Quality Control in Haemodialysis Delivery

European Nephrology, 2011;5(2):132-137

Abstract

Haemodialysis (HD) patients anticipate that all treatments are delivered to their individual needs. However, as the management of HD delivery is complex and every treatment differs, efficient quality control activities are required to ensure that the therapy is effectively provided. Contemporary dialysis machines have integrated tools to support the control process. Ionic clearance measurement alerts when treatment effectiveness is impaired and provides a means to decrease dose variability. Blood volume monitoring and biofeedback control support the achievement of dry weight, treatment by treatment, with reduced risk of intradialytic hypotension and other symptoms related to fluid removal. Available evidence indicates that structured quality control may have a significant effect on patient outcome as well as on the cost efficiency of dialysis care.

Support: The publication of this article was funded by Gambro.
Keywords
Haemodialysis delivery, quality control, dose variability, ionic clearance, Kt/V, dry weight, blood volume monitoring, blood volume tracking
Disclosure Lars-Göran Nilsson, Juan P Bosch and Maria Alquist are all employees of Gambro.
Received: May 30, 2011 | Accepted June 20, 2011 | Citation European Nephrology, 2011;5(2):132-137
Correspondence: Lars-Göran Nilsson, Gambro, PO Box 10101, SE-22010 Lund, Sweden. E: Lars-Goran.Nilsson@gambro.com

Haemodialysis (HD) makes survival possible for more than a million people with end-stage renal disease (ESRD) throughout the world. Still, it is a continuing notion everywhere that the survival rate for prevalent dialysis patients is low and without significant improvement in later years. At the same time, the healthcare spending for ESRD patients on dialysis is immense and the growing population of ESRD patients represents a significant economic burden to countries worldwide.1 Dialysis providers are facing increasing pressure to become more cost efficient; reducing costs for dialysis delivery, while at the same time improving or at least maintaining quality of care.

Older age and a high and increasing rate of co-morbidities, like cardiovascular diseases, inflammation, frequent infections and bleeding disorders, may partly explain the unsatisfactory outcome for patients on chronic dialysis. Age and co-morbid condition are also related to cost-effectiveness in dialysis care, which shows considerable variability between patients.2 In addition, a key variable affecting both outcome and cost in this patient population is the way dialysis care is provided. The time when patients are referred to a nephrologist, what type of dialysis therapy is offered to them and how well that therapy is implemented, all have a profound effect on the therapy results. Implementation of the therapy involves prescription – dialysis dose, fluid removal, dialysis fluid composition, administration of erythropoiesis-stimulating agents, vitamin D analogues, phosphate binders and other drugs – but also consistent delivery of therapy to that prescription.

Like healthcare in general, inability to deliver therapy to the prescription represents a source of inefficiency in dialysis care. A systematic treatment mapping in dialysis clinics has shown that dialysis delivery is often poorly standardised with significant process variability between and within clinics.3 The variability is related to factors such as patient characteristics, dialysis prescription, dialysis equipment design and clinic practices, such as scheduling of patients and staff resources.3,4 When the process is poorly controlled it also becomes difficult to implement individualisation of the therapy.

It is often perceived in medicine that new technologies with potential to improve patient outcomes are contributing to rising health expenditures. However, quality improvements are not necessarily associated with increased costs and there is a substantial cost associated with poor quality. A US analysis on the general Medicare health cost statistics, focusing on key severity-adjusted diagnosis-related groups, supports the concept that poor outcomes lead to greater expenditures and that improving quality can help to reduce costs significantly.5

