Mobile Palliative Care Consultation Service (PCCS): Overview of Hospice and Palliative Care Evaluation (HOPE) Data on In-Patients With End-Stage Cancer, Multiple Sclerosis, and Noncancer, Nonneurological Disease From 4 PCCS Centers in Germany in 2013.

Palliative Care Pub Date : 2018-07-18 eCollection Date: 2018-01-01 DOI:10.1177/1178224218785139
Birgit Basedow-Rajwich, Thomas Montag, Andreas Duckert, Christian Schulz, Gennadij Rajwich, Ingo Kleiter, Jürgen Koehler, Gabriele Lindena
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引用次数: 7

Abstract

Context: During the last decade, numerous in-patient Palliative Care Consultation Service (PCCS) units were established throughout Germany.

Objective: To provide an epidemiological overview on a whole year cohort of palliative patients in terms of demography, complaints, and therapy on admission to PCCS and the impact of PCCS treatment, and identify differences and similarities in different palliative patient subgroups.

Methods: Chi-square, analysis of variance (ANOVA), Kruskal-Wallis followed by Games-Howell analysis of HOspice and Palliative care Evaluation (HOPE 2013) data on 4 PCCS centers and in total 919 patients, with solid tumors (237), metastatic cancer (397), leukemia and lymphoma (99), neurological (109, mostly multiple sclerosis [MS]), and noncancer, nonneurological disease (NCNND, 77).

Results: A mostly uniform block of 3 cancer subgroups in terms of demographics, admission complaints, and initial pharmacological treatment diverged from the neurologic/MS disease subgroup. The "intermediate," NCNND subgroup coalesced with the cancer or the neurologic/MS subgroups in part of the demographics, complaint, and drug parameters. Tetraparesis, requirement for nursing, and help with daily living were more, and pain, dyspnea, weakness, appetite loss, and fatigue were less frequent in neurologic patients compared with the cancer subgroups. Neurologic patients also showed more common use of coanalgetics and antidepressives, less opiates and nonopiate analgetics, corticosteroids, and antiemetics and antacids. NCNND patients had a particularly high rate of disorientation (48%) and death during PCCS (39%). In the 3 cancer subgroups, dyspnea, weakness, appetite loss, and anxiolytic use were less frequent in solid tumor patients. Palliative Care Consultation Service treatment was associated with reduction in symptom severity independent of subgroup entity. All listed differences were significant at P < .05 level.

Conclusion: Despite divergence in demographics, symptoms, and medication, the data underline general usefulness of PCCS care in all end-stage patients and not only the cancer subgroups. Nevertheless, the strong differences revealed in the current study also underscore the need for a carefully tuned, disease-specific therapeutic approach to these subgroups of palliative patients.

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移动姑息治疗咨询服务(PCCS): 2013年来自德国4个PCCS中心的终末期癌症、多发性硬化症和非癌症、非神经疾病住院患者的临终关怀和姑息治疗评估(HOPE)数据概述。
背景:在过去的十年中,许多住院姑息治疗咨询服务(PCCS)单位在德国各地建立。目的:对一整年的姑息治疗患者的人口学、主诉、入院时的治疗以及姑息治疗对姑息治疗的影响进行流行病学综述,并找出不同姑息治疗患者亚组的异同。方法:卡方、方差分析(ANOVA)、Kruskal-Wallis和Games-Howell对4个PCCS中心的临终关怀和姑息治疗评估(HOPE 2013)数据进行分析,共919例患者,其中实体瘤(237例)、转移性癌(397例)、白血病和淋巴瘤(99例)、神经系统疾病(109例,多为多发性硬化症[MS])和非癌症、非神经系统疾病(NCNND, 77例)。结果:3个癌症亚组在人口统计学、入院投诉和初始药物治疗方面基本一致,与神经系统/多发性硬化症疾病亚组不同。“中间”NCNND亚组与癌症或神经系统/多发性硬化症亚组在部分人口统计学、主诉和药物参数上合并。与癌症亚组相比,神经系统患者的四肢麻痹、护理需求和日常生活帮助更多,疼痛、呼吸困难、虚弱、食欲不振和疲劳更少。神经系统患者也更常使用镇痛药和抗抑郁药,较少使用阿片类和非阿片类镇痛药、皮质类固醇、止吐药和抗酸药。NCNND患者在PCCS期间定向障碍(48%)和死亡率(39%)特别高。在3个癌症亚组中,实体瘤患者呼吸困难、虚弱、食欲不振和抗焦虑药的使用较少。姑息治疗咨询服务治疗与症状严重程度的减轻相关,独立于亚组实体。结论:尽管在人口统计学、症状和用药方面存在差异,但数据强调了PCCS治疗对所有终末期患者的普遍有用性,而不仅仅是对癌症亚组。然而,当前研究中揭示的强烈差异也强调了对这些姑息治疗患者亚组进行精心调整的疾病特异性治疗方法的必要性。
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期刊介绍: Palliative Care and Social Practice is an international, peer-reviewed, open access journal that publishes articles on all aspects of palliative care. It welcomes articles from symptom science, clinical practice, and health services research. However, its aim is also to publish cutting-edge research from the realm of social practice - from public health theory and practice, social medicine, and social work, to social sciences related to dying and its care, as well as policy, criticism, and cultural studies. We encourage reports from work with under-represented groups, community development, and studies of civic engagement in end of life issues. Furthermore, we encourage scholarly articles that challenge current thinking about dying, its current care models and practices, and current understandings of grief and bereavement. We want to showcase the next generation of palliative care innovation research and practice - in clinics and in the wider society. Relaunched in July 2019. Partnered with Public Health Palliative Care International (PHPCI) (Title 2008-2018: - Palliative Care: Research and Treatment)
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