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Invited Commentary
July 22, 2013

Clostridium difficile Leaves the Hospital—What’s Next?

Author Affiliations
  • 1Infectious Disease Service, Memorial Sloan-Kettering Cancer Center, and Department of Medicine, Weill Cornell Medical College, New York, New York

Copyright 2013 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.

JAMA Intern Med. 2013;173(14):1367-1368. doi:10.1001/jamainternmed.2013.7940

Since their introduction after World War II, antibiotics have been known to cause gastrointestinal problems, including nausea and diarrhea. By the late 1970s, Clostridium difficile was put forward as the cause of a large proportion of cases of diarrhea,1 and the hunt began for an optimal control strategy. At first, control of the situation seemed easy: clindamycin, an agent with potent anaerobic activity, was implicated, a connection that made biologic sense and was supported by the newly developed hamster model.2 Better yet, less clindamycin use resulted in less C difficile, at least early on, and the problem briefly came under control.3

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