Jump to content

Endoscopic optical coherence tomography imaging

Add links
From Wikipedia, the free encyclopedia

Endoscopic optical coherence tomography
Example of intracoronary optical coherence tomography (OCT) image of atherosclerosis. Between 6 and 8 o'clock it is possible to observe a fibrocalcific atherosclerotic plaque.

Endoscopic optical coherence tomography, also intravascular optical coherence tomography is a catheter-based imaging application of optical coherence tomography (OCT).[1] It is capable of acquiring high-resolution images from inside a blood vessel using optical fibers and laser technology.

One of its main applications is for coronary arteries, which are often treated by endoscopic, minimally invasive surgical procedures.[2] Other applications for peripheral arteries and for neurovascular procedures have been proposed and are being investigated. Neurovascular applications required significant technological developments, due to the highly tortuous anatomy of the cerebrovasculature.

Intravascular OCT rapidly creates three-dimensional images at a resolution of approximately 15 micrometers, an improved resolution with respect to intravascular ultrasound and coronary angiogram, the other imaging techniques.[3] This offers additional information that can be used to optimize the treatment and management of vascular disease.

Theory

[edit]

OCT is analogous to medical ultrasound, measuring the backreflection of infrared light rather than sound. The time for light to be reflected back from the tissue under inspection is used to measure distances. However, due to the high speed of light, the backreflection time cannot be measured directly, but is instead measured using interferometry.[4]

OCT is measured using either time domain (TD-OCT) or frequency domain techniques (FD-OCT). Commercially available coronary OCT technology is based on frequency domain techniques, resulting in rapid acquisition procedures (1 to 2 seconds). Intracoronary OCT uses near-infrared light at 1300 nm and can visualize the microstructure of the arterial wall, its size, and therapeutic devices with high accuracy.

History

[edit]

Intravascular OCT was developed for the imaging of arterial disease at a resolution higher than the other techniques available, such as x-ray angiography and intravascular ultrasounds. OCT allows to assess atherosclerotic plaques characteristics at a resolution of approximately 15 μm (or better) and found applications for the guidance of catheter-based coronary interventions (ie, percutaneous coronary interventions). The first report of endoscopic OCT appeared in 1997 in the journal Science exploring various applications including gastroenterology and airways.[5] The first intravascular in vivo use in a preclinical model was reported in 1994[6] and first in human, clinical imaging in 2003.[7] The first OCT imaging catheter and system was commercialized by LightLab Imaging, Inc., a company based in Massachusetts formed following a technology transfer in 1997 from Fujimoto's lab (MIT).[8]

Early on, time-domain OCT technology required slow acquisitions (>10 seconds long) requiring the use of balloon occlusion techniques to displace the blood from the arterial lumen, opaque to near-infrared light. This prevented a broader adoption for several years. Aroun 2008-2009, the advent of rapid sweep source lasers allowed for the development of intravascular Fourier-Domain OCT (FD-OCT).[9][10] This enabled for the first-time rapid acquisitions of a long coronary segment in a couple of seconds, allowing non occlusive brief contrast injections to clear the arterial lumen from blood. Initial demonstration of FD-OCT for coronary imaging was achieved in 2008-2009[11][3] which significantly accelerated clinical adoption starting in 2009.

Cardiovascular applications

[edit]

Following regulatory clearances in the major geographies between 2009 and 2012 of fast acquisition Fourier domain OCT, the use of intracoronary OCT rapidly increased. It is used to help coronary disease diagnosis, planning of the intervention, assess procedural results, and prevent complications.

In the last decade, clinical benefits of coronary OCT have been systematically investigated. Several studies have linked the use of intravascular imaging such as IVUS and OCT to better stent expansion, a metric strongly correlated to better clinical outcomes in patients suffering from coronary artery disease and myocardial infarction.[12][13][14]

Larger randomized clinical trials have been undertaken. In 2023, a double-blind prospective trial demonstrated improvement in morbidity and mortality in coronary bifurcation interventions: "Among patients with complex coronary-artery bifurcation lesions, OCT-guided PCI was associated with a lower incidence of MACE at 2 years than angiography-guided PCI."[15] Although not every study showed significant results,[16] to date, several studies demonstrated the benefits in patient outcomes of using intravascular imaging during coronary arteries interventions.[17][18] The use of intravascular imaging for coronary intervention is reported on the current cardiology guidelines.

