Respiratory pathogens: assessing resistance patterns in Europe and the potential role of grepafloxacin as treatment of patients with infections caused by these organisms
D. Felmingham, Respiratory pathogens: assessing resistance patterns in Europe and the potential role of grepafloxacin as treatment of patients with infections caused by these organisms, J ANTIMICRO, 45, 2000, pp. 1-8
Although most respiratory tract infections (RTI) are caused by viruses, var
ious bacteria, particularly Streptococcus pneumoniae, Haemophilus influenza
e and Moraxella catarrhalis, are common causes of community-acquired pneumo
nia, acute exacerbations of chronic bronchitis, otitis media and sinusitis.
Empirical antibiotic therapy of patients with RTI must take account of the
increasing prevalence of resistance among the predominant pathogens. Europ
e-wide susceptibility surveillance studies have revealed that resistance to
penicillin and macrolides is highly prevalent among isolates of S. pneumon
iae from France and Spain. Uniquely, in Italy, macrolide resistance is high
ly prevalent while the prevalence of penicillin resistance is low. Resistan
ce to other antibiotic classes, including chloramphenicol, doxycycline and,
in particular, co-trimoxazole, is associated with penicillin resistance in
pneumococci, but resistance to the fluoroquinolones is rare. beta-Lactamas
e production is the principal mechanism of resistance in isolates of H. inf
luenzae and M. catarrhalis, with fluoroquinolone resistance being detected
rarely in these pathogens. In 1998 a surveillance study involving 15 Europe
an countries determined the susceptibilities of many respiratory pathogens
to a range of antimicrobials, including grepafloxacin. The MIC90 of grepafl
oxacin for 1251 isolates of S. pneumoniae was 0.25 mg/L, the MICs for only
five strains being >2 mg/L, and 99.4% of all of the isolates tested were in
hibited by concentrations less than or equal to 0.5 mg/L. The MIC(90)s of g
repafloxacin for 587 isolates of H. influenzae and 323 of Haemophilus parai
nfluenzae were 0.015 and 0.06 mg/L, respectively, while that for 509 isolat
es of M, catarrhalis was 0.03 mg/L. The MIC90S for 1164 isolates of methici
llin-susceptible Staphylococcus aureus and 435 isolates of Klebsiella pneum
oniae were 0.12 and 0.25 mg/L, respectively. Other studies have shown grepa
floxacin to be highly active against clinical isolates of Legionella pneumo
phila (MIC90 0.015 mg/L), Mycoplasma pneumoniae (MIC90 0.5 mg/L) and Chlamy
dia pneumoniae (MICs 0.06-0.12 mg/L). Current susceptibility data indicate
that fluoroquinolone resistance rates among bacterial respiratory tract pat
hogens are low in European countries. The enhanced potency and activity of
grepafloxacin against isolates of S. pneumoniae, including those exhibiting
resistance to unrelated classes of antibiotics, together with its activity
against other respiratory tract pathogens, suggest that this drug has cons
iderable potential as empirical therapy of patients with a wide range of RT
I.