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新加坡将基因分型作为标准治疗方法后卡马西平的使用模式及相关严重皮肤不良反应

Usage Pattern of Carbamazepine and Associated Severe Cutaneous Adverse Reactions in Singapore Following Implementation of Genotyping as Standard-of-Care.

作者信息

Sung Cynthia, Tan Liesbet, Limenta Michael, Ganesan Ganga, Toh Dorothy, Chan Cheng Leng

机构信息

Vigilance and Compliance Branch, Health Products Regulation Group, Health Sciences Authority, Singapore, Singapore.

Health Services & Systems Research Programme, Duke-NUS Medical School, Singapore, Singapore.

出版信息

Front Pharmacol. 2020 May 7;11:527. doi: 10.3389/fphar.2020.00527. eCollection 2020.

DOI:10.3389/fphar.2020.00527
PMID:32457602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7221117/
Abstract

In April 2013, the Ministry of Health and Health Sciences Authority of Singapore jointly issued recommendations for genotyping before starting carbamazepine (CBZ) in new patients of Asian ancestry as standard of care. The Ministry of Health also approved a 75% subsidy for genotyping to all patients on subsidy at public healthcare institutions. To understand the impact of these regulatory decisions, we researched the usage patterns for CBZ and levetiracetam, the trend of Stevens-Johnson syndrome/toxic epidermal necrolysis [Stevens-Johnson syndrome (SJS)/toxic epidermal necrolysis (TEN)] reports associated with antiepileptic drugs and the take-up rates of tests in Singapore. In the 5-year post-policy period, we found that the annual number of reported SJS/TEN cases associated with all antiepileptic drugs was significantly decreased by 57% (p = 0.015); SJS/TEN cases associated with CBZ and phenytoin reduced by 92% and 42% respectively. New CBZ users decreased by 31% while new levetiracetam users approximately doubled. The annual number of tests conducted increased from 444 to approximately 1,200. Regulatory recommendations for genotyping as standard of care coupled with government subsidy for the test had contributed to a reduction in CBZ SJS/TEN in Singapore by >90%, in line with that observed in other Asian countries with similar policies. Additionally, the number of phenytoin-SJS/TEN cases also declined. Taken together, this represents a successful example of precision medicine through implementation of a genotyping program to reduce a rare but serious adverse drug reaction among at-risk individuals, while preserving the availability of an effective and low-cost medicine for the broader population.

摘要

2013年4月,新加坡卫生部和健康科学局联合发布建议,将亚洲血统新患者开始服用卡马西平(CBZ)前进行基因分型作为标准治疗方案。卫生部还批准为所有在公共医疗机构享受补贴的患者提供75%的基因分型补贴。为了解这些监管决策的影响,我们研究了CBZ和左乙拉西坦的使用模式、与抗癫痫药物相关的史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症[史蒂文斯-约翰逊综合征(SJS)/中毒性表皮坏死松解症(TEN)]报告趋势以及新加坡的检测接受率。在政策实施后的5年里,我们发现与所有抗癫痫药物相关的报告SJS/TEN病例年度数量显著下降了57%(p = 0.015);与CBZ和苯妥英相关的SJS/TEN病例分别减少了92%和42%。新的CBZ使用者减少了31%,而新的左乙拉西坦使用者大约增加了一倍。每年进行的检测数量从444增加到了约1200。将基因分型作为标准治疗方案的监管建议以及政府对检测的补贴,使得新加坡CBZ相关的SJS/TEN减少了90%以上,这与其他实施类似政策的亚洲国家观察到的情况一致。此外,苯妥英-SJS/TEN病例数量也有所下降。总体而言,这代表了通过实施基因分型计划来减少高危个体中罕见但严重的药物不良反应,同时为更广泛人群保留有效且低成本药物的可及性,是精准医学成功的一个例子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b5f/7221117/4bbdaf5cc358/fphar-11-00527-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b5f/7221117/561fbf37073c/fphar-11-00527-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b5f/7221117/42aec95a5100/fphar-11-00527-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b5f/7221117/4bbdaf5cc358/fphar-11-00527-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b5f/7221117/561fbf37073c/fphar-11-00527-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b5f/7221117/42aec95a5100/fphar-11-00527-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b5f/7221117/4bbdaf5cc358/fphar-11-00527-g003.jpg

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