Next Article in Journal
Family History of Sudden Cardiac Death of the Young: Prevalence and Associated Factors
Next Article in Special Issue
Spirituality in Renal Supportive Care: A Thematic Review
Previous Article in Journal / Special Issue
Home Palliative Care for Patients with Advanced Chronic Kidney Disease: Preliminary Results
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Ageing Renal Patients: We Need More Collaboration between Geriatric Services and Nephrology Departments

Centre for Nephrology, Royal Free Hospitals NHS Foundation Trust, Pond Street, London NW3 2QG, UK
*
Author to whom correspondence should be addressed.
Healthcare 2015, 3(4), 1075-1085; https://doi.org/10.3390/healthcare3041075
Submission received: 6 September 2015 / Revised: 21 October 2015 / Accepted: 21 October 2015 / Published: 30 October 2015
(This article belongs to the Special Issue Supportive and Palliative Care in Renal Disease)

Abstract

:
There has been a significant increase in the number of frail older patients diagnosed with advanced chronic kidney disease (CKD) over the past thirty years. These elderly patients have high levels of comorbidity, and as a consequence the face of renal medicine is changing—There is an increasing need to focus on traditionally geriatric areas of expertise such as falls prevention and rehabilitation, and to shift our emphasis onto improving patient well-being rather than longevity. Over the past decade, many nephrologists have found that they are already acting as de facto “amateur geriatricians”. This denies patients both the benefits of specialist geriatric assessment, and equally importantly denies them access to the wider geriatric multidisciplinary team. This article describes the prevalence and underlying causes of the so-called “Geriatric Giants” in patients with advanced CKD, and discusses possible improvements in care that closer working with geriatricians could bring.

1. Introduction

There has been a significant expansion in the number of frail older patients diagnosed with advanced chronic kidney disease (CKD) over the past thirty years [1]. Indeed, the burden of CKD disproportionately affects older patients. Despite this, most older patients die with CKD (due to other comorbidities), not from it [2,3,4,5,6]. These elderly patients have high levels of comorbidity, and as a consequence the face of renal medicine is changing—There is an increasing need to focus on traditionally geriatric areas of expertise such as falls prevention and rehabilitation, and shift our emphasis onto improving patient well-being rather than longevity.
In the past, initiatives aimed at improving links between renal medicine and geriatric medicine have been unable to generate sustained enthusiasm [7]. Although nephrologists have long understood the benefits of multidisciplinary working (and are used to working alongside renal dietitians and psychologists) they have been slower to appreciate the expertise that geriatricians, physiotherapists and occupational therapists can provide. This is partly due to cultural barriers and “silo-isation” that exists between hospital departments. As a smaller specialty, most nephrology departments are based in tertiary hospitals and in these large organisations consultants from different specialties may barely know each other, much less understand the skills and services that each has to offer. This lack of knowledge works both ways—Geriatricians are often surprised to discover the breadth of case-mix managed by nephrologists, and the high levels of comorbidity and functional impairment found in our inpatients.
However over the past decade, many nephrologists have realised that they are already acting as de facto “amateur geriatricians” [7], and there has been a push to improve renal training in this area. The American Accreditation Council for Graduate Medical Education (ACGME) now includes mandatory geriatric nephrology training as part of nephrology fellowship programmes, the American Society of Nephrology and UK Renal Association and British Renal Society regularly include geriatric nephrology streams in their annual conferences, and The Kidney Disease in Older People Network (KidoPEN) was established in 2012 to share expertise and good practice in the management of older people with CKD.
Both specialties are very familiar with the concept of patient-centred care. However while renal services often focus on holistic symptom control, dietary changes and the psychological impact of renal disease, geriatric comprehensive assessment focuses on functional status, cognitive impairment and polypharmacy, and aims to maintain or improve quality of life and prevent future hospital readmissions [8,9,10,11,12]. This may also involve guiding patients towards treatment options which will maintain their independence, and initiating Advanced Care Plans to keep patients in their own homes or prevent unwanted escalations in care.
The so-called “Geriatric Giants” (frailty, falls, dementia/delirium and to a lesser extent incontinence) [13] will be extremely familiar to nephrologists in practice, although perhaps the research around their presentation in renal patients is less familiar. This article describes the prevalence and underlying causes of these Geriatric Giants in renal patients, and discusses possible improvements in care that closer working with geriatricians could bring.

