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Jornal Português de Gastrenterologia

versão impressa ISSN 0872-8178

J Port Gastrenterol. v.16 n.2 Lisboa mar. 2009

 

M.E.L.D.-XI: Um factor prognóstico de mortalidade operatória na Cirrose Hepática?

Estudo retrospectivo de 190 doentes

M.E.L.D.-XI na avaliação do risco cirúrgico

 

B. Pinto Costa, F. Castro Sousa, C. Carvalho, M. Serôdio 1

 

RESUMO

Estudos recentes sugerem que o M.E.L.D. (“Model for End-stage Liver Disease”) pode constituir um factor preditivo de mortalidade operatória em doentes cirróticos. Em 2007, foi proposto um índice análogo (M.E.L.D.-XI), determinado a partir da creatininémia e da bilirrubinémia, para definir a prioridade para transplante dos doentes cirróticos medicados com anti-vitamínicos K. Com o objectivo de avaliar o valor do M.E.L.D-XI na quantificação do risco cirúrgico, comparar o seu valor prognóstico com o M.E.L.D. e a classificação de Child-Turcotte-Pugh e determinar se a sua capacidade prognóstica aumenta com a incorporação do sódio (iM.E.L.D.-XI), efectuou-se um estudo retrospectivo de 190 doentes cirróticos operados entre 1993 e 2008. O M.E.L.D.-XI demonstrou uma significativa capacidade prognóstica de mortalidade operatória (aaR.O.C.=71%; p=0,001), comparável à do M.E.L.D. (aaR.O.C.=76%; p=0,0001) e à da classificação de Child-Turcotte-Pugh (aaR.O.C.=72%; p=0,001). O iM.E.L.D.-XI constituiu um significativo factor prognóstico de mortalidade em cirurgia electiva (aaR.O.C.=83%; p=0,024), com potencial preditivo superior ao iM.E.L.D. (aaR.O.C.=80%; p=0,044), ao M.E.L.D. (aaR.O.C.=61%; n.s.) e à classificação de Child-Turcotte-Pugh (aaR.O.C.=54%; n.s.). O M.E.L.D.-XI e o iM.E.L.D.-XI revelaram-se factores preditivos de mortalidade operatória em doentes cirróticos, com boa correlação com o M.E.L.D. e o iM.E.L.D., podendo ser úteis nos casos de eventual dissociação entre o I.N.R. e a função hepática e na normalização das alterações decorrentes da variabilidade inter-laboratorial do I.N.R.

Palavras-chave: M.E.L.D.-XI, M.E.L.D., iM.E.L.D., Child-Turcotte-Pugh, risco cirúrgico, cirrose.

 

SUMMARY

Recent studies suggested that M.E.L.D. (Model for End-stage Liver Disease) may represent a predictive factor of operative mortality in cirrhotic patients. In 2007, a similar parameter was proposed (M.E.L.D.-XI), based on creatininemia and bilirrubinemia, to be used in the definition of priority for transplantation in patients requiring anticoagulant therapy. To evaluate the value of M.E.L.D.-XI in surgical risk evaluation, to compare its prognostic value with M.E.L.D. and Child-Turcotte-Pugh classification and to determine if its prognostic potential increases with incorporation of natremia (iM.E.L.D.-XI) a retrospective study of 190 operated cirrhotic patients was undertaken. IM.E.L.D. revealed a significant predictive capacity of operative mortality (auR.O.C.=71%; p=0,001), similar to M.E.L.D. (auR.O.C.=76%; p=0,0001) and Child-Turcotte-Pugh classification (auR.O.C.=72%; p=0,001). IM.E.L.D.-XI represented a significant prognostic factor of mortality following elective surgery (auR.O.C.=83%; p=0,024) with better predictive potential than iM.E.L.D. (auR.O.C.=80%; p=0,044), M.E.L.D. (auR.O.C.=61%; n.s.) and Child-Turcotte-Pugh classification (auR.O.C.=54%; n.s.). M.E.L.D.-XI and iM.E.L.D.-XI scores revealed to be predictive parameters of operative mortality in cirrhotic patients, with good correlation with M.E.L.D. and iM.E.L.D.; they may be useful in cases of dissociation of I.N.R. in relation to liver function and in normalization of discrepancies associated with interlaboratory variability of I.N.R.. Further studies are needed to clarify the applicability of M.E.L.D.-XI in surgical risk evaluation of cirrhotic patients.

