儿童克罗恩病患者报告结果测量信息系统的临床应用:一项横断面研究

IF 3.2 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Health and Quality of Life Outcomes Pub Date : 2024-12-31 DOI:10.1186/s12955-024-02330-2
Sara Azevedo, Maria Miguel Oliveira, Paulo Nogueira, Ana Isabel Lopes
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引用次数: 0

摘要

目的:本研究通过将患者报告结果测量信息系统(PROMIS®)与客观临床数据和验证的儿童克罗恩病(CD)患者健康相关生活质量(HRQOL)测量进行比较,评估其临床效用。研究设计:横断面研究。儿童乳糜泻患者(8-17岁)从门诊儿科胃肠病学中心前瞻性入组超过8个月。我们评估了PROMIS®儿科短格式测量、人口统计学和疾病相关数据、全球临床评估和HRQOL测量之间的关联。根据PCDAI(缓解vs活动性疾病)进行亚分析。结果:31例患者,平均年龄15.3岁;(58%为女性),平均病程2.7年;80.6%的患者病情缓解或病情轻微。PROMIS®评分与多个因素显著相关:年龄与PROMIS®全球健康量表呈负相关(r=-0.399;p = 0.026)和生活满意度(r=-0.359;p = 0.047);性别与PROMIS®认知功能量表相关(t = 2.20;P = 0.038),有利于男性;学校水平与PROMIS®同伴关系呈负相关(F = 3.90;p = 0.003)。临床评估还显示血红蛋白与PROMIS®Global Health之间存在显著相关性(r = 0.356;P = 0.049)和疼痛干扰(r=-0.360;p = 0.046),铁蛋白与PROMIS®的意义和目的(r = 0.435;P = 0.016)和认知功能(r = 0.450;p = 0.011)。疾病活动性评估与多项PROMIS®措施显著相关,缓解期患者得分更高。治疗变化,特别是皮质类固醇治疗,对PROMIS®焦虑和生活满意度评分有负面影响。IMPACT-III得分与PROMIS®全球健康、意义和目的、生活满意度和同伴关系得分呈正相关,与抑郁、焦虑、疼痛干扰和疲劳得分呈负相关。组分析显示,缓解组的PROMIS®评分和HRQOL评分高于活动性疾病缓解组。结论:与最近的证据一致,PROMIS®评分可靠地反映了疾病活动性和HRQOL。与临床评估和治疗效果的有意义的关联加强了PROs在以患者为中心的儿童IBD管理中的临床相关性和实用性,并强调了自我报告作为评估健康状况的金标准工具的重要性。
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Clinical usefulness of patient-reported-outcome-measurement information system in Pediatric Crohn's Disease: a cross-sectional study.

Objectives: This study evaluated the clinical utility of the Patient-Reported Outcomes Measurement Information System (PROMIS®) by comparing it with objective clinical data and validated health-related quality of life (HRQOL) measures in pediatric Crohn's disease (CD) patients.

Study design: Cross-sectional study. Pediatric CD patients (aged 8-17 years) were enrolled prospectively over eight months from an outpatient pediatric gastroenterology center. We assessed the associations between PROMIS® Pediatric short-form measures, demographic and disease-related data, global clinical assessments, and HRQOL measures. A subanalysis according to the PCDAI (remission versus active disease) was also conducted.

Results: Thirty-one patients (mean age: 15.3; 58% female) with a mean disease duration of 2.7 years were included; 80.6% were in remission or had mild disease. The PROMIS® score was significantly correlated with several factors: age was negatively correlated with the PROMIS® Global Health Scale (r=-0.399; p = 0.026) and Life Satisfaction (r=-0.359; p = 0.047); sex was associated with the PROMIS® Cognitive Function Scale (t = 2.20; p = 0.038), favoring males; and school level was inversely related to the PROMIS® Peer Relationships (F = 3.90; p = 0.003). Clinical assessments also revealed significant correlations between hemoglobin and PROMIS® Global Health (r = 0.356; p = 0.049) and pain interference (r=-0.360; p = 0.046) and between ferritin and PROMIS® Meaning and Purpose (r = 0.435; p = 0.016) and cognitive function (r = 0.450; p = 0.011). Disease activity assessments correlated significantly with multiple PROMIS® measures, with better scores in patients in remission. Treatment changes, particularly corticosteroid treatment, negatively impacted the PROMIS® Anxiety and Life Satisfaction scores. IMPACT-III scores correlated positively with PROMIS® Global Health, Meaning and Purpose, Life Satisfaction, and peer relationships scores and negatively with Depression, Anxiety, Pain interference, and Fatigue scores. Group analysis indicated better PROMIS® scores and HRQOL scores in remission than in active disease remission.

Conclusion: Consistent with recent evidence, PROMIS® scores reliably reflect disease activity and HRQOL. The meaningful associations with clinical assessment and treatment efficacy reinforce the clinical relevance and utility of PROs in the patient-centered management of pediatric IBD and highlight the importance of self-reports as a gold standard tool for assessing health status.

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来源期刊
CiteScore
7.30
自引率
2.80%
发文量
154
审稿时长
3-8 weeks
期刊介绍: Health and Quality of Life Outcomes is an open access, peer-reviewed, journal offering high quality articles, rapid publication and wide diffusion in the public domain. Health and Quality of Life Outcomes considers original manuscripts on the Health-Related Quality of Life (HRQOL) assessment for evaluation of medical and psychosocial interventions. It also considers approaches and studies on psychometric properties of HRQOL and patient reported outcome measures, including cultural validation of instruments if they provide information about the impact of interventions. The journal publishes study protocols and reviews summarising the present state of knowledge concerning a particular aspect of HRQOL and patient reported outcome measures. Reviews should generally follow systematic review methodology. Comments on articles and letters to the editor are welcome.
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