ABSTRACT
Investigators participating in the Epidemiologic Study of Cystic Fibrosis project began to collect microbiological, pulmonary, and nutritional data on cystic fibrosis (CF) patients at 180 North American sites in 1994. Part of this study was a survey undertaken in August 1995 to determine microbiology laboratory practices with regard to pulmonary specimens from CF patients. The survey included a section on test ordering, completed by a site clinician, and a section on test performance and reporting, completed by each site’s clinical microbiology laboratory staff. Seventy-nine percent of the surveys were returned. There was intersite consistency of microbiology laboratory practices in most cases. The majority of sites follow most of the CF Foundation consensus conference recommendations. There were differences in the frequency at which specimens for culture were obtained, in the use of selective media for Staphylococcus aureus andHaemophilus influenzae, and in the use of a prolonged incubation for Burkholderia cepacia. These variations in practice contribute to prevalence differences among sites and may result in differences in clinical care.
Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CF transmembrane regulator gene resulting in abnormal chloride ion transport across epithelia. Affected individuals have defective cyclic AMP-regulated chloride channel activity involving several organs, including the pancreas, biliary tract, gastrointestinal tract, and airways. Pathological findings in the lung include retention of secretions, harboring a variety of microorganisms, in the distal airways. When cultured from the respiratory tracts of CF patients, Staphylococcus aureus, Pseudomonas aeruginosa, and Burkholderia cepacia are associated with increased morbidity and mortality (22). Marked inflammation occurs in these airways, causing progressive bronchiectasis until the loss of functioning airways results in respiratory insufficiency and, eventually, death.
Investigators participating in the Epidemiologic Study of Cystic Fibrosis (ESCF) project began to collect microbiological, pulmonary, and nutritional data on CF patients at 180 North American sites in 1994 in order to describe the disease burden and course, current practice patterns, and safety and effectiveness of dornase alfa (Pulmozyme) in the general CF patient population. All CF patients were invited to enroll regardless of whether they were receiving this medication. Enrollment at the time of the survey included more than 18,000 of the estimated 20,000 to 30,000 CF patients living in North America. The present survey of microbiology practice was undertaken in August 1995 to determine, for each site, the frequencies of performance of sputum and throat cultures, the culture techniques used, and the frequency with which certain organisms are tested for antibiotic susceptibility. These microbiological practice patterns were then correlated with the reported prevalences of S. aureus, P. aeruginosa, and B. cepacia at the participating sites.
Coincident with this survey, the recommendations of a CF Foundation consensus conference on microbiological procedures for evaluation of infectious diseases in CF patients were published (8). This permitted a comparison of the current practices in the participating CF patient care sites with these guidelines as well as those previously published for CF specimens (20).
MATERIALS AND METHODS
Data on the microbiology practices of the ESCF sites were obtained by survey. Surveys were mailed to the 180 enrolled ESCF sites in August 1995. Survey part A, which dealt with clinical data and indications for specific cultures and sensitivities, was completed by the principal investigator and the study coordinator. Part B, which consisted of questions regarding specific culture media, was completed by, or in conjunction with, the director of the site’s clinical microbiology laboratory. Completed surveys were blinded as to site and then forwarded for data management, processing, and analysis. Site confidentiality was maintained throughout the survey.
Of the 180 surveys sent, 142 (79%) were returned within 6 months. These 142 sites represent 15,328 enrolled patients.
The 2-year cumulative prevalences of S. aureus, P. aeruginosa, P. aeruginosa of mucoid phenotype, andB. cepacia were calculated from data on the case report forms submitted to the ESCF by each participating site for the period from 12 months prior to enrollment to 1 year after enrollment in the ESCF. On the ESCF case report form completed at the time of enrollment were recorded the presence or absence of these bacteria for the 12 months prior to enrollment, the source of the cultured sample (throat or sputum), and other clinical information. On the case report form completed at each subsequent encounter were recorded the presence or absence of these bacteria, the source, and clinical information at the time the patient visited the site. A report of at least one culture in each of two successive years (12 months prior to and 1 year following enrollment) was needed for the patient to enter the prevalence analysis. This analysis included patients who enrolled before March 1996. The predicted forced expiratory volume in 1 s (FEV1) percentage was calculated from the FEV1, gender, and height for those 6 years or older at the time of enrollment, using Knudson standards (13). The highest value reported for the period from 6 months prior to enrollment to 1 year after enrollment was used. The age used was that at the midpoint of the period. These data were available for 14,577 patients.
