医疗保健提供者在瘤学中的药物监测实践:一个跨部门研究
Hadeel Alkofide1,2, Haya M Almalag1, Mashael Alromaih1
1Department of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh 1145111, Saudi Arabia.
Pharmaceuticals (Basel, Switzerland)
|June 27, 2024
概括
瘤医疗保健提供者 (HCP) 之间的药物监督 (PV) 实践显示,对药物不良反应 (ADR) 的认识和报告存在差距. 加强光伏教育和简化ADR报告对于癌症护理中的患者安全至关重要.
科学领域:
- 在瘤学瘤学.
- 药物监督 药物监督 药物监督
- 患者安全 患者安全
背景情况:
- 药物监督 (PV) 对瘤学中的患者安全至关重要.
- 了解医疗保健提供者 (HCP) 关于PV的认识,态度和做法是必不可少的.
研究的目的:
- 评估瘤医疗人员的PV意识,态度和实践.
- 在瘤学环境中识别有效报告药物不良反应 (ADR) 的障碍.
主要方法:
- 横截面调查设计. 横截面调查设计.
- 从65名瘤医疗人员收集的关于ADR报告经验,教育和PV协议熟悉度的数据.
主要成果:
- 大约58.9%的医疗人员在内部报告了ADR; 76.9%接受了ADR教育.
- 对于正式的ADR审查程序的认识很低 (38.5%).
- 甲索和帕克利塔克塞尔经常与ADR相关;治疗复杂性是报告障碍.
结论:
- 需要加强光伏教育和标准化报告机制,以改善瘤学护理.
- 加强光伏培训和简化ADR报告流程对于患者安全和结果至关重要.
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