Cristhian Hernández-Gómez
El Bosque University
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Featured researches published by Cristhian Hernández-Gómez.
PLOS ONE | 2016
Maria Virginia Villegas; Christian Pallares; Kevin Escandón-Vargas; Cristhian Hernández-Gómez; Adriana Correa; Carlos Álvarez; Fernando Rosso; Lorena Matta; Carlos M. Luna; Jeannete Zurita; Carlos Mejía-Villatoro; Eduardo Rodríguez-Noriega; Carlos Seas; Manuel Cortesía; Alfonso Guzmán-Suárez; Manuel Guzman-Blanco
Introduction Infections caused by carbapenem-resistant Enterobacteriaceae are a public health problem associated with higher mortality rates, longer hospitalization and increased healthcare costs. We carried out a study to describe the characteristics of patients with carbapenemase-producing Enterobacteriaceae (CPE) and non-CPE bloodstream infection (BSI) from Latin American hospitals and to determine the clinical impact in terms of mortality and antibiotic therapy. Methods Between July 2013 and November 2014, we conducted a multicenter observational study in 11 hospitals from 7 Latin American countries (Argentina, Colombia, Ecuador, Guatemala, Mexico, Peru, Venezuela). Patients with BSI caused by Enterobacteriaceae were included and classified either as CPE or non-CPE based on detection of blaKPC, blaVIM, blaIMP, blaNDM and blaOXA-48 by polymerase chain reaction. Enrolled subjects were followed until discharge or death. Demographic, microbiological and clinical characteristics were collected from medical records. Both descriptive and inferential statistics were used to analyze the information. Results A total of 255 patients with Enterobacteriaceae BSI were included; CPE were identified in 53 of them. In vitro non-susceptibility to all screened antibiotics was higher in the patients with CPE BSI, remaining colistin, tigecycline and amikacin as the most active drugs. Combination therapy was significantly more frequent in the CPE BSI group (p < 0.001). The most common regimen was carbapenem + colistin or polymyxin B. The overall mortality was 37% (94/255). Overall and attributable mortality were significantly higher in patients with CPE BSI (p < 0.001); however, we found that patients with CPE BSI who received combination therapy and those who received monotherapy had similar mortality. After multivariate adjustment, CPE BSI (adjusted odds ratio [aOR] 4; 95% confidence interval [CI] 1.7–9.5; p = 0.002) and critical illness (aOR 6.5; 95% CI 3.1–13.7; p < 0.001) were independently associated with in-hospital mortality. Conclusions This study provides valuable data on the clinical characteristics and mortality risk factors in patients with CPE BSI. We determined that CPE infection is an independent mortality predictor and thus Latin American hospitals should perform campaigns on prevention and control of CPE BSI.
Open Forum Infectious Diseases | 2017
Max Feinstein; Karen Ordóñez; Sergio Reyes; Christian Pallares; Cristhian Hernández-Gómez; Maria Virginia Villegas
Abstract Background The quality of antibiotics is a crucial element in successful treatment of infections. Recently, the use of generic antibiotics has caused controversy because of studies reporting clinical failure and the emergence of antibacterial resistance associated with the sustained use of generic antibiotics. The present study was designed to determine the mortality associated with the use of generic meropenem (GM) and brand-name meropenem (BNM) used to treat Gram-negative infections. Methods We conducted an ambispective cohort study comparing adult patients who received GM and BNM while in the intensive care unit of a tertiary care hospital in Colombia. Patients treated between January 2011 and May 2014 received GM while patients treated between June 2014 and March 2017 received BNM. Patients were included in the study only if the infecting organism was susceptible to meropenem. The GM and BNM cohorts were paired by age, infection type, and infection severity as measured by Sequential Organ Failure Assessment score. Mortality was compared between groups. Data were analyzed using descriptive and inferential statistics. Results A total of 168 patients were included; 68 patients (40%) were treated with GM and 100 (60%) were treated with BNM. The mean age was 57 years old; 72 (43%) women and 96 (57%) men. The most common infecting organism was E. coli (35%) followed by K. pneumoniae (19%). Bacteremia (49%) was the most common infection type, followed by intraabdominal infection (24%). Multivariate analysis demonstrated that patients treated with GM had a risk of death 18 times higher (OR: 18.45 95% CI 1.47-232, P = 0.024) than patients treated with BNM. Patients with a history of cardiovascular disease had an independent risk of death compared with those without cardiovascular disease. Other comorbidities and time between bacterial culture and initiation of treatment with meropenem did not have a statistically significant effect on mortality. Conclusion The present study suggests that patients treated with GM have worse clinical outcomes compared with those treated with BNM. More studies are needed to confirm the clinical superiority of brand-name vs. generic antibiotics, not only for meropenem but also for other commonly-used molecules. Disclosures C. Pallares, Merck Sharp & Dohme, Pfizer: Consultant, Consulting fee. C. Hernández-Gómez, Merck Sharp & Dohme: Consultant, Consulting fee. Pfizer: Consultant, Consulting fee. M. V. Villegas, Merck Sharp & Dohme: Consultant, Consulting fee and Research support. Pfizer: Consultant, Consulting fee and Research support.
