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1.
Infect Dis Now ; 53(5): 104687, 2023 Aug.
Article in English | MEDLINE | ID: mdl-36842502

ABSTRACT

OBJECTIVES: Blood-culture-negative infective endocarditis (BCNE) is found in 2 to 48% of cases of infective endocarditis (IE) (Houpikian and Raoult, 2005) [1].IE and vertebral osteomyelitis due to Chlamydia sp. are difficult to diagnose. PATIENTS AND METHODS: A case report of Chlamydia psittaci IE is provided, associated with a literature review. RESULTS: We report the first case of Chlamydia psittaci IE, revealed by a spondylodiscitis. Questioning of the patient, imaging, serologies and PCR techniques on valves confirmed the diagnosis. CONCLUSION: C. psittaci IE is rare but probably underdiagnosed. In case of negative blood cultures, questioning patients with IE about their contacts with animals is relevant. PCR techniques are reference tools for diagnosis confirmation when valve or vertebral samples are available.


Subject(s)
Chlamydophila psittaci , Endocarditis, Bacterial , Endocarditis , Psittacosis , Humans , Endocarditis, Bacterial/diagnosis , Endocarditis, Bacterial/drug therapy , Bacteria
2.
J Clin Virol ; 82: 1-4, 2016 09.
Article in English | MEDLINE | ID: mdl-27389909

ABSTRACT

While the rapid spread of Zika virus (ZIKV) in South America has been declared a public health emergency few data are available on the kinetics of the virus load and the specific antibodies in individual patients. This report describes the kinetics of ZIKV decay in the body compartments and the kinetics of anti ZIKV IgG and IgM of two people returning from Martinique, French West Indies. ZIKV remained detectable in the plasma for roughly 2 weeks indicating that mosquito control measures should be prolonged accordingly. Remarkably, their urine samples consistently tested positive for even longer. The antibodies responses were different between the two patients but for both the rapid onset of IgM allowed a diagnosis from the end of the first week.


Subject(s)
Communicable Diseases, Imported/virology , Viral Load , Zika Virus Infection/virology , Zika Virus/isolation & purification , Aged , Antibodies, Viral/blood , Family Characteristics , Female , France , Humans , Immunoglobulin G/blood , Immunoglobulin M/blood , Male , Martinique , Middle Aged , Plasma/virology , Saliva/virology , Time Factors , Urine/virology
5.
Int J STD AIDS ; 27(11): 1005-12, 2016 10.
Article in English | MEDLINE | ID: mdl-26429893

ABSTRACT

In France, almost 30,000 people are unaware of their HIV-positive status. Innovative screening strategies are essential to reach this population. The aim of this study was to describe the acceptability of rapid HIV testing (RHT) among French general practitioners (GPs) working in the south of France and barriers for implementing this strategy. We analysed an anonymous questionnaire sent by mail to GPs about demographic data, routine practice, knowledge of RHT and barriers to its use. Between 1 April and 30 September 2013, out of the 165 GPs contacted, 78 returned the questionnaires. The GPs' mean age was 52 years; 49 were men. Fifty-one GPs reported that their registered patients included at least one HIV-infected person and 70 GPs reported taking care of high-risk patients. Sixty-three percent of GPs reported being interested in using RHT in their daily practice. The main reasons reported by uninterested GPs were: greater confidence in standard HIV testing, difficulties including RHT during the routine consultation, difficulties to screen for other sexually transmitted infections simultaneously, and difficulties to deliver a positive result. French National Authorities for Health propose to screen the population at least once in their lifetime and high-risk people at least once a year. In order to achieve this aim, RHT should be included in the GPs' arsenal for HIV testing. We showed a high acceptability of RHT by GPs. If specific and adapted training is developed, and if solutions to barriers reported by GPs are found, RHT could be implemented in to their routine activity.


Subject(s)
AIDS Serodiagnosis/methods , Attitude of Health Personnel , General Practitioners/psychology , HIV Infections/diagnosis , Mass Screening/psychology , AIDS Serodiagnosis/statistics & numerical data , Adult , Aged , Blood Specimen Collection/methods , Blood Specimen Collection/psychology , Cross-Sectional Studies , Feasibility Studies , Female , France , HIV Infections/prevention & control , HIV Seropositivity/diagnosis , HIV Seropositivity/epidemiology , Health Care Surveys , Humans , Male , Middle Aged , Patient Acceptance of Health Care , Surveys and Questionnaires
7.
J Acquir Immune Defic Syndr ; 65(2): 198-206, 2014 Feb 01.
Article in English | MEDLINE | ID: mdl-24220287

