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      Risk factors in early life for developmental coordination disorder: a scoping review

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          Abstract

          Aim

          To perform a scoping literature review of associations between risk factors in early life and developmental coordination disorder (DCD).

          Method

          PubMed, Embase, CINAHL, PsycINFO, and Web of Science (January 1994–March 2019) were searched to identify studies on early risk factors and motor impairment or DCD. The effect of single and multiple risk factors was assessed. Level of evidence was evaluated following the Centre for Evidence‐Based Medicine guidelines. Meta‐analysis on the effect of preterm birth was performed.

          Results

          Thirty‐six studies fulfilled inclusion criteria; 35 had evidence level 3, one had level 4. Highest evidence was available that preterm birth and male sex in term‐born children were associated with DCD. The odds ratio of preterm birth was 2.02 (95% confidence interval: 1.43–2.85). Low to moderate evidence was available that parental subfertility, maternal smoking during pregnancy, postnatal corticosteroid treatment in infants born preterm, extra corporeal membrane oxygenation, retinopathy of prematurity, abnormalities on magnetic resonance imaging scans at term age, and accumulating perinatal or neonatal risk factors were associated with motor impairment.

          Interpretation

          Limited information on early risk factors of DCD is available. Only preterm birth and male sex were consistently associated with an increased risk of DCD.

          What this paper adds

          • Preterm birth is a risk factor for developmental coordination disorder (DCD).

          • In term‐born children, male sex was consistently associated with DCD.

          • Risk factors for DCD are similar to risk factors for cerebral palsy.

          What this paper adds

          • Preterm birth is a risk factor for developmental coordination disorder (DCD).

          • In term‐born children, male sex was consistently associated with DCD.

          • Risk factors for DCD are similar to risk factors for cerebral palsy.

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          Most cited references79

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          PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation

          Scoping reviews, a type of knowledge synthesis, follow a systematic approach to map evidence on a topic and identify main concepts, theories, sources, and knowledge gaps. Although more scoping reviews are being done, their methodological and reporting quality need improvement. This document presents the PRISMA-ScR (Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews) checklist and explanation. The checklist was developed by a 24-member expert panel and 2 research leads following published guidance from the EQUATOR (Enhancing the QUAlity and Transparency Of health Research) Network. The final checklist contains 20 essential reporting items and 2 optional items. The authors provide a rationale and an example of good reporting for each item. The intent of the PRISMA-ScR is to help readers (including researchers, publishers, commissioners, policymakers, health care providers, guideline developers, and patients or consumers) develop a greater understanding of relevant terminology, core concepts, and key items to report for scoping reviews.
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            Scoping studies: towards a methodological framework

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              Guidance for conducting systematic scoping reviews.

              Reviews of primary research are becoming more common as evidence-based practice gains recognition as the benchmark for care, and the number of, and access to, primary research sources has grown. One of the newer review types is the 'scoping review'. In general, scoping reviews are commonly used for 'reconnaissance' - to clarify working definitions and conceptual boundaries of a topic or field. Scoping reviews are therefore particularly useful when a body of literature has not yet been comprehensively reviewed, or exhibits a complex or heterogeneous nature not amenable to a more precise systematic review of the evidence. While scoping reviews may be conducted to determine the value and probable scope of a full systematic review, they may also be undertaken as exercises in and of themselves to summarize and disseminate research findings, to identify research gaps, and to make recommendations for the future research. This article briefly introduces the reader to scoping reviews, how they are different to systematic reviews, and why they might be conducted. The methodology and guidance for the conduct of systematic scoping reviews outlined below was developed by members of the Joanna Briggs Institute and members of five Joanna Briggs Collaborating Centres.

                Author and article information

                Contributors
                m.hadders-algra@umcg.nl
                Journal
                Dev Med Child Neurol
                Dev Med Child Neurol
                10.1111/(ISSN)1469-8749
                DMCN
                Developmental Medicine and Child Neurology
                John Wiley and Sons Inc. (Hoboken )
                0012-1622
                1469-8749
                20 December 2020
                May 2021
                : 63
                : 5 ( doiID: 10.1111/dmcn.v63.5 )
                : 511-519
                Affiliations
                [ 1 ] University of Groningen University Medical Center Groningen Department of Rehabilitation Medicine Groningen the Netherlands
                [ 2 ] University of Groningen University Medical Center Groningen Center for Human Movement Sciences Groningen the Netherlands
                [ 3 ] University of Groningen University Medical Center Groningen Center for Rehabilitation Groningen the Netherlands
                [ 4 ] University of Groningen University Medical Center Groningen Department of Paediatrics – Developmental Neurology Groningen the Netherlands
                Author notes
                [*] [* ] Correspondence to Mijna Hadders‐Algra, Department of Paediatrics – Developmental Neurology, University Medical Center Groningen, Hanzeplein 1, Groningen 9713 GZ, the Netherlands. E‐mail: m.hadders-algra@ 123456umcg.nl

                Author information
                https://orcid.org/0000-0001-6845-5114
                Article
                DMCN14781
                10.1111/dmcn.14781
                8048603
                33345317
                04b0fd64-1d5c-4713-8429-c1a84f567d50
                © 2020 The Authors. Developmental Medicine & Child Neurology published by John Wiley & Sons Ltd on behalf of Mac Keith Press

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 17 November 2020
                Page count
                Figures: 0, Tables: 0, Pages: 9, Words: 8478
                Categories
                Scoping Review
                Reviews
                Custom metadata
                2.0
                May 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.2 mode:remove_FC converted:15.04.2021

                Neurology
                Neurology

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