Rf. Breiman et al., EMERGENCE OF DRUG-RESISTANT PNEUMOCOCCAL INFECTIONS IN THE UNITED-STATES, JAMA, the journal of the American Medical Association, 271(23), 1994, pp. 1831-1835
Objective.-To estimate drug susceptibility patterns of Streptococcus p
neumoniae in selected hospitals in the United States and to characteri
ze the epidemiology of invasive drug-resistant pneumococcal infections
. Design.-Minimum inhibitory concentrations (MICs) for a variety of co
mmonly used antimicrobial drugs were determined for pneumococcal isola
tes submitted to the Centers for Disease Control and Prevention (CDC).
Risk factors for drug-resistant pneumococcal infection were evaluated
. Setting.-Hospital laboratories in the United States submitting pneum
ococcal isolates to the CDC between October 1, 1991, and September 30,
1992. Participants.-A total of 544 persons with pneumococci isolated
from normally sterile sites. Results.-A total of 13 hospitals in 12 st
ates actively participated in an ongoing pneumococcal surveillance stu
dy. Resistance to penicillin was detected in 6.6% of isolates, includi
ng 1.3% of isolates with MICs of 2.0 mu g/mL or more (compared with <0
.02% of isolates with MIC greater than or equal to 2.0 mu g/mL identif
ied by CDC surveillance from 1979 to 1987). A total of 16.4% were resi
stant to at least one of the following drugs or drug classes: penicill
in, cephalosporins, macrolides, combination trimethoprim and sulfameth
oxazole, and chloramphenicol. Six serotypes (6B, 23F, 14, 9V, 19A, and
19F) accounted for nearly 85% of strains resistant to at least one dr
ug class. Children were more likely than adults to be infected with st
rains resistant to trimethoprim-sulfamethoxazole, erythromycin, or chl
oramphenicol. Conclusions.-Emergence of drug-resistant pneumococcal in
fections will present critical challenges to clinicians for treating p
atients with pneumococcal disease. Widened and intensified surveillanc
e is needed. These data suggest that current recommendations for use o
f 23-valent pneumococcal capsular polysaccharide vaccines should be ag
gressively promoted and that development and evaluation of new conjuga
te pneumococcal vaccines may be a crucial part of strategies for preve
ntion.