Multispot and Multiwavelength Lasers for Diabetic Retinopathy

Advanced laser technology allows less damaging, more efficient treatment delivery.

By Manish Nagpal, MS, DO, FRCS; Chaitanya Shukla, DNB; and Kartikey Kothari, MS

Since the ETDRS, panretinal photocoagulation (PRP) or macular laser in the form of focal or grid treatments have been the standard of care for treating patients with diabetic retinopathy. The first lasers were argon and krypton gas in blue-green wavelengths.1,2 Their use was limited because they had short wavelengths, caused light scatter, used high levels of energy, induced photochemical damage, and led to acceleration of cataracts.3 Tunable dye lasers were the next development in laser technology and were available in yellow (577 nm), orange (597 nm to 622 nm), and red wavelengths (622 nm to 680 nm). Maintaining the tunable lasers, however, was expensive and difficult, and some of the dyes were carcinogenic.4 Further research resulted in the introduction of infrared (532 nm) and green (810 nm) wavelengths. The benefits of these lasers include reduced scatter, ease of delivery in dense ocular media, lower cost, and reduced maintenance.5

Further development of solid-state technology brought about the production of 577-nm wavelength lasers4 The combined absorption by both melanin and oxyhemoglobin of 577 nm causes less scatter compared with 532 nm or other yellow wavelengths (561 nm or 568 nm), allows better selective treatment of vasculature, and compensates for the reduction in absorption by retinal pigment epithelium (RPE) melanin compared with 532 nm. The energy concentration to a smaller volume allows use of lower powers and shorter pulse durations. This wavelength provides greater transmittance through some corneal or lenticular opacities,6 and it falls occurs outside the absorption spectrum of retinal xanthophylls, potentially allowing treatment close to the fovea.6 High choriocapillaris absorption should also help to provide more uniform effects in patients with light or irregular fundus pigmentation.7 Studies have shown a higher likelihood that green laser might lead to submacular fibrosis or choroidal neovascularization. Thus, 577-nm wavelength has been described as optimal for macular photocoagulation and treatment of vascular lesions and subretinal vascular proliferations.7,8

Laser light absorbed by melanin of the RPE leads to destruction of mitochondria-rich, and therefore oxygen-demanding, photoreceptors. The resulting mitochondria-deficient glial scars facilitate oxygen diffusion directly from the choroid to the inner retina by reduced oxygen consumption in the outer retina. Relief of inner retinal hypoxia reduces production of VEGF receptors, which limits neovascularization.9,10


Standard laser photocoagulation is performed using single spots with pulse durations of 100 to 200 ms in a continuous mode. The sessions are lengthy and taxing for both patient and surgeon.11 Also, treatments such as PRP carry risk of complications such as macular edema.12

Limitations include the inability to apply laser spots in patterns in the periphery and the tedious burn placement with appropriate spacing.

The multispot laser bypasses some of these limitations.12 Multiple uniform laser burns delivered simultaneously by a single footpedal depression in a variety of patterns using proprietary software create adjustable predetermined square arrays, arcs, and grids with variable spot sizes and variable distance between spots, all controlled through an intuitive interface.11 This defines new strategies in terms of power, software, and hardware technology to formulate safer macular laser applications.10 These devices save time, streamline patient flow for the retina practice, and reduce discomfort from long laser sessions.13,14 These conclusions were drawn from a prospective randomized clinical trial performed to compare the efficacy, collateral damage, and convenience of PRP for proliferative diabetic retinopathy or severe nonproliferative diabetic retinopathy with a 532-nm solid-state green laser (GLx) compared with a 532-nm pattern-scan laser.15 The latter laser showed less collateral damage and similar regression of retinopathy compared with GLx, was less time consuming, and was less painful for patients.16-18

The PASCAL laser (Topcon) uses a proprietary, semiautomated pattern generation technique that allows rapid delivery of laser pulses in a predetermined sequence, with durations of 10 ms to 20 ms at each spot, as opposed to 150 ms to 200 ms with conventional laser. The fluence is only a quarter of that delivered by conventional laser (30 J/cm2 vs conventional, 127 J/cm2). It might be thought that treatment effect would be diminished because of the reduction in fluence, but investigators have not found this to be the case.19

