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Comparison of pain experience and time required for pre-planned navigated peripheral laser versus conventional multispot laser in the treatment of diabetic retinopathy

  • Francesca AmorosoEmail author
  • Alexandre Pedinielli
  • Polina Astroz
  • Oudy Semoun
  • Vittorio Capuano
  • Alexandra Miere
  • Eric H. Souied
Original Article
  • 16 Downloads
Part of the following topical collections:
  1. Eye Complications of Diabetes

Abstract

Purpose

To compare the pain and the duration of a panretinal photocoagulation (PRP) session using a conventional multispot laser (Quantel Medical) versus the Navilas® laser.

Methods

Treatment-naïve patients requiring bilateral PRP for diabetic retinopathy were included. For each patient, PRP was carried out using a conventional multispot laser (Quantel Medical, 577 nm) in one eye and the other eye was treated with the Navilas laser (OD-OS, 577 nm). For both PRP treatments, similar parameters (same power, exposure time, number, size and spacing of the spots) were used. For each eye, the duration of the session and the pain, measured using respectively a chronometer and a visual analogic scale (VAS), were recorded.

Results

Thirty-two eyes of sixteen patients (mean age 57 ± 13 SD, range 28–74), 11 men and 5 women, have been included. A mean of 1289 (1000–1500) spots with a mean power of 352 mW (300–450 mW) and an exposure time of 27 ms (20–30 ms) were delivered. The PRP session with the Navilas laser (mean time of 5.2 ± 0.8 min) was faster than with the conventional multispot laser (6.6 ± 1.1 min) (p = 0.02). Laser-induced pain was significantly reduced (VAS of 2.4 ± 1.6) using the Navilas laser compared to conventional laser (VAS: 7.1 ± 2) (p < 0.001).

Conclusion

The PRP sessions using the Navilas laser were significantly faster and less painful than with a conventional multispot laser in our series.

Keywords

Navilas® Navigated-PRP Conventional multispot laser Diabetic retinopathy 

Notes

Funding

None.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from all individual participants included in the study.

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Copyright information

© Springer-Verlag Italia S.r.l., part of Springer Nature 2019

Authors and Affiliations

  1. 1.Department of Ophthalmology, Centre Hospitalier Intercommunal de CréteilUniversité Paris Est CréteilCreteilFrance

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