TY - JOUR
T1 - Secondary Sclerosing Cholangitis Following Coronavirus Disease 2019 (COVID-19)
T2 - A Multicenter Retrospective Study
AU - Hunyady, Peter
AU - Streller, Lea
AU - Rüther, Darius F.
AU - Groba, Sara Reinartz
AU - Bettinger, Dominik
AU - Fitting, Daniel
AU - Hamesch, Karim
AU - Marquardt, Jens U.
AU - Mücke, Victoria T.
AU - Finkelmeier, Fabian
AU - Sekandarzad, Asieb
AU - Wengenmayer, Tobias
AU - Bounidane, Ayoub
AU - Weiss, Felicitas
AU - Peiffer, Kai Henrik
AU - Schlevogt, Bernhard
AU - Zeuzem, Stefan
AU - Waidmann, Oliver
AU - Hollenbach, Marcus
AU - Kirstein, Martha M.
AU - Kluwe, Johannes
AU - Kütting, Fabian
AU - Mücke, Marcus M.
N1 - Publisher Copyright:
© 2022 The Author(s). Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved.
© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
PY - 2023/2/1
Y1 - 2023/2/1
N2 - Background: Secondary sclerosing cholangitis (SSC) is a rare disease with poor prognosis. Cases of SSC have been reported following coronavirus disease 2019 (COVID-SSC). The aim of this study was to compare COVID-SSC to SSC in critically ill patients (SSC-CIP) and to assess factors influencing transplant-free survival. Methods: In this retrospective, multicenter study involving 127 patients with SSC from 9 tertiary care centers in Germany, COVID-SSC was compared to SSC-CIP and logistic regression analyses were performed investigating factors impacting transplant-free survival. Results: Twenty-four patients had COVID-SSC, 77 patients SSC-CIP, and 26 patients other forms of SSC. COVID-SSC developed after a median of 91 days following COVID-19 diagnosis. All patients had received extensive intensive care treatment (median days of mechanical ventilation, 48). Patients with COVID-SSC and SSC-CIP were comparable in most of the clinical parameters and transplant-free survival was not different from other forms of SSC (P =. 443, log-rank test). In the overall cohort, the use of ursodeoxycholic acid (UDCA) (odds ratio [OR], 0.36 [95% confidence interval {CI},. 16-.80], P =. 013; log-rank P <. 001) and high serum albumin levels (OR, 0.40 [95% CI,. 17-.96], P =. 040) were independently associated with an increased transplant-free survival, while the presence of liver cirrhosis (OR, 2.52 [95% CI, 1.01-6.25], P =. 047) was associated with worse outcome. Multidrug-resistant organism (MDRO) colonization or infection did not impact patients' survival. Conclusions: COVID-SSC and CIP-SSC share the same clinical phenotype, course of the disease, and risk factors for its development. UDCA may be a promising therapeutic option in SSC, though future prospective trials are needed to confirm our findings.
AB - Background: Secondary sclerosing cholangitis (SSC) is a rare disease with poor prognosis. Cases of SSC have been reported following coronavirus disease 2019 (COVID-SSC). The aim of this study was to compare COVID-SSC to SSC in critically ill patients (SSC-CIP) and to assess factors influencing transplant-free survival. Methods: In this retrospective, multicenter study involving 127 patients with SSC from 9 tertiary care centers in Germany, COVID-SSC was compared to SSC-CIP and logistic regression analyses were performed investigating factors impacting transplant-free survival. Results: Twenty-four patients had COVID-SSC, 77 patients SSC-CIP, and 26 patients other forms of SSC. COVID-SSC developed after a median of 91 days following COVID-19 diagnosis. All patients had received extensive intensive care treatment (median days of mechanical ventilation, 48). Patients with COVID-SSC and SSC-CIP were comparable in most of the clinical parameters and transplant-free survival was not different from other forms of SSC (P =. 443, log-rank test). In the overall cohort, the use of ursodeoxycholic acid (UDCA) (odds ratio [OR], 0.36 [95% confidence interval {CI},. 16-.80], P =. 013; log-rank P <. 001) and high serum albumin levels (OR, 0.40 [95% CI,. 17-.96], P =. 040) were independently associated with an increased transplant-free survival, while the presence of liver cirrhosis (OR, 2.52 [95% CI, 1.01-6.25], P =. 047) was associated with worse outcome. Multidrug-resistant organism (MDRO) colonization or infection did not impact patients' survival. Conclusions: COVID-SSC and CIP-SSC share the same clinical phenotype, course of the disease, and risk factors for its development. UDCA may be a promising therapeutic option in SSC, though future prospective trials are needed to confirm our findings.
UR - http://www.scopus.com/inward/record.url?scp=85139831142&partnerID=8YFLogxK
U2 - 10.1093/cid/ciac565
DO - 10.1093/cid/ciac565
M3 - Journal articles
C2 - 35809032
AN - SCOPUS:85139831142
VL - 76
SP - E179-E187
JO - Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
JF - Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
SN - 1058-4838
IS - 3
ER -