Tracking drug-resistant streptococcus pneumoniae in Oregon: an alternative surveillance method.
Streptococcus pneumoniae infections are a major cause of illness and death worldwide. Penicillin-resistant S. pneumoniae were first described in 1967 (1). Since then, the proportions of isolates resistant to penicillin and other antimicrobial agents have increased worldwide (2-5). In the United States, the combined percentage of S. pneumoniae isolates with either intermediate (MIC = 0.1-1.0 [micro]g/ml) or high (MIC 2.0 [micro]g/ml) levels of penicillin resistance is higher than 60% in some areas (5). Strains with multidrug resistance to penicillins, macrolides, sulfonamides, and third-generation cephalosporins have been well documented (3,5-9). Despite the increasing proportion of drug-resistant S. pneumoniae and the importance of knowing the drug resistance status in determining empiric therapy, community-specific surveillance for drug-resistant S. pneumoniae is limited and its proportion is unknown in many areas (10,11). Active surveillance for invasive S. pneumoniae disease includes collection of isolates, centralized susceptibility testing, and collection of patient data (4).
Although such a resource-intensive system for providing community-specific and case-specific S. pneumoniae data is beyond the means of most local and many state health agencies, hospital-specific data already exist in many areas. Many hospital laboratories perform antimicrobial susceptibility testing on S. pneumoniae isolates from sterile and nonsterile sites, and results are often tabulated for local clinicians in a summary table called an antibiogram. Antibiogram data represent invasive and noninvasive S. pneumoniae disease isolates collected from normally sterile and nonsterile sites; may include multiple isolates from the same patient; and are based on hospital laboratory antimicrobial susceptibility testing, a process that may differ between laboratories. In contrast, S. pneumoniae active surveillance data are limited to invasive disease isolates collected from normally sterile sites, specifically exclude duplicate isolates collected from the same patient, and are based on a centralized and standardized susceptibility testing protocol.
We examined preexisting antibiogram data to assess if they could provide local health agencies with an accurate, inexpensive means of estimating the community-specific proportion of drug-resistant S. pneumoniae. The Oregon Health Division performs active surveillance for drug-resistant S. pneumoniae through a cooperative agreement with the Centers for Disease Control and Prevention's Emerging Infections Program. We conducted a cross-sectional survey of the 12 hospital laboratories that serve the Portland Tri-County area (Multnomah, Washington, and Clackamas counties, population 1.2 million) and compared 1996 Portland S. pneumoniae susceptibility results and costs of the aggregated antibiogram surveillance system with the S. pneumoniae susceptibility results and costs of our active surveillance system. We determined the community-specific proportion of S. pneumoniae susceptible to penicillin and performed a limited analysis of hospital-specific susceptibilities to cefotaxime, trimethoprim-sulfamethoxazole, and erythromycin.
Our goal was to determine the proportion of drug-resistant isolates among all S. pneumoniae isolates collected by the active surveillance system in 1996. Therefore, an active surveillance case was defined as an S. pneumoniae isolate from a normally sterile site collected from a Portland Tri-County resident in 1996 and analyzed at a Portland Tri-County hospital microbiology laboratory.
All Portland-area hospital microbiology laboratories were asked to send all S. pneumoniae sterile-site isolates from both inpatients and outpatients to the Oregon State Public Health Laboratory. Health Department staff regularly contacted each laboratory to assess interim isolate recovery rates and to encourage ongoing participation in the surveillance system and (twice a year) performed on-site laboratory audits to compare the number of patients with invasive S. pneumoniae infections with the number of isolates submitted to the state laboratory.
To avoid duplication, only one isolate from each patient was sent to the reference laboratory, even if multiple isolates were obtained from the same person. Isolates were sent twice a year from the Oregon State Public Health Laboratory to a national reference laboratory for antimicrobial susceptibility testing by National Committee for Clinical Laboratory Standards broth microdilution protocols (12). S. pneumoniae antimicrobial-susceptibility percentages for Portland were calculated from the national reference laboratory results. Invasive cases did not have reference laboratory susceptibility testing if the hospital laboratory did not forward the :isolate to the Oregon State Public Health Laboratory or if the isolates received by the Oregon or the reference laboratory were not viable.
Annual costs for this surveillance system included direct and indirect health department staff costs and the expense of isolate storage, processing, and transport incurred by the Oregon State Public Health Laboratory and the national reference laboratory. Hospital laboratory isolate testing, which would have been performed regardless of our request for surveillance data, were not included in these calculations. Time calculations included laboratory audits, patient chart reviews, data entry and analysis, coordination of isolate movement, and communication among hospital laboratories, the health department, the state public health laboratory and the reference laboratory.
