An observational study of adverse drug reactions in hospitalized patients of drug resistance tuberculosis taking PMDT therapy in a tertiary care hospital

P. Naik, A. Pandey, Swati Patel
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Abstract

Background: Drug resistant tuberculosis is an important public health issue in India. The treatment regimen followed is Programmatic Management of Drug resistant Tuberculosis (PMDT) approach. Adverse drug reactions (ADRs) are a serious issue which increases the risk of defaulter rate if poorly managed. Thus study was undertaken to assess the ADRs caused by PMDT therapy in indoor patients of Department of Respiratory Medicine in a tertiary care hospital at Surat.Methods: The prospective and observational study was carried out for one year period. The causality was determined by World Health Organization (WHO) Uppasala Monitoring Centre (UMC) scale and severity was determined by Modified Hartwig and Siegel scale. Fisher exact test was applied for statistical analysis.Results: Among 24 drug resistant tuberculosis patients, 12 (50%) patients developed ADRs due to second line antitubercular drugs. Occurrence of ADRs was more among Category V (100%) as compared to Category IV (36.8%). Occurrence of ADRs was more among females (60%). The commonly involved systems are auditory system (33.3%). Majority of ADRs developed within 61-90 days (66.7%) of initiation of drug therapy. Highest percentage of ADRs causing drugs was pyrazinamide (27.8%). On evaluation of the causality of ADRs, majority were found to be possible (53.3%). The severity assessment showed that most of the patients ADRs were of moderate level (73.3%).Conclusions: PMDT therapy is complicated but early management and reporting of ADRs decreases default rate.
某三级医院耐药结核病住院患者接受PMDT治疗的药物不良反应观察研究
背景:耐药结核病是印度一个重要的公共卫生问题。治疗方案采用耐药结核病规划管理(PMDT)方法。药物不良反应(adr)是一个严重的问题,如果管理不善,会增加违约率的风险。因此,我们对苏拉特某三级医院呼吸内科室内患者进行PMDT治疗引起的不良反应进行了研究。方法:采用前瞻性观察研究,为期1年。因果关系采用世界卫生组织(WHO)乌帕萨拉监测中心(UMC)量表确定,严重程度采用改良Hartwig和Siegel量表确定。采用Fisher精确检验进行统计分析。结果:24例耐药结核患者中,有12例(50%)因二线抗结核药物发生不良反应。第ⅴ类患者adr发生率(100%)高于第ⅳ类患者(36.8%)。不良反应发生率以女性居多(60%)。常见的受累系统为听觉系统(33.3%)。大多数不良反应发生在药物治疗开始后61 ~ 90天(66.7%)。引起不良反应的药物比例最高的是吡嗪酰胺(27.8%)。在评价adr的因果关系时,发现大多数是可能的(53.3%)。严重程度评估显示,大多数患者的不良反应为中度(73.3%)。结论:PMDT治疗复杂,但早期处理和报告不良反应可降低违约率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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