Effectiveness of pharmacological treatments for severe agitation in real-world emergency settings: protocol of individual-participant-data network meta-analysis.

Aggression Agitation Effectiveness Emergency Individual-participant data Network meta-analysis Psychosis Systematic review Tranquilization Violence

Journal

Systematic reviews
ISSN: 2046-4053
Titre abrégé: Syst Rev
Pays: England
ID NLM: 101580575

Informations de publication

Date de publication:
02 Aug 2024
Historique:
received: 03 11 2023
accepted: 20 07 2024
medline: 3 8 2024
pubmed: 3 8 2024
entrez: 2 8 2024
Statut: epublish

Résumé

Severe psychomotor agitation and aggression often require immediate pharmacological intervention, but clear evidence-based recommendations for choosing among the multiple options are lacking. To address this gap, we plan a systematic review and individual-participant-data network meta-analysis to investigate their comparative effectiveness in real-world emergency settings with increased precision. We will include randomized controlled trials investigating intramuscular or intravenous pharmacological interventions, as monotherapy or in combination, in adults with severe psychomotor agitation irrespective of the underlying diagnosis and requiring rapid tranquilization in general or psychiatric emergency settings. We will exclude studies before 2002, those focusing on specific reasons for agitation and placebo-controlled trials to avoid concerns related to the transitivity assumption and potential selection biases. We will search for eligible studies in BIOSIS, CENTRAL, CINAHL Plus, Embase, LILACS, MEDLINE via Ovid, PubMed, ProQuest, PsycINFO, ClinicalTrials.gov, and WHO-ICTRP. Individual-participant data will be requested from the study authors and harmonized into a uniform format, and aggregated data will also be extracted from the studies. At least two independent reviewers will conduct the study selection, data extraction, risk-of-bias assessment using RoB 2, and applicability evaluation using the RITES tool. The primary outcome will be the number of patients achieving adequate sedation within 30 min after treatment, with secondary outcomes including the need for additional interventions and adverse events, using odds ratios as the effect size. If enough individual-participant data will be collected, we will synthesize them in a network meta-regression model within a Bayesian framework, incorporating study- and participant-level characteristics to explore potential sources of heterogeneity. In cases where individual-participant data are unavailable, potential data availability bias will be explored, and models allowing for the inclusion of studies reporting only aggregated data will be considered. We will assess the confidence in the evidence using the Confidence in Network Meta-Analysis (CINeMA) approach. This individual-participant-data network meta-analysis aims to provide a fine-tuned synthesis of the evidence on the comparative effectiveness of pharmacological interventions for severe psychomotor agitation in real-world emergency settings. The findings from this study can greatly be provided clearer evidence-based guidance on the most effective treatments. PROSPERO CRD42023402365.

Sections du résumé

BACKGROUND BACKGROUND
Severe psychomotor agitation and aggression often require immediate pharmacological intervention, but clear evidence-based recommendations for choosing among the multiple options are lacking. To address this gap, we plan a systematic review and individual-participant-data network meta-analysis to investigate their comparative effectiveness in real-world emergency settings with increased precision.
METHODS METHODS
We will include randomized controlled trials investigating intramuscular or intravenous pharmacological interventions, as monotherapy or in combination, in adults with severe psychomotor agitation irrespective of the underlying diagnosis and requiring rapid tranquilization in general or psychiatric emergency settings. We will exclude studies before 2002, those focusing on specific reasons for agitation and placebo-controlled trials to avoid concerns related to the transitivity assumption and potential selection biases. We will search for eligible studies in BIOSIS, CENTRAL, CINAHL Plus, Embase, LILACS, MEDLINE via Ovid, PubMed, ProQuest, PsycINFO, ClinicalTrials.gov, and WHO-ICTRP. Individual-participant data will be requested from the study authors and harmonized into a uniform format, and aggregated data will also be extracted from the studies. At least two independent reviewers will conduct the study selection, data extraction, risk-of-bias assessment using RoB 2, and applicability evaluation using the RITES tool. The primary outcome will be the number of patients achieving adequate sedation within 30 min after treatment, with secondary outcomes including the need for additional interventions and adverse events, using odds ratios as the effect size. If enough individual-participant data will be collected, we will synthesize them in a network meta-regression model within a Bayesian framework, incorporating study- and participant-level characteristics to explore potential sources of heterogeneity. In cases where individual-participant data are unavailable, potential data availability bias will be explored, and models allowing for the inclusion of studies reporting only aggregated data will be considered. We will assess the confidence in the evidence using the Confidence in Network Meta-Analysis (CINeMA) approach.
DISCUSSION CONCLUSIONS
This individual-participant-data network meta-analysis aims to provide a fine-tuned synthesis of the evidence on the comparative effectiveness of pharmacological interventions for severe psychomotor agitation in real-world emergency settings. The findings from this study can greatly be provided clearer evidence-based guidance on the most effective treatments.
SYSTEMATIC REVIEW REGISTRATION BACKGROUND
PROSPERO CRD42023402365.

