Development and external validation of a model to predict multidrug‐resistant bacterial infections in patients with cirrhosis

Author:

Marciano Sebastián1ORCID,Piano Salvatore2ORCID,Singh Virendra3ORCID,Caraceni Paolo45ORCID,Maiwall Rakhi6ORCID,Alessandria Carlo7,Fernandez Javier891011,Kim Dong Joon12ORCID,Kim Sung Eun13ORCID,Soares Elza14ORCID,Marino Mónica15,Vorobioff Julio16,Merli Manuela17ORCID,Elkrief Laure18,Vargas Victor19,Krag Aleksander20,Singh Shivaram21,Elizondo Martín22,Anders Maria M23,Dirchwolf Melisa24,Mendizabal Manuel25,Lesmana Cosmas R. A.262728,Toledo Claudio29,Wong Florence30ORCID,Durand Francois31ORCID,Gadano Adrián1,Giunta Diego H32,Angeli Paolo2,

Affiliation:

1. Liver Unit and Research Department Hospital Italiano Buenos Aires Buenos Aires Argentina

2. Unit of Internal Medicine and Hepatology, Department of Medicine University of Padova Padova Italy

3. Department of Hepatology Postgraduate Institute of Medical Education and Research Chandigarh India

4. Unit of Semeiotics, Liver and Alcohol‐related diseases IRCCS Azienda Ospedaliero‐Universitaria di Bologna Bologna Italy

5. Department of Medical and Surgical Sciences University of Bologna Bologna Italy

6. Institute of Liver and Biliary Sciences New Delhi India

7. Division of Gastroenterology and Hepatology, Città della Salute e della Scienza Hospital University of Turin Turin Italy

8. Liver ICU, Liver Unit, Hospital Clinic University of Barcelona Barcelona Catalonia Spain

9. Institut d'Investigacions Biomèdiques August‐PiSunyer Barcelona Catalonia Spain

10. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas Barcelona Catalonia Spain

11. European Foundation of Chronic Liver Failure (EF‐Clif) Barcelona Catalonia Spain

12. Department of Internal Medicine Hallym University College of Medicine Chuncheon Republic of Korea

13. Division of Gastroenterology and Hepatology, Department of Internal Medicine Hallym Sacred Heart Hospital, College of Medicine, Hallym University Anyang City Republic of Korea

14. Gastroenterology Division, Medicine Department, Faculty of Medical Sciences University of Campinas (UNICAMP) Campinas São Paulo Brazil

15. Liver Unit Hospital Dr. Carlos B. Udaondo Buenos Aires Argentina

16. Medical School Rosario University Rosario Argentina

17. Department of translation and precision medicine University of Rome Sapienza Rome Italy

18. Service de Transplantation, Service d'Hépato‐gastroentérologie Hôpitaux Universitaires de Genève Geneva Switzerland

19. Liver Unit, Department of Internal Medicine, Hospital Vall d'Hebron Universitat Autònoma de Barcelona, CIBERehd Barcelona Spain

20. Department of Gastroenterology and Hepatology Odense University Hospital Odense Denmark

21. Department of Gastroenterology S.C.B. Medical College Cuttack India

22. Bi‐Institutional Liver Transplant Unit Center (Hospital de Clínicas—Military Hospital) Montevideo Uruguay

23. Liver Unit Hospital Aleman Buenos Aires Buenos Aires Argentina

24. Liver Unit Hospital Privado de Rosario Rosario Argentina

25. Liver Unit Hospital Universitario Austral Pilar Argentina

26. Hepatobiliary Division, Department of Internal Medicine Dr. Cipto Mangunkusumo Hospital Jakarta Indonesia

27. Medical Faculty Universitas Indonesia Jakarta Indonesia

28. Digestive Disease & GI Oncology Centre Medistra Hospital Jakarta Indonesia

29. Gastroenterology Unit, Hospital Valdivia Universidad Austral de Chile Valdivia Chile

30. Division of Gastroenterology, Department of Medicine University of Toronto Toronto Ontario Canada

31. Hepatology & Liver Intensive Care, Hospital Beaujon University Paris Diderot Paris France

32. Hospital Italiano Buenos Aires University Buenos Aires Argentina

Abstract

AbstractWith the increasing rate of infections caused by multidrug‐resistant organisms (MDRO), selecting appropriate empiric antibiotics has become challenging. We aimed to develop and externally validate a model for predicting the risk of MDRO infections in patients with cirrhosis.MethodsWe included patients with cirrhosis and bacterial infections from two prospective studies: a transcontinental study was used for model development and internal validation (n = 1302), and a study from Argentina and Uruguay was used for external validation (n = 472). All predictors were measured at the time of infection. Both culture‐positive and culture‐negative infections were included. The model was developed using logistic regression with backward stepwise predictor selection. We externally validated the optimism‐adjusted model using calibration and discrimination statistics and evaluated its clinical utility.ResultsThe prevalence of MDRO infections was 19% and 22% in the development and external validation datasets, respectively. The model's predictors were sex, prior antibiotic use, type and site of infection, MELD‐Na, use of vasopressors, acute‐on‐chronic liver failure, and interaction terms. Upon external validation, the calibration slope was 77 (95% CI .48–1.05), and the area under the ROC curve was .68 (95% CI .61–.73). The application of the model significantly changed the post‐test probability of having an MDRO infection, identifying patients with nosocomial infection at very low risk (8%) and patients with community‐acquired infections at significant risk (36%).ConclusionThis model achieved adequate performance and could be used to improve the selection of empiric antibiotics, aligning with other antibiotic stewardship program strategies.

Publisher

Wiley

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