在患有晚期肾脏病的老年人或成年人及其护理人员中开展姑息治疗干预的可行性和可接受性。

IF 3.2 Q1 UROLOGY & NEPHROLOGY
Kidney360 Pub Date : 2024-10-24 DOI:10.34067/KID.0000000622
Fahad Saeed, Robert K Horowitz, Rebecca J Allen, Peggy Auinger, Ronald M Epstein, Kevin A Fiscella, Peter J Veazie, Paul R Duberstein
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引用次数: 0

摘要

背景:在非肾内科环境中,专业姑息治疗(PC)可改善决策、患者的生活质量(QoL)、预先护理计划(ACP)以及生命末期(EoL)护理质量的某些指标。这项试验性 RCT 探讨了针对 eGFR ≤25 毫升/分钟、年龄≥75 岁的老年人及其护理人员的 PC 干预(CKD-EDU)的可行性和可接受性:方法: 被随机分配到对照组的患者接受标准肾脏病学护理和常规肾脏治疗(KT)教育,而被随机分配到 CKD-EDU 组的患者则接受决策辅助工具,并与 PC 临床医生会面最多三次,讨论 KT 决策和 EoL 规划。患者分别在基线、4-6 周、12-14 周和 24-26 周接受评估。主要结果包括干预的可行性和可接受性、决策冲突和患者生活质量。研究还探讨了减少决策冲突对改善 QOL 的中介效应,以及 CKD-EDU 对 ACP、EoL 治疗强度和 6 个月住院的影响。统计分析包括描述性分析、调整后的重复测量模型、中介分析和逻辑回归模型:在筛选出的 127 名符合条件的患者中,有 58 人(44%)同意接受治疗:30 人被随机分配到 CKD-EUD 治疗组,28 人被分配到对照组。所有患者都完成了基线评估,89%的患者至少完成了一次干预治疗(26/29),这表明干预治疗的依从性和可行性。同样,4 周(83%,n=45/54)、12 周(93%,n=42/45)和 24 周(95%,n=40/42)的评估完成率也很高。所有问题的可接受性评分均超过 85%。接受CKD-EDU治疗的患者在4-6周时决策冲突量表评分有显著改善(P=0.003),在24-26周时生活质量有显著改善(P=0.02)。本试验的探索性分析在统计学上并不显著,但所有效应大小都在预测的方向上:这项研究证明了 CKD-EDU 的可行性和可接受性。结论:这项研究证明了 CKD-EDU 的可行性和可接受性,有必要进行更大规模的试验,以评估其在改善对患者和家属非常重要的关键结果方面的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Feasibility and Acceptability of a Palliative Care Intervention Among Older or Adults with Advanced CKD and their Caregivers.

Background: In non-nephrology settings, specialty Palliative Care (PC) improves decision-making, patient's quality of life (QoL), advance care planning (ACP), and certain indicators of the quality of end-of-life (EoL) care. This pilot RCT explored the feasibility and acceptability of a PC intervention, CKD-EDU, for older adults ≥75 years with eGFR ≤25 ml/min and their caregivers.

Methods: Participants randomized to the control group received standard nephrology care and routine kidney therapy (KT) education, while those randomized to CKD-EDU received a decision aid and met with a PC clinician up to three times to discuss KT decisions and EoL planning. Patients were assessed at baseline, 4-6, 12-14, and 24-26 weeks. Main outcomes included intervention feasibility and acceptability, decision-conflict, and patient QoL. The mediating effects of reduced decision conflict on improved QOL were explored, as were the effects of CKD-EDU on ACP, EoL treatment intensity and 6-month-hospitalization. Statistical analyses encompassed descriptive analyses, adjusted repeated-measure-models, mediation analyses and logistic-regression models.

Results: Among the 127 eligible patients screened, 58 (44%) consented: 30 were randomized to CKD-EUD and 28 to the control arm. All patients completed baseline assessments, and 89% completed at least one intervention session (n=26/29), underscoring intervention adherence and feasibility. Similarly, assessments completion rates at 4 (83%, n=45/54) ), 12 (93%, n=42/45), and 24 (95%, n=40/42) weeks were high. The intervention received over 85% acceptability ratings for all questions. Patients exposed to CKD-EDU exhibited significant improvement in decisional conflict scale scores (P = 0.003) at 4-6 weeks and improvements in QoL at 24-26 weeks (P=0.02). Exploratory analyses were not statistically significant in this pilot, but all effect sizes were in the predicted direction.

Conclusion: This study demonstrates the feasibility and acceptability of CKD-EDU. A larger scale trial is warranted to assess its effectiveness in improving key outcomes important to patients and families.

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来源期刊
Kidney360
Kidney360 UROLOGY & NEPHROLOGY-
CiteScore
3.90
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