期刊论文详细信息
BMC Infectious Diseases
A unique strain of community-acquired Clostridium difficile in severe complicated infection and death of a young adult
Michael R Mulvey1  Kathleen Coard3  Karen Roye-Green2  Orville D Heslop2 
[1]National Microbiology Laboratory, 1015 Arlington Street, Winnipeg MB R3E 3R2, Canada
[2]Department of Microbiology, University of the West Indies, Kingston, Jamaica
[3]Department of Pathology, University of the West Indies, Kingston, Jamaica
关键词: Toxic Megacolon;    Pseudomembranous Colitis;    Clindamycin;    Diarrhoea;    Community-Acquired Infection;    Klebsiella pneumoniae;    Clostridium difficile;   
Others  :  1147274
DOI  :  10.1186/1471-2334-13-299
 received in 2013-01-11, accepted in 2013-06-21,  发布年份 2013
PDF
【 摘 要 】

Background

Clostridium difficile is the major cause of nosocomial antibiotic-associated diarrhoea with the potential risk of progressing to severe clinical outcomes including death. It is not unusual for Clostridium difficile infection to progress to complications of toxic megacolon, bowel perforation and even Gram-negative sepsis following pathological changes in the intestinal mucosa. These complications are however less commonly seen in community-acquired Clostridium difficile infection than in hospital-acquired Clostridium difficile infection. To the best of our knowledge, this was the first case of community-acquired Clostridium difficile infection of its type seen in Jamaica.

Case presentation

We report a case of a 22-year-old female university student who was admitted to the University Hospital of the West Indies, Jamaica with a presumptive diagnosis of pseudomembranous colitis PMC. She presented with a 5-day history of diarrhoea following clindamycin treatment for coverage of a tooth extraction due to a dental abscess. Her clinical condition deteriorated and progressed from diarrhoea to toxic megacolon, bowel perforation and Gram-negative sepsis. Clostridium difficile NAP12/ribotype 087 was isolated from her stool while blood cultures grew Klebsiella pneumoniae. Despite initial treatment intervention with empiric therapy of metronidazole and antibiotic clearance of Klebsiella pneumoniae from the blood, the patient died within 10 days of hospital admission.

Conclusions

We believe that clindamycin used for coverage of a dental abscess was an independent risk factor that initiated the disruption of the bowel micro-flora, resulting in overgrowth of Clostridium difficile NAP12/ribotype 087. This uncommon strain, which is the same ribotype (087) as ATCC 43255, was apparently responsible for the increased severity of the infection and death following toxic megacolon, bowel perforation and pseudomembranous colitis involving the entire large bowel. K. pneumoniae sepsis, resolved by antibiotic therapy was secondary to Clostridium difficile infection. The case registers community-acquired Clostridium difficile infection as producing serious complications similar to hospital-acquired Clostridium difficile infection and should be treated with the requisite importance.

【 授权许可】

   
2013 Heslop et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150403225521735.pdf 203KB PDF download
Figure 1. 36KB Image download
【 图 表 】

Figure 1.

【 参考文献 】
  • [1]Apisarnthanarak A, Khoury H, Reinus WR, Crippin JS, Mundy LM: Severe Clostridium difficile colitis: the role of intracolonic vancomycin? Am J Med 2002, 112:329-329.
  • [2]Aslam S, Musher D: An update diagnosis, treatment, and prevention of Clostridium difficile associated disease. Gastroenterol Clin Am 2006, 35:315-335.
  • [3]Khanna S, Pardi DS, Aronson SL, Kammer PP, Orenstein R, St Sauver JL, Harmsen WS, Zinsmeister AR: The epidemiology of community acquired Clostridium difficile infection: A population based study. Am J Gastroenterol 2012, 107(1):89-95. http://www.endonurse.com/ webcite
  • [4]Bartlett JG, Chang TW, Gurwith M, Gorbach SL, Onderdonk AB: Antibiotic-associated pseudomembranous colitis due to toxin-producing clostridia. N Engl J Med 1978, 298:531-534.
  • [5]Owens RC, Donskey CJ, Gaynes RP, Loo VG, Muto CA: Antimicrobial Associated Risk Factors for Clostridium difficile Infection. Clin Infect Dis 2008, 46(Suppl 1):S19.
  • [6]Mulvey MR, Boyd DA, Gravel D, Hutchinson J, Kelly S, Mcgeer A, Moore D, Simor A, Suh KN, Taylor G, Weese S, Miller M: Hyper-virulent Clostridium difficile strains in hospitalised patients, Canada. Emerg Infect Dis 2010, 16(4):678-681.
  • [7]Cohen SH, Gerding DN, Johnson S, Kelly CP, Loo VG, McDonald LC, Pepin J, Wilcox MH: 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, 31:431-455.
  • [8]Khanna S, Pardi DS, Aronson SL, Kammer PP, Baddour LM: Outcomes in community-acquired Clostridium difficile infection. Aliment Pharmacol Ther 2012, 35(5):613-618.
  • [9]Koss K, Clark MA, Sanders DS, Morton D, Keighley MB, Goh J: The outcome of surgery in fulminant Clostridium difficile colitis. Colorectal Dis 2006, 8(2):149-154.
  • [10]Murray R, Boyd D, Levett PN, Mulvey MR, Alfa MJ: Truncation in the tcdC region of the Clostridium difficile PatLoc of clinical isolates does not predict increased biological activity of Toxin B or Toxin A. BMC Infect Dis 2009, 9:103. BioMed Central Full Text
  • [11]Urbán E, Brazier JS, Sóki J, Nagy E, Duerden BI: PCR ribotyping of clinically important Clostridium difficile strains from Hungary. J Med Microbiol 2001, 50:1082-1086.
  • [12]Sayedy L, Kothari D, Richards RJ: Toxicmegacolon associated Clostridium difficile colitis. World J Gastrointest Endosc 2010, 2(8):293-297.
  文献评价指标  
  下载次数:16次 浏览次数:28次