A preliminary investigation of the reinnervation and return of sensory function in burn patients treated with INTEGRA®

被引:24
作者
Anderson, James R. [2 ]
Fear, Mark W. [1 ,3 ]
Phillips, Jacqueline K. [4 ]
Dawson, Linda F. [5 ]
Wallace, Hilary [6 ]
Wood, Fiona M. [6 ,7 ]
Rea, Suzanne M. [6 ,7 ]
机构
[1] Royal Perth Hosp, Telstra Burns Outcome Ctr, McComb Fdn, Perth, WA 6000, Australia
[2] Univ Western Australia, Fac Med Dent & Hlth Sci, Nedlands, WA 6009, Australia
[3] Univ Notre Dame Australia, Sch Med, Fremantle, WA, Australia
[4] Macquarie Univ, Fac Human Sci, Australian Sch Adv Med, N Ryde, NSW 2109, Australia
[5] Murdoch Univ, Fac Hlth Sci, Perth, WA, Australia
[6] Univ Western Australia, Sch Surg, Burn Injury Res Unit, Nedlands, WA 6009, Australia
[7] Princess Margaret Hosp, Perth, WA, Australia
基金
英国医学研究理事会;
关键词
Nerves; Skin; Burn injury; INTEGRA; Sensory function; ARTIFICIAL SKIN; REGENERATION; WOUNDS; SCARS;
D O I
10.1016/j.burns.2011.04.002
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Background: Loss of sensory function in scar after burn is common, although the basis for this loss is not clear. Additionally, little is known about the effects of different treatment modalities on sensory function and neuroanatomical outcomes'in burn patients. Here, we investigated the effects of the use of the INTEGRA (R) dermal scaffold on neuroanatomy and sensory function in acute burn patients. Hypothesis and objectives: We hypothesized that the use of artificial dermal templates would inhibit or reduce reinnervation after excision, since regrowth of nerves requires complex molecular interactions. Therefore the primary objective of this study was to identify whether there is regrowth of nerve fibres in the INTEGRA (R) dermal scaffold. The secondary objective was to identify whether the INTEGRA (R) dermal scaffold reduced nerve regrowth or limited sensory function outcomes in acute burn patients. Methods: Five patients treated with INTEGRA (R), cultured epithelial autograft spray (prepared using ReCell (R) (CEA)) and split skin graft (SSG) were assessed for sensory function in scar and uninjured contralateral control skin. Neuroanatomy of scar and control sites was assessed using immunohistochemistry for PGP9.5, CGRP and substance P neuronal markers. Nerve density and sensory function was also assessed in a comparative group (n = 8) treated with CEA and SSG only. Results: Neuroanatomy was not significantly different in the INTEGRA (R) patients when compared to the CEA/SSG group only. The patients treated with INTEGRA (R) had worse sensory function than those with CEA/SSG only. Conclusions: Peripheral nerves do reinnervate the INTEGRA (R) dermal scaffold. There is no statistically significant reduction in reinnervation observed when compared to a control group. It is possible that the use of artificial dermal constructs, while permissive for nerve regrowth, limit functionality when compared to nerves that regrow through dermal tissue. Further research to understand the causes of this, and into enhancing reinnervation in dermal scaffolds may improve sensory outcome in the most severely burned patients. (C) 2011 Elsevier Ltd and ISBI. All rights reserved.
引用
收藏
页码:1101 / 1108
页数:8
相关论文
共 23 条
[1]
Nerve outgrowth and neuropeptide expression during the remodeling of human burn wound scars - A 7-month follow-up study of 22 patients [J].
Altun, V ;
Hakvoort, TE ;
van Zuijlen, PPM ;
van der Kwast, TH ;
Prens, EP .
BURNS, 2001, 27 (07) :717-722
[2]
Baryza Mary Jo, 1995, Journal of Burn Care and Rehabilitation, V16, P535, DOI 10.1097/00004630-199509000-00013
[3]
SUCCESSFUL USE OF A PHYSIOLOGICALLY ACCEPTABLE ARTIFICIAL SKIN IN THE TREATMENT OF EXTENSIVE BURN INJURY [J].
BURKE, JF ;
YANNAS, IV ;
QUINBY, WC ;
BONDOC, CC ;
JUNG, WK .
ANNALS OF SURGERY, 1981, 194 (04) :413-428
[4]
Approaches permitting and enhancing motoneuron regeneration after spinal cord, ventral root, plexus and peripheral nerve injuries [J].
Carlstedt, T .
CURRENT OPINION IN NEUROLOGY, 2000, 13 (06) :683-686
[5]
Peripheral regeneration [J].
Chen, Zu-Lin ;
Yu, Wei-Ming ;
Strickland, Sidney .
ANNUAL REVIEW OF NEUROSCIENCE, 2007, 30 :209-233
[6]
UCHL1 (PGP 9.5): Neuronal biomarker and ubiquitin system protein [J].
Day, Ian N. M. ;
Thompson, Rod J. .
PROGRESS IN NEUROBIOLOGY, 2010, 90 (03) :327-362
[7]
Regulation of axonal growth and guidance by the neurotrophin family of neurotrophic factors [J].
Gillespie, LN .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2003, 30 (10) :724-733
[8]
Assessment of cutaneous innervation by skin biopsies [J].
Griffin, JW ;
McArthur, JC ;
Polydefkis, M .
CURRENT OPINION IN NEUROLOGY, 2001, 14 (05) :655-659
[9]
ARTIFICIAL DERMIS FOR MAJOR BURNS - A MULTI-CENTER RANDOMIZED CLINICAL-TRIAL [J].
HEIMBACH, D ;
LUTERMAN, A ;
BURKE, J ;
CRAM, A ;
HERNDON, D ;
HUNT, J ;
JORDAN, M ;
MCMANUS, W ;
SOLEM, L ;
WARDEN, G ;
ZAWACKI, B .
ANNALS OF SURGERY, 1988, 208 (03) :313-320
[10]
SENSORY REINNERVATION AND SENSIBILITY AFTER SUPERFICIAL SKIN WOUNDS IN HUMAN PATIENTS [J].
HERMANSON, A ;
DALSGAARD, CJ ;
BJORKLUND, H ;
LINDBLOM, U .
NEUROSCIENCE LETTERS, 1987, 74 (03) :377-382