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Authors Chen QL, Zhao XY, Wang XM, Lv N, Zhu LL, Xu HM, Zhou Q
Received 8 February 2017
Accepted for publication 6 April 2017
Published 26 April 2017 Volume 2017:13 Pages 565—573
DOI https://doi.org/10.2147/TCRM.S134265
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Colin Mak
Peer reviewer comments 2
Editor who approved publication: Professor Deyun Wang
Abstract: The authors retrospectively analyzed the pattern and characteristics of
non-laboratory-based adverse drug reactions (ADRs) induced by intravenous
radiocontrast agents in a large-scale hospital in China during 2014–2015. There
were 314 ADR cases among 118,208 patients receiving enhanced CT or MRI
examinations. The frequency of moderate/severe ADRs defined by Chinese Society
of Radiology (ie, severe vomiting, systematic urticaria, facial swelling,
dyspnea, vasovagal reaction, laryngeal edema, seizure, trembling, convulsions,
unconsciousness, shock, death, and other unexpected adverse reactions) was rare
(0.0431%), whereas the mild ADRs were uncommon (0.2225%) and accounted for
83.76% of ADRs. Frequency of ADRs induced by iodinated contrast agents was
related with examination site, sex, and type of patient settings (P <0.01) and was higher compared
with gadolinium contrast agents (0.3676% vs 0.0504%, P <0.01). From 2014 to 2015,
frequencies of total and moderate/severe ADRs induced by iodinated contrast
agents decreased significantly (0.4410% vs 0.2947%, P <0.01; 0.0960% vs
0.0282%, P <0.01, respectively).
Frequency of ADRs differed among different iodinated contrast and gadolinium
contrast (P <0.05) agents. Iopromide’s ADR
frequency in 2014 was significantly higher compared with iopamidol, ioversol,
or iohexol (P <0.01). Frequency of
moderate/severe ADRs induced by iodixanol was 4.1–5.4 times that of iohexol,
iopromide, or iopamidol. Rash was the predominant ADR subtype (84.39%) and
occurred more frequently with iodixanol compared with iohexol, iopamidol, or
ioversol (P <0.01). Overall, 21.97% of ADR
cases had allergy history or atopy traits, and these cases experienced ADRs
earlier than the negative ones (17.19 min vs 85.34 min, P <0.01). The mean time to onset
of ADRs was increased in patients receiving iodixanol compared with other
iodinated contrast agents (323.77 min vs 42.36 min, P <0.01). Overall, 37.26% of
ADRs occurred within 5 min and 84.08% of ADRs occurred within 30 min. Efficient
quality improvement in decreasing ADRs induced by radiocontrast agents has been
achieved by multidisciplinary collaboration.
Keywords: allergy, atopy, contrast media, drug monitoring, gadolinium contrast,
iodinated contrast, quality improvements
