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1.
Diagn Microbiol Infect Dis ; 101(2): 115430, 2021 Oct.
Article in English | MEDLINE | ID: mdl-34229244

ABSTRACT

BACKGROUND: This study aimed to assess, by rapid tests, the immune status against COVID-19 among Healthcare Workers (HCW) with history of symptoms, and for whom SARS-CoV-2 detection was either not documented or negative. METHODS: Whole blood by finger prick and serum samples were taken from HCW for use with 2 rapid lateral flow tests and an automated immunoassay. RESULTS: Seventy-two HCWs were included, median duration between symptoms onset and serology sampling was 68 days. Anti-SARS-CoV-2 antibodies were detected by rapid test in 11 HCW (15.3%) and confirmed in the 10 with available serum by the automated immunoassay. The frequency of ageusia or anosmia was higher in participants with SARS-CoV-2 antibodies (P = 0.0006 and P = 0.029, respectively). CONCLUSIONS: This study, among symptomatic HCW during the first wave in France, showed that 15% had IgG anti-SARS-CoV-2, a higher seroprevalence than in the general population. Rapid lateral flow tests were highly concordant with automated immunoassay.


Subject(s)
COVID-19 Serological Testing , COVID-19/diagnosis , Health Personnel , Point-of-Care Testing , SARS-CoV-2/isolation & purification , Adult , Antibodies, Viral/blood , COVID-19/blood , Female , Humans , Immunoassay , Male , Middle Aged , Paris/epidemiology , Pilot Projects , Prospective Studies , SARS-CoV-2/immunology , Sensitivity and Specificity , Seroepidemiologic Studies
2.
AIDS Care ; 32(7): 811-817, 2020 07.
Article in English | MEDLINE | ID: mdl-31431047

ABSTRACT

We evaluated awareness of treatment as prevention (TasP) among adults people living with HIV (PLHIV) in five infectious disease departments in Paris, then how they perceived its impact on their sexual well-being. This cross-sectional multicenter survey was conducted in 2014 during scheduled clinical appointments using a self-administered questionnaire. We analyzed 520 questionnaires (42% women, 54% men of whom 57% were MSM [men who have sex with men]). 75% of women were born abroad, most commonly in sub-Saharan Africa, whereas 64% of men were French-born. The mean time since HIV diagnosis was 12.8 ± 7.8 years. Eighty-seven percent [84-90%]95% reported being aware of the impact of ART on HIV transmission, 94% MSM, 86% women, 83% heterosexual men. PLHIV reported that they gained awareness of TasP through medical doctors (86%). The fear of transmission was perceived as alleviated for 73% [69%;78%]95%, more often among MSM; the sexual life was reported to be improved for 28% [24%;33%]95%; and ART adherence to be improved for 45% [40%;50%]95%, more often among women. The awareness of TasP was relatively high, but it seems important to understand the features of male and female populations of PLHIV to adapt counseling during follow-up appointments, as women's answers differed in various regards.


Subject(s)
HIV Infections , Sexual and Gender Minorities , Cross-Sectional Studies , Female , HIV Infections/prevention & control , Homosexuality, Male , Humans , Male , Paris , Sexual Behavior , Sexual Partners , Surveys and Questionnaires
3.
Antivir Ther ; 20(5): 507-13, 2015.
Article in English | MEDLINE | ID: mdl-25599649

ABSTRACT

BACKGROUND: Atazanavir/ritonavir (ATV/r) is a boosted protease inhibitor recommended to minimize the risk of mother-to-child HIV-1 transmission (MTCT). We aimed to assess the pharmacokinetics, safety and efficacy of ATV/r in HIV-1-infected pregnant women and their neonates. METHODS: A multicentre, cross-sectional, non-interventional cohort of HIV-1-infected pregnant women receiving ATV/r (300/100 mg once daily) who delivered in three Paris hospitals from 2006 to 2013 was designed. We determined antiretroviral trough plasma concentrations using liquid chromatography-mass spectrometry at each of the three trimesters, delivery and post-partum. ATV concentrations at 24 h (C24h) were interpreted by the 150-850 ng/ml efficacy-tolerance thresholds. Safety data and newborn HIV status were recorded. A mother's virological failure was defined as two successive measurements of plasma HIV-1 RNA>50 copies/ml within the 2 months before delivery. RESULTS: 103 pregnant women were included, mostly from sub-Saharan Africa (88%). ATV C24h at each of the three trimesters and delivery remained similar to post-partum values. No dose adjustment was needed during pregnancy. The median plasma ratio of fetal/maternal ATV level was 0.19 (n=28). Only three patients showed two successive detectable viral loads but <400 copies/ml. Among 82 available newborn data, 16 were born preterm. Three in utero deaths occurred. Tolerance was good with one case of maternal grade 3 hyperbilirubinaemia, no cases in neonates at delivery and no clinically relevant adverse event. No case of MTCT was reported. CONCLUSIONS: In this population, an ATV/r-containing antiretroviral regimen demonstrated good pharmacokinetics, virological efficacy and safety. No significant impact of pregnancy on ATV C24h was found. No dose adjustment was required.


