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Dive into the research topics where Susana Peres is active.

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Featured researches published by Susana Peres.


Journal of the International AIDS Society | 2014

The impact of tenofovir disoproxil fumarate on kidney function: four-year data from the HIV-infected outpatient cohort.

Nadine Monteiro; Margarida Branco; Susana Peres; Fernando Borges; Kamal Mansinho

With improvements in survival and disease progression in the era of combined antiretroviral therapy, complications such as kidney disease are becoming increasingly prevalent in HIV‐infected patients. Tenofovir disoproxil fumarate (TDF) has been associated with nephrotoxicity, including decline in glomerular filtration rate, proximal tubular damage and acute kidney injury.


Journal of the International AIDS Society | 2014

Durability of first antiretroviral treatment in HIV chronically infected patients: why change and what are the outcomes?

Patricia Moniz; Filipa Alçada; Susana Peres; Fernando Borges; Teresa Baptista; Ana Cláudia Miranda; Isabel Antunes; Isabel Aldir; Fernando Ventura; Jaime Nina; Kamal Mansinho

First antiretroviral therapy (ART) is often switched to simpler, more potent or better tolerated regimens [ 1 , 2 ]. Although discontinuation rates are frequently studied, the durability of regimens is rarely approached.


Journal of the International AIDS Society | 2014

Evolution trends over three decades of HIV infection late diagnosis: the experience of a Portuguese cohort of 705 HIV-infected patients

Ana Cláudia Miranda; Virginia Moneti; Pedro Brogueira; Susana Peres; Teresa Baptista; Isabel Aldir; Fernando Ventura; Fernando Borges; Kamal Mansinho

Late HIV diagnosis is common and associated with an increased risk of clinical progression, blunted immune response on antiretroviral (ARV) therapy and higher risk of drug toxicity. Across Europe, more than a third of patients are diagnosed late and consequently delay medical care. European Consensus definition group identify as late presentation (LP) persons, presenting for care, with a CD4 count below 350 cell/mm3 or presenting with AIDS‐defining event, regardless of CD4 cell count. Additionally, advanced HIV disease (AD) is defined by a CD4 count below 200 cell/mm3 or an AIDS defining condition in persons presenting to care.


Journal of Antimicrobial Chemotherapy | 2013

The demise of multidrug-resistant HIV-1: the national time trend in Portugal

Jurgen Vercauteren; Kristof Theys; Ap Carvalho; Emília Valadas; Luis Miguel Duque; Eugénio Teófilo; Telo Faria; Domitília Faria; José Vera; Maria João Águas; Susana Peres; Kamal Mansinho; Anne-Mieke Vandamme; Ricardo Jorge Camacho

Objectives Despite a decreasing mortality and morbidity in treated HIV-1 patients, highly active antiretroviral treatment (HAART) can still fail due to the development of drug resistance. Especially, multidrug-resistant viruses pose a threat to efficient therapy. We studied the changing prevalence of multidrug resistance (MDR) over time in a cohort of HIV-1-infected patients in Portugal. Patients and methods We used data of 8065 HIV-1-infected patients followed from July 2001 up to April 2012 in 22 hospitals located in Portugal. MDR at a specific date of sampling was defined as no more than one fully active drug (excluding integrase and entry inhibitors) at that time authorized by the Portuguese National Authority of Medicines and Health Products (INFARMED), as interpreted with the Rega algorithm version 8.0.2. A generalized linear mixed model was used to study the time trend of the prevalence of MDR. Results We observed a statistically significant decrease in the prevalence of MDR over the last decade, from 6.9% (95% CI: 5.7–8.4) in 2001–03, 6.0% (95% CI: 4.9–7.2) in 2003–05, 3.7% (95% CI: 2.8–4.8) in 2005–07 and 1.6% (95% CI: 1.1–2.2) in 2007–09 down to 0.6% (95% CI: 0.3–0.9) in 2009–12 [OR = 0.80 (95% CI: 0.75–0.86); P < 0.001]. In July 2011 the last new case of MDR was seen. Conclusions The prevalence of multidrug-resistant HIV-1 is decreasing over time in Portugal, reflecting the increasing efficiency of HAART and the availability of new drugs. Therefore, in designing a new drug, safety and practical aspects, e.g. less toxicity and ease of use, may need more attention than focusing mainly on efficacy against resistant strains.


Case reports in infectious diseases | 2016

Acute Pyelonephritis with Bacteremia Caused by Enterococcus hirae: A Rare Infection in Humans

Ana Pãosinho; Telma Azevedo; João V. Alves; Isabel A. Costa; Gustavo Carvalho; Susana Peres; Teresa Baptista; Fernando Borges; Kamal Mansinho

Enterococci are one of the usual residents of the microflora in humans. In the last decade this genus has been reported as the third most common cause of bacteremia. We present the case of a 78-year-old female who was admitted to the emergency room because of nausea, lipothymia, and weakness. She was diagnosed with a pyelonephritis with bacteremia, with the isolation in blood and urine cultures of Escherichia coli and Enterococcus hirae. This last microorganism is a rarely isolated pathogen in humans. Currently it is estimated to represent 1–3% of all enterococcal species isolated in clinical practice.


