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  • 1990-1994  (3)
  • 1992  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Australasian journal of dermatology 33 (1992), S. 0 
    ISSN: 1440-0960
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: To determine the effect of bacterial colonization on venous ulcer healing, 82 patients with 100 venous ulcerated limbs were each studied prospectively for six months. Despite bacteriological swab results, topical or systemic antibiotics were not administered unless cellulitis supervened. Initial ulcer size, length of ulcer history and time to complete healing of colonized and uncolonized ulcers were determined and compared.Organisms were cultured from 83 limbs prior to commencement of treatment, the commonest isolates being Staptiytococcus aureaus (48%), mixed coliforms (28%), Pseudomonas aeruginosa (21%) and anaerobes (17%). When compared with ulcers with no bacterial growth, colonized ulcers were of longer duration (P◂0.01), had a larger initial size (p◂0.001) and had significantly longer healing time (p◂0.001). When analysed individually beta-haemolytic streptococci, anaerobes, Staptiylococcus aureus and coliforms were associated with delayed healing. Delayed healing was not found with Pseudomonas aeruginosa, although pseudomonas-colonized ulcers were significantly larger and of longer duration than uncolonized ulcers.Bacterial colonization is associated with delayed venous ulcer healing. To further clarify the pathogenicity of colonizing bacteria, however, the effect of their eradiction on healing of venous ulcers needs to be established.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-601X
    Keywords: 21.10.Dr ; 23.90.+w ; 27.40.+z
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Neutron-deficient isotopes with Z=21 to 26 have been produced as projectile-like fragments of an intense58Ni GANIL beam of 69 MeV/nucleon. The nuclei selected by the upgraded LISE3 spectrometer were identified and implanted in a silicon detector telescope. The43Cr,47Fe and46Fe isotopes were identified for the first time whereas45Fe,45Mn,44Mn and42V were not observed, indicating probable instability of these nuclei against particle emission. Measurements of the half-lives of43Cr and46Mn have been performed and the analysis of their measured beta-delayed proton spectra has given, through the isobaric multiplet mass equation, an empirical estimation of their masses. Half-lives of44Cr,43V,47Fe and46Fe have also been measured. A discussion of various mass predictions for nuclei at the proton drip-line is given.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-904X
    Keywords: anti-human immunotrophic virus (HIV) nucleosides ; drug interactions ; pharmacokinetics ; monkeys
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A pharmacokinetic evaluation of a potential drug interaction between zidovudine (AZT) and dideoxycytidine (ddC) was conducted in monkeys. Each of six animals received 20 mg/kg of AZT intragastrically in the absence and presence of an intravenous steady-state dosage regimen of ddC. The regimen was designed to produce steady-state ddC plasma concentration of 1.77 µg/ml for 30 min. Plasma and urine samples were analyzed for AZT, its major glucuronide metabolite, GAZT, and ddC by HPLC techniques. Pharmacokinetic parameters for AZT and GAZT were calculated by non-compartmental methods. The mean apparent clearance of AZT was 1.40 and 1.78 L/hr/kg in the absence and presence of ddC, respectively. The mean AUC for GAZT was 36.39 µg-hr/ml in the absence of ddC and 28.81 µg-hr/ml in the presence of ddC. No statistical differences were found in these and other pharmacokinetic parameters in the absence and presence of ddC. The absence of an effect on AZT's pharmacokinetics by ddC is attributed to the primary metabolic and renal elimination pathways for AZT and ddC, respectively. The results of this study provide a rational basis to design combined AZT-ddC treatment regimens in AIDS patients.
    Type of Medium: Electronic Resource
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