Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
1.
BMC Pulm Med ; 21(1): 333, 2021 Oct 26.
Article in English | MEDLINE | ID: mdl-34702233

ABSTRACT

BACKGROUND: Recent studies report very low adherence of practitioners to ATS/IDSA recommendations for the treatment of nontuberculous mycobacteria pulmonary disease (NTM-PD), as well as a great variability of practices. Type of management could impact prognosis. METHODS: To evaluate management and prognosis of patients with NTM-PD cases with respect to ATS recommendations, we conducted a multicenter retrospective cohort study (18 sentinel sites distributed throughout France), over a period of six years. We collected clinical, radiological, microbiological characteristics, management and outcome of the patients (especially death or not). RESULTS: 477 patients with NTM-PD were included. Respiratory comorbidities were found in 68% of cases, tuberculosis sequelae in 31.4% of patients, and immunosuppression in 16.8% of cases. The three most common NTM species were Mycobacterium avium complex (60%), M. xenopi (20%) and M. kansasii (5.7%). Smear-positive was found in one third of NTM-PD. Nodulobronchiectatic forms were observed in 54.3% of cases, and cavitary forms in 19.1% of patients. Sixty-three percent of patients were treated, 72.4% of patients with smear-positive samples, and 57.5% of patients with smear-negative samples. Treatment was in adequacy with ATS guidelines in 73.5%. The 2-year mortality was 14.4%. In the Cox regression, treatment (HR = 0.51), age (HR = 1.02), and M. abscessus (3.19) appeared as the 3 significant independent prognostic factors. CONCLUSION: These findings highlight the adequacy between French practices and the ATS/IDSA guidelines. Treatment was associated with a better survival.


Subject(s)
Lung Diseases/epidemiology , Lung Diseases/microbiology , Mycobacterium Infections/epidemiology , Mycobacterium Infections/microbiology , Adolescent , Adult , Aged , Aged, 80 and over , Cohort Studies , Female , France/epidemiology , Guideline Adherence/statistics & numerical data , Humans , Lung Diseases/diagnostic imaging , Lung Diseases/therapy , Male , Middle Aged , Mycobacterium/isolation & purification , Mycobacterium Infections/diagnostic imaging , Mycobacterium Infections/therapy , Prognosis , Retrospective Studies , Sex Distribution , Young Adult
2.
Sci Rep ; 8(1): 5855, 2018 04 11.
Article in English | MEDLINE | ID: mdl-29643428

ABSTRACT

Mycobacterium tuberculosis (Mtb) exhibits a structured phylogeographic distribution worldwide linked with human migrations. We sought to infer how the interactions between distinct human populations shape the global population structure of Mtb on a regional scale. We applied the recently described timescaled haplotypic density (THD) technique on 638 minisatellite-based Mtb genotypes from French tuberculosis patients. THD with a long-term (200 y) timescale indicated that Mtb population in France had been mostly influenced by interactions with Eastern and Southern Europe and, to a lesser extent, Northern and Middle Africa, consistent with historical migrations favored by geographic proximity or commercial exchanges with former French colonies. Restricting the timescale to 20 y, THD identified a sustained influence of Northern Africa, but not Europe where tuberculosis incidence decreased sharply. Evolving interactions between human populations, thus, measurably influence the local population structure of Mtb. Relevant information on such interactions can be inferred using THD from Mtb genotypes.


Subject(s)
Human Migration/statistics & numerical data , Mycobacterium tuberculosis/genetics , Phylogeography/statistics & numerical data , Tuberculosis/microbiology , Africa, Northern/epidemiology , Cross-Sectional Studies , DNA, Bacterial/genetics , DNA, Bacterial/isolation & purification , Datasets as Topic , France/epidemiology , Haplotypes , Humans , Incidence , Minisatellite Repeats/genetics , Mycobacterium tuberculosis/isolation & purification , Retrospective Studies , Tuberculosis/epidemiology , Tuberculosis/transmission
3.
PLoS One ; 12(3): e0173022, 2017.
Article in English | MEDLINE | ID: mdl-28282386

