Arantza Sanvisens

Dr. Arantza Sanvisens

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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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24 January 2011 in European Heart Journal
Verified
Journal Article
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XCXavier Carrillo
Xavier Carrillo
ACAntoni Curós
Antoni Curós
RMRoberto Muga
Roberto Muga
JSJordi Serra
Jordi Serra
ASArantza Sanvisens
Arantza Sanvisens
ABAntoni Bayes
Antoni Bayes
The use of cocaine as a recreational drug has increased in recent years. The aims of this study were to analyse the prevalence and inhospital evolution of acute coronary syndrome (ACS) associated with cocaine consumption (ACS-ACC). Prospective analysis of ACS patients admitted to a coronary care unit from January 2001 to December 2008. During the study period, 2752 patients were admitted for ACS, and among these 479 were ≤50 years of age. Fifty-six (11.7%) patients had a medical history of cocaine use with an increase in prevalence from 6.8% in 2001 to 21.7% in 2008 (P = 0.035). Among patients younger than 30 years of age, 25% admitted to being users compared with 5.5% of those aged 45–50 years (P = 0.007). Similarly, the prevalence of positive urine tests for cocaine was four times higher in the younger patients (18.2 vs. 4.1%, P = 0.035). Acute coronary syndrome associated with cocaine consumption patients (n = 24; those who had a positive urine test for cocaine or who admitted to being users upon admission) had larger myocardial infarcts as indicated by troponin I levels (52.9 vs. 23.4 ng/mL, P < 0.001), lower the left ventricular ejection fraction (44.5 vs. 52.2%, P = 0.049), and increased inhospital mortality (8.3 vs. 0.8%, P = 0.030). The association between cocaine use and ACS has increased significantly over the past few years. Young adults with ACS-ACC that require admission to the coronary care unit have greater myocardial damage and more frequent complications.

1 April 2006 in Drug and Alcohol Dependence
Verified
Journal Article
Closed access
RMRoberto Muga
Roberto Muga
ASArantza Sanvisens
Arantza Sanvisens
FBFerran Bolao
Ferran Bolao
JTJordi Tor
Jordi Tor
JSJavier Santesmases
Javier Santesmases
AMAlvaro Muñoz
Alvaro Muñoz

1 March 2009 in Clinical Gastroenterology and Hepatology
Verified
Journal Article
Closed access
CTCristina Tural
Cristina Tural
JTJordi Tor
Jordi Tor
ASArantza Sanvisens
Arantza Sanvisens
NPNúria Pérez–Alvarez
Núria Pérez–Alvarez
EMElisenda Martínez
Elisenda Martínez
BCBonaventura Clotet
Bonaventura Clotet

15 January 2013 in Alcohol, Clinical and Experimental Research
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Journal Article
Closed access
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IRInmaculada Rivas
Inmaculada Rivas
ASArantza Sanvisens
Arantza Sanvisens
FBFerran Bolao
Ferran Bolao
DFDaniel Fuster
Daniel Fuster
JTJordi Tor
Jordi Tor
RMRoberto Muga
Roberto Muga

1 August 2007 in Clinical Infectious Diseases
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Journal Article
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RMRoberto Muga
Roberto Muga
KLKlaus Langohr
Klaus Langohr
JTJordi Tor
Jordi Tor
ASArantza Sanvisens
Arantza Sanvisens
ISIsabel Serra
Isabel Serra
ÁMÁlvaro Muñoz
Álvaro Muñoz
Background. In the era of highly active antiretroviral therapy (HAART), it remains unclear whether human immunodeficiency virus (HIV)–infected injection drug users (IDUs) have durations of survival similar to those for comparable HIV-uninfected IDUs. The goal of this study was to compare survival durations of HIV-infected and HIV-uninfected IDUs for the period 1987–2004.

2 January 2006 in AIDS
Verified
Journal Article
Closed access
BLBlanca Lumbreras Lacarra
Blanca Lumbreras Lacarra
IJInmaculada Jarrín
Inmaculada Jarrín
JAJulia del Amo
Julia del Amo
SPSantiago Pérez-Hoyos
Santiago Pérez-Hoyos
RMRoberto Muga
Roberto Muga
Ildefonso Hernández AguadoIldefonso Hernández Aguado
Ildefonso Hernández Aguado
To assess the impact of HIV and hepatitis C virus (HCV) infection on long-term mortality in injecting drug users (IDU). Community-based prospective cohort study. Mortality data from follow-up in clinical sites and the Mortality Registry by December 2002 were collected for 3247 IDU who attended three centres for voluntary counselling and testing for HIV/AIDS, HCV and hepatitis B virus (HBV) in 1990–1996. Mortality rates by Poisson regression were adjusting for age, sex, duration of drug use, education, HBV and calendar period (1990–1997 and 1998–2002). Overall, 11.2% were HIV/HCV negative, 43.7% positive only for HCV and 45.1% positive for both. During 26 772 person-years of follow-up, 585 deaths were detected (2.19/100 person-years). Before 1997, HIV/HCV-positive subjects had a five-fold increase in risk of death [relative risk (RR), 5.4; 95% confidence interval (CI), 2.5–11.4] compared with those negative for both; after 1997, a three-fold increase was observed (RR, 2.7; 95% CI, 1.7–4.2). Being HCV positive/HIV negative was not associated with an increase in the risk of death either before (RR, 1.3; 95% CI, 0.6–2.9) or after (RR, 1.2; 95% CI, 0.8–1.9) 1997 compared with HCV/HIV negative. While increases in mortality were seen in those HCV/HIV negative (RR, 1.6; 95% CI, 0.7–3.7) and those only positive for HCV (RR, 1.5; 95% CI, 1.0–2.1), a 20% reduction among coinfected IDUs was observed after 1997 (interaction P = 0.033). HCV/HIV coinfection has had a large impact on mortality in IDU. After 1997, mortality increased in HIV negative/HCV positive subjects and decreased in HIV positive/HCV positive.