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논문검색

Original Article

CYP3A4 기질과 억제제 약물의 병용 고령환자에서 부정맥 부작용 연관성

원문정보

Association of Arrhythmia in the Elderly Patients on Combination Therapy of CYP3A4 Substrates and Inhibitors with the Korean Claims Data

김태우, 장준혁, 추은정, 박래웅, 이숙향

피인용수 : 0(자료제공 : 네이버학술정보)

초록

영어

Background: Arrhythmia due to QT prolongation is one of the most serious adverse events with drug interactions in the elderly. This study aimed to examine the incidence of arrhythmia in Korean elderly patients who administered both cytochrome P450 3A4 (CYP3A4) substrates and inhibitors. Methods: Patients using CYP3A4 substrate and inhibitor were selected from the 2017 elderly patient dataset (the Korean Health Insurance Review and Assessment Service - Aged Population Sample). Selection criteria were patients with a medication possession ratio over 80%, medication duration of at least 7 days, and a follow-up period of 3 months or more. The patient’s basic information is age, gender, health insurance type, and comorbidities. The top 50 drug pairs and comorbidity with high-incidence arrhythmia were presented. Results: In patien ts with drug combinations for over 7 days, there were 981 incidences of arrhythmia, and 351 incidences in those with combinations for over 30 days. The comorbidities of congestive heart failure and myocardial infarction had a significant association with incidence of arrhythmia. Among patients with 7 days or longer, the drug pairs [substrates-inhibitors] with significant adjusted odds ratio (aOR) were [propranolol-cimetidine] (aOR, 2.25; 95% confidence interval [CI], 1.66-3.04). Among patients with 30 days or longer, the drug pairs with significant aOR were [tramadolamiodarone] (aOR, 2.87; 95% CI, 1.97-4.19). Conclusions: In elderly patients, the incidence of arrhythmia was high with drug interactions of CYP3A4 substrates and inhibitors. The comorbidity of congestive heart failure was the risk factor.

목차

ABSTRACT
연구 방법
1. 자료원 및 연구대상
2. 평가변수
3. 통계분석
연구 결과
1. 병용 7일 이상 사용군
2. 병용 30일 이상 사용군
고찰
결론
감사의 말씀
이해상충
References

저자정보

  • 김태우 Tae Woo Kim. 아주대학교 약학대학
  • 장준혁 Junhyuk Chang. 아주대학교 약학대학, 아주대학교 대학원 의생명과학과
  • 추은정 Eunjung Choo. 아주대학교 대학원 바이오헬스규제과학과
  • 박래웅 Rae Woong Park. 아주대학교 대학원 의생명과학과, 아주대학교 의과대학 의료정보학과
  • 이숙향 Sukhyang Lee. 아주대학교 약학대학, 아주대학교 대학원 바이오헬스규제과학과

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