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1.
Infect Dis Now ; 53(1): 104604, 2023 Feb.
Article in English | MEDLINE | ID: mdl-36067948

ABSTRACT

PURPOSE: Data on the microbiological epidemiology of Intra-Abdominal Abscesses (IAAs) are very scarce. We aimed to study the microbiological epidemiology of these infections in order to optimize empirical antibiotic therapy. PATIENTS AND METHODS: Between January 2015 and December 2020, we retrospectively analyzed all IAAs files in our hospital. Clinical and microbiological data such as antibiotic susceptibilities were collected. RESULTS: We studied 243 IAA cases. All in all, 139 (57.2%) IAAs were healthcare-associated and 201 (82.7%) were drained. The highest risk situations for IAAs were appendicitis (n = 69) and diverticulitis (n = 37). Out of the 163 microbiologically documented infections, 136 (81.9%) were polymicrobial. Enterobacterales (n = 192, 36.1%), Enterococcus sp. (n = 84, 17.6%) and anaerobes (n = 66, 16.1%) were the most frequently identified bacteria. Gram-negative bacteria were susceptible to amoxicillin-acid clavulanic, piperacillin-tazobactam, cefotaxime, meropenem in 55.2%, 84.9%, 77.6% and 99.5% of cases, respectively. Concerning Gram-positive bacteria, the susceptibility rate was 81.8% for amoxicillin-clavulanic acid, piperacillin-tazobactam and meropenem, and decreased to 63.4% for cefotaxime. CONCLUSION: This study highlights the polymicrobial profile of IAAs and their low susceptibility to amoxicillin and clavulanic acid. The piperacillin-tazobactam association remained the most appropriate empirical antibiotic therapy.


Subject(s)
Abdominal Abscess , Amoxicillin , Humans , Meropenem , Retrospective Studies , Piperacillin, Tazobactam Drug Combination/therapeutic use , Cefotaxime , Anti-Bacterial Agents/therapeutic use , Abdominal Abscess/drug therapy , Abdominal Abscess/epidemiology
2.
Infect Dis Now ; 52(7): 389-395, 2022 Oct.
Article in English | MEDLINE | ID: mdl-36064101

ABSTRACT

OBJECTIVES: Patients lost to follow-up and treatment failure in tuberculosis disease (TB) are major public health issues. In the absence of appropriate treatment, approximately 70 % of smear-positive patients will die within 10 years of disease progression. This study, conducted in the French region with the highest incidence, aimed to assess tuberculosis treatment outcomes and its determinants. PATIENTS AND METHODS: A prospective, multicenter cohort study (CO1TB) of adults and children treated for TB was conducted in four hospitals in the North of Paris. Treatment outcome at 1 year and associated socioeconomic and clinical factors were studied by multivariate logistic regression. RESULTS: Among 145 TB cases included from May 2018 to January 2020, patients were mainly born abroad and most lived in difficult socioeconomic conditions. During treatment, 25/145 (17 %) patients experienced adverse effects, which were not significantly associated with discontinuation of treatment (p = 0.99). At 1 year, 114 (78 %) had completed treatments, 26 (19 %) were lost to follow-up, three (2.1 %) were still being treated and two (1.4 %) had died. In the multivariate analysis, a history of TB was significantly associated with unfavorable treatment outcome (aOR = 5.3, 95 %CI (1.5;18.6) and a trend towards significance (p < 0.2) was observed among patients aged under 24 years (aOR = 2.9, 95 %-CI 0.95;8.5). CONCLUSION: In this precarious population, socioeconomic conditions were not found to be associated with unfavorable treatment outcome, whereas history of tuberculosis and young age played a role. Increased monitoring is thus required for these patients.


Subject(s)
HIV Infections , Tuberculosis , Adult , Child , Humans , Aged , Antitubercular Agents/therapeutic use , Cohort Studies , Prospective Studies , HIV Infections/drug therapy , Tuberculosis/drug therapy , Tuberculosis/epidemiology , Treatment Outcome , France/epidemiology
3.
Open Forum Infect Dis ; 9(8): ofac353, 2022 Aug.
Article in English | MEDLINE | ID: mdl-35949399

