Adrián Téllez
University of Barcelona
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Adrián Téllez.
Current Infectious Disease Reports | 2017
Juan Ambrosioni; Marta Hernández-Meneses; Adrián Téllez; Juan M. Pericas; C. Falces; José María Tolosana; Barbara Vidal; M. Almela; E. Quintana; Jaume Llopis; Asunción Moreno; José M. Miró
Purpose of the ReviewInfective endocarditis (IE) is a relatively infrequent infectious disease. It does, however, causes serious morbidity, and its mortality rate has remained unchanged at approximately 25%. Changes in IE risk factors have deeply impacted its epidemiology during recent decades but literature from low-income countries is very scarce. Moreover, prophylaxis guidelines have recently changed and the impact on IE incidence is still unknown.Recent FindingsIn high-income countries, the proportion of IE related to prior rheumatic disease has decreased significantly and has been replaced proportionally by cases related to degenerative valvulopathies, prosthetic valves, and cardiovascular implantable electronic devices. Nosocomial and non-nosocomial-acquired cases have risen, as has the proportion caused by staphylococci, and the median age of patients. In low-income countries, in contrast, rheumatic disease remains the main risk factor, and streptococci the most frequent causative agents. Studies performed to evaluate impact of guidelines changes’ have shown contradictory results.SummaryThe increased complexity of cases in high-income countries has led to the creation of IE teams, involving several specialties. New imaging and microbiological techniques may increase sensitivity for diagnosis and detection of IE cases. In low-income countries, IE remained related to classic risk factors. The consequences of prophylaxis guidelines changes are still undetermined.
Clinical Infectious Diseases | 2017
Adrián Téllez; Juan Ambrosioni; Jaume Llopis; Juan M. Pericas; C. Falces; Manel Almela; Cristina Garcia de la Mària; Marta Hernández-Meneses; Barbara Vidal; Elena Sandoval; Eduard Quintana; David Fuster; José María Tolosana; Francesc Marco; Asunción Moreno; José M. Miró; Javier Garcia-Gonzalez; Jordi Vila; Juan C. Paré; Carlos Falces; Daniel Pereda; Ramón Cartañá; Salvador Ninot; Manel Azqueta; Marta Sitges; José L. Pomar; Manuel Castellá; Jose Ortiz; Guillermina Fita; Irene Rovira
Background Infective endocarditis (IE) caused by Abiotrophia (ABI) and Granulicatella (GRA) species is poorly studied. This work aims to describe and compare the main features of ABI and GRA IE. Methods We performed a retrospective study of 12 IE institutional cases of GRA or ABI and of 64 cases published in the literature (overall, 38 ABI and 38 GRA IE cases). Results ABI/GRA IE represented 1.51% of IE cases in our institution between 2000 and 2015, compared to 0.88% of HACEK (Haemophilus, Aggregatibacter, Cardiobacterium, Eikenella, Kingella)-related IE and 16.62% of Viridans group streptococci (VGS) IE. Institutional ABI/GRA IE case characteristics were comparable to that of VGS, but periannular complications were more frequent (P = .008). Congenital heart disease was reported in 4 (10.5%) ABI and in 11 (28.9%) GRA cases (P = .04). Mitral valve was more frequently involved in ABI than in GRA (P < .001). Patient sex, prosthetic IE, aortic involvement, penicillin susceptibility, and surgical treatment were comparable between the genera. New-onset heart failure was the most frequent complication without genera differences (P = .21). Five (13.2%) ABI patients and 2 (5.3%) GRA patients died (P = .23). Factors associated with higher mortality were age (P = .02) and new-onset heart failure (P = .02). The genus (GRA vs ABI) was not associated with higher mortality (P = .23). Conclusions GRA/ABI IE was more prevalent than HACEK IE and approximately one-tenth as prevalent as VGS; periannular complications were more frequent. GRA and ABI genera IE presented similar clinical features and outcomes. Overall mortality was low, and related to age and development of heart failure.
