不同起始时间应用咖啡因对早产儿安全性及有效性的评估:一项江苏省多中心研究

杨洋, 程锐, 吴琦, 乔立兴, 杨祖铭, 顾红兵, 姜善雨, 刘松林, 蒋曙红

中国当代儿科杂志 ›› 2020, Vol. 22 ›› Issue (2) : 130-135.

PDF(1248 KB)
PDF(1248 KB)
中国当代儿科杂志 ›› 2020, Vol. 22 ›› Issue (2) : 130-135. DOI: 10.7499/j.issn.1008-8830.2020.02.009
论著·临床研究

不同起始时间应用咖啡因对早产儿安全性及有效性的评估:一项江苏省多中心研究

  • 杨洋1, 程锐1, 吴琦2, 乔立兴3, 杨祖铭4, 顾红兵5, 姜善雨6, 刘松林7, 蒋曙红8
作者信息 +

Safety and efficacy of caffeine use started at different time in preterm infants: a multicenter study in Jiangsu Province, China

  • YANG Yang1, CHENG Rui1, WU Qi2, QIAO Li-Xing3, YANG Zu-Ming4, GU Hong-Bing5, JIANG Shan-Yu6, LIU Song-Lin7, JIANG Shu-Hong8
Author information +
文章历史 +

摘要

目的 评估早产儿(胎龄≤31周)早期和晚期使用咖啡因的有效性和安全性。方法 从江苏省8家医院的新生儿重症监护室中回顾性选取640例胎龄≤31周的早产儿作为研究对象,其中早期应用咖啡因510例(生后≤72 h开始应用;早期应用组),晚期应用咖啡因130例(生后>72 h开始应用;晚期应用组)。比较两组早产儿的临床资料。结果 早期应用组和晚期应用组在出生体重、Apgar评分、性别、胎龄、入院年龄等方面的比较差异无统计学意义(P > 0.05)。早期应用组咖啡因应用起始日龄和撤除日龄小于晚期应用组(P < 0.05);早期应用组咖啡因应用时间短于晚期应用组(P < 0.05)。两组之间入院时呼吸支持情况的比较差异无统计学意义(P > 0.05)。早期应用组呼吸暂停发生率低于晚期应用组(P < 0.05);早期应用组用氧时间和住院时间短于晚期应用组(P < 0.05)。早期应用组支气管肺发育不良发生率和家庭氧疗率显著低于晚期应用组(P < 0.05)。两组出院时新生儿颅内出血、脑室周围白质软化、坏死性小肠结肠炎、早产儿视网膜病变、动脉导管未闭的发生率和纠正胎龄40周时新生儿神经行为评分的比较差异均无统计学意义(P > 0.05)。两组的病死率比较差异亦无统计学意义(P > 0.05)。结论 早产儿(胎龄≤31周)早期应用咖啡因可显著缩短咖啡因应用时间、用氧时间和住院时间,且无明显不良反应。

Abstract

Objective To study the efficacy and safety of caffeine used in the early (≤ 72 hours after birth) and late (>72 hours after birth) stage in preterm infants with a gestational age of ≤ 31 weeks. Methods A retrospective analysis was performed for 640 preterm infants (with a gestational age of ≤ 31 weeks) who were admitted to the neonatal intensive care unit of eight hospitals in Jiangsu Province, China. Of the 640 preterm infants, 510 were given caffeine in the early stage (≤ 72 hours after birth; early use group) and 130 were given caffeine in the late stage (>72 hours after birth; late use group). The clinical data were compared between the two groups. Results There were no significant differences in birth weight, Apgar score, sex, gestational age, and age on admission between the two groups (P > 0.05). Compared with the late use group, the early use group had a significantly younger age at the beginning and withdrawal of caffeine treatment (P < 0.05) and a significantly shorter duration of caffeine treatment (P < 0.05). There was no significant difference in respiratory support on admission between the two groups (P > 0.05). Compared with the late use group, the early use group had significantly lower incidence rate of apnea (P < 0.05) and significantly shorter oxygen supply time and length of hospital stay (P < 0.05). There were no significant differences between the two groups in the incidence rates of neonatal intracranial hemorrhage, periventricular leukomalacia, necrotizing enterocolitis, retinopathy of prematurity, and patent ductus arteriosus at discharge and NBNA score at the corrected gestational age of 40 weeks (P > 0.05). However, significant differences were found in the incidence of bronchopulmonary dysplasia and the rate of home oxygen therapy, but there was no significant difference in the mortality rate between the two groups (P > 0.05). Conclusions Early use of caffeine can shorten the duration of caffeine treatment, oxygen supply time, and length of hospital stay, with little adverse effect, in preterm infants with a gestational age of ≤ 31 weeks.

