Gregorio Germana Emerita V, Rey Katrina Loren R, Tan-Lim Carol Stephanie C
Division of Pediatric Gastroenterology Hepatology and Nutrition, College of Medicine and Philippine General Hospital, University of the Philippines Manila.
Department of Clinical Epidemiology, College of Medicine, University of the Philippines Manila.
Acta Med Philipp. 2025 Jul 31;59(10):95-109. doi: 10.47895/amp.vi0.10948. eCollection 2025.
Phenobarbital is an inductor of microsomal hepatic enzyme and used as choleretic for cholestatic liver disease to enhance bile flow. It is also used as a premedication for hepatobiliary scintigraphy (HIDA) scan to improve diagnostic accuracy for an obstructive liver disease. We reviewed the available literature on the use of Phenobarbital for treatment of cholestasis and its utility as a premedication for HIDA scan.
All published studies before June 30, 2023 that investigated the efficacy, effectiveness or safety of Phenobarbital in cholestatic jaundice and its effect on the accuracy of hepatobiliary scintigraphy in diagnosis of obstructive jaundice were included. Electronic databases were searched including MEDLINE via PubMed,Cochrane Library, medRxIV, BioRxIV, as well as the following registries for ongoing and completed trials: ClinicalTrials.gov (USA); ChiCTR.org. (China); and the WHO International Clinical Trials Registry Platform. We screened abstracts, reviewed full texts, and extracted relevant information on study design, settings, population, and outcomes. There was no age and language restriction. Two reviewers independently rated the quality of included studies using: Joanna Briggs Institute critical appraisal tool for case reports, case series, and diagnostic accuracy; Newcastle - Ottawa Quality Assessment Scale for cohort studies, and Cochrane Risk of Bias for Randomized Trials. Risk of bias was appraised and GRADE certainty of evidence was judged. Pooled analysis was done using Stata 14 and reported as sensitivity and specificity.
Included were nine reports on Phenobarbital as treatment for cholestasis (one case report, five case series, one cohort and two randomized studies) and seven studies (four diagnostics, two cohorts, one randomized trial) on its use as a premedication for HIDA scan. The quality of case report and case series were considered fair; cohort studies as good; and diagnostic studies were included based on overall assessment. The randomized studies had some or high risk for bias due to concerns in randomization process, measurement of outcome, and risk in the selection of reported results.There were 31 patients (16 adults and 15 children) from case reports and case series. Of the 16 adults, serum total bilirubin concentrations declined from 4 to 70% from baseline in 13 of 15 (87%) patients after Phenobarbital was given at 120 to 250 mg per day from 22 days to five months. Eleven of 14 with pruritus at onset also had improvement in intensity of itching. Of the 15 pediatric patients, ten (67%) showed a decrease from 10 to 60% of the baseline total bilirubin but not a normalization with Phenobarbital intake at a dose of 3 to 12 mg/kg/day from one to 21 months. Five of 14 children also had relief of itching after treatment.Phenobarbital compared to Ursodeoxycholic acid had limited efficacy in reducing the bilirubin levels in neonates and young infants with cholestasis.Moderate certainty evidence showed that with Phenobarbital pretreatment, the hepatobiliary scan done on patients with neonatal cholestasis had 100% (CI 99.2, 100; I = 0.0%) sensitivity and 80.2% (CI 65.4, 92.1; I = 76.6%) specificity while no Phenobarbital pretreatment had 100% (94.9, 100; I = 0.0%) sensitivity and 89.5% (CI 77.0, 98.1; I = 11.4%) specificity. Adverse effects of Phenobarbital were drowsiness, lethargy, poor feeding, and irritability.
There was limited effectiveness of Phenobarbital in decreasing bilirubin levels in cholestatic liver disease. Moderate certainty evidence demonstrated that premedication with Phenobarbital did not improve the specificity of HIDA scan in the diagnosis of obstructive jaundice of infancy. Neurologic symptoms were observed with Phenobarbital intake.
苯巴比妥是一种微粒体肝酶诱导剂,用作胆汁淤积性肝病的利胆剂以增加胆汁流量。它还用作肝胆闪烁显像(HIDA)扫描的术前用药,以提高对梗阻性肝病的诊断准确性。我们回顾了关于使用苯巴比妥治疗胆汁淤积及其作为HIDA扫描术前用药效用的现有文献。
纳入2023年6月30日前发表的所有研究,这些研究调查了苯巴比妥在胆汁淤积性黄疸中的疗效、有效性或安全性及其对肝胆闪烁显像诊断梗阻性黄疸准确性的影响。检索了电子数据库,包括通过PubMed的MEDLINE、Cochrane图书馆、medRxIV、BioRxIV,以及以下正在进行和已完成试验的注册库:ClinicalTrials.gov(美国);ChiCTR.org.(中国);以及世界卫生组织国际临床试验注册平台。我们筛选摘要、审阅全文并提取有关研究设计、背景、人群和结果的相关信息。没有年龄和语言限制。两名审阅者使用以下工具独立评估纳入研究的质量:乔安娜·布里格斯研究所针对病例报告、病例系列和诊断准确性的批判性评估工具;队列研究的纽卡斯尔 - 渥太华质量评估量表,以及随机试验的Cochrane偏倚风险评估。评估偏倚风险并判断证据的GRADE确定性。使用Stata 14进行汇总分析,并报告为敏感性和特异性。
纳入了9篇关于苯巴比妥治疗胆汁淤积的报告(1篇病例报告、5篇病例系列、1篇队列研究和2篇随机研究)以及7篇关于其作为HIDA扫描术前用药的研究(4篇诊断性研究、2篇队列研究、1篇随机试验)。病例报告和病例系列的质量被认为一般;队列研究质量良好;诊断性研究根据总体评估纳入。由于随机化过程、结局测量以及报告结果选择方面的风险,随机研究存在一些或较高的偏倚风险。病例报告和病例系列中有31例患者(16名成人和15名儿童)。在16名成人中,15名患者中的13名(87%)在每天给予120至250毫克苯巴比妥,持续22天至5个月后,血清总胆红素浓度从基线下降了4%至70%。14名起病时有瘙痒的患者中有11名瘙痒强度也有所改善。在15名儿科患者中,10名(67%)在每天服用3至12毫克/千克苯巴比妥,持续1至21个月后,基线总胆红素下降了10%至60%,但未恢复正常。14名儿童中有5名在治疗后瘙痒也有所缓解。与熊去氧胆酸相比,苯巴比妥在降低胆汁淤积新生儿和幼儿胆红素水平方面疗效有限。中等确定性证据表明,对于新生儿胆汁淤积患者,进行苯巴比妥预处理后,肝胆扫描的敏感性为100%(CI 99.2,100;I = 0.0%),特异性为80.2%(CI 65.4,92.1;I = 76.6%),而未进行苯巴比妥预处理时,敏感性为100%(94.9,100;I = 0.0%),特异性为89.5%(CI 77.0,98.1;I = 11.4%)。苯巴比妥的不良反应有嗜睡、无精打采、喂养不佳和易激惹。
苯巴比妥在降低胆汁淤积性肝病胆红素水平方面效果有限。中等确定性证据表明,苯巴比妥预处理并未提高HIDA扫描对婴儿梗阻性黄疸诊断的特异性。服用苯巴比妥时观察到有神经症状。