Acute transcutaneous electrical stimulation (TES) augments esophageal contractility in patients with weak peristalsis
Lung transplantation (LTx) remains controversial in patients with absent peristalsis (AP) given the increased risk for gastroesophageal reflux (GER), and chronic lung allograft dysfunction. Furthermore, specific treatments to facilitate LTx in those with AP have not been widely described. Transcutan...
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Published in | Clinical transplantation Vol. 37; no. 9; p. e15005 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Abstract | Lung transplantation (LTx) remains controversial in patients with absent peristalsis (AP) given the increased risk for gastroesophageal reflux (GER), and chronic lung allograft dysfunction. Furthermore, specific treatments to facilitate LTx in those with AP have not been widely described. Transcutaneous Electrical Stimulation (TES) has been reported to improve foregut contractility in LTx patients and therefore we hypothesize that TES may augment the esophageal motility of patients with ineffective esophageal motility (IEM).
We included 49 patients, 14 with IEM, 5 with AP, and 30 with normal motility. All subjects underwent standard high-resolution manometry and intraluminal impedance (HRIM) with additional swallows as TES was delivered.
TES induced a universal impedance change observable in real-time by a characteristic spike activity. TES significantly augmented the contractile vigor of the esophagus measured by the distal contractile integral (DCI) in patients with IEM [median DCI (IQR) 0 (238) mmHg-cm-s off TES vs. 333 (858) mmHg-cm-s on TES; p = .01] and normal peristalsis [median DCI (IQR) 1545 (1840) mmHg-cm-s off TES vs. 2109 (2082) mmHg-cm-s on TES; p = .01]. Interestingly, TES induced measurable contractile activity (DCI > 100 mmHg-cm-s) in three out of five patients with AP [median DCI (IQR) 0 (0) mmHg-cm-s off TES vs. 0 (182) mmHg-cm-s on TES; p < .001].
TES acutely augmented contractile vigor in patients with normal and weak/ AP. The use of TES may positively impact LTx candidacy, and outcomes for patients with IEM/AP. Nevertheless, further studies are needed to determine the long-term effects of TES in this patient population. |
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AbstractList | Lung transplantation (LTx) remains controversial in patients with absent peristalsis (AP) given the increased risk for gastroesophageal reflux (GER), and chronic lung allograft dysfunction. Furthermore, specific treatments to facilitate LTx in those with AP have not been widely described. Transcutaneous Electrical Stimulation (TES) has been reported to improve foregut contractility in LTx patients and therefore we hypothesize that TES may augment the esophageal motility of patients with ineffective esophageal motility (IEM).BACKGROUNDLung transplantation (LTx) remains controversial in patients with absent peristalsis (AP) given the increased risk for gastroesophageal reflux (GER), and chronic lung allograft dysfunction. Furthermore, specific treatments to facilitate LTx in those with AP have not been widely described. Transcutaneous Electrical Stimulation (TES) has been reported to improve foregut contractility in LTx patients and therefore we hypothesize that TES may augment the esophageal motility of patients with ineffective esophageal motility (IEM).We included 49 patients, 14 with IEM, 5 with AP, and 30 with normal motility. All subjects underwent standard high-resolution manometry and intraluminal impedance (HRIM) with additional swallows as TES was delivered.METHODSWe included 49 patients, 14 with IEM, 5 with AP, and 30 with normal motility. All subjects underwent standard high-resolution manometry and intraluminal impedance (HRIM) with additional swallows as TES was delivered.TES induced a universal impedance change observable in real-time by a characteristic spike activity. TES significantly augmented the contractile vigor of the esophagus measured by the distal contractile integral (DCI) in patients with IEM [median DCI (IQR) 0 (238) mmHg-cm-s off TES vs. 333 (858) mmHg-cm-s on TES; p = .01] and normal peristalsis [median DCI (IQR) 1545 (1840) mmHg-cm-s off TES vs. 2109 (2082) mmHg-cm-s on TES; p = .01]. Interestingly, TES induced measurable contractile activity (DCI > 100 mmHg-cm-s) in three out of five patients with AP [median DCI (IQR) 0 (0) mmHg-cm-s off TES vs. 0 (182) mmHg-cm-s on TES; p < .001].RESULTSTES induced a universal impedance change observable in real-time by a characteristic spike activity. TES significantly augmented the contractile vigor of the esophagus measured by the distal contractile integral (DCI) in patients with IEM [median DCI (IQR) 0 (238) mmHg-cm-s off TES vs. 333 (858) mmHg-cm-s on TES; p = .01] and normal peristalsis [median DCI (IQR) 1545 (1840) mmHg-cm-s off TES vs. 2109 (2082) mmHg-cm-s on TES; p = .01]. Interestingly, TES induced measurable contractile activity (DCI > 100 mmHg-cm-s) in three out of five patients with AP [median DCI (IQR) 0 (0) mmHg-cm-s off TES vs. 0 (182) mmHg-cm-s