Natural history and impact of irritable bowel syndrome‐type symptoms in inflammatory bowel disease during 6 years of longitudinal follow‐up

医学 肠易激综合征 生活质量(医疗保健) 萧条(经济学) 内科学 自然史 疾病 焦虑 门诊部 炎症性肠病 纵向研究 物理疗法 胃肠病学 精神科 病理 护理部 经济 宏观经济学
作者
Keeley M. Fairbrass,PJ Hamlin,David J. Gracie,Alexander C. Ford
出处
期刊:Alimentary Pharmacology & Therapeutics [Wiley]
卷期号:56 (8): 1264-1273 被引量:15
标识
DOI:10.1111/apt.17193
摘要

Summary Background The long‐term natural history and impact of irritable bowel syndrome (IBS)‐type symptoms on outcomes in inflammatory bowel disease (IBD) are uncertain. Aim To assess this in a longitudinal follow‐up study of patients in secondary care Methods We assessed the natural history of IBS‐type symptoms in IBD via Rome III criteria applied at baseline, and 2 and 6 years. We defined longitudinal disease activity as the need for glucocorticosteroids or flare, escalation, hospitalisation or intestinal resection. To assess healthcare utilisation, we recorded the number of outpatient clinic attendances and investigations. We also collected anxiety, depression and somatoform symptom scores and quality of life scores during follow‐up. Results Among 125 individuals with Rome III data at all three time points, only 41 (32.8%) never reported IBS‐type symptoms. Fifteen patients (12.0%) had IBS‐type symptoms at baseline that resolved, 19 (15.2%) had fluctuating symptoms, 35 (28.0%) had new‐onset symptoms, and 15 (12.0%) had persistent symptoms. Among more than 300 patients with IBD activity data, IBS‐type symptoms were not associated with an increased likelihood of the need for glucocorticosteroids or flare, escalation, hospitalisation or intestinal resection. However, the mean numbers of outpatient appointments and endoscopic investigations were significantly higher among those with IBS‐type symptoms. Anxiety, depression and somatoform symptom scores were significantly higher, and quality of life scores were significantly lower, in those reporting IBS‐type symptoms at least once during the study. Conclusions IBS‐type symptoms affected more than two‐thirds of patients with IBD during >6 years of follow‐up and were associated with increased healthcare utilisation, and worse anxiety, depression, somatoform symptom and quality of life scores, but not adverse disease activity outcomes.
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