Journal of the International AIDS Society | 2014

Improve screening of HCV infection by targeting high prevalence aged groups: analysis of a cohort of HCV and HIV co-infected patients

Pedro Brogueira; A.M. Costa; Ana Isabel Miranda; Susana Peres; Teresa Baptista; Isabel Aldir; Isabel Antunes; Fernando Ventura; Fernando Borges; Kamal Mansinho

Hepatitis C constitutes a major public health burden. In Portugal, the prevalence is estimated at 1–1.5% [ 1 ]. Of these, only 30% are presumed to be diagnosed, which reveals that most infections go unknown. The objective of this study is to identify the age‐range distribution at HCV diagnosis and to identify the high‐prevalence birth groups that could be targeted for screening, as a strategy to increase diagnosis and identify patients who would benefit most from treatment.


Journal of the International AIDS Society | 2014

Risk of liver decompensation assessed in HIV/HCV co-infected individuals with advanced liver fibrosis: a faster countdown experience

João Alves; Susana Peres; Fernando Borges; Ana Cláudia Miranda; Teresa Baptista; Fernando Ventura; Isabel Lobo Antunes; Jaime Nina; Maria José Campos; Isabel Aldir; Kamal Mansinho

Cirrhosis secondary to HCV infection is expected to peak in the next decade, particularly in the HIV co‐infected subgroup and has become a leading cause of morbidity among these individuals. Efforts must be done to estimate the risk of liver decompensation (LD) in the short term, in order to define the appropriate time for HCV treatment.


Journal of the International AIDS Society | 2014

Analysis of hepatitis non-treatment causes in a cohort of HCV and HCV/HIV infected patients

Karen Pereira; Ana Cláudia Miranda; Teresa Baptista; Susana Peres; Isabel Antunes; Fernando Ventura; Fernando Borges; Kamal Mansinho

The decision to start hepatitis C virus (HCV) treatment and its timing remains controversial. As new treatment regimens are approved, it is essential to identify patients eligible for each regimen in a timed and tailored approach. This study aims to identify the reasons to defer treatment of chronic hepatitis C infection in both HCV and HCV/HIV infected patients.


Acta Médica Portuguesa | 2017

Anaerobic Bacteria with Clinical Relevance: Morphologic and Taxonomic Classification, Distribution among Human Microbiota and Microbiologic Diagnosis

João Alves; Susana Peres; Elsa Gonçalves; Kamal Mansinho

The wide burden of anaerobic bacteria colonizing human body comprises about 90% of its total biomass. The biotic relationship between humans and its microbiota sets reciprocal benefits, albeit with pathogenic potencial for the human being in particular dysbiosis situations. Infections adjacent to or originating from the skin or mucous membranes of the intestinal, genitourinary and upper respiratory tracts are often polymicrobial in nature, whereby should anaerobes be invariably included in the etiological differential diagnosis of these conditions. Gram negative bacilli such as Bacteroides fragilis group, Fusobacterium spp., Porphyromonas spp., Prevotella spp. and Gram positive cocci such as Peptostreptococcus spp. stand out for their high virulence and frequence of isolation in suppurative infections and abcesses with metastatic or contiguous relation to human microbiota. The fastidious nature of anaerobic bacteria, especially of less aerotolerant species, compels to particular techniques of sample collection, transport and cultural isolation that challenge clinicians and microbiologists for a full efficient practice. Such requirements bring on a poor identification of anaerobic bacteria in the clinical practice and undervaluation of its aetiopathogenic potential amongst common polymicrobial infections. An approach over microbial floras composition in the different human anatomical sites is a primary goal of the present article. Clinicians are intended to recognize the variability and proportion of likely involved anaerobic microorganisms in certain infectious processes related to human microbiota, in order to optimize samples processing and the establishment of an appropriate empirical antibiotic therapy, mindful of anaerobic coverage and according to known susceptibility profiles.


Journal of the International AIDS Society | 2014

Clinical and laboratorial impact of antiretroviral therapy in a cohort of Portuguese patients chronically infected with HIV-2.

Ana Isabel Miranda; Susana Peres; Virginia Moneti; Telma Azevedo; Isabel Aldir; Kamal Mansinho

HIV‐2 infection is endemic in West Africa and some European countries, namely Portugal. HIV‐2 antiretroviral (ARV) treatment presents some restrains related to intrinsic resistance to non‐nucleoside reverse transcriptase inhibitors (NNRTI) and fusion inhibitors, and poorer response to protease inhibitors (PI).

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Dive into the Susana Peres's collaboration.

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Kamal Mansinho

Universidade Nova de Lisboa

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Ap Carvalho

Instituto de Medicina Molecular

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Jurgen Vercauteren

Rega Institute for Medical Research

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Kristof Theys

Rega Institute for Medical Research

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Jaime Nina

Universidade Nova de Lisboa

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João Alves

University of Strasbourg

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Anne-Mieke Vandamme

Rega Institute for Medical Research

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Michiel Debruyne

Katholieke Universiteit Leuven

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