References:
  1. Dor A, Pauly MV, Eichleay MA, Held PJ, End-stage renal disease and economic incentives: the International Study of Health Care Organization and Financing (ISHCOF), Int J Health Care Finance Econ, 2007;7:73–111.
  2. Lee CP, Chertow GM, Zenios SA, An empiric estimate of the value of life: updating the renal dialysis cost-effectiveness standard, Value Health, 2009;12:80–7.
  3. Alquist M, Bosch JP, Treatment mapping--a systematic methodology to assess quality, efficiency and variability in the hemodialysis delivery process, Blood Purif, 2008;26:417–22.
  4. Alquist M, Hegbrant JB, Bosch JP, Monitor turnaround time and time efficiency in hemodialysis delivery--a global comparison, Blood Purif, 2009;28:234–8.
  5. Cleverley WO, Cleverley JO, Is there a cost associated with higher quality?, Healthc Financ Manage, 2011;65:96–102.
  6. Vanholder R, De Smet R, Glorieux G, et al., European Uremic Toxin Work Group (EUTox). Review on uremic toxins: classification, concentration, and interindividual variability, Kidney Int, 2003;63:1934–43.
  7. Daugirdas JT, Simplified equations for monitoring Kt/V, PCRn, eKt/V, and ePCRn, Adv Ren Replace Ther, 1995;2:295–304.
  8. Gotch FA, Levin NW, Port FK, et al., Clinical outcome relative to the dose of dialysis is not what you think: the fallacy of the mean, Am J Kidney Dis, 1997;30:1–15.
  9. Bosch JP, Nabut J, Hegbrant J, et al., Increased Survival for Hemodialysis Patients with a Dialysis Dose above the KDOQI Guidelines, Presented at: ASN 35th Annual Meeting 2002, 30 October – 4 November 2002.
  10. Port FK, Ashby VB, Dhingra RK, et al., Dialysis dose and body mass index are strongly associated with survival in hemodialysis patients, J Am Soc Nephrol, 2002;13:1061–6.
  11. Chertow GM, Owen WF, Lazarus JM, et al., Exploring the reverse J-shaped curve between urea reduction ratio and mortality, Kidney Int, 1999;56:1872–8.
  12. Eknoyan G, Beck GJ, Cheung AK, et al., Hemodialysis (HEMO) Study Group, Effect of dialysis dose and membrane flux in maintenance hemodialysis, N Engl J Med, 2002;347:2010–9.
  13. Depner T, Daugirdas J, Greene T, et al., Hemodialysis Study Group, Dialysis dose and the effect of gender and body size on outcome in the HEMO Study, Kidney Int, 2004;65:1386–94.
  14. Tattersall J, Martin-Malo A, Pedrini L, et al., EBPG guideline on dialysis strategies, Nephrol Dial Transplant, 2007;22(Suppl. 2):ii5–21.
  15. Hemodialysis Adequacy 2006 Work Group, Clinical practice guidelines for hemodialysis adequacy, update 2006, Am J Kidney Dis, 2006;48(Suppl. 1):S2–90.
  16. 2009 Annual Report of the Dialysis Outcomes and Practice Patterns Study: Hemodialysis Data 1999-2008, Arbor Research Collaborative for Health, Ann Arbor, MI. Available from: www.dopps.org (accessed 9 July 2011).
  17. Brimble KS, Treleaven DJ, Onge JS, Carlisle EJ, Risk factors for increased variability in dialysis delivery in haemodialysis patients, Nephrol Dial Transplant, 2003;18:2112–7.
  18. Kloppenburg WD, Stegeman CA, Hooyschuur M, et al., Assessing dialysis adequacy and dietary intake in the individual hemodialysis patient, Kidney Int, 1999;55:1961–9.
  19. McIntyre CW, Lambie SH, Taal MW, Fluck RJ, Assessment of haemodialysis adequacy by ionic dialysance: intra-patient variability of delivered treatment, Nephrol Dial Transplant, 2003;18:559–62.
  20. Teruel JL, Fernández Lucas M, Arambarri M, et al., [Ionic dialysance to control the dose of dialysis. One year experience], Nefrologia, 2003;23:444–50.
  21. Alquist M, Nordgren G, Barlee V, Bosch J, Variability in prescription delivery, Presented at: ASN 38th Annual Meeting 2005, 8–13 November 2005.
  22. Coyne DW, Delmez J, Spence G, Windus DW, Impaired delivery of hemodialysis prescriptions: an analysis of causes and an approach to evaluation, J Am Soc Nephrol, 1997;8:1315–8.
  23. Press MH, Benz RL, Quantifying the role of factors that limit attainment of K/DOQI urea reduction ratio dialytic goal, Clin Nephrol, 2006;66:98–102.