关键词

咖啡因 / 有效性 / 安全性 / 早产儿

Key words

Caffeine / Efficacy / Safety / Preterm infant

引用本文

导出引用
杨洋, 程锐, 吴琦, 乔立兴, 杨祖铭, 顾红兵, 姜善雨, 刘松林, 蒋曙红. 不同起始时间应用咖啡因对早产儿安全性及有效性的评估:一项江苏省多中心研究[J]. 中国当代儿科杂志. 2020, 22(2): 130-135 https://doi.org/10.7499/j.issn.1008-8830.2020.02.009
YANG Yang, CHENG Rui, WU Qi, QIAO Li-Xing, YANG Zu-Ming, GU Hong-Bing, JIANG Shan-Yu, LIU Song-Lin, JIANG Shu-Hong. Safety and efficacy of caffeine use started at different time in preterm infants: a multicenter study in Jiangsu Province, China[J]. Chinese Journal of Contemporary Pediatrics. 2020, 22(2): 130-135 https://doi.org/10.7499/j.issn.1008-8830.2020.02.009

参考文献

[1] Donda K, Vijayakanthi N, Dapaah-Siakwan F, et al. Trends in epidemiology and outcomes of respiratory distress syndrome in the United States[J]. Pediatr Pulmonol, 2019, 54(4):405-414.
[2] Kalikkot Thekkeveedu R, Guaman MC, Shivanna B. Bronchopulmonary dysplasia:a review of pathogenesis and pathophysiology[J]. Respir Med, 2017, 132:170-177.
[3] Sweet DG, Carnielli V, Greisen G, et al. European consensus guidelines on the management of respiratory distress syndrome-2016 update[J]. Neonatology, 2017, 111(2):107-125.
[4] Wielenga JM, van den Hoogen A, van Zanten Henriette A, et al. Protocolized versus non-protocolized weaning for reducing the duration of invasive mechanical ventilation in newborn infants[J]. Cochrane Database Syst Rev, 2016, 3:CD011106.
[5] Steer P, Flenady V, Shearman A, et al. High dose caffeine citrate for extubation of preterm infants:a randomised controlled trial[J]. Arch Dis Child Fetal Neonatal Ed, 2004, 89(6):F499-F503.
[6] Katheria AC, Sauberan JB, Akotia D, et al. A pilot randomized controlled trial of early versus routine caffeine in extremely premature infants[J]. Am J Perinatol, 2015, 32(9):879-886.
[7] Dobson NR, Patel RM, Smith PB, et al. Trends in caffeine use and association between clinical outcomes and timing of therapy in very low birth weight infants[J]. J Pediatr, 2014, 164(5):992-998.
[8] Taha D, Kirkby S, Nawab U, et al. Early caffeine therapy for prevention of bronchopulmonary dysplasia in preterm infants[J]. J Matern Fetal Neonatal Med, 2014, 27(16):1698-1702.
[9] Nagasato A, Nakamura M, Kamimura H. Comparative study of the efficacy and safety of caffeine and aminophylline for the treatment of apnea in preterm infants[J]. Yakugaku Zasshi, 2018, 138(2):237-242.
[10] Schmidt B, Roberts RS, Davis P, et al. Caffeine therapy for apnea of prematurity[J]. N Engl J Med, 2006, 354(20):2112-2121.
[11] Schmidt B, Anderson PJ, Doyle LW, et al. Survival without disability to age 5 years after neonatal caffeine therapy for apnea of prematurity[J]. JAMA, 2012, 307(3):275-282.
[12] Kassim Z, Greenough A, Rafferty GF. Effect of caffeine on respiratory muscle strength and lung function in prematurely born ventilated infants[J]. Eur J Pediatr, 2009, 168(12):1491-1495.
[13] Voynow JA. "New" bronchopulmonary dysplasia and chronic lung disease[J]. Paediatr Respir Rev, 2017, 24:17-18.
[14] Torchin H, Combarel D, Aubelle MS, et al. Association of serum angiogenic factors with bronchopulmonary dysplasia. The ANGIODYS cohort study[J]. Pregnancy Hypertens, 2019, 18:82-87.
