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Predicting clinical decompensation in patients with cirrhosis using the Hepquant-SHUNT test.
Fallahzadeh, Mohammad Amin; Hansen, Daniel J; Trotter, James F; Everson, Gregory T; Saracino, Giovanna; Rahimi, Robert S; Helmke, Steve; Boutte, Jodi; Asrani, Sumeet K.
Afiliação
  • Fallahzadeh MA; Baylor University Medical Center, Dallas, TX, USA.
  • Hansen DJ; Baylor University Medical Center, Dallas, TX, USA.
  • Trotter JF; Baylor University Medical Center, Dallas, TX, USA.
  • Everson GT; University of Colorado Denver School of Medicine, Aurora, CO, USA.
  • Saracino G; HepQuant LLC, Greenwood Village, CO, USA.
  • Rahimi RS; Baylor University Medical Center, Dallas, TX, USA.
  • Helmke S; Baylor University Medical Center, Dallas, TX, USA.
  • Boutte J; University of Colorado Denver School of Medicine, Aurora, CO, USA.
  • Asrani SK; HepQuant LLC, Greenwood Village, CO, USA.
Aliment Pharmacol Ther ; 53(8): 928-938, 2021 04.
Article em En | MEDLINE | ID: mdl-33556192
ABSTRACT

BACKGROUND:

Early identification of risk for decompensation in clinically stable cirrhotic patients helps specialists target early interventions and supports effective referrals from primary care providers to specialty centres.

AIMS:

To examine whether the HepQuant-SHUNT test (HepQuant LLC, Greenwood Village, Colorado, USA) predicts decompensation and the need for liver transplantation, hospitalisation or liver-related death.

METHODS:

Thirty-five compensated and 35 subjects with a previous episode of decompensation underwent the SHUNT Test and were followed for a median of 4.2 years. The disease severity index (DSI) (range 0-50) was examined for association with decompensation in compensated patients; and liver transplantation, liver-related death, and the number and days of liver related hospitalisations in all. DSI prediction of decompensation was also evaluated in 84 subjects with compensated cirrhosis from the Hepatitis C Antiviral Long-Term Treatment against Cirrhosis Trial (HALT-C) followed for a median of 5.8 years.

RESULTS:

At baseline, subjects with prior decompensation had significantly higher DSI than compensated subjects (32.6 vs 20.9, P < 0.001). DSI ≥24 distinguished the decompensated from the compensated patients and independently predicted adverse clinical outcomes (hazard ratio 4.92, 95% confidence interval 1.42-17.06). In the HALT-C cohort, 65% with baseline DSI ≥24 vs 19% with DSI <24 experienced adverse clinical outcomes (relative risk 3.45, P < 0.0001).

CONCLUSIONS:

The SHUNT test is a novel, noninvasive test that predicts risk of decompensation in previously compensated patients. DSI ≥24 is independently associated with risk for clinical decompensation, liver transplantation, death and hospitalisation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hepatite C / Falência Hepática Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Aliment Pharmacol Ther Assunto da revista: FARMACOLOGIA / GASTROENTEROLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hepatite C / Falência Hepática Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Aliment Pharmacol Ther Assunto da revista: FARMACOLOGIA / GASTROENTEROLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos