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Anterior ischemic optic neuropathy in pediatric peritoneal dialysis: risk factors and therapy

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Abstract

Background

Sudden blindness caused by anterior ischemic optic neuropathy (AION) is a rare complication for patients undergoing peritoneal dialysis (PD). Prognosis is generally poor, with AION commonly resulting in permanent visual loss.

Methods

We first describe four case reports of children with AION during PD treatment. We then review ten additional AION cases reported in the literature and compare these 14 affected patients with a control cohort of 59 non-affected patients in the Vienna PD registry.

Results

Significant risk factors for AION were identified as median age (4 vs. 27 months; p < 0.001), autosomal recessive polycystic kidney disease (28.6 vs. 3.4 %; p = 0.01), anephric status (53.8 vs. 6.8 %; p < 0.001) and low to normal blood pressure evidenced by the number of patients having to be treated with antihypertensive medications (14.3 vs. 62.7 %; p = 0.01). Severe hypovolemia was reported in 50 % of all cases. Outcome was visual loss with optic atrophy in nine patients; five patients had a good visual outcome. The major difference in treatment was a rapid bolus of saline within 12 h after the initial symptoms.

Conclusions

Young age, autosomal recessive polycystic kidney disease, anephric status and hypotension are substantial risk factors for AION. Early hospitalization with vascular refilling within a few hours following onset of blindness leads to improved visual outcome.

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Acknowledgments

The authors acknowledge the assistance of A. Chutorian, Columbia University College of Physicians and Surgeons, C. Loirat, CHU Paris–Hôpital Robert Debré, D. Aviles, LSU Health New Orleans and K. Gruber, Department of Pediatrics, Vienna.

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Correspondence to Michael Boehm.

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Dufek, S., Feldkoetter, M., Vidal, E. et al. Anterior ischemic optic neuropathy in pediatric peritoneal dialysis: risk factors and therapy. Pediatr Nephrol 29, 1249–1257 (2014). https://doi.org/10.1007/s00467-013-2747-6

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  • DOI: https://doi.org/10.1007/s00467-013-2747-6

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