在南非各地的耐药结核病设施中,不良事件报告实践
Razia Gaida1,2, Adlai S Davids1,3, Ronel Sewpaul4
1Department of Public Health, Societies and Belonging, Human Sciences Research Council, Pretoria, South Africa.
Southern African journal of infectious diseases
|January 15, 2024
概括
改善南非耐药结核病 (DR-TB) 药物不良反应 (ADR) 报告需要标准化表格和持续培训. 赋予更多的医疗保健工作人员报告不良反应对于更好的药物监测至关重要.
科学领域:
- 药物监督 药物监督 药物监督
- 传染性疾病 传染性疾病
- 公共卫生 公共卫生
背景情况:
- 药物不良反应 (ADR) 报告对于耐药结核病 (DR-TB) 药物监测至关重要,特别是在像南非这样的高负担国家.
- 耐药结核病治疗方案是动态的,需要清楚地了解专业治疗中心的不良事件报告实践.
研究的目的:
- 调查南非DR-TB治疗设施当前的药物不良反应 (ADR) 报告实践.
主要方法:
- 定性研究涉及专业DR-TB设施的医疗保健工作人员的采访.
- 数据收集的重点是人口统计,药物监督培训以及关于不良事件报告的态度/做法.
- 使用一个检查清单来审查记录的不良事件报告表格的完整性和标准化.
主要成果:
- 在正在进行的不良事件报告培训中发现了重大差距,尽管参与者对填写表格表示信心.
- 医疗保健工作者表现出对DR-TB药物主要不良事件的良好了解,但一些错误识别了非不良事件.
- 报告不良事件表格缺乏标准化,参与者表示需要进一步培训和定期反来加强报告.
结论:
- 标准化不良事件报告表格和实施定期报告机制对于改善DR-TB设施的ADR报告率至关重要.
- 持续培训,员工赋权和扩大有资格报告ADR的医疗保健专业人员类别将加强和维持报告实践.
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