Clinical Infectious Diseases | 2018
Juan Ambrosioni; Xabier Urra; Marta Hernández-Meneses; Manel Almela; Carlos Falces; Adrián Téllez; Eduard Quintana; David Fuster; Elena Sandoval; Barbara Vidal; José María Tolosana; Asunción Moreno; Ángel Chamorro; José M. Miró; Juan M. Pericas; Cristina Garcia de la Mària; Javier Garcia-Gonzalez; Francesc Marco; Jordi Vila; Juan C. Paré; Daniel Pereda; Ramón Cartañá; Salvador Ninot; Manel Azqueta; Marta Sitges; José L. Pomar; Manuel Castellá; Jose Ortiz; Guillermina Fita; Irene Rovira
Intravenous thrombolysis is contraindicated in acute ischemic stroke secondary to infective endocarditis. We report our initial experience in 6 cases of proximal vessel occlusion treated with mechanical thrombectomy, which was safe (no bleeding) and effective (significant early neurological improvement) and might be useful in this clinical setting.
PLOS ONE | 2018
Carolina Garcia-Vidal; Celia Cardozo-Espinola; Pedro Puerta-Alcalde; Francesc Marco; Adrián Téllez; Daiana Agüero; Francisco Romero-Santana; Marina Díaz-Beyá; Eva Giné; Laura Morata; Olga Rodríguez-Núñez; Jose A. Martinez; Josep Mensa; Jordi Esteve; Alex Soriano
Objectives We assess the epidemiology and risk factors for mortality of bloodstream infection (BSI) in patients with acute leukemia (AL). Methods Prospectively collected data of a cohort study from July 2004 to February 2016. Multivariate analyses were performed. Results 589 episodes of BSI were documented in 357 AL patients, 55% caused by gram-positive bacteria (coagulase-negative staphylococci 35.7%, Enterococcus spp 10.8%) and 43.5% by gram-negative bacteria (E. coli 21%, PA 12%). We identified 110 (18.7%) multidrug-resistant (MDR) microorganisms, especially MDR-Pseudomonas aeruginosa (7%) and extended-spectrum beta-lactamase producing Enterobacteriaceae (7%). The 30-day mortality was 14.8%. Age (OR 3.1; 95% CI 1.7–5.7); chronic lung disease (4.8; 1.1–21.8); fatal prognosis according to McCabe index (13.9; 6.4–30.3); shock (3.8; 1.9–7.7); pulmonary infection (3.6; 1.3–9.9); and MDR-PA infections with inappropriate treatment (12.8; 4.1–40.5) were related to mortality. MDR-PA BSI was associated to prior antipseudomonal cephalosporin use (9.31; 4.38–19.79); current use of betalactams (2.01; 1.01–4.3); shock (2.63; 1.03–6.7) and pulmonary source of infection (9.6; 3.4–27.21). Conclusions MDR organisms were commonly isolated in BSI in AL. Inappropriate empiric antibiotic treatment for MDR-PA is the primary factor related to mortality that can be changed. New treatment strategies to improve the coverage of MDR-PA BSI should be considered in those patients with risk factors for this infection.
International Journal of Infectious Diseases | 2018
Juan Ambrosioni; Clara Martínez-García; Jaume Llopis; Cristina García-de-la-Mària; Marta Hernández-Meneses; Adrián Téllez; C. Falces; Manel Almela; Barbara Vidal; Elena Sandoval; David Fuster; Eduard Quintana; José María Tolosana; Francesc Marco; Asunción Moreno; José M. Miró
OBJECTIVES The study aimed to describe the epidemiological, microbiological, and clinical features of a population sample of 17 patients with HACEK infective endocarditis (HACEK-IE) and to compare them with matched control patients with IE caused by viridans group streptococci (VGS-IE). METHODS Cases of definite (n=14, 82.2%) and possible (n=3, 17.6%) HACEK-IE included in the Infective Endocarditis Hospital Clinic of Barcelona (IE-HCB) database between 1979 and 2016 were identified and described. Furthermore, a retrospective case-control analysis was performed, matching each case to three control subjects with VGS-IE registered in the same database during the same time period. RESULTS Seventeen out of 1209 IE cases (1.3%, 95% confidence interval 0.69-1.91%) were due to HACEK group organisms. The most frequently isolated HACEK species were Aggregatibacter spp (n=11, 64.7%). Intracardiac vegetations were present in 70.6% of cases. Left heart failure (LHF) was present in 29.4% of cases. Ten patients (58.8%) required in-hospital surgery and none died during hospitalization. In the case-control analysis, there was a trend towards larger vegetations in the HACEK-IE group (median (interquartile range) size 11.5 (10.0-20.0) mm vs. 9.0 (7.0-13.0) mm; p=0.068). Clinical manifestations, echocardiographic findings, LHF rate, systemic emboli, and other complications were all comparable (p>0.05). In-hospital surgery and mortality were similar in the two groups. One-year mortality was lower for HACEK-IE (1/17 vs. to 6/48; p=0.006). CONCLUSIONS HACEK-IE represented 1.3% of all IE cases. Clinical features and outcomes were comparable to those of the VGS-IE control group. Despite the trend towards a larger vegetation size, the embolic event rate was not higher and the 1-year mortality was significantly lower for HACEK-IE.