Data published in late 2016 showed that over 150,000 intracoronary optical coherence tomography procedures are performed every year, and its adoption is rapidly growing at a rate of ~10-20% every year.[19]

Assessment of artery lumen morphology is the cornerstone of intravascular imaging criteria to evaluate disease severity and guide intervention. The high-resolution of OCT imaging allows to assess with high accuracy vessel lumen area, wall microstructure, intracoronary stent apposition and expansion.[20][21] OCT has an improved ability with respect to intravascular ultrasound to penetrate and delineate calcium in the vessel wall that makes it well suited to guide complex interventional strategies in vessels with superficial calcification. OCT has the capability of visualize coronary plaque erosion and fibrotic caps overlying lipid plaques.[22]

Neurovascular applications

[edit]

In the last decade, significant advances have been made in the endovascular treatment of stroke, including brain aneurysms, intracranial atherosclerosis and ischemic stroke.[23] Intravascular OCT has been proposed has a key technology that can improve current procedure and treatments.[24] However, current intracoronary OCT catheters are not designed for navigation and reliable imaging of tortuous cerebrovascular arteries.[25]

Recently, different (wire-like) OCT catheters have been proposed and were specifically designed for the human cerebrovasculature,[26] named neuro optical coherence tomography (nOCT). A first clinical study to investigate safety, feasibility, and clinical potential has been conducted.[27] Initial applications for the treatment of brain aneurysms and intracranial atherosclerosis have been demonstrated[28][29][30] showing future potential.[31][32]

Technology

[edit]

The most critical technological advance was the catheter and the development of fast wavelength sweeping near-infrared lasers. The fiber optic catheter/endoscope required rapid alignment of two optical fibers with 8 μm cores (one rotating) across free space. The distal end has a focusing component (GRIN or ball lens, typically).

State-of-the-art intracoronary optical coherence tomography uses a swept-source laser to make OCT images at high-speed (i.e., approximately 80,000 kHz - A-scan lines per second) to complete acquisition of a 3D OCT volume of coronary segments in a few-seconds.[33] The first intravascular FD-OCT was introduced to the market in 2009 (EU and Asia) and in 2012 (US). In 2018, two intracoronary OCT catheters are clinically available for use in the coronary arteries, having a size in diameter between 2.4F and 2.7F. [citation needed]

The axial resolution of state-of-the-art commercial systems is less than 20 micrometers, which is decoupled from the catheter lateral resolution. The highest resolution of OCT allows for the in vivo imaging of vessel microstructural features at an unprecedented level, enabling visualization of vessel wall atherosclerosis, pathology, and interaction with therapeutic devices at a microscopic level.[34]

Recent developments included the combination of OCT with spectroscopy and fluorescence in a single imaging catheter[35][36] and miniaturization of the imaging catheter.[37]

Safety

[edit]

Safety of intravascular imaging, including intracoronary OCT and intravascular ultrasound, has been investigated by several studies. Recent clinical trials reported a very low rate of self-limiting, minor complications on over 3,000 patients where in all cases no harm or prolongation of hospital stay was observed. Intracoronary optical coherence tomography was demonstrated to be safe among heterogeneous groups of patients presenting varying clinical setting.[38]

See also

[edit]

