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用于耳毒性监测的听阈移位标准评估。

Evaluation of audiometric threshold shift criteria for ototoxicity monitoring.

作者信息

Konrad-Martin Dawn, James Kenneth E, Gordon Jane S, Reavis Kelly M, Phillips David S, Bratt Gene W, Fausti Stephen A

机构信息

VA RR&D National Center for Rehabilitative Auditory Research, Portland VA Medical Center, OR, USA.

出版信息

J Am Acad Audiol. 2010 May;21(5):301-14; quiz 357. doi: 10.3766/jaaa.21.5.3.

Abstract

BACKGROUND

There is disagreement about ototoxicity monitoring methods. Controversy exists about what audiometric threshold shift criteria should be used, which frequencies should be tested, and with what step size. An evaluation of the test performance achieved using various criteria and methods for ototoxicity monitoring may help resolve these issues.

PURPOSE

(1) Evaluate test performance achieved using various significant threshold shift (STS) definitions for ototoxicity monitoring in a predominately veteran population; and (2) determine whether testing in (1/6)- or (1/3)-octave steps improves test performance compared to (1/2)-octave steps.

RESEARCH DESIGN

A prospective, observational study design was used in which STSs were evaluated at frequencies within an octave of each subject's high-frequency hearing limit at two time points, an early monitoring test and the final monitoring test.

STUDY SAMPLE

Data were analyzed from 78 ears of 41 patients receiving cisplatin and from 53 ears of 28 hospitalized patients receiving nonototoxic antibiotics. Cisplatin-treated subjects received a cumulative dosage > or =350 mg by the final monitoring test. Testing schedule, age, and pre-exposure hearing characteristics were similar between the subject groups.

DATA COLLECTION AND ANALYSIS

Threshold shifts relative to baseline were examined to determine whether they met criteria based on magnitudes of positive STS (shifts of > or =5, 10, 15, or 20 dB) and numbers of frequencies affected (shifts at > or =1, 2, or 3 adjacent frequencies) for data collected using approximately (1/6)-, (1/3)-, or (1/2)-octave steps. Thresholds were confirmed during monitoring sessions in which shifts were identified. Test performance was evaluated with receiver operating characteristic (ROC) curves developed using a surrogate "gold standard"; true positive (TP) rates were derived from the cisplatin-exposed group and false positive (FP) rates from the nonexposed, control group. Best STS definitions were identified that achieved the greatest areas under ROC curves or resulted in the highest TP rates for a fixed FP rate near 5%, chosen to minimize the number of patients incorrectly diagnosed with ototoxic hearing loss.

RESULTS

At the early monitoring test, average threshold shifts differed only slightly across groups. Test-frequency step size did not affect performance, and changes at one or more frequencies yielded the best test performance. At the final monitoring test, average threshold shifts were +10.5 dB for the cisplatin group, compared with -0.2 dB for the control group. Compared with the (1/2)-octave step size used clinically, use of smaller frequency steps improved test performance for threshold shifts at > or =2 or > or =3 adjacent frequencies. Best overall test performance was achieved using a criterion cutoff of > or =10 dB threshold shift at > or =2 adjacent frequencies tested in (1/6)-octave steps. Best test performance for the (1/2)-octave step size was achieved for shifts > or =15 dB at one or more frequencies.

CONCLUSIONS

An ototoxicity monitoring protocol that uses an individualized, one-octave range of frequencies tested in (1/6)-octave steps is quick to administer and has an acceptable FP rate. Similar test performance can be achieved using (1/3)-octave test frequencies, which further reduces monitoring test time.

摘要

背景

关于耳毒性监测方法存在分歧。对于应采用何种听阈位移标准、应测试哪些频率以及步长应为多少存在争议。对使用各种标准和方法进行耳毒性监测所取得的测试性能进行评估,可能有助于解决这些问题。

目的

(1)评估在以退伍军人为主的人群中,使用各种显著听阈位移(STS)定义进行耳毒性监测所取得的测试性能;(2)确定与倍频程步长相比,以(1/6)倍频程或(1/3)倍频程步长进行测试是否能提高测试性能。

研究设计

采用前瞻性观察性研究设计,在两个时间点,即早期监测测试和最终监测测试时,对每个受试者高频听力极限一个倍频程范围内的频率进行STS评估。

研究样本

分析了41例接受顺铂治疗患者的78只耳以及28例接受非耳毒性抗生素治疗的住院患者的53只耳的数据。到最终监测测试时,接受顺铂治疗的受试者累积剂量≥350mg。两组受试者的测试时间表、年龄和暴露前听力特征相似。

数据收集与分析

检查相对于基线的听阈位移,以确定根据使用大约(1/6)倍频程、(1/3)倍频程或倍频程步长收集的数据,基于正向STS的幅度(位移≥5、10、15或20dB)和受影响频率的数量(在≥1、2或3个相邻频率处的位移),它们是否符合标准。在确定位移的监测过程中确认阈值。使用替代“金标准”绘制的受试者工作特征(ROC)曲线评估测试性能;真阳性(TP)率来自顺铂暴露组,假阳性(FP)率来自未暴露的对照组。确定了最佳STS定义,这些定义在ROC曲线下面积最大,或者在接近5%的固定FP率下导致最高的TP率,选择该FP率是为了尽量减少被错误诊断为耳毒性听力损失的患者数量。

结果

在早期监测测试中,各组的平均听阈位移仅略有差异。测试频率步长不影响性能,一个或多个频率的变化产生了最佳测试性能。在最终监测测试中,顺铂组的平均听阈位移为+10.5dB,而对照组为-0.2dB。与临床使用的倍频程步长相比,使用较小的频率步长可提高在≥2个或≥3个相邻频率处听阈位移的测试性能。使用(1/6)倍频程步长测试≥2个相邻频率处阈值位移≥10dB的标准截断值可实现最佳总体测试性能。对于倍频程步长,在一个或多个频率处位移≥15dB时可实现最佳测试性能。

结论

一种耳毒性监测方案,即采用以(1/6)倍频程步长测试的个体化一个倍频程频率范围,实施快速且具有可接受的FP率。使用(1/3)倍频程测试频率可实现类似的测试性能,这进一步减少了监测测试时间。

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