European Journal of Cardio-Thoracic Surgery | 2018
Carlos A Mestres; Eduard Quintana; Tomislav Kopjar; Juan Ambrosioni; M. Almela; David Fuster; Salvador Ninot; José M. Miró; Juan M. Pericas; Adrián Téllez; Marta Hernández-Meneses; Asunción Moreno; Cristina Garcia de la Mària; Javier Garcia-Gonzalez; Francesc Marco; Manel Almela; Jordi Vila; Elena Sandoval; Juan C. Paré; Carlos Falces; Daniel Pereda; Ramón Cartañá; Manel Azqueta; Marta Sitges; Barbara Vidal; José L. Pomar; Manuel Castellá; José María Tolosana; Jose Ortiz; Guillermina Fita
OBJECTIVES The aim of this study was to analyse outcomes over 2 decades using cryopreserved vascular allografts to treat vascular infection. METHODS We conducted a retrospective study of patients identified from our institutional database who were treated for primary or secondary vascular infection using implanted allografts. RESULTS Between October 1992 and May 2014, 54 patients underwent surgery for vascular infection out of 118 patients implanted with cryopreserved vascular allografts. The 52 patients for whom we had full information form the basis of the study with a 96% follow-up. The average age was 64 ± 11 years; 87% were men; 65% had previous vascular surgery; 19% had emergency operations. A total of 75% of the patients had aortoiliofemoral infections. Five patients underwent surgery with cardiopulmonary bypass. Fifty percent required more than 1 allograft and 15% had concomitant procedures. Seventy-three percent (38/52) of specimen cultures yielded positive results with polymicrobial flora in 29%. Surgical specimens most frequently grew coagulase-negative staphylococci. The early postoperative reoperation rate was 15% for allograft-related complications. There were 20 (38%) early deaths, including deaths of acute myocardial infarction, anastomosis rupture and persistent sepsis and shock. Uncontrolled infection leading to septic shock and multiple organ failure was the cause of death in 50% of the cases. The mean duration of freedom from allograft reintervention was 12.2 years. The mean duration of freedom from allograft occlusion or limb loss was 12.1 years [95% confidence interval (CI) 9.9-14.4]. Of the 32 surviving patients, we had patency information for 66% obtained by angiography or computed tomography. The mean survival for the cohort was 5.9 years (95% CI 3.9-7.8). Mean freedom from cardiovascular infection-related death was 9.3 years (95% CI 7.2-11.4). CONCLUSIONS Allografts can be indicated for treatment of primary/secondary infection and have remarkable results in multimorbid patients. Patients with vascular infection have a high-risk profile, around 40% mortality during the first 6 months, with reduction in overall mortality thereafter. We believe that allografts may play a role in the surgical treatment of vascular infection.
Medicina Clinica | 2015
Adrián Téllez; Martina Pellicé; Arturo Llobell; José César Milisenda
Medicina Clinica | 2015
Adrián Téllez; Martina Pellicé; Arturo Llobell; José César Milisenda
Clinical Microbiology and Infection | 2018
J.M. Pericàs; A. Moreno; M. Almela; C. García-de-la-Mària; F. Marco; P. Muñoz; C. Peña; A. de Alarcón; A. del Río; A. Eworo; A. Cruceta; J.C. Paré; C.A. Mestres; José Mª Miró; José M. Miró; Asunción Moreno; Juan M. Pericas; Juan Ambrosioni; Adrián Téllez; Marta Hernandez-Meneses; Ana del Río; Carlos Cervera; Francesc Marco; Cristina Garcia de la Mària; Yolanda Armero; Manel Almela; Carlos A. Mestres; Juan C. Paré; David Fuster; Ramón Cartañá
Clinical Infectious Diseases | 2018
Juan Ambrosioni; Adrián Téllez; Marta Hernández-Meneses; Jaume Llopis; Asunción Moreno; José M. Miró