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1.
Am J Gastroenterol ; 93(6): 901-5, 1998 Jun.
Article in English | MEDLINE | ID: mdl-9647015

ABSTRACT

OBJECTIVE: The degree to which patient education in the areas of diet, exercise, and stress management can improve symptoms of irritable bowel syndrome (IBS) through healthier lifestyle behaviors is unknown. The aim of this study was to determine the effects of outpatient education on the short and long term outcomes, and the association between health-promoting behaviors and symptoms. METHODS: Pender's Health Promotion Model provided the theoretical framework. The study had a prospective longitudinal design. A consecutive sample of 52 adult outpatients with IBS attended a structured class that taught health-promoting modifications of lifestyle. Participants completed the Health-Promoting Lifestyle Profile (HPLP) and selected items from a Bowel Disease Questionnaire (BDQ) before the class and 1 month and 6 months later. Spearman rank correlations were used to assess the association between HPLP and symptom scores. Wilcoxon rank sum tests compared changes in scores versus their baseline values. RESULTS: Response rates at 1 and 6 months were 75% and 83%, respectively. Results revealed significant 1- and 6 month-improvements in pain and Manning symptoms (p < 0.01) and in some HPLP scores (exercise at 1 month, p < 0.05; stress management at 6 months, p < 0.01). Significant associations were found between some, but not all, HPLP and symptom scores over time. CONCLUSION: A structured IBS educational class for patients with IBS improved symptoms and some health-promoting behaviors. However, relationships among specific behaviors and specific symptoms did not consistently correspond with this improvement.


Subject(s)
Colonic Diseases, Functional/therapy , Health Behavior , Patient Education as Topic , Adult , Aged , Colonic Diseases, Functional/diet therapy , Colonic Diseases, Functional/psychology , Exercise , Female , Humans , Life Style , Male , Middle Aged , Outpatients , Surveys and Questionnaires
2.
Mayo Clin Proc ; 68(11): 1067-73, 1993 Nov.
Article in English | MEDLINE | ID: mdl-8231271

ABSTRACT

The aims of this study were to investigate a group of patients with achalasia prospectively to determine (1) the relationship between changes in symptoms and esophageal motor function in response to pneumatic dilation and (2) the effects of the balloon size as well as the frequency and duration of inflation on the outcome of treatment. Fourteen patients with achalasia who were symptomatic for a median duration of 27 months participated in the study. The patients were randomized to one combination of the following pneumatic dilation conditions: a 30- or 35-mm balloon dilator, one or two balloon inflations, and 20, 40, or 60 seconds per balloon inflation. A comprehensive assessment of their symptoms and esophageal motility, transit, and diameter were performed before and 3 months after pneumatic dilation. Pneumatic dilation provided significant relief of dysphagia (P < 0.01), but other symptoms (heartburn, regurgitation, and chest pain) remained unchanged. Pneumatic dilation also caused a significant decrease in lower esophageal sphincter pressure and esophageal diameter and improved esophageal emptying of a solid bolus. Nevertheless, no significant association was detected between changes in the symptom score for dysphagia and changes in objective response measures as a result of pneumatic dilation. Changes in the symptom score for dysphagia or objective responses were similar regardless of the size of the dilator used or the frequency and duration of the balloon inflations.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Catheterization , Esophageal Achalasia/physiopathology , Esophageal Achalasia/therapy , Adult , Aged , Deglutition Disorders/etiology , Deglutition Disorders/therapy , Esophageal Achalasia/complications , Esophageal Achalasia/pathology , Esophagogastric Junction/physiopathology , Esophagus/pathology , Esophagus/physiopathology , Female , Humans , Male , Middle Aged , Pressure , Prospective Studies
3.
Am J Gastroenterol ; 86(1): 57-61, 1991 Jan.
Article in English | MEDLINE | ID: mdl-1986556

ABSTRACT

Primary sclerosing cholangitis is a cholestatic liver disease characterized by inflammation and fibrosis of the biliary tract. The cause of the disease is unknown, and no effective medical treatment exists. In this study, 12 patients received a combination of low-dose prednisone (10 mg/day) and colchicine (0.6 mg bid). Their course was compared with that of a group of concurrent historical controls. At 6 and 12 months, there was significantly more improvement in liver test results over baseline values in patients receiving prednisone and colchicine than in the untreated controls. At 24 months, however, no significant differences in biochemical tests were appreciated between treated and untreated patients. Analysis of serial liver biopsies showed no differences in histologic change in the two groups. During the 2 yr of follow-up, there were two deaths in the control group but none in the treated group. Four untreated patients developed ascites; gastrointestinal bleeding developed in three untreated patients, one of whom developed ascites. In contrast, in the treated group, ascites and bleeding developed in only one patient. We conclude that the combination of colchicine and prednisone does not retard histologic progression or progression of standard liver tests after 2 yr of therapy. There is a trend toward less clinical deterioration and improved survival after 2 yr of treatment. On the basis of these findings, we would not advocate empiric use of these drugs for patients with primary sclerosing cholangitis, but suggest that, if they are to be used at all in PSC, they be evaluated in a controlled clinical trial as treatment for this as yet incurable disease.


Subject(s)
Cholangitis, Sclerosing/drug therapy , Colchicine/therapeutic use , Prednisone/therapeutic use , Adult , Cholangitis, Sclerosing/complications , Cholangitis, Sclerosing/pathology , Cholangitis, Sclerosing/physiopathology , Colchicine/administration & dosage , Drug Therapy, Combination , Female , Humans , Liver Function Tests , Male , Middle Aged , Prednisone/administration & dosage , Time Factors
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