FLFaydra I. Lieveld

Faydra I. Lieveld

*This is an algorithmically generated author record based on publicly available information.

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The organizations/institutes from the scholar's latest article


Faydra I. Lieveld has a total of 10 co-authors. Here are the top co-authors by number of shared publications:

  • Andy I. M. Hoepelman

    Department of Internal Medicine and Infectious Diseases, University Medical Center Utrecht, Utrecht, The Netherlands

    1 shared publication
  • Bernhard W. M. Spanier

    Department of Gastroenterology and Hepatology, Rijnstate Hospital, Arnhem, The Netherlands

    1 shared publication
  • Clemens Richter

    Department of Internal Medicine and Infectious Diseases, Rijnstate Hospital, Arnhem, The Netherlands

    1 shared publication
  • Colette Smit

    Stichting HIV Monitoring, Amsterdam, The Netherlands

    1 shared publication
  • Elisabeth H. Gisolf

    Department of Internal Medicine and Infectious Diseases, Rijnstate Hospital, Arnhem, The Netherlands

    1 shared publication
  • Jan M. Vrolijk

    Department of Gastroenterology and Hepatology, Rijnstate Hospital, Arnhem, The Netherlands

    1 shared publication

Latest Publications

  • Liver decompensation in HIV/Hepatitis B coinfection in the combination antiretroviral therapy era does not seem increased compared to hepatitis B mono‐infection

    by Faydra I. Lieveld, Colette Smit, Clemens Richter, Karel J. van Erpecum, Bernhard W. M. Spanier, Elisabeth H. Gisolf, Jan M. Vrolijk, Peter D. Siersema, Andy I. M. Hoepelman, Peter Reiss, et al.

    Background & Aims: HIV/hepatitis B virus (HBV) coinfected subjects are thought to have faster progression to end‐stage liver disease (ESLD) than HBV mono‐infected subjects. We assessed whether this remains in the current cART‐era.Methods: Data from subjects with follow‐up completion post‐2003 were compared between HIV/HBV coinfected subjects in the Dutch HIV Monitoring database and HBV mono‐infected subjects from two centres. The primary outcomes of composite ESLD included portal hypertension, decompensated cirrhosis, hepatocellular carcinoma, liver transplantation and liver‐related mortality. Outcomes were analysed using time‐dependent cause‐specific Cox regression models adjusted for follow‐up time and relevant covariates. Subset‐analyses were done in subjects with follow‐up pre‐2003.Results: In the 1336 co‐ vs 742 mono‐infected subjects, coinfected subjects had no increased probability for ESLD compared to mono‐infected subjects (cHR 0.7 (95% CI 0.4‐1.1), but had increased probabilities for all‐cause (cHR 7.4 [4.9‐11.1]) and liver‐related mortality (cHR 3.4 [1.6‐7.5]). In the current combined cohort, treatment with tenofovir or entecavir was inversely associated with ESLD, all‐cause and liver‐related mortality (cHR 0.4 [95% CI 0.3‐0.7], cHR 0.003 [0.001‐0.01]), cHR 0.007 [0.001‐0.05]). Other predictors for ESLD were older age, being of Sub‐Sahara African descent, increased alanine aminotransferase levels and hepatitis C virus coinfection. While the probability for all‐cause mortality was increased in coinfected subjects, this rate decreased compared to pre‐2003 (HR 40.2 (95% CI: 8.7‐186.2).Conclusions: HIV/HBV coinfected patients no longer seem to be at increased risk for progression to ESLD compared to HBV mono‐infected patients, likely due to widespread use of highly effective cART with dual HBV and HIV activity.