The clinical research unit: a nurse-led unit for patients undergoing early anti-cancer drug trials

MSc, RGN Catherine Cameron (Clinical Nurse Specialist)
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Abstract

Patients participating in phase I and II trials are often treated in busy oncology wards and clinics where it is difficult to monitor them closely and to give them the amount and quality of care that they need. This paper describes the Clinical Research Unit (CRU) which was established to improve patient care and to achieve optimal data collection for such trials. Areas discussed include the structure and layout of the CRU, the staff involved, general functioning of the unit and future development plans. The benefits and potential problems of a nurse-led designated area for phase I and II trial patients are also discussed and it is suggested that the benefits far outweigh the potential problems, most of which can be overcome. It is concluded that the CRU is an optimal environment to treat patients participating in phase I and II trials.

临床研究单位:由护士领导的针对早期抗癌药物试验患者的单位
参加I期和II期试验的患者通常在繁忙的肿瘤病房和诊所接受治疗,很难对他们进行密切监测,也很难向他们提供所需护理的数量和质量。本文描述了临床研究单位(CRU),其建立是为了改善病人的护理和实现这类试验的最佳数据收集。讨论的领域包括CRU的结构和布局、所涉及的工作人员、该单位的一般功能和未来发展计划。本文还讨论了为I期和II期试验患者设立由护士领导的指定区域的好处和潜在问题,认为好处远大于潜在问题,其中大部分问题是可以克服的。因此,CRU是治疗I期和II期临床试验患者的最佳环境。
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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