  24. Lambie SH, Taal MW, Fluck RJ, McIntyre CW, Analysis of factors associated with variability in haemodialysis adequacy, Nephrol Dial Transplant, 2004;19:406–12.
  25. Sehgal AR, Dor A, Tsai AC, Morbidity and cost implications of inadequate hemodialysis, Am J Kidney Dis, 2001;37:1223–31.
  26. Bloembergen WE, Stannard DC, Port FK et al., Relationship of dose of hemodialysis and cause-specific mortality, Kidney Int, 1996;50:557–65.
  27. Walters B, Pennell P, Hegbrant J et al., The frequency of exposure to a dialysis dose of less than single pool (sp)Kt/V of 1.2 predicts decreased survival in hemodialysis patients (abstract), World Congress of Nephrology 2003, 8–12 June 2003.
  28. Mercadal L, Ridel C, Petitclerc T, Ionic dialysance: principle and review of its clinical relevance for quantification of hemodialysis efficiency, Hemodial Int, 2005;9:111–9.
  29. Lindsay RM, Bene B, Goux N, et al., Relationship between effective ionic dialysance and in vivo urea clearance during hemodialysis, Am J Kidney Dis, 2001;38:565–74.
  30. Moret K, Grootendorst DC, Beerenhout C, Kooman JP, Conductivity pulses needed for Diascan measurements: does it cause sodium burden?, NDT Plus, 2009;2:334–5.
  31. Coevoet B, Aazib L, Chlih B, et al., Intérêt du suivi en temps réel de la dialysance ionique dans une démarche d’assurance-qualité en hémodialyse, Dyalog, 1998;92:12–5.
  32. Moret K, Beerenhout CH, van den Wall Bake AW et al., Ionic dialysance and the assessment of Kt/V: the influence of different estimates of V on method agreement, Nephrol Dial Transplant, 2007;22:2276–82.
  33. Mohan S, Madhrira M, Mujtaba M, et al., Effective ionic dialysance/blood flow rate ratio: an indicator of access recirculation in arteriovenous fistulae, ASAIO J, 2010;56:427–33.
  34. Stanescu C, Bene B, Kaba L, et al. Prevention of vascular access complications by weekly surveillance of ionic dialysance and extracorporeal circuit pressures (abstract), Nephrol Dial Transplant, 2007;22(Suppl. 6):vi167.
  35. Menegato MA, Manzini P, Fornasiero G, Mortellato RF, New fistula (AVF) monitoring system by time pattern data analysis in hemodialysis patients, ERA-EDTA 47th Annual Meeting 2010, 2010; abstract Sa360.
  36. Chesterton LJ, Priestman WS, Lambie SH, et al., Continuous online monitoring of ionic dialysance allows modification of delivered hemodialysis treatment time, Hemodial Int, 2006;10:346–50.
  37. Raimann J, Liu L, Ulloa D, et al., Consequences of overhydration and the need for dry weight assessment, Contrib Nephrol, 2008;161:99–107.
  38. McIntyre CW, Haemodialysis-induced myocardial stunning in chronic kidney disease - a new aspect of cardiovascular disease, Blood Purif, 2010;29:105–10.
  39. Charra B, Fluid balance, dry weight, and blood pressure in dialysis, Hemodial Int, 2007;11:21–31.
  40. Agarwal R, Weir MR, Dry-weight: a concept revisited in an effort to avoid medication-directed approaches for blood pressure control in hemodialysis patients, Clin J Am Soc Nephrol, 2010;5:1255–60.
  41. Sinha AD, Why assistive technology is needed for probing of dry weight, Blood Purif, 2011;31:197–202.
  42. Agarwal R, Alborzi P, Satyan S, Light RP, Dry-weight reduction in hypertensive hemodialysis patients (DRIP): a randomized, controlled trial, Hypertension, 2009;53:500–7.
  43. Agarwal R, Bouldin JM, Light RP, Garg A, Probing dry-weight improves left ventricular mass index, Am J Nephrol, 2011;33:373–80.
  44. Paolini F, Mancini E, Bosetto A, Santoro A, Hemoscan: a dialysis machine-integrated blood volume monitor, Int J Artif Organs, 1995;18:487–94.
  45. Lopot F, Kotyk P, Bláha J, Forejt J, Use of continuous blood volume monitoring to detect inadequately high dry weight, Int J Artif Organs, 1996;19:411–4.
  46. Sinha AD, Light RP, Agarwal R, Relative plasma volume monitoring during hemodialysis AIDS the assessment of dry weight, Hypertension, 2010;55:305–11.
  47. Rodriguez HJ, Domenici R, Diroll A, Goykhman I, Assessment of dry weight by monitoring changes in blood volume during hemodialysis using Crit-Line, Kidney Int, 2005;68:854–61.
