A systematic review and meta-analysis of the clinimetric properties of the core outcome measurement instruments for clinical effectiveness trials of nutritional and metabolic interventions in critical illness (CONCISE).


Journal

Critical care (London, England)
ISSN: 1466-609X
Titre abrégé: Crit Care
Pays: England
ID NLM: 9801902

Informations de publication

Date de publication:
20 11 2023
Historique:
received: 14 09 2023
accepted: 09 11 2023
medline: 27 11 2023
pubmed: 21 11 2023
entrez: 21 11 2023
Statut: epublish

Résumé

CONCISE is an internationally agreed minimum set of outcomes for use in nutritional and metabolic clinical research in critically ill adults. Clinicians and researchers need to be aware of the clinimetric properties of these instruments and understand any limitations to ensure valid and reliable research. This systematic review and meta-analysis were undertaken to evaluate the clinimetric properties of the measurement instruments identified in CONCISE. Four electronic databases were searched from inception to December 2022 (MEDLINE via Ovid, EMBASE via Ovid, CINAHL via Healthcare Databases Advanced Search, CENTRAL via Cochrane). Studies were included if they examined at least one clinimetric property of a CONCISE measurement instrument or recognised variation in adults ≥ 18 years with critical illness or recovering from critical illness in any language. The COnsensus-based Standards for the selection of health Measurement INstruments (COSMIN) checklist for systematic reviews of Patient-Reported Outcome Measures was used. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses were used in line with COSMIN guidance. The COSMIN checklist was used to evaluate the risk of bias and the quality of clinimetric properties. Overall certainty of the evidence was rated using a modified Grading of Recommendations, Assessment, Development and Evaluation approach. Narrative synthesis was performed and where possible, meta-analysis was conducted. A total of 4316 studies were screened. Forty-seven were included in the review, reporting data for 12308 participants. The Short Form-36 Questionnaire (Physical Component Score and Physical Functioning), sit-to-stand test, 6-m walk test and Barthel Index had the strongest clinimetric properties and certainty of evidence. The Short Physical Performance Battery, Katz Index and handgrip strength had less favourable results. There was limited data for Lawson Instrumental Activities of Daily Living and the Global Leadership Initiative on Malnutrition criteria. The risk of bias ranged from inadequate to very good. The certainty of the evidence ranged from very low to high. Variable evidence exists to support the clinimetric properties of the CONCISE measurement instruments. We suggest using this review alongside CONCISE to guide outcome selection for future trials of nutrition and metabolic interventions in critical illness. PROSPERO (CRD42023438187). Registered 21/06/2023.

Sections du résumé

BACKGROUND
CONCISE is an internationally agreed minimum set of outcomes for use in nutritional and metabolic clinical research in critically ill adults. Clinicians and researchers need to be aware of the clinimetric properties of these instruments and understand any limitations to ensure valid and reliable research. This systematic review and meta-analysis were undertaken to evaluate the clinimetric properties of the measurement instruments identified in CONCISE.
METHODS
Four electronic databases were searched from inception to December 2022 (MEDLINE via Ovid, EMBASE via Ovid, CINAHL via Healthcare Databases Advanced Search, CENTRAL via Cochrane). Studies were included if they examined at least one clinimetric property of a CONCISE measurement instrument or recognised variation in adults ≥ 18 years with critical illness or recovering from critical illness in any language. The COnsensus-based Standards for the selection of health Measurement INstruments (COSMIN) checklist for systematic reviews of Patient-Reported Outcome Measures was used. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses were used in line with COSMIN guidance. The COSMIN checklist was used to evaluate the risk of bias and the quality of clinimetric properties. Overall certainty of the evidence was rated using a modified Grading of Recommendations, Assessment, Development and Evaluation approach. Narrative synthesis was performed and where possible, meta-analysis was conducted.
RESULTS
A total of 4316 studies were screened. Forty-seven were included in the review, reporting data for 12308 participants. The Short Form-36 Questionnaire (Physical Component Score and Physical Functioning), sit-to-stand test, 6-m walk test and Barthel Index had the strongest clinimetric properties and certainty of evidence. The Short Physical Performance Battery, Katz Index and handgrip strength had less favourable results. There was limited data for Lawson Instrumental Activities of Daily Living and the Global Leadership Initiative on Malnutrition criteria. The risk of bias ranged from inadequate to very good. The certainty of the evidence ranged from very low to high.
CONCLUSIONS
Variable evidence exists to support the clinimetric properties of the CONCISE measurement instruments. We suggest using this review alongside CONCISE to guide outcome selection for future trials of nutrition and metabolic interventions in critical illness.
TRIAL REGISTRATION
PROSPERO (CRD42023438187). Registered 21/06/2023.

Identifiants

pubmed: 37986015
doi: 10.1186/s13054-023-04729-7
pii: 10.1186/s13054-023-04729-7
pmc: PMC10662687
doi:

Types de publication

Meta-Analysis Systematic Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

450

Subventions

Organisme : National Institute of Health Research (NIHR) Academic Clinical Fellowship Award Programme
ID : 2021-19-009
Organisme : National Institute of Health Research (NIHR) Pre-Doctoral Clinical Academic Fellowship Award Programme
ID : NIHR302695

Informations de copyright

© 2023. The Author(s).

