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Number needed to treat with ursodeoxycholic acid therapy to prevent liver transplantation or death in primary biliary cholangitis.
Harms, Maren H; de Veer, Rozanne C; Lammers, Willem J; Corpechot, Christophe; Thorburn, Douglas; Janssen, Harry L A; Lindor, Keith D; Trivedi, Palak J; Hirschfield, Gideon M; Pares, Albert; Floreani, Annarosa; Mayo, Marlyn J; Invernizzi, Pietro; Battezzati, Pier Maria; Nevens, Frederik; Ponsioen, Cyriel Y; Mason, Andrew L; Kowdley, Kris V; Hansen, Bettina E; Buuren, Henk R van; van der Meer, Adriaan J.
  • Harms MH; Department of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • de Veer RC; Department of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Lammers WJ; Department of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Corpechot C; Service d'Hépatologie, Centre de Référence des Maladies Inflammatoires des Voies Biliaires, Hôpital Saint-Antoine, APHP, Paris, France.
  • Thorburn D; The Sheila Sherlock Liver Centre and UCL Institute for Liver and Digestive Health, Royal Free Hospital, London, UK.
  • Janssen HLA; Toronto Centre for Liver Disease, Francis Family Liver Clinic, Toronto Western Hospital Liver Centre, Toronto, Ontario, Canada.
  • Lindor KD; College of Health Solutions, Arizona State University, Phoenix, Arizona, USA.
  • Trivedi PJ; Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.
  • Hirschfield GM; Birmingham NIHR Biomedical Research Centre and Centre for Liver Research, University of Birmingham, Birmingham, UK.
  • Pares A; Toronto Centre for Liver Disease, Francis Family Liver Clinic, Toronto Western Hospital Liver Centre, Toronto, Ontario, Canada.
  • Floreani A; Birmingham NIHR Biomedical Research Centre and Centre for Liver Research, University of Birmingham, Birmingham, UK.
  • Mayo MJ; Liver Unit, Hospital Clínic, CIBERehd, IDIBAPS, University of Barcelona, Barcelona, Spain.
  • Invernizzi P; Department of Surgery, Oncology and Gastroenterology, Universita degli Studi di Padova, Padova, Italy.
  • Battezzati PM; Digestive and Liver Diseases, UT Southwestern Medical Center, Dallas, Texas, USA.
  • Nevens F; Division of Gastroenterology and Program for Autoimmune Liver Diseases, International Center for Digestive Health, Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy.
  • Ponsioen CY; Department of Health Sciences, University of Milan, Milano, Italy.
  • Mason AL; Department of Hepatology, UZ Leuven, Leuven, Belgium.
  • Kowdley KV; Department of Gastroenterology and Hepatology - location Academic Medical Center, Amsterdam University Medical Centres, Amsterdam, The Netherlands.
  • Hansen BE; Division of Gastroenterology and Hepatology, University of Alberta, Edmonton, Alberta, Canada.
  • Buuren HRV; Liver Care Network and Organ Care Research, Swedish Medical Center, Seattle, Washington, USA.
  • van der Meer AJ; Toronto Centre for Liver Disease, Francis Family Liver Clinic, Toronto Western Hospital Liver Centre, Toronto, Ontario, Canada.
Gut ; 69(8): 1502-1509, 2020 08.
Article en En | MEDLINE | ID: mdl-31843787
ABSTRACT

OBJECTIVE:

The clinical benefit of ursodeoxycholic acid (UDCA) in primary biliary cholangitis (PBC) has never been reported in absolute measures. The aim of this study was to assess the number needed to treat (NNT) with UDCA to prevent liver transplantation (LT) or death among patients with PBC.

METHODS:

The NNT was calculated based on the untreated LT-free survival and HR of UDCA with respect to LT or death as derived from inverse probability of treatment weighting-adjusted Cox proportional hazard analyses within the Global PBC Study Group database.

RESULTS:

We included 3902 patients with a median follow-up of 7.8 (4.1-12.1) years. The overall HR of UDCA was 0.46 (95% CI 0.40 to 0.52) and the 5-year LT-free survival without UDCA was 81% (95% CI 79 to 82). The NNT to prevent one LT or death within 5 years (NNT5y) was 11 (95% CI 9 to 13). Although the HR of UDCA was similar for patients with and without cirrhosis (0.33 vs 0.31), the NNT5y was 4 (95% CI 3 to 5) and 20 (95% CI 14 to 34), respectively. Among patients with low alkaline phosphatase (ALP) (≤2× the upper limit of normal (ULN)), intermediate ALP (2-4× ULN) and high ALP (>4× ULN), the NNT5y to prevent one LT or death was 26 (95% CI 15 to 70), 11 (95% CI 8 to 17) and 5 (95% CI 4 to 8), respectively.

CONCLUSION:

The absolute clinical efficacy of UDCA with respect to LT or death varied with baseline prognostic characteristics, but was high throughout. These findings strongly emphasise the incentive to promptly initiate UDCA treatment in all patients with PBC and may improve patient compliance.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ácido Ursodesoxicólico / Colagogos y Coleréticos / Cirrosis Hepática Biliar Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ácido Ursodesoxicólico / Colagogos y Coleréticos / Cirrosis Hepática Biliar Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2020 Tipo del documento: Article