Skip to content

Advertisement

BMC Ophthalmology

  • Research article
  • Open Access
  • Open Peer Review

This article has Open Peer Review reports available.

How does Open Peer Review work?

Noninvasive vascular imaging of ruptured retinal arterial macroaneurysms by Doppler optical coherence tomography

  • 1, 2Email author,
  • 1, 2,
  • 3,
  • 3,
  • 1, 2,
  • 1, 2 and
  • 2
BMC Ophthalmology201515:79

https://doi.org/10.1186/s12886-015-0077-0

©  Miura et al. 2015

Received: 26 March 2015

Accepted: 16 July 2015

Published: 22 July 2015

Open Peer Review reports

Abstract

Background

To describe Doppler optical coherence tomography (OCT) imaging of ruptured retinal arterial macroaneurysms (RAMs).

Methods

Four eyes of four patients with ruptured RAMs were prospectively studied. Vascular imaging was obtained using swept-source Doppler OCT, and compared with indocyanine green angiography images.

Results

En face projection of Doppler OCT images clearly showed RAMs at the corresponding locations of lesions in the indocyanine green angiography images. In Doppler OCT images, RAMs were located in the inner retina in three eyes and in the medium layer of the retina in one eye. In one eye, detection of RAMs by standard OCT was difficult because of the presence of inner retinal hemorrhage. In one eye, disappearance of blood flow after direct laser photocoagulation could be confirmed by Doppler OCT images.

Conclusions

Doppler OCT imaging may potentially function as a noninvasive complementary procedure with indocyanine green angiography.

Keywords

  • Retinal macroaneurysm
  • Doppler
  • Optical coherence tomography
  • Indocyanine green angiography
  • Three dimensional
  • Optical coherence tomography angiography

Background

Retinal arterial macroaneurysms (RAMs) are acquired aneurysmal dilatations of retinal arterioles, and usually develop within the first three orders of the arterial bifurcation [1, 2]. RAMs may remain asymptomatic and spontaneously resolve without treatment. However, rupture of RAMs causes preretinal and intraretinal hemorrhage, which may result in severe visual loss [1]. An accurate and rapid diagnosis is important for treating ruptured RAMs. In current clinical practice, the most reliable methods to detect RAMs are indocyanine green angiography (ICGA) and fluorescein angiography (FA) [1, 3]. However, the clinical applications of ICGA and FA have been limited because of patient discomfort and relatively long measurement times. Optical coherence tomography (OCT) has achieved micrometer-level axial resolution in cross-sectional retinal imaging, and has provided important information about the diagnosis and evaluation of therapeutic effects in RAMs [4–6]. However, standard OCT is only sensitive to backscattered light intensity and cannot provide information about blood flow. Because of this limitation, standard OCT has limited ability to detect RAMs.

Recently, a functional extension of OCT technology for three dimensional (3-D) vascular imaging was developed. This technique was first reported using Doppler OCT and was named optical coherence angiography [7]. Following this development, various 3-D vascular imaging techniques were reported, and were collectively called OCT angiography [8]. The clinical utilities of OCT angiography have been reported for polypoidal choroidal vasculopathy [9–12], choroidal neovascularization, [11–13] macular telangiectasia, [14] and diabetic retinopathy [15, 16]. Unlike standard OCT, OCT angiography can directly evaluate vascular architecture, including a comprehensive evaluation of vascular lesions in RAMs. In this paper, we evaluate the 3-D vascular architecture of RAMs using Doppler OCT angiography, and describe the clinical usefulness of Doppler OCT for RAMs.

Methods

We prospectively evaluated four eyes of four Japanese patients with ruptured RAMs (one male, three females; age range, 67–92 years). The clinical characteristics of these patients are summarized in Table 1. The clinical diagnosis of ruptured RAMs was made by identifying macroaneurysms with ICGA. Eyes with severe cataracts or other eye diseases that interfered with Doppler OCT image quality were excluded from this study. One eye was treated with direct laser photocoagulation.
Table 1

Ruptured retinal macroaneurysm imaged by Doppler optical coherence tomography: Summary of subjects

Case

Gender

Age (years)

Eye

BCVA

Topographic location of retinal macroaneurysm

Associated findings

1

F

75

R

0.3

Medium layer of retina

Vitreous hemorrhage

2

M

73

R

0.6

Inner retina

Vitreous hemorrhage

3

F

92

R

0.05

Inner retina

Vitreous hemorrhage

4

F

67

R

0.9

Inner retina

 

Visual acuity was measured on a Landolt chart. M male; F female; R right; BCVA best corrected visual acuity

