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Jornal Português de Gastrenterologia

versão impressa ISSN 0872-8178

J Port Gastrenterol. v.14 n.1 Lisboa jan. 2007

 

Utilidade da elastografia hepática transitória (FibroScan®) na cirrose hepática

R. Marinho*, F. Serejo*, J. Velosa*, M. Carneiro de Moura*

 

Resumo

Introdução: A elastografia hepática transitória (Fibro-Scan®), é um sistema de ultrasons não invasivo que avalia a fibrose hepática. Objectivo: Avaliar a utilidade do FibroScan® no diagnóstico de cirrose. Métodos: A elastografia (Kilopascals, kPa) realizou-se em 120 doentes: 61 com cirrose de diversas etiologias (31 com cirrose VHC) e 59 sem cirrose (55 com hepatite C crónica) e em 25 controlos. Resultados: A mediana na cirrose foi 16,9 kPa (4,5 - 70,5), naqueles sem cirrose 5,8 kPa (3,8 - 19,6), p < 0,05. Os valores mais altos foram encontrados naqueles com mais de um factor etiológico (VHB, VHC, etanol, VIH), 57 kPa (7,7 - 75) comparativamente com aqueles com apenas um factor, 14 kPa (4,5 - 46,4), p < 0,001. A mediana na cirrose VHC foi 17,1 kPa (6,0 - 40,3), na VHB 13,1 kPa (7,4 - 19,8) e na alcoólica 13,4 kPa (6,8 - 35,8), P = NS. Para um cut-off de 12 kPa a sensibilidade foi 64%, especificidade 98%, o valor predizente positivo 98% (VPP) e o valor predizente negativo 73%, AUROC 0,93. Conclusões: O FibroScan® é um exame não invasivo com utilidade diagnóstica na cirrose. Para valores superiores a 12 kPa o FibroScan® tem um VPP e uma especificidade muito elevados.

 

Clinical usefulness of transitory hepatic elastography (FibroScan®) in the diagnosis of cirrhosis

Summary

Introduction: FibroScan®, is a non-invasive ultrasound device used to quantify liver fibrosis. Aims:Assess clinical usefulness of the FibroScan® in the diagnosis of cirrhosis. Methods: The FibroScan® was performed (kilopascals, kPa) on 120 patients, all with a liver biopsy: 61 with liver cirrhosis of diverse etiologies (31 hepatitis C) and 59 without cirrhosis (55 with chronic hepatitis C). Results: The median in cirrhosis was 16.9 kPa (4.5 - 70.5), and in those without cirrhosis 5.8 kPa (3.8 - 19.6), p < 0,05. The highest values in patients with cirrhosis were found in those with combined causes for liver disease such as hepatitis B, hepatitis C, alcohol, HIV: 57 kPa (7.7 - 75) compared to those with one only factor, 14 kPa (4.5 - 46.4), p <0.001. The median was not different between the different causes of liver cirrhosis. For a cut-off level of 12 kPa and considering all causes of cirrhosis, the sensitivity was 64%, specificity 98%, positive predictive value (PPV) 98% and negative predictive value (NPV) 73%, AUROC 0.93. Conclusions: FibroScan® is a clinically useful non-invasive tool in the assessment of liver cirrhosis. For a cut-off level of 12 kPa the PPV and the specificity were very high.

 

 

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Bibliografia

1. Chiaramonte M, Stroffolini T, Vian A, Stazi MA, Floreani A, Lorenzoni U, et al. Rate of incidence of hepatocellular carcinoma in patients with compensated viral cirrhosis. Cancer 1999;85: 2132-2137.        [ Links ]

2. Bravo AA, Sheth SG, Chopra S. Liver biopsy. N Engl J Med 2001;344: 495-500. 3. Colloredo G, Guido M, Sonzogni A, Leandro G. Impact of liver biopsy size on istological evaluation of chronic viral hepatitis: the smaller the sample, the milder the disease. J Hepatol 2003;39: 239-244.

