Ultrasound in Medicine and Biology
Volume 35, Issue 10 , Pages 1587-1595, October 2009

Real-Time Contrast-Enhanced Ultrasound for the Assessment of Perfusion Dynamics in Skeletal Muscle

  • Martin Krix

      Affiliations

    • German Cancer Research Center, Research Program Imaging and Radiooncology, Department of Radiology, Heidelberg, Germany
    • Bracco Imaging Germany, Konstanz, Germany
    • Corresponding Author InformationAddress correspondence to: Martin Krix, P.D., Dr. med., Dipl. Phys., German Cancer Research Center Heidelberg, INF 280, D-69120 Heidelberg, Germany.
  • ,
  • Holger Krakowski-Roosen

      Affiliations

    • German Cancer Research Center, Department of Immunochemistry, Heidelberg, Germany
  • ,
  • Hans-Ulrich Kauczor

      Affiliations

    • University Hospital of Heidelberg, Department of Diagnostic and Interventional Radiology, Heidelberg, Germany
  • ,
  • Stefan Delorme

      Affiliations

    • German Cancer Research Center, Research Program Imaging and Radiooncology, Department of Radiology, Heidelberg, Germany
  • ,
  • Marc-André Weber

      Affiliations

    • German Cancer Research Center, Research Program Imaging and Radiooncology, Department of Radiology, Heidelberg, Germany
    • University Hospital of Heidelberg, Department of Diagnostic and Interventional Radiology, Heidelberg, Germany

Received 21 January 2009; received in revised form 26 March 2009; accepted 4 May 2009. published online 17 August 2009.

Abstract 

We developed a real-time low-MI contrast-enhanced ultrasound method (CEUS), compared it with venous occlusion plethysmography (VOP) and evaluated its robustness in the quantification of skeletal muscle perfusion during exercise. Contrast pulse sequencing (7MHz) during continuous intravenous infusion of SonoVue (4.8mL/300s) was used repeatedly in eight healthy volunteers to monitor changes of the muscle perfusion before, during and after isometric exercises (10 to 50% of individual maximum strength for 20 to 30 s) of the gastrocnemius muscle in real time. CEUS was correlated with VOP at different time points, and the exactness of several CEUS parameters obtained from ultrasound-signal-intensity-time curves was evaluated. Real-time CEUS depicted a large variability of the skeletal muscle blood volume at rest (mean, 3.48; range, 0.60 to 9.92 [∼mL]), with a significant reproducibility (r=0.72, p<0.05) and correlation with VOP (r=0.59, p<0.001). Mean blood volume during exercise was 1.58(∼mL), increased to a mean maximum after exercise of 8.88(∼mL), the mean change of the local blood volume during and directly after the exercise was –0.10 and +1.57(∼mL/s). The average CEUS signal during exercise decreased (mean area under the curve, –50.4[∼mL·s]) and subsequently increased post exercise (mean 118.6[∼mL·s]). CEUS parameters could be calculated with mean relative errors between 6 and 36%. Continuous assessment of local muscle microcirculation during exercise is possible with real-time CEUS with an acceptable robustness. Its application may be of particular interest in a better understanding of the role of perfusion during muscle training, and the monitoring of pathological vascular response, such as in diabetic microvessel diseases. (E-mail: martin.krix@kabelbw.de)

Key Words: Skeletal muscle perfusion, Real-time contrast-enhanced ultrasound, Venous occlusion plethysmography

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0301-5629(09)00218-X

doi:10.1016/j.ultrasmedbio.2009.05.006

Ultrasound in Medicine and Biology
Volume 35, Issue 10 , Pages 1587-1595, October 2009