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1.
Pediatr Allergy Immunol ; 31(2): 124-132, 2020 02.
Article in English | MEDLINE | ID: mdl-31597224

ABSTRACT

BACKGROUND: Data addressing short- and long-term respiratory morbidity in moderate-late preterm infants are limited. We aim to determine the incidence of recurrent wheezing and associated risk and protective factors in these infants during the first 3 years of life. METHODS: Prospective, multicenter birth cohort study of infants born at 32+0 to 35+0  weeks' gestation and followed for 3 years to assess the incidence of physician-diagnosed recurrent wheezing. Allergen sensitization and pulmonary function were also studied. We used multivariate mixed-effects models to identify risk factors associated with recurrent wheezing. RESULTS: A total of 977 preterm infants were enrolled. Rates of recurrent wheezing during year (Y)1 and Y2 were similar (19%) but decreased to 13.3% in Y3. Related hospitalizations significantly declined from 6.3% in Y1 to 0.75% in Y3. Independent risk factors for recurrent wheezing during Y2 and Y3 included the following: day care attendance, acetaminophen use during pregnancy, and need for mechanical ventilation. Atopic dermatitis on Y2 and male sex on Y3 were also independently associated with recurrent wheezing. Palivizumab prophylaxis for RSV during the first year of life decreased the risk or recurrent wheezing on Y3. While there were no differences in rates of allergen sensitization, pulmonary function tests (FEV0.5 ) were significantly lower in children who developed recurrent wheezing. CONCLUSIONS: In moderate-to-late premature infants, respiratory symptoms were associated with lung morbidity persisted during the first 3 years of life and were associated with abnormal pulmonary function tests. Only anti-RSV prophylaxis exerted a protective effect in the development of recurrent wheezing.


Subject(s)
Asthma/epidemiology , Hypersensitivity/epidemiology , Infant, Premature/physiology , Allergens/immunology , Child, Preschool , Cohort Studies , Female , Follow-Up Studies , Humans , Immunization , Incidence , Infant , Infant, Newborn , Male , Recurrence , Respiratory Function Tests , Respiratory Sounds
2.
Int J Antimicrob Agents ; 50(3): 334-341, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28735882

ABSTRACT

The first Spanish multi-centre study on the microbiology of cystic fibrosis (CF) was conducted from 2013 to 2014. The study involved 24 CF units from 17 hospitals, and recruited 341 patients. The aim of this study was to characterise Pseudomonas aeruginosa isolates, 79 of which were recovered from 75 (22%) patients. The study determined the population structure, antibiotic susceptibility profile and genetic background of the strains. Fifty-five percent of the isolates were multi-drug-resistant, and 16% were extensively-drug-resistant. Defective mutS and mutL genes were observed in mutator isolates (15.2%). Considerable genetic diversity was observed by pulsed-field gel electrophoresis (70 patterns) and multi-locus sequence typing (72 sequence types). International epidemic clones were not detected. Fifty-one new and 14 previously described array tube (AT) genotypes were detected by AT technology. This study found a genetically unrelated and highly diverse CF P. aeruginosa population in Spain, not represented by the epidemic clones widely distributed across Europe, with multiple combinations of virulence factors and high antimicrobial resistance rates (except for colistin).


Subject(s)
Cystic Fibrosis/complications , Drug Resistance, Bacterial , Genetic Variation , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/classification , Pseudomonas aeruginosa/drug effects , Adolescent , Adult , Child , Child, Preschool , Electrophoresis, Gel, Pulsed-Field , Female , Genotype , Humans , Male , Middle Aged , Molecular Epidemiology , Multilocus Sequence Typing , MutL Proteins/genetics , MutS DNA Mismatch-Binding Protein/genetics , Pseudomonas Infections/epidemiology , Pseudomonas aeruginosa/genetics , Pseudomonas aeruginosa/isolation & purification , Spain/epidemiology , Virulence , Young Adult
3.
Pediatr Allergy Immunol ; 26(8): 797-804, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26031206

ABSTRACT

BACKGROUND: Airway diseases are highly prevalent in infants and cause significant morbidity. We aimed to determine the incidence and risk factors for respiratory morbidity in a Spanish cohort of moderate-to-late preterm (MLP) infants prospectively followed during their first year of life. METHODS: SAREPREM is a multicenter, prospective, longitudinal study. Preterm infants born at 32-35 weeks of gestation with no comorbidities were enrolled within 2 weeks of life and followed at 2-4 weeks, 6, and 12 months of age. Multivariate mixed-models were performed to identify independent risk factors associated with (i) development of bronchiolitis, (ii) recurrent wheezing, or (iii) related hospital admissions. RESULTS: Overall, 977 preterm infants were included, and 766 (78.4%) completed follow-up. Of those, 365 (47.7%) developed bronchiolitis during the first year, 144 (18.8%) recurrent wheezing, and 48 (6.3%) were hospitalized. While low birthweight, day care attendance (DCA) and school-age siblings were significantly and independently associated with both the development of bronchiolitis and recurrent wheezing, lower maternal age increased the risk for bronchiolitis and respiratory-related hospitalizations. Lastly, mechanical ventilation was associated with a higher risk of bronchiolitis and history of asthma in any parent increased the likelihood of developing recurrent wheezing. CONCLUSIONS: In this study, several non-modifiable parameters (family history of asthma, low birthweight, need for mechanical ventilation) and modifiable parameters (young maternal age, DCA, or exposure to school-age siblings) were identified as significant risk factors for the development of bronchiolitis and recurrent wheezing during the first year of life in MLP infants.


Subject(s)
Bronchiolitis/epidemiology , Hospitalization/statistics & numerical data , Infant, Premature , Bronchiolitis/complications , Cohort Studies , Female , Follow-Up Studies , Humans , Infant , Infant, Newborn , Male , Prospective Studies , Recurrence , Respiratory Sounds/etiology , Risk Factors , Spain
6.
Int J Cardiovasc Imaging ; 26(3): 253-5, 2010 Mar.
Article in English | MEDLINE | ID: mdl-19866374

ABSTRACT

The diagnosis and treatment of left ventricular apical thrombi after myocardial infarction are still not well established. Fibrinolytic treatment, heparin treatment and surgical removal might be therapeutic options. We present the case of a 37 year old man who came into the Emergency department complaining of pleuritic chest pain. ECG revealed an evolving anterior wall infarction and transthoracic echocardiogram showed a big mobile thrombus in the ventricular apex. In order to confirm diagnosis and to differentiate other entities like pseudoaneurysm, contrast echocardiography and cardiac MRI with late gadolinium enhancement were performed and allowed a definitive diagnosis. Our patient was treated with intravenous heparin and then with oral anticoagulation. Two months later, echocardiogram showed an apical non-mobile and smaller thrombus.


Subject(s)
Anterior Wall Myocardial Infarction/complications , Heart Diseases/diagnosis , Magnetic Resonance Imaging , Thrombosis/diagnosis , Adult , Anterior Wall Myocardial Infarction/diagnosis , Anticoagulants/therapeutic use , Contrast Media , Diagnosis, Differential , Echocardiography , Electrocardiography , Gadolinium , Heart Diseases/drug therapy , Heart Diseases/etiology , Heart Ventricles/pathology , Heparin/administration & dosage , Humans , Male , Predictive Value of Tests , Thrombosis/drug therapy , Thrombosis/etiology , Treatment Outcome
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