Open Forum Infectious Diseases | 2017
Cristhian Hernández-Gómez; Max Feinstein; Karen Ordóñez; Sergio Reyes; Christian Pallares; Sergio Gutiérrez; Lorena Diaz; Obed Suárez; Maria Virginia Villegas
Abstract Background The main goal of an Antimicrobial Stewardship Program (ASP) is to optimize clinical outcomes while minimizing unintended consequences of antimicrobial use. However, the healthcare resource manager’s primary goal for ASP is to reduce the cost of patient care without adversely affecting quality. Globally, generic drugs facilitate access to medication, especially in resource-limited settings, provided that they prove as effective as the brand molecule. Economical evaluation (EE) studies aim to find the most cost effective alternatives. This study was designed to determine the incremental cost-effectiveness ratio (ICER) of generic meropenem (GM) use vs. brand-name meropenem (BNM) to treat Gram-negative infections. Methods We conducted a double cohort EE study of adult patients who received GM vs. patients who received BNM. All patients with meropenem-susceptible infections were treated in the intensive care unit (ICU) of a Colombian acute care hospital. Survival rates were defined as the clinical outcome for effectiveness. Total infection cost was defined by the cost (USD) of antimicrobial consumption, length of stay, and laboratory and imaging exams until infection resolution. ICER was calculated using a decision tree model. Results A total of 168 patients were included; survival rate for the 68 patients treated with GM was 38% vs. 59% for the 100 patients treated with BNM (death risk OR: 18.4 95% CI 1.47–232, P = 0.024). The total antimicrobial consumption cost was lower in the BNM cohort (
Open Forum Infectious Diseases | 2017
Ana Mercedes Rada; Elsa De La Cadena; Nataly Orozco; Carlos Agudelo Restrepo; Cesar Capataz; Marcela Perenguez; Cristhian Hernández-Gómez; Christian Pallares; Paola Porras; Javier Ardila; Rafael Rios; Jinnethe Reyes; Lorena Diaz; Adriana Correa; Maria Virginia Villegas; Cesar A. Arias; Eliana Restrepo
303 vs.
Journal of global antimicrobial resistance | 2017
Elsa De La Cadena; Adriana Correa; Juan S. Muñoz; Laura J. Rojas; Cristhian Hernández-Gómez; Christian Pallares; Federico Perez; Robert A. Bonomo; Maria Virginia Villegas
588) explained by fewer consumption doses. ICU stay costs were higher in the GM cohort (
Infection Control and Hospital Epidemiology | 2017
Max Feinstein; Kevin Escandón-Vargas; Sergio Reyes; Cristhian Hernández-Gómez; Christian Pallares; Maria Virginia Villegas
8,896 vs.
Biomedica | 2013
Cristhian Hernández-Gómez; Victor M. Blanco; Gabriel Motoa; Adriana Correa; Juan José Maya; Laura J. Rojas; Alejandra Hernández; Marta Vallejo; Maria Virginia Villegas
7,705), however, laboratory and imaging exam costs were lower in the GM cohort (
Colombia Medica | 2015
Cristhian Hernández-Gómez; Gabriel Motoa; Marta Vallejo; Victor M. Blanco; Adriana Correa; Elsa De La Cadena; Maria Virginia Villegas
961 vs.
Open Forum Infectious Diseases | 2017
Cristhian Hernández-Gómez; Christian Pallares; Sergio Reyes; Max Feinstein; Sergio Gutiérrez; Soraya Salcedo; Ernesto Martínez; David Aragon; Sara Cobo; Maria Virginia Villegas
1,360). Total infection cost did not show a significant difference between groups (BNM
Open Forum Infectious Diseases | 2016
Cristhian Hernández-Gómez; Christian Pallares; Kevin Escandón-Vargas; Sergio Reyes; Soraya Salcedo; Lorena Matta; Maria Virginia Villegas
10,771 vs. GM