The Doppler OCT system used in this study was a custom-made prototype built by the Computational Optic Group at the University of Tsukuba [11, 16]. This Doppler OCT was based on a swept-source technology, and operated at an axial scan speed of 100,000 A-scans/s, using a swept-source laser at a central wavelength of 1060 nm. The probing beam power was set at 1.85 mW, which is lower than the American National Standards Institute safety limit. The axial resolution in tissues was 6.4 μm. In a single scan, the system simultaneously provided both an intensity-based standard OCT image and a Doppler OCT image. The Doppler signal was calculated from two A-lines in two successive B-scans. Doppler signals were displayed in the form of the squared energy of the Doppler phase shift. Raster scanning protocols with 256 A-lines × 2048 B-scans covering a 6.0 × 6.0-mm region on the retina were used for volumetric scans. The acquisition speed of each measurement was 6.6 s/volume. Composite color Doppler OCT images, in which the Doppler OCT signal was overlaid onto the standard OCT with red color, were created from standard OCT and Doppler OCT images to specify the location of blood flow in the standard OCT image. En face vascular images were calculated from Doppler OCT volume data sets.

This study was performed according to the tenets of the Declaration of Helsinki, and was approved by the Institutional Review Boards of the University of Tsukuba and Tokyo Medical University. Informed consent for the study was obtained from all participants.

Results

All eyes showed retinal hemorrhage around RAMs and three of four eyes were accompanied by vitreous hemorrhage. En face projections of Doppler OCT images clearly showed RAMs at the corresponding locations of lesions in the ICGA images (Figs. 1 and 2). Topographical locations of RAMs were readily determined by Doppler OCT B-scan images. RAMs were located in inner retinas in three eyes (Fig. 2). In these cases, RAMs could be readily detected with standard OCT B-scan images as focal protrusions of the retinal surface. In case 1, the RAM was located in the medium layer of the retina with the presence of inner retinal hemorrhage (Fig. 1). In this case, detection of the RAM in standard OCT B-scan images was difficult because of the absence of a focal change at the retinal surface of the RAM. In standard OCT B-scan images, active RAMs showed round high-intensity areas with low-intensity lumens in all cases.
Figure 1
Fig. 1

Doppler OCT images of the right eye of Subject 1 with ruptured retinal macroaneurysm. a Color fundus photograph shows retinal hemorrhage with a white lesion. Black line indicates scanning area of Doppler OCT (C), and white line specifies the B-scan OCT imaging (D, E). b Indocyanine green angiography image shows retinal macroaneurysm (black arrow). c An en face projection image by Doppler OCT shows retinal macroaneurysm at the corresponding locations of lesions in the indocyanine green angiography image (white arrow). d Standard OCT B-scan image shows inner retinal hemorrhage. e Doppler OCT B-scan image shows blood flow at the retinal macroaneurysm (black arrow)

Figure 2
Fig. 2

Doppler OCT images of the right eye of Subject 2 with ruptured retinal macroaneurysm. a Color fundus photograph shows retinal hemorrhage with a white lesion. b Indocyanine green angiography image shows the retinal macroaneurysm (black arrow). Yellow line indicates scanning area of Doppler OCT (C), and white line specifies the B-scan OCT imaging (D, E). c An en face projection image by Doppler OCT shows retinal macroaneurysms at the corresponding locations of lesions in the indocyanine green angiography image (white arrow). d Standard OCT B-scan image shows retinal macroaneurysm with focal bulge of the retinal surface. e Doppler OCT B-scan image shows blood flow in the retinal macroaneurysm (black arrow)

Case 2 underwent direct laser photocoagulation of the RAM. At 4 months after photocoagulation, ICGA showed occlusion of the RAM, and en face projection of Doppler OCT images clearly showed this occlusion. RAMs were filled with high-intensity areas in standard OCT B-scan images, and the disappearance of blood flow could be confirmed by Doppler OCT B-scan imaging (Fig. 3).
Figure 3
Fig. 3

Doppler OCT images of the right eye of Subject 2 after direct laser photocoagulation at the retinal macroaneurysm. a Color fundus photograph shows decreasing retinal hemorrhage. b Indocyanine green angiography image shows disappearance of the retinal macroaneurysm. Yellow line indicates scanning area of Doppler OCT (C), and white line specifies the B-scan OCT imaging (D, E). c An en face projection image by Doppler OCT shows disappearance of retinal macroaneurysm as the indocyanine green angiography image (white arrow). d Standard OCT B-scan image shows high-intensity mass at the retinal macroaneurysm. e Doppler OCT B-scan image shows disappearance of blood flow at the retinal macroaneurysm (black arrow)

Discussion

The clinical finding of RAMs varied greatly and was described as a masquerade-type syndrome [17]. Ruptured RAMs were accompanied by multilayer retinal hemorrhages, and precise diagnosis was difficult without ICGA or FA [1]. Doppler OCT imaging could noninvasively detect the RAMs without dye injection. The therapeutic effects of RAMs treatment could be readily detected with Doppler OCT imaging. This study shows the possibility of using Doppler OCT as an adjunct method to ICGA or FA.