References

[edit]
  1. ^ Gora MJ, Suter MJ, Tearney GJ, Li X (May 2017). "Endoscopic optical coherence tomography: technologies and clinical applications [Invited]". Biomedical Optics Express. 8 (5): 2405–2444. doi:10.1364/BOE.8.002405. PMC 5480489. PMID 28663882.
  2. ^ Kumar A, Yadav N, Singh S, Chauhan N (July 2016). "Minimally invasive (endoscopic-computer assisted) surgery: Technique and review". Annals of Maxillofacial Surgery. 6 (2): 159–164. doi:10.4103/2231-0746.200348. PMC 5343621. PMID 28299251.
  3. ^ a b Bezerra HG, Costa MA, Guagliumi G, Rollins AM, Simon DI (November 2009). "Intracoronary optical coherence tomography: a comprehensive review clinical and research applications". JACC. Cardiovascular Interventions. 2 (11): 1035–1046. doi:10.1016/j.jcin.2009.06.019. PMC 4113036. PMID 19926041.
  4. ^ Huang D, Swanson EA, Lin CP, Schuman JS, Stinson WG, Chang W, et al. (November 1991). "Optical coherence tomography". Science. 254 (5035): 1178–1181. Bibcode:1991Sci...254.1178H. doi:10.1126/science.1957169. PMC 4638169. PMID 1957169.
  5. ^ Tearney GJ, Brezinski ME, Bouma BE, Boppart SA, Pitris C, Southern JF, et al. (June 1997). "In vivo endoscopic optical biopsy with optical coherence tomography". Science. 276 (5321): 2037–2039. doi:10.1126/science.276.5321.2037. PMID 9197265.
  6. ^ Fujimoto JG, Boppart SA, Tearney GJ, Bouma BE, Pitris C, Brezinski ME (August 1999). "High resolution in vivo intra-arterial imaging with optical coherence tomography". Heart. 82 (2): 128–133. doi:10.1136/hrt.82.2.128. PMC 1729132. PMID 10409522.
  7. ^ Bouma BE, Tearney GJ, Yabushita H, Shishkov M, Kauffman CR, DeJoseph Gauthier D, et al. (March 2003). "Evaluation of intracoronary stenting by intravascular optical coherence tomography". Heart. 89 (3): 317–320. doi:10.1136/heart.89.3.317. PMC 1767586. PMID 12591841.
  8. ^ "Biomedical Optical Imaging and Biophotonics Group". www.rle.mit.edu. Retrieved 2024-05-22.
  9. ^ de Boer JF, Cense B, Park BH, Pierce MC, Tearney GJ, Bouma BE (November 2003). "Improved signal-to-noise ratio in spectral-domain compared with time-domain optical coherence tomography". Optics Letters. 28 (21): 2067–2069. Bibcode:2003OptL...28.2067D. doi:10.1364/OL.28.002067. PMID 14587817.
  10. ^ Adler DC, Chen Y, Huber R, Schmitt J, Connolly J, Fujimoto JG (December 2007). "Three-dimensional endomicroscopy using optical coherence tomography". Nature Photonics. 1 (12): 709–716. Bibcode:2007NaPho...1..709A. doi:10.1038/nphoton.2007.228. ISSN 1749-4885.
  11. ^ Tearney GJ, Waxman S, Shishkov M, Vakoc BJ, Suter MJ, Freilich MI, et al. (November 2008). "Three-dimensional coronary artery microscopy by intracoronary optical frequency domain imaging". JACC. Cardiovascular Imaging. 1 (6): 752–761. doi:10.1016/j.jcmg.2008.06.007. PMC 2852244. PMID 19356512.
  12. ^ Wijns W, Shite J, Jones MR, Lee SW, Price MJ, Fabbiocchi F, et al. (December 2015). "Optical coherence tomography imaging during percutaneous coronary intervention impacts physician decision-making: ILUMIEN I study". European Heart Journal. 36 (47): 3346–3355. doi:10.1093/eurheartj/ehv367. PMC 4677272. PMID 26242713.
  13. ^ Habara M, Nasu K, Terashima M, Kaneda H, Yokota D, Ko E, et al. (April 2012). "Impact of frequency-domain optical coherence tomography guidance for optimal coronary stent implantation in comparison with intravascular ultrasound guidance". Circulation: Cardiovascular Interventions. 5 (2): 193–201. doi:10.1161/CIRCINTERVENTIONS.111.965111. PMID 22456026. S2CID 3025748.
