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Published on: December 8, 2014
Are Antimotility Agents Safe for Use in Clostridioides difficile Infections? Results From an Observational Study in
Carla Kuon1, Rae Wannier1, David Sterken1
1Division of Hospital Medicine, University of California, San Francisco, San Francisco.
Objectives:
To evaluate the safety of antimotility agents (AAs) in a population of patients with hematologic malignancies and concurrent Clostridioides difficile infection (CDI) and to describe the outcomes of AA use in a hospital setting.
Patients And Methods:
We used the electronic health record to identify patients who were hospitalized in the adult malignant hematology service who had 1 or more toxin-positive C difficile stool assay between April 1, 2012, and September 21, 2017. We reviewed medical charts to obtain information on the use of AAs and any subsequent gastrointestinal complications.
Results:
There were 339 patients who were stool toxin positive for CDI during the study period. Of those, 94 patients (27%) were prescribed AAs within 14 days of CDI diagnosis. All patients received CDI antimicrobial therapy within the first 24 hours. There were 2 adverse gastrointestinal events in the group that received AAs and 6 in the group that did not receive AAs. The risk of adverse events did not differ between patients who received AAs and those who did not (adjusted odds ratio, 0.36; 95% CI, 0.06 to 2.10). The mean age of the full cohort was 52.7±15.5 years, and the mean length of stay was 26.7±22.6 days. Early AA use (<48 hours of diagnosis) was not associated with increased adverse effects.
Conclusion:
There was no increase in the incidence of gastrointestinal events in the arm that used AAs compared with the control arm. The evidence suggests that for patients with hematologic malignancies and CDI, the addition of AAs to appropriate antimicrobial therapy poses no additional risk.
Insights
Antimotility agents (AAs) are safe for patients with hematologic malignancies and Clostridioides difficile infection (CDI). Adding AAs to standard antimicrobial therapy did not increase gastrointestinal complications in this patient group.
Area of Science:
- Hematology
- Infectious Diseases
- Pharmacology
Background:
- Clostridioides difficile infection (CDI) is a significant concern in immunocompromised patients, particularly those with hematologic malignancies.
- Antimotility agents (AAs) are sometimes used to manage diarrhea but their safety in the context of CDI in this vulnerable population requires careful evaluation.
Purpose of the Study:
- To assess the safety and outcomes of using antimotility agents (AAs) in patients with hematologic malignancies experiencing Clostridioides difficile infection (CDI).
- To determine if AA use is associated with increased gastrointestinal complications in hospitalized patients with concurrent hematologic malignancy and CDI.
Main Methods:
- Retrospective electronic health record review of patients with hematologic malignancies and positive CDI stool assays between April 2012 and September 2017.
- Chart review to collect data on AA use, timing, and subsequent gastrointestinal complications.
Main Results:
- Out of 339 CDI patients, 94 (27%) received AAs. All patients received appropriate CDI antimicrobial therapy within 24 hours.
- The incidence of adverse gastrointestinal events was similar between patients who received AAs (2 events) and those who did not (6 events).
- Adjusted odds ratio for adverse events was 0.36 (95% CI, 0.06 to 2.10), indicating no significant difference in risk. Early AA use (<48 hours) was also not associated with increased adverse effects.
Conclusions:
- The use of antimotility agents (AAs) in patients with hematologic malignancies and concurrent Clostridioides difficile infection (CDI) did not lead to an increased incidence of gastrointestinal events.
- Adding AAs to standard antimicrobial therapy for CDI in this high-risk population appears to be safe and does not pose additional risks.
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