Non-contact Diffuse Optical Assessment of Pressure Ulcer and Therapy
Non-contact Diffuse Optical Assessment of Pressure Ulcer and Therapy
批准号:
8425042
负责人:
Guoqiang Yu
金额:
$15.64万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-02-15 至 2015-01-31
关键词:
AccountingAdultAffectAmericanBlood CirculationBlood flowClinical ManagementComputersCost SavingsCutaneousDecubitus ulcerDevelopmentDiffuseEarly DiagnosisEarly identificationElectric StimulationEvaluationFiber OpticsForearmGoalsHealedHealthHealthcareHeterogeneityHumanHypoxiaImpairmentIndividualInfectionLong-Term CareMeasurementMeasuresMethodsMonitorMuscleOpticsPain ThresholdPatientsPeripheralPopulationPreventionProceduresPropertyRecruitment ActivityRehabilitation CentersSacral RegionSkinSourceSpinal cord injuryStagingSurfaceSystemTechnologyTherapeuticTissuesTouch sensationTranslatingTreatment CostTreatment outcomeUlcerValidationVariantboneconventional therapycostdetectorhealinghemodynamicshigh riskimprovedinnovationlensnovelpatient populationpressureresponsesacrumtherapy developmenttissue oxygenationtreatment effectwound
中文摘要
描述(由申请人提供):压疮影响着1-3百万美国成年人。长时间的压力导致外周循环不良和组织缺氧,并可能导致严重的组织损伤。电刺激作为一种辅助治疗方法,与传统的溃疡治疗方法相比,其劳动强度较小,成本较低。然而,ES参数通常是任意选择的,治疗结果是通过可见的组织质量和/或伤口体积变化来评估的,而不是溃疡组织内在的血流动力学变化。早期发现压疮是有效管理溃疡和降低后续治疗费用的关键。由于压疮通常起源于附着于骨的深层组织(如骶骨周围的臀肌),因此测量深部组织血流动力学对于溃疡的早期诊断和ES治疗的优化至关重要。然而,目前还没有一种简单的方法能够检测到溃疡在深层组织发展的早期阶段。一项新的先进技术,近红外漫射光学,可以用光纤探头轻轻接触皮肤表面,无创地监测深层组织(高达几厘米)的血流和氧合,最近在我们的初步研究中得到了证明。然而,使用接触探针测量组织血流动力学不适用于容易感染的溃疡组织。本项目旨在开发和验证一种新型的非接触式漫射光学系统(目的1),用于深部组织溃疡发展的早期血流动力学评估。这种非接触式系统将完全避免探针组织接触引起的组织变形和潜在感染。该研究还将整合非接触式系统与ES刺激器,用于压疮的治疗和治疗监测。在集成的非接触式系统在健康肌肉中得到验证,并优化ES治疗参数以最大限度地提高ES的组织血流动力学反应(Aim 2)后,非接触式光学系统将用于检测有或无压疮(I-IV期)患者在ES治疗前、治疗期间和治疗后超过4周(Aim 3)的骶骨周围臀肌的血流和组织氧合。通过对影响组织损伤/愈合的深层组织血流动力学的测量,有望为溃疡发展的早期诊断、ES参数的客观优化以及ES治疗效果的纵向评价提供独特的价值。我们的长期目标是对来自多个康复中心的具有统计意义的人群进行广泛的研究,以转化和商业化这一创新的综合系统,用于有效的压疮临床管理。鉴于压疮长期护理的健康负担,这个转化技术项目有可能显著提高我们对压疮发展和治疗的理解,最终导致人类健康的显著改善和大量的成本节约。
英文摘要
DESCRIPTION (provided by applicant): Pressure ulcers affect 1-3 million American adults. Prolonged pressure results in poor peripheral circulation and tissue hypoxia, and may cause significant tissue damage. As one of the adjunctive therapies, electrical stimulation (ES) is less labor intensive with lower costs compared to conventional therapies for ulcer treatment. However, ES parameters are often selected arbitrarily and treatment outcomes are evaluated by visible estimates of tissue mass and/or wound volume changes rather than intrinsic hemodynamic changes in ulcerous tissues. Early detection of pressure ulcers is the key for effective ulcer management and for reducing subsequent treatment costs. Since pressure ulcers usually originate from deep tissues attached to the bone (e.g., gluteal muscles surrounding the sacrum), measurement of deep tissue hemodynamics is essential for early diagnosis of ulcers and for optimization of ES treatment. However, no easy methods exist yet that are able to detect the early stages of ulcer development in deep tissues. A new advanced technology, near- infrared diffuse optics, can noninvasively monitor blood flow and oxygenation in deep tissues (up to several centimeters) with fiber-optic probes that gently contact the skin surface, and has recently been demonstrated in our preliminary studies. However, measurements of tissue hemodynamics using contact probes are not appropriate for ulcerous tissues that are prone to infection. This proposed project is to develop and validate a novel non-contact diffuse optical system (Aim 1) for early hemodynamic assessment of ulcer development in deep tissues. This non-contact system will completely avoid tissue deformation and potential infections induced by probe-tissue contact. This study will also integrate the non-contact system with an ES stimulator for treatment and therapeutic monitoring of pressure ulcers. After the integrated non-contact system is validated in healthy muscles and ES treatment parameters are optimized to maximize tissue hemodynamic responses to ES (Aim 2), the non-contact optical system will be used to detect blood flow and tissue oxygenation in gluteal muscles surrounding the sacrum in patients with or without pressure ulcers (stages I-IV) before, during and after ES treatments over 4 weeks (Aim 3). It is expected that measurement of deep tissue hemodynamics that affect tissue damage/healing will provide unique value for the early diagnosis of ulcer development, the objective optimization of ES parameters, and the longitudinal evaluation of ES treatment effects. Our long-term goal is to conduct extensive studies on statistically significant populations from multiple rehabilitation centers to translate and commercialize this innovative integrated system for the effective clinical management of pressure ulcers. Given the health burden of long-term care for pressure ulcers, this translational technology project has the potential to significantly advance our understanding of pressure ulcer development and treatment, ultimately leading to significant improvements in human health and substantial cost savings.
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