Luis Mariano Esteban

Prof. Luis Mariano Esteban

Universidad de Zaragoza, Zaragoza, Aragon, Spain
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2017 in Journal of Cleaner Production
Verified
Journal Article
Closed access
ÁSÁngel Salesa
Ángel Salesa
JPJosé A. Pérez-Benedicto
José A. Pérez-Benedicto
DCDavid Colorado-Aranguren
David Colorado-Aranguren
PLPedro Luis Lopez-Julian
Pedro Luis Lopez-Julian
Luis Mariano EstebanLuis Mariano Esteban
Luis Mariano Esteban
DODaniel Olivares
Daniel Olivares

1 October 2017 in Construction and Building Materials
Verified
Journal Article
Closed access
ÁSÁngel Salesa
Ángel Salesa
JPJose Ángel Pérez-Benedicto
Jose Ángel Pérez-Benedicto
Luis Mariano EstebanLuis Mariano Esteban
Luis Mariano Esteban
RVRosa Vicente-Vas
Rosa Vicente-Vas
MOMartín Orna-Carmona
Martín Orna-Carmona

9 May 2022 in Transplant International
Verified
Journal Article
Open access
MSM. Trinidad Serrano
M. Trinidad Serrano
SSSergio Sabroso
Sergio Sabroso
Luis Mariano EstebanLuis Mariano Esteban
Luis Mariano Esteban
MBMarina Berenguer
Marina Berenguer
CFConstantino Fondevila
Constantino Fondevila
MSMagdalena Salcedo
Magdalena Salcedo
In the last few years, several studies have analyzed sex and gender differences in liver transplantation (LT), but none have performed a disaggregated analysis of both mortality and causes of death. Data from 15,998 patients, 11,914 (74.5%) males and 4,069 (25.5%) females, transplanted between 2000 and 2016 were obtained from the Liver Transplantation Spanish Registry. Survival analysis was applied to explore recipient sex as a risk factor for death. The causes of death at different follow-up duration were disaggregated by recipient sex for analysis. Short-term survival was higher in males, whereas long-term survival was higher in females. Survival at 1, 5 and 10 years post-transplant was 87.43%, 73.83%, and 61.23%, respectively, in males and 86.28%, 74.19%, and 65.10%, respectively, in females (p = 0.05). Post-LT mortality related to previous liver disease also presented sex differences. Males had 37% increased overall mortality from acute liver failure (p = 0.035) and 37% from HCV-negative cirrhosis (p < 0.001). Females had approximately 16% increased mortality when the liver disease was HCV-positive cirrhosis (p = 0.003). Regarding causes of death, non-malignancy HCV+ recurrence (6.3% vs. 3.9% of patients; p < 0.001), was more frequently reported in females. By contrast, death because of malignancy recurrence (3.9% vs. 2.2% of patients; p = 0.003) and de novo malignancy (4.8% vs. 2.5% of patients; p < 0.001) were significantly more frequent in male recipients. Cardiovascular disease, renal failure, and surgical complications were similar in both. In summary, male patients have lower short-term mortality than females but higher long-term and overall mortality. In addition, the post-LT mortality risk related to previous liver disease and the causes of mortality differ between males and females.

21 March 2022 in Cancers
Verified
Journal Article
Open access
PDF file
JMJuan Morote
Juan Morote
ABAngel BORQUE-FERNANDO
Angel BORQUE-FERNANDO
MTMarina Triquell
Marina Triquell
ACAnna Celma
Anna Celma
LRLucas Regis
Lucas Regis
EHEnrique Trilla Herrera
Enrique Trilla Herrera
A new and externally validated MRI-PM for csPCa was developed in the metropolitan area of Barcelona, and a web-RC designed with the new option of selecting the csPCa probability threshold. The development cohort comprised 1486 men scheduled to undergo a 3-tesla multiparametric MRI (mpMRI) and guided and/or systematic biopsies in one academic institution of Barcelona. The external validation cohort comprised 946 men in whom the same diagnostic approach was carried out as in the development cohort, in two other academic institutions of the same metropolitan area. CsPCa was detected in 36.9% of men in the development cohort and 40.8% in the external validation cohort (p = 0.054). The area under the curve of mpMRI increased from 0.842 to 0.897 in the developed MRI-PM (p < 0.001), and from 0.743 to 0.858 in the external validation cohort (p < 0.001). A selected 15% threshold avoided 40.1% of prostate biopsies and missed 5.4% of the 36.9% csPCa detected in the development cohort. In men with PI-RADS <3, 4.3% would be biopsied and 32.3% of all existing 4.2% of csPCa would be detected. In men with PI-RADS 3, 62% of prostate biopsies would be avoided and 28% of all existing 12.4% of csPCa would be undetected. In men with PI-RADS 4, 4% of prostate biopsies would be avoided and 0.6% of all existing 43.1% of csPCa would be undetected. In men with PI-RADS 5, 0.6% of prostate biopsies would be avoided and none of the existing 42.0% of csPCa would be undetected. The Barcelona MRI-PM presented good performance on the overall population; however, its clinical usefulness varied regarding the PI-RADS category. The selection of csPCa probability thresholds in the designed RC may facilitate external validation and outperformance of MRI-PMs in specific PI-RADS categories.

15 October 2021 in The Journal of Maternal-Fetal & Neonatal Medicine
Verified
Journal Article
Closed access
CPClara Zamora del Pozo
Clara Zamora del Pozo
MEMarta Chóliz Ezquerro
Marta Chóliz Ezquerro
IMInmaculada Mejía
Inmaculada Mejía
EMElisa Díaz de Terán Martínez-Berganza
Elisa Díaz de Terán Martínez-Berganza
Luis Mariano EstebanLuis Mariano Esteban
Luis Mariano Esteban
RSRicardo Savirón-Cornudella
Ricardo Savirón-Cornudella
Despite its routine use in intrapartum care, the technique of fetal cardiotocography has some limitations. The aim of this study is to analyze the predictive capacity and interobserver agreement in...

14 August 2018 in Prostate Cancer and Prostatic Diseases
Verified
Journal Article
Closed access
PDF file
ABAngel BORQUE-FERNANDO
Angel BORQUE-FERNANDO
JRJosé Rubio-Briones
José Rubio-Briones
Luis Mariano EstebanLuis Mariano Esteban
Luis Mariano Esteban
YDYan Dong
Yan Dong
ACAna Calatrava
Ana Calatrava
DODavid Okrongly
David Okrongly