Background:
Older people with oropharyngeal dysphagia (OD) present a decline in
pharyngeal sensory function. The aim of this proof-of-concept study was to
assess the biomechanical and neurophysiological effects of acute and
subacute oropharyngeal sensory stimulation with transient receptor potential
vanilloid 1 (TRPV1) agonists (capsaicinoids) in older patients with OD.
Methods:
We studied the effect of a single dose
versus
multiple doses
(2 weeks) of oral capsaicin treatment (10
–5
M) or placebo in 28
older patients with OD (81.2 ± 4.6 years) using videofluoroscopy
(penetration-aspiration scale [PAS], timing of swallow response) and
electroencephalography (EEG) (latency and amplitude of pharyngeal
event-related potential [ERP]).
Results:
Acute stimulation by capsaicinoids 10
–5
M did not improve swallow
function and did not produce significant changes in pharyngeal ERP. In
contrast, after 10 days of treatment, patients presented a clinically
relevant and statistically significant reduction in the laryngeal vestibule
closure (LVC) time (22.5%,
p
= 0.042), and in the PAS
(24.2%,
p
= 0.038), compared with the placebo group. EEG
results showed a reduction in the latency of the N1 peak (28.6%,
p
= 0.007) and an increase of the amplitude of the
P1-N2 (59.4%,
p
= 0.038) and the N2-P2 (43.6%,
p
= 0.050) peaks. We observed a strong and significant
correlation between the reduction in the latency of the N1 peak and change
in LVC time after subacute treatment (
r
= 0.750,
p
= 0.003).
Conclusions:
After 2 weeks of treatment, oropharyngeal sensory stimulation with
capsaicinoids induced cortical changes that were correlated with
improvements in swallowing biomechanics in older patients with OD. These
results further show that sensory stimulation by TRPV1 agonists can become a
useful pharmacological treatment for older patients with OD.
Thickened fluids are a therapeutic strategy for oropharyngeal dysphagia (OD). However, its therapeutic effect among different phenotypes of OD patients has not yet been compared. We aimed to assess the therapeutic effect and α-amylase resistance of a mixed gum/starch thickener [Fresubin Clear Thickener® (FCT)] on four phenotypes of OD patients: G1) 36 older; G2) 31 head/neck cancer (HNC); G3) 30 Parkinson’s disease; and G4) 31 chronic post-stroke. Therapeutic effect of FCT was assessed during videofluoroscopy using the Penetration-Aspiration Scale (PAS), for 5/20 mL boluses, at four levels of shear-viscosity (<50, 250, 1000 and 2000 mPa·s). The effect of α-amylase was assessed after 30 s of oral incubation. Patients had high prevalence of VFS signs of impaired efficacy (98.44%) and safety (70.31%) of swallow with a severe PAS score (4.44 ± 0.20). Most severe OD was in HNC (80.6% unsafe swallows). FCT showed a strong therapeutic effect on the safety of swallow at a range between 250–1000 mPa·s (74.19–96.67%, safe swallows in G1, G3, G4, and 58.06% in G2), without increasing pharyngeal residue. Viscosity was unaffected by α-amylase. Increasing shear-viscosity with FCT causes a strong viscosity-dependent therapeutic effect on the safety of swallow. This effect depends on the phenotype and is similar among older, Parkinson’s and post-stroke patients.
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