on TES; p < .001].TES acutely augmented contractile vigor in patients with normal and weak/ AP. The use of TES may positively impact LTx candidacy, and outcomes for patients with IEM/AP. Nevertheless, further studies are needed to determine the long-term effects of TES in this patient population.CONCLUSIONTES acutely augmented contractile vigor in patients with normal and weak/ AP. The use of TES may positively impact LTx candidacy, and outcomes for patients with IEM/AP. Nevertheless, further studies are needed to determine the long-term effects of TES in this patient population. Lung transplantation (LTx) remains controversial in patients with absent peristalsis (AP) given the increased risk for gastroesophageal reflux (GER), and chronic lung allograft dysfunction. Furthermore, specific treatments to facilitate LTx in those with AP have not been widely described. Transcutaneous Electrical Stimulation (TES) has been reported to improve foregut contractility in LTx patients and therefore we hypothesize that TES may augment the esophageal motility of patients with ineffective esophageal motility (IEM). We included 49 patients, 14 with IEM, 5 with AP, and 30 with normal motility. All subjects underwent standard high-resolution manometry and intraluminal impedance (HRIM) with additional swallows as TES was delivered. TES induced a universal impedance change observable in real-time by a characteristic spike activity. TES significantly augmented the contractile vigor of the esophagus measured by the distal contractile integral (DCI) in patients with IEM [median DCI (IQR) 0 (238) mmHg-cm-s off TES vs. 333 (858) mmHg-cm-s on TES; p = .01] and normal peristalsis [median DCI (IQR) 1545 (1840) mmHg-cm-s off TES vs. 2109 (2082) mmHg-cm-s on TES; p = .01]. Interestingly, TES induced measurable contractile activity (DCI > 100 mmHg-cm-s) in three out of five patients with AP [median DCI (IQR) 0 (0) mmHg-cm-s off TES vs. 0 (182) mmHg-cm-s on TES; p < .001]. TES acutely augmented contractile vigor in patients with normal and weak/ AP. The use of TES may positively impact LTx candidacy, and outcomes for patients with IEM/AP. Nevertheless, further studies are needed to determine the long-term effects of TES in this patient population. |
Author | Rogers, Candice Shahmohammadi, Abbas Mindaugas, Rackauskas Machuca, Tiago Estores, David Ayzengart, Alexander Alakrad, Eyad Pelaez, Andres Atkinson, Carl Amaris, Manuel A. Kukrety, Shweta P. Pipkin, Mauricio Nandavaram, Sravanthi |
Author_xml | – sequence: 1 givenname: Manuel A. surname: Amaris fullname: Amaris, Manuel A. organization: Department of Internal Medicine, Division of Gastroenterology, GI Motility Program University of Florida Gainesville Florida USA – sequence: 2 givenname: Carl surname: Atkinson fullname: Atkinson, Carl organization: Department of Internal Medicine Division of Pulmonary Critical Care & Sleep Medicine University of Florida Gainesville Florida USA – sequence: 3 givenname: Tiago surname: Machuca fullname: Machuca, Tiago organization: Miami Transplant Institute Miami Florida USA – sequence: 4 givenname: David surname: Estores fullname: Estores, David organization: Department of Internal Medicine, Division of Gastroenterology, GI Motility Program University of Florida Gainesville Florida USA – sequence: 5 givenname: Eyad surname: Alakrad fullname: Alakrad, Eyad organization: Department of Internal Medicine, Division of Gastroenterology, GI Motility Program University of Florida Gainesville Florida USA – sequence: 6 givenname: Candice surname: Rogers fullname: Rogers, Candice organization: Department of Internal Medicine, Division of Gastroenterology, GI Motility Program University of Florida Gainesville Florida USA – sequence: 7 givenname: Abbas surname: Shahmohammadi fullname: Shahmohammadi, Abbas organization: Department of Internal Medicine Division of Pulmonary Critical Care & Sleep Medicine University of Florida Gainesville Florida USA – sequence: 8 givenname: Shweta P. orcidid: 0000-0003-2680-9863 surname: Kukrety fullname: Kukrety, Shweta P. organization: Department of Internal Medicine Division of Pulmonary Critical Care & Sleep Medicine University of Nebraska Omaha Nebraska USA – sequence: 9 givenname: Alexander surname: Ayzengart fullname: Ayzengart, Alexander organization: Department of Surgery Division of Gastrointestinal Surgery University of Florida Gainesville Florida USA – sequence: 10 givenname: Mauricio surname: Pipkin fullname: Pipkin, Mauricio organization: Miami Transplant Institute Miami Florida USA – sequence: 11 givenname: Rackauskas surname: Mindaugas fullname: Mindaugas, Rackauskas organization: Department of Surgery Division of Thoracic Surgery University of Florida Gainesville Florida USA – sequence: 12 givenname: Sravanthi surname: Nandavaram fullname: Nandavaram, Sravanthi organization: Division of Cardiothoracic Surgery University of Kentucky Lexington Kentucky USA – sequence: 13 givenname: Andres surname: Pelaez fullname: Pelaez, Andres organization: Miami Transplant Institute Miami Florida USA |
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