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1.
Euro Surveill ; 26(18)2021 05.
Artigo em Inglês | MEDLINE | ID: mdl-33960288

RESUMO

Despite social distancing measures implemented in Madrid to prevent the propagation of SARS-CoV-2, a significant increase (57.1%; 28.5 to 38.5 cases/month) in cases of lymphogranuloma venereum was detected during the COVID-19 pandemic. This unusual scenario might have accelerated a shift in Chlamydia trachomatis (CT) epidemiology towards a higher proportion of L genotypes compared with non-L genotypes in CT-positive samples. Our data underscore the importance of surveillance of sexually transmitted infections during the pandemic, in particular among vulnerable populations.


Assuntos
COVID-19 , Linfogranuloma Venéreo , Chlamydia trachomatis/genética , Homossexualidade Masculina , Humanos , Linfogranuloma Venéreo/diagnóstico , Linfogranuloma Venéreo/epidemiologia , Masculino , Pandemias , SARS-CoV-2 , Espanha/epidemiologia
2.
Clin Infect Dis ; 57(3): 458-64, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23575196

RESUMO

BACKGROUND: It is unclear whether pegylated interferon (peg-IFN) -induced neutropenia in subjects coinfected with human immunodeficiency virus (HIV) and hepatitis C virus (HCV) is associated with increased risk of serious infections. METHODS: This was a prospective cohort study conducted between 2000 and 2012 in HIV/HCV-coinfected subjects initiating treatment with peg-IFN plus ribavirin (RBV). Infections were defined as serious when patients required hospitalization, treatment was discontinued, or the patient died. The association between neutropenia (severe, <500 cells/µL; nonsevere, 500 -1500 cells/µL) and infections (serious infections and infections of any severity) was determined by logistic regression analysis. RESULTS: Among 418 subjects (3928 person-weeks of therapy), infections occurred in 123 (29%), accounting for 149 episodes (3.8 infections per 100 person-weeks of therapy). Most infections (47%) involved the upper respiratory tract and were minor. After a multivariate analysis adjusted by age, sex, CD4 count, AIDS, antiretroviral therapy, cirrhosis, neutrophil count, type of peg-IFN, and granulocyte colony-stimulating factor use, none of these variables remained independently associated with the risk of infection. Twenty subjects developed a serious infection (4.8% of all patients). The frequency of serious infections was higher in subjects with severe neutropenia compared to those with nonsevere neutropenia and without neutropenia, although it was not statistically significant (8.6%, 4.8%, and 3.6%, respectively; trend test P = .281). In multivariate analysis, neutropenia was not independently associated with increased risk of serious infections. CONCLUSIONS: In this large prospective cohort of HIV/HCV-coinfected patients treated with peg-IFN plus RBV, serious infections were uncommon, nonfatal, and unrelated to peg-IFN -induced severe neutropenia.


Assuntos
Infecções por HIV/complicações , Hepatite C Crônica/tratamento farmacológico , Interferons/efeitos adversos , Interferons/uso terapêutico , Neutropenia/induzido quimicamente , Infecções Oportunistas/epidemiologia , Ribavirina/uso terapêutico , Adulto , Antivirais/efeitos adversos , Antivirais/uso terapêutico , Estudos de Coortes , Quimioterapia Combinada/efeitos adversos , Infecções por HIV/imunologia , Hepatite C Crônica/complicações , Humanos , Pessoa de Meia-Idade , Neutropenia/imunologia , Estudos Prospectivos , Medição de Risco
5.
Artigo em Inglês | MEDLINE | ID: mdl-19721095

RESUMO

PURPOSE: To evaluate clinical, immunological, and virological outcomes after first-line highly active antiretroviral therapy (HAART) with a regimen including either efavirenz (EFV) or lopinavir/ritonavir (LPV/r) in treatment-naive adult patients in routine clinical care. METHOD: An ongoing prospective, observational follow-up study included all patients starting their first antiretroviral therapy (ART) with any of the studied regimens from July 1998 to July 2004. The follow-up period was finalized in September 2006, when all patients completed an observation of at least 96 weeks. Mortality rates, CD4 counts, viral suppression (HIV RNA below 50 copies/mL), and discontinuation of any component of the regimen were compared at 48 and 96 weeks. RESULTS: Despite the worst immunological status of the LPV/r group patients at baseline, this regimen was at least as effective as the one based on EFV not only in terms of treatment durability but also in terms of virological responses, nevertheless with an apparently quicker immune recovery. In general terms, both regimens present similar tolerability and safety outcomes except for the higher risk of increasing triglyceride (TG) levels in the LPV/r group. Low durability was observed in both regimens. CONCLUSION: In a routine clinical care setting, initial HAART containing LPV/r seems to present an effectiveness, tolerability, and toxicity similar to the one containing EFV.


