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Cystic fibrosis (also known as CF or mucoviscidosis) is an autosomal recessive genetic disorder affecting most critically the lungs, and also the pancreas, liver, and intestine.
The standard precautions synthesize the major features of universal precautions (designed to reduce the risk of transmission of bloodborne pathogens) and body substance isolation (designed to reduce the risk of pathogens from moist body substances) and apply them to all patients receiving care in hospitals regardless of their diagnosis or ...
Dorothy Hansine Andersen (May 15, 1901 – March 3, 1963) was the American physician and researcher who first identified and named cystic fibrosis.During her almost thirty year tenure at Babies Hospital of Columbia-Presbyterian Medical Center (now Morgan Stanley Children's Hospital), Andersen not only identified CF and its inheritance through a recessive gene, she was also at the forefront of ...
Judah, a 14-year-old boy who was diagnosed with cystic fibrosis at just two weeks old has spent his life in and out of the hospital undergoing daily treatments, regular doctor appointments and ...
It is frequently associated with cystic fibrosis and hospital-acquired infections. [14] Salmonella is a genus of bacteria, known to cause gastrointestinal infections. [15] Staphylococcus aureus is a bacterium known to cause skin infections and sepsis, among other pathologies. Notably, S. aureus has evolved several drug-resistant strains ...
The hospital is described to be the "leading cardiothoracic hospital in Australia", and is the hub for specialised services including heart and lung transplants, adult cystic fibrosis, adult congenital heart disease and complex cardiac care. [2]
It was first isolated in patients with cystic fibrosis (CF) in 1977, when it was known as Pseudomonas cepacia. [21] In the 1980s, outbreaks of B. cepacia in individuals with CF were associated with a 35% death rate. B. cepacia has a large genome, containing twice the amount of genetic material as E. coli. [citation needed]
The Cystic Fibrosis Foundation, a non-profit organization dedicated to improving healthcare for people with cystic fibrosis, provided $150 million of the funding for the development for ivacaftor in exchange for royalty rights in the event that the medication was successfully developed and commercialized.
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