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  • Book
    Anna Padoa, Talli Y. Rosenbaum, editors.
    Contents:
    Definitions and Basic Etiology of the Overactive Pelvic Floor
    Overactive Pelvic Floor: Female Sexual Functioning
    The Pelvic Floor and Male Sexual Function
    Female Genital Pain and Penetration Disorders
    Bladder Pain Syndromes/Interstitial Cystitis and the Overactive Pelvic Floor
    Chronic Pelvic Pain Syndromes in Males
    Musculoskeletal Conditions Related to Pelvic Floor Muscle Overactivity
    Female Voiding Dysfunction
    Overactive Pelvic Floor: Gastrointestinal Morbidities
    Subjective Assessment
    Objective Assessment of the Overactive Pelvic Floor
    Electromyography
    Female pelvic floor imaging with emphasis on the overactive pelvic floor
    Urodynamic assessment
    Medical Therapies for the Treatment of Overactive Pelvic Floor
    Treatment Only: A Classical Physical Therapy Approach to an Overactive Pelvic Floor
    An Alternative Physical Therapy Approach to the Overactive Pelvic Floor
    A Tale of Two Pain States- The Integrative Physical Therapy Approach to the Overactive Pelvic Floor
    Complementary and Alternative Therapies for the Overactive Pelvic Floor
    Psychosocial Management.
    Digital Access Springer 2016
  • Article
    Goodwin CS, Hill JP.
    Antimicrob Agents Chemother. 1977 Jan;11(1):26-30.
    Cefoxitin, cefuroxime, and cephalothin were added to dense populations of beta-lactamase-producing enterobacteria, and the subsequent turbidity changes were monitored continuously. Viable counts and antibiotic assays were made at intervals after the addition of antibiotic, and the morphological appearances of the organisms were observed. Cephalothin caused lysis of most of the organisms tested, but even at high concentrations, after a few hours the antibiotic was destroyed and the organisms recommenced logarithmic growth. Cefoxitin produced lysis of all the strains of Escherichia coli and Klebsiella species tested, with supression of regrowth. With cephalothin and cefoxitin the viable counts after the addition of antibiotic correlated with the turbidity measurements. Cefuroxime infrequently caused lysis that suppressed multiplication, and the organisms became long and filamentous while the turbidity readings increased; the viable counts did not correlate with the turbidity measurements. Cefuroxime and cefoxitin were not destroyed by the beta-lactamases of any of the strains of enterobacteria that were studied.
    Digital Access Access Options