1995
DOI: 10.1177/014556139507401004
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The Current Status of Expanded Polytetrafluoroethylene (Gore-Tex) in Facial Plastic Surgery

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Cited by 23 publications
(12 citation statements)
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“…This led to years of experience and experimentation with ePTFE in the facial cosmetic arena. 2 ePTFE comes in different forms and is manufactured by various companies. The most frequently used solid soft tissue implants in the United States for facial augmentation are Gore-Tex, UltraSoft, which has replaced SoftForm (Tissue Technologies Inc., San Francisco, CA, USA), and Advanta (Atrium Medical Corporation, Hudson, NH, USA).…”
Section: Sue Ellen Cox MD Has Indicated No Significant Interest Witmentioning
confidence: 99%
See 1 more Smart Citation
“…This led to years of experience and experimentation with ePTFE in the facial cosmetic arena. 2 ePTFE comes in different forms and is manufactured by various companies. The most frequently used solid soft tissue implants in the United States for facial augmentation are Gore-Tex, UltraSoft, which has replaced SoftForm (Tissue Technologies Inc., San Francisco, CA, USA), and Advanta (Atrium Medical Corporation, Hudson, NH, USA).…”
Section: Sue Ellen Cox MD Has Indicated No Significant Interest Witmentioning
confidence: 99%
“…In 1993, the US Food and Drug Administration (FDA) approved ePTFE (Gore‐Tex, WL Gore & Associates, Flagstaff, AZ, USA) implants for facial defect reconstruction and augmentation. This led to years of experience and experimentation with ePTFE in the facial cosmetic arena 2…”
mentioning
confidence: 99%
“…It is also noncarcinogenic, seldom allergenic, and causes minimal tissue reaction. 6,9 Gore-Tex is available in 1 mm, 2 mm, and 4 mm thick sheets and sutures. The sheets have been used in other surgeries including general, cardiovascular, and urogynecological surgery.…”
Section: Gore-texmentioning
confidence: 99%
“…It is contraindicated for cosmetic lip augmentation, tem-poromandibular joint reconstruction, cardiovascular defects, and dermal placement. [45][46][47] In the present study, the most common complication encountered possibly related to sling placement was seroma formation found in 10% of the patients. This was amenable to aspiration in all cases, although 2 patients required serial aspiration for more than 2 weeks.…”
Section: Commentmentioning
confidence: 78%