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Published in: Health and Quality of Life Outcomes 1/2013

Open Access 01-12-2013 | Research

The development of a patient-reported outcome measure for assessing nighttime symptoms of chronic obstructive pulmonary disease

Authors: Asha Hareendran, Andrew C Palsgrove, Michelle Mocarski, Michael L Schaefer, Juliana Setyawan, Robyn Carson, Barry Make

Published in: Health and Quality of Life Outcomes | Issue 1/2013

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Abstract

Background

The assessment of symptoms of chronic obstructive pulmonary disease (COPD) is important for monitoring and managing the disease and for evaluating outcomes of interventions. COPD patients experience symptoms during the day and night, and symptoms experienced at night often disturb sleep. The aim of this paper is to describe methods used to develop a patient-reported outcome (PRO) instrument for evaluating nighttime symptoms of COPD, and to document evidence for the content validity of the instrument.

Methods

Literature review and clinician interviews were conducted to inform discussion guides to explore patients’ nighttime COPD symptom experience. Data from focus groups with COPD patients was used to develop a conceptual framework and the content of a new PRO instrument. Patient understanding of the new instrument was assessed via cognitive interviews with COPD patients.

Results

The literature review confirmed that there is no instrument with evidence of content validity currently available to assess nighttime symptoms of COPD. Additionally, the literature review and clinician interviews suggested the need to understand patients’ experience of specific symptoms in order to evaluate nighttime symptoms of COPD. Analyses of patient focus group data (N = 27) supported saturation of concepts and aided in development of a conceptual framework. Items were generated using patients’ terminology to collect data on concepts in the framework including the occurrence and severity of COPD symptoms, use of rescue medication at night, and nocturnal awakening. Response options were chosen to reflect concepts that were salient to patients. Subsequent cognitive interviewing with ten COPD patients demonstrated that the items, response options, recall period, and instructions were understandable, relevant, and interpreted as intended.

