Topographic analysis of esophageal double-peaked waves

Slides:



Advertisements
Similar presentations
BioVIEW Suite P Automated Chicago Analysis. Automated Chicago Classification Analysis Advanced Analysis Tutorial.
Advertisements

Date of download: 6/2/2016 Copyright © The American College of Cardiology. All rights reserved. From: Hemodynamic Determinants of Doppler Pulmonary Venous.
Date of download: 6/21/2016 Copyright © ASME. All rights reserved. From: In Vitro Quantification of Time Dependent Thrombus Size Using Magnetic Resonance.
Date of download: 6/22/2016 Copyright © ASME. All rights reserved. From: The Importance of Intrinsic Damage Properties to Bone Fragility: A Finite Element.
Date of download: 9/25/2017 Copyright © ASME. All rights reserved.
Date of download: 10/6/2017 Copyright © ASME. All rights reserved.
Volume 121, Issue 4, Pages (October 2001)
Volume 130, Issue 2, Pages (February 2006)
From: Esophageal motility disorders after gastric banding
Volume 74, Issue 4, Pages (April 1998)
Actions by Angiotensin II on Esophageal Contractility in Humans
Increased frequency of transient lower esophageal sphincter relaxation induced by gastric distention in reflux patients with hiatal hernia  Peter J. Kahrilas*,
Volume 128, Issue 2, Pages (February 2005)
Volume 130, Issue 2, Pages (February 2006)
Volume 8, Issue 9, Pages (September 2011)
Germán Sumbre, Graziano Fiorito, Tamar Flash, Binyamin Hochner 
Volume 121, Issue 2, Pages (August 2001)
Peng Du, Gregory O'Grady, Leo K. Cheng, Andrew J. Pullan 
Volume 114, Issue 4, Pages (April 1998)
Narrow QRS Complex Tachycardias
Volume 130, Issue 1, Pages (January 2006)
Obesity: A Challenge to Esophagogastric Junction Integrity
Volume 142, Issue 4, Pages e7 (April 2012)
Volume 135, Issue 5, Pages (November 2008)
Covering the Cover Gastroenterology
Volume 131, Issue 6, Pages (December 2006)
Contact dynamics during keratocyte motility
Volume 135, Issue 5, Pages (November 2008)
Volume 128, Issue 5, Pages (May 2005)
Volume 57, Issue 5, Pages (March 2008)
Erroneous Diagnosis of Gastroesophageal Reflux Disease in Achalasia
Peter J. Kahrilas, Guy Boeckxstaens  Gastroenterology 
Volume 74, Issue 4, Pages (April 1998)
Yitao Ma, Dinara Shakiryanova, Irina Vardya, Sergey V Popov 
Regulation of Airway Ciliary Activity by Ca2+: Simultaneous Measurement of Beat Frequency and Intracellular Ca2+  Alison B. Lansley, Michael J. Sanderson 
Volume 134, Issue 5, Pages (May 2008)
Electrodiffusion Models of Neurons and Extracellular Space Using the Poisson-Nernst- Planck Equations—Numerical Simulation of the Intra- and Extracellular.
Benjamin Basseri, MD, Jeffrey L
Martin D Bootman, Michael J Berridge, Peter Lipp  Cell 
Challenging the Limits of Esophageal Manometry
Radu Tutuian, Donald O Castell 
Volume 133, Issue 3, Pages (September 2007)
Volume 74, Issue 1, Pages (January 1998)
Mano J. Thubrikar, PhD, Francis Robicsek, MD, Brett L. Fowler, BS 
High-Resolution Manometry and Impedance-pH/Manometry: Valuable Tools in Clinical and Investigational Esophagology  Peter J. Kahrilas, Daniel Sifrim  Gastroenterology 
AGA technical review on the clinical use of esophageal manometry
Volume 84, Issue 3, Pages (March 2003)
Volume 119, Issue 6, Pages (December 2000)
Volume 141, Issue 2, Pages (August 2011)
Development of Esophageal Peristalsis in Preterm and Term Neonates
Khaled Machaca, H. Criss Hartzell  Biophysical Journal 
Feng Han, Natalia Caporale, Yang Dan  Neuron 
Normal Values of Esophageal Distensibility and Distension-Induced Contractility Measured by Functional Luminal Imaging Probe Panometry  Dustin A. Carlson,
Volume 102, Issue 1, Pages (January 2012)
Volume 120, Issue 7, Pages (June 2001)
Clarification of the esophageal function defect in patients with manometric ineffective esophageal motility: studies using combined impedance-manometry 
Volume 66, Issue 2, Pages (August 1974)
Volume 121, Issue 4, Pages (October 2001)
Florian Siegert, Cornelis J. Weijer  Current Biology 
Volume 128, Issue 3, Pages (March 2005)
Reflux Is Unlikely to Occur During Stable Sleep
Cardiac Purkinje cells
Kinetics of P2X7 Receptor-Operated Single Channels Currents
Volume 84, Issue 3, Pages (March 2003)
Electrical Activity of the Stomach: Clinical Implications
Abdominal Pain With Fluctuating Elevation of Amylase and AST
John E. Pickard, Klaus Ley  Biophysical Journal 
Peng Du, Gregory O'Grady, Leo K. Cheng, Andrew J. Pullan 
Synapse-Specific Contribution of the Variation of Transmitter Concentration to the Decay of Inhibitory Postsynaptic Currents  Zoltan Nusser, David Naylor,
Head-Eye Coordination at a Microscopic Scale
Presentation transcript:

