Neural respiratory drive predicts clinical deterioration and safe discharge in exacerbations of COPD. Issue 12 (20th July 2015)
- Record Type:
- Journal Article
- Title:
- Neural respiratory drive predicts clinical deterioration and safe discharge in exacerbations of COPD. Issue 12 (20th July 2015)
- Main Title:
- Neural respiratory drive predicts clinical deterioration and safe discharge in exacerbations of COPD
- Authors:
- Suh, Eui-Sik
Mandal, Swapna
Harding, Rachel
Ramsay, Michelle
Kamalanathan, Meera
Henderson, Katherine
O'Kane, Kevin
Douiri, Abdel
Hopkinson, Nicholas S
Polkey, Michael I
Rafferty, Gerrard
Murphy, Patrick B
Moxham, John
Hart, Nicholas - Abstract:
- Abstract : Rationale: Hospitalised patients with acute exacerbation of COPD may deteriorate despite treatment, with early readmission being common. Objectives: To investigate whether neural respiratory drive, measured using second intercostal space parasternal muscle electromyography (EMGpara ), would identify worsening dyspnoea and physician-defined inpatient clinical deterioration, and predict early readmission. Methods: Patients admitted to a single-site university hospital with exacerbation of COPD were enrolled. Spirometry, inspiratory capacity (IC), EMGpara, routine physiological parameters, modified early warning score (MEWS), modified Borg scale for dyspnoea and physician-defined episodes of deterioration were recorded daily until discharge. Readmissions at 14 and 28 days post discharge were recorded. Measurements and main results: 120 patients were recruited (age 70±9 years, forced expiratory volume in 1 s (FEV1 ) of 30.5±11.2%). Worsening dyspnoea, defined as at least one-point increase in Borg scale, was associated with increases in EMGpara%max and MEWS, whereas an increase in EMGpara%max alone was associated with physician-defined inpatient clinical deterioration. Admission-to-discharge change (Δ) in the normalised value of EMGpara (ΔEMGpara%max ) was inversely correlated with ΔFEV1 (r=−0.38, p<0.001) and ΔIC (r=−0.44, p<0.001). ΔEMGpara%max predicted 14-day readmission (OR 1.13, 95% 1.03 to 1.23) in the whole cohort and 28-day readmission in patients underAbstract : Rationale: Hospitalised patients with acute exacerbation of COPD may deteriorate despite treatment, with early readmission being common. Objectives: To investigate whether neural respiratory drive, measured using second intercostal space parasternal muscle electromyography (EMGpara ), would identify worsening dyspnoea and physician-defined inpatient clinical deterioration, and predict early readmission. Methods: Patients admitted to a single-site university hospital with exacerbation of COPD were enrolled. Spirometry, inspiratory capacity (IC), EMGpara, routine physiological parameters, modified early warning score (MEWS), modified Borg scale for dyspnoea and physician-defined episodes of deterioration were recorded daily until discharge. Readmissions at 14 and 28 days post discharge were recorded. Measurements and main results: 120 patients were recruited (age 70±9 years, forced expiratory volume in 1 s (FEV1 ) of 30.5±11.2%). Worsening dyspnoea, defined as at least one-point increase in Borg scale, was associated with increases in EMGpara%max and MEWS, whereas an increase in EMGpara%max alone was associated with physician-defined inpatient clinical deterioration. Admission-to-discharge change (Δ) in the normalised value of EMGpara (ΔEMGpara%max ) was inversely correlated with ΔFEV1 (r=−0.38, p<0.001) and ΔIC (r=−0.44, p<0.001). ΔEMGpara%max predicted 14-day readmission (OR 1.13, 95% 1.03 to 1.23) in the whole cohort and 28-day readmission in patients under 85 years (OR 1.09, 95% CI 1.01 to 1.18). Age (OR 1.08, 95% CI 1.03 to 1.14) and 12-month admission frequency (OR 1.29, 1.01 to 1.66), also predicted 28-day readmission in the whole cohort. Conclusions: Measurement of neural respiratory drive by EMGpara represents a novel physiological biomarker that may be helpful in detecting inpatient clinical deterioration and identifying the risk of early readmission among patients with exacerbations of COPD. Trial registration: NCT01361451. … (more)
- Is Part Of:
- Thorax. Volume 70:Issue 12(2015)
- Journal:
- Thorax
- Issue:
- Volume 70:Issue 12(2015)
- Issue Display:
- Volume 70, Issue 12 (2015)
- Year:
- 2015
- Volume:
- 70
- Issue:
- 12
- Issue Sort Value:
- 2015-0070-0012-0000
- Page Start:
- 1123
- Page End:
- 1130
- Publication Date:
- 2015-07-20
- Subjects:
- COPD Exacerbations -- Respiratory Muscles -- Lung Physiology
Chest -- Diseases -- Periodicals
Thorax
Chest -- Diseases
Periodicals
Periodicals
617.54 - Journal URLs:
- http://thorax.bmjjournals.com/contents-by-date.0.shtml ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/thoraxjnl-2015-207188 ↗
- Languages:
- English
- ISSNs:
- 0040-6376
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
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