苯巴比妥治疗缺氧缺血性脑病新生儿癫痫发作持续时间的预测因素

Shelim Rumana, Ferdous Jannatul, Mahbuba Sharmin, Jahan Ismat
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摘要

目的:围产期窒息伴缺氧缺血性脑病伴癫痫发作是孟加拉国新生儿死亡和发病的主要原因之一。苯巴比妥仍然是治疗新生儿癫痫发作的首选药物。本研究旨在确定苯巴比妥治疗新生儿缺氧缺血性脑病(HIE)癫痫发作持续时间的预测因素。方法:研究于2016年2月1日至2017年1月31日在东西医学院附属医院新生儿重症监护病房(NICU)对50例HIE合并癫痫发作的新生儿进行研究。记录了苯巴比妥治疗初期控制癫痫发作的剂量和持续时间。在控制癫痫发作以防止进一步复发后,苯巴比妥治疗的总持续时间也被记录下来。随访至3个月大以观察癫痫复发。结果:50例新生儿中,25例(50%)在24小时内反应良好。在癫痫发作初期控制后,苯巴比妥治疗的平均持续时间为4.70±2.93天,在24小时内反应良好的病例中,平均总持续时间为6.89±3.58天。3例(6%)有癫痫复发。复发病例需要72小时以上的初始控制发作(p 0.006),初始控制发作后的原始反射和活动较差(p 0.0002)。癫痫发作初始控制后,苯巴比妥治疗的平均持续时间为6.33±6.11天,苯巴比妥治疗的平均总持续时间也更长,为9.67±7.37天。结论:新生儿初效好,反应较好,需要短时间的苯巴比妥治疗。在癫痫发作得到控制后应立即停用。HIE III型新生儿,初始反应时间超过72小时且癫痫发作初始控制后反射较差的新生儿可能需要更长时间的苯巴比妥治疗(超过7天)以防止癫痫发作复发。因此,明智地使用苯巴比妥可以减少不必要的非特异性治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictors of Duration of Phenobarbitone Therapy in Seizures of Neonates with Hypoxic-Ischemic Encephalopathy
Objective: Perinatal asphyxia with hypoxic-ischemic encephalopathy associated with seizures is one of the leading cause of neonatal mortality and morbidity in Bangladesh. Phenobarbitone remains the drug of choice in treatment of neonatal seizures. This study was conducted to determine the predictors of duration of Phenobarbitone therapy in seizures of neonates with Hypoxic-Ischemic Encephalopathy (HIE). Methodology: The study was conducted in Neonatal Intensive Care Unit (NICU) of East West Medical College Hospital from 1st february 2016 to 31st january 2017 on fifty neonates with HIE and seizures. The dose and duration of phenobarbitone therapy for initial control of seizure was noted. Total duration of phenobarbitone therapy after control of seizure to prevent further recurrences was also noted. Follow up was given up to 3 months of age to see any recurrence of seizures. Results: Out of the 50 neonates,25 cases (50%) responded well within 24 hours. Mean duration of phenobarbitone therapy after initial control of seizure was 4.70 ± 2.93days and Mean total duration of therapy was 6.89 ± 3.58 days in cases who responded well within 24 hours.. 3 (6%) cases had recurrence of seizures. The recurrence cases required more than 72 hours for initial control of seizure (p 0.006) and had poor primitive reflexes and activity after initial control of seizure (p 0.0002). Mean duration of phenobarbitone therapy after initial control of seizures was 6.33 ± 6.11 days and Mean total duration of phenobarbitone therapy was also longer 9.67 ± 7.37 days. Conclusion: Neonates who have good initial response and have better reflexes required short duration of phenobarbitone therapy. It should be discontinued soon after control of seizure. Neonates with HIE III, those requiring more than 72 hours for initial response and poor reflexes after initial control of seizure may require longer duration of phenobarbitone therapy (more than 7 days) to prevent recurrence of seizures. Thus, judicious use of phenobarbitone will minimize the unnecessary non-specific treatment.
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