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Respecto a la jurisprudencia nacional

In document Biblioteca de Derecho y CC. Políticas (página 175-178)

CAPITULO V: “CONTROL DE CONSTITUCIONALIDAD”

III. HALLAZGOS Y DISCUSIÓN

III.2. Discusión

III.2.2. Respecto a la jurisprudencia nacional

Insuffi cient metabolic clearance correlates with inadequate treatment and should be avoided. However, it is not clear what the lowest acceptable dose of acute RRT is.

In the chronic setting, ESRD patients receiving thrice-weekly intermittent haemodi-alysis with URR <60 % had a higher mortality compared to patients with URR of 65–69 % (odds ratio for mortality 1.28 for URR of 55–59 % and 1.39 for URR

<55 %) [ 29 ]. Thrice-weekly IHD with an estimated URR <60 % provides azotemic control similar to that of approximately 10–15 mL/kg/h of CRRT. Since it is unlikely that critically ill patients have a lower requirement for RRT in comparison with stable haemodialysis patients, it has been suggested that CRRT doses of <15 ml/

kg/h are too low in critically ill patients, especially in the acute phases of illness.

High dose CRRT is associated with higher clearance of urea and creatinine but also increased losses of other substances. Some losses may be obvious (ie phos-phate) but others may be hidden and not immediately recognized, for instance trace elements and micronutrients [ 25 ]. There is also increasing recognition that high dose CRRT increases drug clearance and may potentially lead to sub-therapeutic

drug levels, including antibiotics, resulting in treatment failure [ 5 , 30 , 31 ].

The IVOIRE study clearly demonstrated reduced average elimination half-life of administered antibiotics when using high doses of 70 ml/kg/h [ 25 ].

Awareness about the potential dangers of increased clearance is necessary and close drug monitoring is essential when using RRT above the current recommended doses.

References

1. Ronco C, Ricci Z, Bellomo R. Current worldwide practice of dialysis dose prescription in acute renal failure. Curr Opin Crit Care. 2006;12(6):551–6.

2. Ricci Z, Ronco C, Bachetoni A, D’amico G, Rossi S, Alessandri E, et al. Solute removal during continuous renal replacement therapy in critically ill patients: convection versus diffusion. Crit Care. 2006;10(2):R67.

3. Ronco C, Bellomo R, Homel P, Brendolan A, Dan M, Piccinni P, et al. Effects of different doses in continuous veno-venous haemofi ltration on outcomes of acute renal failure: a prospective randomised trial. Lancet. 2000;356(9223):26–30.

4. Bellomo R, Cass A, Cole L, Finfer S, Gallagher M, Lo S, et al. Intensity of continuous renal- replacement therapy in critically ill patients. N Engl J Med. 2009;361(17):1627–38.

5. Bouman CS, Oudemans-van Straaten HM, Tijssen JG, Zandstra DF, Kesecioglu J. Effects of early high-volume continuous venovenous hemofi ltration on survival and recovery of renal function in intensive care patients with acute renal failure: a prospective, randomized trial. Crit Care Med. 2002;30(10):2205–11.

6. Palevsky PM, Zhang JH, O’Connor TZ, Chertow GM, Crowley ST, Choudhury D, et al.

Intensity of renal support in critically ill patients with acute kidney injury. N Engl J Med.

2008;359(1):7–20.

Key Messages

1. CRRT dose is expressed as the amount of dialysis/hemofi ltration fl ow delivered to the patient in ml/kg per hour.

2. Current international guidelines recommend delivering an effl uent volume of 20–25 ml/kg per hour for post-dilution CRRT in AKI, taking into account the degree of ‘pre-dilution’ and ‘fi lter-down’ time.

3. CRRT doses of <15 ml/kg per hour are believed to be too low in critically ill patient, especially in the acute phases of illness.

4. Increasing evidence suggests that fl uid overload is detrimental to both renal outcome and survival in critically ill patients with AKI. It is not possible to recommend a general net ultrafi ltration rate, instead the ultrafi ltration rate should be tailored to the patients’ needs and hemody-namic and fl uid status.

5. The application of high-volume hemofi ltration in severe sepsis and septic shock is not recommended based on the results of human studies.

6. Drug clearance, including antibiotics, is affected by (high dose) CRRT and may potentially lead to sub-therapeutic drug levels resulting in treatment failure.

7. Saudan P, Niederberger M, De SS, Romand J, Pugin J, Perneger T, et al. Adding a dialysis dose to continuous hemofi ltration increases survival in patients with acute renal failure. Kidney Int.

2006;70(7):1312–7.

8. Tolwani AJ, Campbell RC, Stofan BS, Lai KR, Oster RA, Wille KM. Standard versus high- dose CVVHDF for ICU-related acute renal failure. J Am Soc Nephrol. 2008;19(6):1233–8.

9. Lyndon WD, Wille KM, Tolwani AJ. Solute clearance in CRRT: prescribed dose versus actual delivered dose. Nephrol Dial Transplant. 2012;27(3):952–6.

10. Uchino S, Fealy N, Baldwin I, Morimatsu H, Bellomo R. Continuous is not continuous: the incidence and impact of circuit “down-time” on uraemic control during continuous veno- venous haemofi ltration. Intensive Care Med. 2003;29(4):575–8.

11. Faulhaber-Walter R, Hafer C, Jahr N, Vahlbruch J, Hoy L, Haller H, et al. The Hannover Dialysis Outcome study: comparison of standard versus intensifi ed extended dialysis for treatment of patients with acute kidney injury in the intensive care unit. Nephrol Dial Transplant. 2009;24(7):2179–86.

