Efficacy and safety of low-dose hydrocortisone for the prevention and treatment of bronchopulmonary dysplasia in very premature infants: a meta-analysis
返回论文页
|更新时间:2023-05-25
|
Efficacy and safety of low-dose hydrocortisone for the prevention and treatment of bronchopulmonary dysplasia in very premature infants: a meta-analysis
SHI Huiling,JIA Yanping,REN Yi.Efficacy and safety of low-dose hydrocortisone for the prevention and treatment of bronchopulmonary dysplasia in very premature infants: a meta-analysis[J].ZHONGGUO YAOFANG,2023,34(10):1252-1256.
SHI Huiling,JIA Yanping,REN Yi.Efficacy and safety of low-dose hydrocortisone for the prevention and treatment of bronchopulmonary dysplasia in very premature infants: a meta-analysis[J].ZHONGGUO YAOFANG,2023,34(10):1252-1256. DOI: 10.6039/j.issn.1001-0408.2023.10.19.
Efficacy and safety of low-dose hydrocortisone for the prevention and treatment of bronchopulmonary dysplasia in very premature infants: a meta-analysis
计算机检索PubMed、Embase、Web of Science、Cochrane图书馆、中国期刊全文数据库、中文科技期刊数据库、万方数据,收集极早产儿早期预防性使用小剂量HC(试验组)对比安慰剂或多巴胺(对照组)的随机对照试验(RCT)。检索时限均为建库起至2022年6月。筛选文献、提取资料后采用Cochrane系统评价员手册推荐的6.2偏倚风险评估工具对纳入文献质量进行评价;采用RevMan 5.3软件进行Meta分析、敏感性分析和发表偏倚分析。
To systematically evaluate the efficacy and safety of prophylactic use of low-dose hydrocortisone (HC) for the prevention and treatment of bronchopulmonary dysplasia (BPD), and to provide evidence-based reference for clinical treatment.
METHODS
2
PubMed, Embase, Web of Science, Cochrane Library, CJFD, VIP and Wanfang databases were searched by computer; randomized controlled trials (RCT) about prophylactic use of low-dose HC (trial group) versus placebo or dopamine (control group) in very premature infants were collected from the establishment of the database to Jun. 2022. The quality of the included literature was evaluated by using bias risk assessment tool recommended by Cochrane system evaluator’s manual (version 6.2) after screening the literature and extracting the data. Meta-analysis, sensitivity analysis and publication bias analysis were carried out with RevMan 5.3 statistical software.
RESULTS
2
A total of 1 437 very premature infants were included in 9 RCTs. Meta-analysis showed that the incidence of BPD [OR=0.75, 95%CI(0.58,0.95),
P
=0.02] and fatality [OR=0.72, 95%CI (0.54,0.97),
P
=0.03] in trial group were significantly lower than control group; the survival rate without BPD [OR=1.36, 95%CI (1.06,1.74),
P
=0.02], the incidences of gastrointestinal perforation [OR=2.23, 95%CI (1.31,3.78),
P
=0.003] and sepsis [OR=1.27, 95%CI (1.01,1.60),
P
=0.04] in trial group were all significantly higher than control group. There was no significant difference in the incidence of necrotizing enterocolitis, paraventricular leukomalacia, intraventricular hemorrhage, patent ductus arteriosus, hyperglycemia, pneumothorax, retinopathy of premature infants between the two groups (
P
>0.05). Results of sensitivity analysis showed that study results were robust. Results of publication bias analysis showed that there was little possibility of publication bias in this study.
CONCLUSIONS
2
The early prophylactic use of low-dose HC can reduce BPD in very premature infants, reduce fatality, and improve the survival rate without BPD, but we should pay attention to gastrointestinal perforation and sepsis.
HIGGINS R D,JOBE A H,KOSO-THOMAS M,et al. Bronchopulmonary dysplasia:executive summary of a workshop[J]. J Pediatr,2018,197:300-308.
STOLL B J,HANSEN N I,BELL E F,et al. Trends in care practices,morbidity,and mortality of extremely preterm neonates,1993-2012[J]. JAMA,2015,314(10):1039-1051.
TWILHAAR E S,WADE R M,DE KIEVIET J F,et al. Cognitive outcomes of children born extremely or very preterm since the 1990s and associated risk factors:a meta-analysis and meta-regression[J]. JAMA Pediatr,2018,172(4):361-367.