ABSTRACT

Cystic fibrosis (CF) lungs harbor a complex community of interacting microbes, including pathogens like Pseudomonas aeruginosa. Meta-taxogenomic analysis based on V5-V6 rrs PCR products of 52 P. aeruginosa-positive (Pp) and 52 P. aeruginosa-negative (Pn) pooled DNA extracts from CF sputa suggested positive associations between P. aeruginosa and Stenotrophomonas and Prevotella, but negative ones with Haemophilus, Neisseria and Burkholderia. Internal Transcribed Spacer analyses (RISA) from individual DNA extracts identified three significant genetic structures within the CF cohorts, and indicated an impact of P. aeruginosa. RISA clusters Ip and IIIp contained CF sputa with a P. aeruginosa prevalence above 93%, and of 24.2% in cluster IIp. Clusters Ip and IIIp showed lower RISA genetic diversity and richness than IIp. Highly similar cluster IIp RISA profiles were obtained from two patients harboring isolates of a same P. aeruginosa clone, suggesting convergent evolution in the structure of their microbiota. CF patients of cluster IIp had received significantly less antibiotics than patients of clusters Ip and IIIp but harbored the most resistant P. aeruginosa strains. Patients of cluster IIIp were older than those of Ip. The effects of P. aeruginosa on the RISA structures could not be fully dissociated from the above two confounding factors but several trends in these datasets support the conclusion of a strong incidence of P. aeruginosa on the genetic structure of CF lung microbiota.


Subject(s)
Bacteria/genetics , Cystic Fibrosis/complications , DNA, Bacterial/metabolism , Pseudomonas Infections/complications , Sputum/microbiology , Anti-Bacterial Agents/pharmacology , Bacteria/drug effects , Bacteria/isolation & purification , Cluster Analysis , Cystic Fibrosis/diagnosis , DNA, Bacterial/genetics , Electrophoresis, Gel, Pulsed-Field , Genetic Variation , Humans , Incidence , Metagenomics , Microbial Sensitivity Tests , Microbiota , Polymerase Chain Reaction , Pseudomonas Infections/epidemiology , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/drug effects , Pseudomonas aeruginosa/genetics , Pseudomonas aeruginosa/isolation & purification , RNA, Ribosomal/genetics , RNA, Ribosomal/metabolism , RNA, Ribosomal, 16S/genetics , RNA, Ribosomal, 16S/metabolism
4.
Sci Rep ; 7: 45326, 2017 03 28.
Article in English | MEDLINE | ID: mdl-28349973

ABSTRACT

The transmission dynamics of tuberculosis involves complex interactions of socio-economic and, possibly, microbiological factors. We describe an analytical framework to infer factors of epidemic success based on the joint analysis of epidemiological, clinical and pathogen genetic data. We derive isolate-specific, genetic distance-based estimates of epidemic success, and we represent success-related time-dependent concepts, namely epidemicity and endemicity, by restricting analysis to specific time scales. The method is applied to analyze a surveillance-based cohort of 1,641 tuberculosis patients with minisatellite-based isolate genotypes. Known predictors of isolate endemicity (older age, native status) and epidemicity (younger age, sputum smear positivity) were identified with high confidence (P < 0.001). Long-term epidemic success also correlated with the ability of Euro-American and Beijing MTBC lineages to cause active pulmonary infection, independent of patient age and country of origin. Our results demonstrate how important insights into the transmission dynamics of tuberculosis can be gained from active surveillance data.


Subject(s)
Mycobacterium tuberculosis/genetics , Tuberculosis/pathology , Adult , Aged , Female , Genetic Variation , Genotype , Haplotypes , Humans , Male , Middle Aged , Minisatellite Repeats/genetics , Mycobacterium tuberculosis/isolation & purification , Risk Factors , Sputum/microbiology , Tuberculosis/epidemiology , Tuberculosis/microbiology , Tuberculosis/transmission
SELECTION OF CITATIONS
SEARCH DETAIL
...