By Andrew Bush, Diana Bilton, Margaret Hodson
Hodson and Geddes' Cystic Fibrosis presents every thing the breathing clinician, pulmonologist or doctor treating sufferers wishes in one potential quantity. This foreign and authoritative paintings brings jointly present wisdom and has turn into confirmed in prior variants as a number one reference within the box. This fourth version contains a wealth of latest details, figures, worthwhile video clips, and a better half e-book.
The uncomplicated technological know-how that underlies the disorder and its development is printed intimately and positioned right into a scientific context. Diagnostic and scientific elements are lined extensive, in addition to promising advances akin to gene treatments and different novel molecular established remedies. sufferer tracking and the significance of multidisciplinary care also are emphasized.
Throughout, the emphasis is on delivering an updated and balanced overview of either the medical and easy technological know-how elements of the topic and reflecting the multidisciplinary nature of the cystic fibrosis care group.
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Extra resources for Hodson and Geddes' cystic fibrosis
Aureus and P. aeruginosa to any potential pathogen in the CF lung and the interactions between microorganisms, which may be adverse, beneficial, or neutral. 85–87 CYSTIC FIBROSIS REGISTRIES BECOME EVEN MORE IMPORTANT TOOLS As patients with CF become older, many CF-specific complications emerge or their prevalence is better appreciated. 88–91 Not only as outcome parameters in clinical trials, but, also in the clinic more attention went to patient well-being, especially in adults. 94 PARTNERING MOVED THE CYSTIC FIBROSIS FIELD FORWARD More than before, academic groups joined forces.
Arch Pediatr Adolesc Med 2011; 165: 847–56. Rosenfeld M. An overview of endpoints for cystic fibrosis clinical trials: One size does not fit all. Proc Am Thorac Soc 2007; 4: 299–301. Que C, Cullinan P, Geddes D. Improving rate of decline of FEV1 in young adults with cystic fibrosis. Thorax 2006; 61: 155–7. Liou TG, Elkin EP, Pasta DJ, Jacobs JR et al. Year-toyear changes in lung function in individuals with cystic fibrosis. J Cyst Fibros 2010; 9: 250–6. Tiddens HA, de Jong PA. Imaging and clinical trials in cystic fibrosis.
MEDIAN AGE AT DEATH Median age at death is a simple description of the ages of all patients who have died of CF. The calculation only uses data from those patients who have died and is not influenced by the current ages of those patients still living. As such, it is generally lower than the median survival (described in the section “Current Survival”) as survivors are not included. It is dependent on the completeness of the data available, and in patient registries the issue of completeness relates to how well the registry captures the full patient population and therefore all deaths in that population.
Hodson and Geddes' cystic fibrosis by Andrew Bush, Diana Bilton, Margaret Hodson