TY - JOUR
T1 - MELD 3.0 adequately predicts mortality and renal replacement therapy requirements in patients with alcohol-associated hepatitis
AU - Díaz, Luis Antonio
AU - Fuentes-López, Eduardo
AU - Ayares, Gustavo
AU - Idalsoaga, Francisco
AU - Arnold, Jorge
AU - Valverde, María Ayala
AU - Perez, Diego
AU - Gómez, Jaime
AU - Escarate, Rodrigo
AU - Villalón, Alejandro
AU - Ramírez, Carolina A.
AU - Hernandez-Tejero, Maria
AU - Zhang, Wei
AU - Qian, Steve
AU - Simonetto, Douglas A.
AU - Ahn, Joseph C.
AU - Buryska, Seth
AU - Dunn, Winston
AU - Mehta, Heer
AU - Agrawal, Rohit
AU - Cabezas, Joaquín
AU - García-Carrera, Inés
AU - Cuyàs, Berta
AU - Poca, Maria
AU - Soriano, German
AU - Sarin, Shiv K.
AU - Maiwall, Rakhi
AU - Jalal, Prasun K.
AU - Abdulsada, Saba
AU - Higuera-de-la-Tijera, Fátima
AU - Kulkarni, Anand V.
AU - Rao, P. Nagaraja
AU - Salazar, Patricia Guerra
AU - Skladaný, Lubomir
AU - Bystrianska, Natália
AU - Clemente-Sanchez, Ana
AU - Villaseca-Gómez, Clara
AU - Haider, Tehseen
AU - Chacko, Kristina R.
AU - Romero, Gustavo A.
AU - Pollarsky, Florencia D.
AU - Restrepo, Juan Carlos
AU - Castro-Sanchez, Susana
AU - Toro, Luis G.
AU - Yaquich, Pamela
AU - Mendizabal, Manuel
AU - Garrido, Maria Laura
AU - Marciano, Sebastián
AU - Dirchwolf, Melisa
AU - Vargas, Victor
AU - Jiménez, César
AU - Louvet, Alexandre
AU - García-Tsao, Guadalupe
AU - Roblero, Juan Pablo
AU - Abraldes, Juan G.
AU - Shah, Vijay H.
AU - Kamath, Patrick S.
AU - Arrese, Marco
AU - Singal, Ashwani K.
AU - Bataller, Ramon
AU - Arab, Juan Pablo
N1 - Publisher Copyright:
© 2023 The Author(s)
PY - 2023/8
Y1 - 2023/8
N2 - Background & Aims: Model for End-Stage Liver Disease (MELD) score better predicts mortality in alcohol-associated hepatitis (AH) but could underestimate severity in women and malnourished patients. Using a global cohort, we assessed the ability of the MELD 3.0 score to predict short-term mortality in AH. Methods: This was a retrospective cohort study of patients admitted to hospital with AH from 2009 to 2019. The main outcome was all-cause 30-day mortality. We compared the AUC using DeLong's method and also performed a time-dependent AUC with competing risks analysis. Results: A total of 2,124 patients were included from 28 centres from 10 countries on three continents (median age 47.2 ± 11.2 years, 29.9% women, 71.3% with underlying cirrhosis). The median MELD 3.0 score at admission was 25 (20–33), with an estimated survival of 73.7% at 30 days. The MELD 3.0 score had a better performance in predicting 30-day mortality (AUC:0.761, 95%CI:0.732–0.791) compared with MELD sodium (MELD-Na; AUC: 0.744, 95% CI: 0.713–0.775; p = 0.042) and Maddrey's discriminant function (mDF) (AUC: 0.724, 95% CI: 0.691–0.757; p = 0.013). However, MELD 3.0 did not perform better than traditional MELD (AUC: 0.753, 95% CI: 0.723–0.783; p = 0.300) and Age-Bilirubin-International Normalised Ratio-Creatinine (ABIC) (AUC:0.757, 95% CI: 0.727–0.788; p = 0.765). These results were consistent in competing-risk analysis, where MELD 3.0 (AUC: 0.757, 95% CI: 0.724–0.790) predicted better 30-day mortality compared with MELD-Na (AUC: 0.739, 95% CI: 0.708–0.770; p = 0.028) and mDF (AUC:0.717, 95% CI: 0.687–0.748; p = 0.042). The MELD 3.0 score was significantly better in predicting renal replacement therapy requirements during admission compared with the other scores (AUC: 0.844, 95% CI: 0.805–0.883). Conclusions: MELD 3.0 demonstrated better performance compared with MELD-Na and mDF in predicting 30-day and 90-day mortality, and was the best predictor of renal replacement therapy requirements during admission for AH. However, further prospective studies are needed to validate its extensive use in AH. Impact and implications: Severe AH has high short-term mortality. The establishment of treatments and liver transplantation depends on mortality prediction. We evaluated the performance of the new MELD 3.0 score to predict short-term mortality in AH in a large global cohort. MELD 3.0 performed better in predicting 30- and 90-day mortality compared with MELD-Na and mDF, but was similar to MELD and ABIC scores. MELD 3.0 was the best predictor of renal replacement therapy requirements. Thus, further prospective studies are needed to support the wide use of MELD 3.0 in AH.
