2021
DOI: 10.1016/j.transproceed.2021.03.035
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Gastroesophageal Reflux and Esophageal Motility Disorder After Lung Transplant: Influence on the Transplanted Graft

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Cited by 5 publications
(5 citation statements)
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“…1,2 Esophageal dysmotility and gastroesophageal reflux (GER) are common in patients with respiratory disease, thought to be linked to disease progression, and are also common following LTx. The most common esophageal motor disorders include minor disorders of peristalsis, such as ineffective esophageal motility (IEM) and esophago-gastric junction outflow obstruction (EGJOO), [3][4][5][6][7][8][9] along with Jackhammer esophagus seen in some patients, mainly post-LTx, 4,[6][7][8][10][11][12] IEM is associated with greater numbers of proximal reflux events both in respiratory disease 9 and following LTx, 8 while EGJOO is associated with significantly less GER, despite an apparent increased risk of developing CLAD post-LTx. 8 Although studies have suggested that distal contractile integral (DCI) 4,6,7 and aperistalsis prior to LTx can improve following LTx, 13,14 it remains unclear whether certain motility diagnoses prior to LTx either remain the same or change to another diagnosis following LTx, and if this differs with type of respiratory disease.…”
Section: Introductionmentioning
confidence: 99%
“…1,2 Esophageal dysmotility and gastroesophageal reflux (GER) are common in patients with respiratory disease, thought to be linked to disease progression, and are also common following LTx. The most common esophageal motor disorders include minor disorders of peristalsis, such as ineffective esophageal motility (IEM) and esophago-gastric junction outflow obstruction (EGJOO), [3][4][5][6][7][8][9] along with Jackhammer esophagus seen in some patients, mainly post-LTx, 4,[6][7][8][10][11][12] IEM is associated with greater numbers of proximal reflux events both in respiratory disease 9 and following LTx, 8 while EGJOO is associated with significantly less GER, despite an apparent increased risk of developing CLAD post-LTx. 8 Although studies have suggested that distal contractile integral (DCI) 4,6,7 and aperistalsis prior to LTx can improve following LTx, 13,14 it remains unclear whether certain motility diagnoses prior to LTx either remain the same or change to another diagnosis following LTx, and if this differs with type of respiratory disease.…”
Section: Introductionmentioning
confidence: 99%
“…We conducted a search in PubMed, from database inception to January 22, 2023, for reports in any language using the search terms ("lung transplant" OR "lung transplantation" ) AND ( "chronic rejection" OR "chronic lung allograft dysfunction" OR "bronchiolitis obliterans syndrome" OR "CLAD" OR "BOS" ) AND ("esophagus" OR "esophageal" OR "manometry" OR "achalasia" OR "EGJOO" OR "esophagogastric junction outflow obstruction" OR "esophageal motility"), which yielded 53 articles. Of these, only five studies (with 50 to 93 patients) assessed the relationship between post-lung transplant esophageal motility or function and any post-transplant outcomes (11)(12)(13)(14)(15). Of these five, three only investigated symptomatic patients (11,12,14), one did not use CLAD as an outcome (13), and the fifth, while assessing CLAD as an outcome, did not correct for possible confounding variables (15).…”
Section: Introductionmentioning
confidence: 99%
“…Of these, only five studies (with 50 to 93 patients) assessed the relationship between post-lung transplant esophageal motility or function and any post-transplant outcomes (11)(12)(13)(14)(15). Of these five, three only investigated symptomatic patients (11,12,14), one did not use CLAD as an outcome (13), and the fifth, while assessing CLAD as an outcome, did not correct for possible confounding variables (15). We therefore concluded that a larger study was needed to evaluate the association between esophageal disorders and CLAD in better powered multivariable models.…”
Section: Introductionmentioning
confidence: 99%
“…3 AZI diminishes interleukin (IL)-17 stimulated production of IL-8 in human airway smooth muscle cells, reduces other cytokines, and promotes gut motility, all of which may reduce CLAD development. 4-6…”
mentioning
confidence: 99%
“…3 AZI diminishes interleukin (IL)-17 stimulated production of IL-8 in human airway smooth muscle cells, reduces other cytokines, and promotes gut motility, all of which may reduce CLAD development. [4][5][6] Multiple case series reported stabilization of lung function after AZI treatment for bronchiolitis obliterans syndrome (BOS). In these recipients, increased neutrophils in bronchoalveolar lavage (BAL) fluid, were associated with recovery following AZI therapy, leading to the distinction between neutrophilic reversible allograft dysfunction and fibroproliferative.…”
mentioning
confidence: 99%