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Safety of Administering Intravenous CT Contrast Agents Repeatedly or Using Both CT and MRI Contrast Agents on the Same Day: An Animal Study

  • Heejin Bae (Department of Radiology, Severance Hospital, Yonsei University College of Medicine) ;
  • Hyewon Oh (Department of Radiology, Severance Hospital, Yonsei University College of Medicine) ;
  • Ga Bin Park (Department of Radiology, Severance Hospital, Yonsei University College of Medicine) ;
  • Yong Eun Chung (Department of Radiology, Severance Hospital, Yonsei University College of Medicine)
  • Received : 2023.07.27
  • Accepted : 2023.12.21
  • Published : 2024.03.01

Abstract

Objective: To investigate molecular and functional consequences of additional exposures to iodine- or gadolinium-based contrast agents within 24 hours from the initial intravenous administration of iodine-based contrast agents through an animal study. Materials and Methods: Fifty-six Sprague-Dawley male rats were equally divided into eight groups: negative control, positive control (PC) with single-dose administration of CT contrast agent, and additional administration of either CT or MR contrast agents 2, 4, or 24 hours from initial CT contrast agent injection. A 12 µL/g of iodinated contrast agent or a 0.47 µL/g of gadolinium-based contrast agent were injected into the tail vein. Serum levels of blood urea nitrogen, creatinine, cystatin C (Cys C), and malondialdehyde (MDA) were measured. mRNA and protein levels of kidney injury molecule-1 (KIM-1) and neutrophil gelatinase-associated lipocalin (NGAL) were evaluated. Results: Levels of serum creatinine (SCr) were significantly higher in repeated CT contrast agent injection groups than in PC (0.21 ± 0.02 mg/dL for PC; 0.40 ± 0.02, 0.34 ± 0.03, and 0.41 ± 0.10 mg/dL for 2-, 4-, and 24-hour interval groups, respectively; P < 0.001). There was no significant difference in the average Cys C and MDA levels between PC and repeated CT contrast agent injection groups (Cys C, P = 0.256-0.362; MDA, P > 0.99). Additional doses of MR contrast agent did not make significant changes compared to PC in SCr (P > 0.99), Cys C (P = 0.262), and MDA (P = 0.139-0.771) levels. mRNA and protein levels of KIM-1 and NGAL were not significantly different among additional CT or MR contrast agent groups (P > 0.05). Conclusion: A sufficient time interval, probably more than 24 hours, between repeated contrast-enhanced CT examinations may be necessary to avoid deterioration in renal function. However, conducting contrast-enhanced MRI on the same day as contrast-enhanced CT may not induce clinically significant kidney injury.

Keywords

Acknowledgement

This work was supported by the faculty research grant from Yonsei University College of Medicine (grant number: 6-2021-0122).

