Korean J Gastroenterol.  2009 Jul;54(1):13-19. 10.4166/kjg.2009.54.1.13.

Clinical Characteristics and Changing Epidemiology of Clostridium difficile-Associated Disease (CDAD)

Affiliations
  • 1Department of Internal Medicine, Hanyang University College of Medicine, Guri, Korea. hands@hanyang.ac.kr
  • 2Department of Laboratory Medicine, Hanyang University College of Medicine, Guri, Korea.

Abstract

BACKGROUND/AIMS
The spectrum of Clostridium difficile-associated disease (CDAD) ranges from mild diarrhea to life-threatening colitis. Recent studies reported an increase in incidence and severity of CDAD and the presence of severe community-acquired CDAD (CA-CDAD). The aims of this study were to investigate the incidence of CA-CDAD and non-antibiotics-associated CDAD, and to compare the clinical characteristics between hospital-acquired (HA) and CA-CDAD. METHODS: The medical records of 86 patients who were diagnosed as CDAD in Hanyang University Guri Hospital between January 2005 and October 2007 were retrospectively reviewed. RESULTS: Of the 86 patients (mean age 64 years), 53 patients were women. The most frequently prescribed antibiotics were cephalosporins (67.4%), followed by aminoglycosides (38.4%) and quinolones (14%). Of the 86 patients, the average duration of treatment and recovery time of symptoms were 11.5 days and 4.6 days, respectively. Seven percent of patients experienced relapse treatment. The overall incidence rate of CA-CDAD and non-antibiotics-associated CDAD were 10.5% and 22.1%, respectively. CA-CDAD group had lower rate of antimicrobial exposure whilst showing higher rate of complications compared to HA-CDAD group. Three patients in the CA-CDAD progressed towards a severe complicated clinical course, including septic shock. CONCLUSIONS: The incidence rate of CA-CDAD and non-antibiotics-associated CDAD were 10.5% and 22.1%, respectively. CA-CDAD tends to have a higher complication rate compared to HA-CDAD. Community clinicians needs to maintain a high level of suspicion for CDAD, whilst coping with the ever evolving epidemiologic change.

Keyword

Clostridium difficile; Clostridium difficile-associated disease (CDAD); Community-acquired C. difficile-associated disease (CA-CDAD)

MeSH Terms

Adult
Aged
Aged, 80 and over
Aminoglycosides/therapeutic use
Anti-Bacterial Agents/therapeutic use
Bacterial Toxins/analysis
Cephalosporins/therapeutic use
*Clostridium difficile
Community-Acquired Infections/epidemiology
Cross Infection/epidemiology
Enterocolitis, Pseudomembranous/*diagnosis/drug therapy/epidemiology
Enterotoxins/analysis
Female
Humans
Male
Metronidazole/therapeutic use
Middle Aged
Quinolones/therapeutic use
Retrospective Studies

Cited by  2 articles

Current epidemiology and treatment of Clostridium difficile infection
Hyunjoo Pai
Infect Chemother. 2010;42(6):362-368.    doi: 10.3947/ic.2010.42.6.362.

Epidemiology and Clinical Characteristics of Clostridium difficile-associated Disease in Children: Comparison between Community- and Hospital-acquired Infections
Hye Jung Cho, Eell Ryoo, Yong Han Sun, Kang Ho Cho, Dong Woo Son, Hann Tchah
Korean J Pediatr Gastroenterol Nutr. 2010;13(2):146-153.    doi: 10.5223/kjpgn.2010.13.2.146.


