Sassi Fernanda C, Medeiros Gisele C, Zilberstein Bruno, Jayanthi Shri Krishna, de Andrade Claudia R F
Departamento de Fisioterapia, Fonoaudiologia e Terapia Ocupacional, Faculdade de Medicina (FMUSP), Universidade de Sao Paulo, Sao Paulo, SP, BR.
Divisão de Fonoaudiologia, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR.
Clinics (Sao Paulo). 2017 Dec;72(12):718-722. doi: 10.6061/clinics/2017(12)01.
To compare the videofluoroscopic findings of patients with suspected oropharyngeal dysphagia with the results of a clinical screening protocol.
A retrospective observational cohort study was conducted on all consecutive patients with suspected oropharyngeal dysphagia between March 2015 and February 2016 who were assigned to receive a videofluoroscopic assessment of swallowing. All patients were first submitted to videofluoroscopy and then to the clinical assessment of swallowing. The clinical assessment was performed within the first 24 hours after videofluoroscopy. The videofluoroscopy results were analyzed regarding penetration/aspiration using an 8-point multidimensional perceptual scale. The accuracy of the clinical protocol was analyzed using the sensitivity, specificity, likelihood ratios and predictive values.
The selected sample consisted of 50 patients. The clinical protocol presented a sensitivity of 50% and specificity of 95%, with an accuracy of 88%. "Cough" and "wet-hoarse" vocal quality after/during swallowing were clinical indicators that appeared to correctly identify the presence of penetration/aspiration risk.
The clinical protocol used in the present study is a simple, rapid and reliable clinical assessment. Despite the absence of a completely satisfactory result, especially in terms of the sensitivity and positive predictive values, we suggest that lower rates of pneumonia can be achieved using a formal dysphagia screening method.
比较疑似口咽吞咽困难患者的视频透视检查结果与临床筛查方案的结果。
对2015年3月至2016年2月期间所有连续的疑似口咽吞咽困难患者进行回顾性观察队列研究,这些患者被安排接受吞咽的视频透视评估。所有患者首先接受视频透视检查,然后进行吞咽的临床评估。临床评估在视频透视检查后的头24小时内进行。使用8点多维感知量表分析视频透视检查结果中的渗透/误吸情况。使用敏感性、特异性、似然比和预测值分析临床方案的准确性。
所选样本包括50名患者。临床方案的敏感性为50%,特异性为95%,准确性为88%。吞咽后/吞咽期间的“咳嗽”和“湿哑”嗓音质量是似乎能正确识别渗透/误吸风险存在的临床指标。
本研究中使用的临床方案是一种简单、快速且可靠的临床评估。尽管结果并不完全令人满意,尤其是在敏感性和阳性预测值方面,但我们建议使用正式的吞咽困难筛查方法可以降低肺炎发生率。