Validation of MELD3.0 in 2 centers from different continents

Author:

Tejedor Marta1ORCID,Bellón José María23,Fernández de la Varga Margarita4,Peralta Peregrina5,Montalvá Eva6789,Selzner Nazia10ORCID,Berenguer Marina891112ORCID

Affiliation:

1. Hepatology, Hospital Universitario Infanta Elena, Valdemoro, Madrid, Spain

2. Biostatistics, Instituto de Investigación Sanitaria Gregorio Marañón (IISGM), Madrid, Spain

3. CIBERINFEC, ISCIII—CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain

4. Hepatology, Hospital Universitario y Politécnico La Fe, Valencia, Spain

5. Research, Toronto General Hospital, Toronto, Ontario, Canada

6. Department of Hepatobiliopancreatic Surgery and Transplantation Unit, Hospital Universitario y Politécnico La Fe, Valencia, Spain

7. Department of Medicine, University of Valencia, Valencia, Spain

8. Liver and Digestive Diseases Networking Biomedical Research Centre (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain

9. Instituto de Investigación Sanitaria (IIS) La Fe, Valencia, Spain

10. Transplant Hepatology, Ajmera Transplant Center, University of Toronto, Toronto, Ontario, Canada

11. Hepatology and Liver Transplant Unit, Hospital Universitario y Politécnico La Fe, Valencia, Spain

12. Medicine Department, University of Valencia, Valencia, Spain

Abstract

Background: MELD3.0 has been proposed to stratify patients on the liver transplant waiting list (WL) to reduce the historical disadvantage of women in accessing liver transplant. Our aim was to validate MELD3.0 in 2 unique populations. Methods: This study is a 2-center retrospective cohort study from Toronto, Canada, and Valencia, Spain, of all adults added to the liver transplant WL between 2015 and 2019. Listing indications whose short-term survival outcome is not adequately captured by the MELD score were excluded. All patients analyzed had a minimum follow-up of 3 months after inclusion in the WL. Results: Six hundred nineteen patients were included; 61% were male, with a mean age of 56 years. Mean MELD at inclusion was 18.00 ± 6.88, Model for End-Stage Liver Disease Sodium (MELDNa) 19.78 ± 7.00, and MELD3.0 20.25 ± 7.22. AUC to predict 90-day mortality on the WL was 0.879 (95% CI: 0.820, 0.939) for MELD, 0.921 (95% CI: 0.876, 0.967) for MELDNa, and 0.930 (95% CI: 0.888, 0.973) for MELD3.0. MELDNa and MELD3.0 were better predictors than MELD (p = 0.055 and p = 0.024, respectively), but MELD3.0 was not statistically superior to MELDNa (p = 0.144). The same was true when stratified by sex, although the difference between MELD3.0 and MELD was only significant for women (p = 0.032), while no statistical significance was found in either sex when compared with MELDNa. In women, AUC was 0.835 (95% CI: 0.744, 0.926) for MELD, 0.873 (95% CI: 0.785, 0.961) for MELDNa, and 0.886 (95% CI: 0.803, 0.970) for MELD3.0; differences for the comparison between AUC in women versus men for all 3 scores were nonsignificant. Compared to MELD, MELD3.0 was able to reclassify 146 patients (24%), the majority of whom belonged to the MELD 10–19 interval. Compared to MELDNa, it reclassified 68 patients (11%), most of them in the MELDNa 20–29 category. Conclusions: MELD3.0 has been validated in centers with significant heterogeneity and offers the highest mortality prediction for women on the WL without disadvantaging men. However, in these cohorts, it was not superior to MELDNa.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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