Conclusions

A new PRO instrument, the Nighttime Symptoms of COPD Instrument (NiSCI), was developed with documented evidence of content validity. The NiSCI is ready for empirical testing, including item reduction and evaluation of psychometric properties.
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Literature
1.
go back to reference Vestbo J, Hurd SS, Agusti AG, Jones PW, Vogelmeier C, Anzueto A, Barnes PJ, Fabbri LM, Martinez FJ, Nishimura M, et al.: Global Strategy for the Diagnosis, Management and Prevention of Chronic Obstructive Pulmonary Disease, GOLD Executive Summary. Am J Respir Crit Care Med 2013, 187: 347–365. 10.1164/rccm.201204-0596PPPubMedCrossRef Vestbo J, Hurd SS, Agusti AG, Jones PW, Vogelmeier C, Anzueto A, Barnes PJ, Fabbri LM, Martinez FJ, Nishimura M, et al.: Global Strategy for the Diagnosis, Management and Prevention of Chronic Obstructive Pulmonary Disease, GOLD Executive Summary. Am J Respir Crit Care Med 2013, 187: 347–365. 10.1164/rccm.201204-0596PPPubMedCrossRef
2.
go back to reference Rennard S, Decramer M, Calverley PM, Pride NB, Soriano JB, Vermeire PA, Vestbo J: Impact of COPD in North America and Europe in 2000: subjects' perspective of Confronting COPD International Survey. Eur Respir J 2002, 20: 799–805. 10.1183/09031936.02.03242002PubMedCrossRef Rennard S, Decramer M, Calverley PM, Pride NB, Soriano JB, Vermeire PA, Vestbo J: Impact of COPD in North America and Europe in 2000: subjects' perspective of Confronting COPD International Survey. Eur Respir J 2002, 20: 799–805. 10.1183/09031936.02.03242002PubMedCrossRef
3.
go back to reference Agusti A, Hedner J, Marin JM, Barbe F, Cazzola M, Rennard S: Night-time symptoms: a forgotten dimension of COPD. Eur Respir Rev 2011, 20: 183–194. 10.1183/09059180.00004311PubMedCrossRef Agusti A, Hedner J, Marin JM, Barbe F, Cazzola M, Rennard S: Night-time symptoms: a forgotten dimension of COPD. Eur Respir Rev 2011, 20: 183–194. 10.1183/09059180.00004311PubMedCrossRef
4.
go back to reference Partridge MR, Karlsson N, Small IR: Patient insight into the impact of chronic obstructive pulmonary disease in the morning: an internet survey. Curr Med Res Opin 2009, 25: 2043–2048. 10.1185/03007990903103006PubMedCrossRef Partridge MR, Karlsson N, Small IR: Patient insight into the impact of chronic obstructive pulmonary disease in the morning: an internet survey. Curr Med Res Opin 2009, 25: 2043–2048. 10.1185/03007990903103006PubMedCrossRef
5.
go back to reference Cazzola M, MacNee W, Martinez FJ, Rabe KF, Franciosi LG, Barnes PJ, Brusasco V, Burge PS, Calverley PM, Celli BR, et al.: Outcomes for COPD pharmacological trials: from lung function to biomarkers. Eur Respir J 2008, 31: 416–469. 10.1183/09031936.00099306PubMedCrossRef Cazzola M, MacNee W, Martinez FJ, Rabe KF, Franciosi LG, Barnes PJ, Brusasco V, Burge PS, Calverley PM, Celli BR, et al.: Outcomes for COPD pharmacological trials: from lung function to biomarkers. Eur Respir J 2008, 31: 416–469. 10.1183/09031936.00099306PubMedCrossRef
6.
go back to reference Magnussen H, Verkindre C, Jack D, Jadayel D, Henley M, Woessner R, Higgins M, Kramer B: Indacaterol once-daily is equally effective dosed in the evening or morning in COPD. Respir Med 2010, 104: 1869–1876. 10.1016/j.rmed.2010.08.010PubMedCrossRef Magnussen H, Verkindre C, Jack D, Jadayel D, Henley M, Woessner R, Higgins M, Kramer B: Indacaterol once-daily is equally effective dosed in the evening or morning in COPD. Respir Med 2010, 104: 1869–1876. 10.1016/j.rmed.2010.08.010PubMedCrossRef
7.
go back to reference Lofdahl C: Reducing the impact of COPD exacerbations: Clinical efficacy of budesonide/formoterol. Eur Respir Rev 2004, 13: 14–21. Lofdahl C: Reducing the impact of COPD exacerbations: Clinical efficacy of budesonide/formoterol. Eur Respir Rev 2004, 13: 14–21.
8.
go back to reference Make B, Hanania NA, ZuWallack R, Kalberg C, Emmett A, Brown CP, Knobil K: The efficacy and safety of inhaled fluticasone propionate/salmeterol and ipratropium/albuterol for the treatment of chronic obstructive pulmonary disease: an eight-week, multicenter, randomized, double-blind, double-dummy, parallel-group study. Clin Ther 2005, 27: 531–542. 10.1016/j.clinthera.2005.05.009PubMedCrossRef Make B, Hanania NA, ZuWallack R, Kalberg C, Emmett A, Brown CP, Knobil K: The efficacy and safety of inhaled fluticasone propionate/salmeterol and ipratropium/albuterol for the treatment of chronic obstructive pulmonary disease: an eight-week, multicenter, randomized, double-blind, double-dummy, parallel-group study. Clin Ther 2005, 27: 531–542. 10.1016/j.clinthera.2005.05.009PubMedCrossRef
9.
go back to reference Zheng JP, Yang L, Wu YM, Chen P, Wen ZG, Huang WJ, Shi Y, Wang CZ, Huang SG, Sun TY, et al.: The efficacy and safety of combination salmeterol (50 microg)/fluticasone propionate (500 microg) inhalation twice daily via accuhaler in Chinese patients with COPD. Chest 2007, 132: 1756–1763. 10.1378/chest.06-3009PubMedCrossRef Zheng JP, Yang L, Wu YM, Chen P, Wen ZG, Huang WJ, Shi Y, Wang CZ, Huang SG, Sun TY, et al.: The efficacy and safety of combination salmeterol (50 microg)/fluticasone propionate (500 microg) inhalation twice daily via accuhaler in Chinese patients with COPD. Chest 2007, 132: 1756–1763. 10.1378/chest.06-3009PubMedCrossRef
10.
go back to reference Kerwin EM, D'Urzo AD, Gelb AF, Lakkis H, Garcia Gil E, Caracta CF: Efficacy and safety of a 12-week treatment with twice-daily aclidinium bromide in COPD patients (ACCORD COPD I). COPD 2012, 9: 90–101. 10.3109/15412555.2012.661492PubMedCrossRef Kerwin EM, D'Urzo AD, Gelb AF, Lakkis H, Garcia Gil E, Caracta CF: Efficacy and safety of a 12-week treatment with twice-daily aclidinium bromide in COPD patients (ACCORD COPD I). COPD 2012, 9: 90–101. 10.3109/15412555.2012.661492PubMedCrossRef