Precision control, safety, and efficiency of the photocoagulation procedure is combined with optimized patient comfort and convenience20-22

Patient satisfaction questionnaires state a preference for multispot laser over conventional laser with the experience with conventional laser being described as tiring and painful.11,18

In our experience comparing multispot laser in 1 eye and conventional laser in the contralateral eye, we observed less field loss in all eyes treated with multispot laser. Improved ease in treating the extreme periphery was also observed.11

Frequency-domain optical coherence tomography has confirmed that burns from the multispot lasers are confined and localized to the outer retina, and fundus autofluorescence has confirmed the presence of burns that are not always visible on fundus biomicroscop.23,24

In our experience, comparison of burns in lapine eyes with half the fundus lasered with PASCAL and the other half with argon using the same power revealed small blisters in the PASCAL-treated tissue, with minimal disdisruption to the rest of the layers. In the argon lase-treated area, the elevation and destruction of the receptors around the treatment area were greater11,22,25-27

The efficacy of the PASCAL laser in the macular area has been supported by the PETER PAN study, in which barely visible subthreshold laser has been shown to be effective in the macular area or as PRP.22,28


The 577-nm wavelength and the multispot delivery mode combination facilitates lower required energy levels than that of conventional 532-nm laser, resulting in less pain and a milder inflammatory response for the patient.18 Treatment grids are homogeneous and evenly spaced, and similarly intense spot patterns are adjustable for individualized treatment needs. The rapidity of the delivery significantly reduces effects of patient movement.14 The longest bursts last 0.5 seconds, but those consisting of 9 spots are practically instantaneous and avoid the effect of most eye movements.12

A combination of benefits of multispot and multiwavelength lasers is seen with the MC-500 Vixi Multicolor Scan Laser Photocoagulator (Nidek), which allows the user to select from 3 wavelengths either alone or in combination: 532-nm green, 577-nm yellow, and 647-nm red. This enables the user to select the necessary color combination to increase efficiency of treatment for a specific indication.6

The Vixi laser includes 8 preprogrammed scan patterns with a memory function for up to 14 patterns. Available patterns include a single spot, squares, circles, arcs of various dimensions, triple arcs, macular grids, triangles, lines, and curves. The most frequently used scan patterns can be recalled from memory for future use. The scan spot size is continuously variable from 50 μm to 500 μm in single mode and from 100 μm to 500 μm in scan and automanipulation mode. Automanipulation mode delivers repeated laser emissions with variable interval times and conventional coagulation settings in a selectable scan pattern. It allows the surgeon to continue laser emission while confirming spot placement. The scan mode is used for repeated laser emissions with a fixed interval time, high power, and instantaneous speed. It saves time by requiring fewer sessions,14 consumes less energy, and provides more versatility than conventional models.6

Compared with green wavelength, yellow wavelength enables more efficient photocoagulation through opaque media such as cataract. In eyes with retinal hemorrhage, better penetration is achieved with the red wavelength. Hence, with this multi-wavelength, multispot laser, treatment may be started with a particular color and continued with a different color. The laser can be used with existing slit lamps, transforming them into a stage for scanning laser treatments. All units incorporate the safety optics with low impact on cornea (SOLIC) optical design, which ensures low-energy density on the cornea and lens even with large spot sizes.7

In our experience, this laser saves time by requiring fewer sessions, consumes less energy, and provides greater versatility. Laser output can be limited to a single wavelength or modulated to a combination of colors for specific treatments.


We compared the 3 wavelengths in patients with diabetic macular edema who were scheduled for a grid laser treatment. In the area of thickened retina we placed 3 sequential line patterns of laser marks, 1 each with red, green, and yellow wavelength using similar power settings (Figure 1). Following the laser treatment, a spectraldomain optical coherence tomography (SD-OCT) scan using the Spectralis (Heidelberg) was taken through the area containing these 3 rows of laser. The comparative scans of each are shown in Figure 2, which shows that the green wavelength burn tends to cause more collateral damage as compared with yellow, and that red tends to produce a deeper burn. We further carried out repeat scans in the same area after 1 month to examine the involution of these laser burns. The least amount of collateral damage was seen with the yellow wavelength (Figures 3-5).

