Warnecke Tobias, Im Sun, Labeit Bendix, Zwolinskaya Olga, Suntrup-Krüger Sonja, Oelenberg Stephan, Ahring Sigrid, Schilling Matthias, Meuth Sven, Melzer Nico, Wiendl Heinz, Ruck Tobias, Dziewas Rainer
Department of Neurology with Institute of Translational Neurology, University of Muenster, Albert-Schweitzer-Campus 1, Building A1, Münster, 48149, Germany.
Department of Rehabilitation Medicine, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Ther Adv Neurol Disord. 2021 Aug 11;14:17562864211035544. doi: 10.1177/17562864211035544. eCollection 2021.
The flexible endoscopic evaluation of swallowing-tensilon test (FTT) was developed to diagnose myasthenia gravis (MG) in patients with unclear pharyngeal dysphagia. The purpose of this study was to determine sensitivity and specificity of the FTT and compare its diagnostic validity with that of other diagnostic markers.
In this single-centre pragmatic clinical cohort study, a total of 100 patients with unclear pharyngeal dysphagia were eligible to undergo FTT. All patients were subjected to FTT and subsequently followed up clinically. FTT was considered positive if a significant improvement of pharyngeal swallowing function could be objectified endoscopically upon administration of edrophonium chloride. In addition, repetitive nerve stimulation test and serum MG antibody analysis were conducted.
All subjects (mean age 62.5 ± 14.1 years, female 33) underwent FTT without any complications. According to the results of the diagnostic procedures and based on long-term clinical follow-up for at least 3 years, 51 patients were finally diagnosed with MG. The sensitivity and specificity for the FTT was 88.2% and 95.9%, respectively. Application of the Cochran's test showed statistically significant heterogeneity among the diagnostic tests, with results indicating FTT performance to be more accurate than the repetitive nerve stimulation results ( < 0.001) and comparable with serum antibody tests ( > 0.99).
FTT has excellent clinical properties to be used routinely in the assessment of dysphagia with isolated or predominant pharyngeal muscle involvement allowing rapid and accurate diagnosis of MG.
吞咽-腾喜龙试验的柔性内镜评估(FTT)旨在诊断存在咽部吞咽困难且病因不明的重症肌无力(MG)患者。本研究的目的是确定FTT的敏感性和特异性,并将其诊断有效性与其他诊断标志物进行比较。
在这项单中心实用临床队列研究中,共有100例存在咽部吞咽困难且病因不明的患者符合接受FTT的条件。所有患者均接受FTT检查,随后进行临床随访。如果在给予氯化依酚氯铵后可通过内镜客观观察到咽部吞咽功能有显著改善,则FTT被视为阳性。此外,还进行了重复神经电刺激试验和血清MG抗体分析。
所有受试者(平均年龄62.5±14.1岁,女性33例)均接受了FTT检查,未出现任何并发症。根据诊断程序的结果并基于至少3年的长期临床随访,最终有51例患者被诊断为MG。FTT的敏感性和特异性分别为88.2%和95.9%。应用Cochran检验显示诊断试验之间存在统计学上的显著异质性,结果表明FTT的表现比重复神经电刺激结果更准确(<0.001),与血清抗体检测结果相当(>0.99)。
FTT具有出色的临床特性,可常规用于评估孤立性或主要累及咽部肌肉的吞咽困难,能够快速准确地诊断MG。