June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Non-selectivity of ERG reductions in eyes treated for retinoblastoma
Author Affiliations & Notes
  • Catherine Liu
    Ophthalmic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
  • Gowtham Jonna
    Ophthalmic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
  • Jasmine Francis
    Ophthalmic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
  • Brian Marr
    Ophthalmic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
    Weill-Cornell Medical College, New York, NY
  • David Abramson
    Ophthalmic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
    Weill-Cornell Medical College, New York, NY
  • Scott Brodie
    Ophthalmic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
    Ophthalmology, Mt. Sinai Hospital, New York, NY
  • Footnotes
    Commercial Relationships Catherine Liu, None; Gowtham Jonna, None; Jasmine Francis, None; Brian Marr, None; David Abramson, None; Scott Brodie, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 3978. doi:
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    • Get Citation

      Catherine Liu, Gowtham Jonna, Jasmine Francis, Brian Marr, David Abramson, Scott Brodie; Non-selectivity of ERG reductions in eyes treated for retinoblastoma. Invest. Ophthalmol. Vis. Sci. 2013;54(15):3978.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract
 
Purpose
 

We have monitored retinal function in patients treated for retinoblastoma (primarily, but not exclusively by intra-arterial chemotherapy infusion) by ERG recordings for the past six years. We here present data from the subset of patients who underwent a complete ERG protocol including both photopic and scotopic recordings to justify our frequent practice of reporting primarily 30-Hz photopic flicker amplitude data.

 
Methods
 

Patients referred for treatment of retinoblastoma underwent ERG recordings during examination under anesthesia whenever possible at baseline, and following most treatment sessions, especially after intra-arterial chemotherapy. All recordings included photopic single flash (Photopic 3.0, “Phot SF”) and 30-Hz flicker (“Phot 30 Hz”) stimuli; when time permitted, many also underwent dark adaptation for 5 minutes (shorter than the ISCEV standard protocol to minimize anesthesia duration) followed by recordings of responses to scotopic rod-isolating (Scotopic 0.01, “Rod”) and scotopic maximal (Scotopic 3.0, “Scot Max”) flash stimuli. Response amplitudes were measured from averages of 10 replicate records to suppress the effects of unsteady baselines caused by the sevofluorane anesthesia. Correlations were calculated for the complete datasets between the four sets of responses amplitude data.

 
Results
 

Complete photopic and scotopic ERG data was available from over 600 ERG studies of 108 patients. The correlation matrix for these ERG responses are detailed in Table I.

 
Conclusions
 

Under our recording conditions, ERG responses of eyes with untreated retinoblastoma or following intra-arterial treatment for retinoblastoma show very high correlations between 30-Hz flicker amplitude responses and the three other standard photopic and scotopic ERG response amplitudes. The reductions in ERG amplitudes seen in these eyes do not appear to be selective for rod or cone systems. These observations support the use of photopic response amplitudes (especially in response to 30-Hz flicker) as the primary ERG outcome measure in studies of treated and untreated eyes with retinoblastoma when more complete ERG protocols may be impractical.

  
Keywords: 624 oncology • 509 electroretinography: clinical • 744 tumors  
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