In current clinical practice, the most reliable method to detect RAMs is ICGA or FA [1, 3]. However, neither ICGA nor FA could evaluate the topographic locations of RAMs because of their poor axial resolution [18]. Doppler OCT B-scan imaging could provide precise topographic locations of RAMs. In three of four cases, RAMs were located in the inner retina, as previously reported using commercialized spectral-domain OCT [4–6]. In these cases, detection of RAMs with standard OCT was relatively easy because of the presence of protrusions from the retinal surface at the RAMs. In one case, detection of RAMs by standard OCT imaging was made difficult by the lack of changes at the retinal surface. However, standard OCT findings for RAMs could be readily obtained using Doppler OCT images. After direct laser photocoagulation, disappearance of blood flow could be confirmed by Doppler OCT B-scan imaging, and lesions at the RAM were filled with high-intensity area images, indicating thrombus formation at the RAM. The combination Doppler OCT and standard OCT could therefore be useful for clinical evaluations of RAMs.

This study had several limitations. With the small number of subjects in our case series, we evaluated only some of the variations in RAMs. In this study, 6.6 s were required for a single measurement, despite using high-speed 100 kHz OCT. This relatively long measurement time caused motion artifacts in vascular imaging. Clinical applications of ultra-high-speed OCT have already been reported, indicating that the influence of motion artifacts could be minimized by shortening measurement times [19, 20].

This study demonstrated the clinical utility of Doppler OCT to evaluate RAMs. Doppler OCT could detect only some parts of the retinal vasculature; hence, ICGA or FA may still be required to more thoroughly evaluate the entire structure of vascular lesions. Doppler OCT could not detect dye leakage in FA and dye leakage was an important indicator of the activity of RAMs [1, 2]. However, the clinical applications of ICGA and FA have been limited by the possibility of adverse side effects [21]. Doppler OCT imaging is noninvasive, has a short measurement time, and may potentially function as a noninvasive adjunct tool to FA and ICGA for the assessment of RAMs.

Conclusions

The swept-source Doppler OCT was used to evaluate four eyes of four patients with ruptured RAMs. Doppler OCT images clearly delineate the RAMs, and detect the therapeutic effect after direct laser photocoagulation. Doppler OCT imaging could provide important information for diagnosis and treatment of RAMs.

Abbreviations

RAM: 

retinal arterial macroaneurysm

ICGA: 

indocyanine green angiography

FA: 

fluorescein angiography

OCT: 

optical coherence tomography

3-D: 

three dimensional

Declarations

Acknowledgements

This project was partly supported by KAKENHI (24592682) and the Japan Science and Technology Agency through a program of the Development of Systems and Technology for Advanced Measurement and Analysis.

Authors’ Affiliations

(1)
Department of Ophthalmology, Tokyo Medical University, Ibaraki Medical Center, Inashiki, Japan
(2)
Department of Ophthalmology, Tokyo Medical University, Shinjuku, Japan
(3)
Computational Optics Group, University of Tsukuba, Tsukuba, Japan