Topographic analysis of esophageal double-peaked waves Ray E. Clouse, Annamaria Staiano, Aydamir Alrakawi  Gastroenterology  Volume 118, Issue 3, Pages 469-476 (March 2000) DOI: 10.1016/S0016-5085(00)70252-6 Copyright © 2000 American Gastroenterological Association Terms and Conditions

Fig. 1 Normal appearance of esophageal peristalsis on 3-dimensional topographic plots. The peaks in the surface plot (bottom) are represented as concentric lines on the contour plot (top). Pressure data below 10 mm Hg are censored on the contour plot. For these plots, the catheter is positioned so that the distal recording site (position 21) is situated just distal to the lower sphincter, shown in the foreground. Decay of the first topographic segment in the proximal esophagus soon after initiation of the swallow can be seen at the back of the plot. The first trough resumes with contraction in the distal esophagus that is divided into 2 pressure segments before merging with the lower sphincter after-contraction in the foreground.8 Gastroenterology 2000 118, 469-476DOI: (10.1016/S0016-5085(00)70252-6) Copyright © 2000 American Gastroenterological Association Terms and Conditions

Fig. 2 A representative contour plot from a swallow with a double-peaked wave. The plot shows peristalsis entering the distal esophagus (regions of the second and third topographic segments) and reaching the lower sphincter (bottom). The second peak appears as an extension arising from the region of the third segment near its maximal pressure site. Tracings from 5 of the 21 recording sites (5,7,9,11,13) used to create the plot are shown. Numbers on the contour rings indicate amplitude in mm Hg. The retrograde progression of the peak pressures in the second peak is shown with the dashed line extracted from a regression of peak pressures on the topographic plot. Gastroenterology 2000 118, 469-476DOI: (10.1016/S0016-5085(00)70252-6) Copyright © 2000 American Gastroenterological Association Terms and Conditions

Fig. 3 Surface and contour plots from a swallow with a double-peaked wave. (Left) The propagation front appears normal from a distal perspective. (Right) When the plot is rotated 180° with the lower sphincter in the distance, the second peak is seen to extend from the back of the third topographic segment, decaying in pressure as it reaches more proximal sites. The regression line drawn from peak amplitudes at 0.2-cm levels on the surface plot establishes the retrograde progression and velocity of this peak. Gastroenterology 2000 118, 469-476DOI: (10.1016/S0016-5085(00)70252-6) Copyright © 2000 American Gastroenterological Association Terms and Conditions

Fig. 4 Contour plots from 2 swallows with double-peaked waves. The catheter is in the distal position, showing distal esophageal peristalsis and the lower sphincter (bottom). In both swallows, the pressure event responsible for the second peak appears to originate near the maximal pressure in the topographic segment proximal to the lower sphincter (the third topographic segment) and extend cephalad into the esophageal body. Contour rings begin at 10 mm Hg in both panels. (A) The second peak extends >7 cm proximally over the region normally represented by the second topographic segment, a region that was poorly developed on this swallow. (B) The second peak extends for a short distance with retrograde peak progression. The regression lines used to calculate velocities for the onset and peak pressure of the first (primary) wave and the peak pressure of the second peak are shown. Gastroenterology 2000 118, 469-476DOI: (10.1016/S0016-5085(00)70252-6) Copyright © 2000 American Gastroenterological Association Terms and Conditions

Fig. 5 Progression velocities of maximal pressures in the double-peaked waves. Velocities were determined from the slopes of regression lines. The direction was considered uncertain (▵) when the calculated velocity exceeded 50 cm/s in either direction. Gastroenterology 2000 118, 469-476DOI: (10.1016/S0016-5085(00)70252-6) Copyright © 2000 American Gastroenterological Association Terms and Conditions

Fig. 6 Conventional analysis of propagation direction of the second peak using onsets of the second upstroke. (A) Topographic and conventional appearance of a double-peaked wave. Circled numbers represent corresponding catheter recording positions. Onset of contraction producing the second peak propagates in a retrograde direction. (B and C) Two additional swallows from other subjects showing either retrograde or simultaneous onset of the second event. Gastroenterology 2000 118, 469-476DOI: (10.1016/S0016-5085(00)70252-6) Copyright © 2000 American Gastroenterological Association Terms and Conditions

Fig. 7 Frames from the series of propagating axial waveforms taken from the 2 swallows shown in Figure 4. More proximal esophageal locations are represented on the left of each frame. (A) By 5.6 seconds, the peristaltic wave had entered the third topographic region. As pressure climbed at the leading edge, the trailing edge arrested in forward motion (6.8 seconds). Cephalad movement of this trailing edge is well appreciated by 7.4 seconds. (The 6.8-second image is reproduced faintly on the 7.4- and 8.0-second frames for comparison.) With this cephalad movement, isobaric increase in intraesophageal pressure is noted in the proximal esophagus (*), reversing the usual gradient across the propagating waveform produced by the intrabolus pressure at the leading edge (right side of waveform). The trailing edge and cephalad extension responsible for the second peak decay as the leading edge proceeds. (B) The second segment dissipates with appearance of the third segment at 7.0 seconds. Forward progression of the trailing edge is arrested at 7.6 seconds with increasing pressures at the leading edge. Cephalad movement of the trailing edge is appreciated at 8.2 seconds and is maximal at 8.8 seconds. (The 7.6-second image is reproduced on these frames.) The trailing edge decays as antegrade propagation proceeds at 9.4 seconds. The dashed lines show the cephalad margins of the peristaltic front over the time represented by the double-peaked wave. Actual retrograde propagation is not present in either of these swallows. Gastroenterology 2000 118, 469-476DOI: (10.1016/S0016-5085(00)70252-6) Copyright © 2000 American Gastroenterological Association Terms and Conditions