J.J. den Otter
Radboud University Nijmegen
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Journal of Asthma | 1998
J.J. den Otter; B.A. van Dijk; C.P. van Schayck; J. Molema; C. van Weel
The prevalence of asthma and chronic obstructive pulmonary disease (COPD) is rising in most countries, including The Netherlands. It has been suggested that a majority of these cases of (self-reported) symptoms related to asthma/COPD are not diagnosed in general practice. We compared a population screening for underdiagnosed asthma/COPD with a high-risk approach by a questionnaire form with specified questions about asthma/COPD-related symptoms. A case-controlled study including a record review was performed of cases and controls. The results of a population screening were used to classify patients as (a) asthma/COPD, (b) at risk for asthma/COPD, or (c) no asthma/COPD. Eleven hundred fifty-five patients were screened. One hundred fifty-five patients reported previous asthma/COPD-related care (cases). The difference between number of cases and controls in asthma/COPD diagnosis was chosen as main outcome measure. The population screening revealed 85 subjects with a diagnosis of asthma/COPD and 154 subjects with an increased risk. Nineteen diagnoses could be made in cases, and eight diagnoses in controls. The chart review showed that only seven cases and two controls were known to the general practitioner. From this study it can be concluded that in order to reduce the number of un- and underdiagnosed patients, all listed patients in general practice should be screened. However, if screening of all patients is not feasible, active case finding by asking a few questions about shortness of breath or wheezing to all patients in the group of listed individuals is recommended.
European Journal of General Practice | 2007
J.J. den Otter; C.P. van Schayck; H.T.M. Folgering; G. van den Boom; R.P. Akkermans; C. van Weel
Background: Asthma is generally accepted as an inflammatory disease that needs steroid treatment. However, when to start with inhaled steroids remains unclear. A study was undertaken to determine when inhaled corticosteroids should be introduced as the first treatment step. Objective: To investigate the effectiveness of early introduction of inhaled steroids on decline in lung function in steroid-naïve subjects with a rapid decline in lung function in general practice. Subjects: Patients with signs/symptoms suspect of asthma (i.e., persistent and/or recurrent respiratory symptoms) and a decline in forced expiratory volume in 1 s (FEV1) during 1-year monitoring of 0.080 l or more and reversible obstruction (≥10% predicted) or bronchial hyperresponsiveness (PC20≤8 mg/ml) were studied. They had been identified in a population screening aiming to detect subjects at risk for chronic obstructive pulmonary disease (COPD) or asthma. Design: A placebo-controlled, randomized, double-blind study. Methods: 75 subjects out of a random population of 1155 were found eligible, and 45 were willingly to participate. Subjects were randomly treated with placebo or fluticasone propionate 250 µg b.i.d., and FEV1 and PC20 were monitored over a 2-year period. Outcome variables: The primary outcome measure was decline in FEV1; the secondary outcome measure was bronchial hyperresponsiveness (PC20). Results: 22 subjects were randomly allocated to the active group with inhaled corticosteroids and 23 to placebo. Change of FEV1 in the active treated group was +43 ml in post-bronchodilator FEV1 (p =0.341) and +62 ml/year (p =0.237) in pre-bronchodilator FEV1 after 1 year, and −22 ml (p =0.304) for post-bronchodilator FEV1 and −9.4 ml (p =0.691) for pre-bronchodilator FEV1 after 2 years, compared to placebo. The effect on PC20 was almost one dose-step (p =0.627) after 1 year and one dose-step (p =0.989) after 2 years. Conclusion: In this study, the early introduction of inhaled corticosteroids in newly diagnosed asthmatic subjects with rapid decline in lung function did not prove to be either clinically relevant or statistically significant in reversing the decline in FEV1. For PC20, no significant changes were detected.
American Journal of Respiratory and Critical Care Medicine | 1998
G. van den Boom; C.P. van Schayck; M.P.M.H. Rutten; P.R.S. Tirimanna; J.J. den Otter; P.M. van Grunsven; M.J. Buitendijk; C.L.A. van Herwaarden; C. van Weel
British Journal of General Practice | 1996
P.R.S. Tirimanna; C.P. van Schayck; J.J. den Otter; C. van Weel; C.L.A. van Herwaarden; G. van den Boom; P.M. van Grunsven; W.J.H.M. van den Bosch
JAMA | 1995
C.P. van Schayck; P.J.J.A. van den Broek; J.J. den Otter; C.L.A. van Herwaarden; J. Molema; C. van Weel
British Journal of General Practice | 1997
J.J. den Otter; M. Knitel; R.P. Akkermans; C.P. van Schayck; H.T.M. Folgering; C. van Weel
British Journal of General Practice | 1997
J.J. den Otter; G. Reijnen; W.J.H.M. van den Bosch; C.P. van Schayck; J. Molema; C. van Weel
British Journal of General Practice | 1996
P.R.S. Tirimanna; J.J. den Otter; C.P. van Schayck; C.L.A. van Herwaarden; H.T.M. Folgering; C. van Weel
European Respiratory Journal | 1996
J.J. den Otter; H.T.M. Folgering; Marij Knitel; R.P. Akkermans; C.P. van Schayck; C. van Weel
American Journal of Respiratory and Critical Care Medicine | 1996
J.J. den Otter; H. ter Horst; C.P. van Schayck; B.P.A. Thoonen; J. Molema; C. van Weel