Volume 17, Number 10—October 2011
Clostridium difficile Infection in Outpatients, Maryland and Connecticut, USA, 2002–2007
Clostridium difficile, the most commonly recognized diarrheagenic pathogen among hospitalized persons, can cause outpatient diarrhea. Of 1,091 outpatients with diarrhea, we found 43 (3.9%) who were positive for C. difficile toxin. Only 7 had no recognized risk factors, and 3 had neither risk factors nor co-infection with another enteric pathogen.
In the United States, ≈375 million episodes of acute diarrhea occur annually (1). Among hospitalized persons, toxin-producing Clostridium difficile is a primary diarrheagenic pathogen, usually as a consequence of normal bowel flora distortion caused by antimicrobial drug therapy (2,3). C. difficile infection (CDI) complicates and prolongs hospital stays, leading to increases in health care costs, illness, and death. Recent reports suggest increases in community-onset CDI among persons without recent antimicrobial drug treatment or hospitalization. We describe a prospective evaluation of CDI in persons with diarrhea who visited emergency departments (EDs) and ambulatory primary care clinics in Baltimore, Maryland, and New Haven, Connecticut, and identify microbiologic causes and epidemiologic characteristics of diarrhea. This report highlights cases of outpatient CDI, identifies factors associated with infection, and describes molecular strain characterization.
Patients seeking medical attention for community-onset diarrheal illnesses were enrolled from May 2002 through September 2004 in the EDs and ambulatory clinics at Yale–New Haven Hospital (New Haven, CT, USA) and from May 2002 through July 2007 at EDs and clinics affiliated with the University of Maryland (Baltimore, MD, USA) (4).
Informed consent for stool sample collection, initial and follow-up patient interviews, and medical records review was obtained from primarily urban and suburban residents, or parents/guardians for minors, who sought treatment for self-identified primary or secondary diarrhea. This research was approved by the institutional review boards at all participating institutions.
Participants were interviewed at outpatient clinics to assess health status, symptoms, and potential exposures to enteric pathogens, and at follow-up to determine the duration of diarrhea, whether treatment was administered, or whether hospitalization resulted from the initial visit. Stool samples collected during the visit or provided within 48 h and kept cool were homogenized and transferred into multiple vials for storage at –80°C.
An outpatient CDI case was defined as in outpatient with diarrhea whose stool was positive for C. difficile toxins by enzyme immunoassay (TOX A/B II ELISA; TechLab, Blacksburg, VA, USA). Presumptive non–health care–associated (NHA) CDI was defined by the absence of an overnight stay at an inpatient healthcare facility over the previous month.
Traditional risk factors for CDI that were investigated included antimicrobial drug use within the past month, age >65 years, serious underlying illness/weakened immune system, history of bowel or ulcer surgery, colon disease, previous CDI, and recent hospitalization. Statistical analysis was done by using SAS version 9.2 (SAS Institute, Inc., Cary, NC, USA). All p values reported are 2-sided, with no correction for multiple comparisons; p<0.05 was considered significant.
C. difficile toxin–positive stool specimens, in 1-mL aliquots, were shipped frozen to the Centers for Disease Control and Prevention (Atlanta, GA, USA) anaerobe laboratory for culturing by direct inoculation onto cycloserine cefoxitin fructose agar (CCFA) or ethanol shock, followed by CCFA inoculation. Cultures were incubated for 48–72 h at 35°C under anaerobic conditions and examined for characteristic yellow-green fluorescence under long-wave ultraviolet light and CCFAp-cresol odor. C. difficile colonies were confirmed with indole (negative) and PRO disk (positive; Remel, Lenexa, KS, USA) tests.
Pulsed-field gel electrophoresis was performed on C. difficile genomic DNA digested with SmaI, and toxinotyping was performed (5). Binary toxin was assayed by PCR for cdtB (6). Deletions in tcdC were detected (7).
C. difficile toxin tests were performed on 1,091/1,197 stool specimens; 43 (3.9%) of these case-patients met the case definition for outpatient CDI. The mean age of these case-patients was 43.7 years (range 4 months–88 years). Outpatient CDI case-patients were younger at Yale because a significantly greater proportion of toxin-positive children were recruited at Yale (45.5%) than at the University of Maryland (15.6%) (p = 0.04). The 43 outpatient CDI case-patients included 5 infants <1 year of age, 5 children 1–18 years of age, 23 adults 19–64 years of age, and 10 adults >65 years of age; 21 were Caucasian, 18 were African American, and 4 were of other or unknown race/ethnicity (22 male and 21 female case-patients).
