Experimental study on the vascular thermal response to visible laser pulses
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  • 作者:D. Li ; B. Chen ; W. J. Wu ; G. X. Wang ; Y. L. He ; Z. X. Ying
  • 关键词:Port ; wine stain ; Laser irradiation ; Pulsed dye laser ; Dorsal skin chamber ; Vessel thermal responses
  • 刊名:Lasers in Medical Science
  • 出版年:2015
  • 出版时间:January 2015
  • 年:2015
  • 卷:30
  • 期:1
  • 页码:135-145
  • 全文大小:1,314 KB
  • 参考文献:1. Alper JC, Holmes LB (1983) The incidence and significance of birthmarks in a cohort of 4,641 newborns. Pediatr Dermatol 1(1):58-8 CrossRef
    2. Kelly KM, Choi B, McFarlane S et al (2005) Description and analysis of treatments for port-wine stain birthmarks. Arch Facial Plast Surg 7(5):287-4 CrossRef
    3. Minkis K, Geronemus RG, Hale EK (2009) Port wine stain progression: a potential consequence of delayed and inadequate treatment? Lasers Surg Med 41(6):423-26 CrossRef
    4. Anderson RR, Parrish JA (1981) Microvasculature can be selectively damaged using dye laser: a basic theory and experimental evidence in human skin. Lasers Surg Med 1(3):263-76 CrossRef
    5. Tan OT, Morrison P, Kurban AK (1990) 585-nm for the treatment of port-wine stains. Plast Reconstr Surg 86(6):1112-117
    6. Dai T, Pikkula BM, Tunnell JW, Chang DW, Anvari B (2003) Thermal response of human skin epidermis in different skin types to 595-nmlaser irradiation and cryogen spray cooling: an ex-vivo study. Lasers in Surgery: Advanced Characterization, Therapeutics, and Systems XIII, SPIE Proceedings 4949:1-
    7. Dai T, Diagaradjane P, Yaseen MA, Pikkula BM, Thomsen S, Anvari B (2005) Laser-induced thermal injury to dermal blood vessels: analysis of wavelength (585 nm vs. 595 nm), cryogen spray cooling, and wound healing effects. Lasers Surg Med 37(3):210-18
    8. Kimel S, Svaasand LO, Wilson MH, Schell MJ, Milner TE, Neslon JS, Berns MW (1994) Differential vascular response to laser photothermolysis. J Invest Dermatol 103(5):693-00 CrossRef
    9. Kimel S, Svaasand LO, Cao D et al (2002) Vascular response to laser photothermolysis as a function of pulse duration, vessel type, and diameter: implications for port wine stain laser therapy. Lasers Surg Med 30(2):160-69 CrossRef
    10. Kimel S, Svaasand LO, Hammer-Wilson MJ, Nelson JS (2003) Influence of wavelength on response to laser photothermolysis of blood vessels: implications for port wine stain laser therapy. Lasers Surg Med 33(5):288-95 CrossRef
    11. Barton JK, Welch AJ, Izatt JA (1998) Investigating pulsed dye laser-blood vessel interaction with color Doppler optical coherence tomography. Opt Express 3(6):251-56 CrossRef
    12. Barton JK, Frangineas G, Pummer H et al (2001) Cooperative phenomena in two-pulse, two-color laser photocoagulation of cutaneous blood vessels. Photochem Photobiol 73(6):642-50 CrossRef
    13. Babilas P, Shafirstein G, B?umler W, Baier J, Landthaler M, Szeimies R, Abels C (2005) Selective photothermolysis of blood vessels following flashlamp-pumped pulsed dye laser irradiation: in vivo results and mathematical modelling are in agreement. J Invest Dermatol 20(5):343-52
    14. Suthamjariya K, Farinelli WA, Koh W et al (2004) Mechanisms of microvascular response to laser pulses. J Investig Dermatol 122(2):518-25 CrossRef
    15. Shafirstein G, Buckmiller LM, Waner M, B?umler W (2007) Mathematical modeling of selective photothermolysis to aid the treatment of vascular malformations and hemangioma with pulsed dye laser. Lasers Med Sci 22:111-18 CrossRef
    16. Yang MU, Yaroslavsky AN, Farinelli WA et al (2005) Long-pulsed neodymium:yttrium-aluminum-garnet laser treatment for port-wine stains. J Am Acad Dermatol 52(3 Pt 1):480-90 CrossRef
    17. Tierney ER, Hanke CW (2011) Alexandrite laser for the treatment of port wine stains refractory to pulsed dye laser. Dermatol Surg 37(9):1268-8
文摘
Port-wine stains (PWSs) are congenital vascular malformations that progressively darken and thicken with age, and laser therapy is the most effective in clinical practice. Using dorsal skin chamber (DSC), this study evaluated thermal response of blood vessel to a 595-nm pulsed dye laser (PDL) with controlled energy doses and pulse durations. Totally, 32 vessels (30?00?μm in diameter) are selected from the dorsal skin of the mouse to match those in port-wine stain. The experimental results showed that the thermal response of the blood vessels to laser irradiation can be recognized as coagulation, constriction with diameter decrease, disappearance (complete constriction), hemorrhage, and collagen damage in the order of increasing laser radiant exposure. Blood vessels with small diameter would response poorly and survive from the laser heating because their thermal relaxation time is much shorter than the pulse duration. The optimalradiant exposure is from 10 to 12?J/cm2 under 6?ms pulse duration without considering the epidermal light absorption. Numerical simulations were also conducted using a 1,000-μm deep Sprague-Dawley (SD) mouse skinfold. The light transportation and heat diffusion in dorsal skin were simulated with the Monte Carlo method and heat transfer equation, while the blood vessel photocoagulation was evaluated by Arrhenius-type kinetic integral. Both experimental observation and numerical simulation supported that hemorrhage is the dominant thermal response, which occurs due to preferential heating of the superior parts of large blood vessels. In clinical practice for 595?nm PDL, the consequent purpura caused by hemorrhage can be used as a treatment end point.

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