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Auteurs

T W Davies (TW)

Faculty of Medicine & Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK. thomas.davies6@nhs.net.
Critical Care and Perioperative Medicine Research Group, Adult Critical Care Unit, Royal London Hospital, London, E1 1BB, UK. thomas.davies6@nhs.net.

E Kelly (E)

Faculty of Medicine & Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK.
Critical Care and Perioperative Medicine Research Group, Adult Critical Care Unit, Royal London Hospital, London, E1 1BB, UK.

R J J van Gassel (RJJ)

Department of Intensive Care Medicine, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University Medical Centre+, Maastricht, The Netherlands.
Department of Surgery, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University Medical Centre+, Maastricht, The Netherlands.

M C G van de Poll (MCG)

Department of Intensive Care Medicine, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University Medical Centre+, Maastricht, The Netherlands.
Department of Surgery, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University Medical Centre+, Maastricht, The Netherlands.

J Gunst (J)

Clinical Department and Laboratory of Intensive Care Medicine, Department of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, 3000, Louvain, Belgium.

M P Casaer (MP)

Clinical Department and Laboratory of Intensive Care Medicine, Department of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, 3000, Louvain, Belgium.

K B Christopher (KB)

Division of Renal Medicine, Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA.

J C Preiser (JC)

Medical Direction, Erasme University Hospital, Universite Libre de Bruxelles, Brussels, Belgium.

A Hill (A)

Department of Intensive Care Medicine, University Hospital RWTH, 52074, Aachen, Germany.
Department of Anesthesiology, University Hospital RWTH, 52074, Aachen, Germany.

K Gundogan (K)

Division of Intensive Care Medicine, Department of Internal Medicine, Erciyes University School of Medicine, Kayseri, Turkey.

A Reintam-Blaser (A)

Department of Anaesthesiology and Intensive Care, University of Tartu, Tartu, Estonia.
Department of Intensive Care Medicine, Lucerne Cantonal Hospital, Lucerne, Switzerland.

A-F Rousseau (AF)

Department of Intensive Care, University Hospital of Liège, Liege, Belgium.

C Hodgson (C)

Australian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, 3/553 St Kilda Rd, Melbourne, VIC, 3004, Australia.
Department of Intensive Care and Hyperbaric Medicine, The Alfred, Melbourne, VIC, Australia.

D M Needham (DM)

Outcomes After Critical Illness and Surgery (OACIS) Research Group, Johns Hopkins University, Baltimore, MD, USA.
Pulmonary and Critical Care Medicine, Department of Medicine, and Department of Physical Medicine and Rehabilitation, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

S J Schaller (SJ)

Department of Anesthesiology and Intensive Care Medicine (CVK, CCM), Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin, Berlin Institute of Health, Berlin, Germany.
Department of Anesthesiology and Intensive Care, School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, Munich, Germany.

T McClelland (T)

Faculty of Medicine & Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK.
Critical Care and Perioperative Medicine Research Group, Adult Critical Care Unit, Royal London Hospital, London, E1 1BB, UK.

J J Pilkington (JJ)

Centre for Bioscience, Manchester Metropolitan University, John Dalton Building, Chester Street, Manchester, UK.

C M Sevin (CM)

Department of Medicine, Division of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.

P E Wischmeyer (PE)

Department of Anesthesiology, Duke University School of Medicine, DUMC, Box 3094 Mail # 41, 2301 Erwin Road, Durham, NC, 5692 HAFS27710, USA.

Z Y Lee (ZY)

Department of Anesthesiology, University of Malaya, Kuala Lumpur, Malaysia.
Department of Cardiac, Anesthesiology & Intensive Care Medicine, Charité, Berlin, Germany.

D Govil (D)

Institute of Critical Care and Anesthesia, Medanta: The Medicty, Gurugram, Haryana, India.

L Chapple (L)

Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, SA, Australia.

L Denehy (L)

School of Health Sciences, The University of Melbourne, Melbourne, Australia.
Department of Allied Health, Peter McCallum Cancer Centre, Melbourne, Australia.

J C Montejo-González (JC)

Instituto de Investigación I+12, Hospital Universitario, 12 de Octubre, Madrid, Spain.

B Taylor (B)

Department of Research for Patient Care Services, Barnes-Jewish Hospital, St. Louis, MO, USA.

D E Bear (DE)

Department of Critical Care, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Department of Nutrition and Dietetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.

R M Pearse (RM)

Faculty of Medicine & Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK.
Critical Care and Perioperative Medicine Research Group, Adult Critical Care Unit, Royal London Hospital, London, E1 1BB, UK.

A McNelly (A)

Faculty of Medicine & Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK.

J Prowle (J)

Faculty of Medicine & Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK.
Critical Care and Perioperative Medicine Research Group, Adult Critical Care Unit, Royal London Hospital, London, E1 1BB, UK.

Z A Puthucheary (ZA)

Faculty of Medicine & Dentistry, Queen Mary University of London, London, EC1M 6BQ, UK.
Critical Care and Perioperative Medicine Research Group, Adult Critical Care Unit, Royal London Hospital, London, E1 1BB, UK.

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