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1.
Infection ; 42(5): 905-12, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25056129

ABSTRACT

PURPOSE: The aim of this study was to determine the presence of the new Swedish Chlamydia trachomatis (C. trachomatis) variant (nvCT) and the distribution of C. trachomatis ompA genotypes in three geographically distant regions of Spain. METHODS: The genotypes of strains causing 624 episodes of infection (January 2011-September 2012) were studied using a nested PCR that amplifies a fragment of the ompA gene, followed by sequencing. To detect nvCT, a real-time PCR was used that amplifies a fragment of the cryptic plasmid with a 377 base pair deletion, which identifies the nvCT. RESULTS AND CONCLUSION: The ompA genotype was identified in 565 (90.5%) episodes. Eleven genotypes were detected, of which nine were found in all three regions. Only one nvCT strain was detected (0.4%), despite the predominance of genotype E (41%). Other frequent genotypes were genotypes D (19%), F (13%), G (11 %), and J (7%). Genotype L2b, causing lymphogranuloma venereum, was detected in men who have sex with men (MSM) in all three regions. Genotypes E and F were more frequent in women and heterosexual men, and genotypes D, G, J and L2b in MSM. In men, the main factor causing differences in the distribution of C. trachomatis was sexual behavior (MSM versus heterosexual men), while the distribution of C. trachomatis genotypes was similar in women and heterosexual men.


Subject(s)
Bacterial Outer Membrane Proteins/genetics , Chlamydia Infections/epidemiology , Chlamydia Infections/microbiology , Chlamydia trachomatis/genetics , Chlamydia trachomatis/isolation & purification , Adolescent , Adult , Aged , Aged, 80 and over , Bacterial Outer Membrane Proteins/metabolism , Child , Child, Preschool , Chlamydia trachomatis/classification , Chlamydia trachomatis/metabolism , Female , Genotype , Humans , Infant , Infant, Newborn , Male , Middle Aged , Molecular Sequence Data , Real-Time Polymerase Chain Reaction , Risk Factors , Sequence Analysis, DNA , Sexual Behavior , Spain/epidemiology , Young Adult
2.
Clin Microbiol Infect ; 19(9): E424-7, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23656535

ABSTRACT

In a prospective study (2009-2011) in healthcare institutions from the Canary Islands (Spain), 6 out of 298 carbapenem non-susceptible Pseudomonas aeruginosa isolates produced a metallo-ß-lactamase: four IMP-15, two VIM-2 (including one IMP-15-positive isolate) and one VIM-1. Multilocus sequence typing identified the single VIM-1-producing isolate as clone ST111 and two IMP-15-producing isolates as ST606, but, strikingly, bacterial re-identification revealed that the other three isolates (producing IMP-15 and/or VIM-2) were actually Pseudomonas putida. Further retrospective analysis revealed a very high prevalence (close to 50%) of carbapenem resistance in this environmental species. Hence, we report the simultaneous emergence in hospitals on the Canary Islands of P. putida and P. aeruginosa strains producing IMP-15, a metallo-ß-lactamase not previously detected in Europe, and suggest an underestimated role of P. putida as a nosocomial reservoir of worrying transferable resistance determinants.


Subject(s)
Cross Infection/microbiology , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/enzymology , Pseudomonas putida/enzymology , beta-Lactamases/metabolism , Bacterial Typing Techniques , Carbapenems/therapeutic use , Humans , Microbial Sensitivity Tests , Multilocus Sequence Typing , Pseudomonas Infections/drug therapy , Pseudomonas aeruginosa/drug effects , Pseudomonas aeruginosa/genetics , Pseudomonas aeruginosa/isolation & purification , Pseudomonas putida/drug effects , Pseudomonas putida/genetics , Pseudomonas putida/isolation & purification , Retrospective Studies , Spain , beta-Lactamases/genetics
3.
Phys Med Biol ; 52(16): 4749-59, 2007 Aug 21.
Article in English | MEDLINE | ID: mdl-17671333

ABSTRACT

Infants and children are a higher risk population for radiation cancer induction compared to adults. Although some values on pediatric patient doses for cardiac procedures have been reported, data to determine reference levels are scarce, especially when compared to those available for adults in diagnostic and therapeutic procedures. The aim of this study is to make a new contribution to the scarce published data in pediatric cardiac procedures and help in the determination of future dose reference levels. This paper presents a set of patient dose values, in terms of air kerma area product (KAP) and entrance surface air kerma (ESAK), measured in a pediatric cardiac catheterization laboratory equipped with a biplane x-ray system with dynamic flat panel detectors. Cardiologists were properly trained in radiation protection. The study includes 137 patients aged between 10 days and 16 years who underwent diagnostic catheterizations or therapeutic procedures. Demographic data and technical details of the procedures were also gathered. The x-ray system was submitted to a quality control programme, including the calibration of the transmission ionization chamber. The age distribution of the patients was 47 for <1 year; 52 for 1-<5 years; 25 for 5-<10 years and 13 for 10-<16 years. Median values of KAP were 1.9, 2.9, 4.5 and 15.4 Gy cm(2) respectively for the four age bands. These KAP values increase by a factor of 8 when moving through the four age bands. The probability of a fatal cancer per fluoroscopically guided cardiac procedure is about 0.07%. Median values of ESAK for the four age bands were 46, 50, 56 and 163 mGy, which lie far below the threshold for deterministic effects on the skin. These dose values are lower than those published in previous papers.


Subject(s)
Body Burden , Cardiovascular Surgical Procedures/statistics & numerical data , Fluoroscopy/mortality , Neoplasms, Radiation-Induced/mortality , Skin Neoplasms/mortality , Surgery, Computer-Assisted/statistics & numerical data , Whole-Body Counting/statistics & numerical data , Adolescent , Child , Female , Humans , Incidence , Infant , Infant, Newborn , Italy/epidemiology , Male , Pediatrics/statistics & numerical data , Relative Biological Effectiveness , Risk Assessment/methods , Risk Factors , Survival Analysis
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