To assess the association between clinical and laboratory practices and observed bacterial prevalence rates, the sites were divided into two groups, those using a complete protocol and those using a partial protocol. To be categorized as using a complete protocol, a site had to report on its survey the use of the following elements: (i) the procurement and culture of throat swab specimens from patients who did not produce sputum; (ii) inoculation of specimens onto media selective for S. aureus, P. aeruginosa, and B. cepacia; (iii) performance of additional biochemical tests on, or referral to a reference laboratory for, organisms that the site’s routine identification system failed to identify; and (iv) reporting of all isolates of S. aureus, P. aeruginosa, mucoidP. aeruginosa, and B. cepacia to the clinic. These sites were compared with those that did not employ one or more elements of this complete protocol. Because the selective media differed for each organism, a site might use a complete protocol forS. aureus but not P. aeruginosa or B. cepacia; hence the sites were categorized for each of these bacteria and the results were compared. To assess the association of culture frequency with observed prevalence, the culture data from only the year after enrollment were used. The chi-square test of independence was used to determine the significance of differences among the observed prevalences.
RESULTS
Clinical practices.Sixty-four percent of the sites sent 100% of their respiratory tract specimens from CF patients to an on-site laboratory for culture. Of the ESCF sites that sent out respiratory specimens for culture, 64% sent out 25% or less.
All sites requested culturing of CF patients’ sputum specimens. In cases in which sputum could not be produced, 89% of sites requested a throat swab culture. Clinicians at 97% of the sites indicated on the laboratory request form that the specimen was from a CF patient.
Clinicians requested cultures specifically for yeast and fungi at 85% of the sites, for mycobacteria at 86% of the sites, and forAspergillus species at 68% of the sites, primarily when clinically indicated for CF patients. Cultures for yeasts and fungi were requested routinely during all CF patient hospitalizations and clinic visits at 21% of the sites, while such specimens were routinely cultured for mycobacteria at 10% of the sites and forAspergillus species at 4% of the sites.
Clinicians received antibiotic susceptibility reports for all respiratory tract bacteria other than normal flora without a specific request at 85% of the sites, at which 80% of the 15,328 patients were enrolled. At more than 93% of the sites, enrolling 91% of the patients, susceptibility results were received on all S. aureus, P. aeruginosa, and B. cepaciaisolates without request. At 88% of the centers, enrolling 83% of the patients, susceptibility results on all other gram-negative organisms were received without request.
Microbiology laboratory practices.While clinicians at 96% of responding sites indicated on the laboratory request form that the respiratory cultures were from CF patients, only 65% of the laboratories, covering 72% of the patients, required a clinical diagnosis.
Media and culture conditions likely to support the growth of or select for common CF-associated pathogens (6, 9, 10) were used at most sites for all CF patient respiratory specimens (Table1). More than 90% of the laboratories used sheep blood agar for all sputum and throat swab specimens from CF patients. More laboratories used selective media for sputum than for throat swab specimens: 65% (sputum) versus 51% (throat swab) forS. aureus-selective media and 95% (sputum) versus 80% (throat swab) for gram-negative-selective media. Importantly, only 17% of laboratories cultured sputum specimens on media or under conditions selective for Haemophilus influenzae. This was reduced to 13% for throat cultures. A much larger proportion of laboratories used chocolate agar under aerobic conditions, which will allow H. influenzae to grow but will also allow overgrowth by P. aeruginosa (5). Seventy-three percent of laboratories used B. cepacia-selective media for primary culture of sputum, but only 46% carried out longer-term incubation at a reduced temperature. All CF respiratory specimens were cultured on media selective for yeasts and fungi at 11% of sites, while at 87% of the sites, fungal media were used only if requested.
Percentage of laboratories using specified media on all cystic fibrosis respiratory specimens
Responding laboratories routinely employed several systems to identify gram-negative organisms. Automated systems were used by 80% of the laboratories, biochemical strips were employed by 45%, and standard biochemical methods were used by 35% of the laboratories. Many of the sites used multiple systems routinely. When the routine systems failed to identify organisms, laboratories performed the following practices: 66% set up additional biochemical tests involving incubations of 48 h or more, 51% set up additional biochemical tests without extended incubation, 50% sent the organisms to a reference laboratory, 25% used information from prior isolates, and 4% conducted no further tests. Most sites (96%) used combinations of these practices.
Specimens for culture of mycobacteria, including those classified as atypical, were sent to a reference laboratory by 66% of the site laboratories. Fifty-eight percent of these sites indicated that the specimens were from CF patients and were likely to have high numbers ofP. aeruginosa.
Several methods for bacterial quantification were reportedly used. A semiquantitative estimation for a swabbed primary plate was performed by 92% of the laboratories routinely and by 2% of the laboratories only upon request. Four percent of the laboratories performed serial dilutions of sputum routinely, while 8% used this method upon request only.
