Cystic Fibrosis

Cystic Fibrosis PDF

Author: David M. Orenstein

Publisher: Lippincott Williams & Wilkins

Published: 2012-03-28

Total Pages: 788

ISBN-13: 1451154380

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This one-of-a-kind guide offers easy-to-understand explanations, advice, and management options for patients or parents of patients with cystic fibrosis. The book explains the disease process, outlines the fundamentals of diagnosing and screening, and addresses the challenges of treatment for those living with CF. As one reviewer said, this book “is the only complete answer book for everyone living with the disease. It is an indispensable resource for families of children with CF, adolescent and adult patients, and physicians, nurses, respiratory therapists, and social workers involved in the care of CF patients.”

Cystic Fibrosis

Cystic Fibrosis PDF

Author: Daniel Markovich

Publisher:

Published: 2008-11

Total Pages: 0

ISBN-13: 9780981469522

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A guide to cystic fibrosis for patients and their families that provides information on the genetic cause of the disorder; its effects on the respiratory, gastrointestinal, and reproductive systems; unusual manifestation; issues of respiratory therapy, eating, and nutrition; lung transplantation; and gene therapy.

Cystic Fibrosis

Cystic Fibrosis PDF

Author: David M. Orenstein

Publisher: Lippincott Williams & Wilkins

Published: 2004

Total Pages: 504

ISBN-13: 9780781741521

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Explains the how and why behind the disease process, outlines the fundamentals of diagnosis and screening, and addresses the challenges of treatment for those living with CF.

Handbook of Cystic Fibrosis

Handbook of Cystic Fibrosis PDF

Author: Amy G. Filbrun

Publisher: Springer

Published: 2016-10-06

Total Pages: 99

ISBN-13: 3319325043

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This concise manual provides clinicians and other related health care professionals with an essential reference tool to the background of cystic fibrosis, and the management and treatment of this disease. The latest guidelines are reviewed and current and emerging treatments are discussed in the latter chapters. Cystic fibrosis is an inherited condition where a mutation in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) causes loss of function. The dysfunction of CFTR results in the production of thick mucus in the lungs and digestive tract, causing pulmonary and gastrointestinal manifestations. The incidence of cystic fibrosis in Europe and the US ranges between 1 in 2,000 and 1 in 25,000.

Understanding Cystic Fibrosis

Understanding Cystic Fibrosis PDF

Author: Karen Hopkin

Publisher: Univ. Press of Mississippi

Published: 2010-02-11

Total Pages: 144

ISBN-13: 1604739525

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Cystic Fibrosis (CF) is the most common genetic disorder in the white population. Since the discovery of the CF gene in 1989, scientists have learned a great deal about the biology of this disease, which strikes one child in every 3.300 births. With the gene pinpointed, scientists are now working on ways to replace it and are developing better tests for early diagnosis. Understanding Cystic Fibrosis charts the progress that has been made in identifying the mutations that cause CF and in understanding how these genetic errors cause a disease whose symptoms can range from mild respiratory distress to life-threatening lung infections. This book features a review of current available treatments; research that can lead to therapies and perhaps a cure; advice and resources for families and patients; how to work best with health-care providers and HMOs; the history and diagnosis of CF; who gets CF and why; how CF affects the lungs, intestines, and other organs; and a list of organizations, support groups, and resources.

Cystic Fibrosis in Primary Care

Cystic Fibrosis in Primary Care PDF

Author: Douglas Lewis, MD, FAAFP

Publisher: Springer Nature

Published: 2020-01-28

Total Pages: 184

ISBN-13: 3030259099

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Cystic fibrosis is a disease that affects the entire body. It tends to be thought of as primarily a pulmonary disease since pulmonary decline is the main factor in early mortality. Because of the multi-system nature of the disease, a better understanding of cystic fibrosis expands the family physician's understanding of subjects ranging from genetics to pulmonary function to nutrition to colon transport to hydration to electrolyte management. The primary care philosophy is unique in that it always considers how a narrow problem can affect an individual globally. Cystic Fibrosis care can often feel fractured to patients as they are sent to multiple specialists to deal with problems outside of the comfort level of a prior or current specialist. With a broad medical philosophy, care is more inclusive as clinicians can manage topics such as diabetes and preventive care without multiple referrals and additional appointments. Family physicians are well-positioned and well-qualified to competently meet many of the care needs of those with cystic fibrosis. This book is edited by a family medicine physician who has specialist level experience with the disease. It opens with a background on cystic fibrosis foundations and centers to familiarize the reader. The next chapter gives a basic overview of the disease. Each of the subsequent chapters provide a comprehensive look at how cystic fibrosis affects other areas of the body that the primary care physician should be familiar with. Major components of cystic fibrosis such as physiology, spirometry, inflammation, airway clearance, chronic infection, cystic fibrosis related diabetes and pancreatic insufficiency, among others, are thoroughly explained. Written by experts in the field, Cystic Fibrosis in Primary Care appeals to all family physicians as well as specialists, residents, medical students physician assistants and nurse practitioners alike.

Cystic Fibrosis

Cystic Fibrosis PDF

Author: David M. Orenstein

Publisher:

Published: 2000

Total Pages: 406

ISBN-13:

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ritten by well-known experts in the clinical management of cystic fibrosis, this practical book is a complete guide to caring for the patient with cystic fibrosis. The authors offer pragmatic advice on every problem arising during the course of the disease--from treatment of symptoms to referral for lung and liver transplants. This volume is an essential reference for any health care provider treating persons with CF, including pediatricians, pulmonologists, internists, residents, nurses, respiratory therapists, and nutritionists