AB - Background & Aims: Model for End-Stage Liver Disease (MELD) score better predicts mortality in alcohol-associated hepatitis (AH) but could underestimate severity in women and malnourished patients. Using a global cohort, we assessed the ability of the MELD 3.0 score to predict short-term mortality in AH. Methods: This was a retrospective cohort study of patients admitted to hospital with AH from 2009 to 2019. The main outcome was all-cause 30-day mortality. We compared the AUC using DeLong's method and also performed a time-dependent AUC with competing risks analysis. Results: A total of 2,124 patients were included from 28 centres from 10 countries on three continents (median age 47.2 ± 11.2 years, 29.9% women, 71.3% with underlying cirrhosis). The median MELD 3.0 score at admission was 25 (20–33), with an estimated survival of 73.7% at 30 days. The MELD 3.0 score had a better performance in predicting 30-day mortality (AUC:0.761, 95%CI:0.732–0.791) compared with MELD sodium (MELD-Na; AUC: 0.744, 95% CI: 0.713–0.775; p = 0.042) and Maddrey's discriminant function (mDF) (AUC: 0.724, 95% CI: 0.691–0.757; p = 0.013). However, MELD 3.0 did not perform better than traditional MELD (AUC: 0.753, 95% CI: 0.723–0.783; p = 0.300) and Age-Bilirubin-International Normalised Ratio-Creatinine (ABIC) (AUC:0.757, 95% CI: 0.727–0.788; p = 0.765). These results were consistent in competing-risk analysis, where MELD 3.0 (AUC: 0.757, 95% CI: 0.724–0.790) predicted better 30-day mortality compared with MELD-Na (AUC: 0.739, 95% CI: 0.708–0.770; p = 0.028) and mDF (AUC:0.717, 95% CI: 0.687–0.748; p = 0.042). The MELD 3.0 score was significantly better in predicting renal replacement therapy requirements during admission compared with the other scores (AUC: 0.844, 95% CI: 0.805–0.883). Conclusions: MELD 3.0 demonstrated better performance compared with MELD-Na and mDF in predicting 30-day and 90-day mortality, and was the best predictor of renal replacement therapy requirements during admission for AH. However, further prospective studies are needed to validate its extensive use in AH. Impact and implications: Severe AH has high short-term mortality. The establishment of treatments and liver transplantation depends on mortality prediction. We evaluated the performance of the new MELD 3.0 score to predict short-term mortality in AH in a large global cohort. MELD 3.0 performed better in predicting 30- and 90-day mortality compared with MELD-Na and mDF, but was similar to MELD and ABIC scores. MELD 3.0 was the best predictor of renal replacement therapy requirements. Thus, further prospective studies are needed to support the wide use of MELD 3.0 in AH.
KW - Alcohol
KW - Alcoholic hepatitis
KW - Cirrhosis
KW - End-stage liver disease
KW - Female
KW - MELD
KW - Outcome prediction
UR - http://www.scopus.com/inward/record.url?scp=85165989420&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85165989420&partnerID=8YFLogxK
U2 - 10.1016/j.jhepr.2023.100727
DO - 10.1016/j.jhepr.2023.100727
M3 - Article
AN - SCOPUS:85165989420
SN - 2589-5559
VL - 5
JO - JHEP Reports
JF - JHEP Reports
IS - 8
M1 - 100727
ER -