4. Maharaj B, Maharaj RJ, Leary WP, Cooppan RM, Naran AD, Pirie D, et al. Sampling variability and its influence on the diagnostic yield of percutaneous needle biopsy of the liver. Lancet 1986;1: 523-525.

5. Intraobserver and interobserver variations in liver biopsy interpretation in patients with chronic hepatitis C. The French METAVIR Cooperative Study Group. Hepatology 1994;20(1 Pt 1): 15-20.

6. Mukherjee S, Sorrell MF. Noninvasive tests for liver fibrosis. Semin Liver Dis 2006;26: 337-347.

7. Imbert-Bismut F, Ratziu V, Pieroni L, Charlotte F, Benhamou Y, Poynard T, et al. MULTIVIRC Group. Biochemical markers of liver fibrosis in patients with hepatitis C virus infection: a prospective study. Lancet 2001;357:1069-1075.

8. Le Calvez S, Thabut D, Messous D, Munteanu M, Ratziu V, Imbert-Bismut F, et al. The predictive value of Fibrotest vs. APRI for the diagnosis of fibrosis in chronic hepatitis C. Hepatology 2004;39: 862-863

9. Wai CT, Greenson JK, Fontana RJ, Kalbfleisch JD, Marrero JA, Conjeevaram HS, et al. A simple noninvasive index can predict both significant fibrosis and cirrhosis in patients with chronic hepatitis C. Hepatology 2003;38: 518-526.

10. Forns X, Ampurdanes S, Llovet JM, Aponte J, Quinto L, Martinez-Bauer E, et al. Identification of chronic hepatitis C patients without hepatic fibrosis by a simple predictive model. Hepatology 2002;36(4 Pt 1): 986-992.

11. Saito H, Tada S, Nakamoto N, Kitamura K, Horikawa H, Kurita S, et al. Efficacy of non-invasive elastometry on staging of hepatic fibrosis. Hepatol Res 2004;29: 97-103.

12. Sandrin L, Fourquet B, Hasquenoph JM, Yon S, Fournier C, Mal F, et al. Transient elastography: a new noninvasive method for assessment of hepatic fibrosis. Ultrasound Med Biol 2003;29:1705-1713.

13. Castera L, Vergniol J, Foucher J, Le Bail B, Chanteloup E, Haaser M, et al. Prospective comparison of transient elastography, Fibrotest, APRI, and liver biopsy for the assessment of fibrosis in chronic hepatitis C. Gaatroenterology 2005;128: 343-350.

14. Ziol M, Handra-Luca A, Kettaneh A, Christidis C, Mal F, Kazemi F, et al Noninvasive assessment of liver fibrosis by measurement of stiffness in patients with chronic hepatitis C. Hepatology 2005;41: 48-54.

15. Zeuzem S, Diago M, Gane E, Reddy KR, Pockros P, Prati D, Et al. Peginterferon alfa-2a (40 kilodaltons) and ribavirin in patients with chronic hepatitis C and normal aminotransferase levels. Gastroenterology 2004;127: 1724-1732.

16. Moreno-Otero R, Trapero-Marugan M, Mendoza J. Liver fibrosis assessment by transient elastography in hepatitis C patients with normal alanine aminotransferase. Gut 2006;55: 1055-1066.

17. Bedossa P, Dargere D, Paradis V. Sampling variability of liver fibrosis in chronic hepatitis C. Hepatology 2003;38: 1449-1457.

18. Strassburg CP, Manns MP. Approaches to liver biopsy techniquesrevisited. Semin Liver Dis 2006;26: 318-327.

19. Colletta C, Smirne C, Fabris C, Toniutto P, Rapetti R, Minisini R, et al. Value of two noninvasive methods to detect progression of fibrosis among HCV carriers with normal aminotransferases. Hepatology 2005;42: 838-845.

20. de Ledinghen V, Douvin C, Kettaneh A, Ziol M, Roulot D, Marcellin P, et al. Diagnosis of hepatic fibrosis and cirrhosis by transient elastography in HIV/hepatitis C virus-coinfected patients. J Acquir Immune Defic Syndr 2006;41: 175-179.

