Neonatal Medicine, Imperial College London, London, UK.
Neonatal Medicine, School of Public Health, Imperial College London, London, UK.
BMJ Open. 2022 Nov 17;12(11):e063835. doi: 10.1136/bmjopen-2022-063835.
Describe the population of babies who do and do not receive postnatal corticosteroids for prevention or treatment of bronchopulmonary dysplasia (BPD).
Retrospective cohort study using data held in the National Neonatal Research Database.
National Health Service neonatal units in England and Wales.
Babies born less than 32 weeks gestation and admitted to neonatal units from 1 January 2012 to 31 December 2019.
Proportion of babies given postnatal corticosteroid; type of corticosteroid; age at initiation and duration, trends over time.
Survival to discharge, treatment for retinopathy of prematurity, BPD, brain injury, severe necrotising enterocolitis, gastrointestinal perforation.
8% (4713/62019) of babies born <32 weeks and 26% (3525/13527) born <27 weeks received postnatal corticosteroids for BPD. Dexamethasone was predominantly used 5.3% (3309/62019), followed by late hydrocortisone 1.5%, inhaled budesonide 1.5%. prednisolone 0.8%, early hydrocortisone 0.3% and methylprednisolone 0.05%. Dexamethasone use increased over time (2012: 4.5 vs 2019: 5.8%, p=0.04). Median postnatal age of initiation of corticosteroid course was around 3 weeks for late hydrocortisone, 4 weeks for dexamethasone, 6 weeks for inhaled budesonide, 12 weeks for prednisolone and 16 weeks for methylprednisolone. Babies who received postnatal corticosteroids were born more prematurely, had a higher incidence of comorbidities and a longer length of stay.
In England and Wales, around 1 in 12 babies born less than 32 weeks and 1 in 4 born less than 27 weeks receive postnatal corticosteroids to prevent or treat BPD. Given the lack of convincing evidence of efficacy, challenges of recruiting to and length of time taken to conduct randomised controlled trial, our data highlight the need to monitor long-term outcomes in children who received neonatal postnatal corticosteroids.
描述接受或未接受产后皮质类固醇治疗以预防或治疗支气管肺发育不良(BPD)的婴儿人群。
使用国家新生儿研究数据库中的数据进行回顾性队列研究。
英格兰和威尔士的国民保健服务新生儿单位。
胎龄小于 32 周且于 2012 年 1 月 1 日至 2019 年 12 月 31 日期间入住新生儿单位的婴儿。
接受产后皮质类固醇治疗的婴儿比例;皮质类固醇的类型;起始年龄和持续时间,随时间的趋势。
出院存活率、早产儿视网膜病变治疗、BPD、脑损伤、严重坏死性小肠结肠炎、胃肠穿孔。
出生胎龄<32 周的婴儿中,有 8%(4713/62019)接受了 BPD 的产后皮质类固醇治疗,而胎龄<27 周的婴儿中,有 26%(3525/13527)接受了治疗。地塞米松的使用最为普遍(5.3%,3309/62019),其次是晚期氢化可的松 1.5%、吸入布地奈德 1.5%、泼尼松龙 0.8%、早期氢化可的松 0.3%和甲泼尼龙 0.05%。地塞米松的使用随着时间的推移而增加(2012 年:4.5% vs 2019 年:5.8%,p=0.04)。晚期氢化可的松开始皮质类固醇疗程的平均出生后年龄约为 3 周,地塞米松为 4 周,吸入布地奈德为 6 周,泼尼松龙为 12 周,甲泼尼龙为 16 周。接受产后皮质类固醇治疗的婴儿出生时更不成熟,合并症的发生率更高,住院时间更长。
在英格兰和威尔士,大约每 12 个胎龄小于 32 周的婴儿和每 4 个胎龄小于 27 周的婴儿接受产后皮质类固醇治疗以预防或治疗 BPD。鉴于缺乏令人信服的疗效证据,以及招募参与和进行随机对照试验所需的时间长,我们的数据强调需要监测接受新生儿产后皮质类固醇治疗的儿童的长期结局。