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临床试验/NCT01584765
NCT01584765已完成不适用

Rechallenge Analysis: Detection of Potential Drug-Induced Liver Injury Using Kaiser California Database

GlaxoSmithKline0 个研究点目标入组 1 人开始时间: 2012年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
1
主要终点
Liver injury rechallenge

研究概览

简要总结

Drug re-administration or rechallenge should be avoided after drug-induced liver injury (DILI) to avoid recurrent and fatal injury. Rechallenge outcomes vary considerably by drug and patient subjects. In order to better predict these outcomes, the objective of this analysis is to assess clinical outcomes of positive drug rechallenge following possible drug-induced liver injury. Electronic medical records from Kaiser Permanente California (KPSC), a managed care organization, will be utilized to identify patients who experience possible drug-induced liver injury following exposure to medications associated with hepatotoxicity, and who are then rechallenged with the medication.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who received at least one prescription for a suspect drug between Jan 1, 2003 and June 30, 2009 (drug initiation period)
  • Patients who experienced incident DILI event (identified by ALT ≥3xULN or AP ≥2xULN within 6 months of suspect drug administration) during the first exposure period that:
  • Resolved to within normal limits of ALT (for hepatocellular & mixed) or AP (for cholestatic) within 180 days or
  • Resolved to ALT < 3xULN (for hepatocellular & mixed) within 90 days or AP<2xULN (for cholestatic) within 180 days or
  • Dropped by ≥50% of (Peak ALT - ULN) for hepatocellular or of (Peak AP - ULN) for cholestatic or mixed within 180 days
  • Patients who were rechallenged with the same suspect drug; rechallenge will include first rechallenge event for the analysis.
  • Patients who had at least of 12 months of continuous membership and drug benefit prior to and on the dispensing index date (inclusive). There is no minimum restriction of continuous membership plus drug benefit after the start date.
  • Patients who were 18 years of age or older at the time of the first drug dispensing (index date) during the drug initiation period Jan 1, 2003 and June 30,
  • Each patient's first prescription for the study drugs during the drug initiation period will be identified as index prescription.
  • Patients who had health insurance coverage with full medical, pharmacy and lab benefits at the index date.

排除标准

  • Patients meeting the definition of chronic liver injury and exhibiting persistent ALT≥3xULN or AP or bilirubin ≥2xULN within 90 days after initial injury
  • Patients with chronic liver injury diagnostic codes or included in KPSC disease registries preceding the initial or rechallenge liver injury

研究组 & 干预措施

Rechallenge

positive, negative, indeterminate and intermediate rechallenge subtypes

干预措施: Prescription drugs with known hepatotoxicity (Drug)

Severe positive rechallenge

Subtype of positive rechallenge is defined as: ALT≥5 xULN or AP ≥2 xULN and bilirubin ≥2 xULN with one of the following: INR ≥1.5, Ascites, or Encephalopathy where time from liver chemistry elevation to INR≥1.5,ascites, or encephalopathy is less than 26 weeks in the absence of underlying cirrhosis; other organ failure considered due to DILI; liver-related hospitalization

干预措施: Prescription drugs with known hepatotoxicity (Drug)

结局指标

主要结局

Liver injury rechallenge

时间窗: Up to seven and a half years

Liver injury in relation to rechallenge types (positive, negative, indeterminate and intermediate) for hepatocellular, cholestatic and mixed DILI, respectively, defined according to Danan \& Benichou, 1993, J Clin Epidemiol, 46(11): p. 1323-30.

次要结局

  • Severe positive rechallenge(Up to seven and a half years)

研究者

申办方类型
Industry
责任方
Sponsor

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