ABSTRACT

Background: The rationale behind the use of ethambutol in the standard tuberculosis treatment is to prevent the emergence of resistance to rifampicin in case of primary resistance to isoniazid. We evaluated whether early detection of isoniazid resistance using molecular testing allows the use an ethambutol-free regimen. Methods: FAST-TB, a phase 4, French, multicenter, open-label, non-inferiority trial, compared 2 strategies: (1) polymerase chain reaction (PCR)-based detection of isoniazid and rifampicin resistance at baseline using Genotype MTBDRplus version 2.0 followed by ethambutol discontinuation if no resistance was detected (PCR arm) and (2) a standard 4-drug combination, pending phenotypic drug-susceptibility results (C arm). Adult patients with smear-positive pulmonary tuberculosis were enrolled. The primary endpoint was the proportion of patients with treatment success defined as bacteriological or clinical cure at the end of treatment. A non-inferiority margin of 10% was used. Results: Two hundred three patients were randomized, 104 in the PCR arm and 99 in the C arm: 26.6% were female, median age was 37 (interquartile range, 28-51) years, 72.4% were born in Africa, and 5.4% were infected with human immunodeficiency virus. Chest x-ray showed cavities in 64.5% of the cases. Overall, 169 patients met criteria of treatment success: 87 of 104 (83.7%) in the PCR arm and 82 of 99 (82.8%) in the C arm with a difference of +0.8% (90% confidence interval, -7.9 to 9.6), meeting the noninferiority criteria in the intention-to-treat population (P = .02). Conclusions: In a setting with low prevalence of primary isoniazid resistance, a 3-drug combination with isoniazid, rifampicin, and pyrazinamide, based on rapid detection of isoniazid resistance using molecular testing, was noninferior to starting the recommended 4-drug regimen.

4.
Int J Tuberc Lung Dis ; 25(11): 903-910, 2021 11 01.
Article in English | MEDLINE | ID: mdl-34686232

ABSTRACT

SETTING: Migrants to Europe face a disproportionate burden of infections, including TB, yet little is known about the approach taken by primary and secondary care providers to screening and treatment. We therefore explored policy and practice relating to screening of active TB and latent TB infection (LTBI) in France.METHODS: We conducted an online national survey of French primary and secondary care physicians regarding their practices in relation to TB/LTBI screening among migrants.RESULTS: 367 physicians responded to the questionnaire among which 195 (53.1%) were primary care physicians, 126 (34.3%) were TB specialists in secondary care, and 46 (12.5%) other physicians; 303 (85.5%) were involved daily in the care of migrants. Most respondents recommended systematic TB screening with chest X-ray for migrants from medium and high-incidence countries (71.9%). Primary care physicians were less likely to offer screening than physicians in other settings (aOR 0.21, 95% CI 0.09-0.48). 220 (61.8%) offered LTBI screening for children (<15 years) and 34.0% for all migrants from high incidence countries.CONCLUSION: Improving awareness on TB screening is a critical next step to improve health outcomes in migrant groups and meet regional targets for tackling TB.


Subject(s)
Latent Tuberculosis , Transients and Migrants , Child , Europe , France/epidemiology , Humans , Latent Tuberculosis/diagnosis , Latent Tuberculosis/epidemiology , Mass Screening
5.
Infect Dis Now ; 51(3): 273-278, 2021 May.
Article in English | MEDLINE | ID: mdl-33069842

ABSTRACT

OBJECTIVE: To identify tools that will result in faster diagnosis, making the current pulmonary tuberculosis strategy more efficient. PATIENTS AND METHODS: A 4-year (2015-2018) retrospective study. The gold standard for diagnosis was a positive culture from a respiratory specimen. All sputum, fibroscopy and post-fibroscopy specimens (for smear negative patients) were collected. Each specimen was analyzed through smear examination and culture. All nucleic acid amplification testing results were included. Analyses looked at the incremental yield of positive cases of each successive specimen collection, and time to diagnosis. RESULTS: A total of 354 patients had at least one positive culture. Sputum allowed a diagnosis in 92% of cases (including a gain in sensitivity of around 7% for the third sputum specimen), with 160 smear-positive patients (45%). Among smear-negative patients, 109 underwent a fibroscopy procedure (culture sensitivity of 75%), and 59 had a post-fibroscopy specimen collected, which together identified the rest of the patients (8%). Molecular testing was used in 237 specimens. Median time to diagnosis was 11 days, which was significantly reduced among smear-negative patients when molecular testing was used (P<0.001). Shortening the delay between sputum specimen collections did not alter procedure sensitivity. CONCLUSIONS: We identified several aspects of the French tuberculosis diagnosis algorithm that could be improved, and posed the basis for a prospective study. Centers in higher incidence areas could benefit from a dedicated, predefined procedure exploring suspicions of tuberculosis. A high suspicion score of tuberculosis could drive the reasoned use of molecular testing in such settings.