Identifiants

pubmed: 39095865
doi: 10.1186/s13643-024-02623-z
pii: 10.1186/s13643-024-02623-z
doi:

Substances chimiques

Antipsychotic Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

205

Subventions

Organisme : Bundesministerium für Bildung und Forschung
ID : 01KG2208

Informations de copyright

© 2024. The Author(s).

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Auteurs

Spyridon Siafis (S)

Technical University of Munich, TUM School of Medicine and Health, Department of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Munich, Germany. spyridon.siafis@tum.de.
German Center for Mental Health (DZPG), Partner site München/Augsburg, Munich, Germany. spyridon.siafis@tum.de.

Hui Wu (H)

Technical University of Munich, TUM School of Medicine and Health, Department of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Munich, Germany.

Nobuyuki Nomura (N)

Technical University of Munich, TUM School of Medicine and Health, Department of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Munich, Germany.
German Center for Mental Health (DZPG), Partner site München/Augsburg, Munich, Germany.
Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Johannes Schneider-Thoma (J)

Technical University of Munich, TUM School of Medicine and Health, Department of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Munich, Germany.
German Center for Mental Health (DZPG), Partner site München/Augsburg, Munich, Germany.

Irene Bighelli (I)

Technical University of Munich, TUM School of Medicine and Health, Department of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Munich, Germany.
German Center for Mental Health (DZPG), Partner site München/Augsburg, Munich, Germany.

Carolin Lorenz (C)

Technical University of Munich, TUM School of Medicine and Health, Department of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Munich, Germany.

Joseph E Dib (JE)

Division of Psychiatry & Applied Psychology, Institute of Mental Health, School of Medicine, University of Nottingham, Nottingham, Nottinghamshire, UK.

Prathap Tharyan (P)

Clinical Epidemiology Unit, Christian Medical Centre, Vellore, India.

Leonie A Calver (LA)

School of Nursing and Midwifery, University of Newcastle, Callaghan, NSW, Australia.

Geoffrey K Isbister (GK)

Clinical Toxicology Research Group, University of Newcastle, Newcastle, NSW, Australia.

Esther W Y Chan (EWY)

Department of Pharmacology and Pharmacy, University of Hong Kong, Pok Fu Lam, Hong Kong SAR, China.
Laboratory of Data Discovery for Health (D24H), Science Park, Hong Kong SAR, China.
Department of Pharmacy, HKU-Shenzhen Hospital, Shenzhen, China.
HKU-SZ Institute of Research and Innovation (SIRI), Shenzhen, China.

Jonathan C Knott (JC)

Department of Critical Care, The University of Melbourne, Melbourne, VIC, Australia.

Celene Y L Yap (CYL)

Department of Nursing, Faculty of Medicine, Dentistry and Health Sciences, Melbourne School of Health Sciences, The University of Melbourne, Melbourne, VIC, Australia.

Célia Mantovani (C)

Department of Neurosciences and Behavior, Ribeirao Preto School of Medicine, Universidade de Sao Paulo, São Paulo, Brazil.

Marc L Martel (ML)

Department of Emergency Medicine, Hennepin County Medical Center, Minneapolis, MN, USA.

David Barbic (D)

Department of Emergency Medicine, University of British Columbia, Vancouver, BC, Canada.
Centre for Health Evaluation & Outcomes Sciences, St. Paul's Hospital, Vancouver, BC, Canada.

William G Honer (WG)

Department of Psychiatry, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
BC Mental Health and Substance Use Services Research Institute, Vancouver, BC, Canada.

Wulf-Peter Hansen (WP)

BASTA-Das Bündnis für psychisch erkrankte Menschen, Munich, Germany.

Gisele Huf (G)

National Institute of Quality Control in Health, Oswaldo Cruz Foundation, Av. Brasil 4365, Manguinhos, Rio de Janeiro, Brazil.

Jacob Alexander (J)

SA Health, Adelaide, Australia.

Nirmal S Raveendran (NS)

Department of Psychiatry, Christian Medical College, Vellore, Tamil Nadu, India.

Evandro S F Coutinho (ESF)

Department of Epidemiology, Institute of Social Medicine, State University of Rio de Janeiro, Rio de Janeiro, Brazil.

Josef Priller (J)

Technical University of Munich, TUM School of Medicine and Health, Department of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Munich, Germany.
German Center for Mental Health (DZPG), Partner site München/Augsburg, Munich, Germany.
Neuropsychiatry and Laboratory of Molecular Psychiatry, Charité - Universitätsmedizin Berlin and DZNE, Berlin, Germany.
University of Edinburgh and UK DRI, Edinburgh, UK.

Clive E Adams (CE)

Institute of Mental Health, University of Nottingham, Nottingham, Nottinghamshire, UK.

Georgia Salanti (G)

Institute of Social and Preventive Medicine (ISPM), University of Bern, Bern, Switzerland.

Stefan Leucht (S)

Technical University of Munich, TUM School of Medicine and Health, Department of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Munich, Germany.
German Center for Mental Health (DZPG), Partner site München/Augsburg, Munich, Germany.

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