Avoidant Restrictive Food Intake Disorder in Childhood and Adolescence : A Clinical Guide

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Avoidant Restrictive Food Intake Disorder in Childhood and Adolescence : A Clinical Guide

  • 言語:ENG
  • ISBN:9780367224387
  • eISBN:9781000032819

ファイル: /

Description

Avoidant Restrictive Food Intake Disorder, more commonly known as ARFID, is a relatively newly introduced diagnostic category. Research in the field, although growing, remains limited, with clinical knowledge and expertise varying across clinicians. There may be uncertainty how to correctly identify and diagnose the disorder as well as how best to direct treatment.

This clinical guide sets out to be a trailblazer in the field, providing up-to-date information and comprehensive clinical guidance on ARFID in childhood and adolescence. Chapters in the book are divided into five sections, the first focussing on the importance of attending to the perspectives of those directly affected by ARFID. Three subsequent sections cover diagnosis and presentation, including chapters on aetiology, epidemiology, assessment, and outcome measures; clinical assessment, including psychological, family, nutritional, medical, and sensory components; and management, discussing nutritional, medical, psychological, and wider system approaches. The final section discusses prognosis and outcomes, and considers future research directions.

This clinically focussed book, with contributions from a multi-disciplinary authorship, is intended to function as an accessible, practical guide, and reference resource. It includes summaries of available evidence, with related recommendations for clinical practice. The advice and suggestions included will assist clinicians in targeting their attention appropriately, to ensure that children, adolescents, and their families receive the best possible care.

Table of Contents

List of Illustrations

Contributors

Preface

Acknowledgements

PART 1

Perspectives

  1. Young people’s perspectives – LOUISE BRADBURY
  2. Parent and carer views and experiences – SARA MILNE
  3. Information from qualitative research – LUCY COOKE
  4. PART II

    Diagnosis and presentation

  5. Overview of diagnosis and presentation – RACHEL BRYANT-WAUGH
  6. Aetiology and epidemiology – NADIA MICALI AND CHRISTINE E. COOPER-VINCE
  7. Baseline and outcome measures – LUCY COOKE
  8. PART III

    Assessment

  9. Psychological assessment of child and family – CLAIRE HIGGINS AND PRABSHNY PILLAY
  10. Nutritional and feeding assessment – SARAH CAWTHERLEY AND ELEANOR CONWAY
  11. Physical assessment – LEE HUDSON AND EMMA PARISH
  12. Assessment of sensory processing – HEATHER SCOTT AND KAREN RAY
  13. PART IV

    Management

  14. Overview of treatment and management – RACHEL BRYANT-WAUGH
  15. Nutritional management and tube weaning – SARAH CAWTHERLEY, CLAIRE HIGGINS AND ÚNA MCCRANN
  16. Medical management – LEE HUDSON
  17. Individual interventions –AMY SIDDALL, LOUISE BRADBURY AND SARA MILNE
  18. Parent/carer and family interventions –PRABASHNY PILLAY AND CLAIRE HIGGINS
  19. Group interventions – CATHERINE FROGLEY AND KAREN TAYLOR
  20. Working with schools, nurseries and other agencies– AMY SIDDALL
  21. PART V

    Progress and future directions

  22. Prognosis and outcome – ELAINE CHUNG
  23. Future research directions – RACHEL BRYANT-WAUGH

Appendix - What Matters to Me?

Glossary

Subject Index

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