Most sites routinely reported the common pathogens associated with CF as being distinct from normal flora (Table2). S. aureus, P. aeruginosa, B. cepacia, and H. influenzaeisolates were reported routinely by at least 94% of the laboratories. Distinction between mucoid and nonmucoid P. aeruginosaisolates was reported routinely by 89% of the laboratories, only on request by 4%, and not at all by 4% of the laboratories. MucoidPseudomonas isolates that could not be speciated were reported routinely by 62% of the laboratories, only on request by 4%, and not at all by 18%. Fungi and yeasts were reported routinely by varying numbers of laboratories, with as many as 15% of sites reporting these organisms only upon request and up to 5% not reporting them at all.
Percentage of laboratories reporting specific organisms as distinct from normal flora in CF patient respiratory tract cultures
All but two laboratories reported growth of other nonfermentative gram-negative rods, such as Stenotrophomonas(Xanthomonas) maltophilia andAlcaligenes and Acinetobacter species, with 97% identifying them to the genus or species level. All but three sites reported growth of fermentative gram-negative rods (Escherichia coli, Klebsiella spp., Proteus spp.,Serratia spp., etc.), with 96% identifying them to the genus or species level.
Association of clinical and laboratory practices with observed bacterial prevalences.The reported 2-year cumulative prevalences of several organisms of clinical interest in CF were significantly different for sites using complete protocols and those using partial protocols. For the purposes of this analysis, we focused on S. aureus, P. aeruginosa, and B. cepacia since patients whose airway secretions yielded these organisms upon culture have been documented to have increased airway obstruction compared with similar CF patients in whom these organisms have not been detected (1, 7, 12, 15, 16, 21, 23, 24).
For S. aureus, 35% of the sites used complete protocols and 65% did not. The 2-year cumulative prevalence was 54% at sites using complete protocols, versus 48% at sites using partial protocols (P = 0.0001) . The largest difference in S. aureus cumulative prevalence occurred in patients aged 6 to 12 years with more-severe airway obstruction (FEV1, <70% [predicted]). The prevalence of S. aureus in these patients, at sites using complete protocols, was 58.2%, versus 49.7% at centers using partial protocols (Table3).
Comparison of 2-year cumulative prevalences of sites using complete protocols and those using partial protocols to detect bacteria of interest
For P. aeruginosa, 57% of the sites used complete protocols. The 2-year cumulative prevalence was 66% for sites using complete protocols, versus 63% for those using partial protocols (P = 0.0001) . This difference in prevalence was most pronounced in those aged 6 to 12 years with FEV1 of ≥70% (predicted). Those sites using complete protocols detected P. aeruginosa in 60.3% of these patients, compared with a detection rate of 55.6% for these patients at sites using partial protocols (Table 3).
The 2-year cumulative prevalence rates for mucoid P. aeruginosa isolates were 44 and 36% at sites performing complete and partial protocols, respectively (P = 0.0001). Complete protocols were used at 55% of the sites. The differences in prevalence of mucoid P. aeruginosa isolates were greatest in those under 17 years of age with more-severe airway obstruction (Table3).
Sites performing complete protocols for B. cepacia had a prevalence rate of 4.6%, versus 3.6% for sites using a partial protocol (P = 0.005), with the greatest differences being in the 6- to 12-year age group and those over 18 with less-severe airway obstruction (Table 3).
For S. aureus and mucoid P. aeruginosa, only part of these differences was accounted for by differences in culture frequency alone. After adjustment for the number of cultures performed, sites that used complete protocols still detected more patients withS. aureus or mucoid P. aeruginosa than those that did not. Twenty percent more S. aureus cultures per patient per year and 12% more B. cepacia cultures per patient per year were performed by sites using complete protocols than by sites using partial protocols. In the case of P. aeruginosa, essentially all of the difference in prevalence rates between sites performing complete protocols and those using partial protocols was explained by differences in culture frequency. Forty percent more cultures for P. aeruginosa (2.3 versus 1.6 cultures) were performed per patient per year at sites using complete protocols for that organism than at sites using partial protocols.
DISCUSSION
This survey describes the variation in the microbiology practices of 142 of 180 sites participating in a large multicenter study of CF. This variation in practice affects detection of these bacteria and, hence, the prevalence rates of microbes important in CF and must be taken into account when such rates are estimated and used to assess the impact of bacteria on disease status in CF patients. In particular, denominator data for epidemiological studies of the impact of H. influenzae, mycobacteria, yeasts, and fungi on disease progression in CF patients must be limited to sites performing routine culturing for the bacteria in question on selective media under optimal conditions.