12. Schiffl H, Lang SM, Fischer R. Daily hemodialysis and the outcome of acute renal failure. N Engl J Med. 2002;346(5):305–10.

13. Jun M, Heerspink HJ, Ninomiya T, Gallagher M, Bellomo R, Myburgh J, et al. Intensities of renal replacement therapy in acute kidney injury: a systematic review and meta-analysis. Clin J Am Soc Nephrol. 2010;5(6):956–63.

14. Jorres A, John S, Lewington A, ter Wee PM, Vanholder R, Van BW, et al. A European Renal Best Practice (ERBP) position statement on the Kidney Disease Improving Global Outcomes (KDIGO) Clinical Practice Guidelines on Acute Kidney Injury: part 2: renal replacement therapy. Nephrol Dial Transplant. 2013;28(12):2940–5.

15. Khwaja A. KDIGO clinical practice guidelines for acute kidney injury. Nephron Clin Pract.

2012;120(4):179–84.

16. Bouchard J, Soroko SB, Chertow GM, Himmelfarb J, Ikizler TA, Paganini EP, et al. Fluid accumulation, survival and recovery of kidney function in critically ill patients with acute kidney injury. Kidney Int. 2009;76(4):422–7.

17. Payen D, de Pont AC, Sakr Y, Spies C, Reinhart K, Vincent JL. A positive fl uid balance is associated with a worse outcome in patients with acute renal failure. Crit Care. 2008;12(3):R74.

18. Bellomo R, Cass A, Cole L, Finfer S, Gallagher M, Lee J, et al. An observational study fl uid balance and patient outcomes in the Randomized Evaluation of Normal vs. Augmented Level of Replacement Therapy trial. Crit Care Med. 2012;40(6):1753–60.

19. Vaara ST, Korhonen AM, Kaukonen KM, Nisula S, Inkinen O, Hoppu S, et al. Fluid overload is associated with an increased risk for 90-day mortality in critically ill patients with renal replacement therapy: data from the prospective FINNAKI study. Crit Care. 2012;16(5):R197.

20. Bouman CS, Oudemans-van Straaten HM, Schultz MJ, Vroom MB. Hemofi ltration in sepsis and systemic infl ammatory response syndrome: the role of dosing and timing. J Crit Care.

2007;22(1):1–12.

21. Grootendorst AF, van Bommel EF, van der Hoven B, van Leengoed LA, van Osta AL. High volume hemofi ltration improves right ventricular function in endotoxin-induced shock in the pig. Intensive Care Med. 1992;18(4):235–40.

22. Boussekey N, Chiche A, Faure K, Devos P, Guery B, d’Escrivan T, et al. A pilot randomized study comparing high and low volume hemofi ltration on vasopressor use in septic shock.

Intensive Care Med. 2008;34(9):1646–53.

23. Cole L, Bellomo R, Journois D, Davenport P, Baldwin I, Tipping P. High-volume haemofi ltra-tion in human septic shock. Intensive Care Med. 2001;27(6):978–86.

24. Ghani RA, Zainudin S, Ctkong N, Rahman AF, Wafa SR, Mohamad M, et al. Serum IL-6 and IL-1-ra with sequential organ failure assessment scores in septic patients receiving high- volume haemofi ltration and continuous venovenous haemofi ltration. Nephrology (Carlton).

2006;11(5):386–93.

25. Joannes-Boyau O, Honore PM, Perez P, Bagshaw SM, Grand H, Canivet JL, et al. High- volume versus standard-volume haemofi ltration for septic shock patients with acute kidney injury (IVOIRE study): a multicentre randomized controlled trial. Intensive Care Med.

2013;39(9):1535–46.

26. Zhang P, Yang Y, Lv R, Zhang Y, Xie W, Chen J. Effect of the intensity of continuous renal replacement therapy in patients with sepsis and acute kidney injury: a single-center random-ized clinical trial. Nephrol Dial Transplant. 2012;27(3):967–73.

27. Clark E, Molnar AO, Joannes-Boyau O, Honore PM, Sikora L, Bagshaw SM. High-volume hemofi ltration for septic acute kidney injury: a systematic review and meta-analysis. Crit Care.

2014;18(1):R7.

28. Lehner G, Wiedermann C, Joannidis M. High volume hemofi ltration in critically ill patients – a systematic review and meta-analysis. Minerva Anestesiol. 2014;80(5):595–609.

29. Owen Jr WF, Lew NL, Liu Y, Lowrie EG, Lazarus JM. The urea reduction ratio and serum albumin concentration as predictors of mortality in patients undergoing hemodialysis. N Engl J Med. 1993;329(14):1001–6.

30. Jamal JA, Economou CJ, Lipman J, Roberts JA. Improving antibiotic dosing in special situa-tions in the ICU: burns, renal replacement therapy and extracorporeal membrane oxygenation.

Curr Opin Crit Care. 2012;18(5):460–71.

31. Roberts DM, Roberts JA, Roberts MS, Liu X, Nair P, Cole L, et al. Variability of antibiotic concentrations in critically ill patients receiving continuous renal replacement therapy: a multicentre pharmacokinetic study. Crit Care Med. 2012;40(5):1523–8.

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H.M. Oudemans-van Straaten et al. (eds.), Acute Nephrology for the Critical Care Physician, DOI 10.1007/978-3-319-17389-4_14

In document Biblioteca de Derecho y CC. Políticas (página 175-178)