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Oral intake of tablets and capsules in patients with dysphagia: Naming the risks

3rd International Conference and Exhibition on Rhinology & Otology

Heike Penner and Julia Schiele

Agaplesion Bethanien Krankenhaus, Germany University of Heidelberg, Germany

Posters & Accepted Abstracts: Otolaryngology

DOI: 10.4172/2161-119X.C1.014

Abstract
Lodging of tablets or capsules in the pharynx or their aspiration may result in reduced absorption, mucosal ulcerations, aspiration pneumonia or even suffocation. To facilitate swallowing, tablets are frequently split or crushed and capsules are opened which can impair efficacy and safety of drug treatment. Although it can be expected that swallowing solid medication is especially difficult for patients suffering from dysphagia, this issue has not been investigated thoroughly before. Therefore we investigated the prevalence of difficulties swallowing solid dosage forms in patients with stroke-induced dysphagia, whether the risk of aspiration for the accompanying bolus increases during oral intake of solid medication, whether routinely performed assessment tests help identify patients at risk and the prevalence of inappropriate manipulation of solid dosage forms. Using video endoscopy, we evaluated how 52 patients swallowed four placebos of different shapes with texture-modified water (TMW, pudding consistency) and milk. Lodging of placebos was observed and swallowing performance was rated according to the Penetration Aspiration Scale (PAS). Additionally, the Daniels Test, the Bogenhausener Dysphagie score, the Scandinavian Stroke Scale, the Barthel Index and Tinetti�s Mobility Test were conducted. Finally, the patients� medication was checked for inappropriate modification. A substantial proportion of the patients (>40%), experienced severe difficulties swallowing solid oral dosage forms. Compared to the administration of TMW/milk alone, the placebos increased the PAS values for the accompanying bolus in the majority of the patients (p 0.0001) and residue values were significantly higher (p 0.05) as well. There was no correlation to any of the routinely performed bedside tests. Of the drugs that were modified before video-endoscopic evaluation 20.8% were crushed inappropriately. As a consequence we suggest that safety and effectiveness of swallowing tablets and capsules should be evaluated routinely in video-endoscopic examinations.
Biography

Email: hpenner@bethanien-heidelberg.de

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