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      Validation of the DECAF score to predict hospital mortality in acute exacerbations of COPD

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          Abstract

          Background

          Hospitalisation due to acute exacerbations of COPD (AECOPD) is common, and subsequent mortality high. The DECAF score was derived for accurate prediction of mortality and risk stratification to inform patient care. We aimed to validate the DECAF score, internally and externally, and to compare its performance to other predictive tools.

          Methods

          The study took place in the two hospitals within the derivation study (internal validation) and in four additional hospitals (external validation) between January 2012 and May 2014. Consecutive admissions were identified by screening admissions and searching coding records. Admission clinical data, including DECAF indices, and mortality were recorded. The prognostic value of DECAF and other scores were assessed by the area under the receiver operator characteristic (AUROC) curve.

          Results

          In the internal and external validation cohorts, 880 and 845 patients were recruited. Mean age was 73.1 (SD 10.3) years, 54.3% were female, and mean (SD) FEV 1 45.5 (18.3) per cent predicted. Overall mortality was 7.7%. The DECAF AUROC curve for inhospital mortality was 0.83 (95% CI 0.78 to 0.87) in the internal cohort and 0.82 (95% CI 0.77 to 0.87) in the external cohort, and was superior to other prognostic scores for inhospital or 30-day mortality.

          Conclusions

          DECAF is a robust predictor of mortality, using indices routinely available on admission. Its generalisability is supported by consistent strong performance; it can identify low-risk patients (DECAF 0–1) potentially suitable for Hospital at Home or early supported discharge services, and high-risk patients (DECAF 3–6) for escalation planning or appropriate early palliation.

          Trial registration number

          UKCRN ID 14214.

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          Most cited references15

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          BTS guideline for emergency oxygen use in adult patients.

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            John LIZARS. Centenary of a forgotten pioneer of the surgery of trigeminal neuralgia.

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              Dyspnoea severity and pneumonia as predictors of in-hospital mortality and early readmission in acute exacerbations of COPD.

              Rates of mortality and readmission are high in patients hospitalised with acute exacerbations of chronic obstructive pulmonary disease (AECOPD). In this population, the prognostic value of the Medical Research Council Dyspnoea Scale (MRCD) is uncertain, and an extended MRCD (eMRCD) scale has been proposed to improve its utility. Coexistent pneumonia is common and, although the CURB-65 prediction tool is used, its discriminatory value has not been reported. Clinical and demographic data were collected on consecutive patients hospitalised with AECOPD. The relationship of stable-state dyspnoea severity to in-hospital mortality and 28-day readmission was assessed. The discriminatory value of CURB-65, MRCD and eMRCD, in the prediction of in-hospital mortality, was assessed and compared. 920 patients were recruited. 10.4% died in-hospital and 19.1% of the 824 survivors were readmitted within 28 days of discharge. During their stable state prior to admission, 34.2% of patients were too breathless to leave the house. Mortality was significantly higher in pneumonic than in non-pneumonic exacerbations (20.1% vs 5.8%, p<0.001). eMRCD was a significantly better discriminator than either CURB-65 or the traditional MRCD scale for predicting in-hospital mortality, and was a stronger prognostic tool than CURB-65 in the subgroup of patients with pneumonic AECOPD. The severity of dyspnoea in the stable state predicts important clinical outcomes in patients hospitalised with AECOPD. The eMRCD scale identifies a subgroup of patients at a particularly high risk of in-hospital mortality and is a better predictor of mortality risk than CURB-65 in exacerbations complicated by pneumonia.
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                Author and article information

                Journal
                Thorax
                Thorax
                thoraxjnl
                thorax
                Thorax
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                0040-6376
                1468-3296
                February 2016
                : 71
                : 2
                : 133-140
                Affiliations
                [1 ]Department of Respiratory Medicine, North Tyneside General Hospital , North Shields, UK
                [2 ]Institute of Cellular Medicine, Newcastle University , Newcastle Upon Tyne, UK
                [3 ]Chest Clinic, Royal Victoria Infirmary , Newcastle Upon Tyne, UK
                [4 ]Department of Respiratory Medicine, Northern General Hospital , Sheffield, South Yorkshire, UK
                [5 ]Department of Respiratory Medicine, Royal Cornwall Hospital , Truro, Cornwall, UK
                [6 ]Department of Respiratory Medicine, University Hospital of North Tees, Hardwick Hall , Stockton-on-Tees, Cleveland, UK
                [7 ]Institute of Health and Society, Baddiley-Clark Building, Newcastle University , Newcastle Upon Tyne, UK
                Author notes
                [Correspondence to ] Dr SC Bourke, Department of Respiratory Medicine, North Tyneside General Hospital, Rake Lane, North Shields, Tyne and Wear NE29 8NH, UK; Stephen.Bourke@ 123456nhct.nhs.uk
                Article
                thoraxjnl-2015-207775
                10.1136/thoraxjnl-2015-207775
                4752621
                26769015
                e8dff581-e8cf-44cf-b296-5c350aa174b2
                Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

                This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

                History
                : 1 September 2015
                : 19 October 2015
                : 10 November 2015
                Categories
                1506
                Chronic Obstructive Pulmonary Disease
                Original article
                Custom metadata
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                Surgery
                copd exacerbations
                Surgery
                copd exacerbations

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