I-CoPE: A pilot study of structured supportive care delivery to people with newly diagnosed high-grade glioma and their carers

被引:23
作者
Philip, Jennifer [1 ,2 ]
Collins, Anna [1 ]
Staker, Jane [3 ]
Murphy, Michael [3 ]
机构
[1] Univ Melbourne, Dept Med, Parkville, Vic, Australia
[2] St Vincents Hosp Melbourne, Palliat Care Serv, Melbourne, Vic, Australia
[3] St Vincents Hosp Melbourne, Dept Neurosurg, Melbourne, Vic, Australia
关键词
high-grade glioma; quality of life; supportive care; QUALITY-OF-LIFE; PALLIATIVE CARE; FUNCTIONAL ASSESSMENT; FAMILY CAREGIVER; NEEDS; VALIDATION; INTERVENTION; SATISFACTION; PREFERENCES; DISTRESS;
D O I
10.1093/nop/npy010
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background. There is limited evidence to guide best approaches to supportive care delivery to patients with highgrade glioma. I-CoPE (Information, Coordination, Preparation and Emotional) is a structured supportive care approach for people with newly diagnosed high-grade glioma and their family carers. Delivered by a cancer care coordinator, I-CoPE consists of (1) staged information, (2) regular screening for needs, (3) communication and coordination, and (4) family carer engagement. This pilot study tested acceptability and preliminary effectiveness of I-CoPE, delivered over 3 transitions in the illness course, for people newly diagnosed with high-grade glioma and their carers. Methods. I-CoPE was delivered at the identified transition times (at diagnosis, following the diagnostic hospitalization, following radiotherapy), with associated data collection (enrollment, 2 weeks, 12 weeks). Outcomes of interest included: acceptability/feasibility (primary); quality of life; needs for support; disease-related information needs; and carer preparedness to care (secondary). Descriptive statistics were used to assess acceptability outcomes, while patient and carer outcomes were assessed using repeated measures ANOVA. Results. Thirty-two patients (53% male, mean age 60) and 31 carers (42% male) participated. I-CoPE was highly acceptable: 86% of eligible patients enrolled, and of these 88% completed the study. Following I-CoPE patients and carers reported fewer information needs (P < .001), while carers reported fewer unmet supportive care needs (P < .01) and increased preparedness to care (P = .04). Quality of life did not significantly change. Conclusion. A model of supportive care delivered based upon illness transitions is feasible, acceptable, and suggests preliminary efficacy in some areas. Formal randomized studies are now required.
引用
收藏
页码:61 / 70
页数:10
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