2. Frailty and Multiple Comorbidities

Frailty, defined by Clegg et al. as “a cumulative decline in multiple physiological systems and impairment of homeostasis leading to increased vulnerability to external stressors” [14], is an area of great interest in current geriatric research. It is a concept which has long been widely understood as a marker of decreased physiological reserve and increased mortality by clinicians.
There are two main models of frailty—The Rockwood Frailty Index, which views frailty as an accumulation of deficits, with patients moving along a continuum from non-frail to frail [15], and the Fried Frailty Phenotype, which sees frailty as a syndrome which is either present or absent [16], based on the presence of three or more of the following criteria: unintentional weight loss, self-reported exhaustion, weakness, slow walking speed, and low physical activity. In both models, this cumulative decline depletes homoeostatic reserves until minor stressor events trigger disproportionate changes in health status (for example, a minor urinary tract infection may lead to delirium and bedfastness in a frail patient, while the same illness would have minimal effect on a robust patient of the same age).
A high proportion of renal patients are frail. Indeed, some studies have shown that over 78% of dialysis patients aged over 70 would meet the Fried frailty criteria [17,18,19,20], compared with 6.9% of Fried’s original cohort of older patients with normal renal function [21]. There are a number of possible reasons for the extremely high proportion of frail dialysis patients—in a later study, Fried found an association between protein-energy wasting and both impaired renal function and chronic inflammation [22]. This may be exacerbated by poor intake due to uraemia and dietary restrictions. High levels of comorbidities, frequent infections and regular hospital admissions in this population will also predispose to frailty. This has a number of implications for nephrologists—should we screen for frailty, if it is so prevalent? And how should we intervene when we find it [8]?
The intervention for frailty with the strongest evidence base is the comprehensive geriatric assessment (CGA), defined as “a multidimensional interdisciplinary diagnostic process focused on determining a frail older person’s medical, psychological and functional capability in order to develop a coordinated and integrated plan for treatment and long term follow up” [23]. The resources are not currently in place to allow a comprehensive geriatric assessment for 80% of our prevalent dialysis patients, but pilot studies by Jassal and others which offered CGA to older new starters on dialysis have shown promising early results [24,25,26]. Another option might be the wider use of “Cause for Concern” screening tools to identify the failing dialysis patient and to intervene early. The British Geriatric Society’s excellent “Fit for Frailty” guidelines [27] are both comprehensive and easy to read, and are highly recommended for all clinicians who care for older patients.

3. Functional Status

Cook and Jassal [28] found that in a cohort of 168 prevalent haemodialysis patients aged over 65 years, only 5% were independent in all Activities of Daily Life (ADLs) and Instrumented Activities of Daily Life (IADLs), and 53% were dependent in at least one of the six basic ADLs. Almost half were unable to wash without assistance. Only a quarter could rise from a chair without using their arms, and less than a third had normal balance. Over 30% had fallen at least once in the previous year. Functional status is somewhat better in peritoneal dialysis (PD) patients [29], but this may be due to patient selection (if assisted PD is not available, only patients with relatively good functional status will be offered PD).
Kurella Tamura et al. [30] found that physical function declined rapidly in the three months before initiation of haemodialysis, which might be expected due to increasing uraemia. However, contrary to expectation physical function did not appear to recover following initiation of dialysis, and patients remained significantly functionally impaired. Jassal et al. [31] found that 30% of new starters on dialysis became more functionally dependent within the first six months of being on haemodialysis, including those patients who had previously lived independently. Although functional status did not worsen after the first six months, it did not improve either.
In contrast, Murtagh [32] found that patients managed conservatively maintained functional status until the last month of life. There is admittedly the possibility of lead-time bias here—patients were included in the study when estimated glomerular filtration rate (eGFR) was < 15mls/min (i.e., long before dialysis would usually be initiated) and eGFR at point of death was not recorded, so it is quite possible that “last month of life” is equivalent to (or even earlier than) “time at which patient would have started dialysis if they had not been managed conservatively”. However Hussain et al. [33], a much larger study following patients from eGFR < 20mls/min, reported similar findings.

4. Falls and Fractures

Older dialysis patients frequently fall [34,35,36], when they do fall they are at increased risk of fractures [37,38,39,40,41], and they are more likely to have poor outcomes than similar-aged patients with normal renal function [41,42,43,44]. Cook and Jassal found that over 30% of dialysis patients aged over 65 had fallen at least once in the previous year, and only 20% of patients had normal timed functional mobility scores [28]. Post-dialysis hypotension, underlying cerebrovascular and cardiovascular disease, polypharmacy, autonomic dysfunction and peripheral neuropathy (due to co-existing diabetes and deposition of B2 microglobulin) are just some of the potential causes of these falls. There is an association between vitamin D deficiency, somatic muscular weakness and falls risk in both renal patients and the general population [35,45,46,47]. Many patients have amputations [48,49,50,51]. Many patients also have visual [52] or cognitive problems [53], and trying to climb off and onto the bed for dialysis and then to negotiate a busy, noisy dialysis unit can be a disorientating experience for many older patients. In addition, patients with cognitive problems have higher rates of falls when their attention is distracted [54,55], and dialysis units are generally rather distracting places.
Awareness of some of these problems can lead to risk reduction [41]—For example, regular medication reviews, omitting antihypertensives on the morning of dialysis to prevent hypotension, removing trip hazards in the dialysis unit and offering assistance with transfers, and early screening and referral to physiotherapy or occupational therapy for walking aids and grab rails. Simple screening tools such as the sit-to-stand test and the timed up-and-go are effective at predicting falls risk [56], and can easily be carried out in clinic or on the dialysis unit.

