Section of Geriatrics and Palliative Medicine, University of Chicago, Chicago, Illinois 60637, USA.
J Palliat Med. 2009 Sep;12(9):779-83. doi: 10.1089/jpm.2009.0059.
Cholinesterase inhibitors and N-methyl-D-aspartic acid (NMDA) receptor antagonists are Food and Drug Administration (FDA) approved for the treatment of moderate to severe Alzheimer's disease. As dementia progresses to the end stage and patients become hospice-eligible, clinicians consider whether or not to continue these therapies without the benefit of scientific evidence. We sought to describe hospice medical directors practice patterns and experiences in the use and discontinuation of cholinesterase inhibitors and NMDA receptor antagonists in hospice patients that meet the Medicare hospice criteria for dementia.
Mail survey of hospice medical directors from a random sample from the National Hospice and Palliative Care Organization.
Of the 413 eligible participants, 152 completed surveys were returned, yielding a response rate of 37%. Of the respondents, 75% and 33% reported that at least 20% of their patients were taking a cholinesterase inhibitor or memantine, respectively, at the time of hospice admission. The majority of respondents do not consider these therapies effective in persons with end-stage dementia, however, a subset believe that these medications improved patient outcomes including stabilization of cognition (22%), decrease in challenging behaviors (28%), and maintenance of patient function (22%) as well as caregiver outcomes namely reduced caregiver burden (20%) and improved caregiver quality of life (20%). While 80% of respondents recommended discontinuing these therapies to families at the time of hospice enrollment, 72% of respondents reported that families experienced difficulty stopping these therapies. A subset of respondents observed accelerated cognitive (30%) and functional decline (26%) or emergence of challenging behaviors (32%) with medication discontinuation.
The findings from this survey indicate that cholinesterase inhibitors and/or NMDA receptor antagonists are prescribed for a subset of patients with advanced dementia and that a proportion of hospice medical directors report clinical benefit from the ongoing use of these agents. In addition, physician preferences for discontinuing these therapies are frequently at odds with the wishes of family members. Prospective studies are needed to evaluate the clinical impact of the discontinuation of these therapies on patient and caregiver outcomes.
乙酰胆碱酯酶抑制剂和 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂已获得美国食品和药物管理局(FDA)批准,用于治疗中重度阿尔茨海默病。随着痴呆症进展到终末期,患者符合医疗保险临终关怀标准,临床医生会考虑是否在缺乏科学证据的情况下继续使用这些疗法。我们旨在描述临终关怀医疗主任在符合医疗保险临终关怀标准的痴呆症患者中使用和停止乙酰胆碱酯酶抑制剂和 NMDA 受体拮抗剂的实践模式和经验。
对全国临终关怀和姑息治疗组织的随机样本中的临终关怀医疗主任进行邮件调查。
在 413 名符合条件的参与者中,有 152 名完成了调查,应答率为 37%。在回答者中,75%和 33%的人报告说,他们的患者中至少有 20%在进入临终关怀时正在服用乙酰胆碱酯酶抑制剂或美金刚,分别。大多数受访者认为这些疗法对终末期痴呆患者无效,但有一部分人认为这些药物改善了患者的预后,包括认知稳定(22%)、减少挑战性行为(28%)和维持患者功能(22%)以及照顾者的结果,即减轻照顾者的负担(20%)和提高照顾者的生活质量(20%)。虽然 80%的受访者建议在临终关怀登记时向家属推荐停止这些治疗,但 72%的受访者报告说,家属在停止这些治疗方面遇到困难。一部分受访者观察到停药后认知(30%)和功能下降(26%)或出现挑战性行为(32%)加速。
这项调查的结果表明,乙酰胆碱酯酶抑制剂和/或 NMDA 受体拮抗剂被开给了一部分晚期痴呆症患者,并且一部分临终关怀医疗主任报告说,这些药物的持续使用有临床获益。此外,医生停止这些治疗的偏好经常与家属的愿望相悖。需要前瞻性研究来评估这些治疗的停药对患者和照顾者结局的临床影响。