Héctor Jesús Maldonado Garza
Universidad Autónoma de Nuevo León
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Featured researches published by Héctor Jesús Maldonado Garza.
Digestive and Liver Disease | 2011
Diego Garcia-Compean; José G. González; César Antonio Marrufo García; Juan Pablo Flores Gutiérrez; Oralia Barboza Quintana; Gabriela Galindo Rodríguez; Miguel Angel Mar Ruiz; David de León Valdez; Joel Omar Jáquez Quintana; Héctor Jesús Maldonado Garza
BACKGROUND Eosinophilic esophagitis (EoE) is not routinely considered in the differential diagnosis of refractory gastroesophageal reflux disease (GERD). AIMS To prospectively evaluate the prevalence of EoE and describe the clinical features and predictors of EoE in patients with refractory symptoms of GERD. METHODS Esophageal biopsies were obtained in patients with symptoms of GERD refractory to 8 weeks of conventional antisecretory therapy. Diagnosis of EoE was defined as at least 20 eosinophils × high power field and clinical unresponsiveness to proton pump inhibitors. Clinical and manometric features were compared. Independent risk factors predicting EoE were identified. RESULTS Six out of 150 included patients (4%) met the diagnostic criteria for EoE. Patients with EoE were significantly younger, had significantly more dysphagia, atopy, ineffective esophageal peristalsis, esophageal rings and esophageal strictures than patients without EoE. Independent predictors of EoE were: age under 45 years (OR 4.8, 95% CI 2.4-8.6), dysphagia (OR 12.2, 95% CI 4.3-19.4), and atopy (OR 3.4, 95% CI 1.5-7.4). CONCLUSIONS EoE is an uncommon condition (4%) in patients with refractory symptoms of GERD. Age under 45 years, atopy or dysphagia may warrant suspicion of EoE in this subset of patients.
PLOS ONE | 2015
Adrián Camacho-Ortiz; Daniel López-Barrera; Raúl Hernández-García; Alejandra M. Galván-De los Santos; Samantha Flores-Treviño; Jorge Llaca-Díaz; Héctor Jesús Maldonado Garza; Francisco Javier Bosques-Padilla; Elvira Garza-González
Background and Objective Clostridium difficile NAP1/ribotype 027 is associated with severe disease and high mortality rates. Our aim was to determine the prevalence of NAP1/ribotype 027 among C. difficile isolates in a tertiary care hospital, and review the main clinical data. Methods We included 106 stool samples from 106 patients. Samples were tested for A&B toxins and were cultured on CCFA agar. The genes tcdA, tcdB, tcdC, cdtA, and cdtB were amplified using PCR in clinical isolates. The tcdA 3’-end deletion analysis, PCR-ribotyping, and pulsed-field gel electrophoresis (PFGE) were also performed. Stool samples that were positive for culture were tested by the GeneXpert C. difficile assay. Clinical data were collected. Results Thirty-six patients tested positive for A&B toxins; and 22 patients had positive culture for C. difficile, 14 of which tested positive for the A&B toxins and all 22 patients tested positive by the GeneXpert C. difficile assay. Risk factors included an average hospital stay of 16.1 days prior to toxin detection, average antibiotic use for 16.2 days, and a median of 3 antibiotics used. The 30-day crude mortality rate was 8.4%. Six of the 22 patients died, and 3 of those deaths were directly attributed to C. difficile infection. The majority of isolates, 90.9% (20/22), carried genes tcdB, tcdA, cdtA, and cdtB; and these strains carried the corresponding downregulator gene tcdC, with an 18-bp deletion. PFGE was performed on 17 isolates, and one main pattern was observed. Analysis of the ribotyping data showed similar results. Conclusion The above findings represent the clonal spread of C. difficile in our institution, which mainly includes the NAP1/027 strain. This is the first report of C. difficile ribotype NAP1/027 in Mexico.
Revista Espanola De Enfermedades Digestivas | 2016
Rodrigo Manuel Nárvaez Rivera; José G. González; Roberto Monreal Robles; Diego García Compeán; Jonathan Paz Delgadillo; Aldo Azael Garza Galindo; Héctor Jesús Maldonado Garza
BACKGROUND/AIMS Few studies have validated the performance of guidelines for the prediction of choledocholithiasis (CL). Our objective was to prospectively assess the accuracy of the American Society for Gastrointestinal Endoscopy (ASGE) guidelines for the identification of CL. METHODS A two-year prospective evaluation of patients with suspected CL was performed. We evaluated the ASGE guidelines and its component variables in predicting CL. RESULTS A total of 256 patients with suspected CL were analyzed. Of the 208 patients with high-probability criteria for CL, 124 (59.6%) were found to have a stone/sludge at endoscopic retrograde cholangiopancreatography (ERCP). Among 48 patients with intermediate-probability criteria, 21 (43.8%) had a stone/sludge. The performance of ASGE high- and intermediate-probability criteria in our population had an accuracy of 59.0% (85.5% sensitivity, 24.3% specificity) and 41.0% (14.4% sensitivity, 75.6% specificity), respectively. The mean ERCP delay time was 6.1 days in the CL group and 6.4 days in the group without CL, p = 0.638. The presence of a common bile duct (CBD) > 6 mm (OR 2.21; 95% CI, 1.20-4.10), ascending cholangitis (OR 2.37; 95% CI, 1.01-5.55) and a CBD stone visualized on transabdominal US (OR 3.33; 95% CI, 1.48-7.52) were stronger predictors of CL. The occurrence of biliary pancreatitis was a strong protective factor for the presence of a retained CBD stone (OR 0.30; 95% CI, 0.17-0.55). CONCLUSIONS Irrespective of a patients ASGE probability for CL, the application of current guidelines in our population led to unnecessary performance of ERCPs in nearly half of cases.
Annals of Hepatology | 2011
Joel Omar Jáquez Quintana; Diego Garcia-Compean; José G. González; Jesús Zacarías Villarreal Pérez; Fernando Javier Lavalle González; Linda E. Muñoz Espinosa; Pedro Hernández; Erick Reyes Cabello; Edgar Redondo Villarreal; Ricardo Flores Rendon; Héctor Jesús Maldonado Garza
World Journal of Gastroenterology | 2008
Diego Garcia-Compean; Héctor Jesús Maldonado Garza
Archives of Medical Research | 2006
Jaime Raúl Zúñiga-Noriega; Francisco Javier Bosques-Padilla; Guillermo I. Perez-Perez; Rolando Tijerina-Menchaca; Juan Pablo Flores-Gutiérrez; Héctor Jesús Maldonado Garza; Elvira Garza-González
Gastroenterology | 2016
Luis A. Rodriguez Robles; Roberto Monreal Robles; Jose Maria Remes Troche; Francisco Javier Bosques Padilla; Héctor Jesús Maldonado Garza; Manuel Martinez-Vazquez
Medicina Universitaria | 2001
Francisco Javier Bosques Padilla; Omar Alanís Aguilar; Elvira Garza González; Héctor Jesús Maldonado Garza; Rolando Tijerina Menchaca
Endoscopia | 2018
Martín Wah Suárez; Roberto Monreal Robles; Omar David Borjas Almaguer; Héctor Jesús Maldonado Garza; Diego García Compeán; Jonathan Paz Delgadillo; Emmanuel I. González Moreno; José G. González
Gastrointestinal Endoscopy | 2017
Emmanuel I. González-Moreno; Roberto Monreal Robles; Omar D. Borjas-Almaguer; Diego Garcia-Compean; Héctor Jesús Maldonado Garza; Jose A Gonzalez