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Skin reactions after photodynamic therapy are unaffected by 839nm photobiomodulation therapy: A randomized, double-blind, placebo-controlled, clinical trial

Background and Objective Photodynamic therapy (PDT) is associated with erythema and edema. Photobiomodulation (PBM) therapy may stimulate the skin recovery process. We investigated the potential of PBM to reduce PDT-induced skin reactions. Study Design and Methods Healthy volunteers (n=20) were rand...

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Published in:Lasers in surgery and medicine 2017-11, Vol.49 (9), p.810
Main Authors: Bay, Christiane, Vissing, Anne-Cathrine, Thaysen-Petersen, Daniel, Lerche, Catharina Margrethe, Togsverd-Bo, Katrine, Heydenreich, Jakob, Haedersdal, Merete
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container_issue 9
container_start_page 810
container_title Lasers in surgery and medicine
container_volume 49
creator Bay, Christiane
Vissing, Anne-Cathrine
Thaysen-Petersen, Daniel
Lerche, Catharina Margrethe
Togsverd-Bo, Katrine
Heydenreich, Jakob
Haedersdal, Merete
description Background and Objective Photodynamic therapy (PDT) is associated with erythema and edema. Photobiomodulation (PBM) therapy may stimulate the skin recovery process. We investigated the potential of PBM to reduce PDT-induced skin reactions. Study Design and Methods Healthy volunteers (n=20) were randomized to receive left- or right side PBM (near-infrared 839/595nm) or placebo-PBM (595nm) on their buttocks. Corresponding test areas were exposed to standardized PDT reactions, using ablative fractional laser-assisted PDT (AFXL-PDT) with methyl-aminolevulinate (MAL) incubated for 30, 90, and 180 minutes before red-light illumination. Each buttock received PBM and placebo-PBM for five consecutive days, starting one day before PDT interventions. Follow-up visits were performed 4 and 11 days after PDT. Outcome measure included blinded, observer-assessed skin reactions, substantiated by objectively measured erythema and pigment percentages and skin temperatures. Results PDT interventions induced a standardized range of erythema and edema in all subjects. Skin reactions were clinically unaffected by PBM throughout the active treatment period and at all subsequent follow-up visits (PBM vs. placebo-PBM, P=1.000). Clinical results were supported by similar erythema intensities and skin temperatures in PBM and placebo-PBM treated skin: median erythema 28.1% versus 30.3% (AFXL-PDT with 30minutes MAL-incubation), 36.1% versus 35.2% (90minutes MAL-incubation) and 39.4% versus 40.9% (180minutes MAL-incubation) (Day 4, P>0.05). No differences in clinical hyperpigmentation or pigment percentages were observed between corresponding test areas in any subject on the final 11-day follow-up. Conclusion Under the current study conditions, PDT-induced skin reactions were unaffected by PBM. Lasers Surg. Med. 49:810-818, 2017. © 2017 Wiley Periodicals, Inc.
doi_str_mv 10.1002/lsm.22690
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Photobiomodulation (PBM) therapy may stimulate the skin recovery process. We investigated the potential of PBM to reduce PDT-induced skin reactions. Study Design and Methods Healthy volunteers (n=20) were randomized to receive left- or right side PBM (near-infrared 839/595nm) or placebo-PBM (595nm) on their buttocks. Corresponding test areas were exposed to standardized PDT reactions, using ablative fractional laser-assisted PDT (AFXL-PDT) with methyl-aminolevulinate (MAL) incubated for 30, 90, and 180 minutes before red-light illumination. Each buttock received PBM and placebo-PBM for five consecutive days, starting one day before PDT interventions. Follow-up visits were performed 4 and 11 days after PDT. Outcome measure included blinded, observer-assessed skin reactions, substantiated by objectively measured erythema and pigment percentages and skin temperatures. Results PDT interventions induced a standardized range of erythema and edema in all subjects. Skin reactions were clinically unaffected by PBM throughout the active treatment period and at all subsequent follow-up visits (PBM vs. placebo-PBM, P=1.000). Clinical results were supported by similar erythema intensities and skin temperatures in PBM and placebo-PBM treated skin: median erythema 28.1% versus 30.3% (AFXL-PDT with 30minutes MAL-incubation), 36.1% versus 35.2% (90minutes MAL-incubation) and 39.4% versus 40.9% (180minutes MAL-incubation) (Day 4, P&gt;0.05). No differences in clinical hyperpigmentation or pigment percentages were observed between corresponding test areas in any subject on the final 11-day follow-up. Conclusion Under the current study conditions, PDT-induced skin reactions were unaffected by PBM. Lasers Surg. Med. 49:810-818, 2017. © 2017 Wiley Periodicals, Inc.