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Originally Posted by Soton Pod
I would have to say, in response to your comments, that using liquid nitrogen as an alternative to phenol is viable. You mention the issue of pain. This has never been something I have encountered bearing in mind that the freeze times required are short when compared with plantar wart treatments. Matrix tissue is much more suseptable to cold injury than the plantar epidermis and so freeze times are brief. Also, immediate pain is less as the toe is already anaesthetised but of course as the anaesthetic wears off some discomfort may return but this needs to be properly investigated to make a fair comparison.
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Between 1987 and 1989, sixty-eight patients underwent bi-lateral (both hallux) nail surgery where phenol was used as the chemical agent on one digit, whilst LN2 (either by direct or indirect application of the cryogen) was used on the other. Post-operative care was provided up to eight weeks after surgery and an additional two review appointments were scheduled at six and twelve-month intervals following complete healing.
From those patients:
· With phenol, two patients reported mild to moderate post-operative discomfort (both TNAs)
· With LN2, twelve patients reported mild to moderate pain (8 TNAs and 4 PNAs) and nine patients reported moderate to severe pain (6 TNAs and 3 PNAs)
· With phenol, healing times were between 14 and 28 days for PNAs; 33 and 58 days for TNAs
· With LN2, healing times were between 13 and 21 days for PNAs; 28 and 48 days for TNAs (healing times were measured by closure of the wound with no exudate)
· With phenol there were no regrowths of nail at the 12 month review
· With LN2 there were 12 partial regrowths (with TNAs) and 1 regrowth (with PNA)
Phenol was applied by the standard three and four minutes irrigation via a cotton bud applicator. LN2 was applied as a direct cryogen through a fine spray for all TNAs (23 in total) and indirect application via a 4mm dia closed cryo-probe for all PNAs (45 in total) in two freeze/thaw cycles between 10 and 20 seconds (until the formation of a visible iceball at 3mm beyond the margin of the target tissue).
Post-operative discomfort/pain is difficult to measure objectively for comparative analysis as no two patients have the same pain threshold, however it was observed that there was an elevated level of discomfort when the cryogen was applied directly to the matrix and nail bed tissue and especially so when there was formation of a haemorrhagic bullae (5 TNAs and 1 PNA).
I would concur that freeze times are much less than those used in VP treatments, especially with planter verrucae, however it is very difficult to measure the iceball formation unless thermocouples are inserted into the adjacent tissue. If thermocouples are not used then you run the risk of inadequate iceball formation (leading to regrowth) or excessive iceball formation (leading to severe post-operative pain - and malformation of the remaining nail matrix when used for PNAs).
Mark Russell