-200x.2003.01797.x.
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Ibuprofen for the treatment of a patent ductus arteriosus in preterm and/or low birth weight infants.布洛芬用于治疗早产儿和/或低出生体重儿的动脉导管未闭。
不同剂量静脉注射对早产儿动脉导管未闭(胎龄<32 周)闭合效果的比较:一项前瞻性观察研究。
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Clinical Dilemma Involving Treatments for Very Low-Birth-Weight Infants and the Potential Risk of Necrotizing Enterocolitis: A Narrative Literature Review.极低出生体重儿治疗相关的临床困境及坏死性小肠结肠炎的潜在风险:一篇叙述性文献综述
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Physiol Rep. 2023 Jun;11(12):e15749. doi: 10.14814/phy2.15749.
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Children (Basel). 2022 Jan 10;9(1):89. doi: 10.3390/children9010089.
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Survey of PDA management in very low birth weight infants across Italy.意大利极低出生体重儿 PDA 管理调查。
Ital J Pediatr. 2020 Feb 14;46(1):22. doi: 10.1186/s13052-020-0773-0.
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Neonatal necrotizing enterocolitis with intestinal perforation in extremely premature infants receiving early indomethacin treatment for patent ductus arteriosus.在接受早期吲哚美辛治疗动脉导管未闭的极早产儿中发生的伴有肠穿孔的新生儿坏死性小肠结肠炎。
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Eur J Pediatr. 2002 Apr;161(4):202-7. doi: 10.1007/s00431-002-0915-y.
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A comparison of ibuprofen and indomethacin for closure of patent ductus arteriosus.布洛芬与吲哚美辛用于动脉导管未闭封堵的比较。
N Engl J Med. 2000 Sep 7;343(10):674-81. doi: 10.1056/NEJM200009073431001.
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Prophylactic ibuprofen therapy of patent ductus arteriosus in preterm infants.早产儿动脉导管未闭的预防性布洛芬治疗
Eur J Pediatr. 2000 May;159(5):364-8. doi: 10.1007/s004310051288.