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Pragmatic randomised controlled trial of a personalised intervention for carers of people requiring home oxygen therapy

机译:针对需要家庭氧气疗法的护理人员的个性化干预的实用随机对照试验

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摘要

We used a pragmatic randomised controlled trial to evaluate a behavioural change strategy targeting carers of chronically hypoxaemic patients using long-term home oxygen therapy. Intervention group carers participated in personalised educational sessions focusing on motivating carers to take actions to assist patients. All patients received usual care. Effectiveness was measured through a composite event of patient survival to hospitalisation, residential care admission or death to 12 months. Secondary outcomes at baseline, 3, 6 and 12 months included carer and patient emotional and physical well-being. No difference between intervention ( = 100) and control ( = 97) patients was found for the composite outcome (hazard ratio (HR) 1.22, 95% confidence interval (CI) = 0.89, 1.68; = 0.22). Improved fatigue, mastery, vitality and general health occurred in intervention group patients (all values < 0.05). No benefits were seen in carer outcomes. Mortality was significantly higher in intervention patients (HR = 2.01, 95% CI = 1.00, 4.14; = 0.05; adjusted for Australia-modified Karnofsky Performance Status), with a significant diagnosis–intervention interaction ( = 0.028) showing higher mortality in patients with COPD (HR 4.26; 95% CI = 1.60, 11.35) but not those with interstitial lung disease (HR 0.83; 95% CI = 0.28, 2.46). No difference was detected in the primary outcome, but patient mortality was higher when carers had received the intervention, especially in the most disabled patients. Trials examining behavioural change interventions in severe disease should stratify for functionality, and both risks and benefits should be independently monitored. Australian New Zealand Clinical Trials Registry (ACTRN12607000177459).
机译:我们使用了一项务实的随机对照试验来评估针对使用长期家庭氧气疗法治疗慢性低氧血症患者的护理人员的行为改变策略。干预小组护理人员参加了个性化的教育会议,重点是激发护理人员采取行动协助患者。所有患者均接受常规护理。通过患者存活至住院,住院治疗或死亡至12个月的复合事件来衡量有效性。在基线,3、6和12个月时的次要结果包括护理人员和患者的情绪和身体健康。综合结果未发现干预(= 100)和对照组(= 97)患者之间的差异(危险比(HR)1.22,95%置信区间(CI)= 0.89,1.68; = 0.22)。干预组患者的疲劳,精通,活力和总体健康状况得到改善(所有值均<0.05)。护理结果未见益处。干预组患者的死亡率显着更高(HR = 2.01,95%CI = 1.00,4.14; = 0.05;针对澳大利亚修改的卡诺夫斯基绩效状态进行校正),显着的诊断-干预相互作用(= 0.028)显示,接受治疗的患者死亡率更高COPD(HR 4.26; 95%CI = 1.60,11.35),但不是间质性肺疾病的患者(HR 0.83; 95%CI = 0.28,2.46)。在主要结局方面未发现差异,但是当护理人员接受干预后,患者死亡率更高,尤其是在最残疾的患者中。检验重症患者行为改变干预措施的试验应按功能进行分层,并且应独立监控风险和收益。澳大利亚新西兰临床试验注册中心(ACTRN12607000177459)。

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