Most case-patients (36/43, 83.7%) had a recognized underlying risk factor. Twenty-seven (62.8%) had received systemic antimicrobial drugs, including ciprofloxacin, gaitifloxacin, amoxicillin, ampicillin/sulbactam, piperacillin/tazobactam, cefpodoxime, vancomycin, clindamycin, metronidazole, erythromycin, or trimethoprim/sulfamethoxazole within the preceding month; 14 (32.6%) had been hospitalized; and 15 (34.9%) had chronic illnesses or had undergone bowel surgery that potentially affect immune status or gastrointestinal function (Table 1). Two persons, 1 with AIDS and 1 who underwent a previous bowel resection for diverticulitis, had been treated in the past month for CDI. Only 7 (16.3%) patients had NHA-CDI infections without identified risk factors; 3 were infants (<1 year), 1 was a child (1–18 years), 3 were adults (19–64 years), and none were elderly (>65 years) (Table 2).
The 43 outpatient CDI case-patients were compared with the other 1,048 persons in which C. difficile toxin had not been detected. Persons with CDI were, on average, significantly older than others with diarrhea, 43.7 years vs. 29.2 years, respectively (p<0.01). Outpatient CDI case-patients were more likely than C. difficile–negative patients to have medical or surgical conditions (34.9% vs.16.8%, p<0.001), been recently hospitalized (32.6% vs. 8.8%, p<0.001), or to have used antimicrobial drugs (62.8% vs. 22.0%, p<0.001).
Co-infections with other enteric pathogens were common among CDI case-patients, including C. perfringens (3), rotavirus (5), norovirus (3), sapovirus (2), and 1 each with hookworm, Bacillus cereus, astrovirus, and adenovirus. The likelihood of co-infection was similar in patients with (12/36 [33.3%]) and without (3/7 [42.9%]) risk factors (p>0.1).
Of 43 C. difficile toxin–positive stools initially tested, 39 stool samples were submitted to the Centers for Disease Control and Prevention for anaerobic culture and C. difficile was isolated from 31 samples. Binary toxin was identified in 12 (38.7%). Pulsed-field gel electrophoresis identified 15 different types (Figure). No associations were found between risk factors, including age, and strain or toxinotype (data not shown).
NHA-CDI has been recognized for >12 years, and recent reports suggest that disease occurs without patient’s known exposure to antimicrobial drugs or other previously identified risk factors (2,8–13). Although we found a proportion of C. difficile–positive diarrheal stools similar to that of 2 other recent prospective studies that used confirmatory culture (i.e., 1.5%–3.9%) for outpatient CDI (7,13,14), we also found a lower proportion of outpatient CDI cases without recognized risk factors of recent hospitalization, chronic medical conditions, recent antimicrobial drug exposure, or co-infection than did those studies.
One limitation of our study was using retrospective self-reporting for assessment of hospitalizations or antimicrobial drug use in the previous month, which potentially can result in recall bias. Also, antimicrobial drug therapy was assessed for only 4 weeks before diarrhea onset; exposure to antimicrobial drugs for a period longer than 1 month before patient seeks treatment may present a risk for CDI. In addition, this study was conducted at 2 urban centers in the eastern United States and may not be generalizable to other locations or clinical settings. Finally, although enzyme immunoassay detection for C. difficile was the standard of care at the time of the study, it is now considered too insensitive to be used as a stand-alone diagnostic test (15).
In summary, we detected toxigenic C. difficile in a similar proportion of patients to those reported in other studies of CDI. However, all but 3 patients had either known risk factors for CDI or other pathogens potentially responsible for their illness; 1 was <1 year of age. C. difficile isolates responsible for outpatient CDI are genetically diverse. An evolving picture of widespread, frequent CDI among outpatients without risk factors should be tempered by these findings.
Dr Hirshon is an associate professor in the Departments of Emergency Medicine and Epidemiology and Public Health at the University of Maryland School of Medicine. His research interests include developing emergency departments as sites for surveillance and hypothesis- driven research in public health.
We thank Susan Bell, Shirley Tirrell, Carol Lyons, Judith Johnson, Baiba Pironis, Kathy Strauss, and Sandra Strauss for specimen testing and processing and Terry Rabatsky-Ehr, Janet Laymann, Jill Heckendorf, Sue Henderson, Jennifer Withrow, and Kawthar Muhammad for participant enrollment and data collection.
