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      Systematic Review of Antimicrobial Drug Prescribing in Hospitals

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          Abstract

          Standardizing methods and reporting could improve interventions that reduce Clostridium difficile–associated diarrhea and antimicrobial drug resistance.

          Abstract

          Prudent prescribing of antimicrobial drugs to hospital inpatients may reduce incidences of antimicrobial drug resistance and healthcare-associated infection. We reviewed the literature from January 1980 to November 2003 to identify rigorous evaluations of interventions to improve hospital prescribing of antimicrobial drugs. We identified 66 studies with interpretable data, of which 16 reported 20 microbiologic outcomes: gram-negative resistant bacteria, 10 studies; Clostridium difficile–associated diarrhea, 5 studies; vancomycin-resistant enterococci, 3 studies; and methicillin-resistant Staphylococcus aureus, 2 studies. Four studies provided strong evidence that the intervention changed microbial outcomes with low risk for alternative explanations, 8 studies provided less convincing evidence, and 4 studies provided no evidence. The strongest and most consistent evidence was for C. difficile–associated diahrrea, but we were able to analyze only the immediate impact of interventions because of nonstandardized durations of follow-up. The ability to compare results of studies could be substantially improved by standardizing methods and reporting.

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          Most cited references18

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          Interrupted time series designs in health technology assessment: lessons from two systematic reviews of behavior change strategies.

          In an interrupted time series (ITS) design, data are collected at multiple instances over time before and after an intervention to detect whether the intervention has an effect significantly greater than the underlying secular trend. We critically reviewed the methodological quality of ITS designs using studies included in two systematic reviews (a review of mass media interventions and a review of guideline dissemination and implementation strategies). Quality criteria were developed, and data were abstracted from each study. If the primary study analyzed the ITS design inappropriately, we reanalyzed the results by using time series regression. Twenty mass media studies and thirty-eight guideline studies were included. A total of 66% of ITS studies did not rule out the threat that another event could have occurred at the point of intervention. Thirty-three studies were reanalyzed, of which eight had significant preintervention trends. All of the studies were considered "effective" in the original report, but approximately half of the reanalyzed studies showed no statistically significant differences. We demonstrated that ITS designs are often analyzed inappropriately, underpowered, and poorly reported in implementation research. We have illustrated a framework for appraising ITS designs, and more widespread adoption of this framework would strengthen reviews that use ITS designs.
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            Compensatory mutations, antibiotic resistance and the population genetics of adaptive evolution in bacteria.

            In the absence of the selecting drugs, chromosomal mutations for resistance to antibiotics and other chemotheraputic agents commonly engender a cost in the fitness of microorganisms. Recent in vivo and in vitro experimental studies of the adaptation to these "costs of resistance" in Escherichia coli, HIV, and Salmonella typhimurium found that evolution in the absence of these drugs commonly results in the ascent of mutations that ameliorate these costs, rather than higher-fitness, drug-sensitive revertants. To ascertain the conditions under which this compensatory evolution, rather than reversion, will occur, we did computer simulations, in vitro experiments, and DNA sequencing studies with low-fitness rpsL (streptomycin-resistant) mutants of E. coli with and without mutations that compensate for the fitness costs of these ribosomal protein mutations. The results of our investigation support the hypothesis that in these experiments, the ascent of intermediate-fitness compensatory mutants, rather than high-fitness revertants, can be attributed to higher rates of compensatory mutations relative to that of reversion and to the numerical bottlenecks associated with serial passage. We argue that these bottlenecks are intrinsic to the population dynamics of parasitic and commensal microbes and discuss the implications of these results to the problem of drug resistance and adaptive evolution in parasitic and commmensal microorganisms in general.
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              Society for Healthcare Epidemiology of America and Infectious Diseases Society of America Joint Committee on the Prevention of Antimicrobial Resistance: guidelines for the prevention of antimicrobial resistance in hospitals.

              Antimicrobial resistance results in increased morbidity, mortality, and costs of health care. Prevention of the emergence of resistance and the dissemination of resistant microorganisms will reduce these adverse effects and their attendant costs. Appropriate antimicrobial stewardship that includes optimal selection, dose, and duration of treatment, as well as control of antibiotic use, will prevent or slow the emergence of resistance among microorganisms. A comprehensively applied infection control program will interdict the dissemination of resistant strains.
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                Author and article information

                Journal
                Emerg Infect Dis
                Emerging Infect. Dis
                EID
                Emerging Infectious Diseases
                Centers for Disease Control and Prevention
                1080-6040
                1080-6059
                February 2006
                : 12
                : 2
                : 211-216
                Affiliations
                [* ]University of Dundee Medical School, Dundee, United Kingdom;
                []Ninewells Hospital, Dundee, United Kingdom;
                []Frenchay Hospital, Bristol, United Kingdom;
                [§ ]St Vincent's University Hospital, Dublin, Ireland;
                []Nottingham City Hospital, Nottingham, United Kingdom;
                [# ]University of Nottingham, Nottingham, United Kingdom;
                [** ]Aberdeen Royal Infirmary, Aberdeen, United Kingdom;
                [†† ]Hammersmith Hospital, London, United Kingdom;
                [‡‡ ]University of Aberdeen Health Services Research Unit, Aberdeen, United Kingdom;
                [§§ ]Inverclyde Royal Hospital, Greenock, United Kingdom;
                [¶¶ ]United Kingdom Cochrane Centre, Oxford, United Kingdom;
                [## ]Leeds General Infirmary, Leeds, United Kingdom;
                [*** ]University of Leeds, Leeds, United Kingdom
                Author notes
                Address for correspondence: Peter Davey, Health Informatics Centre, University of Dundee Medical School, Mackenzie Building, Kirsty Semple Way, Dundee DD2 4BF, United Kingdom; fax: 44-1382-420-010; email: p.g.davey@ 123456chs.dundee.ac.uk
                Article
                05-0145
                10.3201/eid1202.05145
                3373108
                16494744
                5a743aee-517a-4d32-9e64-875e3aab199a
                History
                Categories
                Synopsis

                Infectious disease & Microbiology
                synopsis,clostridium difficile,antimicrobial drug policy,antimicrobial drug resistance,systematic review,hospital-acquired infection

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