{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T17:10:26Z","timestamp":1785431426099,"version":"3.56.0"},"reference-count":22,"publisher":"Cambridge University Press (CUP)","issue":"3","license":[{"start":{"date-parts":[[2025,12,19]],"date-time":"2025-12-19T00:00:00Z","timestamp":1766102400000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["cambridge.org"],"crossmark-restriction":true},"short-container-title":["Infect. Control Hosp. Epidemiol."],"published-print":{"date-parts":[[2026,3]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec id=\"S0899823X25103772_as1\">\n                    <jats:title>Objective:<\/jats:title>\n                    <jats:p>\n                      To identify host and clinical risk factors contributing to the development of\n                      <jats:italic>Clostridioides difficile<\/jats:italic>\n                      infection (CDI) among colonized patients.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X25103772_as2\">\n                    <jats:title>Design:<\/jats:title>\n                    <jats:p>Retrospective, matched case-control study.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X25103772_as3\">\n                    <jats:title>Setting:<\/jats:title>\n                    <jats:p>Duke University Health System, including 3 hospitals and affiliated outpatient clinics.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X25103772_as4\">\n                    <jats:title>Participants:<\/jats:title>\n                    <jats:p>\n                      Adult patients who underwent \u22652 two-step\n                      <jats:italic>C. difficile<\/jats:italic>\n                      tests (nucleic acid amplification test (NAAT) followed by toxin enzyme immunoassay) between 03\/15\/2020\u201312\/31\/2023. Cases were patients with\n                      <jats:italic>C. difficile<\/jats:italic>\n                      colonization (NAAT+\/toxin\u2013) who converted to CDI (NAAT+\/toxin+) within 90 days; controls were colonized patients who remained toxin-negative. Cases were matched to controls by date of index testing (\u00b11 year).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X25103772_as5\">\n                    <jats:title>Methods:<\/jats:title>\n                    <jats:p>Data collection encompassed a 90-day \u201cpre-exposure\u201d period preceding index testing and a \u2264 90-day \u201cexposure\u201d period between index and repeat testing. Antibiotic use was stratified by risk for each period. Multivariate conditional logistic regression with forward selection was used to identify predictors of progression.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X25103772_as6\">\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>\n                      Among 2,212 colonized patients, 71 cases and 133 matched controls were identified. Several host and clinical characteristics were independently associated with progression to CDI in our multivariate model. Notably, high-risk antibiotic use across the pre-exposure and exposure periods was associated with greater odds of progression to CDI compared to other patterns of antibiotic use (adjusted odds ratio 2.70;\n                      <jats:italic>P<\/jats:italic>\n                      = .03).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X25103772_as7\">\n                    <jats:title>Conclusions:<\/jats:title>\n                    <jats:p>\n                      Sustained exposure to high-risk antibiotics was a strong predictor of the progression from\n                      <jats:italic>C. difficile<\/jats:italic>\n                      colonization to infection, underscoring the need for further research on longitudinal stewardship strategies for CDI prevention, particularly among patients previously identified as colonized.\n                    <\/jats:p>\n                  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