Subject(s)
Bacteremia/complications , Pericarditis/microbiology , Pneumonia, Pneumococcal/complications , Adult , Humans , Male , SuppurationABSTRACT
No disponible
Subject(s)
Humans , Male , Adult , Pericarditis/microbiology , Pneumonia, Pneumococcal/complications , Streptococcus pneumoniae/pathogenicity , Bacteremia/complicationsABSTRACT
Insulin resistance (IR) is a common condition in chronic hepatitis C. Recent studies have reported that IR is associated with liver fibrosis progression in these patients. However, there is no information available on this issue in human immunodeficiency virus (HIV)/hepatitis C virus (HCV)-coinfected patients. For these reasons, we investigate the relationship between IR and liver fibrosis in patients with HIV and HCV infections. This was a cross-sectional study where patients from an Infectious Diseases Unit with HIV/HCV coinfection who underwent a liver biopsy, with available frozen sera samples at the time of biopsy and a known or estimated date of infection were included. IR was determined by the homeostasis model assessment (HOMA-IR) method. The relationship between histological findings and several variables, including HOMA-IR values, was examined. Seventy-nine patients fulfilled the inclusion criteria. Age at HCV infection >21 years was the only variable independently associated with advanced liver fibrosis (stages F3 and F4) [adjusted odds ratio (AOR) 4.15; 95% confidence interval (CI) 1.5-11.3]. The variables associated with a fibrosis progression rate above the median were age at HCV infection >21 years (AOR 6.41; 95% CI 2.16-27.96) and previous exposure to nevirapine (AOR 8.9; 95% CI 2.01-39.36). There was no association between HOMA-IR values and the presence of advanced fibrosis or a faster fibrosis progression. Thus IR is not associated with liver damage or fibrosis progression in HIV/HCV-coinfected individuals.
Subject(s)
HIV Infections/metabolism , HIV , Hepatitis C/metabolism , Insulin Resistance , Liver Cirrhosis/metabolism , Adult , Cross-Sectional Studies , Female , HIV Infections/complications , HIV Infections/pathology , HIV Infections/virology , Hepatitis C/complications , Hepatitis C/pathology , Hepatitis C/virology , Humans , Liver Cirrhosis/pathology , Liver Cirrhosis/virology , MaleABSTRACT
The prevalence of osteopenia in HIV-infected patients is high. However, the mechanisms implicated in bone mass loss in HIV infection are unclear. Because of this, we analyzed serum free testosterone and vitamin D3 hydroxylated metabolites in HIV-infected patients, with and without antiretroviral treatment, and the relation between them and osteopenia. Seventy-four HIV-infected patients were selected because they had frozen sera available at a date close to a DEXA evaluation. Free testosterone, 25(OH)D3, and 1,25(OH)2D3 were determined in frozen serum. There were no differences in free testosterone, 25(OH)D3, and 1,25(OH)2D3 levels between patients with and without osteopenia. 25(OH)D3 levels in naive and HAART-treated patients were 26.2 (10.3-32.8) and 33.1 (20.6-46.8) ng/ml, respectively (p = 0.04). 1,25(OH)2D3 levels in naive and HAART treated patients were 60.3 (49.2-80.8) and 85.5 (68-111.6) pmol/liter (p = 0.01). Free testosterone levels in 9 naive men and in 50 HAART-treated men were 42.6 (24.1-67.3) and 69.2 (47.5-112.1) pmol/liter, respectively (p = 0.04). In conclusion, HIV-infected patients with and without osteopenia showed similar levels of vitamin D metabolites and free testosterone. However, antiretroviral drug-naive patients showed lower serum levels of vitamin D metabolites and free testosterone than HAART-treated patients.
Subject(s)
Antiretroviral Therapy, Highly Active , Bone Diseases, Metabolic/etiology , Calcifediol/blood , Calcitriol/blood , HIV Infections/complications , HIV Infections/drug therapy , Testosterone/blood , Vitamin D/blood , Adult , Anti-HIV Agents/therapeutic use , Female , Humans , Male , Middle AgedABSTRACT
No disponible
Subject(s)
Adult , Male , Humans , Cerebrospinal Fluid , Meningitis , Skull Fracture, Basilar , Acute Disease , Fistula , Brain Injuries, TraumaticSubject(s)
AIDS-Related Opportunistic Infections/microbiology , Bartonella Infections/complications , Hemoperitoneum/microbiology , Liver Diseases/complications , AIDS-Related Opportunistic Infections/diagnosis , Adult , Antibodies, Bacterial/blood , Bartonella Infections/diagnosis , Bartonella Infections/microbiology , Bartonella henselae/immunology , Humans , Liver Diseases/diagnosis , Liver Diseases/microbiology , MaleSubject(s)
Fingers/blood supply , Gangrene/etiology , Osteomyelitis/etiology , Pneumonia, Bacterial/etiology , Radiography, Thoracic , Streptococcal Infections/diagnosis , Streptococcus pyogenes , Substance Abuse, Intravenous/complications , Adult , Empyema, Pleural/etiology , Female , Humans , Pneumonia, Bacterial/diagnostic imaging , Streptococcal Infections/complicationsSubject(s)
Ciprofloxacin/adverse effects , IgA Vasculitis/chemically induced , Aged , Aged, 80 and over , Humans , MaleABSTRACT
We report on an outbreak of laboratory-acquired brucellosis involving four technicians working at a microbiology laboratory. All cases occurred in a period of 4 months. Blood cultures and the Rose Bengal test were positive for Brucella spp. in all cases. Microagglutination was positive for Brucella spp. at titers of between 1/40 and 1/160. All patients were cured after treatment.
