https://www.selleckchem.com/pr....oducts/cepharanthine
Validated scales were used to assess dysphagia severity for all time points as primary outcome measures. A total of 34 patients were randomized 19 to the intervention group and 15 to the control group. The key findings of the repeated-measures between-group comparisons were significant increases in the intervention group for the following dysphagia measures (1) secretion severity score (immediately after TEE P0.001; 24h after TEE P0.001) and (2) Penetration-Aspiration Scale score for saliva (immediately after TEE P0.00
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