An antibiogram case was defined as any S. pneumoniae isolate identified in 1996 by a Portland Tri-County hospital microbiology laboratory that was tabulated on the respective 1996 S. pneumoniae antibiogram. Specimens were submitted from inpatients and outpatients and from sterile and nonsterile sites.
We requested antibiograms from all 12 Portland Tri-County hospital laboratories. Antibiogram data were aggregated to produce antimicrobial susceptibility percentages for the Portland area. All susceptibility testing was performed at individual hospital laboratories. We did not routinely survey laboratory techniques or reporting criteria, nor did the Oregon State Public Health Laboratory perform confirmation susceptibility testing of any hospital isolates.
The cost of the antibiogram method included direct and indirect health department staff expenses but excluded the cost of hospital laboratory isolate testing, a process performed regardless of our surveillance requests. Time calculations included staff time spent requesting antibiograms and performing data entry and analysis.
The Mantel-Haenzel chi-square and Fisher's exact tests were used to compare the proportions of susceptible S. pneumoniae isolates determined by the two surveillance methods. P values [is less than or equal to] 0.05 were considered statistically significant. Statistical calculations were performed by using Epi-Info (Epi-Info version 6.04b; Centers for Disease Control and Prevention, Atlanta, GA).
Of the 12 Portland-area hospital laboratories participating in the active surveillance system, 10 (83%) submitted isolates to our active surveillance system in 1996. One hospital (A) had no sterile-site isolates in 1996. A second hospital (F) had two sterile-site isolates but did not submit them to the state laboratory. Of 266 invasive S. pneumoniae infections identified by health department staff through audits, 178 (67%) S. pneumoniae isolates were tested by the reference laboratory. Of the 88 identified cases that were not analyzed by the reference laboratory, in 81 cases the hospital did not submit an isolate to the state laboratory, and in 7 the isolate submitted was not viable. The number of isolates collected from each hospital was 2 to 59 (Table 1). The mean and median numbers of active surveillance isolates collected per hospital were 18 and 9.5, respectively. Of the 178 isolates tested, 153 (86% [95% CI = 80% to 91%]) were susceptible to penicillin (MIC 0.06 [micro]g/ml).
Table 1. Streptococcus pneumoniae penicillin susceptibility as determined by two surveillance methods, Portland, Oregon, 1996
Active surveillance Antiobiograms No. Susceptible No. Susceptible Hospital isolates N % isolates N % A (a) 20 17 85 B 34 29 85 134 112 84 C 59 52 88 274 227 83 D 6 4 67 120 89 74 E 12 11 92 41 34 83 F (a) 61 58 95 G 33 28 85 110 100 91 H 11 10 91 161 137 85 I 8 6 75 64 56 88 J 7 6 86 107 91 85 K 6 5 83 (b) L 2 2 100 (b) Total 178 153 86 1,092 921 84
(a) No isolates submitted to the Oregon Public Health Laboratory.
(b) Antibiogram data not available from hospital.
Penicillin antibiogram data were collected from 10 (83%) of 12 Portland-area hospitals (Table 1). Eight of the 10 hospitals listed only the proportion of susceptible S. pneumoniae isolates on their antibiogram and did not specify the number of intermediate- or high-resistance isolates. Of the aggregated 1,092 S. pneumoniae isolates used by Portland-area hospitals to generate penicillin antibiogram data, 921 (84% [95% CI = 82% to 86%]) were listed as susceptible to penicillin.
The proportion of penicillin-susceptible isolates at each hospital was 67% to 100% by the active surveillance method and 74% to 95% by antibiogram data (Figure). The median hospital-specific difference between the two methods was 6%. In no instance did hospital-specific penicillin-susceptibility estimates from the two methods differ statistically (p [is greater than] 0.05). We found no statistical difference between the overall S. pneumoniae penicillin-susceptibility proportion determined by active surveillance and by the antibiogram method (p [is greater than] 0.05).
[Figure ILLUSTRATION OMITTED]
We compared active surveillance and antibiogram S. pneumoniae susceptibilities to cefotaxime, trimethoprim-sulfamethoxazole, and erythromycin (Table 2). Of the 178 isolates collected and tested through the active surveillance system, 165 (93% [95% CI = 88% to 96%]) were susceptible to cefotaxime (MIC 0.50 [micro]g/ml), 141 (79% [95% CI = 73% to 85%]) were susceptible to trimethoprim (MIC 0.50 [micro]g/ml)-sulfamethoxazole (MIC 9.50 [micro]g/ml), and 169 (95% [95% CI = 91% to 98%]) were susceptible to erythromycin (MIC 0.50 [micro]g/ml).