11.
go back to reference Terzano C, Petroianni A, Conti V, Ceccarelli D, Graziani E, Sanduzzi A, D'Avelli S: Rational timing of combination therapy with tiotropium and formoterol in moderate and severe COPD. Respir Med 2008, 102: 1701–1707. 10.1016/j.rmed.2008.07.012PubMedCrossRef Terzano C, Petroianni A, Conti V, Ceccarelli D, Graziani E, Sanduzzi A, D'Avelli S: Rational timing of combination therapy with tiotropium and formoterol in moderate and severe COPD. Respir Med 2008, 102: 1701–1707. 10.1016/j.rmed.2008.07.012PubMedCrossRef
12.
go back to reference United States Food and Drug Administration: Guidance for industry on patient-reported outcome measures: use in medical product development to support labeling claims. Fed Regist 2009, 74: 65132–65133. United States Food and Drug Administration: Guidance for industry on patient-reported outcome measures: use in medical product development to support labeling claims. Fed Regist 2009, 74: 65132–65133.
13.
go back to reference Patrick DL, Burke LB, Gwaltney CJ, Leidy NK, Martin ML, Molsen E, Ring L: Content validity–establishing and reporting the evidence in newly developed patient-reported outcomes (PRO) instruments for medical product evaluation: ISPOR PRO good research practices task force report: part 1–eliciting concepts for a new PRO instrument. Value Health 2011, 14: 967–977. 10.1016/j.jval.2011.06.014PubMedCrossRef Patrick DL, Burke LB, Gwaltney CJ, Leidy NK, Martin ML, Molsen E, Ring L: Content validity–establishing and reporting the evidence in newly developed patient-reported outcomes (PRO) instruments for medical product evaluation: ISPOR PRO good research practices task force report: part 1–eliciting concepts for a new PRO instrument. Value Health 2011, 14: 967–977. 10.1016/j.jval.2011.06.014PubMedCrossRef
14.
go back to reference Patrick DL, Burke LB, Gwaltney CJ, Leidy NK, Martin ML, Molsen E, Ring L: Content validity–establishing and reporting the evidence in newly developed patient-reported outcomes (PRO) instruments for medical product evaluation: ISPOR PRO Good Research Practices Task Force report: part 2–assessing respondent understanding. Value Health 2011, 14: 978–988. 10.1016/j.jval.2011.06.013PubMedCrossRef Patrick DL, Burke LB, Gwaltney CJ, Leidy NK, Martin ML, Molsen E, Ring L: Content validity–establishing and reporting the evidence in newly developed patient-reported outcomes (PRO) instruments for medical product evaluation: ISPOR PRO Good Research Practices Task Force report: part 2–assessing respondent understanding. Value Health 2011, 14: 978–988. 10.1016/j.jval.2011.06.013PubMedCrossRef
15.
go back to reference Meguro M, Barley EA, Spencer S, Jones PW: Development and validation of an improved, COPD-specific version of the St. George Respiratory Questionnaire. Chest 2007, 132: 456–463. 10.1378/chest.06-0702PubMedCrossRef Meguro M, Barley EA, Spencer S, Jones PW: Development and validation of an improved, COPD-specific version of the St. George Respiratory Questionnaire. Chest 2007, 132: 456–463. 10.1378/chest.06-0702PubMedCrossRef
16.
go back to reference Jones PW, Quirk FH, Baveystock CM, Littlejohns P: A self-complete measure of health status for chronic airflow limitation. The St. George's Respiratory Questionnaire. Am Rev Respir Dis 1992, 145: 1321–1327. 10.1164/ajrccm/145.6.1321PubMedCrossRef Jones PW, Quirk FH, Baveystock CM, Littlejohns P: A self-complete measure of health status for chronic airflow limitation. The St. George's Respiratory Questionnaire. Am Rev Respir Dis 1992, 145: 1321–1327. 10.1164/ajrccm/145.6.1321PubMedCrossRef
17.
go back to reference Zigmond AS, Snaith RP: The hospital anxiety and depression scale. Acta Psychiatr Scand 1983, 67: 361–370. 10.1111/j.1600-0447.1983.tb09716.xPubMedCrossRef Zigmond AS, Snaith RP: The hospital anxiety and depression scale. Acta Psychiatr Scand 1983, 67: 361–370. 10.1111/j.1600-0447.1983.tb09716.xPubMedCrossRef
19.
go back to reference Polit DF, Hungler BP: Nursing research: principles and methods. 6th edition. Philadelphia: Lippincott Williams and Wilkins; 1995. Polit DF, Hungler BP: Nursing research: principles and methods. 6th edition. Philadelphia: Lippincott Williams and Wilkins; 1995.
20.
21.
go back to reference Muhr T: User's Manual for ATLAS.ti 5.0. Berlin: ATLAS.ti Scientific Software Development GmbH; 2004. Muhr T: User's Manual for ATLAS.ti 5.0. Berlin: ATLAS.ti Scientific Software Development GmbH; 2004.
22.
go back to reference Rabe KF, Hurd S, Anzueto A, Barnes PJ, Buist SA, Calverley P, Fukuchi Y, Jenkins C, Rodriguez-Roisin R, van Weel C, Zielinski J: Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am J Respir Crit Care Med 2007, 176: 532–555. 10.1164/rccm.200703-456SOPubMedCrossRef Rabe KF, Hurd S, Anzueto A, Barnes PJ, Buist SA, Calverley P, Fukuchi Y, Jenkins C, Rodriguez-Roisin R, van Weel C, Zielinski J: Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am J Respir Crit Care Med 2007, 176: 532–555. 10.1164/rccm.200703-456SOPubMedCrossRef
Metadata
Title
The development of a patient-reported outcome measure for assessing nighttime symptoms of chronic obstructive pulmonary disease
Authors
Asha Hareendran
Andrew C Palsgrove
Michelle Mocarski
Michael L Schaefer
Juliana Setyawan
Robyn Carson
Barry Make
Publication date
01-12-2013
Publisher
BioMed Central
Published in
Health and Quality of Life Outcomes / Issue 1/2013
Electronic ISSN: 1477-7525
DOI
https://doi.org/10.1186/1477-7525-11-104

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