Basic fibroblast growth factor reduces scar formation in acute incisional wounds

ABSTRACT In order to identify a means to reduce scar formation of the skin after incision, this study examined the effect of local administration of basic fibroblast growth factor (bFGF) in humans. bFGF was administered to a sutured wound immediately after an operation. The drug was injected once in...

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Published inWound repair and regeneration Vol. 15; no. 5; pp. 617 - 623
Main Authors Ono, Ichiro, Akasaka, Yoshikiyo, Kikuchi, Risa, Sakemoto, Akiko, Kamiya, Takafumi, Yamashita, Toshiharu, Jimbow, Kowichi
Format Journal Article
LanguageEnglish
Published Malden, USA Blackwell Publishing Inc 01.09.2007
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Summary:ABSTRACT In order to identify a means to reduce scar formation of the skin after incision, this study examined the effect of local administration of basic fibroblast growth factor (bFGF) in humans. bFGF was administered to a sutured wound immediately after an operation. The drug was injected once into the dermis of the margins of wounds using a 27G needle or rinsing after performing dermostitches. The lengths of the treated wounds varied from 1 to 32 cm, and the subjects were 2–86 years old. Sutured wounds after excision of skin tumors from the face, trunk, and limbs and sutured wounds such as those at the donor sites of full‐thickness skin grafts were treated with low‐dose bFGF injections (0.1 μg/cm wound; Group 2), high‐dose bFGF injections (1 μg/cm wound; Group 3), and rinsed with high‐dose bFGF (1 μg/cm wound; Group 4). No patient treated with bFGF had hypertrophic scars, while some patients had hypertrophic or very wide scars in the control group (Group 1), and the ratios of minimum scarring of Group 2 ( p<0.001), Group 3 ( p<0.0001), and Group 4 ( p<0.0001) were statistically significantly higher than those of Group 1. Postoperative administration of bFGF inhibited hypertrophic scarring and widening of remaining scars without any serious side effects.
Bibliography:ark:/67375/WNG-25HN8RK6-6
ArticleID:WRR293
istex:6B33ED02D6019CF745A80C101C02E37C22A4002C
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1067-1927
1524-475X
DOI:10.1111/j.1524-475X.2007.00293.x