Subject(s)
Tuberculosis, Pulmonary/diagnosis , Adult , Algorithms , Early Diagnosis , Female , France , Humans , Male , Middle Aged , Mycobacterium tuberculosis/isolation & purification , Nucleic Acid Amplification Techniques/methods , Retrospective Studies , Sensitivity and Specificity , Specimen Handling , Sputum/microbiology
7.
Rev Neurol (Paris) ; 175(7-8): 451-457, 2019.
Article in English | MEDLINE | ID: mdl-31383464

ABSTRACT

Tuberculous meningitis (TBM) is the most lethal and disabling form of tuberculosis. In 2017, approximately 10 million people developed TB worldwide, of whom more than 100,000 new cases of TBM are estimated to occur per year. In patients who are co-infected with HIV-1, TBM has a mortality approaching 50%. Diagnosis of TBM is often delayed by the insensitive and lengthy culture technique required for disease confirmation. GeneXpert represents the most significant advance in TBM diagnostics over the past decade, but it lacks sensitivity and cannot be used to rule out the diagnosis. Higher volume of cerebrospinal fluid (CSF) seems to be interesting to improve the diagnosis performances. New rapid and accurate diagnostic tools are necessary. Better advances have been made concerning the anti-tuberculosis chemotherapy of TBM, with the publication of clinical trials and pharmacokinetic studies exploring the use of higher rifampicin doses and fluoroquinolones. The rise of drug-resistant TBM is another challenge for management because TBM caused by multidrug resistant organisms results in death or severe disability in almost all sufferers.


Subject(s)
Tuberculosis, Meningeal/diagnosis , Tuberculosis, Meningeal/therapy , Humans
8.
Rev Mal Respir ; 36(1): 22-30, 2019 Jan.
Article in French | MEDLINE | ID: mdl-30236440

ABSTRACT

OBJECTIVES: To describe the residual broncho-pulmonary lesions and evaluate the role of CT scanning at the end of treatment of pulmonary tuberculosis. MATERIALS AND METHODS: Analysis of the initial and end of treatment CT scans of 56 patients with pulmonary tuberculosis according to a reading grid including parenchymatous and airways lesions. The CT data at the end of treatment were analysed in relation to the clinical and microbiological data, and the original CT scan. RESULTS: Active lesions (thick walled cavities and/or centrilobular micronodules) persisted in 24 patients (43%) after a mean treatment period of 7 months. The persistence of these signs of activity was correlated with the initial presence of a cavitary syndrome (p=0.027), with predominant sub-segmentary bronchial involvement, with extensive micronodular spread (p=0.024) and with bronchiectasis (p=0.04). These residual lesions were not associated with an increased risk of relapse. CONCLUSION: The persistence of signs of activity on the CT scan at the end of treatment of tuberculosis do not necessarily correspond to an absence of cure but to a radiological delay. This imaging is nevertheless useful to make an assessment of any subsequent changes in the bronchial tree and to estimate the risk of later complications.


Subject(s)
Bronchi/diagnostic imaging , Lung/diagnostic imaging , Tomography, X-Ray Computed/methods , Tuberculosis, Pulmonary/diagnostic imaging , Adolescent , Adult , Aged , Bronchi/pathology , Female , France , Humans , Lung/pathology , Male , Middle Aged , Retrospective Studies , Treatment Outcome , Tuberculosis, Pulmonary/drug therapy , Tuberculosis, Pulmonary/pathology , Young Adult
10.
New Microbes New Infect ; 12: 31-4, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27222715

ABSTRACT

Melioidosis is an endemic disease in Southeast Asia and northern Australia. An increasing number of cases are being reported in nonendemic countries, making the diagnosis less obvious. We discuss the identification of Burkholderia pseudomallei using matrix-assisted desorption ionization-time of flight mass spectrometry on the occasion of recent cases of imported melioidosis in French travellers.