References

  1. Pitkanen L, Tommila P, Kaarniranta K, Jaaskelainen JE, Kinnunen K. Retinal arterial macroaneurysms. Acta Ophthalmol. 2014;92:101–4.View ArticlePubMedGoogle Scholar
  2. Rabb MF, Gagliano DA, Teske MP. Retinal arterial macroaneurysms. Surv Ophthalmol. 1988;33:73–96.View ArticlePubMedGoogle Scholar
  3. Gomez-Ulla F, Gonzalez F, Torreiro MG, Perez R, Des J. Indocyanine green angiography in isolated primary retinal arterial macroaneurysms. Acta Ophthalmol Scand. 1988;76:671–4.View ArticleGoogle Scholar
  4. Lee EK, Woo SJ, Ahn J, Park KH. Morphologic characteristics of retinal arterial macroaneurysm and its regression pattern on spectral-domain optical coherence tomography. Retina. 2011;31:2095–101.View ArticlePubMedGoogle Scholar
  5. Goldenberg D, Soiberman U, Loewenstein A, Goldstein M. Heidelberg spectral-domain optical coherence tomographic findings in retinal artery macroaneurysm. Retina. 2012;32:990–5.View ArticlePubMedGoogle Scholar
  6. Shah VA, Poulose A, Cassell M, Sabates NR. Spectral domain optical coherence tomography findings of retinal macroaneurysm. Ophthalmic Surg Lasers Imaging. 2010;41:1–4.Google Scholar
  7. Makita S, Hong Y, Yamanari M, Yatagai T, Yasuno Y. Optical coherence angiography. Opt Express. 2006;14:7821–40.View ArticlePubMedGoogle Scholar
  8. Leitgeb RA, Werkmeister RM, Blatter C, Schmetterer L. Doppler optical coherence tomography. Prog Retin Eye Res. 2014;41:26–43.View ArticlePubMedPubMed CentralGoogle Scholar
  9. Makita S, Jaillon F, Yamanari M, Miura M, Yasuno Y. Comprehensive in vivo micro-vascular imaging of the human eye by dual-beam-scan Doppler optical coherence angiography. Opt Express. 2011;19:1271–83.View ArticlePubMedGoogle Scholar
  10. Miura M, Makita S, Iwasaki T, Yasuno Y. Three-dimensional visualization of ocular vascular pathology by optical coherence angiography in vivo. Invest Ophthalmol Vis Sci. 2011;52:2689–95.View ArticlePubMedGoogle Scholar
  11. Hong YJ, Miura M, Makita S, Ju MJ, Lee BH, Iwasaki T, et al. Noninvasive investigation of deep vascular pathologies of exudative macular diseases by high-penetration optical coherence angiography. Invest Ophthalmol Vis Sci. 2013;54:3621–31.View ArticlePubMedGoogle Scholar
  12. Hong YJ, Miura M, Ju MJ, Makita S, Iwasaki T, Yasuno Y. Simultaneous investigation of vascular and retinal pigment epithelial pathologies of exudative macular diseases by multifunctional optical coherence tomography. Invest Ophthalmol Vis Sci. 2014;55:5016–31.View ArticlePubMedGoogle Scholar
  13. Jia Y, Bailey ST, Wilson DJ, Tan O, Klein ML, Flaxel CJ, et al. Quantitative optical coherence tomography angiography of choroidal neovascularization in age-related macular degeneration. Ophthalmology. 2014;121:1435–44.View ArticlePubMedPubMed CentralGoogle Scholar
  14. Chin EK, Kim DY, Hunter 3rd AA, Pilli S, Wilson M, Zawadzki RJ, et al. Staging of macular telangiectasia: power-Doppler optical coherence tomography and macular pigment optical density. Invest Ophthalmol Vis Sci. 2013;54:4459–70.View ArticlePubMedPubMed CentralGoogle Scholar
  15. Schwartz DM, Fingler J, Kim DY, Zawadzki RJ, Morse LS, Park SS, et al. Phase-variance optical coherence tomography: a technique for noninvasive angiography. Ophthalmology. 2014;121:180–7.View ArticlePubMedGoogle Scholar
  16. Miura M, Hong Y, Yasuno Y, Muramatsu D, Iwasaki T, Goto H. Three-dimensional Vascular Imaging of Proliferative Diabetic Retinopathy by Doppler Optical Coherence Tomography. Am J Ophthalmol. 2015;159:528–38.View ArticlePubMedGoogle Scholar
  17. Spalter HF. Retinal macroaneurysms: a new masquerade syndrome. Trans Am Ophthalmol Soc. 1982;80:113–30.PubMedPubMed CentralGoogle Scholar
  18. Bartsch DU, Freeman WR. Axial intensity distribution analysis of the human retina with a confocal scanning laser tomograph. Exp Eye Res. 1994;58:161–73.View ArticlePubMedGoogle Scholar
  19. Choi W, Mohler KJ, Potsaid B, Lu CD, Liu JJ, Jayaraman V, et al. Choriocapillaris and choroidal microvasculature imaging with ultrahigh speed OCT angiography. PLoS One. 2013;8:e81499.View ArticlePubMedPubMed CentralGoogle Scholar
  20. Blatter C, Klein T, Grajciar B, Schmoll T, Wieser W, Andre R, et al. Ultrahigh-speed non-invasive widefield angiography. J Biomed Opt. 2012;17:070505.View ArticlePubMedGoogle Scholar
  21. Yannuzzi LA, Rohrer KT, Tindel LJ, Sobel RS, Costanza MA, Shields W, et al. Fluorescein angiography complication survey. Ophthalmology. 1986;93:611–7.View ArticlePubMedGoogle Scholar

Copyright

© Miura et al. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Advertisement

BMC Ophthalmology

ISSN: 1471-2415

Contact us