5. Cognitive Function

An estimated 30%–70% of haemodialysis patients have been shown to have some degree of cognitive impairment [53,57,58,59,60,61], and incidence of new cognitive impairment has been associated with both severity of CKD [58,62,63] and with both rate of decline of renal function and albuminuria [64]. This is probably due to a combination of comorbidity (presence of diabetes, vascular disease and hypertension are all independent risk factors [65,66]) and factors unique to CKD, such as the presence of uraemia.
Cognitive function is worse during dialysis sessions [67], presumably due to reduced cerebral perfusion, and best either just before or the day after a dialysis session. It does not seem to improve with more frequent haemodialysis [68], and there is conflicting evidence regarding improvement following transplantation [69,70,71], suggesting that some of this damage may be permanent.
Visuospatial and executive functions are disproportionately affected in these patients [65,72,73], and the NHANES III study found slower learning speeds and impaired visual concentration even in otherwise healthy, younger CKD patients (aged 20–59), compared with standardised populations [74]. This has obvious implications for pre-dialysis counselling and patient education programmes, as well as with treatment compliance. Importantly, these deficits may not be immediately obvious to clinicians in the way that loss of short-term memory or orientation might be, and will also not be detected using short screening tools such as the Abbreviated Mental Test (AMT), which is widely used to screen for dementia and delirium in patients acutely admitted to NHS hospitals.
The presence of cognitive impairment has been linked with an increased risk of hospitalisation [75] and death [60] in dialysis populations, and there are several plausible reasons for this. Firstly, the presence of comorbidities such as diabetes and vascular disease will predispose patients to both cognitive impairment and higher rates of hospitalisation and death. However, difficulties in taking medications or following dietary or fluid restrictions due to impaired executive function may also play a role.

6. Conclusions

As the population ages, renal patients are increasingly presenting with one of the “Geriatric Giants” alongside their nephrological diagnoses. However, their underlying renal disease mandates ongoing specialist renal input—nephrologists cannot simply abdicate responsibility for the care of these complex patients to geriatric services. Indeed few would wish to—There is a long tradition of inpatient care for dialysis and renal transplant patients being provided by nephrologists regardless of the admission diagnosis, and indeed dialysis patients often see the renal team as their first port of call for any medical problems.
These patients should already be known to renal services, so it makes obvious sense for the nephrology department to maintain responsibility for identifying patients who they feel would benefit from geriatric input, rather than simply referring everybody for assessment (of course when people are NOT known to renal services, i.e., the older patient with CKD as an incidental finding, it is important to emphasise that there is good evidence that early nephrology input reduces progression [76]).
There will be some aspects of care that can only be managed by the nephrologists—For example a dialysis patient with falls due to postural hypotension may simply need their target dry weight adjusting. However the current solution, nephrologists becoming “amateur geriatricians”, denies patients both the benefits of specialist geriatric assessment, and equally importantly denies them access to the wider geriatric multidisciplinary team, including hospital at home/admission avoidance, community geriatrics, day hospitals, falls clinics, memory clinics and other specialist services. Protocols for referral to renogeriatric clinics should be developed locally to make the best use of the resources available.
From the geriatricians’ point of view, closer links with nephrology would provide expertise in the management and prevention of both CKD and acute kidney injuries (AKIs), which disproportionately affect older adults [77] and are often poorly managed [78].
Nephrology has an excellent track record of working with palliative care services to develop conservative management programmes in the UK, and with diabetologists and cardiologists to develop joint diabetic nephropathy and cardiorenal clinics respectively. The future aim for the specialty should be the establishment of joint geriatric nephrology services to ensure that our frail older patients have access to the full spectrum of services, and are not disadvantaged by their co-existing renal disease.

