{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,3]],"date-time":"2026-09-03T15:28:30Z","timestamp":1788449310706,"version":"build-2803163510"},"reference-count":10,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2019,4,30]],"date-time":"2019-04-30T00:00:00Z","timestamp":1556582400000},"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":["Echocardiography"],"published-print":{"date-parts":[[2019,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Introduction<\/jats:title><jats:p>Ultrasound enhancing agents (<jats:styled-content style=\"fixed-case\">UEA<\/jats:styled-content>s) are often utilized to enhance ultrasound image quality; however, concerns about adverse reactions have limited their use. Moreover, these agents had been either contraindicated or are labeled with a warning in patients with intra\u2010cardiac shunts because of a theoretic risk of systemic microvascular obstruction. This labeling was recently removed in the United States, but data in these patients are lacking.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Over a 15\u2010month period, patients receiving three different <jats:styled-content style=\"fixed-case\">FDA<\/jats:styled-content>\u2010approved <jats:styled-content style=\"fixed-case\">UEA<\/jats:styled-content>s at our center were prospectively evaluated for clinically significant adverse events (<jats:styled-content style=\"fixed-case\">AE<\/jats:styled-content>s).<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>A total of 5521 <jats:styled-content style=\"fixed-case\">UEA<\/jats:styled-content> administrations were performed (Definity<jats:sup>\u00ae<\/jats:sup>: 3306, Lumason<jats:sup>\u00ae<\/jats:sup>: 2137, Optison<jats:sup>\u00ae<\/jats:sup>: 78). There were 14 <jats:styled-content style=\"fixed-case\">AE<\/jats:styled-content>s (0.25%) reported (Lumason<jats:sup>\u00ae<\/jats:sup>: 0.05% [n\u00a0=\u00a01] vs Definity<jats:sup>\u00ae<\/jats:sup>: 0.39% [n\u00a0=\u00a013], <jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.02). Back pain was the most common complaint (n\u00a0=\u00a09), followed by headache (n\u00a0=\u00a02), rash (n\u00a0=\u00a02), dyspnea (n\u00a0=\u00a02), and palpitations (n\u00a0=\u00a01). Among the 33 patients known to have intra\u2010cardiac shunts, there were no <jats:styled-content style=\"fixed-case\">AE<\/jats:styled-content>s. Known right\u2010to\u2010left shunts with positive saline bubble study were present in 20 patients (Lumason<jats:sup>\u00ae<\/jats:sup>: n\u00a0=\u00a09, Definity<jats:sup>\u00ae<\/jats:sup>: n\u00a0=\u00a011). Left\u2010to\u2010right atrial shunts based on color Doppler were present in 10 patients (Lumason<jats:sup>\u00ae<\/jats:sup>: n\u00a0=\u00a05, Definity<jats:sup>\u00ae<\/jats:sup> n\u00a0=\u00a05). Three patients were known to have ventricular septal defect with left\u2010to\u2010right flow (Definity<jats:sup>\u00ae<\/jats:sup>: n\u00a0=\u00a02, Optison<jats:sup>\u00ae<\/jats:sup>: n\u00a0=\u00a01).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Adverse events were significantly higher with Definity<jats:sup>\u00ae<\/jats:sup>; however, overall incidences were low, and <jats:styled-content style=\"fixed-case\">AE<\/jats:styled-content>s were minor. Furthermore, no <jats:styled-content style=\"fixed-case\">AE<\/jats:styled-content>s were reported in patients with known intra\u2010cardiac shunts. <jats:styled-content style=\"fixed-case\">UEA<\/jats:styled-content>s showed a good safety profile in our study and should be afforded to all appropriate patients, including those with known intra\u2010cardiac shunts.<\/jats:p><\/jats:sec>","DOI":"10.1111\/echo.14344","type":"journal-article","created":{"date-parts":[[2019,5,1]],"date-time":"2019-05-01T03:06:06Z","timestamp":1556679966000},"page":"1041-1044","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":15,"title":["Safety profile of ultrasound enhancing agents in echocardiography"],"prefix":"10.1111","volume":"36","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5027-6548","authenticated-orcid":false,"given":"Suwen","family":"Kumar","sequence":"first","affiliation":[{"name":"Oregon Health and Science University Portland 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