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1.
Chron Respir Dis ; 14(4): 360-369, 2017 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-28393532

RESUMEN

Diagnostic delay is common in most respiratory diseases, particularly in bronchiectasis. However, sex bias in diagnostic delay has not been studied to date. OBJECTIVE: Assessment of diagnostic delay in bronchiectasis by sex. METHODS: The Spanish Historical Registry of Bronchiectasis recruited adults diagnosed with bronchiectasis from 2002 to 2011 in 36 centres in Spain. From a total of 2113 patients registered we studied 2099, of whom 1125 (53.6%) were women. RESULTS: No differences were found for sex or age (61.0 ± 20.6, p = 0.88) or for localization of bronchiectasis ( p = 0.31). Bronchiectasis of unknown aetiology and secondary to asthma, childhood infections and tuberculosis was more common in women (all ps < 0.05). More men than women were chronic obstructive pulmonary disease-related bronchiectasis and colonized by Haemophilus influenzae ( p < 0.001 for both). Onset of symptoms was earlier in women. The diagnostic delay for women with bronchiectasis was 2.1 years more than for men ( p = 0.001). DISCUSSION: We recorded a substantial delay in the diagnosis of bronchiectasis. This delay was significantly longer in women than in men (>2 years). Independent factors associated with this sex bias were age at onset of symptoms, smoking history, daily expectoration and reduced lung function.


Asunto(s)
Bronquiectasia/diagnóstico , Bronquiectasia/etiología , Diagnóstico Tardío/estadística & datos numéricos , Adulto , Edad de Inicio , Anciano , Anciano de 80 o más Años , Asma/complicaciones , Sesgo , Bronquios/microbiología , Bronquiectasia/fisiopatología , Femenino , Haemophilus influenzae/aislamiento & purificación , Humanos , Masculino , Persona de Mediana Edad , Enfermedad Pulmonar Obstructiva Crónica/complicaciones , Sistema de Registros , Factores Sexuales , Fumar , España , Esputo , Factores de Tiempo , Tuberculosis Pulmonar/complicaciones
2.
Rev Esp Quimioter ; 28 Suppl 1: 19-24, 2015 Sep.
Artículo en Español | MEDLINE | ID: mdl-26365729

RESUMEN

Nebulized antibiotic therapy is an attractive therapeutic option given the high concentration obtained from the drug at the site of infection, minimizing the adverse effects and possible drug interactions. Inhalation of drugs as treatment of cystic fibrosis (CF) related lung disease has been proven to be highly effective. Consequently, an increasing number of drugs and devices have been developed for CF lung disease or are currently under development. Other limited areas of experience in this field are lung transplant recipients, immunosuppressed patients, bronchiectasis and ventilated patients. In this review document we analyse the current status of the inhaled medications, their modes of administration and indications and their results as well as side effects. Specifically we address antibiotics, and additionally, we review the current knowledge on devices for inhalation therapy with regard to optimal particle sizes and characteristics of wet nebulisers, dry powder and metered dose inhalers. Several factors contribute to a highly variable pulmonary drug deposition as the devices, the physical properties of the administered antimicrobial agent, the type of respiratory disease and the inhalation technique. Despite many clinicians have obtained a valuable experience from the aerosolized administration of antimicrobials and persuaded of their efficacy and safety. However, RCTs out of CF are needed to answer important clinical questions, such as what is the appropriate dose, the optimal delivery device, the optimal way of drug administration, as well as the exact therapeutic role and pharmacokinetic profile of aerosolized drug.


Asunto(s)
Administración por Inhalación , Enfermedades Pulmonares/terapia , Nebulizadores y Vaporizadores , Aerosoles , Fibrosis Quística/complicaciones , Humanos , Enfermedades Pulmonares/tratamiento farmacológico , Enfermedades Pulmonares/etiología
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