Subject(s)
Atazanavir Sulfate , HIV Protease Inhibitors , HIV-1/drug effects , Pregnancy Complications, Infectious/drug therapy , Ritonavir , Adult , Atazanavir Sulfate/adverse effects , Atazanavir Sulfate/pharmacokinetics , Atazanavir Sulfate/therapeutic use , CD4 Lymphocyte Count , Cross-Sectional Studies , Drug Administration Schedule , Drug Combinations , Female , HIV Protease Inhibitors/adverse effects , HIV Protease Inhibitors/pharmacokinetics , HIV Protease Inhibitors/therapeutic use , Humans , Hyperbilirubinemia/chemically induced , Infant, Newborn , Pregnancy , Ritonavir/adverse effects , Ritonavir/pharmacokinetics , Ritonavir/therapeutic use , Viral Load/drug effects
4.
PLoS One ; 7(9): e44442, 2012.
Article in English | MEDLINE | ID: mdl-22970218

ABSTRACT

BACKGROUND: Exposure to hepatitis B virus (HBV) remains a serious risk to healthcare workers (HCWs) in endemic developing countries owing to the strong prevalence of HBV in the general and hospital populations, and to the high rate of occupational blood exposure. Routine HBV vaccination programs targeted to high-risk groups and especially to HCWs are generally considered as a key element of prevention strategies. However, the high rate of natural immunization among adults in such countries where most infections occur perinatally or during early childhood must be taken into account. METHODOLOGY/PRINCIPAL FINDINGS: We conducted a cross sectional study in 207 personnel of 4 occupational groups (medical, paramedical, cleaning staff, and administrative) in Niamey's National Hospital, Niger, in order to assess the prevalence of HBV markers, to evaluate susceptibility to HBV infection, and to identify personnel who might benefit from vaccination. The proportion of those who declared a history of occupational blood exposure ranged from 18.9% in the administrative staff to 46.9% in paramedical staff. Only 7.2% had a history of vaccination against HBV with at least 3 injections. Ninety two percent were anti-HBc positive. When we focused on170 HCWs, only 12 (7.1%) showed no biological HBV contact. Twenty six were HBsAg positive (15,3%; 95% confidence interval: 9.9%-20.7%) of whom 8 (32%) had a viral load >2000 IU/ml. CONCLUSIONS/SIGNIFICANCE: The very small proportion of HCWs susceptible to HBV infection in our study and other studies suggests that in a global approach to prevent occupational infection by bloodborne pathogens, a universal hepatitis B vaccination of HCWs is not priority in these settings. The greatest impact on the risk will most likely be achieved by focusing efforts on primary prevention strategies to reduce occupational blood exposure. HBV screening in HCWs and treatment of those with chronic HBV infection should be however considered.


Subject(s)
Hepatitis B Vaccines/administration & dosage , Hospitals, University , Personnel, Hospital , Adult , Cross-Sectional Studies , Developing Countries , Endemic Diseases , Female , Humans , Male , Middle Aged , Niger
5.
J Med Virol ; 69(1): 7-17, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12436472

ABSTRACT

The aims of this study were to assess the sociodemographic, epidemiological, clinical, and biological characteristics of French patients co-infected with human immunodeficiency virus-hepatitis C virus (HIV-HCV), as well as the management of their HCV infection. Data on 509 HIV-HCV co-infected patients, followed up at six French University Hospitals, were collected using a questionnaire. Student's t-test, Pearson's chi-square, Fisher's exact, and Fisher-Freeman-Halton's exact tests were used. The mean age of the patients was 38.3 years, and the male to female sex ratio 2.08; 88% of patients were born in Metropolitan France, and 20% were dependent on health benefits; 74% were intravenous drug users and 14% blood or blood product recipients. Forty-seven percent were in CDC classification stage A, 18% had a CD4+ count of <200, and 79% were undergoing current antiretroviral treatment. HCV RNA was positive in 84% (50% type 1, 13% untypable). Forty-four percent had normal alanine aminotransferase (ALT) levels, 24% alcohol consumption >15 g/day, and 51% had undergone liver biopsy (10% of which had cirrhosis). Histological grade was not related to ALT level or CD4+ count. Overall, 40% of patients had been treated for HCV infection. HCV treatment was significantly associated with performance of liver biopsy, histological grade, ALT level, CD4+ count, Centers for Disease Control (CDC) classification, but not with age or alcohol consumption. Rate of early response to treatment was fifty percent among patients treated with bitherapy. Eighty-nine percent of all patients with previous or current anti-HCV treatment had undergone liver biopsy. In conclusion, despite the difficulties in managing hepatitis C in HIV-infected patients, almost one-half of all patients in this study had received anti-HCV treatment.


Subject(s)
HIV Infections/complications , Hepacivirus/physiology , Hepatitis C/complications , Liver/virology , RNA, Viral/analysis , Substance Abuse, Intravenous/complications , Adult , Alanine Transaminase/blood , Antiviral Agents/therapeutic use , Female , France , Genotype , HIV Infections/drug therapy , HIV Infections/immunology , HIV Infections/virology , Hepacivirus/genetics , Hepacivirus/isolation & purification , Hepatitis C/blood , Hepatitis C/drug therapy , Hepatitis C/pathology , Hepatitis C/virology , Hospitals, University , Humans , Interferons/therapeutic use , Liver/pathology , Male , RNA, Viral/blood , Risk Factors , Surveys and Questionnaires
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