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1.
Med Mal Infect ; 46(6): 318-21, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27235009

ABSTRACT

OBJECTIVE: To evaluate the efficacy of amikacin on sputum conversion during initial sputum smear positive tuberculosis treatment. MATERIAL AND METHODS: Single-center observational cohort study (2012-2013) evaluating time to sputum smear conversion with standard treatment (ST) versus standard treatment+amikacin (IV 15mg/kg/day) for seven days (STamK). RESULTS: Forty-five patients were included. Median time to smear negative samples was 26.5 days (14-56) for the 30 (66.7%) patients included in the ST group and 48 days (19.5-69.5) for the 15 patients (33.3%) included in the STamK group (P=0.76). Time to negative culture was only known for 27 patients (61.4%): 47.5 days (26-58) for 18 patients in the ST group and 40 days (14-77) for nine patients in the STamK group. CONCLUSION: Despite our small sample size, the addition of amikacin in active tuberculosis treatment did not seem to impact time to smear conversion or period of contagiousness.


Subject(s)
Amikacin/therapeutic use , Antitubercular Agents/therapeutic use , Tuberculosis, Pulmonary/drug therapy , Adult , Amikacin/administration & dosage , Antitubercular Agents/administration & dosage , Bacterial Load , Drug Administration Schedule , Drug Therapy, Combination , Female , Humans , Male , Middle Aged , Mycobacterium tuberculosis/drug effects , Mycobacterium tuberculosis/isolation & purification , Patient Isolation , Sputum/microbiology , Time Factors
2.
Eur J Clin Microbiol Infect Dis ; 32(6): 729-34, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23370968

ABSTRACT

Pyomyositis is a primary purulent infection of skeletal muscles mostly described in tropical areas. Staphylococcus aureus is by far the main causative microorganisms. In temperate areas, pyomyositis more frequently affects male adults with immunodeficiency. Gram-negative bacilli pyomyositis are uncommon and occur mainly in this context of immunodeficiency. Only one case of Enterobacter cloacae pyomyositis has been reported so far. Chronic Granulomatous Disease (CGD) is a rare inherited immunodeficiency characterized by a loss of NADPH oxidase activity in phagocytic cells that favors infections due to catalase-positive microorganisms. Pyomyositis has only been described once as a complication of CGD. We report here a case of Enterobacter cloacae-associated pyomyositis of the left thigh in a patient with CGD, and review the literature on Gram-negative pyomyositis.


Subject(s)
Enterobacter cloacae , Enterobacteriaceae Infections/complications , Granulomatous Disease, Chronic/complications , Pyomyositis/complications , Adult , Chronic Disease , Enterobacteriaceae Infections/diagnosis , Enterobacteriaceae Infections/drug therapy , Gram-Negative Bacteria , Humans , Male , Pyomyositis/diagnosis , Pyomyositis/drug therapy , Pyomyositis/microbiology , Treatment Outcome
3.
J Med Microbiol ; 60(Pt 2): 249-251, 2011 Feb.
Article in English | MEDLINE | ID: mdl-20965920

ABSTRACT

Corynebacterium jeikeium, a member of the non-diphtheria corynebacteria, has been rarely reported as being responsible for cardiovascular-device infection. Here, we report what is believed to be the first case of C. jeikeium pacemaker infection associated with the presence of proteinase-3 antineutrophil cytoplasmic antibodies. The diagnosis was established based on the positivity of a single positive blood culture and led to pacemaker extraction. This observation highlights the difficulty in the diagnosis of cardiac-device infection in the presence of a single positive blood culture with a fastidious microorganism that could be considered as a contaminant. It also underscores the need for device extraction to ensure healing.