Keywords: M.E.L.D.-XI, M.E.L.D., iM.E.L.D., Child-Turcotte-Pugh, surgical risk, cirrhosis

 

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Bibliografia

1. Freeman RB: MELD: the holy grail of organ allocation? J Hepato 2005: 42:16-20

2. Malinchoc M, Kamath PS, Gordon FD, Peine CJ, Rank J, ter Borg PC: A model to predict poor survival in patients undergoing transjugular intrahepatic portosystemic shunts. Hepatology 2000; 31:864-71

3. Teh SH, Nagorney DM, Stevens SR, Offord KP, Terneau TM, Plevak DJ, et al.: Risk factors for mortality after surgery in patients with cirrhosis. Gastroenterology 2007; 132:1261-9

4. Northup PG, Wanomaker RC, Lee VD, Adams RB, Berg CL: Model for End-Stage Liver Disease (MELD) predicts nontransplant surgical mortality in patients with cirrhosis. Ann Surg 2005; 242:244-51

5. Befeler AS, Palmer DE, Hoffman M, Longo W, Solomon H, Di Bisceglia AM: The safety of intra-abdominal surgery in patients with cirrhosis: Model for End-Stage Liver Disease is superior to Child-Turcotte-Pugh classification in predicting outcome. Arch Surg 2005; 140:650-4

6. Farnsworth N, Fagan SP, Berger DH, Awad SS: Child-Turcotte-Pugh versus MELD score as a predictor of outcome after elective and emergent surgery in cirrhotic patients. Am J Surg 2004; 188:580-3

7. Perkins L, Jeffries M, Patel T: Utility of preoperative scores for predicting morbidity after cholecystectomy in patients with cirrhosis. Clin Gastroenterol Hepatol 2004; 2:1123-8

8. Cucchetti A, Ercolani G, Vivarelli M, Cescon M, Ravaioli M, La Barba G, et al.: Impact of Model for End-Stage Liver Disease (MELD) score on prognosis after hepatectomy for hepatocellular carcinoma on cirrhosis. Liver Transpl 2006; 12:966-71

9. Pugh RN, Murray-Lyon IM, Dawson JL, Pietroni MC, Williams R: Transection of the oesophagus for bleeding oesophageal varices. Br J Surg 1973; 60:646-9

10. Durand F, Valla D: Assessment of the prognosis of cirrhosis: Child-Pugh versus MELD. J Hepatol 2005; 42:S100-7.

11. Huo TI, Lee SD, Lin HC: Selecting an optimal prognostic system for liver cirrhosis: the model for end-stage liver disease and beyond. Liver Int 2008; 28:606-13

12. Kamath PS, Kim WR, Advanced Liver Disease Study Group: The model for end-stage liver disease (MELD). Hepatology 2007; 45:797-805

13. Durand F; Valla D: Assessment of prognosis of cirrhosis. Semin Liver Dis 2008; 28:110-22

14. Cholongitas E, Papatheodoridis GV, Vangeli M, Terreni N, Patch D, Burroughs AK: Systematic review: the model for end-stage liver disease – should it replace Child-Pugh’s classification for assessing prognosis in cirrhosis? Aliment Pharmacol Ther 2005;22:1079-89

15. Luca A, Angermayr B, Bertolini G, Koening F, Vizzini G, Ploner M, et al.: An integrated Meld Model including serum sodium and age improves the prediction of early mortality in patients with cirrhosis. Liver Transp 2007; 13:1174-80

16. Huo T, Lin H, Huo SC, Lee P, Wu J, Lee F, et al.: Comparison of four model for end-stage liver disease-based prognostic systems for cirrhosis. Liver Transpl 2008; 14:837-44

17. Biggins SW, Kim WR, Terrault NA, Saab S, Balan V, Schiano T, et al.: Evidence-based incorporation of serum sodium concentration into MELD. Gastroenterology 2006; 130:1652-60

18. Londoño M, Cárdenas A, Guevara M, Quintó L, Heras D, Navasa M, et al: MELD score and serum sodium in the prediction of survival of patients with cirrhosis awaiting liver transplantation. Gut 2007; 56:1283-90.

