Interventional multispectral photoacoustic imaging with a clinical linear array ultrasound probe for guiding nerve blocks

Accurate identification of tissue structures such as nerves and blood vessels is critically important for interventional procedures such as nerve blocks. Ultrasound imaging is widely used as a guidance modality to visualize anatomical structures in real-time. However, identification of nerves and small blood vessels can be very challenging, and accidental intra-neural or intra-vascular injections can result in significant complications. Multi-spectral photoacoustic imaging can provide high sensitivity and specificity for discriminating hemoglobin- and lipid-rich tissues. However, conventional surface-illumination-based photoacoustic systems suffer from limited sensitivity at large depths. In this study, for the first time, an interventional multispectral photoacoustic imaging (IMPA) system was used to image nerves in a swine model in vivo. Pulsed excitation light with wavelengths in the ranges of 750 - 900 nm and 1150 - 1300 nm was delivered inside the body through an optical fiber positioned within the cannula of an injection needle. Ultrasound waves were received at the tissue surface using a clinical linear array imaging probe. Co-registered B-mode ultrasound images were acquired using the same imaging probe. Nerve identification was performed using a combination of B-mode ultrasound imaging and electrical stimulation. Using a linear model, spectral-unmixing of the photoacoustic data was performed to provide image contrast for oxygenated and de-oxygenated hemoglobin, water and lipids. Good correspondence between a known nerve location and a lipid-rich region in the photoacoustic images was observed. The results indicate that IMPA is a promising modality for guiding nerve blocks and other interventional procedures. Challenges involved with clinical translation are discussed.

[1]  P. Beard Biomedical photoacoustic imaging , 2011, Interface Focus.

[2]  M. B. van der Mark,et al.  Estimation of lipid and water concentrations in scattering media with diffuse optical spectroscopy from 900 to 1,600 nm. , 2010, Journal of biomedical optics.

[3]  T. V. van Leeuwen,et al.  Design and evaluation of a laboratory prototype system for 3D photoacoustic full breast tomography. , 2013, Biomedical optics express.

[4]  Vasilis Ntziachristos,et al.  Unmixing Molecular Agents From Absorbing Tissue in Multispectral Optoacoustic Tomography , 2014, IEEE Transactions on Medical Imaging.

[5]  Marjolein van der Voort,et al.  Optical Detection of the Brachial Plexus for Peripheral Nerve Blocks: An In Vivo Swine Study , 2011, Regional Anesthesia & Pain Medicine.

[6]  Shaoqun Zeng,et al.  Confocal imaging reveals three-dimensional fine structure difference between ventral and dorsal nerve roots. , 2011, Journal of biomedical optics.

[7]  Adrien E. Desjardins,et al.  Interventional Photoacoustic Imaging of the Human Placenta with Ultrasonic Tracking for Minimally Invasive Fetal Surgeries , 2015, MICCAI.

[8]  Yebin Jiang,et al.  Musculoskeletal sonography: important imaging pitfalls. , 2010, AJR. American journal of roentgenology.

[9]  J. Mari,et al.  Interventional multispectral photoacoustic imaging with a clinical ultrasound probe for discriminating nerves and tendons: an ex vivo pilot study. , 2015, Journal of biomedical optics.

[10]  Marjolein van der Voort,et al.  Needle stylet with integrated optical fibers for spectroscopic contrast during peripheral nerve blocks. , 2011, Journal of biomedical optics.

[11]  Wiendelt Steenbergen,et al.  Photoacoustic needle: minimally invasive guidance to biopsy , 2013, Journal of biomedical optics.

[12]  Alejandro F. Frangi,et al.  Medical Image Computing and Computer-Assisted Intervention -- MICCAI 2015 , 2015, Lecture Notes in Computer Science.

[13]  Adrien E. Desjardins,et al.  An interventional multispectral photoacoustic imaging platform for the guidance of minimally invasive procedures , 2015, European Conference on Biomedical Optics.

[14]  L. Helen,et al.  Nerve localization techniques for peripheral nerve block and possible future directions , 2015, Acta anaesthesiologica Scandinavica.

[15]  Beth Friedman,et al.  Fluorescent peptides highlight peripheral nerves during surgery in mice , 2011, Nature Biotechnology.

[16]  Changhuei Yang,et al.  Images of spinal nerves and adjacent structures with optical coherence tomography: preliminary animal studies. , 2007, The journal of pain : official journal of the American Pain Society.

[17]  Stephen T. C. Wong,et al.  Label-free high-resolution imaging of prostate glands and cavernous nerves using coherent anti-Stokes Raman scattering microscopy , 2011, Biomedical optics express.

[18]  Marjolein van der Voort,et al.  Optical Detection of Peripheral Nerves: An In Vivo Human Study , 2012, Regional Anesthesia & Pain Medicine.

[19]  S. Ourselin,et al.  In-plane ultrasonic needle tracking using a fiber-optic hydrophone. , 2015, Medical physics.

[20]  Sebastien Ourselin,et al.  Performance characteristics of an interventional multispectral photoacoustic imaging system for guiding minimally invasive procedures , 2015, Journal of biomedical optics.

[21]  B T Cox,et al.  k-Wave: MATLAB toolbox for the simulation and reconstruction of photoacoustic wave fields. , 2010, Journal of biomedical optics.

[22]  C. L. Jeng,et al.  Complications of peripheral nerve blocks. , 2010, British journal of anaesthesia.