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  • 2005-2009  (3)
  • 2007  (3)
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  • 2005-2009  (3)
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  • 2007  (3)
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  • 1
    Online Resource
    Online Resource
    Wiley ; 2007
    In:  Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy Vol. 27, No. 1 ( 2007-01), p. 53-67
    In: Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, Wiley, Vol. 27, No. 1 ( 2007-01), p. 53-67
    Abstract: The echinocandins represent the newest class of antifungals to combat infections caused by Candida sp. Micafungin is an echinocandin recently approved by the United States Food and Drug Administration. It is indicated in adults for esophageal candidiasis and prophylaxis against candidal infections in hematopoietic stem cell transplant recipients. Micafungin exhibits in vitro fungicidal activity against Candida sp, including fluconazole‐resistant isolates. Its in vivo efficacy is comparable to that of fluconazole in the treatment of esophageal candidiasis and superior to that of fluconazole for prophylaxis of invasive candidal infections. Because it is not significantly metabolized by the cytochrome P450 3A system, micafungin is associated with few drug interactions. Micafungin does not require adjustment in patients with renal and/or hepatic impairment, and it has been shown to be well tolerated in both adult and pediatric patients. Its efficacy against Candida sp, coupled with its overall safety and drug interaction profiles, makes it an attractive option in the treatment against esophageal candidiasis and prophylaxis against invasive candidal infections.
    Type of Medium: Online Resource
    ISSN: 0277-0008 , 1875-9114
    Language: English
    Publisher: Wiley
    Publication Date: 2007
    detail.hit.zdb_id: 2061167-5
    SSG: 15,3
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  • 2
    Online Resource
    Online Resource
    SAGE Publications ; 2007
    In:  Annals of Pharmacotherapy Vol. 41, No. 6 ( 2007-06), p. 965-972
    In: Annals of Pharmacotherapy, SAGE Publications, Vol. 41, No. 6 ( 2007-06), p. 965-972
    Abstract: To review the literature on tigecycline, a novel antibiotic. DATA SOURCES: References were identified through MEDLINE (1966–February 2007) and International Pharmaceutical Abstracts(1970–February 2007) databases, using the key words tigecycline, glycylcycline, complicated skin and skin structure infections (cSSSI), complicated intraabdominal infections (cIAI), and in vitro. Additional articles for this review were identified by reviewing the bibliographies of articles cited. The package insert was also used as a reference. STUDY SELECTION AND DATA EXTRACTION: In vitro, clinical, and pharmacokinetic studies evaluating tigecycline's safety and efficacy were selected. DATA SYNTHESIS: A tigecycline 100 mg intravenous loading dose followed by an intravenous infusion of 50 mg every 12 hours was shown in clinical trials to be as effective as comparator antibiotics in treating cSSSI and cIAI. Tigecycline has a broad spectrum of activity that includes many resistant bacteria with few treatment options, such as methicillin-resistant Staphylococcus aureus and extended-spectrum β-lactamase—producing bacteria such as Escherichia coli and Klebsiella pneumoniae. In cSSSI studies, tigecycline was found to be noninferior to vancomycin plus aztreonam with test-of-cure rates of 86.5% and 88.6%, respectively. Tigecycline was also found to be noninferior to imipenem/ cilastatin in cIAI studies; clinical cure rates were 86.1% and 86.2%, respectively. In vitro activity has been demonstrated against other multidrug-resistant microorganisms of concern, such as Acinetobacterspp. Although it has a broad spectrum of activity, tigecycline has inadequate activity against Pseudomonasspp. Nausea and vomiting were the most frequently reported adverse effects. CONCLUSIONS: Tigecycline is approved for the treatment of cSSSI and cIAI infections. To date, little resistance to tigecycline has been reported; however, with widespread use of the drug, resistance will likely occur. Since published studies have not dealt with seriously ill patients, it is recommended that, until further studies have been completed, other agents be used in the treatment of these patients unless no option other than tigecycline exists.
    Type of Medium: Online Resource
    ISSN: 1060-0280 , 1542-6270
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2007
    detail.hit.zdb_id: 2053518-1
    SSG: 15,3
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  • 3
    In: Respiration, S. Karger AG, Vol. 74, No. 3 ( 2007), p. 329-333
    Abstract: 〈 i 〉 Background: 〈 /i 〉 A large tertiary referral hospital in inner-city Chicago. 〈 i 〉 Objectives: 〈 /i 〉 To determine whether the IS 〈 i 〉 6110 〈 /i 〉 repetitive DNA element of 〈 i 〉 Mycobacterium tuberculosis 〈 /i 〉 is detected in exhaled breath condensate of patients with newly diagnosed active pulmonary tuberculosis. 〈 i 〉 Methods: 〈 /i 〉 Ten hospitalized patients with positive Ziehl-Neelson-stained sputum smears were studied. Concurrent sputum cultures for mycobacteria were performed as well. Exhaled breath condensate was collected from each patient within 6 days of initiating antituberculosis chemotherapy (median 1.5 days). These samples were analyzed by polymerase chain reaction (PCR) using primers designed to amplify the IS 〈 i 〉 6110 〈 /i 〉 DNA fragment of 〈 i 〉 M. tuberculosis 〈 /i 〉 . Exogenous 〈 i 〉 M. tuberculosis 〈 /i 〉 DNA was added to exhaled breath condensate samples to detect PCR inhibitors. Concurrent cultures of exhaled breath condensate for mycobacteria were performed. 〈 i 〉 Results: 〈 /i 〉 〈 i 〉 M. tuberculosis 〈 /i 〉 was identified in 9 of 10 sputum cultures. One isolate was identified as 〈 i 〉 Mycobacterium kansasii 〈 /i 〉 . The IS 〈 i 〉 6110 〈 /i 〉 repetitive DNA element of 〈 i 〉 M. tuberculosis 〈 /i 〉 was not detected in any of the 10 exhaled breath condensate samples. Exogenous 〈 i 〉 M. tuberculosis 〈 /i 〉 DNA added to these samples elicited the characteristic band pattern of 〈 i 〉 M. tuberculosis 〈 /i 〉 on agarose gel electrophoresis. No PCR inhibitors were detected. Cultures of exhaled breath condensate showed no growth of mycobacteria. 〈 i 〉 Conclusions: 〈 /i 〉 The IS 〈 i 〉 6110 〈 /i 〉 repetitive DNA element of 〈 i 〉 M. tuberculosis 〈 /i 〉 is not detected in exhaled breath condensate of patients with newly diagnosed active pulmonary tuberculosis.
    Type of Medium: Online Resource
    ISSN: 0025-7931 , 1423-0356
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2007
    detail.hit.zdb_id: 1464419-8
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