Leeds Gastroenterology Institute, St. James's University Hospital, Leeds, UK.
Leeds Institute of Medical Research at St. James's, University of Leeds, Leeds, UK.
Aliment Pharmacol Ther. 2022 Oct;56(8):1264-1273. doi: 10.1111/apt.17193. Epub 2022 Aug 22.
The long-term natural history and impact of irritable bowel syndrome (IBS)-type symptoms on outcomes in inflammatory bowel disease (IBD) are uncertain.
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.
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.
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.
肠易激综合征(IBS)样症状在炎症性肠病(IBD)中的长期自然史和对结局的影响尚不确定。
通过对二级保健患者进行的纵向随访研究来评估这一点。
我们通过在基线、2 年和 6 年时应用罗马 III 标准来评估 IBD 中 IBS 样症状的自然史。我们将纵向疾病活动定义为需要糖皮质激素或发作、升级、住院或肠道切除术。为了评估医疗保健的利用情况,我们记录了门诊就诊次数和检查次数。我们还在随访期间收集了焦虑、抑郁和躯体症状评分以及生活质量评分。
在 125 名具有所有三个时间点罗马 III 数据的个体中,只有 41 名(32.8%)从未报告过 IBS 样症状。15 名患者(12.0%)基线时有 IBS 样症状但已缓解,19 名(15.2%)症状波动,35 名(28.0%)出现新发症状,15 名(12.0%)症状持续存在。在 300 多名有 IBD 活动数据的患者中,IBS 样症状与需要糖皮质激素或发作、升级、住院或肠道切除术的可能性增加无关。然而,有 IBS 样症状的患者的门诊预约和内镜检查次数明显更多。报告至少一次研究期间有 IBS 样症状的患者的焦虑、抑郁和躯体症状评分显著升高,生活质量评分显著降低。
在超过 6 年的随访期间,IBS 样症状影响了超过三分之二的 IBD 患者,与更高的医疗保健利用、更差的焦虑、抑郁、躯体症状和生活质量评分相关,但与不良疾病活动结局无关。