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首页> 外文期刊>Rheumatology >Validation of the Dudley inflammatory bowel symptom questionnaire for the assessment of bowel symptoms in axial SpA: Prevalence of clinically relevant bowel symptoms and association with disease activity
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Validation of the Dudley inflammatory bowel symptom questionnaire for the assessment of bowel symptoms in axial SpA: Prevalence of clinically relevant bowel symptoms and association with disease activity

机译:验证Dudley炎症性肠症状问卷以评估轴向SpA的肠症状:临床相关肠症状的普遍性以及与疾病活动的关系

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Objectives: To validate the Dudley Inflammatory Bowel Disease Questionnaire (DISQ) for determining the presence and severity of bowel symptoms in axial SpA. Methods: Seventy-seven SpA patients were assessed for disease activity using the BASDAI. All participants, including 32 healthy controls and 29 patients with Crohn's Disease (CD), completed the DISQ and an assessment of stool form and frequency. Validation of the DISQ was undertaken in accordance with OMERACT criteria. Results: Validity of the DISQ for measuring bowel symptoms in SpA was confirmed (Cronbach's α 0.79). Mean DISQ scores (s.d.) were: controls 2.6 (2.6), SpA 8.7 (6.1) and CD 17.1 (10.2). Differences were significant between controls and SpA, and SpA and CD, and correlated with disease activity (ρ 0.27, P = 0.02). In SpA, DISQ scores of those taking NSAIDs (n = 59) did not differ from those not taking NSAIDs (n = 18) (P = 0.31). Stool form and frequency differed significantly between SpA patients and healthy controls (P < 0.001). Using the DISQ the prevalence of clinically relevant bowel symptoms in SpA is 31%, and 7.8% experience bowel symptoms equivalent to active CD. Conclusion: The DISQ is a valid measure of bowel symptoms in SpA. Bowel symptoms are prevalent in SpA and correlate with disease activity. Symptoms do not relate to treatment with NSAIDs. We conclude that bowel symptoms should be included as a domain in the clinical assessment of patients with SpA and that the DISQ has potential as an outcome measure in clinical trials.
机译:目的:验证Dudley炎症性肠病问卷(DISQ)以确定轴向SpA中肠症状的存在和严重程度。方法:使用BASDAI对77名SpA患者进行了疾病活动评估。所有参与者,包括32名健康对照者和29名克罗恩病(CD)患者,均完成了DISQ并评估了大便的形式和频率。 DISQ的验证是根据OMERACT标准进行的。结果:确认DISQ可以测量SpA肠症状的有效性(Cronbach'sα0.79)。平均DISQ得分(标准差)为:对照2.6(2.6),SpA 8.7(6.1)和CD 17.1(10.2)。对照组与SpA,SpA和CD之间存在显着差异,并且与疾病活动性相关(ρ0.27,P = 0.02)。在SpA中,服用NSAID的人(n = 59)的DISQ得分与未服用NSAID的人(n = 18)的DISQ得分没有差异(P = 0.31)。 SpA患者和健康对照之间的粪便形式和频率显着不同(P <0.001)。使用DISQ,SpA中临床相关肠症状的患病率为31%,而7.8%的肠症状相当于活性CD。结论:DISQ是SpA中肠症状的有效量度。肠症状在SpA中很普遍,并且与疾病活动相关。症状与NSAID的治疗无关。我们得出结论,肠道症状应作为SpA患者的临床评估中的一个领域,并且DISQ有潜力作为临床试验中的结局指标。

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