BHANDARI V. Postnatal inflammation in the patho-genesis of bronchopulmonary dysplasia[J]. Birth Defects Res A Clin Mol Teratol,2014,100(3):189-201.
DELARA M,CHAUHAN B F,LE M L,et al. Efficacy and safety of pulmonary application of corticosteroids in preterm infants with respiratory distress syndrome:a systematic review and meta-analysis[J]. Arch Dis Child Fetal Neonatal Ed,2019,104(2):F137-F144.
PHAROAH P D. Dexamethasone treatment and cerebral palsy[J]. Arch Dis Child Fetal Neonatal Ed,2001,84(2):140Fa-140.
HALLIDAY H L. Early postnatal dexamethasone and cerebral palsy[J]. Pediatrics,2002,109(6):1168-1169.
SHINWELL E S,KARPLUS M,BADER D,et al. Neonatologists are using much less dexamethasone[J]. Arch Dis Child Fetal Neonatal Ed,2003,88(5):F432-F433.
DOYLE L W,CHEONG J L,EHRENKRANZ R A,et al. Early(< 8 days)systemic postnatal corticosteroids for prevention of bronchopulmonary dysplasia in preterm infants[J]. Cochrane Database Syst Rev,2017,10(10):CD001146.
OFMAN G,PEREZ M,FARROW K N. Early low-dose hydrocortisone:is the neurodevelopment affected?[J]. J Perinatol,2018,38(6):636-638.
WATTERBERG K L,GERDES J S,COLE C H,et al. Prophylaxis of early adrenal insufficiency to prevent bronchopulmonary dysplasia:a multicenter trial[J]. Pediatrics,2004,114(6):1649-1657.
BAUD O,MAURY L,LEBAIL F,et al. Effect of early low-dose hydrocortisone on survival without bronchopulmonary dysplasia in extremely preterm infants(PREMILOC):a double-blind,placebo-controlled,multicentre,randomised trial[J]. Lancet,2016,387(10030):1827-1836.
BONSANTE F,LATORRE G,IACOBELLI S,et al. Early low-dose hydrocortisone in very preterm infants:a randomized,placebo-controlled trial[J]. Neonatology,2007,91(4):217-221.
BOURCHIER D,WESTON P J. Randomised trial of dopamine compared with hydrocortisone for the treatment of hypotensive very low birthweight infants[J]. Arch Dis Child Fetal Neonatal Ed,1997,76(3):F174-F178.
EFIRD M M,HEERENS A T,GORDON P V,et al. A randomized-controlled trial of prophylactic hydrocor-tisone supplementation for the prevention of hypotension in extremely low birth weight infants[J]. J Perinatol,2005,25(2):119-124.
HOCHWALD O,PALEGRA G,OSIOVICH H. Adding hydrocortisone as 1st line of inotropic treatment for hypotension in very low birth weight infants[J]. Indian J Pediatr,2014,81(8):808-810.
PARIKH N A,KENNEDY K A,LASKY R E,et al. Pilot randomized trial of hydrocortisone in ventilator-dependent extremely preterm infants:effects on regional brain volumes[J]. J Pediatr,2013,162(4):685-690.e1.
PELTONIEMI O,KARI M A,HEINONEN K,et al. Pretreatment cortisol values may predict responses to hydrocortisone administration for the prevention of bronchopulmonary dysplasia in high-risk infants[J]. J Pediatr,2005,146(5):632-637.
PATEL R M. Short- and long-term outcomes for extremely preterm infants[J]. Am J Perinatol,2016,33(3):318-328.
JOBE A H,BANCALARI E. Bronchopulmonary dysplasia[J]. Am J Respir Crit Care Med,2001,163(7):1723-1729.
HIGGINS J P T,ALTMAN D G,GØTZSCHE P C,et al. The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials[J]. BMJ,2011,343:d5928.
SHAFFER M L,BAUD O,LACAZE-MASMONTEIL T,et al. Effect of prophylaxis for early adrenal insufficiency using low-dose hydrocortisone in very preterm infants:an individual patient data meta-analysis[J]. J Pediatr,2019,207:136-142.e5.
MORRIS I P,GOEL N,CHAKRABORTY M. Efficacy and safety of systemic hydrocortisone for the prevention of bronchopulmonary dysplasia in preterm infants:a systematic review and meta-analysis[J]. Eur J Pediatr,2019,178(8):1171-1184.