Surgery
Volume 148, Issue 1 , Pages 78-86, July 2010

Real-time, near-infrared, fluorescence-guided identification of the ureters using methylene blue

  • Aya Matsui, MD

      Affiliations

    • Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA
    • Division of Cancer Diagnostics and Therapeutics, Hokkaido University Graduate School of Medicine, Sapporo, Japan
  • ,
  • Eiichi Tanaka, MD, PhD

      Affiliations

    • Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA
    • Division of Cancer Diagnostics and Therapeutics, Hokkaido University Graduate School of Medicine, Sapporo, Japan
  • ,
  • Hak Soo Choi, PhD

      Affiliations

    • Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA
  • ,
  • Vida Kianzad, PhD

      Affiliations

    • Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA
  • ,
  • Sylvain Gioux, PhD

      Affiliations

    • Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA
  • ,
  • Stephen J. Lomnes, MS

      Affiliations

    • GE Healthcare, Princeton, NJ
  • ,
  • John V. Frangioni, MD, PhD

      Affiliations

    • Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA
    • Department of Radiology, Beth Israel Deaconess Medical Center, Boston, MA
    • Corresponding Author InformationReprint requests: John V. Frangioni, MD, PhD, Department of Medicine, Division of Hematology/Oncology, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Room SL-B05, Boston, MA 02215.

Accepted 7 December 2009. published online 01 February 2010.

Background

The aim of this study was to determine whether the invisible near-infrared (NIR) fluorescence properties of methylene blue (MB), a dye already approved by the U.S. Food and Drug Administration for other indications, could be exploited for real-time, intra-operative identification of the ureters.

Methods

The optical properties of MB were quantified in vitro. Open surgery and laparoscopic NIR fluorescence imaging systems were employed. Yorkshire pigs were injected intravenously with 0.1-mg/kg MB (n = 8), 10-mg furosemide followed by 0.1-mg/kg MB (n = 6), or 0.5-mg/kg MB (n = 6). The contrast-to-background ratio (CBR) of the kidney and ureters, and the MB concentration in the urine, were quantified.

Results

Peak MB absorbance, emission, and intensity in urine occurred at 668 nm, 688 nm, and 20 μmol/L, respectively. After intravenous injection, doses as low as 0.1-mg/kg MB provided prolonged imaging of the ureters, and a dose of 0.5 mg/kg provided statistically significant improvement of CBR. The preinjection of furosemide increased urine volume but did not improve CBR. Laparoscopic identification of the ureter using MB NIR fluorescence was demonstrated.

Conclusion

Ureteral imaging using MB NIR fluorescence provides sensitive, real-time, intra-operative identification of the ureters during open and laparoscopic surgeries.

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 Supported by National Institutes of Health (National Cancer Institute) Grant #R01-CA-115296 and a sponsored research agreement from GE Healthcare.

PII: S0039-6060(09)00794-6

doi:10.1016/j.surg.2009.12.003

Surgery
Volume 148, Issue 1 , Pages 78-86, July 2010