  14. ^ Vergallo R, Porto I, D'Amario D, Annibali G, Galli M, Benenati S, et al. (April 2019). "Coronary Atherosclerotic Phenotype and Plaque Healing in Patients With Recurrent Acute Coronary Syndromes Compared With Patients With Long-term Clinical Stability: An In Vivo Optical Coherence Tomography Study". JAMA Cardiology. 4 (4): 321–329. doi:10.1001/jamacardio.2019.0275. PMC 6484796. PMID 30865212.
  15. ^ Holm NR, Andreasen LN, Neghabat O, Laanmets P, Kumsars I, Bennett J, et al. (October 2023). "OCT or Angiography Guidance for PCI in Complex Bifurcation Lesions". The New England Journal of Medicine. 389 (16): 1477–1487. doi:10.1056/NEJMoa2307770. PMID 37634149. S2CID 261231045.
  16. ^ Ali ZA, Landmesser U, Maehara A, Matsumura M, Shlofmitz RA, Guagliumi G, et al. (October 2023). "Optical Coherence Tomography-Guided versus Angiography-Guided PCI". The New England Journal of Medicine. 389 (16): 1466–1476. doi:10.1056/NEJMoa2305861. PMID 37634188.
  17. ^ Kang DY, Ahn JM, Yun SC, Hur SH, Cho YK, Lee CH, et al. (October 2023). "Optical Coherence Tomography-Guided or Intravascular Ultrasound-Guided Percutaneous Coronary Intervention: The OCTIVUS Randomized Clinical Trial". Circulation. 148 (16): 1195–1206. doi:10.1161/CIRCULATIONAHA.123.066429. PMID 37634092.
  18. ^ Stone GW, Christiansen EH, Ali ZA, Andreasen LN, Maehara A, Ahmad Y, et al. (March 2024). "Intravascular imaging-guided coronary drug-eluting stent implantation: an updated network meta-analysis". Lancet. 403 (10429): 824–837. doi:10.1016/S0140-6736(23)02454-6. PMID 38401549.
  19. ^ Swanson EA, Fujimoto JG (March 2017). "The ecosystem that powered the translation of OCT from fundamental research to clinical and commercial impact [Invited]". Biomedical Optics Express. 8 (3): 1638–1664. doi:10.1364/BOE.8.001638. PMC 5480569. PMID 28663854.
  20. ^ Ughi GJ, Adriaenssens T, Onsea K, Kayaert P, Dubois C, Sinnaeve P, et al. (February 2012). "Automatic segmentation of in-vivo intra-coronary optical coherence tomography images to assess stent strut apposition and coverage". The International Journal of Cardiovascular Imaging. 28 (2): 229–241. doi:10.1007/s10554-011-9824-3. PMID 21347593.
  21. ^ Yabushita H, Bouma BE, Houser SL, Aretz HT, Jang IK, Schlendorf KH, et al. (September 2002). "Characterization of human atherosclerosis by optical coherence tomography". Circulation. 106 (13): 1640–1645. doi:10.1161/01.CIR.0000029927.92825.F6. PMID 12270856.
  22. ^ Kini AS, Vengrenyuk Y, Yoshimura T, Matsumura M, Pena J, Baber U, et al. (February 2017). "Fibrous Cap Thickness by Optical Coherence Tomography In Vivo". Journal of the American College of Cardiology. 69 (6): 644–657. doi:10.1016/j.jacc.2016.10.028. PMID 27989887.
  23. ^ Nogueira RG, Ribó M (September 2019). "Endovascular Treatment of Acute Stroke". Stroke. 50 (9): 2612–2618. doi:10.1161/STROKEAHA.119.023811. PMID 31340728.
  24. ^ Chen CJ, Kumar JS, Chen SH, Ding D, Buell TJ, Sur S, et al. (April 2018). "Optical Coherence Tomography: Future Applications in Cerebrovascular Imaging". Stroke. 49 (4): 1044–1050. doi:10.1161/STROKEAHA.117.019818. PMID 29491139.
  25. ^ Gounis MJ, Ughi GJ, Marosfoi M, Lopes DK, Fiorella D, Bezerra HG, et al. (January 2019). "Intravascular Optical Coherence Tomography for Neurointerventional Surgery". Stroke. 50 (1): 218–223. doi:10.1161/STROKEAHA.118.022315. PMC 6541539. PMID 30580737.
  26. ^ Ughi GJ, Marosfoi MG, King RM, Caroff J, Peterson LM, Duncan BH, et al. (July 2020). "A neurovascular high-frequency optical coherence tomography system enables in situ cerebrovascular volumetric microscopy". Nature Communications. 11 (1): 3851. Bibcode:2020NatCo..11.3851U. doi:10.1038/s41467-020-17702-7. PMC 7395105. PMID 32737314.
