| Literature DB >> 33328164 |
Luís Carlos Lopes-Júnior1, Emiliana Bomfim2, Karin Olson3, Eliane Tatsch Neves4, Denise Sayuri Calheiros Silveira5, Michelle Darezzo Rodrigues Nunes6, Lucila Castanheira Nascimento7, Gabriela Pereira-da-Silva7, Regina Aparecida Garcia Lima7.
Abstract
OBJECTIVE: To evaluate evidence from randomised controlled trials and non-randomised controlled trials on the effectiveness of hospital clowns for a range of symptom clusters in children and adolescents admitted to hospital with acute and chronic conditions.Entities:
Mesh:
Year: 2020 PMID: 33328164 PMCID: PMC7737653 DOI: 10.1136/bmj.m4290
Source DB: PubMed Journal: BMJ ISSN: 0959-8138
Fig 1Illustration of hospital clowns, shown on the front cover of the September 1908 issue of Parisian newspaper Le Petit Journal 25
Fig 2Flowchart of studies selected according to PRISMA (preferred reporting items for systematic reviews and meta-analyses).32 Medline=Medical Literature Analysis and Retrieval System Online (via Pubmed); APA PsycINFO=American Psychological Association Psychology Information; LILACS=Latin American and Caribbean Health Sciences Literature; CINAHL=Cumulative Index to Nursing and Allied Health Literature; CENTRAL=Cochrane Central Register of Controlled Trials; ReBEC=Brazilian Registry of Clinical Trials; SciELO=Scientific Electronic Library Online
Fig 3Internal validity and risk-of-bias assessment of included randomised controlled trials,46 47 48 51 52 53 56 57 58 60 61 62 67 according to RoB 2 (revised Cochrane risk-of-bias tool for randomised trials).23 Plus sign (+) indicates low risk of bias; minus sign (−) indicates some concerns; cross (×) indicates high risk of bias
Fig 4Percentage of risk of bias among included randomised controlled trials,46 47 48 51 52 53 56 57 58 60 61 62 67 by domains of RoB 2 (revised Cochrane risk-of-bias tool for randomised trials)23
Consensus ROBINS-I judgments between two reviewers by domain of bias
| Study | ROBINS-I* domains | Overall ROBINS-I judgment* | ||||||
|---|---|---|---|---|---|---|---|---|
| Bias due to confounding | Bias in selection of participants | Bias in measurement of interventions | Bias due to departures from intended interventions | Bias due to missing data | Bias in measurement of outcomes | Bias in selection of reports results | ||
| Meisel et al 2010 | Moderate | Moderate | Moderate | Moderate | Low | Serious | Low | Serious |
| Fernandes et al 2010 | Moderate | Moderate | Low | Low | Low | Moderate | Low | Moderate |
| Kingsnorth et al 2011 | Moderate | Moderate | Moderate | Serious | Low | Moderate | Low | Serious |
| Tener et al 2012 | Serious | Moderate | Moderate | Moderate | Low | Moderate | Low | Serious |
| Yun et al 2015 | Low | Moderate | Low | Low | Low | Low | Low | Moderate |
| Saliba et al 2016 | Moderate | Serious | Low | Low | Low | Serious | Low | Serious |
| Dionigi et al 2017 | Moderate | Moderate | Low | Low | Low | Low | Low | Moderate |
| Sánchez et al 2017 | Moderate | Moderate | Low | Low | Low | Moderate | Low | Moderate |
| Lopes-Júnior et al 2018 | Low | Low | Low | Low | Low | Low | Low | Low |
| Arriaga et al 2020 | Low | Moderate | Low | Low | Low | Low | Low | Moderate |
| Lopes-Júnior et al 2020 | Low | Moderate | Low | Low | Low | Low | Low | Moderate |
ROBINS-I=risk of bias in non-randomised studies.24
Overall judgment includes the following categories: low risk of bias (the study is comparable to a well performed randomised trial with regard to this domain (the study is judged to have a low risk of bias for all domains)); moderate risk of bias (the study is sound for a non-randomised study with regard to this domain but cannot be considered comparable to a well performed randomised trial (the study is judged to have a low or moderate risk of bias for all domains)); serious risk of bias (the study has some important problems in this domain (the study is judged to have a low or moderate risk of bias for most domains but is at serious risk of bias in at least one domain)); critical risk of bias (the study is too problematic in this domain to provide any useful evidence (the study is judged to have a critical risk of bias in at least one domain)); no information (no information on which to base a judgment about risk of bias for this domain (there is a lack of information in one or more key domains of bias for the outcome)).24