11.
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
13.
Int J Tuberc Lung Dis ; 19(2): 205-9, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25574920

ABSTRACT

OBJECTIVES: To evaluate isolation practices and management of sputum smear-positive tuberculosis (TB) in France. METHODS: A survey was conducted using a questionnaire e-mailed in 2011 and 2012 to physicians of the French Society of Infectious Diseases, the French Respiratory Society and the French National Society of Internal Medicine. RESULTS: Of 311 responders, a quarter stated they treated more than 25 TB cases per year. A total of 87.8% declared they routinely used a four-drug regimen in the initial intensive phase. Of the 311 physicians who responded, 31.9% removed isolation precautions after three negative acid-fast bacilli (AFB) sputum results, 19.0% after 15 days of treatment and 34.1% only in case of clinical improvement. According to 71% of the responders, discharge from hospital despite positive AFB sputum smear results was 'possible'. A routine AFB sputum smear was performed after 2 months of treatment by only 21% of the responders. CONCLUSION: Despite recent national guidelines, the management of isolation precautions for sputum smear-positive TB remains heterogeneous, and a significant proportion of physicians use a three-drug regimen. Further efforts should be made to implement TB guidelines, mainly by raising awareness through national scientific institutions, but also by obtaining better evidence.


Subject(s)
Antitubercular Agents/administration & dosage , Practice Patterns, Physicians'/statistics & numerical data , Sputum/microbiology , Tuberculosis/drug therapy , Drug Therapy, Combination , France , Health Care Surveys , Humans , Practice Guidelines as Topic , Surveys and Questionnaires , Tuberculosis/prevention & control
14.
Springerplus ; 4: 824, 2015.
Article in English | MEDLINE | ID: mdl-26753112

ABSTRACT

BACKGROUND: Vascular graft infections are infrequent complications with important morbidity and mortality rates. Pasteurella multocida, a Gram negative bacillus, is a normal oral commensal of many animals. For mankind, it is a pathogenous bacillus which is rarely implicated in vascular grafts. CASE REPORT: We report hereafter the fourth case introduced in the international literature about vascular graft infections caused by P. multocida. The patient was successfully treated with a combination of a surgical graft change and a 6 weeks bi-antibiotic therapy. DISCUSSION: There is fours case reported in litterature with quite different antibiotic drugs and duration. CONCLUSION: P. multicoda graft infection should be long with initial intravenous drug and mainteance traitement should not be required.

16.
Int J Tuberc Lung Dis ; 15(8): 1131-2, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21740681

ABSTRACT

Mycobacterium bovis is responsible for a zoonosis originating in cattle. This disease has rarely affected man in industrialised countries since the establishment of veterinary surveillance in cattle. We report the case of a young female patient who developed a Mycobacterium bovis primary infection revealed by erythema nodosum. Infection was probably due to the consumption of non-pasteurised milk in Morocco. This clinical manifestation is rare and physicians ought to be aware of this imported pathology.


Subject(s)
Erythema Nodosum/microbiology , Milk/microbiology , Mycobacterium bovis/isolation & purification , Tuberculosis, Bovine/microbiology , Tuberculosis/diagnosis , Zoonoses , Animals , Antitubercular Agents/therapeutic use , Cattle , Erythema Nodosum/drug therapy , Female , Humans , Treatment Outcome , Tuberculosis/drug therapy , Tuberculosis/microbiology , Tuberculosis, Bovine/transmission , Young Adult
17.
Med Trop (Mars) ; 71(1): 7-10, 2011 Feb.
Article in French | MEDLINE | ID: mdl-21585080

ABSTRACT

INTRODUCTION: Giant hydatid cyst located in the retroperitoneal space is rare. The purpose of this report is to present a case cured by surgery in an adult traveller. CASE REPORT: In August 2009, a 67-year-old female who traveled frequently to Lebanon was admitted for assessment of a giant retroperitoneal hydatid cyst discovered coincidentally following palpation of an abdominal mass in 1997. From 1966 to 1975, the patient had undergone several surgical procedures for pulmonary and hepatic hydatidosis, complicated by vomica and anaphylactic shock. In 1997, computed tomography showed that the retroperitoneal cyst measured 100 mm at the widest point. At that time, the patient refused to undergo further surgery and was treated medically using albendazole initially in association with praziquantel. In 2009, the cyst had expanded to 180 mm at the widest point and the patient finally consented to perikystectomy. Excision was total and recovery was uneventful. Histology examination confirmed the viability of the cyst. Follow-up examination at 12 months indicated no relapse. COMMENTS: The retroperitoneal space is a rare location for hydatidosis. Occurrence in this location is generally primary. In case of discovery of a liquid-filled retroperitoneal mass, a history of travel to an endemic area for hydatid disease should be elicited. Diagnosis relies on radiological findings and positive serology. Since retroperitoneal cysts are often giant, they respond poorly to medical treatment. Similarly radiological treatment is difficult due to retroperitoneal location. Surgery, preferably perikystectomy, is the treatment of choice.