Author Contributions

Helen Alston carried out the literature review and produced the first and final drafts, Aine Burns edited the final draft.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Rao, A.; Casula, A.; Castledine, C. UK Renal Registry 17th annual report: Chapter 1 UK renal replacement therapy incidence in 2013: National and centre-specific analyses. Nephron 2015, 129, 31–56. [Google Scholar] [CrossRef] [PubMed]
  2. End-Stage Kidney Disease in Australia: Total Incidence 2003–2007. Available online: http://www.aihw.gov.au/publication-detail/?id=10737419269 (accessed on 20 September 2015).
  3. Locatelli, F.; Pozzoni, P. Chronic kidney disease in the elderly: Is it really a premise for overwhelming renal failure? Kidney Int. 2006, 69, 2118–2120. [Google Scholar] [CrossRef] [PubMed]
  4. El‐Ghoul, B.; Elie, C.; Sqalli, T.; Jungers, P.; Daudon, M.; Grünfeld, J.P.; Lesavre, P.; Joly, D. Nonprogressive kidney dysfunction and outcomes in older adults with chronic kidney disease. J. Am. Geriatr. Soc. 2009, 57, 2217–2223. [Google Scholar] [CrossRef] [PubMed]
  5. Hemmelgarn, B.R.; Zhang, J.; Manns, B.J.; Tonelli, M.; Larsen, E.; Ghali, W.A.; Southern, D.A.; McLaughlin, K.; Mortis, G.; Culleton, B.F. Progression of kidney dysfunction in the community-dwelling elderly. Kidney Int. 2006, 69, 2155–2161. [Google Scholar] [CrossRef] [PubMed]
  6. Keith, D.S.; Nichols, G.A.; Gullion, C.M.; Brown, J.B.; Smith, D.H. Longitudinal follow-up and outcomes among a population with chronic kidney disease in a large managed care organization. Arch. Intern. Med. 2004, 164, 659–663. [Google Scholar] [CrossRef] [PubMed]
  7. Oreopoulos, D.G.; Dimkovic, N. Geriatric nephrology is coming of age. J. Am. Soc. Nephrol. 2003, 14, 1099–1101. [Google Scholar] [CrossRef] [PubMed]
  8. Wiggins, J.; Bitzer, M. Geriatric assessment for the nephrologist. Semin. Dial. 2012, 25, 623–627. [Google Scholar] [CrossRef] [PubMed]
  9. Caplan, G.A.; Williams, A.J.; Daly, B.; Abraham, K.; Abraham, K. A randomized, controlled trial of comprehensive geriatric assessment and multidisciplinary intervention after discharge of elderly from the emergency department—The DEED II study. J. Am. Geriatr. Soc. 2004, 52, 1417–1423. [Google Scholar] [CrossRef] [PubMed]
  10. Conroy, S.P.; Ansari, K.; Williams, M.; Laithwaite, E.; Teasdale, B.; Dawson, J.; Mason, S.; Banerjee, J. A controlled evaluation of comprehensive geriatric assessment in the emergency department: The ‘Emergency Frailty Unit’. Age Ageing 2014, 43, 109–114. [Google Scholar] [CrossRef] [PubMed]
  11. Conroy, S.P.; Stevens, T.; Parker, S.G.; Gladman, J.R. A systematic review of comprehensive geriatric assessment to improve outcomes for frail older people being rapidly discharged from acute hospital: ‘Interface geriatrics’. Age Ageing 2011, 40, 436–443. [Google Scholar] [CrossRef] [PubMed]
  12. Li, C.M.; Chen, C.Y.; Li, C.Y.; Wang, W.D.; Wu, S.C. The effectiveness of a comprehensive geriatric assessment intervention program for frailty in community-dwelling older people: A randomized, controlled trial. Arch. Gerontol. Geriatr. 2010, 50, S39–S42. [Google Scholar] [CrossRef]
  13. Woo, J. 2013: That was the year that was. Age Ageing 2014, 43, 152–156. [Google Scholar] [CrossRef] [PubMed]
  14. Clegg, A.; Young, J.; Iliffe, S.; Rikkert, M.O.; Rockwood, K. Frailty in elderly people. Lancet 2013, 381, 752–762. [Google Scholar] [CrossRef]
  15. Rockwood, K.; Stadnyk, K.; MacKnight, C.; McDowell, I.; Hébert, R.; Hogan, D.B. A brief clinical instrument to classify frailty in elderly people. Lancet 1999, 353, 205–206. [Google Scholar] [CrossRef]
  16. Fried, L.P.; Tangen, C.M.; Walston, J.; Newman, A.B.; Hirsch, C.; Gottdiener, J.; Seeman, T.; Tracy, R.; Kop, W.J.; Burke, G.; et al. Frailty in older adults: Evidence for a phenotype. J. Gerontol. Biol. Sci. Med. Sci. 2001, 56, M146–M156. [Google Scholar] [CrossRef]