Assuntos
Terapia Antirretroviral de Alta Atividade , Infecções por HIV/tratamento farmacológico , Adulto , Alcinos , Fármacos Anti-HIV/uso terapêutico , Benzoxazinas/uso terapêutico , Contagem de Linfócito CD4 , Ciclopropanos , Feminino , Seguimentos , Infecções por HIV/sangue , Infecções por HIV/mortalidade , Humanos , Lopinavir , Masculino , Estudos Prospectivos , Pirimidinonas/uso terapêutico , Ritonavir/uso terapêutico , Triglicerídeos/sangue , Carga Viral
6.
Asian Cardiovasc Thorac Ann ; 25(3): 226-228, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28325073

RESUMO

Despite the high frequency of gastrointestinal complications and opportunistic infections in HIV-1 infected patients, tracheoesophageal (TEF) and bronchoesophageal (BEF) fístulas are rare. Our objective is to comunicate an additional and unusual case of TEF in an HIV-1-infected patient whose immunologic status was good with complete suppression of viral replication, so although uncommon, TEF/BEF of an infectious origen should be considered in AIDS. Endoscopic treatment with tracheal/esophageal stents is not without morbidity and mortality. As long as the patient can undergo reconstructive surgery, this should be the technique of choice.


Assuntos
Síndrome da Imunodeficiência Adquirida/complicações , Broncoscopia/métodos , Endoscopia Gastrointestinal/métodos , Esôfago/cirurgia , HIV , Traqueia/cirurgia , Fístula Traqueoesofágica/cirurgia , Adulto , Anastomose Cirúrgica/métodos , Humanos , Masculino , Stents , Tomografia Computadorizada por Raios X , Fístula Traqueoesofágica/complicações
7.
PLoS One ; 9(1): e85798, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24497929

RESUMO

BACKGROUND: A low CD4/CD8 ratio has been identified in the general population as a hallmark of inmmunosenescence and a surrogate of all-cause mortality. We aimed to investigate in treated HIV-infected individuals the relationship between the CD4/CD8 ratio and serious non-AIDS events. METHODS: Case-control study within a prospective hospital-based cohort of HIV-infected subjects during at least one year of ART-mediated viral suppression. Cases were patients with serious non-AIDS events (non-AIDS malignancies, cardiovascular disease, and end-stage kidney disease), and controls individuals who did not developed non-AIDS events during follow-up. Data were analyzed using ROC analysis and multivariate logistic regression. Conditional logistic regression was performed in 200 cases/controls matched by age, sex, nadir CD4 and proximal CD4 counts. RESULTS: We analyzed 407 subjects (109 cases, 298 controls). The CD4/CD8 ratio was lower in cases (0.44 vs. 0.70, P<0.0001), with higher discriminatory ability for the detection of non-AIDS events than the CD4 count, CD8 count and nadir CD4. Multivariate analyses (adjusted for age, sex, nadir CD4, proximal CD4 count, year of ART initiation and ART duration) confirmed the independent association of a low CD4/CD8 ratio with the risk of non-AIDS morbidity (per CD4/CD8 ratio quartile decrease, OR, 2.9; 95% CI, 1.3-6.2) and non-AIDS mortality (OR, 2.8; 95% CI, 1.5-5.3). CONCLUSIONS: The CD4/CD8 ratio provides additional information to the CD4 counts and nadir CD4 in treated HIV-infected individuals, since it is independently associated with the risk of non-AIDS-related morbidity and mortality. This association is robust and maintained within different subgroups of patients.


Assuntos
Fármacos Anti-HIV/uso terapêutico , Doenças Cardiovasculares/virologia , Infecções por HIV/imunologia , Neoplasias/virologia , Adulto , Relação CD4-CD8 , Doenças Cardiovasculares/imunologia , Estudos de Casos e Controles , Feminino , Infecções por HIV/complicações , Infecções por HIV/tratamento farmacológico , Humanos , Masculino , Pessoa de Meia-Idade , Análise Multivariada , Neoplasias/imunologia , Estudos Prospectivos , Curva ROC , Risco
8.
J Antimicrob Chemother ; 59(4): 794-8, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17392354

RESUMO

BACKGROUND: Limited data are available to predict the length of time required for a patient to achieve sputum culture conversion after starting therapy for pulmonary tuberculosis. METHODS: Rates of sputum smear and culture conversion were determined at weeks 2, 4, 8 and 16 after initiating therapy in patients admitted to our Respiratory Isolation Unit from January 1997 to December 2003. RESULTS: For the 184 patients included in the analysis, the mean time from the initiation of appropriate therapy to sputum culture and smear conversion were 34 +/- 26 and 38 +/- 32 days (mean +/- SD) respectively. Only 53% of patients obtained negative sputum cultures within the first 4 weeks of therapy. Multivariate analysis showed that the persistence of positive cultures during the first 4 weeks of therapy was associated with high bacillary counts in sputum smears at diagnosis [OR: 2.86; 95% confidence interval (95% CI): 1.20-6.66], lung cavitations (OR: 4.0; 95% CI: 1.63-9.09) and a prolonged period of symptoms (OR: 3.57; 95% CI: 1.43-3.57). The only factor associated with the persistence of positive cultures after more than 16 weeks of therapy was infection with a multidrug-resistant strain. CONCLUSIONS: High initial sputum bacillary counts and drug resistance result in delayed culture conversion. This should be taken into account when decisions regarding the potential discontinuation of isolation are made. The early identification of drug resistance is important for effective infection control in hospitals.


Assuntos
Mycobacterium tuberculosis/efeitos dos fármacos , Isolamento de Pacientes , Escarro/microbiologia , Tuberculose Pulmonar/microbiologia , Adulto , Idoso , Antituberculosos/farmacologia , Contagem de Colônia Microbiana , Farmacorresistência Bacteriana Múltipla , Feminino , Infecções por HIV/complicações , Humanos , Isoniazida/farmacologia , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Análise Multivariada , Fatores de Risco
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