{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T10:58:04Z","timestamp":1790852284904,"version":"4.1.0"},"reference-count":32,"publisher":"Cambridge University Press (CUP)","license":[{"start":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T00:00:00Z","timestamp":1790812800000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/"}],"content-domain":{"domain":["cambridge.org"],"crossmark-restriction":true},"short-container-title":["Infect. Control Hosp. Epidemiol."],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec id=\"S0899823X26105571_as1\">\n                    <jats:title>Objective:<\/jats:title>\n                    <jats:p>\n                      Leukemic and hematopoietic cell transplant patients have one of the highest incidences of\n                      <jats:italic>Clostridioides difficile<\/jats:italic>\n                      infection (CDI). Although CDI patients are considered the primary source of transmission, asymptomatic colonized (AC) patients can progress to CDI or contribute to in-unit transmission. We aim to quantify the roles of CDI and AC patients in\n                      <jats:italic>C. difficile<\/jats:italic>\n                      importation and transmission within oncological units.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X26105571_as2\">\n                    <jats:title>Design:<\/jats:title>\n                    <jats:p>Prospective cohort study<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X26105571_as3\">\n                    <jats:title>Setting:<\/jats:title>\n                    <jats:p>Two leukemia and hematopoietic cell transplant units in a large tertiary care hospital in the United States for a 6-month period.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X26105571_as4\">\n                    <jats:title>Methods:<\/jats:title>\n                    <jats:p>\n                      We developed a stochastic, individual-based network model to simulate\n                      <jats:italic>C. difficile<\/jats:italic>\n                      acquisition and transmission. Data from cultures and nucleic acid amplification testing obtained at admission and weekly, and toxin enzyme immunoassay tests used for CDI diagnosis were used to calibrate the model. Healthcare worker room assignments informed the network structure. Key parameters were estimated via particle filtering.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X26105571_as5\">\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>The model reproduced observed weekly test counts and transmission pairs. Only 23% of new colonization events were observed via testing. AC patients were the primary source of new colonizations: 51% (range: 38%\u201370%) were due to importation (of those, 87% were admitted as AC), and 49% (30%\u201362%) were due to transmission (AC was the source in 92% of transmissions that resulted in new colonizations).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0899823X26105571_as6\">\n                    <jats:title>Conclusions:<\/jats:title>\n                    <jats:p>\n                      These findings reinforce the role of AC, particularly via admission importation, in sustaining\n                      <jats:italic>C. difficile<\/jats:italic>\n                      transmission in high-risk hospital settings. Infection control focused on CDI effectively reduced onward transmission, as indicated by CDI\u2019s low contribution to new colonizations.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1017\/ice.2026.10557","type":"journal-article","created":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T10:23:15Z","timestamp":1790850195000},"page":"1-7","update-policy":"https:\/\/doi.org\/10.1017\/policypage","source":"Crossref","is-referenced-by-count":0,"title":["Quantifying the contributions of asymptomatic and symptomatic colonized patients to\n                    <i>Clostridioides difficile<\/i>\n                    acquisition in oncological units"],"prefix":"10.1017","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6947-2098","authenticated-orcid":false,"given":"Savannah","family":"Curtis","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/04tj63d06","id-type":"ROR","asserted-by":"publisher"}],"name":"North Carolina State 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Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America","name":"copyright","label":"Copyright","group":{"name":"copyright_and_licensing","label":"Copyright and Licensing"}},{"value":"This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike licence (https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the same Creative Commons licence is used to distribute the re-used or adapted article and the original article is properly cited. The written permission of Cambridge University Press or the rights holder(s) must be obtained prior to any commercial use.","name":"license","label":"License","group":{"name":"copyright_and_licensing","label":"Copyright and Licensing"}},{"value":"This content has been made available to all.","name":"free","label":"Free to read"}]}}