1.Psychiatric, Somatic and Other Functional Gastrointestinal Disorders in Patients With Irritable Bowel Syndrome at a Tertiary Care Center.
Prashant SINGH ; Abhishek AGNIHOTRI ; Manish K PATHAK ; Asef SHIRAZI ; Rajeew P TIWARI ; V SREENIVAS ; Rajesh SAGAR ; Govind K MAKHARIA
Journal of Neurogastroenterology and Motility 2012;18(3):324-331
BACKGROUND/AIMS: To study the prevalence of somatic and psychiatric co-morbidities in the patients of irritable bowel syndrome (IBS) and to assess the quality of life (QOL) of these patients. METHODS: One hundred and eighty-four IBS patients and 198 controls were included. Diagnosis of IBS, its sub-classification and assessment of other functional gastrointestinal disorders (FGIDs) was made on basis of Rome III criteria. Severity of IBS was assessed using IBS severity scoring system. Psychiatric evaluation was done using Patient Heath Questionnaire. QOL was evaluated using WHO QOL-BREF. RESULTS: One hundred and forty-seven (79.9%) and 158 (85.9%) patients with IBS had at least one other FGID or at least one somatic co-morbidity, respectively. Higher number of patients had at least one psychiatric co-morbidity compared to controls (79.9% vs 34.3%; P < 0.001). Major depressive syndrome (47.3% vs 5.1%; P < 0.001), somatoform disorder (50% vs 14.6%; P < 0.001) and panic syndrome (44% vs 11.6%; P < 0.001) were more common in IBS than controls. Only 14 (7.6%) patients were receiving drug treatment for their psychiatric illness. Severe IBS symptoms were present in significantly higher number of patients with constipation predominant IBS than diarrhea predominant IBS. Those with severe disease had higher prevalence of psychiatric (95.1%) and somatic (96.7%) co-morbidities compared with mild disease. QOL of IBS patients was significantly lower in all four domains compared to controls. Presence of at least one other FGID was significantly associated with presence of one or more psychiatric co-morbidity (P < 0.001). CONCLUSIONS: Majority of IBS patients presenting to a tertiary care center had associated psychiatric, somatic co-morbidities and reduced QOL. Very few of them received specific psychiatric treatment.
Anxiety Disorders
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Constipation
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Depression
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Depressive Disorder
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Diarrhea
;
Gastrointestinal Diseases
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Humans
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Irritable Bowel Syndrome
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Panic
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Prevalence
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Quality of Life
;
Surveys and Questionnaires
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Rome
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Somatoform Disorders
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Tertiary Care Centers
;
Tertiary Healthcare
2.Role of random biopsies in surveillance of dysplasia in ulcerative colitis patients with high risk of colorectal cancer.
Sawan BOPANNA ; Maitreyee ROY ; Prasenjit DAS ; S DATTAGUPTA ; V SREENIVAS ; V Pratap MOULI ; Saurabh KEDIA ; Rajan DHINGRA ; Rajesh PRADHAN ; N Suraj KUMAR ; Dawesh P YADAV ; Govind MAKHARIA ; Vineet AHUJA
Intestinal Research 2016;14(3):264-269
BACKGROUND/AIMS: Recent data suggest that the incidence of ulcerative colitis (UC) related colorectal cancer (CRC) in India is similar to that of West. The optimum method for surveillance is still a debate. Surveillance with random biopsies has been the standard of care, but is a tedious process. We therefore undertook this study to assess the yield of random biopsy in dysplasia surveillance. METHODS: Between March 2014 and July 2015, patients of UC attending the Inflammatory Bowel Disease clinic at the All India Institute of Medical Sciences with high risk factors for CRC like duration of disease >15 years and pancolitis, family history of CRC, primary sclerosing cholangitis underwent surveillance colonoscopy for dysplasia. Four quadrant random biopsies at 10 cm intervals were taken (33 biopsies). Two pathologists examined specimens for dysplasia, and the yield of dysplasia was calculated. RESULTS: Twenty-eight patients were included. Twenty-six of these had pancolitis with a duration of disease greater than 15 years, and two patients had associated primary sclerosing cholangis. No patient had a family history of CRC. The mean age at onset of disease was 28.89±8.73 years and the duration of disease was 19.00±8.78 years. Eighteen patients (64.28%) were males. A total of 924 biopsies were taken. None of the biopsies revealed any evidence of dysplasia, and 7/924 (0.7%) were indefinite for dysplasia. CONCLUSIONS: Random biopsy for surveillance in longstanding extensive colitis has a low yield for dysplasia and does not suffice for screening. Newer techniques such as chromoendoscopy-guided biopsies need greater adoption.
Age of Onset
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Biopsy*
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Cholangitis, Sclerosing
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Colitis
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Colitis, Ulcerative*
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Colonoscopy
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Colorectal Neoplasms*
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Humans
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Incidence
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India
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Inflammatory Bowel Diseases
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Male
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Mass Screening
;
Methods
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Risk Factors
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Standard of Care
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Ulcer*