  17. Painter, P.; Kuskowski, M. A closer look at frailty in ESRD: Getting the measure right. Hemodial. Int. 2013, 17, 41–49. [Google Scholar] [CrossRef] [PubMed]
  18. Johansen, K.L.; Chertow, G.M.; Jin, C.; Kutner, N.G. Significance of frailty among dialysis patients. J. Am. Soc. Nephrol. 2007, 18, 2960–2967. [Google Scholar] [CrossRef] [PubMed]
  19. Collins, A.J.; Foley, R.N.; Chavers, B.; Gilbertson, D.; Herzog, C.; Ishani, A.; Johansen, K.; Kasiske, B.L.; Kutner, N.; Liu, J.; et al. US Renal Data System 2013 Annual Data Report. Am. J. Kidney Dis. 2014, 63, E1–E460. [Google Scholar] [CrossRef] [PubMed]
  20. Johansen, K.L.; Delgado, C.; Bao, Y.; Tamura, M.K. Frailty and dialysis initiation. Semin Dial. 2013, 26, 690–696. [Google Scholar] [CrossRef] [PubMed]
  21. Fried, L.P.; Kronmal, R.A.; Newman, A.B.; Bild, D.E.; Mittelmark, M.B.; Polak, J.F.; Robbins, J.A.; Gardin, J.M. Risk factors for 5-year mortality in older adults: The cardiovascular health study. JAMA 1998, 279, 585–592. [Google Scholar] [CrossRef] [PubMed]
  22. Fried, L.F.; Boudreau, R.; Lee, J.S.; Chertow, G.; Kurella-Tamura, M.; Shlipak, M.G.; Ding, J.Z.; Sellmeyer, D.; Tylavsky, F.A.; Simsonick, E.; et al. Kidney function as a predictor of loss of lean mass in older adults: Health, aging and body composition Study. J. Am. Geriatr. Soc. 2007, 55, 1578–1584. [Google Scholar] [CrossRef] [PubMed]
  23. Stuck, A.E.; Siu, A.L.; Wieland, G.D.; Rubenstein, L.Z.; Adams, J. Comprehensive geriatric assessment: A meta-analysis of controlled trials. Lancet 1993, 342, 1032–1036. [Google Scholar] [CrossRef]
  24. Farragher, J.; Jassal, S.V. Rehabilitation of the geriatric dialysis patient. Semin Dial. 2012, 25, 649–656. [Google Scholar] [CrossRef] [PubMed]
  25. Jassal, S.V.; Chiu, E.; Li, M. Geriatric hemodialysis rehabilitation care. Adv. Chronic Kidney Dis. 2008, 15, 115–122. [Google Scholar] [CrossRef] [PubMed]
  26. Nonoyama, M.L.; Brooks, D.; Ponikvar, A.; Jassal, S.V.; Kontos, P.; Devins, G.M.; Spanjevic, L.; Heck, C.; Laprade, J.; Naglie, G. Exercise program to enhance physical performance and quality of life of older hemodialysis patients: A feasibility study. Int. Urol. Nephrol. 2010, 42, 1125–1130. [Google Scholar] [CrossRef] [PubMed]
  27. Fit for Frailty. Avaiable online: http://www.bgs.org.uk/index.php/fit-for-frailty (accessed on 20 September 2015).
  28. Cook, W.L.; Jassal, S.V. Functional dependencies among the elderly on hemodialysis. Kidney Int. 2008, 73, 1289–1295. [Google Scholar] [CrossRef]
  29. Văcăroiu, I.A.; Rădulescu, D.; Ciocâlteu, A.; Peride, I.; Ardeleanu, S.; Checheriţă, I.A. Functional status of chronic renal replacement therapy in elderly patients—Comparison between hemodialysis and peritoneal dialysis. Rev. Med. Chir. Soc. Med. Nat. Iasi. 2012, 116, 375–382. [Google Scholar] [PubMed]
  30. Kurella Tamura, M.; Covinsky, K.E.; Chertow, G.M.; Yaffe, K.; Landefeld, C.S.; McCulloch, C.E. Functional status of elderly adults before and after initiation of dialysis. N. Engl. J. Med. 2009, 361, 1539–1547. [Google Scholar] [CrossRef] [PubMed]
  31. Jassal, S.V.; Chiu, E.; Hladunewich, M. Loss of independence in patients starting dialysis at 80 years of age or older. N. Engl. J. Med. 2009, 361, 1612–1613. [Google Scholar] [CrossRef] [PubMed]
  32. Murtagh, F.E.M.; Addington-Hall, J.M.; Higginson, I.J. End-stage renal disease: A new trajectory of functional decline in the last year of life. J. Am. Geriatr. Soc. 2011, 59, 304–308. [Google Scholar] [CrossRef] [PubMed]
  33. Hussain, J.A.; Mooney, A.; Russon, L. Comparison of survival analysis and palliative care involvement in patients aged over 70 years choosing conservative management or renal replacement therapy in advanced chronic kidney disease. Palliat. Med. 2013, 27, 829–839. [Google Scholar] [CrossRef] [PubMed]
