Clinical pilot study of intense ultrasound therapy to deep dermal facial skin and subcutaneous tissues.
APA
Gliklich RE, White WM, et al. (2007). Clinical pilot study of intense ultrasound therapy to deep dermal facial skin and subcutaneous tissues.. Archives of facial plastic surgery, 9(2), 88-95. https://doi.org/10.1001/archfaci.9.2.88
MLA
Gliklich RE, et al.. "Clinical pilot study of intense ultrasound therapy to deep dermal facial skin and subcutaneous tissues.." Archives of facial plastic surgery, vol. 9, no. 2, 2007, pp. 88-95.
PMID
17372061
Abstract
[OBJECTIVE] To evaluate the clinical safety of intense ultrasound in the treatment of the dermis and subcutaneous tissues of the face and neck in terms of skin inflammation, pain, adverse events, and histologic features.
[DESIGN] In an open-label, phase 1 study, patients scheduled to undergo a rhytidectomy were enrolled into immediate (face-lift surgery within 24 hours of intense ultrasound treatment) and delayed (face-lift surgery 4-12 weeks after treatment) treatment groups. Intense ultrasound treatments were performed as a series of several linear exposures delivered 1.5 to 2.0 mm apart with the use of 1 of 3 available handpieces with different focal depths. Subject pain ratings and standardized digital photographs were obtained at uniform points. Photographs were blindly rated for inflammation. Histologic evaluation of treated tissues was performed with nitroblue tetrazolium chloride viability stain.
[RESULTS] Fifteen subjects with a mean +/- SD age of 53 +/- 7 years were enrolled. Seven subjects were nonrandomly assigned to the immediate group and 8 were in the delayed group. On histologic examination, thermal injury zones were consistently identified in the dermis at exposure levels greater than 0.5 J as focal areas of denatured collagen. At this threshold level or above, most patient exposures were associated with transient superficial skin erythema and slight to mild discomfort on a standardized pain scale. No other adverse effects were noted in any case. Thermal injury zones were produced in the expected linear pattern and were consistent in size and depth from zone to zone. Increasing source power did not increase the depth of the epicenter of the thermal injury zone. Epidermis was spared in all cases.
[CONCLUSION] In this first clinical study of intense ultrasound therapy to facial tissues, the intense ultrasound system allowed for the safe and well-tolerated placement of targeted, precise, and consistent thermal injury zones in the dermis and subcutaneous tissues with sparing of the epidermis.
[DESIGN] In an open-label, phase 1 study, patients scheduled to undergo a rhytidectomy were enrolled into immediate (face-lift surgery within 24 hours of intense ultrasound treatment) and delayed (face-lift surgery 4-12 weeks after treatment) treatment groups. Intense ultrasound treatments were performed as a series of several linear exposures delivered 1.5 to 2.0 mm apart with the use of 1 of 3 available handpieces with different focal depths. Subject pain ratings and standardized digital photographs were obtained at uniform points. Photographs were blindly rated for inflammation. Histologic evaluation of treated tissues was performed with nitroblue tetrazolium chloride viability stain.
[RESULTS] Fifteen subjects with a mean +/- SD age of 53 +/- 7 years were enrolled. Seven subjects were nonrandomly assigned to the immediate group and 8 were in the delayed group. On histologic examination, thermal injury zones were consistently identified in the dermis at exposure levels greater than 0.5 J as focal areas of denatured collagen. At this threshold level or above, most patient exposures were associated with transient superficial skin erythema and slight to mild discomfort on a standardized pain scale. No other adverse effects were noted in any case. Thermal injury zones were produced in the expected linear pattern and were consistent in size and depth from zone to zone. Increasing source power did not increase the depth of the epicenter of the thermal injury zone. Epidermis was spared in all cases.
[CONCLUSION] In this first clinical study of intense ultrasound therapy to facial tissues, the intense ultrasound system allowed for the safe and well-tolerated placement of targeted, precise, and consistent thermal injury zones in the dermis and subcutaneous tissues with sparing of the epidermis.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 해부 | subcutaneous
|
피하조직 | dict | 3 | |
| 시술 | rhytidectomy
|
안면거상술 | dict | 1 | |
| 해부 | skin
|
scispacy | 1 | ||
| 해부 | subcutaneous tissues
|
scispacy | 1 | ||
| 해부 | dermis
|
scispacy | 1 | ||
| 해부 | focal
|
scispacy | 1 | ||
| 해부 | tissues
|
scispacy | 1 | ||
| 해부 | nitroblue tetrazolium chloride
|
scispacy | 1 | ||
| 해부 | Epidermis
|
scispacy | 1 | ||
| 해부 | facial tissues
|
scispacy | 1 | ||
| 합병증 | dermal facial
|
scispacy | 1 | ||
| 약물 | nitroblue tetrazolium chloride
|
C0298621
2,2'-di-p-nitrophenyl-5,5'-diphenyl-3,3'-(3,3'-dimethoxy-4,4'-diphenylene)ditetrazolium chloride
|
scispacy | 1 | |
| 약물 | [DESIGN] In
|
scispacy | 1 | ||
| 질환 | pain
|
C0030193
Pain
|
scispacy | 1 | |
| 질환 | Subject pain
|
scispacy | 1 | ||
| 질환 | inflammation
|
C0021368
Inflammation
|
scispacy | 1 | |
| 질환 | skin erythema
|
C0041834
Erythema
|
scispacy | 1 | |
| 기타 | dermis
|
scispacy | 1 | ||
| 기타 | collagen
|
scispacy | 1 | ||
| 기타 | skin erythema
|
scispacy | 1 |
MeSH Terms
Adult; Dermis; Equipment Design; Face; Female; Humans; Inflammation; Male; Middle Aged; Pilot Projects; Prospective Studies; Rhytidoplasty; Subcutaneous Tissue; Treatment Outcome; Ultrasonic Therapy
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