Subject(s)
Antibodies, Antineutrophil Cytoplasmic/blood , Blood/microbiology , Corynebacterium Infections/diagnosis , Corynebacterium/isolation & purification , Pacemaker, Artificial/microbiology , Prosthesis-Related Infections/diagnosis , Aged , Blood/immunology , Corynebacterium/classification , Corynebacterium Infections/microbiology , Humans , Male , Myeloblastin/immunology , Prosthesis-Related Infections/microbiology
4.
Rev Med Interne ; 30(9): 754-68, 2009 Sep.
Article in French | MEDLINE | ID: mdl-19615793

ABSTRACT

Idiopathic capillary leak syndrome (ICLS) is a rare and poorly known condition. Since the first description in 1960, about hundred cases have been reported. A French register that was initiated in 1997 provides a better knowledge of the natural course of the disease and highlights some therapeutic issues. ICLS mainly affects middle-aged adults. The prognosis is poor with a 10-year mortality rate around 34%. Severe crisis and complications occurring in intensive care units account for 80% of the mortality. Diagnosis relies on an almost pathognomonic association: recurrent attacks of hypotension and hemoconcentration with paradoxical hypoalbuminemia. A monoclonal gammopathy is found in about 80% of patients. Physiopathology still remains unclear. Paraprotein toxicity has never been demonstrated. As a result, no evidence-based treatment is available neither for acute crisis nor for prophylaxis. Management of acute episodes is mainly symptomatic. Fluid infusion must be cautious because it can induce complications during the recovery phase. Patient education is a major measure to prevent recurrent attacks. Beta-2 stimulants were reported to reduce the frequency and severity of episodes and were considered as the recommended prophylactic measure. However, early data from the French register suggest that intravenous immunoglobulins are more effective in reducing both frequency and severity of the attacks. Inclusion of patients with ICLS in a register is crucial to improve the knowledge about aetiology and treatment of this disorder.


Subject(s)
Capillary Leak Syndrome , Registries , Acute Disease , Adolescent , Adult , Aged , Capillary Leak Syndrome/diagnosis , Capillary Leak Syndrome/drug therapy , Capillary Leak Syndrome/epidemiology , Capillary Leak Syndrome/etiology , Capillary Leak Syndrome/mortality , Capillary Leak Syndrome/physiopathology , Capillary Leak Syndrome/prevention & control , Diuretics/therapeutic use , Female , Follow-Up Studies , France , Humans , Immunoglobulins, Intravenous/therapeutic use , Immunologic Factors/therapeutic use , Male , Middle Aged , Patient Education as Topic , Prognosis , Time Factors
6.
Rev Med Interne ; 29(1): 15-27, 2008 Jan.
Article in French | MEDLINE | ID: mdl-18054122

ABSTRACT

PURPOSE: Granulomatous diseases are defined by specific histological features, following the local recruitment of macrophages and lymphocytes. Many infections can lead to the development of granuloma. CURRENT KNOWLEDGE AND KEY POINTS: Microorganisms responsible for granuloma include mainly mycobacteria, many viral and fungal species, as well as schistosoma in endemic areas. Nevertheless, almost all microorganisms can lead to granuloma, especially if their clearance needs macrophages pathway. New immunosuppressive drugs such as tumor necrosis factor antagonists are associated with a high risk of infectious granulomatous complications. All patients with granuloma must be carefully screened to find a potential underlying infection, since an immunosuppressive therapy could be otherwise considered. We here review the general diagnostic process with a specific glance to the main organs. FUTURE PROSPECTS AND PROJECTS: Without clinical or epidemiological clue, diagnosis can be very tedious. New molecular tools now assist classical microbiological and histological techniques. Their specificity and sensitivity have recently been better characterized, and their use will probably increase in the near future for the diagnosis of infectious granuloma. They may also lead to discover new infectious aetiologies of granulomatous diseases formerly considered as idiopathic. We describe here the main microorganisms that can be responsible for granuloma, with a specific focus on the use of new diagnostic tools.


Subject(s)
Granuloma/diagnosis , Granuloma/microbiology , Immunocompromised Host , Diagnosis, Differential , Granuloma/parasitology , Granuloma/virology , Humans , Tuberculosis/diagnosis
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