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在病学中实施遗传检测的护理模式
Dervla M Connaughton1, Andrew J Mallett2
1Department of Medicine, Division of Nephrology, University Hospital, London Health Sciences Centre, London, ON, Canada; Schulich School of Medicine and Dentistry, Western University, London, ON, Canada.
Seminars in nephrology
|July 16, 2025
概括
基因检测可以改善病的诊断和管理,但采用速度很慢. 本综述提出了护理模式,将遗传检测纳入常规科实践,以获得更好的患者结果.
科学领域:
- 腎臟病學 (nephrology) 是一種醫學專業.
- 遗传学 遗传学 是一个
- 医疗保健提供 医疗保健提供
背景情况:
- 基因检测为诊断和管理病提供了显著的潜力.
- 目前将其纳入常规科护理是有限的,尽管其已被证明具有临床效用和成本效益,但仍有延迟.
研究的目的:
- 检查将遗传检测纳入科实践的护理模式.
- 提出改善慢性病患者获得基因检测的策略.
主要方法:
- 审查现有和拟议的护理模式,用于遗传检测在科.
- 确定实施的基本组成部分,障碍物和促进者.
主要成果:
- 关键的方法包括加强遗传服务,建立遗传学诊所,利用虚拟咨询和组建多学科团队.
- 将基因检测纳入科护理的主流化至关重要.
结论:
- 需要实用,可扩展和以患者为中心的解决方案来改变科护理范式.
- 基因检测应该成为病管理的标准组成部分,以改善结果并促进公平的全球护理.
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