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Domiciliary pulse-oximetry at exacerbation of chronic obstructive pulmonary disease: prospective pilot study

BACKGROUND: The ability to objectively differentiate exacerbations of chronic obstructive pulmonary disease (COPD) from day-to-day symptom variations would be an important development in clinical practice and research. We assessed the ability of domiciliary pulse oximetry to achieve this. METHODS: 4...

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Autores principales: Hurst, John R, Donaldson, Gavin C, Quint, Jennifer K, Goldring, James JP, Patel, Anant RC, Wedzicha, Jadwiga A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978135/
https://www.ncbi.nlm.nih.gov/pubmed/20961450
http://dx.doi.org/10.1186/1471-2466-10-52
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author Hurst, John R
Donaldson, Gavin C
Quint, Jennifer K
Goldring, James JP
Patel, Anant RC
Wedzicha, Jadwiga A
author_facet Hurst, John R
Donaldson, Gavin C
Quint, Jennifer K
Goldring, James JP
Patel, Anant RC
Wedzicha, Jadwiga A
author_sort Hurst, John R
collection PubMed
description BACKGROUND: The ability to objectively differentiate exacerbations of chronic obstructive pulmonary disease (COPD) from day-to-day symptom variations would be an important development in clinical practice and research. We assessed the ability of domiciliary pulse oximetry to achieve this. METHODS: 40 patients with moderate-severe COPD collected daily data on changes in symptoms, heart-rate (HR), oxygen saturation (SpO(2)) and peak-expiratory flow (PEF) over a total of 2705 days. 31 patients had data suitable for baseline analysis, and 13 patients experienced an exacerbation. Data were expressed as multiples of the standard deviation (SD) observed from each patient when stable. RESULTS: In stable COPD, the SD for HR, SpO(2 )and PEF were approximately 5 min(-1), 1% and 10l min(-1). There were detectable changes in all three variables just prior to exacerbation onset, greatest 2-3 days following symptom onset. A composite Oximetry Score (mean magnitude of SpO(2 )fall and HR rise) distinguished exacerbation onset from symptom variation (area under receiver-operating characteristic curve, AUC = 0.832, 95%CI 0.735-0.929, p = 0.003). In the presence of symptoms, a change in Score of ≥1 (average of ≥1SD change in both HR and SpO(2)) was 71% sensitive and 74% specific for exacerbation onset. CONCLUSION: We have defined normal variation of pulse oximetry variables in a small sample of patients with COPD. A composite HR and SpO(2 )score distinguished exacerbation onset from symptom variation, potentially facilitating prompt therapy and providing validation of such events in clinical trials.
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spelling pubmed-29781352010-11-11 Domiciliary pulse-oximetry at exacerbation of chronic obstructive pulmonary disease: prospective pilot study Hurst, John R Donaldson, Gavin C Quint, Jennifer K Goldring, James JP Patel, Anant RC Wedzicha, Jadwiga A BMC Pulm Med Research Article BACKGROUND: The ability to objectively differentiate exacerbations of chronic obstructive pulmonary disease (COPD) from day-to-day symptom variations would be an important development in clinical practice and research. We assessed the ability of domiciliary pulse oximetry to achieve this. METHODS: 40 patients with moderate-severe COPD collected daily data on changes in symptoms, heart-rate (HR), oxygen saturation (SpO(2)) and peak-expiratory flow (PEF) over a total of 2705 days. 31 patients had data suitable for baseline analysis, and 13 patients experienced an exacerbation. Data were expressed as multiples of the standard deviation (SD) observed from each patient when stable. RESULTS: In stable COPD, the SD for HR, SpO(2 )and PEF were approximately 5 min(-1), 1% and 10l min(-1). There were detectable changes in all three variables just prior to exacerbation onset, greatest 2-3 days following symptom onset. A composite Oximetry Score (mean magnitude of SpO(2 )fall and HR rise) distinguished exacerbation onset from symptom variation (area under receiver-operating characteristic curve, AUC = 0.832, 95%CI 0.735-0.929, p = 0.003). In the presence of symptoms, a change in Score of ≥1 (average of ≥1SD change in both HR and SpO(2)) was 71% sensitive and 74% specific for exacerbation onset. CONCLUSION: We have defined normal variation of pulse oximetry variables in a small sample of patients with COPD. A composite HR and SpO(2 )score distinguished exacerbation onset from symptom variation, potentially facilitating prompt therapy and providing validation of such events in clinical trials. BioMed Central 2010-10-20 /pmc/articles/PMC2978135/ /pubmed/20961450 http://dx.doi.org/10.1186/1471-2466-10-52 Text en Copyright ©2010 Hurst et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hurst, John R
Donaldson, Gavin C
Quint, Jennifer K
Goldring, James JP
Patel, Anant RC
Wedzicha, Jadwiga A
Domiciliary pulse-oximetry at exacerbation of chronic obstructive pulmonary disease: prospective pilot study
title Domiciliary pulse-oximetry at exacerbation of chronic obstructive pulmonary disease: prospective pilot study
title_full Domiciliary pulse-oximetry at exacerbation of chronic obstructive pulmonary disease: prospective pilot study
title_fullStr Domiciliary pulse-oximetry at exacerbation of chronic obstructive pulmonary disease: prospective pilot study
title_full_unstemmed Domiciliary pulse-oximetry at exacerbation of chronic obstructive pulmonary disease: prospective pilot study
title_short Domiciliary pulse-oximetry at exacerbation of chronic obstructive pulmonary disease: prospective pilot study
title_sort domiciliary pulse-oximetry at exacerbation of chronic obstructive pulmonary disease: prospective pilot study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978135/
https://www.ncbi.nlm.nih.gov/pubmed/20961450
http://dx.doi.org/10.1186/1471-2466-10-52
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