Prevalence of the risk factors for QT prolongation and associated drug-drug interactions in a cohort of medical inpatients

被引:17
作者
Khan, Qasim [1 ,2 ]
Ismail, Mohammad [1 ]
Haider, Iqbal [3 ]
Ali, Zahid [1 ]
机构
[1] Univ Peshawar, Dept Pharm, Khyber Pakhtunkhwa, Pakistan
[2] COMSATS Inst Informat Technol, Dept Pharm, Abbottabad, Pakistan
[3] Khyber Teaching Hosp, Dept Med, Peshawar, Pakistan
关键词
Medical ward; QT prolongation; QT prolonging drugs; QT prolonging drug-drug interactions; torsades de pointes;
D O I
10.1016/j.jfma.2018.01.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Purpose: Medical inpatients are at increased risk of QT interval prolongation due to multiple risk actors and QT prolonging drugs. This study aimed to identify the prevalence of risk factors for QT prolongation; QT prolonging medications; associated drug-drug interactions (QT-DDIs); their predictors; and TdP (torsades de pointes) risks of drugs. Methods: This cohort study was carried out in medical wards of two tertiary hospitals in Khyber Pakhtunkhwa, Pakistan. The QT-DDIs were identified using Micromedex DrugReax (R) and AZCERT (Arizona Center for Education and Research on Therapeutics) QT drugs lists. AZCERT QT drugs lists were used to identify TdP risks. Logistic regression analysis was performed to identify predictors of QT-DDIs. Results: Total 400 patients were included in this study. The most frequent QT prolonging risk factors included use of >= 1 QT prolonging drugs (74.5%), female gender (55%) and diabetes mellitus (36.3%). Total 487 QT prolonging drugs were identified. According to AZCERT classification, 33.8% of the interacting drugs were included in list-1 (known risk of TdP), 0.9% in list-2 (possible risk of TdP) and 58.8% in list-3 (conditional risk of TdP). The occurrence of QT-DDIs was significantly associated with >= 10 prescribed medications (p = 0.01), chronic liver disease (p = 0.05), chronic obstructive pulmonary disease (p = 0.03), gastroenteritis (p = 0.02), antimicrobials (p < 0.001), antiemetics (p < 0.001) and antinausea (p < 0.001). Conclusion: A substantial number of patients were exposed to risk factors for QT prolongation; and QT prolonging drugs such as proton pump inhibitors, antimicrobials and diuretics which may lead to serious outcomes. Copyright (c) 2018, Formosan Medical Association. Published by Elsevier Taiwan LLC.
引用
收藏
页码:109 / 115
页数:7
相关论文
共 21 条
[1]  
[Anonymous], MICR DRUG REAX
[2]   Drug-drug interactions contributing to QT prolongation in cardiac intensive care units [J].
Armahizer, Michael J. ;
Seybert, Amy L. ;
Smithburger, Pamela L. ;
Kane-Gill, Sandra L. .
JOURNAL OF CRITICAL CARE, 2013, 28 (03) :243-249
[3]   Risk factors for prolonged QTc among US adults: Third National Health and Nutrition Examination Survey [J].
Benoit, SR ;
Mendelsohn, AB ;
Nourjah, P ;
Staffa, JA ;
Graham, DJ .
EUROPEAN JOURNAL OF CARDIOVASCULAR PREVENTION & REHABILITATION, 2005, 12 (04) :363-368
[4]  
*COMM PROPR MED PR, 1997, CPMP98696 EUR AG EV
[5]  
DAY CP, 1993, LANCET, V341, P1423
[6]   Heart rate-corrected QT interval prolongation predicts risk of coronary heart disease in black and white middle-aged men and women - The ARIC study [J].
Dekker, JM ;
Crow, RS ;
Hannan, PJ ;
Schouten, EG ;
Folsom, AR .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 43 (04) :565-571
[7]  
Drew BJ, 2010, J AM COLL CARDIOL, V55, P934, DOI [10.1016/j.jacc.2010.01.001, 10.1161/CIRCULATIONAHA.109.192704]
[8]   Serious ventricular arrhythmias among users of cisapride and other QT-prolonging agents in the United States [J].
Enger, C ;
Cali, C ;
Walker, AM .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2002, 11 (06) :477-486
[9]   Multivariate analysis of risk factors for QT prolongation following subarachnoid hemorrhage [J].
Fukui, S ;
Katoh, H ;
Tsuzuki, N ;
Ishihara, S ;
Otani, N ;
Ooigawa, H ;
Toyooka, T ;
Ohnuki, A ;
Miyazawa, T ;
Nawashiro, H ;
Shima, K .
CRITICAL CARE, 2003, 7 (03) :R7-R12
[10]   Long QT syndrome: Diagnosis and management [J].
Khan, IA .
AMERICAN HEART JOURNAL, 2002, 143 (01) :7-14