...
首页> 外文期刊>International Journal of Basic & Clinical Pharmacology >A prospective observational pharmacovigilance study of adverse drug reaction monitoring in patients of MDR-TB at tertiary care hospital
【24h】

A prospective observational pharmacovigilance study of adverse drug reaction monitoring in patients of MDR-TB at tertiary care hospital

机译:三级医院耐多药结核病患者药物不良反应监测的前瞻性观察药物警戒性研究

获取原文
           

摘要

Background: The emergence of drug resistant mycobacteria has become a significant public health problem world over creating an obstacle to effective TB control. ADRs are common in patients of MDR-TB on DOTs-Plus drug regimen. Present study was carried out in tertiary care hospital. Identification of types and frequency of adverse drug reactions in Intensive and continuation phase of MDR-TB Patients. Methods: It was a prospective observational study conducted in Department of TB- Chest and Medicine, Govt. Medical College, Aurangabad, Maharashtra, India. All the MDR-TB patients admitted at the directly observed treatment, short course plus (DOTS plus) Center at Medical College Hospital were enrolled and were monitored for ADRs. The causality and severity of the reactions were determined using Naranjo algorithm and Hartwig questionnaire, respectively. Results: A total of 121 tuberculosis patients of MDR-TB on DOTS therapy were enrolled for the study. Out of 121 patients, 13 were dropouts, 6 died, 7 defaulted so 108 patients assessed for ADRs, 48 patients developed 61 (56.48%) adverse drug reactions. The higher numbers of ADRs were observed in age group 31-40yrs followed by 21-30yrs which were more common in men. Majority of adverse drug reactions were Gastrointestinal (GI) problems 32 (52.45%), followed by Ototoxicity 7 (11.48%) and Psychiatric Manifestations 6 (9.84%) and skin problems 3 (4.92%). On evaluation of the causality of ADRs, majority were found to be Possible (59.02%). The severity assessment showed that most of the patients ADRs were of moderate level (50.82%).Some patients required treatment withdrawal and replacement with other drug and most of the patients were managed with supportive medication without removing anti-tubercular drug from their treatment regimen. Conclusions: ADRs are major factor limiting completion of drug therapy under RNTCP and occurrence of drug resistance which requires attention of all health care professionals.
机译:背景:耐药性分枝杆菌的出现已经成为一个严重的公共卫生问题,已经成为有效控制结核病的障碍。在DOTs-Plus药物治疗方案中,MDR-TB患者常见ADR。目前的研究是在三级医院进行的。识别耐多药结核病患者密集和持续阶段药物不良反应的类型和频率。方法:这是一项在政府结核病与胸腔内科进行的前瞻性观察研究。印度马哈拉施特拉邦奥兰加巴德医学院。登记了所有在直接观察到的治疗,Medical College Hospital的短疗期加(DOTS加)中心接受治疗的耐多药结核病患者,并进行了ADR监测。分别使用Naranjo算法和Hartwig调查表确定反应的因果关系和严重程度。结果:共纳入121名接受DOTS治疗的耐多药结核病患者。在121例患者中,有13例辍学,6例死亡,7例违约,因此对108名患者进行了ADR评估,其中48例发生了61例(56.48%)药物不良反应。在31-40岁年龄组中观察到较高的ADR数量,其后在男性中更为常见的是21-30岁。药物不良反应的大多数是胃肠道(GI)问题32(52.45%),其次是耳毒性7(11.48%)和精神病表现6(9.84%)和皮肤问题3(4.92%)。在评估ADR的因果关系时,发现多数是可行的(59.02%)。严重程度评估表明,大多数患者的ADR处于中等水平(50.82%)。一些患者需要停药并用其他药物替代,并且大多数患者在不从治疗方案中去除抗结核药的情况下接受了支持药物治疗。结论:ADR是限制RNTCP下药物治疗的完成和耐药性发生的主要因素,这需要所有医疗保健专业人员的注意。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号