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Cystic Fibrosis (CF) is a multi-system disorder, requiring not just respiratory expertise but also management of nutrition, diabetes, musculoskeletal and psychosocial issues. This pocketbook is a concise companion for all health care professionals who manage patients with CF. The book covers all aspects of care, including both paediatric and adult-specific issues, and summarizes up-to-date literature in a concise and focussed style. There is an emphasis on the practical aspects of management with separate chapters covering the effects of CF in the lung, the microbiology of pulmonary CF, and management of exacerbations. Psychosocial aspects of CF care, end of life care and lung transplantation are also covered, and potential future therapies reviewed. This second edition has been extensively updated to reflect the UK CF Trust Standards of Care, treatment guidelines and Cochrane reviews. There are updates on emerging organisms; an expanded section on physiotherapy; and a new Pharmacopeia that covers all common CF medications.
This text investigates the comprehensive clinical management of cystic fibrosis across multiple physiological systems and patient age groups. The author, a specialist in respiratory medicine, synthesizes current literature, treatment guidelines, and standards of care to provide a practical framework for healthcare professionals. The book serves as a clinical reference for navigating the complexities of CF, from pulmonary microbiology to psychosocial support and end-of-life care.
What You Will Find
Scope Limits
Medical professionals frequently cite this text as a reliable, portable reference for daily clinical practice. Experts highlight the book's adherence to updated standards of care and its utility as a concise resource for multidisciplinary teams.
Page Count:
187
Publication Date:
2015-01-01
Publisher:
OUP Oxford
ISBN-10:
0191007455
ISBN-13:
9780191007453
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