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Correspondence  |   August 2012
Could the Open Door Crack on Perioperative Visual Loss Be Even Bigger?
Author Notes
  • University of Iowa, Iowa City, Iowa.
Article Information
Correspondence
Correspondence   |   August 2012
Could the Open Door Crack on Perioperative Visual Loss Be Even Bigger?
Anesthesiology 8 2012, Vol.117, 432-433. doi:10.1097/ALN.0b013e31825fb5d4
Anesthesiology 8 2012, Vol.117, 432-433. doi:10.1097/ALN.0b013e31825fb5d4
To the Editor: 
The recent study of postoperative visual loss after spinal surgery identified long duration anesthesia, male gender, obesity, and the need for larger blood transfusion as risk factors for postoperative visual loss.1 The authors believe the core mechanism for visual loss is a vascular one causing optic nerve ischemia. The accompanying editorial emphasized the possible role anesthesia-associated inflammation may play in visual loss and referenced the article of Staff et al.,  who first described postoperative inflammatory neuropathy.2,3 The inflammatory neuropathy cases described by Staff et al.  all involved peripheral nerves. Perhaps there is a common risk factor in perioperative visual loss and postoperative inflammatory peripheral neuropathy. That factor could be the use of nitrous oxide. It would be interesting if information on the use of nitrous oxide were available from these two reports' databases.
Nitrous oxide anesthesia increases plasma homocysteine.4 Nitrous oxide does this by disrupting a metabolic chain involving folate, vitamin B6, and vitamin B12. Speculatively, the nitrous-oxide–induced increase in homocysteine effects could be greater in individuals who have a preexisting deficiency of these vitamins or a subclinical or undiagnosed variant of the known congenital biochemical abnormalities involving these vitamins, such as hyperhomocystinemia.
Nitrous-oxide–induced increases in plasma homocysteine have been correlated positively with altered endothelial function.4 Increased plasma homocysteine concentration have strong association with increased inflammation.5,6 Increased homocysteine concentrations are strongly correlated with the microvascular complications of diabetes, including neuropathy.7 The ENIGMA trail suggested that if nitrous oxide is used for more than 2 h in patients, it increases their long-term myocardial infarction risk.8 Hyperhomocystinemia is also well described as a factor for central retinal artery occlusion and central retinal vein occlusion.9  11 This is precisely what the injury in perioperative visual loss seems to be.
If this speculated link between nitrous oxide use and perioperative vision loss should ever find any more supporting scientific evidence, it could suggest utility of simple protective strategies to avoid both postoperative visual loss and inflammatory peripheral neuropathy. One remedy could be to administer folate and vitamins B6 and B12 as premedication to patients before they undergo long duration surgery, especially spinal surgery, when using nitrous oxide in the anesthetic. In one preoperative study of 390 patients scheduled for major surgery, 0.2% individuals had a preexisting folate deficiency and 7.5% individuals had preexisting increased plasma homocysteine concentrations.12 Those individuals could possibly be a higher risk for blindness or postoperative inflammatory neuropathy than are the other patients. The authors proposed administering routine preanesthetic folate and vitamin supplements when nitrous oxide was planned to be used on patients undergoing major surgery. The alternative protective remedy would be to avoid use of nitrous oxide surgeries that present the risk of vision loss.
Nitrous oxide is not devoid of benefits and has been shown to reduce long-term pain, possibly via  its N  -methyl-D-aspartic acid receptor blocking effects.13 Thus, the overall place of nitrous oxide use in anesthesia remains a matter of debate.
It is likely that multiple risk factors for visual loss after long duration spinal surgery will remain, and all have a complex interplay with no single remedy being able to eliminate the risk of blindness.
References
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