Cargando…
Cauda Equina Syndrome Core Outcome Set (CESCOS): An international patient and healthcare professional consensus for research studies
BACKGROUND: Cauda Equina Syndrome (CES) is an emergency condition that requires acute intervention and can lead to permanent neurological deficit in working age adults. A Core Outcome Set (COS) is the minimum set of outcomes that should be reported by a research study within a specific disease area....
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953762/ https://www.ncbi.nlm.nih.gov/pubmed/31923259 http://dx.doi.org/10.1371/journal.pone.0225907 |
_version_ | 1783486671232172032 |
---|---|
author | Srikandarajah, Nisaharan Noble, Adam Clark, Simon Wilby, Martin Freeman, Brian J. C. Fehlings, Michael G. Williamson, Paula R. Marson, Tony |
author_facet | Srikandarajah, Nisaharan Noble, Adam Clark, Simon Wilby, Martin Freeman, Brian J. C. Fehlings, Michael G. Williamson, Paula R. Marson, Tony |
author_sort | Srikandarajah, Nisaharan |
collection | PubMed |
description | BACKGROUND: Cauda Equina Syndrome (CES) is an emergency condition that requires acute intervention and can lead to permanent neurological deficit in working age adults. A Core Outcome Set (COS) is the minimum set of outcomes that should be reported by a research study within a specific disease area. There is significant heterogeneity in outcome reporting for CES, which does not allow data synthesis between studies. The hypothesis is that a COS for CES can be developed for future research studies using patients and healthcare professionals (HCPs) as key stakeholders. METHODS AND FINDINGS: Qualitative semi-structured interviews with CES patients were audio-recorded, transcribed and analysed using NVivo to identify the outcomes of importance. These were combined with the outcomes obtained from a published systematic literature review of CES patients. The outcomes were grouped into a list of 37, for rating through two rounds of an international Delphi survey according to pre-set criteria. The Delphi survey had an overall response rate of 63% and included 172 participants (104 patients, 68 HCPs) from 14 countries who completed both rounds. Thirteen outcomes reached consensus at the end of the Delphi survey and there was no attrition bias detected. The results were discussed at an international consensus meeting attended by 34 key stakeholders (16 patients and 18 HCPs) from 8 countries. A further three outcomes were agreed to be included. There was no selection bias detected at the consensus meeting. There are 16 outcomes in total in the CESCOS. DISCUSSION: This is the first study in the literature that has determined the core outcomes in CES using a transparent international consensus process involving healthcare professionals and CES patients as key stakeholders. This COS is recommended as the most important outcomes to be reported in any research study investigating CES outcomes and will allow evidence synthesis in CES. |
format | Online Article Text |
id | pubmed-6953762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69537622020-01-21 Cauda Equina Syndrome Core Outcome Set (CESCOS): An international patient and healthcare professional consensus for research studies Srikandarajah, Nisaharan Noble, Adam Clark, Simon Wilby, Martin Freeman, Brian J. C. Fehlings, Michael G. Williamson, Paula R. Marson, Tony PLoS One Research Article BACKGROUND: Cauda Equina Syndrome (CES) is an emergency condition that requires acute intervention and can lead to permanent neurological deficit in working age adults. A Core Outcome Set (COS) is the minimum set of outcomes that should be reported by a research study within a specific disease area. There is significant heterogeneity in outcome reporting for CES, which does not allow data synthesis between studies. The hypothesis is that a COS for CES can be developed for future research studies using patients and healthcare professionals (HCPs) as key stakeholders. METHODS AND FINDINGS: Qualitative semi-structured interviews with CES patients were audio-recorded, transcribed and analysed using NVivo to identify the outcomes of importance. These were combined with the outcomes obtained from a published systematic literature review of CES patients. The outcomes were grouped into a list of 37, for rating through two rounds of an international Delphi survey according to pre-set criteria. The Delphi survey had an overall response rate of 63% and included 172 participants (104 patients, 68 HCPs) from 14 countries who completed both rounds. Thirteen outcomes reached consensus at the end of the Delphi survey and there was no attrition bias detected. The results were discussed at an international consensus meeting attended by 34 key stakeholders (16 patients and 18 HCPs) from 8 countries. A further three outcomes were agreed to be included. There was no selection bias detected at the consensus meeting. There are 16 outcomes in total in the CESCOS. DISCUSSION: This is the first study in the literature that has determined the core outcomes in CES using a transparent international consensus process involving healthcare professionals and CES patients as key stakeholders. This COS is recommended as the most important outcomes to be reported in any research study investigating CES outcomes and will allow evidence synthesis in CES. Public Library of Science 2020-01-10 /pmc/articles/PMC6953762/ /pubmed/31923259 http://dx.doi.org/10.1371/journal.pone.0225907 Text en © 2020 Srikandarajah et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Srikandarajah, Nisaharan Noble, Adam Clark, Simon Wilby, Martin Freeman, Brian J. C. Fehlings, Michael G. Williamson, Paula R. Marson, Tony Cauda Equina Syndrome Core Outcome Set (CESCOS): An international patient and healthcare professional consensus for research studies |
title | Cauda Equina Syndrome Core Outcome Set (CESCOS): An international patient and healthcare professional consensus for research studies |
title_full | Cauda Equina Syndrome Core Outcome Set (CESCOS): An international patient and healthcare professional consensus for research studies |
title_fullStr | Cauda Equina Syndrome Core Outcome Set (CESCOS): An international patient and healthcare professional consensus for research studies |
title_full_unstemmed | Cauda Equina Syndrome Core Outcome Set (CESCOS): An international patient and healthcare professional consensus for research studies |
title_short | Cauda Equina Syndrome Core Outcome Set (CESCOS): An international patient and healthcare professional consensus for research studies |
title_sort | cauda equina syndrome core outcome set (cescos): an international patient and healthcare professional consensus for research studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953762/ https://www.ncbi.nlm.nih.gov/pubmed/31923259 http://dx.doi.org/10.1371/journal.pone.0225907 |
work_keys_str_mv | AT srikandarajahnisaharan caudaequinasyndromecoreoutcomesetcescosaninternationalpatientandhealthcareprofessionalconsensusforresearchstudies AT nobleadam caudaequinasyndromecoreoutcomesetcescosaninternationalpatientandhealthcareprofessionalconsensusforresearchstudies AT clarksimon caudaequinasyndromecoreoutcomesetcescosaninternationalpatientandhealthcareprofessionalconsensusforresearchstudies AT wilbymartin caudaequinasyndromecoreoutcomesetcescosaninternationalpatientandhealthcareprofessionalconsensusforresearchstudies AT freemanbrianjc caudaequinasyndromecoreoutcomesetcescosaninternationalpatientandhealthcareprofessionalconsensusforresearchstudies AT fehlingsmichaelg caudaequinasyndromecoreoutcomesetcescosaninternationalpatientandhealthcareprofessionalconsensusforresearchstudies AT williamsonpaular caudaequinasyndromecoreoutcomesetcescosaninternationalpatientandhealthcareprofessionalconsensusforresearchstudies AT marsontony caudaequinasyndromecoreoutcomesetcescosaninternationalpatientandhealthcareprofessionalconsensusforresearchstudies |