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Individualised patient care as an adjunct to standard care for promoting adherence to ocular hypotensive therapy: An exploratory randomised controlled trial

机译:个性化患者护理作为标准护理的辅助措施,以促进对眼压治疗的依从性:一项探索性随机对照试验

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Purpose: To evaluate the impact of individualised patient care, as an adjunct to standard care, on adherence to ocular hypotensive therapy. Methods: A two-arm, single-masked exploratory randomised controlled trial recruited patients newly prescribed ocular hypotensive therapy. The intervention involved an individual assessment of health-care needs and beliefs and a 1-year follow-up period according to need. The primary outcome was refill adherence, measured by collating prescription and dispensing data for 12 months. Secondary outcomes included self-reported adherence, glaucoma knowledge, beliefs about illness and medicines, quality of care, intraocular pressure (IOP) fluctuation, and changes in clinical management assessed at 12 months. The strength of the intervention was measured following withdrawal by reviewing clinical outcomes for a further 12 months. Results: In all, 127 patients were recruited (91% response rate). Intervention-arm patients collected significantly more prescriptions than control-arm patients. Self-report adherence was significantly better in the intervention-arm for patients who forgot drops and those who intentionally missed drops. The intervention group demonstrated significantly more glaucoma knowledge, expressed a significantly stronger belief in the necessity of eye drops and believed that they had more personal control over managing their condition. Control-arm patients had more IOP fluctuation and changes in clinical management. However, this finding only reached significance at 24 months. Conclusion: Modelling patient care according to health-care needs and beliefs about illness and medicines can have a significant impact on improving adherence to therapy for this patient group, with the potential benefit of improving clinical outcomes.
机译:目的:评估作为标准护理的辅助措施的个性化患者护理对坚持降压治疗的影响。方法:一项两臂,单掩盖探索性随机对照试验,招募了新开了眼压治疗的患者。干预措施包括对医疗保健需求和信念的个人评估,并根据需要进行为期1年的随访。主要结果是笔芯依从性,通过整理处方和分配12个月的数据进行测量。次要结局包括自我报告的依从性,青光眼知识,对疾病和药物的信念,护理质量,眼压(IOP)波动以及在12个月时评估的临床管理变化。停药后通过回顾12个月的临床结果来测量干预的强度。结果:总共招募了127例患者(有效率91%)。干预组患者比对照组有更多的处方。对于遗忘掉药和故意遗漏的患者,干预组的自我报告依从性明显更好。干预组显示出更多的青光眼知识,对滴眼剂的必要性表示出更强烈的信念,并相信他们对自己的病情控制有更多的个人控制权。对照组患者的眼压波动更大,临床管理发生变化。但是,这一发现仅在24个月时才有意义。结论:根据医疗保健需求以及对疾病和药物的信念对病人的护理进行建模,可以大大改善该患者对治疗的依从性,并具有改善临床疗效的潜在益处。

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