Victoria González

Dr. Victoria González


Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

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1 September 2007 in International Journal of Infectious Diseases
Verified
Journal Article
Closed access
ABArístides Aguilar Betancourt
Arístides Aguilar Betancourt
CDC.A. González Delgado
C.A. González Delgado
ZEZ. Cinza Estévez
Z. Cinza Estévez
JMJ. Cabrera Martínez
J. Cabrera Martínez
GRG. Véliz Ríos
G. Véliz Ríos
JRJ.C. Aguilar Rubido
J.C. Aguilar Rubido

1 July 2004 in Journal of Clinical Microbiology
Verified
Journal Article
Open access
PDF file
EPEduardo Padilla
Eduardo Padilla
VGVictoria González
Victoria González
JMJose María Manterola
Jose María Manterola
APAndrés Pérez
Andrés Pérez
MQMaría Dolores Quesada
María Dolores Quesada
VAVicente Ausina
Vicente Ausina
The performance of two DNA line probe assays, a new version of INNO-LiPA Mycobacteria (Innogenetics, Ghent, Belgium) and the GenoType Mycobacterium (Hain Diagnostika, Nehren, Germany), were evaluated for identification of mycobacterial species isolated from liquid cultures. Both tests are based on a PCR technique and designed for simultaneous identification of different mycobacterial species by reverse hybridization and line probe technology. The INNO-LiPA Mycobacteria v2 targeting the 16S-23S rRNA gene spacer region was developed for the simultaneous identification of 16 different mycobacterial species. The GenoType Mycobacterium, which targets the 23S rRNA gene, allows simultaneous identification of 13 mycobacterial species. Both tests were evaluated on 110 mycobacterial strains belonging to 22 different mycobacterial species (20 reference strains, 83 clinical strains, and 4 Mycobacterium kansasii strains isolated from tap water) that were previously inoculated into MB/BacT bottles. The sensitivity of both methods, defined as the number of positive results obtained with the Mycobacterium genus probe together with an interpretable result on the number of samples tested was 110 of 110 (100%) for INNO-LiPA and 102 of 110 (92.7%) for GenoType. For samples with interpretable results, INNO-LiPA was able to correctly identify 109 of 110 samples (99.1%), whereas the GenoType correctly identified 100 of 102 samples (98.0%). Both tests were easy to perform, rapid, and reliable when applied to mycobacterial identification directly from MB/BacT bottles.

1 May 2004 in European Journal of Clinical Microbiology & Infectious Diseases
Verified
Journal Article
Closed access
PDF file
EPE. Padilla
E. Padilla
CVCris Vilaplana
Cris Vilaplana
MQM. D. Quesada
M. D. Quesada
VAV. Ausina
V. Ausina
VGVictoria González
Victoria González
MPM. A. Pallarés
M. A. Pallarés

1 January 2014 in World Journal of Gastroenterology
Verified
Journal Article
Open access
VSVerónica Saludes
Verónica Saludes
VGVictoria González
Victoria González
RPRamon Planas
Ramon Planas
LMLurdes Matas
Lurdes Matas
VAVicente Ausina
Vicente Ausina
EMElisa Martró
Elisa Martró
Hepatitis C virus (HCV) infection represents a major public health issue. Hepatitis C can be cured by therapy, but many infected individuals are unaware of their status. Effective HCV screening, fast diagnosis and characterization, and hepatic fibrosis staging are highly relevant for controlling transmission, treating infected patients and, consequently, avoiding end-stage liver disease. Exposure to HCV can be determined with high sensitivity and specificity with currently available third generation serology assays. Additionally, the use of point-of-care tests can increase HCV screening opportunities. However, active HCV infection must be confirmed by direct diagnosis methods. Additionally, HCV genotyping is required prior to starting any treatment. Increasingly, high-volume clinical laboratories use different types of automated platforms, which have simplified sample processing, reduced hands-on-time, minimized contamination risks and human error and ensured full traceability of results. Significant advances have also been made in the field of fibrosis stage assessment with the development of non-invasive methods, such as imaging techniques and serum-based tests. However, no single test is currently available that is able to completely replace liver biopsy. This review focuses on approved commercial tools used to diagnose HCV infection and the recommended hepatic fibrosis staging tests.

1 September 2013 in Journal of Clinical Virology
Verified
Journal Article
Closed access
VGVictoria González
Victoria González
MGMeissiner Gomes-Fernandes
Meissiner Gomes-Fernandes
EBElisabet Bascuñana
Elisabet Bascuñana
SCSònia Casanovas
Sònia Casanovas
VSVerónica Saludes
Verónica Saludes
EMElisa Martró
Elisa Martró

28 January 2016 in Substance Use & Misuse
Verified
Journal Article
Closed access
PDF file
CFCinta Folch
Cinta Folch
JCJordi Casabona
Jordi Casabona
AEAlbert Espelt
Albert Espelt
XMXavier Majó
Xavier Majó
MMMercè Meroño
Mercè Meroño
RGREDAN Study Group
REDAN Study Group
Objectives: The aim of this study was to assess differences in the prevalence of HIV and HCV infection and associated risk factors between new (injecting for ≤5 years) and long-term injectors and to estimate HIV/HCV incidence among new injectors. Methods: Cross-sectional study among people who inject drugs (PWID) who attended harm reduction centers in Catalonia in 2010–11. Anonymous questionnaires and oral fluid samples were collected. Poisson regression models were applied to determine the association between HIV/HCV infection and risk factors. Results: Of the 761 participants, 21.4% were new injectors. New injectors were younger than long-term injectors (mean age = 31.6 vs. 37.8) and were more likely to be immigrants (59.0% vs. 33.4%). HIV and HCV prevalence was 20.6% and 59.4% among new injectors, and estimated HIV and HCV incidence 8.7 and 25.1 /100 person-years, respectively. Among new injectors, HIV infection was associated with homelessness (PR = 3.10) and reporting a previous sexually transmitted infection (PR = 1.79). Reporting front/backloading (PR = 1.33) and daily injection (PR = 1.35) were risk-factors for HCV infection. For long-term injectors, HIV risk factors were: having shared syringes (PR = 1.85), having injected cocaine (PR = 1.38), reporting front/backloading (PR = 1.30) and ever having been in prison (PR = 2.03). Conclusion: A large proportion of PWID in Catalonia are new injectors, a subgroup with a high level of both sexual and parenteral exposure and a high incidence rate of HIV/ HCV infections. It is important to improve early diagnosis of these infections among this group, in particular among migrants. To identify and address risk factors for homelessness PWID should be a priority.