Generalization of the Bolus Volume Effect on Piezoelectric Sensor Signals during Pharyngeal Swallowing in Normal Subjects

2011 ◽  
Vol 53 (1) ◽  
pp. 65-71 ◽  
Author(s):  
Yozo Miyaoka ◽  
Ichiro Ashida ◽  
Shin-ya Kawakami ◽  
Yuko Tamaki ◽  
Satomi Miyaoka
2016 ◽  
Vol 40 (6) ◽  
pp. 1018 ◽  
Author(s):  
Jin-Woo Park ◽  
Gyu-Jeong Sim ◽  
Dong-Chan Yang ◽  
Kyoung-Hwan Lee ◽  
Ji-Hea Chang ◽  
...  

2006 ◽  
Vol 57 (4) ◽  
pp. 351-362 ◽  
Author(s):  
Yuko Matsumura ◽  
Takehiro Karaho ◽  
Tetsuya Tanabe ◽  
Satoshi Kitahara

1988 ◽  
Vol 150 (6) ◽  
pp. 1307-1309 ◽  
Author(s):  
WJ Dodds ◽  
KM Man ◽  
IJ Cook ◽  
PJ Kahrilas ◽  
ET Stewart ◽  
...  

1998 ◽  
Vol 107 (4) ◽  
pp. 344-348 ◽  
Author(s):  
Yukio Ohmae ◽  
Masami Ogura ◽  
Satoshi Kitahara ◽  
Takehiro Karaho ◽  
Tetsuzo Inouye

This study quantified the effects of head rotation on pharyngeal swallowing in healthy subjects. Videofluoroscopic and oropharyngeal manometric examinations of pharyngeal swallowing were performed on seven volunteers with the head in neutral and rotated positions. Videofluoroscopic study revealed that head rotation swallow causes the bolus to lateralize away from the direction of head rotation. Pharyngeal manometric study indicated that the pharyngeal peak pressures toward the side of head rotation were significantly increased, whereas the pharyngeal pressures opposite the side of head rotation were not affected. Head rotation swallow produced a significant fall in upper esophageal sphincter (UES) resting pressure and a delay in UES closing. We concluded that the head rotation swallow in normal subjects not only alters the bolus pathway, but also has a useful effect on both pharyngeal clearance and UES dynamics.


Gut ◽  
1997 ◽  
Vol 41 (3) ◽  
pp. 285-290 ◽  
Author(s):  
R K Mittal ◽  
C Chiareli ◽  
J Liu ◽  
R H Holloway ◽  
W Dixon

Background—Atropine decreases the frequency of transient lower oesophageal sphincter relaxation (TLOSR) through an unknown mechanism. Gastric distension and pharyngeal receptor excitation are two possible sources for the afferent stimulus responsible for TLOSR.Aims—To determine whether atropine affects gastric distension induced TLOSR and pharyngeal receptor mediated lower oesophageal sphincter (LOS) relaxation.Methods—Oesophageal manometry and pH recordings were performed in 10 healthy volunteers on two separate days in the postprandial setting, following either atropine (15 μg/kg intravenous bolus and 4 μg/kg/h as a maintenance dose) or placebo. Pharyngeal receptor mediated LOS relaxation was studied in nine subjects by rapid injection of minute amounts of water (0.05, 0.1, 0.2, 0.3, and 0.4 ml) in the pharynx before and after atropine. Gastric distension mediated TLOSR was studied in eight subjects by insufflating the stomach with 300, 600 and 900 ml of CO2 before and after atropine.Results—Atropine reduced the frequency of spontaneous gastro-oesophageal reflux and TLOSR compared with placebo (p<0.05). Pharyngeal stimulation resulted in bolus volume dependent LOS relaxation. Atropine decreased the frequency and amplitude of pharyngeal receptor mediated LOS relaxation at bolus volumes of 0.05, 0.1, and 0.2 ml. Gastric distension resulted in intermittent episodes of TLOSR. The frequency of gastric distension induced TLOSR was significantly decreased by atropine.Conclusion—(1) Atropine reduces the frequency of spontaneous reflux and TLOSR in normal subjects; and (2) gastric distension induced TLOSR and pharyngeal receptor mediated LOS relaxation is inhibited by atropine.


