5 results on '"van den Berg, Jan"'
Search Results
2. The validity and precision of the leicester cough questionnaire in COPD patients with chronic cough
- Author
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Berkhof Farida F, Boom Lisenka N, ten Hertog Nynke E, Uil Steven M, Kerstjens Huib AM, and van den Berg Jan WK
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LCQ ,COPD ,validity ,cough ,health status ,Computer applications to medicine. Medical informatics ,R858-859.7 - Abstract
Abstract Background A validated instrument to assess the effects of chronic cough on health status in patients with chronic obstructive pulmonary disease (COPD) is currently not available. The Leicester Cough Questionnaire (LCQ) is a cough-specific health status questionnaire which is originally validated for a population of general patients presenting with chronic cough. We examined the psychometric performance of the LCQ in patients with COPD and chronic productive cough. Methods Concurrent validity, internal consistency, reproducibility and responsiveness were determined. The St. George's Respiratory Questionnaire (SGRQ) and the Short Form-36 (SF-36) were used as external criteria. Questionnaires were completed at the start of the study. After 2 and 12 weeks the LCQ was repeated, together with a global rating of change. Results In total 54 patients were included. Concurrent validity analysis showed significant correlations between corresponding domains of the LCQ and the SGRQ (rs -0.31 to -0.60). Corresponding domains of the LCQ and the SF-36 showed weaker correlations (rs 0.04 to 0.41). Internal consistency was adequate for two of the three domains (Cronbach's α 0.74 - 0.86). Test-retest reliability in stable patients was high (intraclass correlation coefficients 0.79 - 0.93). The mean difference after two weeks was 0.73 (± 1.75). Responsiveness analysis indicated that the LCQ was able to detect changes after 12 weeks. Conclusion The LCQ is a valid, reliable, responsive instrument to measure health status in COPD patients with chronic productive cough. Trial Registration ClinicalTrials.gov: NCT01071161
- Published
- 2012
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3. Oral or IV prednisolone in the treatment of COPD exacerbations - A randomized, controlled, double-blind study
- Author
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de Jong, Ynze P., Uil, Steven M., Grotjohan, Hans P., Postma, Dirkje S., Kerstjens, Huib A. M., van den Berg, Jan W. K., and Groningen Research Institute for Asthma and COPD (GRIAC)
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METHYLPREDNISOLONE ,CONTROLLED CLINICAL-TRIAL ,OBSTRUCTIVE PULMONARY-DISEASE ,THERAPY ,INTRAVENOUS CORTICOSTEROIDS ,exacerbation ,CHRONIC-BRONCHITIS ,MANAGEMENT ,COPD ,IV prednisolone ,oral prednisolone ,STRATEGY ,RESPIRATORY QUESTIONNAIRE ,EMERGENCY TREATMENT - Abstract
Background: Treatment with systemic corticosteroids for exacerbations of COPD results in improvement in clinical outcomes. On hospitalization, corticosteroids are generally administered IV. It has not been established whether oral administration is equally effective. We conducted a study to demonstrate that therapy with oral prednisolone was not inferior to therapy with IN prednisolone using a double-blind, double-dummy design. Methods: Patients hospitalized for an exacerbation of COPD were randomized to receive 5 days of therapy with prednisolone, 60 mg IV or orally. Treatment failure, the primary outcome, was defined as death, admission to the ICU, readmission to the ICU because of COPD, or the intensification of pharmacologic therapy during a 90-day follow-up period. Results: A total of 435 patients were referred for a COPD exacerbation warranting hospitalization; 107 patients were randomized to receive IV therapy, and 103 to receive oral therapy. Overall treatment failure within 90 days was similar, as follows: IV prednisolone, 61.7%; oral prednisolone, 56.3% (one-sided lower bound of the 95% confidence interval [CI], -5.8%). There were also no differences in early (ie, within 2 weeks) treatment failure (17.8% and 18.4%, respectively; one-sided lower bound of the 95% CI, -9.4%), late (ie, after 2 weeks) treatment failure (54.0% and 47.0%, respectively; one-sided lower bound of the 95% CI, -5.6%), and mean (+/- SD) length of hospital stay (11.9 +/- 8.6 and 11.2 +/- 6.7 days, respectively). Over I week, clinically relevant improvements were found in spirometry and health-related quality of life, without significant differences between the two treatment groups. Conclusion: Therapy with oral prednisolone is not inferior to IV treatment in the first 90 days after starting therapy. We suggest that the oral route is preferable in the treatment of COPD exacerbations. Trial registration: Clinicaltrials.gov Identifier: NCT00311961.
