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Picot J, Hartwell D, Harris P, et al. The Effectiveness of Interventions to Treat Severe Acute Malnutrition in Young Children: A Systematic Review. Southampton (UK): NIHR Journals Library; 2012 Apr. (Health Technology Assessment, No. 16.19.)

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The Effectiveness of Interventions to Treat Severe Acute Malnutrition in Young Children: A Systematic Review.

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Appendix 2The Preferred Reporting Items for Systematic Reviews and Meta-Analyses checklist

Section/topicItemChecklist itemReported on page number(s)
Title
Title1Identify the report as a systematic review, meta-analysis or bothi, iii
Abstract
Structured summary2Provide a structured summary including, as applicable: background; objectives; data sources; study eligibility criteria, participants and interventions; study appraisal and synthesis methods; results; limitations; conclusions and implications of key findings; systematic review registration numberAbstract iii–iv

Executive summary ix–xiii
Introduction
Rationale3Describe the rationale for the review in the context of what is already known1–9
Objectives4Provide an explicit statement of questions being addressed with reference to PICOS8
Methods
Protocol and registration5Indicate if a review protocol exists, if and where it can be accessed (e.g. web address), and, if available, provide registration information including registration number11, Appendix 1
Eligibility criteria6Specify study characteristics (e.g. PICOS, length of follow-up) and report characteristics (e.g. years considered, language, publication status) used as criteria for eligibility, giving rationale12–14
Information sources7Describe all information sources (e.g. databases with dates of coverage, contact with study authors to identify additional studies) in the search and date last searched11, Appendix 3
Search8Present full electronic search strategy for at least one database, including any limits used, such that it could be repeatedAppendix 3
Study selection9State the process for selecting studies (i.e. screening, eligibility, included in systematic review, and, if applicable, included in the meta-analysis)12–14
Data collection process10Describe method of data extraction from reports (e.g. piloted forms, independently, in duplicate) and any processes for obtaining and confirming data from investigators14
Data items11List and define all variables for which data were sought (e.g. PICOS, funding sources) and any assumptions and simplifications made12–14, Appendices 712
Risk of bias in individual studies12Describe methods used for assessing risk of bias of individual studies (including specification of whether this was done at the study or outcome level) and how this information is to be used in any data synthesis14, Appendix 4
Summary measures13State the principal summary measures (e.g. RR, difference in means)N/A, narrative synthesis
Synthesis of results14Describe the methods of handling data and combining results of studies, if done, including measures of consistency (e.g. I2) for each meta-analysisN/A, narrative synthesis
Risk of bias across studies15Specify any assessment of risk of bias that may affect the cumulative evidence (e.g. publication bias, selective reporting within studies)14, Appendix 4
Additional analyses16Describe methods of additional analyses (e.g. sensitivity or subgroup analyses, meta-regression), if done, indicating which were pre-specifiedN/A, narrative synthesis
Results
Study selection17Give numbers of studies screened, assessed for eligibility, and included in the review, with reasons for exclusions at each stage, ideally with a flow diagram17, 19
Study characteristics18For each study, present characteristics for which data were extracted (e.g. study size, PICOS, follow-up period) and provide the citations19–20, 20–22, 26–29, 36–39, 45–47, 50–51, 54–57, 63–67, 81–82, Appendices 712
Risk of bias within studies19Present data on risk of bias of each study and, if available, any outcome level assessment (see Item 12)23, 31, 40,48, 53, 58, 70, 83, Appendices 712
Results of individual studies20For all outcomes considered (benefits or harms), present, for each study: (1) simple summary data for each intervention group and (2) effect estimates and CIs, ideally with a forest plot20, 22–25, 30–36, 39–45, 47–50, 51–54, 59–63, 69–79, 84–87, Appendices 712
Synthesis of results21Present results of each meta-analysis done, including CIs and measures of consistencyN/A
Risk of bias across studies22Present results of any assessment of risk of bias across studies (see Item 15)23, 31, 40, 48, 53, 58, 70, 83
Additional analysis23Give results of additional analyses, if done [e.g. sensitivity or subgroup analyses, meta-regression (see Item 16)]N/A
Discussion
Summary of evidence24Summarise the main findings including the strength of evidence for each main outcome; consider their relevance to key groups (e.g. health-care providers, users and policy-makers)89–95, 99
Limitations25Discuss limitations at study and outcome level (e.g. risk of bias), and at review level (e.g. incomplete retrieval of identified research, reporting bias)95–98
Conclusions26Provide a general interpretation of the results in the context of other evidence, and implications for future research89–95, 99, 100
Funding
Funding27Describe sources of funding for the systematic review and other support (e.g. supply of data); role of funders for the systematic reviewiv

N/A, not applicable; PICOS, participants, interventions, comparisons, outcomes and study design; RR, risk ratio.

From: Moher D, Liberati A, Tetzlaff J, Altman DG, The PRISMA Group. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: the PRISMA statement. PLoS Med 2009;6(7):e1000097. doi:10.1371/journal.pmed1000097.

© 2012, Crown Copyright.

Included under terms of UK Non-commercial Government License.

Bookshelf ID: NBK98563

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