  27. ^ Pereira VM, Lylyk P, Cancelliere N, Lylyk PN, Lylyk I, Anagnostakou V, et al. (May 2024). "Volumetric microscopy of cerebral arteries with a miniaturized optical coherence tomography imaging probe". Science Translational Medicine. 16 (747): eadl4497. doi:10.1126/scitranslmed.adl4497. PMID 38748771.
  28. ^ King RM, Peker A, Anagnostakou V, Raskett CM, Arends JM, Dixit HG, et al. (September 2023). "High-frequency optical coherence tomography predictors of aneurysm occlusion following flow diverter treatment in a preclinical model". Journal of NeuroInterventional Surgery. 15 (9): 919–923. doi:10.1136/jnis-2022-019275. PMID 36002288.
  29. ^ Anagnostakou V, Epshtein M, Ughi GJ, King RM, Valavanis A, Puri AS, et al. (May 2022). "Transvascular in vivo microscopy of the subarachnoid space". Journal of NeuroInterventional Surgery. 14 (5): 420–428. doi:10.1136/neurintsurg-2021-018544. PMID 35115394.
  30. ^ Caroff J, King RM, Ughi GJ, Marosfoi M, Langan ET, Raskett C, et al. (November 2020). "Longitudinal Monitoring of Flow-Diverting Stent Tissue Coverage After Implant in a Bifurcation Model Using Neurovascular High-Frequency Optical Coherence Tomography". Neurosurgery. 87 (6): 1311–1319. doi:10.1093/neuros/nyaa208. PMC 7666887. PMID 32463884.
  31. ^ Siddiqui AH, Andersson T (2024-09-26). "Shining light on neurovascular disease". Interventional Neuroradiology: 15910199241285962. doi:10.1177/15910199241285962. ISSN 1591-0199. PMC 11559757. PMID 39324217.
  32. ^ Cooney E (2024-05-15). "To detect risk of stroke, tiny probe acts 'like a microscope' inside brain's blood vessels". STAT. Retrieved 2024-05-17.
  33. ^ Yun SH, Tearney G, de Boer J, Bouma B (November 2004). "Pulsed-source and swept-source spectral-domain optical coherence tomography with reduced motion artifacts". Optics Express. 12 (23): 5614–5624. Bibcode:2004OExpr..12.5614Y. doi:10.1364/opex.12.005614. PMC 2713045. PMID 19488195.
  34. ^ Tearney GJ, Regar E, Akasaka T, Adriaenssens T, Barlis P, Bezerra HG, et al. (March 2012). "Consensus standards for acquisition, measurement, and reporting of intravascular optical coherence tomography studies: a report from the International Working Group for Intravascular Optical Coherence Tomography Standardization and Validation". Journal of the American College of Cardiology. 59 (12): 1058–1072. doi:10.1016/j.jacc.2011.09.079. PMID 22421299.
  35. ^ Fard AM, Vacas-Jacques P, Hamidi E, Wang H, Carruth RW, Gardecki JA, et al. (December 2013). "Optical coherence tomography--near infrared spectroscopy system and catheter for intravascular imaging". Optics Express. 21 (25): 30849–30858. Bibcode:2013OExpr..2130849F. doi:10.1364/OE.21.030849. PMC 3926541. PMID 24514658.
  36. ^ Ughi GJ, Wang H, Gerbaud E, Gardecki JA, Fard AM, Hamidi E, et al. (November 2016). "Clinical Characterization of Coronary Atherosclerosis With Dual-Modality OCT and Near-Infrared Autofluorescence Imaging". JACC. Cardiovascular Imaging. 9 (11): 1304–1314. doi:10.1016/j.jcmg.2015.11.020. PMC 5010789. PMID 26971006.
  37. ^ Bezerra HG, Quimby DL, Matar F, Mohanty BD, Bassily E, Ughi GJ (July 2023). "High-Frequency Optical Coherence Tomography (HF-OCT) for Preintervention Coronary Imaging: A First-in-Human Study". JACC. Cardiovascular Imaging. 16 (7): 982–984. doi:10.1016/j.jcmg.2023.01.013. PMID 37407126.
  38. ^ van der Sijde JN, Karanasos A, van Ditzhuijzen NS, Okamura T, van Geuns RJ, Valgimigli M, et al. (April 2017). "Safety of optical coherence tomography in daily practice: a comparison with intravascular ultrasound". European Heart Journal - Cardiovascular Imaging. 18 (4): 467–474. doi:10.1093/ehjci/jew037. PMID 26992420.
Retrieved from "http://en.wiki.x.io/w/index.php?title=Endoscopic_optical_coherence_tomography_imaging&oldid=1263590477"