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The treatments objective is to reduce the patient's symptoms through the re-establishing of nasosinusal ventilation and draining, to control infections, eliminate the pulmonary infection reservoir and improve the patient s nutritional state. Despite the use of medications or even surgery, the patients with Cystic Fib rosis are not cured. Basically treating patients with Cystic Fibrosis means to improve the quality of life, not suf fering from recurring infections. Hence, various treatments and therapy are done cautiously to the people suffering with Cystic Fibrosis, such are the nasal treatment consists of washing with saline solution, intranasal corticosteroids antimicrobial therapy and Functional Endoscopic Sinus Surgery(FESS). Another treatment is the saline solution is aimed at liquid ifying the secretion and providing nasal hygiene. It may be used in isotonic or hypertonic imigations with the advantage of decongesting the nose The most significant Cystic fibrosis available is the antibiotics and it should prevent the bacterias such Pseudomonas, Staphylococcus, as well as the anaerobe germs. The mostly used are the aminosidine and quinolone antibiotics, despite these are not released for children by the FDA. other antibiotics used are piperacillin, ceftazidime and imipenem. Moreover, there are a lot of risks on undertaking the surgery since the patients situation isn,'t stable because of their advanced pulmonary disorder, extensive sinusal disease, anatomic changes caused by prior surgeries, coagulopathy for vitamin K deficiency, pancreatic and hepatic diseases, as well as nutritional deficiency. In spite of rigorous treatment, the recurrence is a rule and the average of free time from symptoms ranges from 1 to 4 years Despite respiratory manifestations arent the main cause of death in the Cystic Fibrosis patients; however, it does bring a significant morbidity. With the extensive research going on for decades, the life expectancy of Cystic Fibrosis patients has increased dramatically especially when the antibiotic therapy and improvement of surgical techniques was administered to the patients. As per today there is no exact cure for Cystic FibrosisThe treatments objective is to reduce the patient's symptoms through the re-establishing of nasosinusal ventilation and draining, to control infections, eliminate the pulmonary infection reservoir and improve the patient's nutritional state. Despite the use of medications or even surgery, the patients with Cystic Fib rosis are not cured. Basically treating patients with Cystic Fibrosis means to improve the quality of life, not suffering from recurring infections. Hence, various treatments and therapy are done cautiously to the people suffering with Cystic Fibrosis, such are the nasal treatment consists of washing with saline solution, intranasal corticosteroids, antimicrobial therapy and Functional Endoscopic Sinus Surgery (FESS). Another treatment is the saline solution is aimed at liquidifying the secretion and providing nasal hygiene. It may be used in isotonic or hypertonic irrigations with the advantage of decongesting the nose. The most significant Cystic fibrosis available is the antibiotics and it should prevent the bacterias such as Pseudomonas, Staphylococcus, as well as the anaerobe germs. The mostly used are the aminosidine and quinolone antibiotics, despite these are not released for children by the FDA. Other antibiotics used are piperacillin, ceftazidime and imipenem. Moreover, there are a lot of risks on undertaking the surgery since the patients situation isn’t stable because of their advanced pulmonary disorder, extensive sinusal disease, anatomic changes caused by prior surgeries, coagulopathy for vitamin K deficiency, pancreatic and hepatic diseases, as well as nutritional deficiency. In spite of rigorous treatment, the recurrence is a rule and the average of free time from symptoms ranges from 1 to 4 years. Despite respiratory manifestations aren’t the main cause of death in the Cystic Fibrosis patients; however, it does bring a significant morbidity. With the extensive research going on for decades, the life expectancy of Cystic Fibrosis patients has increased dramatically especially when the antibiotic therapy and improvement of surgical techniques was administered to the patients. As per today, there is no exact cure for Cystic Fibrosis
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