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Titlebook: Cystic Fibrosis Pulmonary Infections: Lessons from Around the World; Adolf Bauernfeind,Melvin I. Marks (Professor and V Book 1996 Springer

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发表于 2025-3-21 19:44:07 | 显示全部楼层 |阅读模式
书目名称Cystic Fibrosis Pulmonary Infections: Lessons from Around the World
编辑Adolf Bauernfeind,Melvin I. Marks (Professor and V
视频videohttp://file.papertrans.cn/243/242597/242597.mp4
丛书名称Respiratory Pharmacology and Pharmacotherapy
图书封面Titlebook: Cystic Fibrosis Pulmonary Infections: Lessons from Around the World;  Adolf Bauernfeind,Melvin I. Marks (Professor and V Book 1996 Springer
描述Infection of the lower respiratory tract is a major determinant of the course of cystic fibrosis. Although numerous efforts have been made to elucidate the specific mechanisms predisposing the respiratory mucosa of cystic fibrosis patients to infection, so far no clinically relevant procedures for completely effective prevention or control of infection have resulted. Hence, in dealing with infections in cystic fibrosis, we continue to rely mainly on antimicrobials. Antiinfective measures are inseparably correlated with microbiology, and the quality of antiinfec­ tive therapy directly reflects the quality of microbial monitoring. Vali­ dated guidelines for microbiologic testing and antiinfective use need to be developed and made available to all health providers and their cystic fibrosis patients. Several years ago, the editors cochaired a symposium at the Interna­ tional Congress of Chemotherapy on the Global Perspectives of Micro­ biological and Clinical Infectious Diseases in Patients with Cystic Fibrosis. During this half-day symposium, the editors heard reports from several countries around the world with an alarming range of survival for patients with cystic fibrosis. This sen
出版日期Book 1996
关键词Respiratory system; infectious disease; infectious diseases; microbiology; pediatrics
版次1
doihttps://doi.org/10.1007/978-3-0348-7359-8
isbn_softcover978-3-0348-7361-1
isbn_ebook978-3-0348-7359-8
copyrightSpringer Basel AG 1996
The information of publication is updating

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Microbial Resistanceion of multiply resistant organisms within the lungs of these patients. With seeming predictability, . becomes progressively resistant to several classes of antimicrobial agents including .-lactam antibiotics, aminoglycosides, and the fluoroquinolones [1].
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Cystic Fibrosis in Japanese population. Twenty-eight percent of the total cases presented symptoms of meconium ileus, which is a higher frequency than that seen in the Caucasian population. This might probably reflect a genetic difference between CF of Northern Europe and Japan.
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Anisotropic Behaviour of Damaged Materialster transplantation [1]. The first successful heart-lung transplants (HLT) for CF were performed in the United Kingdom in 1985 [2] and encouraging intermediate term (51/2 year experience) results have been reported [3] which compare favorably with results of HLT performed for diseases other than CF [4].
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Anion Carriers of Mitochondrial Membranesf . increases with age. Of the CF-patients with ., 73% showed elevated specific serum IgG to this fungus. No correlation was found between culture, specified IgG to . and either specific Aspergillus IgE or total serum IgE. Maintaining good pulmonary condition and reduction of exposure to . may prevent colonization and infection with this mold.
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Infinite Space, Half Space and Bi-materials,approximate annual cost of treatment in Venezuela is US$10 000 per patient, making it very difficult to provide adequate therapy to low income patients without financial assistance from public and private institutions.
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