{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,2]],"date-time":"2026-02-02T23:00:54Z","timestamp":1770073254107,"version":"3.49.0"},"reference-count":28,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2019,3,28]],"date-time":"2019-03-28T00:00:00Z","timestamp":1553731200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Mycoses"],"published-print":{"date-parts":[[2019,6]]},"abstract":"<jats:title>Summary<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Isavuconazole use in the real\u2010world setting has not been extensively described. Subgroups of patients with particular prognostic significance, such as previous triazole prophylaxis or treatment and the important subgroup treated empirically for invasive fungal infection, have beforehand been excluded from trials.<\/jats:p><\/jats:sec><jats:sec><jats:title>Objectives<\/jats:title><jats:p>We aimed to determine treatment response and safety in these patients at a large US transplant and cancer centre.<\/jats:p><\/jats:sec><jats:sec><jats:title>Patients\/Methods<\/jats:title><jats:p>We conducted a retrospective cohort study of all adult inpatients administered \u22653 doses of isavuconazole between June 2015 and October 2017.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Ninety\u2010one adults were identified. Six (7%) received primary prophylaxis, 10 (11%) treatment then secondary prophylaxis and 75 (82%) treatment only. Overall treatment response was 62%. Six\u2010week mortality was 24%. Sixty\u2010three per cent of 32 patients treated with isavuconaozle following prophylaxis with another antifungal agent exhibited a treatment response. Among 49 patients switched from treatment with another agent, 53% had a treatment response. Thirty\u2010four patients received isavuconazole empirically, and 65% demonstrated a treatment response. Individuals given isavuconazole prophylaxis developed no breakthrough invasive fungal infections. One patient discontinued isavuconazole due to hepatotoxicity.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Real\u2010world isavuconazole use appears safe and is associated with treatment responses in varied patients including critically important subgroups previously unreported.<\/jats:p><\/jats:sec>","DOI":"10.1111\/myc.12910","type":"journal-article","created":{"date-parts":[[2019,3,9]],"date-time":"2019-03-09T19:07:55Z","timestamp":1552158475000},"page":"534-541","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":23,"title":["Real\u2010world use\u2014Isavuconazole at a large academic medical center"],"prefix":"10.1111","volume":"62","author":[{"given":"Habiba","family":"Hassouna","sequence":"first","affiliation":[{"name":"Department of Infectious Disease Cleveland Clinic Cleveland Ohio"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Vasilios","family":"Athans","sequence":"additional","affiliation":[{"name":"Department of Pharmacy Cleveland Clinic Cleveland Ohio"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9862-1929","authenticated-orcid":false,"given":"Kyle D.","family":"Brizendine","sequence":"additional","affiliation":[{"name":"Department of Infectious Disease Cleveland Clinic Cleveland 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