References

  1. Hasebroock KM, Serkova NJ. Toxicity of MRI and CT contrast agents. Expert Opin Drug Metab Toxicol 2009;5:403-416
  2. Wichmann JL, Katzberg RW, Litwin SE, Zwerner PL, De Cecco CN, Vogl TJ, et al. Contrast-induced nephropathy. Circulation 2015;132:1931-1936
  3. European Society of Urogenital Radiology. ESUR guidelines on contrast agents 10.0 [accessed on May 25, 2022]. Available at: https://www.esur.org/wp-content/uploads/2022/03/ESUR-Guidelines-10_0-Final-Version.pdf
  4. American College of Radiology. ACR manual on contrast media 2022 [accessed on May 25, 2022]. Available at: https://www.acr.org/-/media/ACR/files/clinical-resources/contrast_media.pdf
  5. Mohammed NM, Mahfouz A, Achkar K, Rafie IM, Hajar R. Contrast-induced nephropathy. Heart Views 2013;14:106-116
  6. Tao SM, Wichmann JL, Schoepf UJ, Fuller SR, Lu GM, Zhang LJ. Contrast-induced nephropathy in CT: incidence, risk factors and strategies for prevention. Eur Radiol 2016;26:3310-3318
  7. Mitchell AM, Kline JA, Jones AE, Tumlin JA. Major adverse events one year after acute kidney injury after contrast-enhanced computed tomography. Ann Emerg Med 2015;66:267-274.e4
  8. Rudnick M, Feldman H. Contrast-induced nephropathy: what are the true clinical consequences? Clin J Am Soc Nephrol 2008;3:263-272
  9. Mitchell AM, Jones AE, Tumlin JA, Kline JA. Incidence of contrast-induced nephropathy after contrast-enhanced computed tomography in the outpatient setting. Clin J Am Soc Nephrol 2010;5:4-9
  10. Park JH, Shin HJ, Choi JY, Lim JS, Park MS, Kim MJ, et al. Is there association between statin usage and contrast-associated acute kidney injury after intravenous administration of iodine-based contrast media in enhanced computed tomography? Eur Radiol 2020;30:5261-5271
  11. van der Molen AJ, Reimer P, Dekkers IA, Bongartz G, Bellin MF, Bertolotto M, et al. Post-contrast acute kidney injury - Part 1: definition, clinical features, incidence, role of contrast medium and risk factors: recommendations for updated ESUR Contrast Medium Safety Committee guidelines. Eur Radiol 2018;28:2845-2855
  12. Abujudeh HH, Gee MS, Kaewlai R. In emergency situations, should serum creatinine be checked in all patients before performing second contrast CT examinations within 24 hours? J Am Coll Radiol 2009;6:268-273
  13. Trivedi H, Foley WD. Contrast-induced nephropathy after a second contrast exposure. Ren Fail 2010;32:796-801
  14. Geenen RW, Kingma HJ, van der Molen AJ. Contrast-induced nephropathy: pharmacology, pathophysiology and prevention. Insights Imaging 2013;4:811-820
  15. Bellin MF. MR contrast agents, the old and the new. Eur J Radiol 2006;60:314-323
  16. Perazella MA. Current status of gadolinium toxicity in patients with kidney disease. Clin J Am Soc Nephrol 2009;4:461-469
  17. Currie GM. Pharmacology, part 5: CT and MRI contrast media. J Nucl Med Technol 2019;47:189-202
  18. Akdeniz D, Celik HT, Kazanci F, Yilmaz H, Yalcin S, Bilgic MA, et al. Is kidney injury molecule 1 a valuable tool for the early diagnosis of contrast-induced nephropathy? J Investig Med 2015;63:930-934
  19. Wang ZY, Wang YL, Wei J, Jin L, Wang ZC. Role of serum cystatin C in the prediction of contrast-induced nephropathy after intra-arterial interventions. Chin Med J (Engl) 2020;133:408-414
  20. Quintavalle C, Anselmi CV, De Micco F, Roscigno G, Visconti G, Golia B, et al. Neutrophil gelatinase-associated lipocalin and contrast-induced acute kidney injury. Circ Cardiovasc Interv 2015;8:e002673
  21. Wacker-Gussmann A, Buhren K, Schultheiss C, Braun SL, Page S, Saugel B, et al. Prediction of contrast-induced nephropathy in patients with serum creatinine levels in the upper normal range by cystatin C: a prospective study in 374 patients. AJR Am J Roentgenol 2014;202:452-458
  22. Murty MS, Sharma UK, Pandey VB, Kankare SB. Serum cystatin C as a marker of renal function in detection of early acute kidney injury. Indian J Nephrol 2013;23:180-183
  23. Kellum JA, Romagnani P, Ashuntantang G, Ronco C, Zarbock A, Anders HJ. Acute kidney injury. Nat Rev Dis Primers 2021;7:52
  24. Ronco C, Bellomo R, Kellum JA. Acute kidney injury. Lancet 2019;394:1949-1964
  25. Oh H, Choi A, Seo N, Lim JS, You JS, Chung YE. Protective effect of glycyrrhizin, a direct HMGB1 inhibitor, on post-contrast acute kidney injury. Sci Rep 2021;11:15625
  26. Oh SW, Park SY, Yong HS, Choi YH, Cha MJ, Kim TB, et al. Korean clinical practice guidelines for adverse reactions to intravenous iodinate and MRI-gadolinium contrast agents: revised clinical consensus and recommendations (3rd edition, 2022). J Korean Soc Radiol 2022;83:254-264
  27. Fahling M, Seeliger E, Patzak A, Persson PB. Understanding and preventing contrast-induced acute kidney injury. Nat Rev Nephrol 2017;13:169-180