Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
University of Toronto, Toronto, Ontario, Canada.
J Clin Oncol. 2020 Mar 20;38(9):926-936. doi: 10.1200/JCO.19.00018. Epub 2020 Feb 5.
Family caregivers provide substantial care for patients with advanced cancer, while suffering from hidden morbidity and unmet needs. The objectives of this review were to examine risk factors associated with caregiving for patients with advanced cancer, evaluate the evidence for pertinent interventions, and provide a practical framework for palliative care of caregivers in oncology settings. We reviewed studies examining the association of factors at the level of the caregiver, patient, caregiver-patient relationship, and caregiving itself, with adverse outcomes. In addition, we reviewed randomized controlled trials of interventions targeting the caregiver, the caregiver-patient dyad, or the patient and their family. Risk factors for adverse mental health outcomes included those related to the patient's declining status, symptom distress, and poor prognostic understanding; risk factors for adverse bereavement outcomes included unfavorable circumstances of the patient's death. Among the 16 randomized trials, the most promising results showed improvement of depression resulting from early palliative care interventions; results for quality of life were generally nonsignificant or showed an effect only on some subscales. Caregiving outcomes included burden, appraisal, and competence, among others, and showed mixed findings. Only three trials measured bereavement outcomes, with mostly nonsignificant results. On the basis of existent literature and our clinical experience, we propose the CARES framework to guide care for caregivers in oncology settings: Considering caregivers as part of the unit of care, Assessing the caregiver's situation and needs, Referring to appropriate services and resources, Educating about practical aspects of caregiving, and Supporting caregivers through bereavement. Additional trials are needed that are powered specifically for caregiver outcomes, use measures validated for advanced cancer caregivers, and test real-world interventions.
家庭照顾者为晚期癌症患者提供大量的照顾,但自身却承受着隐性疾病和未满足需求的痛苦。本综述的目的是检查与照顾晚期癌症患者相关的风险因素,评估相关干预措施的证据,并为肿瘤学环境中照顾者的姑息治疗提供一个实用框架。我们回顾了研究,这些研究检查了照顾者、患者、照顾者-患者关系以及照顾本身的水平上的因素与不良结局之间的关联。此外,我们还回顾了针对照顾者、照顾者-患者二人组或患者及其家庭的干预措施的随机对照试验。心理健康不良结局的风险因素包括与患者病情恶化、症状困扰和预后理解不佳相关的因素;不良丧亲结局的风险因素包括患者死亡的不利情况。在 16 项随机试验中,最有希望的结果显示,早期姑息治疗干预可改善抑郁症状;生活质量的结果通常不显著,或者仅在某些子量表上显示出效果。照顾者的结局包括负担、评估和能力等,结果参差不齐。只有三项试验测量了丧亲结局,结果大多不显著。基于现有文献和我们的临床经验,我们提出 CARES 框架来指导肿瘤学环境中的照顾者护理:将照顾者视为护理单元的一部分,评估照顾者的情况和需求,转介给适当的服务和资源,教育照顾者实际护理方面的知识,并通过丧亲之痛支持照顾者。需要更多的试验,这些试验专门针对照顾者的结局,使用针对晚期癌症照顾者验证的措施,并测试实际的干预措施。