延长咖啡因治疗中度早产儿呼吸暂停:MoCHA随机临床试验。

JAMA Pub Date : 2025-04-28 DOI:10.1001/jama.2025.5791
Waldemar A Carlo,Eric C Eichenwald,Benjamin A Carper,Edward F Bell,Martin Keszler,Ravi M Patel,Pablo J Sánchez,Ronald N Goldberg,Carl T D'Angio,Krisa P Van Meurs,Anna Maria Hibbs,Namasivayam Ambalavanan,Shirley S Cosby,Nancy S Newman,Betty R Vohr,Michele C Walsh,Abhik Das,Robin K Ohls,Janell Fuller,Matthew A Rysavy,Sarvin Ghavam,Luc P Brion,Karen M Puopolo,Ryan Moore,Michelle L Baack,Tarah T Colaizy,Mariana Baserga,Ahmed F Osman,Stephanie L Merhar,Brenda B Poindexter,Sara B DeMauro,Vasanth Kumar,C Michael Cotten,
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引用次数: 0

摘要

重要性中度早产婴儿在停用咖啡因后等待早产呼吸暂停缓解的住院时间可能会延长。目的评价延长咖啡因治疗是否能缩短住院时间。从2019年2月到2022年12月,这项随机临床试验在29家美国医院进行,招募了妊娠29至33周出生的婴儿,这些婴儿在经后33至35周接受咖啡因治疗,并计划停止咖啡因治疗,同时接受全饲(≥120 mL/kg/d)。随访于2023年3月20日完成。干预措施:婴儿在出院后28天随机接受口服枸橼酸咖啡因(10mg /kg/d)或安慰剂治疗。主要结局和测量主要结局是随机分组后的出院天数。次要结局包括生理成熟天数(连续5天无呼吸暂停,接受全口喂养,离开培养箱至少48小时)、月经后出院年龄、全因住院再入院、全因生病和急诊就诊、安全结局和死亡。结果共827例患儿(中位胎龄31周;414名女性[51%])随机选取(咖啡因组416名;在达到预定的无效阈值之前,计划的878例中有411例(安慰剂)。随机分组后两组住院天数无差异(咖啡因组18.0天[IQR, 10至30天],安慰剂组16.5天[IQR, 10至27天];调整中位差,0天[95% CI, -1.7天至1.7天]),到生理成熟的天数也没有差异(14.0天对15.0天,调整中位差,-1天[95% CI, -2.4天至0.4天])。接受咖啡因治疗的婴儿呼吸暂停消失得更快(6.0天vs 10.0天;调整中位差为-2.7天[95% CI, -3.4至-2.0天]),但与完全口服喂养的天数相似(7.5天vs 6.0天,调整中位差为0天[95% CI, -0.1至0.1])。再入院率和住院率在两组之间没有差异。两组患者不良事件发生率差异无统计学意义。结论及相关性在中度早产儿中,与安慰剂相比,继续使用咖啡因治疗并没有缩短住院时间。临床试验注册号:NCT03340727。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extended Caffeine for Apnea in Moderately Preterm Infants: The MoCHA Randomized Clinical Trial.
Importance Hospitalization of moderately preterm infants may be prolonged while waiting for apnea of prematurity to resolve after discontinuing caffeine. Objective To evaluate whether extending caffeine treatment reduces the duration of hospitalization. Design, Setting, and Participants From February 2019 to December 2022, this randomized clinical trial in 29 US hospitals enrolled infants born at 29 to 33 weeks' gestation who at 33 to 35 weeks' postmenstrual age were receiving caffeine treatment with plans to discontinue it plus receiving full feeds (≥120 mL/kg/d). Follow-up was completed on March 20, 2023. Interventions Infants were randomized to oral caffeine citrate (10 mg/kg/d) or placebo until 28 days after discharge. Main Outcomes and Measures The primary outcome was days to discharge after randomization. Secondary outcomes included days to physiological maturity (apnea free for 5 consecutive days, receiving full oral feeds, and out of the incubator for at least 48 hours), postmenstrual age at discharge, all-cause hospital readmissions, all-cause sick and emergency department visits, safety outcomes, and death. Results A total of 827 infants (median gestational age, 31 weeks; 414 female [51%]) were randomized (416, caffeine; 411, placebo) out of the 878 planned before reaching the prespecified futility threshold. Days of hospitalization after randomization did not differ between groups (18.0 days [IQR, 10 to 30 days] for caffeine vs 16.5 [IQR, 10 to 27 days] for placebo; adjusted median difference, 0 days [95% CI, -1.7 to 1.7 days]), nor did days to physiological maturity differ (14.0 vs 15.0 days, adjusted median difference, -1 day [95% CI, -2.4 to 0.4 days]). Infants receiving caffeine were apnea free sooner (6.0 vs 10.0 days; adjusted median difference, -2.7 days [95% CI, -3.4 to -2.0 days ]) but had similar days to full oral feeding (7.5 vs 6.0 days, adjusted median difference, 0 days [95% CI, -0.1 to 0.1]). Rates of readmissions and sick visits did not differ between groups. There was no statistically significant difference in adverse events between the 2 groups. Conclusions and Relevance In moderately preterm infants, continuation of caffeine treatment compared with placebo did not shorten hospitalization. Trial Registration ClinicalTrials.gov Identifier: NCT03340727.
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