Kumar Lokesh, Thakar Alok, Thakur Bhaskar, Sikka Kapil
*Department of Otolaryngology †Department of Biostatistics, All India Institute of Medical Sciences, New Delhi, India.
Otol Neurotol. 2017 Oct;38(9):e378-e383. doi: 10.1097/MAO.0000000000001525.
To evaluate clinic based and laboratory tests of otolith function for their sensitivity and specificity in demarcating unilateral compensated complete vestibular deficit from normal.
Prospective cross-sectional study.
Tertiary care hospital vestibular physiology laboratory.
Control group-30 healthy adults, 20-45 years age; Case group-15 subjects post vestibular shwannoma excision or post-labyrinthectomy with compensated unilateral complete audio-vestibular loss.
Otolith function evaluation by precise clinical testing (head tilt test-HTT; subjective visual vertical-SVV) and laboratory testing (headroll-eye counterroll-HR-ECR; vesibular evoked myogenic potentials-cVEMP).
Sensitivity and specificity of clinical and laboratory tests in differentiating case and control subjects.
Measurable test results were universally obtained with clinical otolith tests (SVV; HTT) but not with laboratory tests. The HR-ECR test did not indicate any definitive wave forms in 10% controls and 26% cases. cVEMP responses were absent in 10% controls.HTT test with normative cutoff at 2 degrees deviations from vertical noted as 93.33% sensitive and 100% specific. SVV test with normative cutoff at 1.3 degrees noted as 100% sensitive and 100% specific. Laboratory tests demonstrated poorer specificities owing primarily to significant unresponsiveness in normal controls.
Clinical otolith function tests, if conducted with precision, demonstrate greater ability than laboratory testing in discriminating normal controls from cases with unilateral complete compensated vestibular dysfunction.
评估基于临床和实验室的耳石功能测试在区分单侧代偿性完全前庭功能缺失与正常情况时的敏感性和特异性。
前瞻性横断面研究。
三级医疗医院前庭生理学实验室。
对照组——30名年龄在20至45岁之间的健康成年人;病例组——15名前庭神经鞘瘤切除术后或迷路切除术后伴有代偿性单侧完全听觉-前庭功能丧失的受试者。
通过精确的临床测试(头倾斜试验-HTT;主观视觉垂直线-SVV)和实验室测试(头滚动-眼反向转动-HR-ECR;前庭诱发肌源性电位-cVEMP)评估耳石功能。
临床和实验室测试区分病例组和对照组受试者的敏感性和特异性。
临床耳石测试(SVV;HTT)普遍获得了可测量的测试结果,但实验室测试未获得。HR-ECR测试在10%的对照组和26%的病例组中未显示任何明确的波形。10%的对照组中未检测到cVEMP反应。HTT测试以与垂直方向偏差2度为标准界限,敏感性为93.33%,特异性为100%。SVV测试以1.3度为标准界限,敏感性和特异性均为100%。实验室测试的特异性较差,主要原因是正常对照组中存在明显的无反应性。
如果精确进行,临床耳石功能测试在区分正常对照组与单侧完全代偿性前庭功能障碍病例方面比实验室测试具有更强的能力。