Time to response and predictors of seizure response to phenobarbitone therapy among neonates admitted with hypoxic-ischemic encephalopathy at Nekemte Comprehensive Specialized Hospital, Ethiopia

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY Journal of Clinical Neuroscience Pub Date : 2025-04-01 Epub Date: 2025-02-05 DOI:10.1016/j.jocn.2025.111104
Wase Benti Hailu , Getnet Yimer , Serawit Deyno , Lensa Tamiru Bacha
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Abstract

Background

Hypoxic-ischemic encephalopathy is a brain injury that occurs in newborns when there is not enough blood flow to the brain. Recent studies have raised concerns about how well phenobarbitone works for treating seizures in newborns, as it may not effectively control seizures with the initial loading and repeated doses.

Objective

This study evaluated the time to respond and predictors of seizure response to phenobarbitone therapy among neonates admitted with hypoxic-ischemic encephalopathy.

Methods and Materials

A retrospective cohort study was conducted at Nekemte Comprehensive Specialized Hospital, using randomly selected medical records of 284 neonates who were treated between January 2020 and December 31, 2023. The study included neonates diagnosed with perinatal asphyxia stage II and III hypoxic-ischemic encephalopathy, who were treated with nasogastric phenobarbitone. The treatment included an initial loading dose of 20 mg/kg and two repeated doses of 10 mg/kg. Survival analysis was conducted. Predictor variables with a p-value ≤ 0.25 in bivariate Cox regression were included in the multivariable Cox regression analysis. Adjusted Hazard Ratios with 95 % confidence intervals were computed, and a p-value < 0.05 was considered statistically significant.

Results

Out of the 284 neonates, 210 (73.9 %) responded to the phenobarbitone treatment. The incidence rate of response was 27.73 per 1000 person-hours of observation, with a median time to response of 29 h (IQR 26.5–32 h). Low birth weight (AHR = 0.59; 95 %CI 0.58, 0.98), subtle seizure type (AHR: 2.35; 95 % CI 1.09, 5.08), severe hypothermia (AHR = 0.23; 95 % CI 0.052, 0.26), and seizure frequency of twice or more (AHR = 0.436, 95 % CI 0.31, 0.61) were identified as predictors of seizure response.

Conclusion and recommendations

The overall incidence rate of response was low. Having a history of twice or more frequency of seizure insult, severe hypothermia and low birth weight decreased the response rate while subtle types of seizure increased the likelihood of response to phenobarbitone therapy. Electroencephalogram-confirmed seizure treatment and combined management with therapeutic hypothermia for high-risk newborns need to be started for better response and reduced response time. Further controlled studies utilizing both clinical and neuroimaging for definitive outcome measurement are recommended.
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埃塞俄比亚Nekemte综合专科医院收治的缺氧缺血性脑病新生儿对苯巴比妥治疗的反应时间和癫痫发作反应的预测因素
背景:缺氧缺血性脑病是一种新生儿脑损伤,发生在脑供血不足的情况下。最近的研究引起了人们对苯巴比妥治疗新生儿癫痫发作效果的关注,因为它在初始负荷和重复剂量下可能无法有效控制癫痫发作。目的评价新生儿缺氧缺血性脑病对苯巴比妥治疗的反应时间和癫痫发作反应的预测因素。方法与材料采用回顾性队列研究方法,随机选取2020年1月至2023年12月31日在Nekemte综合专科医院就诊的284例新生儿病历。该研究包括诊断为围产期窒息II期和III期缺氧缺血性脑病的新生儿,并给予鼻胃苯巴比妥治疗。治疗包括初始负荷剂量为20 mg/kg和两次重复剂量为10 mg/kg。进行生存分析。将双变量Cox回归中p值≤0.25的预测变量纳入多变量Cox回归分析。计算95%置信区间的校正风险比,p值<;0.05认为有统计学意义。结果284例新生儿中,210例(73.9%)对苯巴比妥治疗有应答。应答发生率为27.73 / 1000人-小时观察,中位应答时间为29小时(IQR为26.5-32小时)。95% CI 0.58, 0.98),轻微发作型(AHR: 2.35;95% CI 1.09, 5.08),严重低温(AHR = 0.23;95% CI 0.052, 0.26)和两次或两次以上癫痫发作频率(AHR = 0.436, 95% CI 0.31, 0.61)被确定为癫痫发作反应的预测因子。结论与建议总有效率较低。有两次或两次以上癫痫发作、严重低温和低出生体重的病史会降低反应率,而轻微类型的癫痫发作会增加对苯巴比妥治疗的反应可能性。需要开始对高危新生儿进行脑电图证实的癫痫发作治疗和治疗性低温联合管理,以获得更好的反应并缩短反应时间。建议进一步的对照研究利用临床和神经影像学来确定结果的测量。
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来源期刊
Journal of Clinical Neuroscience
Journal of Clinical Neuroscience 医学-临床神经学
CiteScore
4.50
自引率
0.00%
发文量
402
审稿时长
40 days
期刊介绍: This International journal, Journal of Clinical Neuroscience, publishes articles on clinical neurosurgery and neurology and the related neurosciences such as neuro-pathology, neuro-radiology, neuro-ophthalmology and neuro-physiology. The journal has a broad International perspective, and emphasises the advances occurring in Asia, the Pacific Rim region, Europe and North America. The Journal acts as a focus for publication of major clinical and laboratory research, as well as publishing solicited manuscripts on specific subjects from experts, case reports and other information of interest to clinicians working in the clinical neurosciences.
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