Pediatric contrast-enhanced ultrasound in the United States: a survey by the Contrast-Enhanced Ultrasound Task Force of the Society for Pediatric Radiology
Background The United States Food and Drug Administration (FDA) recently approved an ultrasound (US) contrast agent for intravenous and intravesical administration in children. Objective Survey the usage, interest in and barriers for contrast-enhanced US among pediatric radiologists. Materials and m...
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Published in: | Pediatric radiology Vol. 48; no. 6; pp. 852 - 857 |
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Main Authors: | , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Berlin/Heidelberg
Springer Berlin Heidelberg
01-06-2018
Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
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Summary: | Background
The United States Food and Drug Administration (FDA) recently approved an ultrasound (US) contrast agent for intravenous and intravesical administration in children.
Objective
Survey the usage, interest in and barriers for contrast-enhanced US among pediatric radiologists.
Materials and methods
The Contrast-Enhanced Ultrasound Task Force of the Society for Pediatric Radiology (SPR) surveyed the membership of the SPR in January 2017 regarding their current use and opinions about contrast-enhanced US in pediatrics.
Results
The majority (51.1%, 166) of the 325 respondents (26.7% of 1,218) practice in either a university- or academic affiliated group. The most widely used US contrast agent was Lumason® 52.3% (23/44). While lack of expertise and training were reported barriers, all respondents who are not currently using US contrast agents are considering future use.
Conclusion
Interest in pediatric contrast US is very high. Education and training are needed to support members who plan to adopt contrast US into practice. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0301-0449 1432-1998 |
DOI: | 10.1007/s00247-018-4088-x |