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使用更新后的罗塞尔·优克福因果关系评估方法对新生儿和重症监护病房儿童药物性肝损伤进行因果关系评估。

Causality Evaluation of Drug-Induced Liver Injury in Newborns and Children in the Intensive Care Unit Using the Updated Roussel Uclaf Causality Assessment Method.

作者信息

Ye Ling, Feng Zeying, Huang Longjian, Guo Chengjun, Wu Xiong, He Li, Tan Wei, Wang Yi, Wu Xuehong, Hu Biwen, Li Tong, Yang Guoping, Chengxian Guo, He Qingnan

机构信息

Center of Clinical Pharmacology, The Third Xiangya Hospital, Central South University, Changsha, China.

Youjiang Medical University for Nationalities, Baise, China.

出版信息

Front Pharmacol. 2021 Dec 20;12:790108. doi: 10.3389/fphar.2021.790108. eCollection 2021.

Abstract

Drug-induced liver injury (DILI) is a common adverse reaction in the clinic; however, there are relatively few reports of DILI in critically ill newborns and children. Making use of the Pediatric Intensive Care database (PIC), this study identifies which drugs are related to DILI in neonates and children in China. Using the PIC, we screened for patients whose liver was suspected of being injured by drugs during hospitalization. The medicine they used was then assessed by the Roussel Uclaf Causality Assessment Method (RUCAM). At the same time, we also collated drug combinations that may affect CYP (Cytochrome P) enzyme metabolism, which may cause DILI. A total of 13,449 patients were assessed, of whom 77 newborns and 261 children were finally included. The main type of liver injury in neonates was mixed (83.1%), while the hepatic injury types of children were mostly distributed between hepatocellular (59.4%) and cholestatic (28.4%). In terms of the RUCAM assessment, the drugs that were most considered to cause or be associated with hepatic injury in newborns were medium and long chain fat emulsions (17%), sodium glycerophosphate (12%), and meropenem (9%); while omeprazole (11%), methylprednisolone sodium succinate (10%), and meropenem (8%) were the primary culprits of DILI in children. Drug combinations frequently seen in neonates that may affect CYP enzyme metabolism are omeprazole + budesonide (16.9%), dexamethasone + midazolam (10.4%), and midazolam + sildenafil (10.4%). In children, the commonly used drug combinations are fentanyl + midazolam (20.7%), ibuprofen + furosemide (18.4%), and diazepam + omeprazole (15.3%). In this study, medium and long chain fat emulsions and sodium glycerophosphate have been strongly associated with DILI in newborns, while omeprazole and methylprednisolone sodium succinate play an important role in the DILI of children. Also, attention should be paid to the effect on CYP enzymes when using multiple drugs at the same time. In future DILI cases, it is advisable to use the latest RUCAM for prospective study design so that complete case data and high RUCAM scores can be collected.

摘要

药物性肝损伤(DILI)是临床上常见的不良反应;然而,关于危重新生儿和儿童发生DILI的报道相对较少。本研究利用儿科重症监护数据库(PIC),确定在中国新生儿和儿童中哪些药物与DILI有关。我们使用PIC筛选住院期间肝脏疑似受药物损伤的患者。然后采用乌氏因果关系评估法(RUCAM)对他们使用的药物进行评估。同时,我们还整理了可能影响细胞色素P(CYP)酶代谢、进而可能导致DILI的药物组合。共评估了13449例患者,最终纳入77例新生儿和261例儿童。新生儿肝损伤的主要类型为混合型(83.1%),而儿童肝损伤类型大多分布在肝细胞型(59.4%)和胆汁淤积型(28.4%)之间。在RUCAM评估方面,新生儿中最常被认为导致或与肝损伤相关的药物是中长链脂肪乳剂(17%)、甘油磷酸钠(12%)和美罗培南(9%);而儿童DILI的主要罪魁祸首是奥美拉唑(11%)、甲泼尼龙琥珀酸钠(10%)和美罗培南(8%)。新生儿中常见的可能影响CYP酶代谢的药物组合是奥美拉唑+布地奈德(16.9%)、地塞米松+咪达唑仑(10.4%)和咪达唑仑+西地那非(10.4%)。在儿童中,常用的药物组合是芬太尼+咪达唑仑(20.7%)、布洛芬+呋塞米(18.4%)和地西泮+奥美拉唑(15.3%)。在本研究中,中长链脂肪乳剂和甘油磷酸钠与新生儿DILI密切相关,而奥美拉唑和甲泼尼龙琥珀酸钠在儿童DILI中起重要作用。此外,同时使用多种药物时应注意对CYP酶的影响。在未来的DILI病例中,建议使用最新的RUCAM进行前瞻性研究设计,以便收集完整的病例数据和获得较高的RUCAM评分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c0/8721278/9f74c2940c51/fphar-12-790108-g001.jpg

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