Funding for this study was provided by the National Center for Infectious Diseases of the Centers for Disease Control and Prevention (grant no. U01CI000296), the American Association of Medical Colleges (grant no. MM0205-02/02).
- Herikstad H, Yang S, Van Gilder TJ, Vugia D, Hadler J, Blake P, A population-based estimate of the burden of diarrhoeal illness in the United States: FoodNet, 1996–7. Epidemiol Infect. 2002;129:9–17.
- Kelly CP, LaMont JT. Clostridium difficile—more difficult than ever. N Engl J Med. 2008;359:1932–40.
- McDonald LC, Coignard B, Dubberke E, Song X, Horan T, Kutty PK. Ad Hoc Clostridium difficile Surveillance Working Group. Recommendations for surveillance of Clostridium difficile–associated disease. Infect Control Hosp Epidemiol. 2007;28:140–5. Epub 2007 Jan 25.
- Nataro JP, Mai V, Johnson J, Blackwelder WC, Heimer R, Tirrell S, Diarrheagenic E. coli in Baltimore and New Haven. Clin Infect Dis. 2006;43:402–7. Epub 2006 Jul 11.
- Rupnik M, Avesani V, Janc M, von Eichel-Streiber C, Delmée M. A novel toxinotyping scheme and correlation of toxinotypes with serogroups of Clostridium difficile isolates. J Clin Microbiol. 1998;36:2240–7.
- Stubbs S, Rupnik M, Gibert M, Brazier J, Duerden B, Popoff M. Production of actin-specific ADP-ribosyltransferase (binary toxin) by strains of Clostridium difficile. FEMS Microbiol Lett. 2000;186:307–12.
- Killgore G, Thompson A, Johnson S, Brazier J, Kuijper E, Pepin J, Comparison of seven techniques for typing international epidemic strains of Clostridium difficile: restriction endonuclease analysis, pulsed-field gel electrophoresis, PCR-ribotyping, multilocus sequence typing, multilocus variable-number tandem-repeat analysis, amplified fragment length polymorphism, and surface layer protein A gene sequence typing. J Clin Microbiol. 2008;46:431–7. Epub 2007 Nov 26.
- Blossom DB, McDonald LC. The challenges posed by reemerging Clostridium difficile infection. Clin Infect Dis. 2007;45:222–7. Epub 2007 Jun 4.
- Centers for Disease Control and Prevention. Surveillance for community-associated Clostridium difficile—Connecticut, 2006. MMWR Morb Mortal Wkly Rep. 2008;57:340–3.
- Karlström O, Fryklund B, Tullus K, Burman LG, and the Swedish C. difficile Study Group. A prospective nationwide study of Clostridium difficile–associated diarrhea in Sweden. Clin Infect Dis. 1998;26:141–5.
- Kutty PK, Benoit SR, Woods CW, Sena AC, Naggie S, Frederick J, Assessment of Clostridium difficile–associated disease surveillance definitions, North Carolina, 2005. Infect Control Hosp Epidemiol. 2008;29:197–202.
- Lambert PJ, Dyck M, Thompson LH, Hammond GW. Population-based surveillance of Clostridium difficile infection in Manitoba, Canada, by using interim surveillance definitions. Infect Control Hosp Epidemiol. 2009;30:945–51.
- Bauer MP, Veenendaal D, Verhoef L, Bloembergen P, van Dissel JT, Kuijper EJ. Clinical and microbiological characteristics of community-onset Clostridium difficile infection in The Netherlands. Clin Microbiol Infect. 2009;15:1087–92.
- Wilcox MH, Mooney L, Bendall R, Settle CD, Fawley WN. A case-control study of community-associated Clostridium difficile infection. J Antimicrob Chemother. 2008;62:388–96.
- Cohen SH, Gerding DN, Johnson S, Kelly CP, Loo VG, McDonald LC, Clinical practice guidelines for Clostridium difficile infection in adults: 2010 update by the Society for Healthcare Epidemiology of America (SHEA) and the Infectious Diseases Society of America (IDSA). Infect Control Hosp Epidemiol. 2010;31:431–55.
Suggested citation for this article: Hirshon JM, Thompson AD, Limbago B, McDonald LC, Bonkosky M, Heimer R, et al. Clostridium difficile infection in outpatients, Maryland and Connecticut, USA, 2002–2007. Emerg Infect Dis [serial on the Internet]. 2011 Oct [date cited]. http://dx.doi.org/10.3201/eid1710.110069
- Page created: September 26, 2011
- Page last updated: September 26, 2011
- Page last reviewed: September 26, 2011
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)