  48. Santoro A, Mancini E, Hemodialysis and the elderly patient: complications and concerns, J Nephrol, 2010;23(Suppl. 15):S80–9.
  49. Kimmel PL, Varela MP, Peterson RA, et al., Interdialytic weight gain and survival in hemodialysis patients: effects of duration of ESRD and diabetes mellitus, Kidney Int, 2000;57:1141–51.
  50. Kalantar-Zadeh K, Regidor DL, Kovesdy CP, et al., Fluid retention is associated with cardiovascular mortality in patients undergoing long-term hemodialysis, Circulation, 2009;119:671–9.
  51. Flythe JE, Kimmel SE, Brunelli SM, Rapid fluid removal during dialysis is associated with cardiovascular morbidity and mortality, Kidney Int, 2011;79:250–7.
  52. Movilli E, Gaggia P, Zubani R, et al., Association between high ultrafiltration rates and mortality in uraemic patients on regular haemodialysis. A 5-year prospective observational multicentre study, Nephrol Dial Transplant, 2007;22:3547–52.
  53. Brunelli SM, Chertow GM, Ankers ED, et al., Shorter dialysis times are associated with higher mortality among incident hemodialysis patients, Kidney Int, 2010;77:630–6.
  54. Dasselaar JJ, Slart RH, Knip M, et al., Haemodialysis is associated with a pronounced fall in myocardial perfusion, Nephrol Dial Transplant, 2009;24:604–10.
  55. Flythe JE, Brunelli SM, The Risks of High Ultrafiltration Rate in Chronic Hemodialysis: Implications for Patient Care, Semin Dial, 2011;24(3):259–65.
  56. McIntyre CW, Recurrent circulatory stress: the dark side of dialysis, Semin Dial, 2010;23:449–51.
  57. Kooman J, Basci A, Pizzarelli F, et al., EBPG guideline on haemodynamic instability, Nephrol Dial Transplant, 2007;22(Suppl. 2):ii22–44.
  58. Lindley EJ, Reducing sodium intake in hemodialysis patients, Semin Dial, 2009;22:260–3.
  59. Kayikcioglu M, Tumuklu M, Ozkahya M, et al., The benefit of salt restriction in the treatment of end-stage renal disease by haemodialysis, Nephrol Dial Transplant, 2009;24:956–62.
  60. Charra B, Chazot C, The neglect of sodium restriction in dialysis patients: a short review, Hemodial Int, 2003;7:342–7.
  61. Penne EL, Sergeyeva O, Sodium gradient: a tool to individualize dialysate sodium prescription in chronic hemodialysis patients?, Blood Purif, 2011;31:86–91.
  62. Song JH, Park GH, Lee SY, et al., Effect of sodium balance and the combination of ultrafiltration profile during sodium profiling hemodialysis on the maintenance of the quality of dialysis and sodium and fluid balances, J Am Soc Nephrol, 2005;16:237–46.
  63. Santoro A, Mancini E, Paolini F, et al., Automatic control of blood volume trends during hemodialysis, ASAIO J, 1994;40:M419–22.
  64. Santoro A, Mancini E, Basile C, et al., Blood volume controlled hemodialysis in hypotension-prone patients: a randomized, multicenter controlled trial, Kidney Int, 2002;62:1034–45.
  65. Franssen CF, Dasselaar JJ, Sytsma P, et al., Automatic feedback control of relative blood volume changes during hemodialysis improves blood pressure stability during and after dialysis, Hemodial Int, 2005;9:383–92.
  66. Déziel C, Bouchard J, Zellweger M, Madore F, Impact of hemocontrol on hypertension, nursing interventions, and quality of life: a randomized, controlled trial, Clin J Am Soc Nephrol, 2007;2:661–8.
  67. Basile C, Giordano R, Vernaglione L, et al., Efficacy and safety of haemodialysis treatment with the Hemocontrol biofeedback system: a prospective medium-term study, Nephrol Dial Transplant, 2001;16:328–34.
  68. Selby NM, Lambie SH, Camici PG, et al., Occurrence of regional left ventricular dysfunction in patients undergoing standard and biofeedback dialysis, Am J Kidney Dis, 2006;47:830–41.
  69. Dasselaar JJ, Huisman RM, de Jong PE, et al., Effects of relative blood volume-controlled hemodialysis on blood pressure and volume status in hypertensive patients, ASAIO J, 2007;53:357–64.
  70. Santoro A, Rindi P, Capriolo R, et al., Automatic blood volume control (BVT): a technological tool for hypertension therapy in HD patients, Presented at: ASN 39th Annual Meeting 2006, San Diego, California, 14–19 November, 2006.

Suggest a topic for future coverage