S. Mehnaz, M. Chowdhury, B. Yasmeen, Masudur Rahman, R. Akter, Manifa Afrin, M. Begum
{"title":"人重组红细胞生成素(rHuEPO)在围产期窒息中的作用——一项随机对照试验","authors":"S. Mehnaz, M. Chowdhury, B. Yasmeen, Masudur Rahman, R. Akter, Manifa Afrin, M. Begum","doi":"10.3329/NIMCJ.V10I1.39326","DOIUrl":null,"url":null,"abstract":"Background : Perinatal asphyxia is an insult to the fetus or newborn infant due to lack of oxygen (hypoxia) and/or a lack of perfusion (ischemia) to various organs, which will manifest as difficulty in establishing spontaneous respiration evident by delayed cry after birth, at least after one minute. World-wide, perinatal asphyxia accounts for about 900,000 deaths each year. In Bangladesh it is a major cause of neonatal death. A substantial proportion of the children that survive suffer late effects such as cerebral palsy and epilepsy. \nObjective : To determine the efficacy of erythropoietin in improving the neurological outcome of term neonates with perinatal asphyxia (HIE stage II and III). \nMaterials and methods : A Randomized Controll Trial was carried out in the Neonatal ward and NICU of Dhaka Shishu Hospital from 1st April 2014 to 30th Sep 2015. A total 68 neonates with perinatal asphyxia (both HIE stage II and III) who fulfill the inclusion criteria were enrolled and randomly assigned to intervention group (n=35) and control group (n=33). Intervention group received rHuEPO 300- 500 U/kg/dose daily subcutaneously for 5 days within first 48 hours of birth along with the standard treatment protocol and control group received standard treatment protocol only. \nResults : Baseline clinical characteristics, USG of brain during hospital stay were almost similar in both groups. Statistically significant effect was noted in seizure control, tolerance of oral feeding, hospital stay and neurological outcome at 3 months of age (p=008). USG of brain at 3 months of age also improved significantly (p=0.027). \nConclusion : This study demonstrates the effectiveness of early administration of rHuEPO to term neonates with moderate to severe asphyxia, beneficial effect on short term outcomes like seizure control, tolerance of oral feeding and neurological outcome at 3 months of age. A large multicenter study would be done for further evaluation of these findings. \nNorthern International Medical College Journal Vol.10(1) Jul 2018: 330-334","PeriodicalId":389586,"journal":{"name":"Northern International Medical College Journal","volume":"48 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Role of Human Recombinant Erythropoietin (rHuEPO) in Perinatal Asphyxia-a randomized controlled trial\",\"authors\":\"S. Mehnaz, M. Chowdhury, B. Yasmeen, Masudur Rahman, R. Akter, Manifa Afrin, M. 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引用次数: 0
摘要
背景:围产期窒息是对胎儿或新生儿的一种侮辱,由于缺氧和/或各器官缺乏灌注(缺血),表现为建立自主呼吸困难,明显表现为出生后延迟哭泣,至少在一分钟后。全世界每年约有90万人死于围产期窒息。在孟加拉国,它是新生儿死亡的一个主要原因。存活下来的儿童中有相当一部分患有脑瘫和癫痫等后期影响。目的:探讨促红细胞生成素对围产儿窒息期(HIE II期和III期)足月新生儿神经预后的改善效果。材料与方法:2014年4月1日至2015年9月30日在达卡石树医院新生儿病房和新生儿重症监护病房进行随机对照试验。入选符合入选标准的围产期窒息新生儿(HIE II期和III期)68例,随机分为干预组(n=35)和对照组(n=33)。干预组在出生后48小时内每日皮下注射rHuEPO 300- 500 U/kg剂量,连续5天,并给予标准治疗方案,对照组仅给予标准治疗方案。结果:两组患者住院期间脑USG及基线临床特征基本相似。在癫痫发作控制、口服喂养耐受性、住院时间和3月龄神经预后方面均有统计学意义(p=008)。3月龄时脑USG也显著改善(p=0.027)。结论:本研究表明,早期给予rHuEPO对中重度窒息足月新生儿有效,对癫痫发作控制、口服喂养耐受性和3月龄时神经学预后等短期预后有有益影响。将进行一项大型多中心研究以进一步评估这些发现。北方国际医学院学报Vol.10(1) july 2018: 330-334
Role of Human Recombinant Erythropoietin (rHuEPO) in Perinatal Asphyxia-a randomized controlled trial
Background : Perinatal asphyxia is an insult to the fetus or newborn infant due to lack of oxygen (hypoxia) and/or a lack of perfusion (ischemia) to various organs, which will manifest as difficulty in establishing spontaneous respiration evident by delayed cry after birth, at least after one minute. World-wide, perinatal asphyxia accounts for about 900,000 deaths each year. In Bangladesh it is a major cause of neonatal death. A substantial proportion of the children that survive suffer late effects such as cerebral palsy and epilepsy.
Objective : To determine the efficacy of erythropoietin in improving the neurological outcome of term neonates with perinatal asphyxia (HIE stage II and III).
Materials and methods : A Randomized Controll Trial was carried out in the Neonatal ward and NICU of Dhaka Shishu Hospital from 1st April 2014 to 30th Sep 2015. A total 68 neonates with perinatal asphyxia (both HIE stage II and III) who fulfill the inclusion criteria were enrolled and randomly assigned to intervention group (n=35) and control group (n=33). Intervention group received rHuEPO 300- 500 U/kg/dose daily subcutaneously for 5 days within first 48 hours of birth along with the standard treatment protocol and control group received standard treatment protocol only.
Results : Baseline clinical characteristics, USG of brain during hospital stay were almost similar in both groups. Statistically significant effect was noted in seizure control, tolerance of oral feeding, hospital stay and neurological outcome at 3 months of age (p=008). USG of brain at 3 months of age also improved significantly (p=0.027).
Conclusion : This study demonstrates the effectiveness of early administration of rHuEPO to term neonates with moderate to severe asphyxia, beneficial effect on short term outcomes like seizure control, tolerance of oral feeding and neurological outcome at 3 months of age. A large multicenter study would be done for further evaluation of these findings.
Northern International Medical College Journal Vol.10(1) Jul 2018: 330-334