Clostridium difficile infection: epidemiology, risk factors and management

被引:247
作者
Ananthakrishnan, Ashwin N. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA 02114 USA
关键词
INFLAMMATORY-BOWEL-DISEASE; ANTIBIOTIC-ASSOCIATED DIARRHEA; PCR RIBOTYPE 027; INTRAVENOUS IMMUNOGLOBULIN; HYPERVIRULENT STRAIN; TREATMENT STRATEGIES; TOXIN-A; COLITIS; VANCOMYCIN; METRONIDAZOLE;
D O I
10.1038/nrgastro.2010.190
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The epidemiology of Clostridium difficile infection (CDI) has changed over the past decade. There has been a dramatic worldwide increase in its incidence, and new CDI populations are emerging, such as those with community-acquired infection and no previous exposure to antibiotics, children, pregnant women and patients with IBD. Diagnosis of CDI requires identification of C. difficile toxin A or B in diarrheal stool. The accuracy of current diagnostic tests remains inadequate and the optimal diagnostic testing algorithm has not been defined. The first-line agents for CDI treatment are metronidazole and vancomycin, with the latter being the preferred agent in patients with severe disease as it has significantly superior efficacy. The incidence of metronidazole treatment failures has increased, emphasizing the need to find alternative treatment options. Disease recurrence continues to occur in 20-40% of patients and its treatment remains challenging. In patients with CDI who develop fulminant colitis, early surgical consultation is essential. Intravenous immunoglobulin and tigecycline have been used in patients with severe refractory disease but delaying surgery may be associated with worse outcomes. Infection control measures are key to prevent horizontal transmission of infection. Ongoing research into effective treatment protocols and prevention is essential.
引用
收藏
页码:17 / 26
页数:10
相关论文
共 90 条
  • [1] Abougergi Marwan S, 2010, J Hosp Med, V5, pE1, DOI 10.1002/jhm.542
  • [2] Excess hospitalisation burden associated with Clostridium difficile in patients with inflammatory bowel disease
    Ananthakrishnan, A. N.
    McGinley, E. L.
    Binion, D. G.
    [J]. GUT, 2008, 57 (02) : 205 - 210
  • [3] Clostridium Difficile and Inflammatory Bowel Disease
    Ananthakrishnan, Ashwin N.
    Issa, Mazen
    Binion, David G.
    [J]. GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 2009, 38 (04) : 711 - +
  • [4] Treatment of Clostridium difficile-associated disease:: old therapies and new strategies
    Aslam, S
    Hamill, R
    Musher, DM
    [J]. LANCET INFECTIOUS DISEASES, 2005, 5 (09) : 549 - 557
  • [5] Clinical features of Clostridium difficile-associated diarrhoea due to binary toxin (actin-specific ADP-ribosyltransferase)-producing strains
    Barbut, F
    Decré, D
    Lalande, V
    Burghoffer, A
    Noussair, L
    Gigandon, A
    Espinasse, F
    Raskine, L
    Robert, J
    Mangeol, A
    Branger, C
    Petit, JC
    [J]. JOURNAL OF MEDICAL MICROBIOLOGY, 2005, 54 (02) : 181 - 185
  • [6] ANTIBIOTIC-ASSOCIATED PSEUDOMEMBRANOUS COLITIS DUE TO TOXIN-PRODUCING CLOSTRIDIA
    BARTLETT, JG
    CHANG, TW
    GURWITH, M
    GORBACH, SL
    ONDERDONK, AB
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (10) : 531 - 534
  • [7] Antibiotic-associated diarrhea
    Bartlett, JG
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (05) : 334 - 339
  • [8] The case for vancomycin as the preferred drug for treatment of Clostridium difficile infection
    Bartlett, John G.
    [J]. CLINICAL INFECTIOUS DISEASES, 2008, 46 (10) : 1489 - 1492
  • [9] Historical perspectives on studies of Clostridium difficile and C difficile infection
    Bartlett, John G.
    [J]. CLINICAL INFECTIOUS DISEASES, 2008, 46 : S4 - S11
  • [10] Clinical recognition and diagnosis of Clostridium difficile infection
    Bartlett, John G.
    Gerding, Dale N.
    [J]. CLINICAL INFECTIOUS DISEASES, 2008, 46 : S12 - S18