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1.
Pneumologie ; 69(3): 147-64, 2015 Mar.
Artículo en Alemán | MEDLINE | ID: mdl-25750095

RESUMEN

Spirometry is a simple test and considered the gold standard in lung function. An obstructive ventilatory defect is a disproportionate reduction of maximal airflow from the lung in relation to the maximal volume that can be displaced from the lung. It implies airway narrowing and is defined by a reduced FEV1/FVC ratio below the 5th percentile of the predicted value (lower limit of normal, LLN). A restrictive disorder may be suspected when vital capacity (FVC) is reduced and FEV1/FVC is normal. It is definitely proven, however, only by a decrease in TLC below the 5th percentile of predicted value (LLN). The measurement of TLC by body plethysmography is necessary to confirm or exclude a restrictive defect or hyperinflation of the lung when FVC is below the LLN. 2012 a task force of the ERS published new reference values based on 74,187 records from healthy non-smoking males and females from 26 countries. The new reference equations for the 3-95 age range are now available that include appropriate age-dependent mean values and lower limits of normal (LLN). This presentation aims at providing the reader with recommendations dealing with standardization and interpretation of spirometry.


Asunto(s)
Diagnóstico por Computador/normas , Medicina Ambiental/normas , Medicina del Trabajo/normas , Guías de Práctica Clínica como Asunto , Neumología/normas , Espirometría/normas , Alemania
2.
Respir Med ; 105(7): 959-71, 2011 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-21356587

RESUMEN

Body plethysmography allows to assess functional residual capacity (FRC(pleth)) and specific airway resistance (sRaw) as primary measures. In combination with deep expirations and inspirations, total lung capacity (TLC) and residual volume (RV) can be determined. Airway resistance (Raw) is calculated as the ratio of sRaw to FRC(pleth). Raw is a measure of airway obstruction and indicates the alveolar pressure needed to establish a flow rate of 1 L s(-1). In contrast, sRaw can be interpreted as the work to be performed by volume displacement to establish this flow rate. These measures represent different functional aspects and should both be considered. The measurement relies on the fact that generation of airflow needs generation of pressure. Pressure generation means that a mass of air is compressed or decompressed relative to its equilibrium volume. This difference is called "shift volume". As the body box is sealed and has rigid walls, its free volume experiences the same, mirror image-like shift volume as the lung. This shift volume can be measured via the variation of box pressure. The relationship between shift volume and alveolar pressure is assessed in a shutter maneuver, by identifying mouth and alveolar pressure under zero-flow conditions. These variables are combined to obtain FRC(pleth), sRaw and Raw. This presentation aims at providing the reader with a thorough and precise but non-technical understanding of the working principle of body plethysmography. It also aims at showing that this method yields significant additional information compared to spirometry and even bears a potential for further development.


Asunto(s)
Obstrucción de las Vías Aéreas/fisiopatología , Resistencia de las Vías Respiratorias/fisiología , Capacidad Residual Funcional/fisiología , Pletismografía Total/instrumentación , Capacidad Pulmonar Total/fisiología , Humanos , Espirometría/instrumentación
3.
Pneumologie ; 63(1): 49-55, 2009 Jan.
Artículo en Alemán | MEDLINE | ID: mdl-19137503

RESUMEN

BACKGROUND: A standard outcome parameter for pharmacological trials in COPD has not yet been defined. Therefore, it is the aim of this review to evaluate frequently used parameters for their eligibility as assessment and outcome parameters in COPD. METHODS: A review of the actual scientific literature was performed. RESULTS: It is recommended to continue to rely primarily on the FEV (1), which has been used as a primary variable in the vast majority of trials. In addition, further parameters, such as FVC and IC/TLC should be determined. If available, additional information is provided by RV/TLC, K (co), PaO (2) and PaCO (2). FEV (1) is not a surrogate parameter for dyspnoea, quality of life, and exercise tolerance, which should therefore be assessed separately. Frequency and severity of exacerbations and mortality are important outcome parameters in long-term trials. Complex indices, such as the BODE index, may be superior to single variables. CONCLUSIONS: No single additional parameter has been evaluated sufficiently in order to substitute FEV (1) as the standard parameter for the assessment and outcome in COPD.


