| 000 | 02579na a2200421 4500 | ||
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| 999 |
_c370 _d370 |
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| 003 | PC370 | ||
| 005 | 20210625062753.0 | ||
| 008 | 130622s2013 xxx||||| |||| 00| 0 eng d | ||
| 040 | _cH12O | ||
| 041 | _aeng | ||
| 100 |
_aLópez Campos, José Luis _92612 _eInstituto de Investigación i+12 |
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| 100 |
_aPozo Rodríguez, Francisco _9702 _eNeumología _eInstituto de Investigación i+12 (2013-) |
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| 245 | 0 | 0 |
_aEuropean CORD Audit: design, organisation of work and methodology _h[artículo] |
| 260 |
_c2013 _bEuropean Respiratory Journal, |
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| 300 | _a41(2):270–6. | ||
| 500 | _aFormato Vancouver: López-Campos JL, Hartl S, Pozo-Rodríguez F, Roberts CM; European COPD Audit team. European COPD Audit: design, organisation of work and methodology. Eur Respir J. 2013;41(2):270–6. | ||
| 501 | _aPMID: 2259936 | ||
| 504 | _aContiene 18 referencias | ||
| 520 | _aClinical audit has an important role as an indicator of the clinical practice in a given community. The European Respiratory Society (ERS) chronic obstructive pulmonary disease (COPD) audit was designed as a pilot study to evaluate clinical practice variability as well as clinical and organisational factors related to outcomes for COPD hospital admissions across Europe. The study was designed as a prospective observational noninterventional cohort trial, in which 422 hospitals from 13 European countries participated. There were two databases: one for hospital's resources and organisation and one for clinical information. The study was comprised of an initial 8-week phase during which all consecutive cases admitted to hospital due to an exacerbation of COPD were identified and information on clinical practice was gathered. During the 90-day second phase, mortality and readmissions were recorded. Patient data were anonymised and encrypted through a multi-lingual web-tool. As there is no pan-European Ethics Committee for audits, all partners accepted the general ethical rules of the ERS and ensured compliance with their own national ethical requirements. This paper describes the methodological issues encountered in organising and delivering a multi-national European audit, highlighting goals, barriers and achievements, and provides valuable information for those interested in developing clinical audits. | ||
| 710 |
_988 _aServicio de Neumología |
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| 710 |
_9625 _aInstituto de Investigación imas12 |
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| 856 |
_uhttp://pc-h12o-es.m-hdoct.a17.csinet.es/pdf/pc/3/pc370.pdf _ySolicitar documento |
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| 942 |
_n0 _2ddc _cART |
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