ABSTRACT

BACKGROUND: Malaria during pregnancy has serious consequences that are worsened by HIV infection. Malaria preventive measures for HIV-infected pregnant women include cotrimoxazole (CTX) prophylaxis given to prevent HIV-related opportunistic infections and also protective against malaria, or intermittent preventive treatment (IPTp) with an antimalarial drug. Here, we present the first study evaluating CTX efficacy versus mefloquine (MQ)-IPTp, alone and in combination, in HIV-infected pregnant women. METHODS: We conducted 2 randomized, open-label, noninferiority trials in Benin. In the CTX-mandatory trial, HIV-infected women with CD4 counts of <350 per cubic millimeter received CTX either alone or with MQ-IPTp (N = 292). In the CTX-not-mandatory trial (CD4 count >350/mm), CTX was compared with MQ-IPTp (N = 140). In both the trials, the primary end point was microscopic placental parasitemia. RESULTS: At delivery, 1 woman in each CTX-alone treatment group exhibited placental parasitemia, versus no women in the groups receiving MQ. CTX alone demonstrated noninferiority in the CTX-mandatory trial. However, polymerase chain reaction-detected placental parasitemia was markedly reduced in the CTX + MQ group compared with CTX alone (0/105 vs. 5/103, P = 0.03). Because of insufficient recruitment in the CTX-not-mandatory trial, noninferiority could not be conclusively assessed. Dizziness and vomiting of moderate intensity were reported by 34%-37% of women receiving MQ in both the trials, versus 0%-3% in CTX groups (P < 0.0001). No serious adverse events related to these drugs were found. CONCLUSIONS: CTX alone provided adequate protection against malaria in HIV-infected pregnant women, although MQ-IPTp showed higher efficacy against placental infection. Although more frequently associated with dizziness and vomiting, MQ-IPTp may be an effective alternative given concerns about parasite resistance to CTX.


Subject(s)
Antimalarials/administration & dosage , Chemoprevention/methods , HIV Infections/complications , Malaria/prevention & control , Mefloquine/administration & dosage , Pregnancy Complications, Parasitic/prevention & control , Trimethoprim, Sulfamethoxazole Drug Combination/administration & dosage , Adult , Antimalarials/adverse effects , Benin , Chemoprevention/adverse effects , Dizziness/chemically induced , Dizziness/epidemiology , Drug Therapy, Combination/adverse effects , Drug Therapy, Combination/methods , Drug-Related Side Effects and Adverse Reactions/epidemiology , Drug-Related Side Effects and Adverse Reactions/pathology , Female , Humans , Infant , Infant, Newborn , Mefloquine/adverse effects , Parasitemia/prevention & control , Pregnancy , Treatment Outcome , Trimethoprim, Sulfamethoxazole Drug Combination/adverse effects , Young Adult
8.
PLoS One ; 8(3): e59446, 2013.
Article in English | MEDLINE | ID: mdl-23555035

ABSTRACT

OBJECTIVE: To investigate the factors associated with HIV1 RNA plasma viral load (pVL) below 40 copies/mL at the third trimester of pregnancy, as part of prevention of mother-to-child transmission (PMTCT) in Benin. DESIGN: Sub study of the PACOME clinical trial of malaria prophylaxis in HIV-infected pregnant women, conducted before and after the implementation of the WHO 2009 revised guidelines for PMTCT. METHODS: HIV-infected women were enrolled in the second trimester of pregnancy. Socio-economic characteristics, HIV history, clinical and biological characteristics were recorded. Malaria prevention and PMTCT involving antiretroviral therapy (ART) for mothers and infants were provided. Logistic regression helped identifying factors associated with virologic suppression at the end of pregnancy. RESULTS: Overall 217 third trimester pVLs were available, and 71% showed undetectability. Virologic suppression was more frequent in women enrolled after the change in PMTCT recommendations, advising to start ART at 14 weeks instead of 28 weeks of pregnancy. In multivariate analysis, Fon ethnic group (the predominant ethnic group in the study area), regular job, first and second pregnancy, higher baseline pVL and impaired adherence to ART were negative factors whereas higher weight, higher antenatal care attendance and longer ART duration were favorable factors to achieve virologic suppression. CONCLUSIONS: This study provides more evidence that ART has to be initiated before the last trimester of pregnancy to achieve an undetectable pVL before delivery. In Benin, new recommendations supporting early initiation were well implemented and, together with a high antenatal care attendance, led to high rate of virologic control.


Subject(s)
Anti-HIV Agents/pharmacology , HIV Infections/blood , HIV Infections/transmission , HIV-1/physiology , Infectious Disease Transmission, Vertical/prevention & control , Pregnancy Complications/blood , RNA, Viral/blood , Adult , Benin , Cohort Studies , Female , HIV-1/drug effects , Humans , Logistic Models , Malaria/prevention & control , Multivariate Analysis , Pregnancy , Pregnancy Trimester, Third/blood , Prospective Studies , Viral Load/drug effects
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