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1.
Clin Infect Dis ; 33(3): 338-43, 2001 Aug 01.
Article in English | MEDLINE | ID: mdl-11438899

ABSTRACT

The incidence of anaerobic bloodstream infections (BSI) in patients who underwent bone marrow transplantation (BMT) recently increased at our institution. A retrospective case-control study of patients undergoing BMT from January 1995 through December 1998 was performed to determine the microbiological characteristics, epidemiology, and outcome of anaerobic BSI and to identify independent risk factors for infection. Anaerobic BSI occurred in 23 patients, for a rate of 4 BSIs per 100 BMT procedures, and it accounted for 17% of all BSIs that occurred during the study period. Infection occurred at a mean (+/- standard deviation) of 7+/-4 days after BMT and 7+/-5 days after the onset of neutropenia. Fusobacterium nucleatum was the most frequently isolated pathogen (in 17 patients), followed by Leptotrichia buccalis (in 4), Clostridium septicum (in 1), and Clostridium tertium (in 1). Two case patients (9%) died. Severity of mucositis was an independent predictor of anaerobic BSI (odds ratio, 4.4; P=.01). Controlling mucositis is critical for the prevention of anaerobic BSI in this patient population.


Subject(s)
Bacteremia/etiology , Bacteria, Anaerobic , Bone Marrow Transplantation/adverse effects , Adult , Agranulocytosis/complications , Case-Control Studies , Female , Humans , Immunocompromised Host , Logistic Models , Male , Mucous Membrane/immunology , Retrospective Studies , Risk Factors
2.
JAMA ; 271(24): 1913-8, 1994.
Article in English | MEDLINE | ID: mdl-8201735

ABSTRACT

OBJECTIVE--To determine the safety and efficacy of a new combination treatment for patients with Clostridium difficile-associated disease (CDD). The treatment combines the yeast Saccharomyces boulardii with an antibiotic (vancomycin hydrochloride or metronidazole). DESIGN--A double-blind, randomized, placebo-controlled, parallel-group intervention study in patients with active CDD. Patients received standard antibiotics and S boulardii or placebo for 4 weeks, and were followed up for an additional 4 weeks after therapy. Effectiveness was determined by comparing the recurrence of CDD in the two groups using multivariate analysis to control for other risk factors for CDD. SETTING--National referral study of ambulatory or hospitalized patients from three main study coordinating centers. PATIENTS--A total of 124 eligible consenting adult patients, including 64 who were enrolled with an initial episode of CDD, and 60 who had a history of at least one prior CDD episode. Patients who were immunosuppressed due to acquired immunodeficiency syndrome or cancer chemotherapy within 3 months were not eligible. INTERVENTION--Treatment with oral S boulardii (1 g/d for 4 weeks) or placebo in combination with a standard antibiotic. MAIN OUTCOME MEASURE--Recurrence of active CDD. RESULTS--A history of CDD episodes dramatically increased the likelihood of further recurrences. Multivariate analysis revealed that patients treated with S boulardii and standard antibiotics had a significantly lower relative risk (RR) of CDD recurrence (RR, 0.43; 95% confidence interval, 0.20 to 0.97) compared with placebo and standard antibiotics. The efficacy of S boulardii was significant (recurrence rate 34.6%, compared with 64.7% on placebo; P = .04) in patients with recurrent CDD, but not in patients with initial CDD (recurrence rate 19.3% compared with 24.2% on placebo; P = .86). There were no serious adverse reactions associated with S boulardii. CONCLUSIONS--The combination of standard antibiotics and S boulardii was shown to be an effective and safe therapy for these patients with recurrent CDD; no benefit of S boulardii was demonstrated for those with an initial episode of CDD.


Subject(s)
Enterocolitis, Pseudomembranous/drug therapy , Metronidazole/therapeutic use , Vancomycin/therapeutic use , Yeast, Dried/therapeutic use , Adult , Aged , Clostridioides difficile , Double-Blind Method , Drug Therapy, Combination , Female , Humans , Male , Middle Aged , Recurrence
3.
J Am Med Rec Assoc ; 58(7): 18-20, 1987 Jul.
Article in English | MEDLINE | ID: mdl-10282653

ABSTRACT

This article describes the process of obtaining funds from a foundation in order to purchase capital equipment and is based on the authors' experience in obtaining grant support for a medical record department at a 503-bed not-for-profit hospital in Chicago, IL. The steps involved in obtaining philanthropic support and delineation of the participating roles of the medical record manager and development officer are discussed.


Subject(s)
Capital Expenditures/methods , Economics/methods , Financial Management/methods , Fund Raising/methods , Hospital Departments/economics , Medical Records Department, Hospital/economics , Chicago , Foundations , Hospital Bed Capacity, 500 and over , Role , Time Factors
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