Walavalkar Anisha, Craswell Alison, Gray Nicholas A
Renal Unit, Department of Nephrology, Sunshine Coast University Hospital, Birtinya, Queensland, Australia.
University of the Sunshine Coast, Sippy Downs, Queensland, Australia.
Can J Kidney Health Dis. 2022 Apr 15;9:20543581221089080. doi: 10.1177/20543581221089080. eCollection 2022.
Older people with kidney failure often choose conservative kidney care. The experiences and quality of life (QOL) of caregivers who support them are incompletely characterized.
To determine the burden, QOL, and understand experiences of caregivers supporting patients managed conservatively.
Systematic review of quantitative and qualitative studies.
PubMed, Embase, PsycINFO, CINAHL, and MEDLINE electronic databases were systematically searched for quantitative and qualitative studies published between January 2000 and July 2020.
Caregivers of adults with kidney failure (estimated glomerular filtration rate < 15 mL/min/1.73 m) managed conservatively.
Data were extracted by 2 independent reviewers using a prespecified extraction tool. Study quality was assessed using the Critical Appraisal Skills Program (CASP) tool.
Descriptive reports of demographics, measurement scales, and outcomes. Thematic synthesis of qualitative data.
Six studies met inclusion criteria, including 3 quantitative and 3 descriptive qualitative studies. Caregivers of patients receiving conservative kidney management (CKM) experienced significant caregiver burden and similar impacts to their QOL as those caring for patients receiving dialysis. Thematic synthesis revealed 5 themes: Understanding the concept of CKM, Need for involvement in the decision for CKM, Identifying available supports, Uncertainty about the future and negotiating deteriorations and dying, and Burden of care impacting on QOL.
Low numbers of included studies, data collection and recruitment biases in qualitative studies and small caregiver numbers in quantitative studies, limit transferability of findings. Heterogeneity in study design and outcome measures precluded meta-analysis.
Caregivers of patients with conservatively managed kidney failure suffer significant burden and experience QOL comparable with those caring for patients on dialysis. Limited understanding and involvement in conservative management decision making, and a fear of deterioration and dying, result in anxiety in caregivers. Further research into the experiences of caregivers will help support both caregivers and the patients who choose conservative management.
PROSPERO registration number CRD42021209811.
老年肾衰竭患者通常选择保守的肾脏护理方式。对支持他们的照料者的经历和生活质量(QOL)的了解并不全面。
确定照料负担、生活质量,并了解支持接受保守治疗患者的照料者的经历。
对定量和定性研究的系统评价。
对PubMed、Embase、PsycINFO、CINAHL和MEDLINE电子数据库进行系统检索,以查找2000年1月至2020年7月期间发表的定量和定性研究。
接受保守治疗的成年肾衰竭患者(估计肾小球滤过率<15 mL/min/1.73 m²)的照料者。
由2名独立评审员使用预先指定的提取工具提取数据。使用批判性评估技能计划(CASP)工具评估研究质量。
人口统计学的描述性报告、测量量表和结果。定性数据的主题综合分析。
六项研究符合纳入标准,包括三项定量研究和三项描述性定性研究。接受肾脏保守治疗(CKM)患者的照料者经历了显著的照料负担,并且在生活质量方面受到的影响与照料接受透析治疗患者的照料者相似。主题综合分析揭示了五个主题:理解CKM的概念、参与CKM决策的必要性、确定可用的支持、对未来的不确定性以及应对病情恶化和死亡,以及照料负担对生活质量的影响。
纳入研究数量较少,定性研究中的数据收集和招募偏差以及定量研究中照料者数量较少,限制了研究结果的可转移性。研究设计和结果测量的异质性排除了进行荟萃分析的可能性。
接受保守治疗的肾衰竭患者的照料者承受着巨大的负担,其生活质量与照料接受透析治疗患者的照料者相当。对照护管理决策的理解和参与有限,以及对病情恶化和死亡的恐惧,导致照料者产生焦虑情绪。进一步研究照料者的经历将有助于为照料者和选择保守治疗的患者提供支持。
PROSPERO注册号CRD42021209811。