ABSTRACT
Over the past 3 decades, antimicrobial resistance among Streptococcus pneumoniae, the most common cause of community-acquired pneumonia (CAP), has escalated dramatically
worldwide. In the late 1970s, strains of pneumococci displaying resistance to penicillin
were described in South Africa and Spain. By the early 1990s, penicillin-resistant
clones of S. pneumoniae spread rapidly across Europe and globally. Additionally, resistance to macrolides
and other antibiotic classes escalated in tandem with penicillin resistance. Six international
clones (serotypes 6A, 6B, 9V, 14, 19F, 23F) were responsible for most of these resistant
isolates. Currently, 15 to 30% of S. pneumoniae worldwide are multidrug-resistant (MDR) (i.e., resistant to ≥ 3 classes of antibiotics).
Despite the dramatic escalation in the rate of antimicrobial resistance among pneumococci
worldwide, the clinical impact of antimicrobial resistance is difficult to define. Treatment failures due to antibiotic-resistant
pneumococci have been reported with meningitis, otitis media, and lower respiratory
tract infections, but the relation between drug resistance and treatment failures
has not been convincingly established. Clinical failures often reflect factors independent of antimicrobial susceptibility of the infecting organisms. Host factors (e.g., extremes
of age; underlying immunosuppressive or debilitating disease; comorbidities), or factors
that affect intrinsic virulence of the organisms (e.g., capsular subtype) strongly
influence prognosis. Mortality rates are higher in the presence of: multilobar involvement,
renal insufficiency, need for intensive care unit (ICU) care, hypoxemia, severe derangement
in physiological parameters, and comorbidities. Given these confounding factors, dissecting
out the impact of antimicrobial resistance on clinical outcomes is difficult, if not
impossible. Prospective, randomized trials designed to assess the clinical significance
of antimicrobial resistance among pneumococci are lacking, and for logistical reasons,
will never be done. Does in vitro resistance translate into clinical failures? Should
changing resistance patterns modify our choice of therapy for CAP or for suspected
pneumococcal pneumonia? In this review, we discuss several facets, including mechanisms
of antimicrobial resistance among specific antibiotic classes, epidemiology and spread
of antimicrobial resistance determinants regionally and worldwide, risk factors for
acquisition and dissemination of resistance, the impact of key international clones
displaying multidrug resistance, the clinical impact of antimicrobial resistance,
and strategies to limit or curtail antimicrobial resistance among this key respiratory
tract pathogen.
KEYWORDS
Streptococcus pneumoniae
- pneumococcus - invasive pneumococcal disease (IPD) - antimicrobial resistance -
penicillin resistance - macrolide resistance
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Joseph P LynchIII M.D.
Division of Pulmonary, Critical Care Medicine, Allergy, and Clinical Immunology, The
David Geffen School of Medicine at UCLA
10833 Le Conte Ave., Rm. 37-131 CHS, Los Angeles, CA 90095
eMail: jplynch@mednet.ucla.edu