scholarly journals Health service use and costs associated with aggressiveness or agitation and containment in adult psychiatric care: a systematic review of the evidence

2015 ◽  
Vol 15 (1) ◽  
Author(s):  
Maria Rubio-Valera ◽  
Juan V Luciano ◽  
José Miguel Ortiz ◽  
Luis Salvador-Carulla ◽  
Alfredo Gracia ◽  
...  
2011 ◽  
Vol 96 (Supplement 1) ◽  
pp. A94-A95
Author(s):  
J. Woodman ◽  
M. Brandon ◽  
D. Glaser ◽  
R. Gilbert

Author(s):  
Manjula Manikandan ◽  
Claire Kerr ◽  
Grace Lavelle ◽  
Michael Walsh ◽  
Aisling Walsh ◽  
...  

The Lancet ◽  
2005 ◽  
Vol 365 (9456) ◽  
pp. 312-317 ◽  
Author(s):  
Gopalakrishnan Netuveli ◽  
Brian Hurwitz ◽  
Mark Levy ◽  
Monica Fletcher ◽  
Greta Barnes ◽  
...  

BMJ Open ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. e035892
Author(s):  
Manjula Manikandan ◽  
Aisling Walsh ◽  
Claire Kerr ◽  
Michael Walsh ◽  
Jennifer M Ryan

IntroductionCerebral palsy (CP) is a neurodisability that primarily results in motor impairments and activity limitations, but is often associated with epilepsy and disturbances of sensation, perception, cognition, behaviour and speech. Most children with CP survive well into adulthood. Adults with CP experience increased risk of age-related chronic conditions such as arthritis, stroke, cardiorespiratory and mental health conditions in addition to the ongoing disabilities experienced from childhood. Therefore, adults with CP often require extensive health services. However, health service use among adults with CP has not been well documented. This mixed method review aims to identify, appraise and synthesise quantitative and qualitative literature examining health service use among adults with CP.Methods and analysisThe mixed method systematic review will be conducted in accordance with the Joanna Briggs Institute (JBI) methodology. A systematic search of MEDLINE (Ovid), CINAHL, Embase, PsycINFO and Cochrane Library from inception to March 2020 will be conducted. Quantitative observational studies, qualitative studies and mixed method studies examining health service use among adults with CP (≥18 years) will be included. Outcomes of interest are the proportion of adults using health services frequency of use and experiences of health services from the perspectives of adults with CP, caregivers and health service providers. Two reviewers will independently screen titles, abstracts and full-texts, extract data and assess the quality of included studies using JBI instruments. Where possible a pooled analysis and aggregation of findings will be performed for quantitative and qualitative data, respectively, and Grading of Recommendations Assessment, Development and Evaluation (GRADE)/GRADE-CERQual (Confidence in Evidence from Reviews of Qualitative research) employed. Quantitative and qualitative findings will be integrated using a triangulation approach at the synthesis stage. A narrative synthesis will be carried out where this is not possible.Ethics and disseminationEthical approval is not required for this review. The findings will be disseminated through a peer-reviewed journal and conferences.PROSPERO registration numberCRD42020155 380.


The Lancet ◽  
2005 ◽  
Vol 365 (9456) ◽  
pp. 312-317 ◽  
Author(s):  
G NETUVELI ◽  
B HURWITZ ◽  
M LEVY ◽  
M FLETCHER ◽  
G BARNES ◽  
...  

PLoS ONE ◽  
2019 ◽  
Vol 14 (4) ◽  
pp. e0216029 ◽  
Author(s):  
Laura S. M. Kuula ◽  
Kati M. Viljemaa ◽  
Janne T. Backman ◽  
Marja Blom

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