Guest guest Posted July 18, 2002 Report Share Posted July 18, 2002 > , I think you've raised an interesting and important point. My > theoretical concerns are not only with the best method of zapping > vessels as you discussed above, but (even with ideal equipment and > practitioner) the short- and long-term consequences of zapping > vessels. It may well be that zapping vessels may not result in > permanent change in some or even most rosaceans, and that repeated > treatments will be needed. It's entirely possible that, with the > body's compensatory mechanisms, original or continued treatments may > make rosacea worse. I think you're right that certain forms of IPL or laser treatment have the capability to make things worse. Dr. Nase underwent pulsed- dye laser treatment, which reduced his redness by ~50% and eliminated much of his telangiectasia (he reports all this in his book). However, he found that his skin sensitivity to skincare products and also to the environment, and flushing associated with that, was much worsened. This evidence, albeit anecdotal, reminds me a little of the laser abstract you recently posted where the doctors were pleased with improvement, but patients weren't. Anything that causes an insult to the skin has the potential to cause angiogenesis (e.g. blistering, bruising, swelling). This is why the newer lasers, and Photoderm in particular, are of theoretical benefit because they are more selective for the blood vessel. Dr. Nase has *always* cautioned against casuing deep bruising or blistering of the skin, because it will likely cause angiogenesis -- i.e. more redness and flushing. In fact, Nase also cautioned against only having 2 or 3 treatments because of the potential for angiogenesis. <questions about aretries and veins snipped - pass!> > You know, , the more we all discuss this, the more convinced I > am that IPL and related treatments are so in their infancy. This is > really experimental stuff. I'm also reminded here of Rick's > insightful hammer/nail analogy. We know that laser treatments work > best for specific, visible skin conditions and imperfections. Using > laser-related technologies for anti-aging and rosacea is wholly > different. (Below you mention psoriasis, but I assume you're > referring to post-PUVA therapy, oral medication that is then > activated by UV light; I wasn't aware that angiogenesis is a problem there.) Dr. Ormerod's study on psoriasis followed the topical treatment of psoriasis patients with an NO inhibitor (L-NAME). I believe it was double-blind placebo controlled but don't have access to the full text any more. Dr. Ormerod used laser-doppler to measure blood flow through the cheeks where topical L-NAME was applied. He found a 40% reduction in blood flow using laser-doppler. He also meausured the production of VEGF and found a significant decrease (can't remember the exact figures). > out of it? But if I'm reading this right, then theoretically topical > NOI might help stave off facial edema and inflammation, but not > flushing. The reasons why it's hypothesised that NO inhibition could reduce flushing is that NO is involved in many forms of skin flushing and redness, including to heat, irritation, etc. (Nase's book has a lot of references on this). In addition, simply blocking endothelial NO production which occurs continuously from vessel walls leads to reduction in blood-flow through those vessels (this is what the Ormerod paper documented). This obviously has potential to reduce residual redness and discomfort. I have had discussions with doctors (other than Ethan Lerner) who have run preliminary trials with NO inhibitors on rosacea with no visible benefit (I don't know whether they used laser-doppler). This raises more questions than it answers. Was there still the reduction in blood flow as measured on Psoriasis patients? Why did this not reduce redness? Was the NO inhibitor getting to the larger feed vessels where it was needed? Was the cream base optimised? Was the NO inhibitor the lasest and most potent? etc. etc. . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 18, 2002 Report Share Posted July 18, 2002 > , I think you've raised an interesting and important point. My > theoretical concerns are not only with the best method of zapping > vessels as you discussed above, but (even with ideal equipment and > practitioner) the short- and long-term consequences of zapping > vessels. It may well be that zapping vessels may not result in > permanent change in some or even most rosaceans, and that repeated > treatments will be needed. It's entirely possible that, with the > body's compensatory mechanisms, original or continued treatments may > make rosacea worse. I think you're right that certain forms of IPL or laser treatment have the capability to make things worse. Dr. Nase underwent pulsed- dye laser treatment, which reduced his redness by ~50% and eliminated much of his telangiectasia (he reports all this in his book). However, he found that his skin sensitivity to skincare products and also to the environment, and flushing associated with that, was much worsened. This evidence, albeit anecdotal, reminds me a little of the laser abstract you recently posted where the doctors were pleased with improvement, but patients weren't. Anything that causes an insult to the skin has the potential to cause angiogenesis (e.g. blistering, bruising, swelling). This is why the newer lasers, and Photoderm in particular, are of theoretical benefit because they are more selective for the blood vessel. Dr. Nase has *always* cautioned against casuing deep bruising or blistering of the skin, because it will likely cause angiogenesis -- i.e. more redness and flushing. In fact, Nase also cautioned against only having 2 or 3 treatments because of the potential for angiogenesis. <questions about aretries and veins snipped - pass!> > You know, , the more we all discuss this, the more convinced I > am that IPL and related treatments are so in their infancy. This is > really experimental stuff. I'm also reminded here of Rick's > insightful hammer/nail analogy. We know that laser treatments work > best for specific, visible skin conditions and imperfections. Using > laser-related technologies for anti-aging and rosacea is wholly > different. (Below you mention psoriasis, but I assume you're > referring to post-PUVA therapy, oral medication that is then > activated by UV light; I wasn't aware that angiogenesis is a problem there.) Dr. Ormerod's study on psoriasis followed the topical treatment of psoriasis patients with an NO inhibitor (L-NAME). I believe it was double-blind placebo controlled but don't have access to the full text any more. Dr. Ormerod used laser-doppler to measure blood flow through the cheeks where topical L-NAME was applied. He found a 40% reduction in blood flow using laser-doppler. He also meausured the production of VEGF and found a significant decrease (can't remember the exact figures). > out of it? But if I'm reading this right, then theoretically topical > NOI might help stave off facial edema and inflammation, but not > flushing. The reasons why it's hypothesised that NO inhibition could reduce flushing is that NO is involved in many forms of skin flushing and redness, including to heat, irritation, etc. (Nase's book has a lot of references on this). In addition, simply blocking endothelial NO production which occurs continuously from vessel walls leads to reduction in blood-flow through those vessels (this is what the Ormerod paper documented). This obviously has potential to reduce residual redness and discomfort. I have had discussions with doctors (other than Ethan Lerner) who have run preliminary trials with NO inhibitors on rosacea with no visible benefit (I don't know whether they used laser-doppler). This raises more questions than it answers. Was there still the reduction in blood flow as measured on Psoriasis patients? Why did this not reduce redness? Was the NO inhibitor getting to the larger feed vessels where it was needed? Was the cream base optimised? Was the NO inhibitor the lasest and most potent? etc. etc. . Quote Link to comment Share on other sites More sharing options...
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