Subject(s)
Echinococcosis , Travel , Aged , Echinococcosis/diagnosis , Echinococcosis/surgery , Female , Humans , Retroperitoneal Space
18.
Pathol Biol (Paris) ; 59(1): 29-31, 2011 Feb.
Article in French | MEDLINE | ID: mdl-21277703

ABSTRACT

From March 1998 to August 2009, 1538 non-respiratory samples collected from 1182 patients, were tested using the Gen-Probe Amplified Mycobacterium Direct Test™ (AMTD). After decontamination procedure, every sample was tested by AMTD and by culture on solid and liquid media. The "Gold-standard" was considered by the combination of culture results and clinical diagnosis. Tuberculosis was present in 17,59 % (208 patients). For theses 1538 non-respiratory samples (225 culture positive samples, 248 AMTD positive), 279 corresponded to tuberculosis. After resolving the discordant results, the sensitivity, specificity, positive and negative values were 89, 99, 99,6 and 97,3 %.


Subject(s)
Mycobacterium tuberculosis/isolation & purification , Nucleic Acid Amplification Techniques , RNA, Bacterial/analysis , Tuberculosis/diagnosis , Humans , In Vitro Techniques , Microscopy , Mycobacterium tuberculosis/genetics , Mycobacterium tuberculosis/growth & development , Organ Specificity , Predictive Value of Tests , Sensitivity and Specificity , Specimen Handling , Staining and Labeling
19.
Pathol Biol (Paris) ; 59(1): 26-8, 2011 Feb.
Article in French | MEDLINE | ID: mdl-21277702

ABSTRACT

The purpose of this study was to evaluate the SD Bioline Ag MPT64 Rapid(®) for identification of the Mycobacterium tuberculosis complex. The method uses an immunochromatographic assay and needs 100 µl of sample taken from liquid culture or colonies suspended. The sensitivity was determined using 99 strains of M. tuberculosis complex and the specificity using 10 nontuberculous mycobacteria and 85 strains other than mycobacteria genus. The test showed excellent sensitivity (99%) and specificity (100%). This technique displays several advantages and is destined to spread in all laboratories and particularly in endemic areas.


Subject(s)
Antigens, Bacterial/analysis , Chromatography/methods , Immunoblotting/methods , Mycobacterium tuberculosis/immunology , Tuberculosis/diagnosis , Antibodies, Bacterial/immunology , Antibodies, Immobilized , Antigens, Bacterial/genetics , Bacterial Proteins/analysis , Bacterial Proteins/genetics , Enterobacteriaceae/immunology , False Positive Reactions , Female , Gram-Positive Bacteria/immunology , Humans , In Vitro Techniques , Male , Mutation , Mycobacterium/genetics , Mycobacterium/immunology , Mycobacterium/isolation & purification , Mycobacterium tuberculosis/genetics , Mycobacterium tuberculosis/isolation & purification , Sensitivity and Specificity , Species Specificity , Suspensions , Time Factors
20.
Rev Med Interne ; 32(3): 173-80, 2011 Mar.
Article in French | MEDLINE | ID: mdl-20951474

ABSTRACT

Candida species is the fourth most common cause of bloodstream infection and is the leading cause of invasive fungal infection among hospitalized patients. Acute disseminated candidiasis remains a life-threatening disease that now occurs mainly in intensive care units hospitalized patients. Delay in treatment of Candida bloodstream infections could be minimized by the development of more rapid and sensitive diagnostic techniques for the identification of Candida bloodstream infections. Current guidelines for the management of invasive candidiasis recommend fluconazole or an echinocandin as the primary therapeutic option. The optimal choice of the antifungal agent should depend on local epidemiology, prior antifungal therapy and patient's characteristics.


Subject(s)
Candidemia/drug therapy , Candidiasis/drug therapy , Candidemia/epidemiology , Candidiasis/epidemiology , Candidiasis/microbiology , Decision Trees , Humans
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