Literature DB >> 30450343

Is There an Association Between Hyperbaric Oxygen Therapy and Improved Outcome of Deep Chemical Peeling? A Randomized Pilot Clinical Study.

Itay Wiser1,2, Averbuch Sagie Roni1, Ella Ziv1,2, Mony Friedman2,3, Shay Efraty2,3, Lior Heller1,2, Marina Landau2,4, Tali Friedman1,2.   

Abstract

BACKGROUND: Phenol chemical peeling (PCP) treatment is associated with prolonged recovery and sustained adverse events. Hyperbaric oxygen therapy (HBOT) is known to accelerate wound healing. The purpose of the current study was to evaluate the effect of HBOT on PCP recovery period and adverse events.
METHODS: This is a pilot randomized controlled clinical study. Women following PCP underwent 5 consecutive daily HBOT sessions, compared with PCP alone. Pain, pruritus, erythema, crusting, scaling, and edema were daily evaluated up to 28 days following PCP. Photographs taken on days 14 and 35 following PCP were assessed. Confidence to appear in public was assessed 14 days following PCP.
RESULTS: Eight participants equally assigned to HBOT and control groups. Lower severity scores for erythema, scaling, and pruritus were documented in the HBOT group (mean difference 1.19, P = .006; .84, P = .04; and 2.19, P = .001, respectively). Photographic assessment severity score was higher for skin tightness, edema, erythema, crusting, and scaling in the control group on day 14 post PCP (P < .05) and for erythema on day 35 post PCP (P < .05). Epithelialization percentage was higher in the HBOT group on day 14 post PCP compared with controls (98.5% ± 1% vs 94.2% ± 1%; P = .021). The HBOT group scored higher in confidence to appear in public (20.8 ± 1.7 vs 14.5 ± 1.3; P = .029).
CONCLUSION: Hyperbaric oxygen therapy following PCP is associated with faster recovery as assessed by both patients and caregivers. So far, HBOT was mainly used in the treatment of problematic or chronic wounds. Our study suggests expanding the indications in which hyperbaric oxygen treatment is applicable and recommended.

Entities:  

Keywords:  chemical peels; clinical trials; dermatologic therapy; hyperbaric oxygen treatment

Year:  2018        PMID: 30450343      PMCID: PMC6236503          DOI: 10.1177/2292550317749511

Source DB:  PubMed          Journal:  Plast Surg (Oakv)        ISSN: 2292-5503            Impact factor:   0.947


  23 in total

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Authors:  J V Boykin
Journal:  Wound Repair Regen       Date:  2001 Sep-Oct       Impact factor: 3.617

Review 2.  Hyperbaric oxygen: its uses, mechanisms of action and outcomes.

Authors:  A L Gill; C N A Bell
Journal:  QJM       Date:  2004-07

3.  Chemical peels.

Authors:  Marina Landau
Journal:  Clin Dermatol       Date:  2008 Mar-Apr       Impact factor: 3.541

Review 4.  Hyperbaric oxygen therapy.

Authors:  R M Leach; P J Rees; P Wilmshurst
Journal:  BMJ       Date:  1998-10-24

Review 5.  Acute peripheral ischaemia and compartment syndromes: a role for hyperbaric oxygenation.

Authors:  F Wattel; D Mathieu; R Nevière; N Bocquillon
Journal:  Anaesthesia       Date:  1998-05       Impact factor: 6.955

Review 6.  Gas gangrene.

Authors:  G B Hart; R C Lamb; M B Strauss
Journal:  J Trauma       Date:  1983-11

Review 7.  Phenol peeling and the history of phenol peeling.

Authors:  J M Stuzin
Journal:  Clin Plast Surg       Date:  1998-01       Impact factor: 2.017

8.  Hyperbaric oxygenation accelerates the healing rate of nonischemic chronic diabetic foot ulcers: a prospective randomized study.

Authors:  Laurence Kessler; Pascal Bilbault; Francoise Ortéga; Claire Grasso; Raphael Passemard; Dominique Stephan; Michel Pinget; Francis Schneider
Journal:  Diabetes Care       Date:  2003-08       Impact factor: 19.112

9.  Hyperbaric oxygen attenuates apoptosis and decreases inflammation in an ischemic wound model.

Authors:  Qixu Zhang; Qing Chang; Robert A Cox; Xuemei Gong; Lisa J Gould
Journal:  J Invest Dermatol       Date:  2008-03-13       Impact factor: 8.551

Review 10.  Chemical peels in aesthetic dermatology: an update 2009.

Authors:  T C Fischer; E Perosino; F Poli; M S Viera; B Dreno
Journal:  J Eur Acad Dermatol Venereol       Date:  2009-09-08       Impact factor: 6.166

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