Asunto(s)
Enfermedad Pulmonar Obstructiva Crónica/terapia , Volumen Espiratorio Forzado , Humanos , Evaluación de Resultado en la Atención de Salud , Pronóstico , Enfermedad Pulmonar Obstructiva Crónica/fisiopatología , Trastornos del Sueño-Vigilia/etiología
4.
Eur J Med Res ; 14 Suppl 4: 27-31, 2009 Dec 07.
Artículo en Inglés | MEDLINE | ID: mdl-20156720

RESUMEN

INTRODUCTION: In utero and/or childhood environmental tobacco smoke exposure is well known to adversely affect lung function and to depreciate child's health in many ways. Fewer studies have assessed the long-term effects on COPD development and disease severity in later adulthood. METHODS: COPD patients were interviewed using a structured questionnaire regarding their personal as well as the smoking habits of their parents. Data were compared with the disease history, e.g. COPD exacerbation rate, and their lung function data. RESULTS: Between 2003 and 2004 COPD patients were recruited a) in a private practice specialized in pulmonary medicine (n = 133) and b) in a hospital (n = 158). 75% of their fathers and only 15.4 of all mothers smoked regularly. COPD patients from smoking mothers had lower FEV1 predicted than those raised in household without maternal smoking exposure: 39.4 +/- 9.5% vs. 51.9 +/- 6.0% (P = 0.037). Fathers had no effect on FEV1 regardless if they are smokers or non-smokers. Rate of severe exacerbations requiring hospitalization remained unaffected by parental second hand smoke exposure. CONCLUSION: Maternal smoking negatively affects lung function of their offspring even in late adulthood when they develop COPD. It even aggravates the cumulative effect of active cigarette consumption. Clinical course of the COPD remained unaffected.


Asunto(s)
Efectos Tardíos de la Exposición Prenatal , Enfermedad Pulmonar Obstructiva Crónica/etiología , Fumar/efectos adversos , Adulto , Anciano , Femenino , Volumen Espiratorio Forzado , Humanos , Masculino , Persona de Mediana Edad , Embarazo
5.
Pneumologie ; 62(9): 520-6, 2008 Sep.
Artículo en Alemán | MEDLINE | ID: mdl-18546084

RESUMEN

INTRODUCTION: Smoking parents are the main source of passive smoke exposure in childhood. Only few studies have assessed the effect of maternal or paternal cigarette smoke exposure in childhood on the development and severity of COPD. PATIENTS AND METHODS: We recruited n = 251 COPD-patients, n = 113 were clinically stable (no exacerbations for up to 24 years backdated from the day of interview), and - according to their history - n = 138 had more than one exacerbation during this time period. All COPD-patients were interviewed by a physician using a structured questionnaire on main health outcomes, social status, smoking history of their parents and themselves. Furthermore, pulmonary function was measured, and concomitant lung diseases were excluded. RESULTS: Both COPD groups were comparable in age, gender, smoking history at the beginning of the disease, and cigarette pack-years smoked. Patients whose mothers smoked during childhood had poorer lung function values: FEV (1) 45.2 % vs. 54 % (p = 0.037). Non-smoking patients with a history of maternal smoking had a 7-times higher exacerbation rate compared to patients without passive smoke exposure (p = 0.073). Paternal cigarette smoke exposure had no effect. CONCLUSION: Maternal cigarette smoke exposure in childhood aggravates the COPD disease and predisposes the patient for a higher disease severity.


Asunto(s)
Exposición Materna/estadística & datos numéricos , Exposición Paterna/estadística & datos numéricos , Enfermedad Pulmonar Obstructiva Crónica/epidemiología , Medición de Riesgo/métodos , Fumar/epidemiología , Contaminación por Humo de Tabaco/estadística & datos numéricos , Adolescente , Adulto , Distribución por Edad , Causalidad , Niño , Preescolar , Femenino , Alemania/epidemiología , Humanos , Incidencia , Masculino , Factores de Riesgo , Distribución por Sexo
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