  34. Anderson, K.N.; Catt, M.; Collerton, J.; Davies, K.; von Zglinicki, T.; Kirkwood, T.B.; Jagger, C. Assessment of sleep and circadian rhythm disorders in the very old: The Newcastle 85+ Cohort Study. Age Ageing 2014, 43, 57–63. [Google Scholar] [CrossRef] [PubMed]
  35. Boudville, N.; Inderjeeth, C.; Elder, G.J.; Glendenning, P. Association between 25-hydroxyvitamin D, somatic muscle weakness and falls risk in end-stage renal failure. Clin. Endocrinol. 2010, 73, 299–304. [Google Scholar] [CrossRef] [PubMed]
  36. Cook, W.L.; Tomlinson, G.; Donaldson, M.; Markowitz, S.N.; Naglie, G.; Sobolev, B.; Jassal, S.V. Falls and fall-related injuries in older dialysis patients. Clin. J. Am. Soc. Nephrol. 2006, 1, 1197–1204. [Google Scholar] [CrossRef] [PubMed]
  37. Ball, A.M.; Gillen, D.L.; Sherrard, D.; Weiss, N.S.; Emerson, S.S.; Seliger, S.L.; Kestenbaum, B.R.; Stehman-Breen, C. Risk of hip fracture among dialysis and renal transplant recipients. J. Am. Med. Assoc. 2002, 288, 3014–3018. [Google Scholar] [CrossRef]
  38. Bruce, D.G.; John, A.; Nicklason, F.; Goldswain, P.R. Secondary hyperparathyroidism in patients from Western Australia with hip fracture: relationship to type of hip fracture, renal function, and vitamin D deficiency. J. Am. Geriatr. Soc. 1999, 47, 354–359. [Google Scholar] [CrossRef] [PubMed]
  39. Iimori, S.; Mori, Y.; Akita, W.; Kuyama, T.; Takada, S.; Asai, T.; Kuwahara, M.; Sasaki, S.; Tsukamoto, Y. Diagnostic usefulness of bone mineral density and biochemical markers of bone turnover in predicting fracture in CKD stage 5D patients-a single-center cohort study. Nephrol. Dial. Transplant. 2012, 27, 345–351. [Google Scholar] [CrossRef] [PubMed]
  40. Ma, M.K.; Yap, D.Y.; Yip, T.P.; Lui, S.L.; Lo, W.K. Charlson Co-morbidity Index and albumin significantly associated with fracture risk in peritoneal dialysis patients. Nephrology 2013, 18, 365–368. [Google Scholar] [PubMed]
  41. Toussaint, N.D.; Elder, G.J.; Kerr, P.G. A rational guide to reducing fracture risk in dialysis patients. Semin. Dial. 2010, 23, 43–54. [Google Scholar] [CrossRef] [PubMed]
  42. Akushevich, I.; Kravchenko, J.; Ukraintseva, S.; Arbeev, K.; Yashin, A.I. Time trends of incidence of age-associated diseases in the US elderly population: Medicare-based analysis. Age Ageing 2013, 42, 494–500. [Google Scholar] [CrossRef] [PubMed]
  43. Khan, S.K.; Rushton, S.P.; Courtney, M.; Gray, A.C.; Deehan, D.J. Elderly men with renal dysfunction are most at risk for poor outcome after neck of femur fractures. Age Ageing 2013, 42, 76–81. [Google Scholar] [CrossRef] [PubMed]
  44. Mittalhenkle, A.; Gillen, D.L.; Stehman-Breen, C.O. Increased risk of mortality associated with hip fracture in the dialysis population. Am. J. Kidney Dis. 2004, 44, 672–679. [Google Scholar] [CrossRef]
  45. Li, Y.C. Vitamin D: Roles in renal and cardiovascular protection. Curr. Opin. Nephrol. Hypertens. 2012, 21, 72–79. [Google Scholar] [CrossRef] [PubMed]
  46. Macdonald, H.M. Is ankle strength as important as vitamin D status in helping to prevent falls in winter? Age Ageing 2013, 42, 154–155. [Google Scholar] [CrossRef] [PubMed]
  47. Taskapan, H.; Baysal, O.; Karahan, D.; Durmus, B.; Altay, Z.; Ulutas, O. Vitamin D and muscle strength, functional ability and balance in peritoneal dialysis patients with vitamin D deficiency. Clin. Nephrol. 2011, 76, 110–116. [Google Scholar] [CrossRef] [PubMed]
  48. Lavery, L.A.; Lavery, D.C.; Hunt, N.A.; La Fontaine, J.; Ndip, A.; Boulton, A.J. Amputations and foot-related hospitalisations disproportionately affect dialysis patients. Int. Wound J. 2013, 12, 523–526. [Google Scholar] [CrossRef] [PubMed]
  49. Ndip, A.; Lavery, L.A.; Boulton, A.J. Diabetic foot disease in people with advanced nephropathy and those on renal dialysis. Curr. Diab. Rep. 2010, 10, 283–290. [Google Scholar] [CrossRef] [PubMed]