Based on these findings, we conducted a study comparing the morphologic effects of the yellow and green wavelengths using the Vixi laser for patients undergoing laser for diabetic retinopathy.29 Fifty-six eyes of 28 patients received PRP in this prospective study. The green laser was applied to the right eye and yellow to the left. The study areas were imaged on the same day and after 1 month with color fundus photography and SD-OCT.

We found more morphologic changes in the retinal layers in the form of hyperreflectivity, subretinal fluid, and intraretinal vacuoles on OCT scans of the right eyes. At 1 month, SD-OCT scans of the right eyes showed greater alteration in the form of hyperreflectivity involving the RPE and neurosensory retina compared with the left eyes. Hence, yellow was seen to cause less collateral damage to the neuroretina and permit a level of reorganization in the outer retina.15


The pattern scan yellow laser uses less power and decreases patient discomfort.18,22,30 The treatment is delivered in minimal time with a gentle effect on the targeted area; there is minimal effect on the surrounding retinal tissue and an absence of late scarring. Treatment can be delivered through opaque media, and we believe there is potential synergy when combined with intravitreal anti-VEGF therapies.31

Manish Nagpal, MS, DO, FRCS, is a vitreoretinal consultant at Retina Foundation in Ahmedabad, India. Dr. Nagpal is a consultant for Nidek and Topcon. Dr. Nagpal may be reached at

Chaitanya Shukla, DNB, is a fellow at Retina Foundation in Ahmedabad, India. Dr. Shukla may be reached at

Kartikey Kothari, MS, is a fellow at Retina Foundation in Ahmedabad, India. Dr. Kothari may be reached at

