Influence of Contrast Material Temperature on Patient Comfort and Image Quality in Computed Tomography of the Abdomen A Randomized Controlled Trial

被引:3
|
作者
Martens, Bibi [1 ,2 ]
Wildberger, Joachim E. [1 ,2 ]
Van Kuijk, Sander M. J. [3 ]
De Vos-Geelen, Judith [4 ,5 ]
Jeukens, Cecile R. L. P. N. [1 ]
Mihl, Casper [1 ,2 ]
机构
[1] Maastricht Univ, Med Ctr, Dept Radiol & Nucl Med, P Debyelaan 25 POB 5800, NL-6202 AZ Maastricht, Netherlands
[2] Maastricht Univ, CARIM Sch Cardiovasc Dis, Maastricht, Netherlands
[3] Maastricht Univ, Med Ctr, Dept Clin Epidemiol & Med Technol Assessment, Maastricht, Netherlands
[4] Maastricht UMC, Div Med Oncol, Dept Internal Med, Maastricht, Netherlands
[5] Maastricht UMC, GROW Sch Oncol & Dev Biol, Maastricht, Netherlands
关键词
multidetector computed tomography; diagnostic imaging; abdomen; contrast media; image quality; contrast material warming; discomfort; HEPATIC DYNAMIC CT; MEDIA VISCOSITY; ANGIOGRAPHY; ENHANCEMENT; INJECTION; FLOW;
D O I
10.1097/RLI.0000000000000807
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: International guideline recommendations on safe use of contrast media (CM) are conflicting regarding the necessity to prewarm iodinated CM. Purpose: Aim of the study was to evaluate the effects of room temperature CM compared with prewarmed CM on image quality, safety, and patient comfort in abdominal computed tomography (CT). Methods: CATCHY (Contrast Media Temperature and Patient Comfort in Computed Tomography of the Abdomen) is a double-blinded, randomized noninferiority trial. Between February and August 2020, 218 participants referred for portal venous abdominal CTwere prospectively and randomly assigned to 1 of 2 groups. All patients received iopromide at 300 mg I/mL: group 1 at room temperature (similar to 23 degrees C [similar to 73 degrees F]) and group 2 prewarmed to body temperature (37 degrees C [99 degrees F]). A state-of-the-art individualized CM injection protocol was used, based on body weight and adapted to tube voltage. Primary outcome was absolute difference in mean liver attenuation between groups, calculated with a 2-sided 95% confidence interval. The noninferiority margin was set at -10 HU. Secondary outcomes were objective (signal-to-noise ratio and contrast-to-noise ratio) and subjective image quality; CMextravasations and other adverse events; and participant comfort (5-point scale questionnaire) and pain (numeric rating scale). This trial is registered with ClinicalTrials.gov (NCT04249479). Results: The absolute difference in mean attenuation between groups was + 4.23 HU (95% confidence interval, +0.35 to +8.11; mean attenuation, 122.2 +/- 13.1 HU in group 1, 118.0 +/- 15.9 HU in group 2; P = 0.03). Signalto-noise ratio, contrast-to-noise ratio, and subjective image quality were not significantly different between groups (P = 0.53, 0.23, and 0.99 respectively). Contrast extravasation occurred in 1 patient (group 2), and no other adverse events occurred. Comfort scores were significantly higher in group 1 than in group 2 (P = 0.03); pain did not significantly differ (perceived P > 0.99; intensity P = 0.20). Conclusions: Not prewarming iodinated CM was found noninferior in abdominal CT imaging. Prewarming conferred no beneficial effect on image quality, safety, and comfort, and might therefore no longer be considered a prerequisite in state-of-the art injection protocols for parenchymal imaging.
引用
收藏
页码:85 / 89
页数:5
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