</description><identifier>ISSN: 0196-8092</identifier><identifier>EISSN: 1096-9101</identifier><identifier>DOI: 10.1002/lsm.22690</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Clinical trials ; Double-blind studies ; Edema ; Erythema ; Hyperpigmentation ; I.R. radiation ; Lasers ; Light ; Light therapy ; Photodynamic therapy ; Randomization ; Skin</subject><ispartof>Lasers in surgery and medicine, 2017-11, Vol.49 (9), p.810</ispartof><rights>2017 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Bay, Christiane</creatorcontrib><creatorcontrib>Vissing, Anne-Cathrine</creatorcontrib><creatorcontrib>Thaysen-Petersen, Daniel</creatorcontrib><creatorcontrib>Lerche, Catharina Margrethe</creatorcontrib><creatorcontrib>Togsverd-Bo, Katrine</creatorcontrib><creatorcontrib>Heydenreich, Jakob</creatorcontrib><creatorcontrib>Haedersdal, Merete</creatorcontrib><title>Skin reactions after photodynamic therapy are unaffected by 839nm photobiomodulation therapy: A randomized, double-blind, placebo-controlled, clinical trial</title><title>Lasers in surgery and medicine</title><description>Background and Objective Photodynamic therapy (PDT) is associated with erythema and edema. Photobiomodulation (PBM) therapy may stimulate the skin recovery process. We investigated the potential of PBM to reduce PDT-induced skin reactions. Study Design and Methods Healthy volunteers (n=20) were randomized to receive left- or right side PBM (near-infrared 839/595nm) or placebo-PBM (595nm) on their buttocks. Corresponding test areas were exposed to standardized PDT reactions, using ablative fractional laser-assisted PDT (AFXL-PDT) with methyl-aminolevulinate (MAL) incubated for 30, 90, and 180 minutes before red-light illumination. Each buttock received PBM and placebo-PBM for five consecutive days, starting one day before PDT interventions. Follow-up visits were performed 4 and 11 days after PDT. Outcome measure included blinded, observer-assessed skin reactions, substantiated by objectively measured erythema and pigment percentages and skin temperatures. Results PDT interventions induced a standardized range of erythema and edema in all subjects. Skin reactions were clinically unaffected by PBM throughout the active treatment period and at all subsequent follow-up visits (PBM vs. placebo-PBM, P=1.000). Clinical results were supported by similar erythema intensities and skin temperatures in PBM and placebo-PBM treated skin: median erythema 28.1% versus 30.3% (AFXL-PDT with 30minutes MAL-incubation), 36.1% versus 35.2% (90minutes MAL-incubation) and 39.4% versus 40.9% (180minutes MAL-incubation) (Day 4, P&gt;0.05). No differences in clinical hyperpigmentation or pigment percentages were observed between corresponding test areas in any subject on the final 11-day follow-up. Conclusion Under the current study conditions, PDT-induced skin reactions were unaffected by PBM. Lasers Surg. 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Photobiomodulation (PBM) therapy may stimulate the skin recovery process. We investigated the potential of PBM to reduce PDT-induced skin reactions. Study Design and Methods Healthy volunteers (n=20) were randomized to receive left- or right side PBM (near-infrared 839/595nm) or placebo-PBM (595nm) on their buttocks. Corresponding test areas were exposed to standardized PDT reactions, using ablative fractional laser-assisted PDT (AFXL-PDT) with methyl-aminolevulinate (MAL) incubated for 30, 90, and 180 minutes before red-light illumination. Each buttock received PBM and placebo-PBM for five consecutive days, starting one day before PDT interventions. Follow-up visits were performed 4 and 11 days after PDT. Outcome measure included blinded, observer-assessed skin reactions, substantiated by objectively measured erythema and pigment percentages and skin temperatures. Results PDT interventions induced a standardized range of erythema and edema in all subjects. Skin reactions were clinically unaffected by PBM throughout the active treatment period and at all subsequent follow-up visits (PBM vs. placebo-PBM, P=1.000). Clinical results were supported by similar erythema intensities and skin temperatures in PBM and placebo-PBM treated skin: median erythema 28.1% versus 30.3% (AFXL-PDT with 30minutes MAL-incubation), 36.1% versus 35.2% (90minutes MAL-incubation) and 39.4% versus 40.9% (180minutes MAL-incubation) (Day 4, P&gt;0.05). No differences in clinical hyperpigmentation or pigment percentages were observed between corresponding test areas in any subject on the final 11-day follow-up. Conclusion Under the current study conditions, PDT-induced skin reactions were unaffected by PBM. Lasers Surg. Med. 49:810-818, 2017. © 2017 Wiley Periodicals, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/lsm.22690</doi></addata></record>
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subjects Clinical trials
Double-blind studies
Edema
Erythema
Hyperpigmentation
I.R. radiation
Lasers
Light
Light therapy
Photodynamic therapy
Randomization
Skin
title Skin reactions after photodynamic therapy are unaffected by 839nm photobiomodulation therapy: A randomized, double-blind, placebo-controlled, clinical trial
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