  1. Tasman W, Jaeger EA. Duane’s Clinical Ophthalmology. Philadelphia: Lippincott Williams & Wilkins, 2005.
  2. Bessette FM, Nguyen LC. Laser light: its nature and its action on the eye. CMAJ (Ottawa). 1989;141:1141-1148.
  3. Freeman WR, Bartsch DU. New ophthalmic lasers for the evaluation and treatment of retinal disease. Aust N Z J Ophthalmol. 1993;21:139-146.
  4. Kent C. Laser Evolution: True Yellow Meets Solid State. Review of Ophthalmology. 2007;7(24). Available at:
  5. Fankhauser F 2nd, Giger H, Niederer P, Seiler T. Transpupillary laser phototherapy of tumors and vascular anomalies of retina and choroid: theoretical approach and clinical implications. Technol Health Care. 2000;8:93-112.
  6. Papavasileiou E, Prasad S. Multicolor scan laser photocoagulator provides efficiencies in the clinic. Retina Today. 2012;7(3):69-71.
  7. Joondeph BC, Joondeph HC, Blair NP. Retinal macroaneurysms treated with the yellow dye laser. Retina. 1989;9(3):187-192.
  8. Bressler SB, Almukhtar T, Aiello LP. Green or yellow laser treatment for diabetic macular edema: exploratory assessment within the Diabetic Retinopathy Clinical Research Network. Retina. 2013;33(10):2080-2088.
  9. Glickman RD. Phototoxicity to the retina: mechanisms of damage. Int J Toxicol. 2002;21(6):473-490.
  10. Ip M, Puliafito CA. Laser photocoagulation. In: Yanoff M, Duker JS. Ophthalmology. 3rd ed. Mosby; 2008:522- 523.
  11. Nagpal M. Clinical experience with a high-speed multispot laser. Retina Today. 2008:3(5):76-78.
  12. Rosen R, Lumbroso B. Practical guide for the use of Quantel medical 577nm multispot laser: supra scan 577.
  13. Blumenkranz MS, Yellachich D, Andersen DE, et al. Semiautomated patterned scanning laser for retinal photocoagulation. Retina. 2006;26(3):370-376.
  14. Muqit MM, Marcellino GR, Henson DB, et al. Single-session vs multiple-session pattern scanning laser panretinal photocoagulation in proliferative diabetic retinopathy: The Manchester Pascal Study. Arch Ophthalmology. 2010;128(5):525-533.
  15. Nagpal M, Marlecha S, Nagpal K. Comparison of laser photocoagulation for diabetic retinopathy using 532-nm standard laser versus multispot pattern scan laser. Retina. 2010;30(3):452-458.
  16. Sanghvi C, McLauchlan R, Delgado C, et al. Initial experience with the Pascal photocoagulator: a pilot study of 75 procedures. Br J Ophthalmol. 2008;92(8):1061-1064.
  17. Haller JA. PASCAL laser for retinal disease treatment. Retina Today. 2006:1(4).
  18. Muqit MM, Marcellino GR, Gray JC, et al. Pain Responses of Pascal 20 ms multi-spot and 100 ms single-spot panretinal photocoagulation: Manchester Pascal Study, MAPASS report 2. Br J Ophthalmol. 2010;94(11):1493- 1498.
  19. Al-Hussainy S, Dodson PM, Gibson JM. Pain response and follow-up of patients undergoing panretinal laser photocoagulation with reduced exposure times. Eye (Lond.). 2008;22(1):96-99.
  20. Modi D, Chiranand P, Akduman L. Efficacy of patterned scan laser in treatment of macular edema and retinal neovascularization. Clin Ophthalmol. 2009;3:465-470.
  21. Velez-Montoya R, Guerrero-Naranjo JL, Gonzalez-Mijares CC, et al. Pattern scan laser photocoagulation: safety and complications, experience after 1301 consecutive cases. Br J Ophthalmol. 2010;94(6):720-724.
  22. Salman AG. Pascal laser versus conventional laser for treatment of diabetic retinopathy. Saudi J Ophthalmol. 2011;25(2):175-179.
  23. Sanghvi C, McLauchlan R, Delgado C, et al. Initial experience with the PASCAL photocoagulator: a pilot study of 75 procedures. Br J Ophthalmol. 2008;92(8):1061-1064.
  24. Muqit MM, Gray JC, Marcellino, GR, et al. Fundus autofluorescence and fourier-domain optical coherence tomography imaging of 10 and 20 millisecond PASCAL retinal photocoagulation treatment. Br J Ophthalmol. 2009;93(4):518-525.
  25. Nagpal M, S. Jain, Nagpal K et al. Comparison of Histopathological changes of the retinal layers using standard Argon green laser (GLx) single-spot laser versus multispot Pattern Laser (PASCAL) in Indian rabbit retinas with light microscopy. Paper presented at: Asia ARVO; Hyderabad, India; January 15-18, 2009.
  26. Muqit MM, Gray JC, Marcellino GR, et al. Fundus autofluorescence and Fourier-domain optical coherence tomography imaging of 10 and 20 millisecond Pascal retinal photocoagulation treatment. Br J Ophthalmol. 2008:93(4):518-525.
  27. Muqit MM, Henson DB, Young LB, et al. Laser tissue interactions. Ophthalmology. 2010;117(10):2039.
  28. Mugit MM, Young LB, McKenzie R, et al. Pilot randomised clinical trial of Pascal TargETEd Retinal versus variable fluence PANretinal 20 ms laser in diabetic retinopathy: PETER PAN study. Br J Ophthalmol. 2013;97(2):220-227.
  29. Nagpal M, Kothari K, Mehrotra N. Comparison of effect of yellow and green wavelength of laser on morphological changes in retinal layers using spectral-domain optical coherence tomography (SD-OCT). Paper presented at: VRSI meeting; Pune, Maharashtra, India; December 12, 2013.
  30. Al-Hussainy S, Dodson PM, Gibson JM. Pain response and follow-up of patients undergoing panretinal laser photocoagulation with reduced exposure times. Eye (Lond.). 2008:22(1);96-99.
  31. Muqit MM, Gray JG, Marcellino GR, et al. Barely visible 10-millisecond Pascal laser photocoagulation for diabetic macular edema: observations of clinical effect and burn localization. Am J Ophthalmol. 2010;149(6):979-986

Contact Info

Bryn Mawr Communications LLC
1008 Upper Gulph Road, Suite 200
Wayne, PA 19087

Phone: 484-581-1800
Fax: 484-581-1818

Karen Roman

Janet Burk

About Retina Today

Retina Today is a publication that delivers the latest research and clinical developments from areas such as medical retina, retinal surgery, vitreous, diabetes, retinal imaging, posterior segment oncology and ocular trauma. Each issue provides insight from well-respected specialists on cutting-edge therapies and surgical techniques that are currently in use and on the horizon.