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Consultant physicians working with patients - Royal College of ...

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2 Specialties Renal medicineLocal and regional servicesClinical networksThe level <strong>of</strong> renal service provision in different hospitalsvaries considerably. Some district general hospitals(DGHs) do not have a consultant renal physician.Others have a renal physician on a sessional basis,perhaps providing support for a satellite haemodialysisunit and outpatient clinic work, <strong>with</strong> 24-hour cover forrenal problems provided by the nearest renal unit. Agrowing number <strong>of</strong> DGHs have renal units that havesufficient consultant renal <strong>physicians</strong> to provide both24-hour specialist cover for renal medicine and on-callcover for general internal medicine (GIM), but requireaccess to a tertiary centre for renal transplantation.Continuous RRT (by haem<strong>of</strong>iltration or haemodiafiltration)for the urgent management <strong>of</strong> AKI can beperformed in many intensive care units (ICUs); <strong>patients</strong>who require continuous RRT may need to betransferred to a renal unit if RRT is still needed whenintensive care is no longer required. Delay in transfer isassociated <strong>with</strong> poorer outcomes and there is increasingdemand for formal agreements between hospitals in aclinical network to ensure timely and safe transfer <strong>of</strong><strong>patients</strong> <strong>with</strong> AKI.3 Working <strong>with</strong> <strong>patients</strong>: patient-centredcareWhat you do <strong>with</strong> <strong>patients</strong>Involving <strong>patients</strong> in decisions about theirtreatmentThe diagnosis <strong>of</strong> progressive CKD will be a majorlife-changing event. The needs <strong>of</strong> <strong>patients</strong> and theirfamilies and carers should be assessed on a regular basisto ensure that appropriate support is provided so thatthey can be involved in decisions about treatment. Theconsultant renal physician is central to ensuring thatoptimum support is provided by the multipr<strong>of</strong>essionalteam and that <strong>patients</strong> have access to the knowledge andexpertise that they require. Many decisions facing<strong>patients</strong> <strong>with</strong> kidney disease are ‘preference sensitive’ –the choice depends not just on clinical outcomes butalso on the patient’s values and preferences. Elicitingthese, and ensuring that the patient ‘shares’ thedecision, rather than passively accepting a decisionmade by the healthcare team, requires specificconsultation skills. This is particularly important whenconsidering RRT for <strong>patients</strong> <strong>with</strong> end-stage kidneyfailure. Older <strong>patients</strong> <strong>with</strong> significant comorbidityother than CKD derive minimal or no survival benefitfrom dialysis: for such <strong>patients</strong>, the decision whether tostart dialysis is analogous to deciding whether to havechemotherapy to extend life in incurable cancer.Renal units provide information to <strong>patients</strong> and theircarers through direct discussions <strong>with</strong> members <strong>of</strong> themultipr<strong>of</strong>essional team – individually or in groupsessions – and through written and audiovisualmaterials. Patient decision aids are used as part <strong>of</strong> the‘shared decision-making approach’ and can be paper orweb based. Patients who feel ‘in control’ <strong>of</strong> their illnessdo better than those who feel that their illness controlsthem, so investment <strong>of</strong> effort to ‘empower’ <strong>patients</strong> payslarge dividends. Most UK renal units <strong>of</strong>fer <strong>patients</strong>access to their own test results and clinic letters usingRenal Patient View 5 – an award-winning, web-basedaccess system that so far is unique to renal medicine.Patients should be <strong>of</strong>fered opportunities for self-carewhenever possible. Peritoneal dialysis and homehaemodialysis <strong>of</strong>fer greater opportunities forindependence and self-determination, but decisionsabout treatment must take into account the impact oncarers and the patient’s home and family life.Patient choice: cultural considerationsPatients need time and expert advice to help them deal<strong>with</strong> diverse choices, which may include opting forhome-based dialysis treatment, hospital-based dialysisor pre-emptive living donor transplant or, for some,choosing not to receive dialysis or a transplant whenkidney failure supervenes and instead opting forconservative care. Such discussions can be complex andtime-consuming. The need to provide information in arange <strong>of</strong> languages appropriate to the local populationandtotakeaccount<strong>of</strong>religiousneeds–egwhenconsidering dietary advice – is widely recognised.Patient support groupsMany renal units have active kidney disease associationsthat provide local information and support. Thecontrolling council <strong>of</strong> the National Kidney Federation(NKF, www.kidney.org.uk) brings together 63 kidney<strong>patients</strong>’ associations. The NKF campaigns forimprovements to renal provision and treatment, andprovides support and information for <strong>patients</strong> throughits website, information leaflets on kidney disease andthe National Kidney Patients’ Helpline. The BritishKidney Patient Association (www.britishkidney-pa.co.uk) provides support, information and grant aidboth to individuals and to renal centres, as well assupporting research that is likely to be <strong>of</strong> direct benefitC○ <strong>Royal</strong> <strong>College</strong> <strong>of</strong> Physicians 2013 215

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