19. Heuman DM, Mihas AA, Habib A, Gilles HS, Stravitz RT, Sanyal AJ, et al: MELD-XI: a rational approach to “sickest first” liver transplantation in cirrhotic patients requiring anticoagulant therapy. Liver Transp 2007; 13:30-7

20. Ferenci P, Lockwood A, Mullen K, Tarter R, Weissenborn K, Blei AT and Members of the Working Party: Hepatic encephalopathy - definition, nomenclature, diagnosis, and quantification: final report of the working party at the 11th World Congress of Gastroenterology, Vienna, 1998: Hepatology 2002; 35:716-21

21. ASA Physical Status Classification System. [American Society of Anaesthesiologists website]: www.asahq.org/clinical/physicalstatus.htm.2008. Accessed in February 28th, 2008.

22. Lorimer JW, Doumit G: Comorbidity is a major determinant of severity in acute diverticulitis. Am J Surg 2007; 193:681-5

23. Charlson ME, Szatrowski TP, Peterson J, Gold J: Validation of a combined comorbidity index. J Clin Epidemiol 1994; 47:1245-51

24. Sutton R, Bann S, Brooks M, Srin S: The surgical risk scale as an improved tool for risk-adjusted analysis in comparative surgical audit. Br J Surg 2002; 89:763-8

25. Neary WD, Prytherch D, Foy C, Heather BP, Earnshaw JJ: Comparison of different methods of risk stratification in urgent and emergency surgery. Br J Surg 2007; 94:1300-5

26. World Medical Association Declaration of Helsinki – Ethical principles for medical research involving human subjects. [World Medical Association’s website]: www.wma.net/e/policy/b3.htm. Accessed in December 23rd, 2008.

27. Durand F: Risk scores in cirrhotic patients: from non-transplant surgery to transplantation and back. J Hepatol 2006; 44:620-1

28. Pinto Costa B, Castro Sousa F, Carvalho C, Serôdio M, Moreira J: Importância do M.E.L.D. na avaliação do risco cirúrgico de doentes cirróticos – Análise preliminar de 98 casos. Revista Portuguesa de Cirurgia 2008; 5:7-18        [ Links ]

29. Ravaioli M, Masette M, Ridolfi L, Capelli M, Grazi GL, Venturoli N, et al: Laboratory test variability and model for end-stage liver disease score calculation: effect on liver allocation and proposal for adjustment. Transplantation 2007; 83:919-24

30. Lisman T, van Leeuwen Y, Adelmeijer J, Pereboom IT, Haagsma EB, van den Berg AP, et al: Interlaboratory variability in assessment of the model of end-stage liver disease score. Liver Int 2008; 28:1344-51

31. Trotter JF, Brimhall B, Arjal R, Phillips C: Specific laboratory methodologies achive higher Model for Endstage Liver Disease (MELD) scores for patients listed for liver transplantation. Liver Transpl 2004; 10:995-1000

32. Trotter JF, Olson J, Lefkowitz J, Smith AD, Arjal R, Kenison J: Changes in International Normalized Ratio (INR) and Model for Endstage Liver Disease (MELD) based on selection of clinical laboratory. Am J Transp 2007; 7:1624-8

33. Kenison J, Arjal R, Smith A, Brimhall B, Phillips C, Olson J et al.: Interlaboratory variation in INR leads to clinically relevant changes in MELD score: survey of US clinical laboratories. Am J Transpl 2006; 6 Suppl 2:333

34. Tripodi A, Caldwell SH, Hoffman M, Trotter JF, Sanyal AJ: Review article: the prothrombin time test as a measure of bleeding risk and prognosis in liver disease. Aliment Pharmacol Ther 2007; 26:141-8

35. Tripodi A, Chantarangkul V, Mannucci PM: The international normalized ratio to prioritize patients for liver transplantation: problems and possible solutions. J Thromb Haemost 2008; 6:243-8

 

1 Serviço de Cirurgia III dos Hospitais da Universidade de Coimbra

 

Correspondência:

Beatriz Pinto da Costa

Clínica Universitária de Cirurgia III

Hospitais da Universidade de Coimbra

Praceta Prof. Mota Pinto

3000-075 Coimbra

Telefone: 239400417

Fax: 239402111

beatrizpcosta@huc.min-saude.pt

 

Recebido para publicação: 29/11/2008

Aceite para publicação: 12/02/2009