Khan Farman Ullah, Khan Amjad, Khan Faiz Ullah, Hayat Khezar, Rehman Asim Ur, Chang Jie, Khalid Waseem, Noor Sidra, Khan Asad, Fang Yu
Department of Pharmacy Administration and Clinical Pharmacy, Xi'an Jiaotong University, Xi'an, China.
Center for Drug Safety and Policy Research, Xi'an Jiaotong University, Xi'an, China.
Front Pharmacol. 2022 May 17;13:876955. doi: 10.3389/fphar.2022.876955. eCollection 2022.
Multidrug-resistant tuberculosis (MDR-TB) is a growing public health problem. Treatment regimens used against MDR-TB are costly, prolonged, and associated with more side effects as compared with the drug-susceptible tuberculosis. This study was framed to determine the incidence of adverse drug events, risk factors, and their management in MDR-TB patients. This prospective follow-up cohort study was conducted at the site of programmatic management of drug-resistant TB located at the Pakistan Institute of Medical Sciences, Islamabad. All patients, irrespective of their age, gender, and ethnicity, were included in the study. Adverse drug events were observed in patients at different time points during the study. Patients enrolled for the treatment from January 2018 were prospectively followed till December 2020 up to their end treatment outcomes. Out of 126 MDR-TB patients enrolled for treatment, 116 met the inclusion criteria and were included in the final analysis. Most patients (50.9%) were between 18 and 45 years of age. A minimum of one adverse event was experienced by (50.9%) patients. Of all the adverse events, gastrointestinal disorders were more frequent (47.4%), followed by arthralgia (28.4%) and psychiatric disturbance (20.6%). Furthermore, multivariate analysis showed a significant association with the incidence of adverse events in patients with age group above 60 years (odds ratio (OR) 4.50; 95% CI 1.05-19.2), active smokers (OR 4.20; 95% CI 1.31-13.4), delayed reporting to the TB center (OR 4.03; 95% CI 1.34-12.1), and treatment without bedaquiline regime (OR 3.54; 95% CI 1.23-10.1). Most of the patients (94.6%), counseled by the pharmacist, were found to be satisfied with the information provided and looked for more pharmacist counseling opportunities in the management of MDR-TB. Current findings recommend that ADEs might be well managed by timely identification and reporting. Bedaquiline coupled with other active medications lowered the chance of ADEs in MDR-TB patients. Elderly patients, active smoking behavior, and those who have a delay in the treatment initiation are more prone to ADEs. Clinical pharmacist's contribution to TB control programs may help caregivers and patients concerning the rational use of medication, early detection, and management of ADEs.
耐多药结核病(MDR-TB)是一个日益严重的公共卫生问题。与药物敏感型结核病相比,用于治疗耐多药结核病的治疗方案成本高、疗程长且副作用更多。本研究旨在确定耐多药结核病患者药物不良事件的发生率、危险因素及其管理方法。这项前瞻性随访队列研究在位于伊斯兰堡的巴基斯坦医学科学研究所的耐药结核病规划管理地点进行。所有患者,无论年龄、性别和种族,均纳入研究。在研究期间的不同时间点观察患者的药物不良事件。2018年1月开始治疗的患者前瞻性随访至2020年12月,直至其最终治疗结局。在126名登记接受治疗的耐多药结核病患者中,116名符合纳入标准并纳入最终分析。大多数患者(50.9%)年龄在18至45岁之间。(50.9%)的患者至少经历了一次不良事件。在所有不良事件中,胃肠道疾病更为常见(47.4%),其次是关节痛(28.4%)和精神障碍(20.6%)。此外,多变量分析显示,60岁以上年龄组患者(优势比(OR)4.50;95%置信区间1.05-19.2)、现吸烟者(OR 4.20;95%置信区间1.31-13.4)、延迟向结核病中心报告(OR 4.03;95%置信区间1.34-12.1)以及未采用含贝达喹啉方案治疗(OR 3.54;95%置信区间1.23-10.1)与不良事件的发生率显著相关。在接受药剂师咨询的患者中,大多数(94.6%)对所提供的信息感到满意,并希望在耐多药结核病管理中有更多接受药剂师咨询的机会。目前的研究结果表明,通过及时识别和报告,药物不良事件可能得到很好的管理。贝达喹啉与其他有效药物联用可降低耐多药结核病患者发生药物不良事件的几率。老年患者、现吸烟行为以及治疗开始延迟的患者更容易发生药物不良事件。临床药剂师对结核病控制项目的贡献可能有助于护理人员和患者合理用药、早期发现和管理药物不良事件。