Table 2. Streptococcus pneumoniae susceptibility to cefotaxime, trimethoprim-sulfamethoxazole, and erythromycin, by two surveillance methods, Portland, Oregon, 1996
Cefotaxime Active surveillance Antibiograms No. Susceptible No. Susceptible iso- iso- Hospital lates N % lates N % A (a) (b) B 34 32 94 10 8 80 C 59 54 92 274 255 93 D 6 4 67 120 112 93 E 12 12 100 (b) F (a) 61 59 97 G 33 31 94 110 105 95 H 11 11 100 -- I 8 7 88 -- J 7 6 86 -- K 6 6 100 -- L 2 2 100 -- Total 178 165 93 575 539 94 Trimethoprim-Sulfamethoxazole Active surveillance Antibiograms No. Susceptible No. Susceptible iso- iso- Hospital lates N % lates N % A (a) (b) B 34 26 76 (b) C 59 49 83 274 230 84 D 6 3 50 E 12 9 75 16 13 81 F (a) (b) G 33 27 82 (b) H 11 10 91 (b) I 8 6 75 (b) J 7 5 71 10 8 80 K 6 4 67 (b) L 2 2 100 (b) Total 178 141 79 300 251 84 Erythromycin Active surveillance Antibiograms No. Susceptible No. Susceptible iso- iso- Hospital lates N % lates N % A (a) (b) B 34 33 97 134 126 94 C 59 57 97 274 230 84 D 6 5 83 120 88 73 E 12 12 100 42 39 93 F (a) 61 56 92 G 33 30 91 110 100 91 H 11 11 100 (b) I 8 8 100 (b) J 7 6 86 10 10 100 K 6 5 83 (b) L 2 2 100 (b) Total 178 169 95 751 649 86
(a) Isolates submitted to the Oregon Public Health Laboratory.
(b) Antibiogram data not available from hospital.
In hospitals where antibiogram data were available for cefotaxime, trimethoprim-sulfamethoxazole, and erythromycin, 539 (94%) of 575 aggregated isolates (95% CI = 91% to 95%) were susceptible to cefotaxime, 251 (84%) of 300 isolates (95% CI = 79% to 88%) were susceptible to trimethoprim-sulfamethoxazole, and 649 (86%) of 751 isolates (95% CI = 84% to 89%) were susceptible to erythromycin. Hospital-specific antibiogram and active surveillance data from four institutions were available for direct comparison for cefotaxime and from three institutions for trimethoprim-sulfamethoxazole. In each instance, the hospital-specific proportion of S. pneumoniae isolates susceptible to cefotaxime or trimethoprim-sulfamethoxazole did not differ significantly by surveillance method. We were able to directly compare S. pneumoniae erythromycin susceptibility by antibiogram and active surveillance at six hospitals. The proportions of erythromycin-susceptible S. pneumoniae isolates determined by each surveillance method were statistically comparable in five of' the six hospitals (p [is greater than] 0.05). One hospital (C) had a significantly higher proportion (p = 0.01) of erythromycin-susceptible isolates determined by active surveillance (97% [95% CI = 88% to 100%]) than reported by the corresponding antibiogram (84% [95% CI = 79% to 88%]).
The antibiogram survey required 20 hours of health department staff time, for a total cost of $700:$650 for personnel expenses and $50 for miscellaneous support expenses. The active surveillance method required 570 hours of staff time and cost $52,000:$40,000 for direct and indirect personnel expenses and $12,000 for laboratory costs.
Accurate, community-specific drug-resistant S. pneumoniae data are important for several reasons. First, most outpatient illnesses caused by S. pneumoniae are treated empirically, without identification of the organism. Community-specific data may be a valuable determinant of empiric therapy for these infections and of initial empiric therapy for invasive disease. Second, communities with a high percentage of drug-resistant S. pneumoniae may benefit from efforts to reduce inappropriate antibiotic prescriptions. Increased drug-resistant S. pneumoniae carriage is directly related to antibiotic therapy, and reduced antimicrobial use in the community can decrease rates of antimicrobial resistance (13-16). Finally, clinicians in areas with a low percentage of drug-resistant S. pneumoniae and minimal penicillin resistance might gain confidence in treating presumptive outpatient infections with empiric penicillin therapy, thereby reducing the risk for multidrug resistance.
Despite the clinical and public health importance of drug-resistant S. pneumoniae surveillance, community-specific surveillance data are not uniformly available. A 1996 study determined that 54% of states either conducted or were planning to implement surveillance for drug-resistant S. pneumoniae by June 1997 (17). Our study supports the usefulness of S. pneumoniae antibiogram data, commonly available at many hospitals, in estimating the community-specific proportion of penicillin-susceptible S. pneumoniae. In no instance did hospital-specific penicillin susceptibility estimates from the two methods differ statistically. More importantly, the overall Portland penicillin susceptibility proportions determined by the active surveillance and antibiogram methods were statistically comparable.