Dysphagia ◽  
2022 ◽  
Author(s):  
Kannit Pongpipatpaiboon ◽  
Yoko Inamoto ◽  
Keiko Aihara ◽  
Hitoshi Kagaya ◽  
Seiko Shibata ◽  
...  

2014 ◽  
Vol 128 ◽  
pp. 46-51 ◽  
Author(s):  
Tuo Lin ◽  
Guangqing Xu ◽  
Zulin Dou ◽  
Yue Lan ◽  
Fan Yu ◽  
...  

1992 ◽  
Vol 263 (3) ◽  
pp. R624-R630 ◽  
Author(s):  
H. G. Preiksaitis ◽  
S. Mayrand ◽  
K. Robins ◽  
N. E. Diamant

The coordination of swallowing and respiration, as measured by nasal airflow, and the effect of changes in the volume of the swallow bolus (0-20 ml) were investigated in 12 normal subjects. Both nonbolus and bolus swallows were usually preceded and followed by expiratory airflow. Swallows followed by inspiratory airflow accounted for 20% of nonbolus swallows but decreased further in frequency in the presence of a bolus. Swallowing was associated with an apneic period lasting 1.90 +/- 0.26 s for nonbolus swallows. Based on the apneic period response to bolus volume, the subjects were divided into two groups. The apneic period decreased by 60% in seven of the subjects regardless of bolus volume. The remaining five subjects gradually increased swallow apnea as bolus volume was increased. At larger bolus volumes, the latter group also exhibited an earlier onset of the swallow apnea and an increase in the number of swallows preceded by inspiration. The duration of the swallow-associated respiratory cycle was similarly prolonged by an increase in bolus volume in both groups. The results indicate that the respiratory pattern associated with swallowing is modulated by the volume of the swallow bolus. Within the normal population, at least two different patterns of response to bolus volume are identified.


Author(s):  
Per Cajander ◽  
Taher I. Omari ◽  
Charles Cock ◽  
Anders Magnuson ◽  
Mika Scheinin ◽  
...  

Background Remifentanil impairs swallowing, and disturbed accommodation to bolus volume may be one of the underlying causes. It is not fully understood whether remifentanil-induced swallowing dysfunction is mediated by peripheral or central mechanisms. Aims To investigate if remifentanil-induced swallowing dysfunction is dependent on the bolus volume and whether the effect of remifentanil could be counteracted by methylnaltrexone, a peripherally acting opioid antagonist. Methods Nineteen healthy volunteers were included in this double-blinded, randomized, placebo-controlled, crossover study. Study participants received target-controlled remifentanil infusions and placebo infusions in a randomized order. Methylnaltrexone was administered by intravenous injection of doses of 0.3 mg/kg. Recordings of pressure and impedance data were acquired using a combined manometry and impedance solid state catheter. Data was analyzed from three series of bolus swallows, baseline, during remifentanil exposure, and 15 min after methylnaltrexone. Results Remifentanil induced significant effects on multiple pharyngeal and esophageal function parameters. No significant differences in remifentanil-induced swallowing dysfunction related to different bolus volumes were found. Pharyngeal effects of remifentanil were not significantly counteracted by methylnaltrexone, whereas on the distal esophageal level, effects on distension pressures were counteracted. Conclusions Changes in pharyngeal and esophageal pressure flow variables were consistent with previous results on remifentanil-induced swallowing dysfunction, and uniform across all bolus volumes. The effects of remifentanil on the pharyngeal level and on the proximal esophagus appear to be predominantly centrally mediated, whereas the effects of remifentanil on the distal esophagus may be mediated by both central and peripheral mechanisms.


Sign in / Sign up

Export Citation Format

Share Document