This proposal presents an innovative and effective solution to the problem of ischemia derived injuries to the skin and nerves as a consequence of applied cold therapy. Cooling is commonly used after orthopedic surgery and in sports medicine to reduce pain, swelling, inflammation, and metabolism. Although cryotherapy has been widely practiced for centuries, and its benefits are recognized intuitively even within the lay community, it is rather amazing that there is no definitive understanding of the risk factors associated with ts use. These risks are significant as evidenced by an annual occurrence of some 1,500 cases of cryotherapy injury involving extensive tissue necrosis and/or severe neuropathy. More than 120 preliminary studies have documented that even brief exposures to circulating ice water cause a deep state of ischemia that persists for hours after the removal of cold. Our studies have also documented the alteration of local availability and action of vasoactive molecules in conjunction with creating and sustaining the ischemic state. We have invented a proprietary technology that includes special devices and application methods that deliver cryotherapy with all of its benefits while also greatly lowering the risk of ischemia induced injury. The technology works by periodically stimulating blood flow in affected areas during the application of cryotherapy. We also apply the refrigeration source directly to the treatment area via solid state cooling technology with greatly increased thermal efficiency and control. We have assembled an exceptional interdisciplinary research team with expertise in human thermal physiology, bioheat transfer engineering, device design, and cardiovascular flow control mechanisms. The research plan will consist of three aims to: (a) characterize the problem: map the depression of skin blood perfusion as a function of the temperature and exposure time to cryotherapy, (b) define the mechanism of action: apply microdialysis technology to identify and measure the action of candidate vasoactive agents that govern the vascular response to cryotherapy, and (c) design, implement, and verify the solution: build and test prototype devices to stimulate blood flow in skin during cryotherapy and measure the effect on ischemia induction. We have already demonstrated the efficacy of multiple modes of stimulating blood flow that can be combined with cryotherapy. We believe that this technology will have a transformative benefit to the practice of cryotherapy and will enable its benefits to be realized with a greatly reduced risk of collateral injury in skin and nerves.

Public Health Relevance

Cryotherapy is applied widely for the treatment of soft tissue trauma in contexts such as orthopedic surgery, rehabilitation, and sports medicine. Most procedures are ice based, resulting in skin temperatures as low 10?C. An undesired outcome is that cold induced tissue ischemia may result in tissue necrosis and neuropathy, and more than a thousand such occurrences occur annually. We have conducted studies that quantify the cold induction of ischemia with the attendant risk of injury. We have also devised new device designs and methods for cryotherapy that will provide more effective treatments and be safer to use.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
1R01EB015522-01A1
Application #
8504618
Study Section
Bioengineering, Technology and Surgical Sciences Study Section (BTSS)
Program Officer
Krosnick, Steven
Project Start
2013-04-15
Project End
2017-03-31
Budget Start
2013-04-15
Budget End
2014-03-31
Support Year
1
Fiscal Year
2013
Total Cost
$449,186
Indirect Cost
$123,913
Name
University of Texas Austin
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
170230239
City
Austin
State
TX
Country
United States
Zip Code
78712
Christmas, Kevin M; Patik, Jordan C; Khoshnevis, Sepideh et al. (2018) Pronounced and sustained cutaneous vasoconstriction during and following cyrotherapy treatment: Role of neurotransmitters released from sympathetic nerves. Microvasc Res 115:52-57
Christmas, Kevin M; Patik, Jordan C; Khoshnevis, Sepideh et al. (2016) Sustained cutaneous vasoconstriction during and following cyrotherapy treatment: Role of oxidative stress and Rho kinase. Microvasc Res 106:96-100
Khoshnevis, Sepideh; Craik, Natalie K; Matthew Brothers, R et al. (2016) Cryotherapy-Induced Persistent Vasoconstriction After Cutaneous Cooling: Hysteresis Between Skin Temperature and Blood Perfusion. J Biomech Eng 138:4032126
Mejia, Natalia; Dedow, Karl; Nguy, Lindsey et al. (2015) An On-Site Thermoelectric Cooling Device for Cryotherapy and Control of Skin Blood Flow. J Med Device 9:0445021-445026
Diller, Kenneth R (2015) Heat Transfer in Health and Healing. J Heat Transfer 137:1030011-10300112
Khoshnevis, Sepideh; Craik, Natalie K; Diller, Kenneth R (2015) Cold-induced vasoconstriction may persist long after cooling ends: an evaluation of multiple cryotherapy units. Knee Surg Sports Traumatol Arthrosc 23:2475-83
Lee, Joshua F; Christmas, Kevin M; Harrison, Michelle L et al. (2014) Cerebral vasoreactivity: impact of heat stress and lower body negative pressure. Clin Auton Res 24:135-41
Khoshnevis, Sepideh; Nordhauser, Jennifer E; Craik, Natalie K et al. (2014) Quantitative evaluation of the thermal heterogeneity on the surface of cryotherapy cooling pads. J Biomech Eng 136: