Staphylococcus Aureus Clinical Trial
Official title:
Retrospective Chart Review of the Outcome of Treatment for Staphylococcus Aureus Bacteremia
The purpose of this study is to review medical records at MEDVAMC in order to relate the outcome of bacteremic MRSA infection to the antibiotics selected for treatment.
Treatment of bacteremic infection (infection associated with positive blood cultures) due to
Staphylococcus aureus has become increasingly problematic as a result of the increasing
prevalence of strains that are resistant to beta-lactam antibiotics (so-called
methicillin-resistant Staphylococcus aureus, MRSA). About 70% of hospital-related strains of
S. aureus are MRSA, and, in the past 4 years, the incidence of MRSA in community-acquired
infection has risen to about 50%; these data are quite representative of what is being seen
elsewhere in the United States and other parts of the world.
Bacteremic MRSA infections are highly problematic for at least two reasons: (1)they are
serious, with substantial morbidity and about a 25% rate of mortality in middle-aged adults,
the principal patients in our system; and (2)available antibiotic therapy is suboptimal.
In the pre-MRSA era (before 1982 in the United States), treatment of bacteremic S. aureus
infection with a beta-lactam antibiotic such as nafcillin produced a uniform microbiological
cure (Musher DM, McKenzie SO: Infections due to Staphylococcus aureus. Medicine 56:383-409,
1977). This means that, in the absence of an untreated focus of infection that required
surgical removal (such as a myocardial abscess), antibiotics rapidly sterilized the blood
stream. This does not mean that no one died; deaths from complications of infection remained
common. But, at autopsy, there was generally no evidence for active infection. Extensive
literature examined the question of whether gentamicin should be added to nafcillin to treat
this kind of disease (reviewed critically in DM, Verner EF: Treatment of Infections due to
Staphylococcus aureus. IN The Staphylococci, Ed. by J Jeljascewicz, Gustave Fischer Verlag,
Stuttgart, New York, pp.407-419, 1986). Gentamicin produced a synergistic bactericidal
effect agains S. aureus in vitro and in animal models. In humans, the addition of gentamicin
was associated with more rapid sterilization of the blood stream, but prolonged gentamicin
therapy was also associated with nephrotoxicity.
In contrast, in the MRSA era, treatment with vancomycin is associated with persistence of
bacteremia (positive blood cultures) and death from active infection. The investigators have
recently participated in a prospective observational study that documented the association
between vancomycin treatment, persistently positive blood cultures, and persistence of
active infection during treatment of S. aureus bacteremia with vancomycin (Chang F-Y,
McDonald BB, Peacock, Jr. JE, Musher DM, et al. Staphylococcus aureus bacteremia: recurrence
and the impact of antibiotic treatment in a prospective multicenter study. Medicine
82:333-339, 2003).
There appears to be a very close correlation between the outcome of treatment for serious S.
aureus infection and the bactericidal activity of the treating antibiotic in vitro using
conventional techniques (Musher DM, Verner EF: Treatment of infections due to Staphylococcus
aureus. IN The Staphylococci, Ed. by J Jeljascewicz, Gustave Fischer Verlag, Stuttgart, New
York, pp.407-419, 1986). We recently showed that adding low concentrations of gentamicin to
vancomycin led to substantial synergistic bactericidal activity against MRSA (Shelburne SA,
Musher DM, Hulten K, Ceasar H, Lu MY, Bhaila I, Hamill RJ. In-vitro killing of
community-associated methicillin-resistant Staphylococcus aureus with drug combinations.
Antimicrob Agents Chemother 48:4016-9, 2004).
Based in part on the analogy of nafcillin for treating methicillin-susceptible S. aureus
infection, and in part of in vitro studies such as ours (cited above), some physicians
regularly add gentamicin to vancomycin for treating MRSA infection. Others, without even the
in vitro support, add rifampin either instead of gentamicin or together with gentamicin.
There are no clinical studies to support or to refute any of these clinically motivated
usages.
Thus, at present, about one-third of patients with MRSA bacteremia at VAMC are treated with
vacomycin plus gentamicin, and two-thirds receive vancomycin alone; some in each group
receive rifampin. The decisionto add gentamicin is made a haphazard fashion, generally
reflecting the interpretation of the literature by the attending physician and/or the
residents.
Our proposal is, simply to systematically review records from the past two years in order to
relate treatment of MRSA bacteremic infection to outcome.
;
Observational Model: Ecologic or Community, Time Perspective: Retrospective
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