  50. Ndip, A.; Lavery, L.A.; LaFontaine, J.; Rutter, M.K.; Vardhan, A.; Vileikyte, L.; Boulton, A.J. High levels of foot ulceration and amputation risk in a multiracial cohort of diabetic patients on dialysis therapy. Diabetes Care 2010, 33, 878–880. [Google Scholar] [CrossRef] [PubMed]
  51. Ndip, A.; Rutter, M.K.; Vileikyte, L.; Vardhan, A.; Asari, A.; Jameel, M.; Tahir, H.A.; Lavery, L.A.; Boulton, A.J.M. Dialysis treatment is an independent risk factor for foot ulceration in patients with diabetes and stage 4 or 5 chronic kidney disease. Diabetes Care 2010, 33, 1811–1816. [Google Scholar] [CrossRef] [PubMed]
  52. Chiu, E.; Markowitz, S.N.; Cook, W.L.; Jassal, S.V. Visual impairment in elderly patients receiving long-term hemodialysis. Am. J. Kidney Dis. 2008, 52, 1131–1138. [Google Scholar] [CrossRef] [PubMed]
  53. Kurella, M.; Chertow, G.M.; Luan, J.; Yaffe, K. Cognitive impairment in chronic kidney disease. J. Am. Geriatr. Soc. 2004, 52, 1863–1869. [Google Scholar] [CrossRef] [PubMed]
  54. Martin, K.L.; Blizzard, L.; Wood, A.G.; Srikanth, V.; Thomson, R.; Sanders, L.M.; Callisaya, M.L. Cognitive function, gait, and gait variability in older people: A population-based study. J. Gerontol. Biol. Sci. Med. Sci. 2013, 68, 726–732. [Google Scholar] [CrossRef] [PubMed]
  55. Lundin-Olsson, L.; Nyberg, L.; Gustafson, Y. Attention, frailty, and falls: The effect of a manual task on basic mobility. J. Am. Geriatr. Soc. 1998, 46, 758–761. [Google Scholar] [CrossRef] [PubMed]
  56. Soangra, R.; Lockhart, T.E.; Lach, J.; Abdel-Rahman, E.M. Effects of hemodialysis therapy on sit-to-walk characteristics in end stage renal disease patients. Ann. Biomed. Eng. 2013, 41, 795–805. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Anand, S.; Johansen, K.L.; Kurella Tamura, M. Aging and chronic kidney disease: The impact on physical function and cognition. J. Gerontol. A 2013, 69, 315–322. [Google Scholar] [CrossRef] [PubMed]
  58. Kurella, M.; Chertow, G.M.; Fried, L.F.; Cummings, S.R.; Harris, T.; Simonsick, E.; Satterfield, S.; Ayonayon, H.; Yaffe, K. Chronic kidney disease and cognitive impairment in the elderly: The health, aging, and body composition study. J. Am. Soc. Nephrol. 2005, 16, 2127–2133. [Google Scholar] [CrossRef] [PubMed]
  59. Murray, A.M.; Knopman, D.S. Cognitive impairment in CKD: No longer an occult burden. Am. J. Kidney Dis. 2010, 56, 615–618. [Google Scholar] [CrossRef] [PubMed]
  60. Griva, K.; Stygall, J.; Hankins, M.; Davenport, A.; Harrison, M.; Newman, S.P. Cognitive impairment and 7-year mortality in dialysis patients. Am. J. Kidney Dis. 2010, 56, 693–703. [Google Scholar] [CrossRef] [PubMed]
  61. Murray, A.M.; Tupper, D.E.; Knopman, D.S.; Gilbertson, D.T.; Pederson, S.L.; Li, S.; Smith, E.; Hochhalter, A.K.; Collins, A.J.; Kane, R.L. Cognitive impairment in hemodialysis patients is common. Neurology 2006, 67, 216–223. [Google Scholar] [CrossRef] [PubMed]
  62. Buchman, A.S.; Tanne, D.; Boyle, P.A.; Shah, R.C.; Leurgans, S.E.; Bennett, D.A. Kidney function is associated with the rate of cognitive decline in the elderly. Neurology 2009, 73, 920–927. [Google Scholar] [CrossRef] [PubMed]
  63. Etgen, T.; Sander, D.; Chonchol, M.; Briesenick, C.; Poppert, H.; Förstl, H.; Bickel, H. Chronic kidney disease is associated with incident cognitive impairment in the elderly: The INVADE study. Nephrol. Dial. Transplant. 2009, 24, 3144–3150. [Google Scholar] [CrossRef] [PubMed]
  64. Etgen, T.; Sander, D.; Chonchol, M.; Briesenick, C.; Poppert, H.; Förstl, H.; Bickel, H. Chronic kidney disease, cognitive decline, and incident dementia: The 3C study. Neurology 2011, 77, 2043–2051. [Google Scholar]
  65. Sarnak, M.J.; Tighiouart, H.; Scott, T.M.; Lou, K.V.; Sorensen, E.P.; Giang, L.M.; Drew, D.A.; Shaffi, S.K.; Strom, J.M.; Singh, A.K.; et al. Frequency of and risk factors for poor cognitive performance in hemodialysis patients. Neurology 2013, 80, 471–480. [Google Scholar] [CrossRef] [PubMed]
