Department of Pharmacy, University of Peshawar, Khyber Pakhtunkhwa, Pakistan; Department of Pharmacy, COMSATS Institute of Information Technology, Abbottabad, Pakistan.
Department of Pharmacy, University of Peshawar, Khyber Pakhtunkhwa, Pakistan.
J Formos Med Assoc. 2019 Jan;118(1 Pt 1):109-115. doi: 10.1016/j.jfma.2018.01.016. Epub 2018 Feb 17.
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.
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® 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.
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).
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.
背景/目的:由于多种风险因素和 QT 延长药物,住院患者存在 QT 间期延长的风险增加。本研究旨在确定 QT 延长的风险因素、QT 延长药物、相关药物-药物相互作用(QT-DDIs)及其预测因素、以及药物致尖端扭转型室性心动过速(TdP)的风险。
本队列研究在巴基斯坦开伯尔-普赫图赫瓦省的两家三级医院的内科病房进行。使用 Micromedex DrugReax®和 AZCERT(亚利桑那州治疗教育与研究中心)QT 药物清单来识别 QT-DDIs。使用 AZCERT QT 药物清单来识别 TdP 风险。采用 logistic 回归分析识别 QT-DDIs 的预测因素。
本研究共纳入 400 例患者。最常见的 QT 延长风险因素包括使用≥1 种 QT 延长药物(74.5%)、女性(55%)和糖尿病(36.3%)。共发现 487 种 QT 延长药物。根据 AZCERT 分类,相互作用药物中有 33.8%属于清单 1(已知致 TdP 风险),0.9%属于清单 2(可能致 TdP 风险),58.8%属于清单 3(致 TdP 条件风险)。QT-DDIs 的发生与服用≥10 种处方药(p=0.01)、慢性肝病(p=0.05)、慢性阻塞性肺疾病(p=0.03)、肠胃炎(p=0.02)、抗菌药物(p<0.001)、止吐药(p<0.001)和止恶心药(p<0.001)显著相关。
大量患者面临 QT 延长的风险因素以及质子泵抑制剂、抗菌药物和利尿剂等 QT 延长药物的暴露,这可能导致严重后果。