Randeberg L L, Bonesrønning J H, Dalaker M, Nelson J S, Svaasand L O
Department of Electronics and Telecommunications, Norwegian University of Science and Technology, N-7491 Trondheim, Norway.
Lasers Surg Med. 2004;34(5):414-9. doi: 10.1002/lsm.20042.
Monitoring dynamic changes during laser induced photothermolysis of vascular skin lesions is essential for obtaining an optimal therapeutic result. Rapid photoinduced thermal damage occurs at a threshold temperature of about 70 degrees C. It is therefore, relevant to identify markers to indicate if this threshold temperature has been reached. Methemoglobin, which is formed by a photo-induced oxidation of hemoglobin, indicates that the temperature has reached this threshold value. This study presents a proof of concept of a method for monitoring the in vivo presence of methemoglobin immediately after laser exposure.
STUDY DESIGN/MATERIALS AND METHODS: The present study was designed to investigate the in vivo temperature dependence of hemoglobin absorption in the 450-800 nm spectrum range. In vivo diffuse reflectance measurements of port-wine stain (PWS) and telangiectasia were performed prior to, and immediately after, laser treatment with a pulsed dye laser (PDL) at 585 nm wavelength.
In vivo measurements following laser treatment of vascular skin lesions showed an immediate increase in the optical absorption of blood. This effect, caused by thermal stress, is a result of an increased dermal blood volume fraction and methemoglobin formation. The effect is light dose dependent, and reflectance spectra revealed methemoglobin formation in patients treated with fluences above 5 J/cm2 at 585 nm wavelength.
It was proved that methemoglobin can be measured in vivo by reflectance spectroscopy. Measurements of the average methemoglobin concentrations immediately after laser exposure may be a valuable diagnostic tool to verify that the blood temperature has been sufficiently high to induce thermal damage to the vessel wall.
监测血管性皮肤病变激光诱导光热解过程中的动态变化对于获得最佳治疗效果至关重要。在约70摄氏度的阈值温度下会迅速发生光致热损伤。因此,识别指示是否已达到该阈值温度的标志物具有重要意义。高铁血红蛋白由血红蛋白的光诱导氧化形成,表明温度已达到该阈值。本研究提供了一种在激光照射后立即监测体内高铁血红蛋白存在情况的方法的概念验证。
研究设计/材料与方法:本研究旨在研究450 - 800纳米光谱范围内血红蛋白吸收的体内温度依赖性。在用波长为585纳米的脉冲染料激光(PDL)对葡萄酒色斑(PWS)和毛细血管扩张进行激光治疗之前和之后,进行体内漫反射测量。
血管性皮肤病变激光治疗后的体内测量显示血液的光吸收立即增加。这种由热应激引起的效应是真皮血容量分数增加和高铁血红蛋白形成的结果。该效应与光剂量有关,反射光谱显示在585纳米波长下,能量密度高于5 J/cm² 的患者中形成了高铁血红蛋白。
已证明可通过反射光谱法在体内测量高铁血红蛋白。激光照射后立即测量平均高铁血红蛋白浓度可能是一种有价值的诊断工具,用于验证血液温度是否足够高以对血管壁造成热损伤。