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1.
Neurogastroenterol Motil ; 28(1): 116-26, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26517978

ABSTRACT

BACKGROUND: Esophagogastric junction outflow obstruction (EGJOO) is a newly described diagnostic entity growing in importance due to the use of high resolution manometry (HRM). There is little knowledge regarding its incidence, etiopathogeny, long-term evolution, and most suitable treatment. Our objective was to increase the awareness of EGJOO to optimize the management of these patients. METHODS: We conducted a historical (retrospective and prospective) study of patients diagnosed with EGJOO using HRM combined with multichannel intraluminal impedance, comparing their manometric and impedance characteristics with those of a control group. Symptoms, etiology of obstruction, acid exposure, clinical course (and its associated factors), and response to treatment were also evaluated in the EGJOO group. KEY RESULTS: Forty-four subjects were included (28 patients and 16 controls). Esophagogastric junction outflow obstruction patients presented incomplete esophageal transit more frequently than controls. Patients with structural obstruction had dysphagia more frequently than patients with functional obstruction, and different manometric, impedance, and pH-metric patterns. Over one-third of the EGJOO patients presented a spontaneous resolution of symptoms without EGJOO treatment. In the multivariate analysis, the variables associated with this spontaneous symptomatic resolution included typical symptoms of gastro-esophageal reflux disease or epigastralgia as the main symptom and resting or basal pressure of the upper esophageal sphincter <50 mmHg. CONCLUSIONS & INFERENCES: The majority of EGJOO patients presented intact peristalsis which may compensate for the lack of EGJ relaxation. In the EGJOO patients presenting favorable factors associated with a spontaneous resolution of symptoms, invasive treatments should be considered with special caution. Structural etiologies are more amenable to management, while the remainder may improve without intervention.


Subject(s)
Deglutition Disorders/physiopathology , Esophageal Motility Disorders/physiopathology , Esophagogastric Junction/physiopathology , Gastroesophageal Reflux/physiopathology , Acetylcholine Release Inhibitors/therapeutic use , Adult , Aged , Botulinum Toxins/therapeutic use , Case-Control Studies , Cohort Studies , Dilatation/methods , Disease Progression , Endoscopy, Digestive System/methods , Esophageal Motility Disorders/complications , Esophageal Motility Disorders/therapy , Esophageal Sphincter, Lower/physiopathology , Female , Gastroesophageal Reflux/complications , Humans , Male , Manometry , Middle Aged , Prospective Studies , Retrospective Studies
2.
Rev Esp Enferm Dig ; 100(8): 481-9, 2008 Aug.
Article in Spanish | MEDLINE | ID: mdl-18942901

ABSTRACT

OBJECTIVE: To assess the effect of pentoxiphylline (a potent inhibitor of tumor necrosis factor alpha) on survival, on systemic and portal hemodynamics, and on cardiac function in patients with alcoholic cirrhosis. DESIGN: A randomized double-blind placebo-controlled trial. SETTING: A single center using parallel groups of patients to compare pentoxiphylline with placebo. PATIENTS: We recruited 24 patients with alcoholic cirrhosis (8 Child-Pugh B and 16 Child-Pugh C). INTERVENTIONS: Patients were randomly assigned to receive pentoxiphylline (400 mg tid; n = 12) or placebo (n = 12) over a 4-week period. OUTCOME MEASURES: The primary outcome was to extend short-term and long-term survival. Secondary outcomes included hemodynamic benefits (improvement in cardiac function and/or systemic vascular resistance index, or decrease in portal pressure). RESULTS: Portal pressure and cardiac function remained unchanged and there were no significant differences in short-term or long-term survival between treatment and placebo groups. The group on pentoxiphylline increased systemic vascular resistance and decreased cardiac indices (from 1,721 +/- 567 to 2,082 +/- 622 dyn.sec(-1) cm(-5) m(-2) and from 4.17 +/- 1.4 to 3.4 +/- 0.9 l.m(-2), p = 0.05). CONCLUSIONS: Although pentoxiphylline seems to provide some short-term hemodynamic benefits in patients with advanced alcoholic cirrhosis, this drug has no effect on survival or portal pressure in these patients.


Subject(s)
Liver Cirrhosis, Alcoholic/drug therapy , Liver Cirrhosis, Alcoholic/physiopathology , Pentoxifylline/therapeutic use , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Double-Blind Method , Female , Heart/drug effects , Heart/physiopathology , Hemodynamics/drug effects , Humans , Liver Cirrhosis, Alcoholic/mortality , Male , Middle Aged , Portal System/drug effects , Portal System/physiopathology , Severity of Illness Index , Survival Rate
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