Antibiogram data also hold promise for estimating S. pneumoniae susceptibilities to other antimicrobial drugs. The hospital-specific proportion of S. pneumoniae isolates susceptible to cefotaxime and trimethoprim-sulfamethoxazole did not differ for the two methods in hospitals where comparisons were possible. The erythromycin susceptibility proportions by antibiogram and active surveillance were statistically comparable at each of the hospitals for which erythromycin data were available, except for hospital C. The reason for this discordance is not clear but may be influenced by statistical chance.
Time and financial requirements for the antibiogram method were minimal and probably within reach of many local health departments. Laboratory effort was limited to mailing a current antibiogram to the health department. However, the antibiogram method can only estimate the proportion of drug-resistant S. pneumoniae in a community. The active surveillance system collects patient-specific (e.g., risk factors, demographics) and infection-specific information, permits serotyping and molecular analysis of isolates, provides data on the actual S. pneumoniae disease effect in the population, permits evaluation of targeted vaccination campaigns and antimicrobial guideline efforts, provides specific MIC data for a range of antimicrobial agents, and allows for validation of alternative surveillance methods.
Prior surveillance studies have documented equal or greater proportions of penicillin-resistant isolates collected from nonsterile sites than from sterile sites (18,19). Our active surveillance system captures only isolates from sterile sites collected from invasive S. pneumoniae disease. Most isolates in the antibiograms were from noninvasive diseases and nonsterile sites. Our study showed no statistical difference between the proportion of penicillin-susceptible S. pneumoniae determined by either method and therefore no difference between the penicillin-susceptible proportion of invasive and noninvasive isolates. Ninety-six percent of our active surveillance isolates were from outpatients or inpatients hospitalized less than 48 hours and are unlikely to represent nosocomial infections. These data support the traditional epidemiologic characterization of S. pneumoniae as a community rather than nosocomially acquired organism.
Several potential limitations deserve comment. The active surveillance system had a case-isolate recovery rate of 67%. The current performance indicator for the active surveillance system, instituted in 1998, is a case-isolate recovery rate of 85% (A. Schuchat, pers. comm.) We were unable to characterize the susceptibilities of the missing isolates, which may have biased our active surveillance results. Antibiograms were tabulated from all isolates submitted to a particular hospital laboratory. Multiple isolates from a single patient may have disproportionately influenced these results. Unlike the active surveillance system, in which chart reviews excluded nonresidents, antibiogram data may have included isolates from patients who were not Portland-area residents and should not have been included in Portland S. pneumoniae antimicrobial-susceptibility results. We were unable to estimate the number of duplicate isolates or non-Portland-area residents in our antibiogram data.
This study suggests that antibiogram data already available in hospitals may be useful in estimating the community-specific proportion of drug-resistant S. pneumoniae. We recommend further validation of these results at sites where active surveillance and antibiogram data can be directedly compared. The most effective use of antibiogram drug-resistant S. pneumoniae surveillance may require that hospitals routinely and consistently perform S. pneumoniae susceptibility testing to multiple antimicrobial drugs. Communities considering this surveillance method may need to work with local hospitals to develop a cost-effective susceptibility testing regimen. Although yielding less information than active surveillance, antibiogram surveillance might be most useful in communities where hospital antibiogram data are available but more intensive surveillance is limited by a lack of financial or personnel resources.
We thank the laboratory directors, managers, and staff at the Oregon State Public Health Laboratory and the Portland Tri-County hospital microbiology laboratories for their work in this study and Drs. Anne Schuchat, Thomas Van Gilder, and Andrew Pelletier for manuscript review.
This study was funded, in part, by a cooperative agreement between the Oregon Health Division and the Centers for Disease Control and Prevention's Emerging Infections Program.
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At the time this study was performed, Dr. Chin was an Epidemic Intelligence Service Officer with the Centers for Disease Control and Prevention, assigned to the Oregon Health Division. He currently practices emergency medicine in Sharon, Connecticut.
Arthur E. Chin,(*)([dagger]) Katrina Hedberg,(*) Paul R. Cieslak,(*) Maureen Cassidy,(*) Karen R. Stefonek,(*) and David W. Fleming(*)
(*) Oregon Health Division, Portland, Oregon, USA; and ([dagger]) Centers for Disease Control and Prevention, Atlanta, Georgia, USA
Address for correspondence: Arthur E. Chin, 63 Indian Mountain Road, Lakeville, CT 06039, USA; fax: 860-364-4427; e-mail: firstname.lastname@example.org <mailto:email@example.com.
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|Author:||Fleming, David W.|
|Publication:||Emerging Infectious Diseases|
|Article Type:||Statistical Data Included|
|Date:||Sep 1, 1999|
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