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Understanding tensions and identifying clinician agreement on improvements to early-stage chronic kidney disease monitoring in primary care: a qualitative study

机译:定性研究:了解紧张状况并确定临床医生对改善早期慢性肾脏病监测的基本共识

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Objectives Since 2006, general practitioners (GPs) in England, UK, have been incentivised to keep a register and monitor patients with chronic kidney disease (CKD) stages 3–5. Despite tensions and debate around the merit of this activity, there has been little qualitative research exploring clinician perspectives on monitoring early-stage CKD in primary care. This study aimed to examine and understand a range of different healthcare professional views and experiences of identification and monitoring in primary care of early-stage CKD, in particular stage 3. Design Qualitative design using semistructured interviews. Setting National Health Service (NHS) settings across primary and secondary care in South West England, UK. Participants 25 clinicians: 16 GPs, 3 practice nurses, 4 renal consultants and 2 public health physicians. Results We identified two related overarching themes of dissonance and consonance in clinician perspectives on early-stage CKD monitoring in primary care. Clinician dissonance around clinical guidelines for CKD monitoring emanated from different interpretations of CKD and different philosophies of healthcare and moral decision-making. Clinician consonance centred on the need for greater understanding of renal decline and increasing proteinuria testing to reduce overdiagnosis and identify those patients who were at risk of progression and further morbidity and who would benefit from early intervention. Clinicians recommended adopting a holistic approach for patients with CKD representing a barometer of overall health. Conclusions The introduction of new National Institute for Health and Care Excellence (NICE) CKD guidelines in 2014, which focus the meaning and purpose of CKD monitoring by increased proteinuria testing and assessment of risk, may help to resolve some of the ethical and moral tensions clinicians expressed regarding the overmedicalisation of patients with a CKD diagnosis.
机译:目的自2006年以来,英国,英国的全科医生(GPs)受到激励,要进行登记并监测3至5期慢性肾脏病(CKD)患者。尽管围绕这项活动的价值存在紧张和争论,但很少有定性研究探索临床医生对初级保健中早期CKD监测的观点。这项研究旨在检查和理解早期CKD(尤其是第3阶段)初级保健中一系列不同的医疗保健专业人士的观点以及鉴定和监测的经验。设计使用半结构化访谈进行定性设计。在英国西南英格兰,在初级保健和二级保健中设置国家卫生服务(NHS)设置。参与者25名临床医生:16名全科医生,3名执业护士,4名肾脏顾问和2名公共卫生医生。结果我们从临床医生的角度对基层医疗早期CKD监测中确定了两个相关的总体失调和共鸣主题。临床医生对CKD监测的临床指导意见不一致,是由于对CKD的不同解释以及医疗保健和道德决策的不同哲学产生的。临床医生的共鸣集中于对肾脏下降和增加蛋白尿测试的更多了解的需要,以减少过度诊断,并确定那些有发展和进一步发病风险并将从早期干预中受益的患者。临床医生建议对代表整体健康状况的CKD患者采取整体治疗方法。结论2014年新引入的美国国立卫生研究院卓越CKD指南着重于通过增加蛋白尿测试和风险评估来监测CKD的意义和目的,这可能有助于解决临床医生的某些道德和道德压力对于CKD诊断的患者过度用药表示反对。

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