Reference

1. Larson HE, Price AB, Honour P, et al. Clostridium difficile and the aetiology of pseudomembranous colitis. Lancet. 1978; 1:1063–1066.
2. Bartlett JG, Chang TW, Gurwith M, et al. Antibiotic-associated pseudomembranous colitis due to toxin-producing clostridia. N Engl J Med. 1978; 298:531–534.
Article
3. Fekety R, Shah A. Diagnosis and treatment of C. difficile colitis. JAMA. 1993; 269:71–75.
4. Kelly CP, Pothoulakis C, LaMont JT. Clostridium difficile colitis. N Engl J Med. 1994; 330:257–262.
5. Loo VG, Poirier L, Miller MA, et al. A predominantly clonal multiinstitutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality. N Engl J Med. 2005; 353:2442–2449.
6. Pepin J, Valiquette L, Cossette B. Mortality attributable to nosocomial Clostridium difficile-associated disease during an epidemic caused by a hypervirulent strain in Quebec. Can Med Assoc J. 2005; 173:1037–1042.
7. Pepin J, Valiquette L, Alary ME, et al. Clostridium difficile-associated diarrhea in a region of Quebec from 1991 to 2003: a changing pattern of disease severity. Can Med Assoc J. 2004; 171:466–472.
8. Hubert B, Loo VG, Bourgault AM, et al. Portrait of the geo-graphic dissemination of the Clostridium difficile North American pulsed-field type 1 strain and the epidemiology of C. difficile-associated disease in Quebec. Clin Infect Dis. 2007; 44:238–244.
9. McDonald LC, Killgore GE, Thompson A, et al. An epidemic, toxin genevariant strain of Clostridium difficile. N Engl J Med. 2005; 353:2433–2441.
10. Muto CA, Pokrywka M, Shutt K, et al. A large outbreak of Clostridium difficile-associated disease with an unexpected proportion of deaths and colectomies at a teaching hospital following increased fluoroquinolone use. Infect Control Hosp Epidemiol. 2005; 26:273–280.
11. Kazakova SV, Ware K, Baughman B, et al. A hospital outbreak of diarrhea due to an emerging epidemic strain of Clostridium difficile. Arch Intern Med. 2006; 166:2518–2524.
12. Morinville V, McDonald J. Clostridium difficile-associated diarrhea in 200 Canadian children. Can J Gastroenterol. 2005; 19:497–501.
13. MMWR. Severe Clostridium difficile-associated disease in populations previously at low risk - four states, 2005. MMWR Morb Mortal Wkly Rep. 2005; 54:1201–1205.
14. Dial S, Delaney JAC, Barkun AN, Suissa S. Use of gastric acid-suppressive agents and the risk of community-acquired Clostridium difficile-associated disease. JAMA. 2005; 294:2989–2995.
15. Warny M, Pepin J, Fang A, et al. Toxin production by an emerging strain of Clostridium difficile associated with outbreaks of severe disease in North America and Europe. Lancet. 2005; 366:1079–1084.
16. Voth DE, Ballard JD. Clostridium difficile toxins: mechanism of action and role in disease. Clin Microbiol Rev. 2005; 18:247–263.
17. Spigaglia P, Mastrantonio P. Molecular analysis of the patho-genicity locus and polymorphism in the putative negative reg-ulator of toxin production (TcdC) among Clostridium difficile clinical isolates. J Clin Microbiol. 2002; 40:3470–3475.
18. 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; 186:307–312.
19. Geric B, Johnson S, Gerding DN, Grabnar M, Rupnik M. Frequency of binary toxin genes among Clostridium difficile strains that do not produce large clostridial toxins. J Clin Microbiol. 2003; 41:5227–5232.
20. Goncalves C, Decre D, Barbut F, Burghoffer B, Petit JC. Prevalence and characterization of a binary toxin (actin-spe-cific ADP-ribosyltransferase) from Clostridium difficile. J Clin Microbiol. 2004; 42:1933–1939.
21. Rupnik M GM, Geric B. Binary toxin producing Clostridium difficile strains. Anaerobes. 2003; 9:289–294.
22. Kim JH, Kim HJ, Ku NS, et al. Prognosis factors of Clostridium difficile associated diarrhea. Infect Chemother. 2007; 39:71–77.
23. Brazier JS. The diagnosis of Clostridium difficile-associated disease. J Antimicrob Chemother. 1998; 41:29–40.
24. Riley TV, Cooper M, Bell B, Golledge CL. Community-acquired Clostridium difficile-associated diarrhea. Clin Infect Dis. 1995; 20:S263–265.
25. Barbut F, Decre D, Lalande V, et al. Clinical features of Clostridium difficile-associated diarrhoea due to binary toxin (actin-specific ADP-ibosyltransferase)-producing strains. J Med Microbiol. 2005; 54:181–185.
26. CDC. Surveillance for community-associated Clostridium difficile–Connecticut, 2006. MMWR Morb Mortal Wkly Rep. 2008; 57:340–343.
27. Songer JG, Anderson MA. Clostridium difficile: an important pathogen of food animals. Anaerobe. 2006; 12:1–4.
28. Baverud V. Clostridium difficile infections in animals with special reference to the horse. A review. Vet Q. 2002; 24:203–219.
29. Hammitt MC, Bueschel DM, Keel MK, et al. A possible role for Clostridium difficile in the etiology of calf enteritis. Vet Microbiol. 2007; 127:343–352.
30. Lee CR, Lee JK, Cho YS, Yoo HM, Kim WH, Lee KW. A clinical investigation of Clostridium difficile-associated disease. Korean J Gastroenterol. 1999; 33:338–347.
31. Cheong HS, Kim JK, Lim TK, et al. Therapeutic efficacy of metronidazole for patients with Clostridium difficile-associated diarrhea. Korean J Med. 2007; 72:639–646.
32. Shin BM, Kuak EY, Yoo HM, et al. Multicentre study of the prevalence of toxigenic Clostridium difficile in Korea: results of a retrospective study 2000-2005. J Med Microbiol. 2008; 57:697–701.
Full Text Links
  • KJG
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr