Skip to main content

Advertisement

Log in

Repeatability and clinical use of pupillary light reflex measurement using RAPDx® pupillometer

  • Original Paper
  • Published:
International Ophthalmology Aims and scope Submit manuscript

Abstract

Objective

To evaluate the repeatability of pupillary light reflex metrics measured by the RAPDx® dynamic pupillometer in healthy subjects and clinical application in patients with unilateral optic neuritis (ON).

Methods

Sixty eyes of 30 healthy volunteers were measured three times consecutively by the same technician. The amplitude of constriction (AC), the latency of constriction (LOC), the velocity of peak constriction (VC) of light-evoked pupillary constriction, RAPD score for amplitude and latency were measured using RAPDx® dynamic pupillometer. The repeatability of above metrics was assessed by the intraclass correlation coefficient (ICC) and coefficient of variation (Cov). Furthermore, pupillary light reflex measurements were performed in 48 eyes of 24 patients diagnosed with unilateral optic neuritis (ON). Interocular symmetry was evaluated both in the healthy subjects and the ON-involved patients.

Results

High repeatability of AC, LOC, and VC in healthy subjects was displayed, presenting with the ICC value over 0.80 and the Cov less than 8.00%. But the RAPD score for amplitude (ICC: 0.67) and RAPD score for latency (ICC: 0.65) showed only moderate repeatability. Furthermore, a slight declining trend was found in amplitude and peak velocity when continuous and multiple measurements in the healthy subjects. Good symmetry of the AC, LOC, and VC of pupillary light constriction between the two eyes was displayed in the healthy subjects (P > 0.05). By contrast, there was a distinct decrease of AC and VC (P < 0.01), and a mild increase of LOC (P < 0.01) in the ON-involved eye in direct pupillary light reflex.

Conclusions

Pupillary light reflex measured by the RAPDx® pupillometer achieved overall good repeatability and interocular symmetry in healthy subjects. The device also presented decent preliminary results in patients with unilateral ON, suggesting its potential value to be developed as a tool in optic nerve diseases.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

Code availability

Not applicable.

References

  1. Levatin P (1959) Pupillary escape in disease of the retina or optic nerve. Arch Ophthalmol 62:768–779

    Article  CAS  Google Scholar 

  2. Johnson LN, Hill RA, Bartholomew MJ (1988) Correlation of afferent pupillary defect with visual field loss on automated perimetry. Ophthalmology 95(12):1649–1655

    Article  CAS  Google Scholar 

  3. Dacey DM, Liao HW, Peterson BB et al (2005) Melanopsin-expressing ganglion cells in primate retina signal colour and irradiance and project to the LGN. Nature 433(7027):749–754

    Article  CAS  Google Scholar 

  4. McDougal DH, Gamlin PD (2015) Autonomic control of the eye. Compr Physiol 5(1):439–473

    PubMed  PubMed Central  Google Scholar 

  5. Gamlin PD (2006) The pretectum: connections and oculomotor-related roles. Prog Brain Res 151:379–405

    Article  Google Scholar 

  6. Kozicz T, Bittencourt JC, May PJ et al (2011) The Edinger-Westphal nucleus: a historical, structural, and functional perspective on a dichotomous terminology. J Comp Neurol 519(8):1413–1434

    Article  Google Scholar 

  7. Loewenfeld IE (1999) Otto Lowenstein: neurologic and ophthalmologic testing methods during his lifetime. Doc Ophthalmol 98(1):3–20

    Article  CAS  Google Scholar 

  8. Kawasaki A, Moore P, Kardon RH (1995) Variability of the relative afferent pupillary defect. Am J Ophthalmol 120(5):622–633

    Article  CAS  Google Scholar 

  9. Loewenfeld I, Newsome D (1971) Iris mechanics. I. Influence of pupil size on dynamics of pupillary movements. Am J Ophthalmol. 71:347–362

    Article  CAS  Google Scholar 

  10. Thompson HS, Corbett JJ, Cox TA (1981) How to measure the relative afferent pupillary defect. Surv Ophthalmol 26(1):39–42

    Article  CAS  Google Scholar 

  11. Takizawa G, Miki A, Maeda F et al (2015) Association between a relative afferent pupillary defect using pupillography and inner retinal atrophy in optic nerve disease. Clin Ophthalmol 9:1895–1903

    Article  Google Scholar 

  12. Yoo YJ, Hwang JM (2017) Differences in pupillary light reflex between optic neuritis and ischemic optic neuropathy. PLOS ONE. 12(10):e0186741

    Article  Google Scholar 

  13. Najjar RP, Sharma S, Atalay E et al (2018) Pupillary responses to full-field chromatic stimuli are reduced in patients with early-stage primary open-angle glaucoma. Ophthalmology 125(9):1362–1371

    Article  Google Scholar 

  14. Rukmini AV, Milea D, Baskaran M et al (2015) Pupillary responses to high-irradiance blue light correlate with glaucoma severity. Ophthalmology 122(9):1777–1785

    Article  Google Scholar 

  15. Ba-Ali S, Brøndsted AE, Andersen HU et al (2020) Pupillary light responses in type 1 and type 2 diabetics with and without retinopathy. Acta Ophthalmol. https://doi.org/10.1111/aos.14348

    Article  PubMed  Google Scholar 

  16. Landis JR, Koch GG (1977) The measurement of observer agreement for categorical data. Biometrics 33(1):159–174

    Article  CAS  Google Scholar 

  17. Tatham AJ, Meira-Freitas D, Weinreb RN et al (2014) Detecting glaucoma using automated pupillography. Ophthalmology 121(6):1185–1193

    Article  Google Scholar 

  18. Satou T, Ishikawa H, Goseki T et al (2018) Evaluation of a Relative Afferent Pupillary Defect using the RAPDx(®) device before and after treatment in patients with optic nerve disease. Neuroophthalmology 42(3):146–149

    Article  Google Scholar 

  19. Ozeki N, Yuki K, Shiba D et al (2013) Pupillographic evaluation of relative afferent pupillary defect in glaucoma patients. Br J Ophthalmol 97(12):1538–1542

    Article  Google Scholar 

  20. Satou T, Ishikawa H, Asakawa K et al (2016) Evaluation of Relative Afferent Pupillary Defect Using RAPDx device in patients with optic nerve disease. Neuro ophthalmology 40(3):120–124

    Article  Google Scholar 

  21. Lawlor M, Quartilho A, Bunce C et al (2017) Patients with normal tension glaucoma have relative sparing of the relative afferent pupillary defect compared to those with open angle glaucoma and elevated intraocular pressure. Invest Ophthalmol Vis Sci 58(12):5237–5241

    Article  Google Scholar 

  22. Fan X, Miles JH, Takahashi N et al (2009) Sex-specific lateralization of contraction anisocoria in transient pupillary light reflex. Invest Ophthalmol Vis Sci 50(3):1137–1144

    Article  Google Scholar 

  23. Carle CF, Maddess T, James AC (2011) Contraction anisocoria: segregation, summation, and saturation in the pupillary pathway. Invest Ophthalmol Vis Sci 52(5):2365–2371

    Article  Google Scholar 

  24. Smith SA, Ellis CJ, Smith SE (1979) Inequality of the direct and consensual light reflexes in normal subjects. Br J Ophthalmol 63(7):523–527

    Article  CAS  Google Scholar 

  25. Hutchins B, Weber JT (1985) The pretectal complex of the monkey: a reinvestigation of the morphology and retinal terminations. J Comp Neurol 232(4):425–442

    Article  CAS  Google Scholar 

  26. Clarke RJ, Blanks RH, Giolli RA (2003) Midbrain connections of the olivary pretectal nucleus in the marmoset (Callithrix jacchus): implications for the pupil light reflex pathway. Anat Embryol (Berl) 207(2):149–155

    Article  Google Scholar 

  27. Tabatabaei SA, Soleimani M, Alizadeh M et al (2011) Predictive value of visual evoked potentials, relative afferent pupillary defect, and orbital fractures in patients with traumatic optic neuropathy. Clin Ophthalmol 5:1021–1026

    PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This project is supported by the Intramural Research Fund of Joint Shantou International Eye Center. (NO.18–014).

Author information

Authors and Affiliations

Authors

Contributions

All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by Dezhi Zheng, Qi Zhang, Yi Shi, Jialin Chen. The first draft of the manuscript was written by Dezhi Zheng, and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Dezhi Zheng.

Ethics declarations

Conflicts of interest

The authors declare that they have no conflict of interest.

Consent to participate

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

Consent for publication

The participant has consented to the submission of the paper to the journal.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the Joint Shantou International Eye Center (JSIEC) Ethic committee and with the 1964 Declaration of HELSINKI and its later amendments or comparable ethical standards.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zheng, D., Huang, Z., Chen, W. et al. Repeatability and clinical use of pupillary light reflex measurement using RAPDx® pupillometer. Int Ophthalmol 42, 2227–2234 (2022). https://doi.org/10.1007/s10792-022-02222-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10792-022-02222-8

Keywords

Navigation