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      Associations between gender and health‐related quality of life in people with IgE‐mediated food allergy and their caregivers: A systematic review

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          Abstract

          Objective

          Understanding factors that impact health‐related quality of life (HRQL) is essential to inform personalised food allergy management. However, there are inconsistencies about the impact of gender on HRQL in food allergy. This review aimed to collate all investigations of the association between gender and total or subdomain HRQL scores of individuals with food allergy and their caregivers.

          Design

          This is a narrative systematic review. We descriptively synthesised and compared HRQL outcomes by participant and parent genders according to statistical and clinical significance. Study quality was assessed using the ROBINS‐I, inclusive of all domains. Sensitivity analysis of non‐interventional studies was conducted using the ROBINS‐E.

          Data Sources

          A systematic search of Medline and Embase databases was conducted on 4 April 2022 and updated on 5 December 2023.

          Eligibility Criteria

          Studies were eligible for inclusion if they reported original data on the association between any sex and/or gender and HRQL, as measured with any validated instrument, in populations with IgE‐mediated food allergy. Interventional and non‐interventional studies were eligible.

          Results

          A comparison of 34 eligible studies (10 interventional and 24 non‐interventional) indicated females with food allergy (62.5% of studies of children, 83.3% of studies of adults) and mothers of children with food allergy (50% of studies of caregivers) experienced poorer self‐reported baseline HRQL than their counterparts, notably in domains of physical, emotional or food anxiety‐related well‐being. Gender differences in child HRQL after food allergen immunotherapy were observed. However, selective reporting in included interventional studies meant the direction of this association could not be determined. The proxy‐reported total HRQL of participants was not affected by caregiver gender, nor was caregiver HRQL likely impacted by child gender.

          Conclusions

          Gender should be considered an important modifier of participant HRQL outcomes in food allergy studies. Purposeful exploration of HRQL in all genders is needed to fully understand the implications of this construct on the lived experience of food allergy.

          Systematic Review Registration

          PROSPERO (CRD42022329901).

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          Most cited references81

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          The PRISMA 2020 statement: an updated guideline for reporting systematic reviews

          The Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) statement, published in 2009, was designed to help systematic reviewers transparently report why the review was done, what the authors did, and what they found. Over the past decade, advances in systematic review methodology and terminology have necessitated an update to the guideline. The PRISMA 2020 statement replaces the 2009 statement and includes new reporting guidance that reflects advances in methods to identify, select, appraise, and synthesise studies. The structure and presentation of the items have been modified to facilitate implementation. In this article, we present the PRISMA 2020 27-item checklist, an expanded checklist that details reporting recommendations for each item, the PRISMA 2020 abstract checklist, and the revised flow diagrams for original and updated reviews.
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            ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions

            Non-randomised studies of the effects of interventions are critical to many areas of healthcare evaluation, but their results may be biased. It is therefore important to understand and appraise their strengths and weaknesses. We developed ROBINS-I (“Risk Of Bias In Non-randomised Studies - of Interventions”), a new tool for evaluating risk of bias in estimates of the comparative effectiveness (harm or benefit) of interventions from studies that did not use randomisation to allocate units (individuals or clusters of individuals) to comparison groups. The tool will be particularly useful to those undertaking systematic reviews that include non-randomised studies.
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              Methodological quality (risk of bias) assessment tools for primary and secondary medical studies: what are they and which is better?

              Methodological quality (risk of bias) assessment is an important step before study initiation usage. Therefore, accurately judging study type is the first priority, and the choosing proper tool is also important. In this review, we introduced methodological quality assessment tools for randomized controlled trial (including individual and cluster), animal study, non-randomized interventional studies (including follow-up study, controlled before-and-after study, before-after/ pre-post study, uncontrolled longitudinal study, interrupted time series study), cohort study, case-control study, cross-sectional study (including analytical and descriptive), observational case series and case reports, comparative effectiveness research, diagnostic study, health economic evaluation, prediction study (including predictor finding study, prediction model impact study, prognostic prediction model study), qualitative study, outcome measurement instruments (including patient - reported outcome measure development, content validity, structural validity, internal consistency, cross-cultural validity/ measurement invariance, reliability, measurement error, criterion validity, hypotheses testing for construct validity, and responsiveness), systematic review and meta-analysis, and clinical practice guideline. The readers of our review can distinguish the types of medical studies and choose appropriate tools. In one word, comprehensively mastering relevant knowledge and implementing more practices are basic requirements for correctly assessing the methodological quality.
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                Author and article information

                Contributors
                Journal
                Clinical & Experimental Allergy
                Clin Experimental Allergy
                Wiley
                0954-7894
                1365-2222
                February 07 2024
                Affiliations
                [1 ] Allergy Immunology Murdoch Children's Research Institute Parkville Victoria Australia
                [2 ] School of Population and Global Health University of Melbourne Parkville Victoria Australia
                [3 ] Department of Paediatrics University of Melbourne Parkville Victoria Australia
                [4 ] National Allergy Centre of Excellence (NACE) Parkville Victoria Australia
                [5 ] Centre for Medicine Use and Safety Monash University Parkville Victoria Australia
                [6 ] Department of Allergy and Immunology The Royal Children's Hospital Parkville Victoria Australia
                [7 ] Monash Children's Hospital Monash Health Clayton Victoria Australia
                Article
                10.1111/cea.14450
                38321912
                790e24db-4bc3-4424-b82e-16f9f5b18fa9
                © 2024

                http://creativecommons.org/licenses/by/4.0/

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