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- 2007
4. Undetected chronic obstructive pulmonary disease and asthma in people over 50 years with persistent cough.
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Broekhuizen, Berna D. L., Sachs, Alfred P. E., Hoes, Arno W., Moons, Karel G. M., van den Berg, Jan W. K., Dalinghaus, Willem H., Lammers, Ernst, and Verheij, Theo J. M.
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OBSTRUCTIVE lung diseases ,ELDER care ,ASTHMA ,COUGH ,PHYSICIAN-patient relations - Abstract
Background Chronic obstructive pulmonary disease (COPD) and asthma are underdiagnosed in primary care. Aim To determine how often COPD or asthma are present in middle-aged and older patients who consult their GP for persistent cough. Design of study A cross-sectional study in 353 patients older than 50 years, visiting their GP for persistent cough and not known to have COPD or asthma. Setting General practice in the Netherlands. Method All participants underwent extensive diagnostic workup, including symptoms, signs, spirometry, and body plethysmography. All results were studied by an expert panel to diagnose or exclude COPD and/or asthma. The reproducibility of the panel diagnosis was assessed by calculation of Cohen's K statistic in a sample of 41 participants. Results Of the 353 participants, 102 (29%, 95% confidence interval [CI] = 24 to 34%) were diagnosed with COPD. In 14 of these 102 participants, both COPD and asthma were diagnosed (4%, 95% CI = 2 to 7%). Asthma (without COPD) was diagnosed in 23 (7%, 95% CI = 4 to 10%) participants. Mean duration of cough was 93 days (median 40 days). The reproducibility of the expert panel was good (Cohen's K = 0.90). Conclusion In patients aged over 50 years who consult their GP for persistent cough, undetected COPE) or asthma is frequently present. [ABSTRACT FROM AUTHOR]
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- 2010
- Full Text
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5. A Prospective Cohort Study on the Effects of Geriatric Rehabilitation Following Acute Exacerbations of COPD.
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van Dam van Isselt, Eléonore F., van Eijk, Monica, van Geloven, Nan, Groenewegen-Sipkema, Karin H., van den Berg, Jan-Willem K., Nieuwenhuys, Cécile M.A., Chavannes, Niels H., and Achterberg, Wilco P.
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HEALTH status indicators , *HOSPITALS , *LONGITUDINAL method , *OBSTRUCTIVE lung diseases , *REGRESSION analysis , *TREATMENT effectiveness , *GERIATRIC rehabilitation , *VITAL capacity (Respiration) , *DISEASE exacerbation , *EVALUATION of human services programs - Abstract
Older patients with chronic obstructive pulmonary disease (COPD), hospitalized for an acute exacerbation, often do not receive recommended post-acute pulmonary rehabilitation. This underuse might be related to the impaired clinical and functional status of these patients, who are more likely to present with frailty, comorbidities, and disability. Having developed and implemented a geriatric rehabilitation program for these patients (GR_COPD), the primary aim of this study was to investigate the effectiveness of this program. A prospective cohort study with a 3-month follow-up period. Patients who declined the GR_COPD program were considered as controls. The study was conducted at the pulmonary department of 2 hospitals. Patients were eligible when hospitalized as a result of an acute exacerbation of COPD and indicated for the GR_COPD program based on standardized criteria. Primary outcome was defined as change in disease-specific health status measured with the clinical COPD questionnaire (CCQ), secondary outcome as the exacerbation rate ratio during follow-up. To balance potential confounders between the intervention and control group, propensity score–based weighted linear regression analyses were performed. Of the 158 included patients [78 (49.4%) male, mean age 70.8 (±8.1) years, mean forced expiratory volume in 1 second: 35.5 (±12.8) as % of predicted], 78 received the GR_COPD program. The results of the CCQ showed a significant and clinically relevant treatment effect of −0.56 points [95% confidence interval (CI) −0.89, −0.23; P =.001). Patients in the control group had 2.77 times more exacerbations compared with the intervention group (95% CI 2.13, 3.58; P <.001). This study shows a clinically relevant effect of the GR_COPD program on disease-specific health status and exacerbation rate. Implementation of the program for older patients with severe COPD hospitalized for an acute exacerbation is recommended. [ABSTRACT FROM AUTHOR]
- Published
- 2019
- Full Text
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