All of the 142 sites request culturing of sputum produced by CF patients. However, if sputum cannot be produced, many sites do not request a throat swab culture. This is an important issue, since throat swab and sputum culture yields are similar for S. aureus andP. aeruginosa (9) and the frequency of detection of S. aureus and/or P. aeruginosa by throat swab culture in children under 2 years is associated with significantly increased morbidity and mortality in the following 10 years (12).
Ninety-six percent of the sites specify that the specimen is from a CF patient, although only 65% of the laboratories (representing 72% of the patients) require a clinical diagnosis. It is important that the diagnosis of CF be specified so that the laboratories are alerted to use appropriate media to enhance the detection of clinically important organisms (25).
Tablan et al. (20) showed that B. cepacia was isolated from simulated CF sputum by 95% of the laboratories usingB. cepacia-selective medium (P. cepacia agar or oxidative-fermentative polymyxin B-bacitracin-lactose agar) but was detected by only 22% of the laboratories not using a selective medium. Our data show that the use of B. cepacia-selective media has increased significantly in the past 9 years, from 12% in Tablan’s study to 73% in our study. Unfortunately, over half of the laboratories still do not carry out long-term incubation at a reduced temperature, conditions which may increase the yield of B. cepacia by allowing slower-growing colonies to become apparent. Further complicating matters, other organisms, such asStenotrophomonas maltophilia, can grow on B. cepacia-selective media and be difficult to distinguish fromB. cepacia, even with further biochemical testing (2). Early detection of B. cepacia in CF patients is extremely important with respect to both the individual patient and the CF population, since this organism appears to be spread from person to person among CF patients. Non-culture-based methods of identifyingB. cepacia and P. aeruginosa, such as detection of species-specific DNA by PCR (4, 17), have been developed and may have more-widespread application in the future.
Routine culturing for organisms of clinical and prognostic importance in CF (S. aureus, P. aeruginosa, and B. cepacia) is carried out at most, but not all, sites. Most laboratories report these organisms routinely as being distinct from normal flora, and they almost all routinely report antimicrobial agent susceptibilities for these organisms. Mucoid Pseudomonasspecies are not reported as distinct from Pseudomonasspecies by over one-third of the laboratories. The presence of mucoidPseudomonas species in respiratory secretions may have significant clinical implications (11, 14), making it potentially important to recognize these isolates as a distinct entity.
This survey indicates the degree to which practice currently follows the CF Foundation consensus conference recommendations. The sites follow these recommendations to various degrees. For example, 81% of the sites use protocols recommended for detection of P. aeruginosa, but only 65% follow the recommendation to useS. aureus-selective media for all CF patient sputum specimens. Less than half of the centers employ B. cepacia-selective culture media or incubate the cultures for extended periods, both of which improve the yield of this bacterium. These variations in laboratory practices contribute significantly to differences in the observed 2-year cumulative prevalences of several clinically important organisms in CF patients. These differences are most pronounced in the young. The contribution of each specific part of the complete protocol that accounted for the differences cannot be entirely determined because a site that completed one part of the protocol often completed the other parts as well and sample sizes allowing comparison of sites that used one part, with all other parts being equally employed or not employed, became too small. One specific part did, however, independently account for much of the variance: the more frequently cultures were obtained, the higher the observed prevalences for these bacteria. It appears likely that these differences in practice will affect estimates of the effect of these organisms on the clinical outcome.
This is the first large-scale survey of actual microbiological practices at a large number of CF patient care sites, representing over 14,000 CF patients. Several conclusions can be drawn from this survey. Substantial between-site differences exist in the protocols used for culturing the respiratory tracts of CF patients. This is particularly true for the use of throat swabs and thus affects the detection ofS. aureus, P. aeruginosa, and B. cepacia most in the young CF patient. This results in significant differences in 2-year cumulative prevalences of bacteria between sites using complete protocols and those using partial protocols. Early detection of these organisms in this young CF patient population may significantly alter the therapy prescribed. In recent antibiotic trials, the degree of reduction of sputum bacterial colony counts correlated with the degree of reversal of airway obstruction in CF patients (18, 19). Hence, early detection of those microbes associated with greater airway obstruction at an earlier age in these patients (12) may motivate earlier appropriate antibiotic intervention and slow the development of airway obstruction in these patients. Finally, further communication among sites to routinely employ standard practices, as recommended by the CF Foundation and by a recent study by Burns et al. (3), will be valuable in improving the rates of detection of potentially pathogenic organisms associated with CF and may lead to improved infection control practices and allow for more-accurate measurement of the impact of new antimicrobial therapies in CF.
ACKNOWLEDGMENTS
This work was financially supported by Genentech, Inc.
We thank Paul Quie and C. Carlyle Clawson for their assistance with this article.
FOOTNOTES
- Received 14 September 1998.
- Accepted 17 November 1998.
- Copyright © 1999 American Society for Microbiology
