Bencardino Sarah, D'Amico Ferdinando, Ciliberto Ambra, Danese Silvio
Gastroenterology and Endoscopy, IRCCS Ospedale San Raffaele and Vita-Salute San Raffaele University, 20132 Milan, Italy.
J Clin Med. 2025 Aug 9;14(16):5648. doi: 10.3390/jcm14165648.
Crohn's disease (CD) is a chronic inflammatory bowel disease that significantly affects patients' quality of life. Nutrition is increasingly recognized as a modifiable factor influencing disease activity and symptom management. Despite growing interest, structured dietary guidelines for CD are lacking, and patients often rely on personal experience or fragmented advice. This study aimed to investigate patients' perceptions of diet, the support they receive, and the psychosocial burden of dietary management in CD. : A nationwide online survey was conducted in Italy from April to May 2025 among individuals diagnosed with CD. The questionnaire, developed in line with the CROSS reporting guidelines, comprised 30 multiple-choice questions across five sections: demographics, disease characteristics, dietary habits during remission, dietary habits during flare-ups, and psychological impact. Invitations were distributed through patient associations, webinars, and gastroenterology professionals. Responses were anonymized. A total of 222 participants completed the survey (59.5% female, most aged 30-39 years). Fatigue was the most common symptom (71.6%), frequently persisting even during remission. Nearly half of respondents reported diet as "very important" in disease management, yet only 32% had received a formal referral to a nutritionist. The most commonly adopted dietary approach was a low-fiber diet, while awareness of evidence-based protocols like the Crohn's disease exclusion diet (CDED) was limited (11.7%). Social and psychological burdens were significant, with 79.2% reporting anxiety when outside their home. : Dietary education and psychological support are unmet needs for CD patients. Improved access to tailored nutritional counseling and greater awareness of validated dietary approaches may enhance disease management and quality of life.
克罗恩病(CD)是一种慢性炎症性肠病,严重影响患者的生活质量。营养越来越被认为是影响疾病活动和症状管理的一个可改变因素。尽管人们对此的兴趣日益浓厚,但针对克罗恩病的结构化饮食指南却很缺乏,患者往往依赖个人经验或零散的建议。本研究旨在调查患者对饮食的看法、他们获得的支持以及克罗恩病饮食管理的心理社会负担。2025年4月至5月在意大利对被诊断为克罗恩病的个体进行了一项全国性在线调查。该问卷是根据CROSS报告指南制定的,包括五个部分的30个多项选择题:人口统计学、疾病特征、缓解期饮食习惯、发作期饮食习惯以及心理影响。邀请通过患者协会、网络研讨会和胃肠病学专业人员进行分发。回答进行了匿名处理。共有222名参与者完成了调查(59.5%为女性,大多数年龄在30 - 39岁)。疲劳是最常见的症状(71.6%),即使在缓解期也经常持续存在。近一半的受访者表示饮食在疾病管理中“非常重要”,但只有32%的人得到了转介至营养师的正式推荐。最常采用的饮食方法是低纤维饮食,而对克罗恩病排除饮食(CDED)等循证方案的认知有限(11.7%)。社会和心理负担较重,79.