<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>55(5)</volume><submitter>Truong CY</submitter><pubmed_abstract>Health care-onset health care facility-associated &lt;i>Clostridium difficile&lt;/i> infection (HO-CDI) is overdiagnosed for several reasons, including the high prevalence of &lt;i>C. difficile&lt;/i> colonization and the inability of hospitals to limit testing to patients with clinically significant diarrhea. We conducted a quasiexperimental study from 22 June 2015 to 30 June 2016 on consecutive inpatients with &lt;i>C. difficile&lt;/i> test orders at an academic hospital. Real-time electronic patient data tracking was used by the laboratory to enforce testing criteria (defined as the presence of diarrhea [?3 unformed stools in 24 h] and absence of laxative intake in the prior 48 h). Outcome measures included &lt;i>C. difficile&lt;/i> test utilization, HO-CDI incidence, oral vancomycin utilization, and clinical complications. During the intervention, 7.1% (164) and 9.1% (211) of 2,321 &lt;i>C. difficile&lt;/i> test orders were canceled due to absence of diarrhea and receipt of laxative therapy, respectively. &lt;i>C. difficile&lt;/i> test utilization decreased upon implementation from an average of 208.8 tests to 143.0 tests per 10,000 patient-days (&lt;i>P&lt;/i> &lt; 0.001). HO-CDI incidence rate decreased from an average of 13.0 cases to 9.7 cases per 10,000 patient-days (&lt;i>P&lt;/i> = 0.008). Oral vancomycin days of therapy decreased from an average of 13.8 days to 9.4 days per 1,000 patient-days (&lt;i>P&lt;/i> = 0.009). Clinical complication rates were not significantly different in patients with 375 canceled orders compared with 869 episodes with diarrhea but negative &lt;i>C. difficile&lt;/i> results. Real-time electronic clinical data tracking is an effective tool for verification of &lt;i>C. difficile&lt;/i> clinical testing criteria and safe reduction of inflated HO-CDI rates.</pubmed_abstract><journal>Journal of clinical microbiology</journal><pagination>1276-1284</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5405247</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Real-Time Electronic Tracking of Diarrheal Episodes and Laxative Therapy Enables Verification of Clostridium difficile Clinical Testing Criteria and Reduction of Clostridium difficile Infection Rates.</pubmed_title><pmcid>PMC5405247</pmcid><pubmed_authors>Schroeder LF</pubmed_authors><pubmed_authors>Banaei N</pubmed_authors><pubmed_authors>Wilson R</pubmed_authors><pubmed_authors>Shah N</pubmed_authors><pubmed_authors>Holubar M</pubmed_authors><pubmed_authors>Deresinski S</pubmed_authors><pubmed_authors>Sundararajan G</pubmed_authors><pubmed_authors>Madison A</pubmed_authors><pubmed_authors>Shepard J</pubmed_authors><pubmed_authors>Gombar S</pubmed_authors><pubmed_authors>Tekic N</pubmed_authors><pubmed_authors>Tompkins L</pubmed_authors><pubmed_authors>Truong CY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Real-Time Electronic Tracking of Diarrheal Episodes and Laxative Therapy Enables Verification of Clostridium difficile Clinical Testing Criteria and Reduction of Clostridium difficile Infection Rates.</name><description>Health care-onset health care facility-associated &lt;i>Clostridium difficile&lt;/i> infection (HO-CDI) is overdiagnosed for several reasons, including the high prevalence of &lt;i>C. difficile&lt;/i> colonization and the inability of hospitals to limit testing to patients with clinically significant diarrhea. We conducted a quasiexperimental study from 22 June 2015 to 30 June 2016 on consecutive inpatients with &lt;i>C. difficile&lt;/i> test orders at an academic hospital. Real-time electronic patient data tracking was used by the laboratory to enforce testing criteria (defined as the presence of diarrhea [?3 unformed stools in 24 h] and absence of laxative intake in the prior 48 h). Outcome measures included &lt;i>C. difficile&lt;/i> test utilization, HO-CDI incidence, oral vancomycin utilization, and clinical complications. During the intervention, 7.1% (164) and 9.1% (211) of 2,321 &lt;i>C. difficile&lt;/i> test orders were canceled due to absence of diarrhea and receipt of laxative therapy, respectively. &lt;i>C. difficile&lt;/i> test utilization decreased upon implementation from an average of 208.8 tests to 143.0 tests per 10,000 patient-days (&lt;i>P&lt;/i> &lt; 0.001). HO-CDI incidence rate decreased from an average of 13.0 cases to 9.7 cases per 10,000 patient-days (&lt;i>P&lt;/i> = 0.008). Oral vancomycin days of therapy decreased from an average of 13.8 days to 9.4 days per 1,000 patient-days (&lt;i>P&lt;/i> = 0.009). Clinical complication rates were not significantly different in patients with 375 canceled orders compared with 869 episodes with diarrhea but negative &lt;i>C. difficile&lt;/i> results. Real-time electronic clinical data tracking is an effective tool for verification of &lt;i>C. difficile&lt;/i> clinical testing criteria and safe reduction of inflated HO-CDI rates.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 May</publication><modification>2021-02-20T20:53:47Z</modification><creation>2019-03-27T02:42:05Z</creation></dates><accession>S-EPMC5405247</accession><cross_references><pubmed>28250001</pubmed><doi>10.1128/JCM.02319-16</doi><doi>10.1128/jcm.02319-16</doi></cross_references></HashMap>