21. Foucher J, Chanteloup E, Vergniol J, Castera L, Le Bail B, Adhoute X, et al. Diagnosis of cirrhosis by transient elastography (FibroScan): a prospective study. Gut 2006;55: 403-408.

22. Ganne-Carrie N, Ziol M, de Ledinghen V, Douvin C, Marcellin P, Castera L, et al. Accuracy of liver stiffness measurement for the diagnosis of cirrhosis in patients with chronic liver diseases. Hepatology 2006;44: 1511-1517.

23. Corpechot C, El Naggar A, Poujol-Robert A, Ziol M, Wendum D, Chazouilleres O, et al. Assessment of biliary fibrosis by transient elastography in patients with PBC and PSC. Hepatology 2006;43:1118-1124.

24. Foucher J, Castera L, Bernard PH, Adhoute X, Laharie D, Bertet J, et al. Prevalence and factors associated with failure of liver stiffness measurement using FibroScan in a prospective study of 2114 examinations. Eur J Gastroenterol Hepatol 2006;18: 411-412.

25. Kazemi F, Kettaneh A, N'kontchou G, Pinto E, Ganne-Carrie N, Trinchet JC, et al. Liver stiffness measurement selects patients with cirrhosis at risk of bearing large oesophageal varices. J Hepatol 2006;45: 230-235.

26. Lu SN, Wang JH, Liu SL, Hung CH, Chen CH, Tung HD, et al. Thrombocytopenia as a surrogate for cirrhosis and a marker for the identification of patients at high-risk for hepatocellular carcinoma. Cancer 2006;107: 2212-22.

27. Graham CS, Baden LR, Yu E, Mrus JM, Carnie J, Heeren T, et al. Influence of human immunodeficiency virus infection on the course of hepatitis c virus infection: a meta-analysis. Clin Infect Dis 2001;33: 562-569.

28. Marcellin P, de Ledinghen V, Dhumeaux D, Poupon R, Ziol M, Bedossa P, et al. Non-invasive assessment of liver fibrosis in chronic hepatitis B using FibroScan®. Hepatology 2005; 42(Suppl): 715A-716A.

29. Barreiro P, Martin-Carbonero L, Nunez M, Rivas P, Morente A, Simarro N, et al. Predictors of liver fibrosis in HIV-infected patients with chronic hepatitis C virus (HCV) infection: assessment using transient elastometry and the role of HCV genotype 3. Clin Infect Dis 2006;42: 1032-1039.

30. Laharie D, Zerbib F, Adhoute X, Boue-Lahorgue X, Foucher J, Castera L, et al. Diagnosis of liver fibrosis by transient elastography (FibroScan) and non-invasive methods in Crohn's disease patients treated with methotrexate. Aliment Pharmacol Ther 2006;23: 1621-1628.

31. Melin P, Dacon A, Gauchet A, Schoeny M, Diebold MD. Dépistage non invasif de la fibrose hépatique. Intérêt du FibroScan® en consultation d'alcoologie. Alcoologie et Addictologie 2005;27: 191-196.

32. Masaki N, Imamura M, Kikuchi Y, Oka S. Usefulness of elastometry in evaluating the extents of liver fibrosis in hemophiliacs coinfected with hepatitis C virus and human immunodeficiency virus. Hepatol Res 2006;35: 135-139.

33. Ghany MG, Doo E. Assessment of liver fibrosis: palpate, poke or pulse? Hepatology 2005;42: 759-761.

 

Correspondência:

Rui Tato Marinho

Av. Prof. Egas Moniz

1600 Lisboa, Portugal

Tel.: 916984040

E-mail: rui.marinho@mail.telepac.pt

 

* Serviço de Gastrenterologia e Hepatologia, Hospital Santa Maria de Lisboa, Faculdade de Medicina de Lisboa, Instituto de Medicina Molecular, Lisboa, Portugal.

 

Recebido para publicação: 12/01/2007

Aceite para publicação: 22/01/2007