Informed consent, dementia and oral health care provision.

Graeme Ting
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Abstract

Managing patients with dementia requires a practitioner to exercise diverse skills. Communicating with the patient (as their dementia allows), relatives, caregivers and medical personnel are essential elements in the care process. Diagnosis of oral health problems may not be straightforward, clinical examination and treatment planning may be hampered by poor cooperation from the person with dementia. Practitioners must view any treatment from the patient's perspective and balance this with the requirements for sound clinical care. The consent process must be approached in a manner that fulfils the ethical responsibilities that acknowledge patient rights. This can be difficult when managing a patient with dementia. This paper will explore issues surrounding the consent process and the provision of oral health care to people suffering from dementia. It is hoped that readers will be stimulated to review their practice; especially related to informed consent, whether they routinely manage patients with dementia or not. Such practice evaluation should consider the wants and needs of patients and families on a broader than clinical basis and thus enhance the care that is brought to this group of interesting and often challenging patients.

知情同意、痴呆和口腔保健提供。
管理痴呆症患者需要从业人员锻炼多种技能。与患者(在痴呆症允许的情况下)、亲属、照顾者和医务人员进行沟通是护理过程中的基本要素。口腔健康问题的诊断可能并不直截了当,临床检查和治疗计划可能因痴呆症患者的不配合而受到阻碍。从业人员必须从患者的角度看待任何治疗,并将其与良好的临床护理要求相平衡。同意过程必须以履行承认患者权利的伦理责任的方式进行。在管理痴呆症患者时,这可能很困难。本文将探讨的问题周围的同意过程和提供口腔保健的人患有痴呆症。希望读者能被激励去回顾他们的实践;尤其是在知情同意方面,无论他们是否对痴呆症患者进行常规管理。这种实践评估应该考虑患者和家属的需求,而不是临床基础,从而提高对这群有趣且经常具有挑战性的患者的护理。
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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