[15] Naeem A, Ahmed I, Silveyra P. Bronchopulmonary dysplasia:an update on experimental therapeutics[J]. Eur Med J (Chelmsf), 2019, 4(1):20-29.
[16] 早产儿支气管肺发育不良调查协作组. 早产儿支气管肺发育不良发生率及高危因素的多中心回顾调查分析[J]. 中华儿科杂志, 2011, 49(9):655-662.
[17] Hand I, Zaghloul N, Barash L, et al. Timing of caffeine therapy and neonatal outcomes in preterm infants:a retrospective study[J]. Int J Pediatr, 2016, 2016:9478204.
[18] Álvarez-Fuente M, Moreno L, Mitchell JA, et al. Preventing bronchopulmonary dysplasia:new tools for an old challenge[J]. Pediatr Res, 2019, 85(4):432-441.
[19] Mueni E, Opiyo N, English M. Caffeine for the management of apnea in preterm infants[J]. Int Health, 2009, 1(2):190-195.
[20] 邱洁, 封云, 程锐, 等. 早期或晚期使用枸橼酸咖啡因防治极低出生体重儿呼吸暂停的临床分析[J]. 中国当代儿科杂志, 2018, 20(12):979-984.
[21] Lodha A, Entz R, Synnes A, et al. Early caffeine administration and neurodevelopmental outcomes in preterm infants[J]. Pediatrics, 2019, 143(1). pii:e20181348.
[22] Moya FR, Mazela J, Shore PM, et al. Prospective observational study of early respiratory management in preterm neonates less than 35 weeks of gestation[J]. BMC Pediatr, 2019, 19(1):147.
[23] Belkhatir K, Zivanovic S, Lumgair H, et al. Variations in preterm stabilisation practices and caffeine therapy between two European tertiary level neonatal units[J]. Acta Paediatr, 2019. doi:10.1111/apa.15011[Epub ahead of print].
[24] Park HW, Lim G, Chung SH, et al. Early caffeine use in very low birth weight infants and neonatal outcomes:a systematic review and meta-analysis[J]. J Korean Med Sci, 2015, 30(12):1828-1835.
[25] Scanlon JE, Chin KC, Morgan ME, et al. Caffeine or theophylline for neonatal apnoea?[J]. Arch Dis Child, 1992, 67(4 Spec No):425-428.
[26] Skouroliakou M, Bacopoulou F, Markantonis SL. Caffeine versus theophylline for apnea of prematurity:a randomised controlled trial[J]. J Paediatr Child Health, 2009, 45(10):587-592.
[27] Zulqarnain A, Hussain M, Suleri KM, et al. Comparison of caffeine versus theophylline for apnea of prematurity[J]. Pak J Med Sci, 2019, 35(1):113-116.
[28] Welsh C, Pan J, Belik J. Caffeine impairs gastrointestinal function in newborn rats[J]. Pediatr Res, 2015, 78(1):24-28.
[29] 孙慧清, 康文清, 熊虹. 小剂量氨茶碱对早产儿脑神经发育的影响[J]. 中国新生儿科杂志, 2012, 27(5):320-324.
[30] Hwang J, Kim YS, Shin JH, et al. Hemodynamic effects on systemic blood flow and ductal shunting flow after loading dose of intravenous caffeine in preterm infants according to the patency of ductus arteriosus[J]. J Korean Med Sci, 2018, 33(4):e25.
[31] Gupte AS, Gupta D, Ravichandran S, et al. Effect of early caffeine on neurodevelopmental outcome of very low-birth weight newborns[J]. J Matern Fetal Neonatal Med, 2016, 29(8):1233-1237.
[32] Fleiss B, Gressens P. Neuroprotection of the preterm brain[J]. Handb Clin Neurol, 2019, 162:315-328.
[33] Atik A, Harding R, De Matteo R, et al. Caffeine for apnea of prematurity:effects on the developing brain[J]. Neurotoxicology, 2017, 58:94-102.


PDF(1248 KB)

Accesses

Citation

Detail

段落导航
相关文章

/