  66. Kalaitzidis, R.G.; Karasavvidou, D.; Tatsioni, A.; Balafa, O.; Pappas, K.; Spanos, G.; Pelidou, S.H.; Siamopoulos, K.C. Risk factors for cognitive dysfunction in CKD and hypertensive subjects. Int. Urol. Nephrol. 2013, 45, 1637–1646. [Google Scholar] [CrossRef] [PubMed]
  67. Murray, A.M.; Pederson, S.L.; Tupper, D.E.; Hochhalter, A.K.; Miller, W.A.; Li, Q.; Zaun, D.; Collins, A.J.; Kane, R.; Foley, R.N. Acute variation in cognitive function in hemodialysis patients: A cohort study with repeated measures. Am. J. Kidney Dis. 2007, 50, 270–278. [Google Scholar] [CrossRef] [PubMed]
  68. Tamura, M.K.; Unruh, M.L.; Nissenson, A.R.; Larive, B.; Eggers, P.W.; Gassman, J.; Mehta, R.L.; Kliger, A.S.; Stokes, J.B. Effect of more frequent hemodialysis on cognitive function in the frequent hemodialysis network trials. Am. J. Kidney Dis. 2013, 61, 228–237. [Google Scholar] [CrossRef] [PubMed]
  69. Gelb, S.; Shapiro, R.J.; Hill, A.; Thornton, W.L. Cognitive outcome following kidney transplantation. Nephrol. Dial. Transplant. 2008, 23, 1032–1038. [Google Scholar] [CrossRef] [PubMed]
  70. Harciarek, M.; Biedunkiewicz, B.; Lichodziejewska-Niemierko, M.; Dębska-Ślizień, A.; Rutkowski, B. Continuous cognitive improvement 1 year following successful kidney transplant. Kidney Int. 2011, 79, 1353–1360. [Google Scholar] [CrossRef] [PubMed]
  71. Radić, J.; Ljutić, D.; Radić, M.; Kovačić, V.; Dodig-Ćurković, K.; Šain, M. Kidney transplantation improves cognitive and psychomotor functions in adult hemodialysis patients. Am. J. Nephrol. 2011, 34, 399–406. [Google Scholar] [CrossRef] [PubMed]
  72. Elias, M.F.; Dore, G.A.; Davey, A. Kidney disease and cognitive function. Contrib. Nephrol. 2013, 179, 42–57. [Google Scholar] [PubMed]
  73. Lee, J.J.; Chin, H.J.; Byun, M.S.; Choe, J.Y.; Park, J.H.; Lee, S.B.; Choi, E.A.; Chae, D.W.; Kim, K.W. Impaired frontal executive function and predialytic chronic kidney disease. J. Am. Geriatr. Soc. 2011, 59, 1628–1635. [Google Scholar] [CrossRef] [PubMed]
  74. Hailpern, S.M.; Melamed, M.L.; Cohen, H.W.; Hostetter, T.H. Moderate chronic kidney disease and cognitive function in adults 20 to 59 years of age: Third National Health and Nutrition Examination Survey (NHANES III). J. Am. Soc. Nephrol. 2007, 18, 2205–2213. [Google Scholar] [CrossRef] [PubMed]
  75. Collins, A.J. Excerpts from the United States renal data system 2006 annual data report. Am. J. Kidney Dis. 2007, 49, S1–S296. [Google Scholar] [CrossRef] [PubMed]
  76. National Clinical Guideline Centre. Early Identification and Management of Chronic Kidney Disease in Adults in Primary and Secondary Care; National Clinical Guideline Center: London, England, 2014.
  77. Chertow, G.M.; Burdick, E.; Honour, M.; Bonventre, J.V.; Bates, D.W. Acute kidney injury, mortality, length of stay, and costs in hospitalized patients. J. Am. Soc. Nephrol. 2005, 16, 3365–3370. [Google Scholar] [CrossRef] [PubMed]
  78. Ftouh, S.; Lewington, A. Prevention, detection and management of acute kidney injury: Concise guideline. Clin. Med. 2014, 14, 61–65. [Google Scholar] [CrossRef] [PubMed]

Share and Cite

MDPI and ACS Style

Alston, H.; Burns, A. Ageing Renal Patients: We Need More Collaboration between Geriatric Services and Nephrology Departments. Healthcare 2015, 3, 1075-1085. https://doi.org/10.3390/healthcare3041075

AMA Style

Alston H, Burns A. Ageing Renal Patients: We Need More Collaboration between Geriatric Services and Nephrology Departments. Healthcare. 2015; 3(4):1075-1085. https://doi.org/10.3390/healthcare3041075

Chicago/Turabian Style

Alston, Helen, and Aine Burns. 2015. "Ageing Renal Patients: We Need More Collaboration between Geriatric Services and Nephrology Departments" Healthcare 3, no. 4: 1075-1085. https://doi.org/10.3390/healthcare3041075

Article Metrics

Back to TopTop