患有幼年特发性关节炎、炎症性肠病和健康同龄人的疫苗接种覆盖率:横断面电子调查数据

Elizaveta Makarova, Aygul Khabirova, Natalia Volkova, Tatiana Gabrusskaya, Natalia Ulanova, Larisa Sakhno, Maria Revnova, Mikhail Kostik
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引用次数: 1

摘要

背景:儿童特发性关节炎(JIA)和炎症性肠病(IBD)等免疫介导性疾病的患者,由于疾病相关的免疫功能障碍和免疫抑制药物的应用,发生感染的风险增加。目的:评价IBD和JIA患者的疫苗覆盖率,并与健康儿童进行比较。方法:在横断面研究中,我们纳入了190名JIA儿童(n = 81)、IBD儿童(n = 51)和HC儿童(n = 58)的法定代理人的问卷调查数据。为这项调查制作了一份电子在线问卷。结果:JIA患者以女性为主,发病年龄较小。JIA的父母受教育程度较高。三个研究组的就业水平和家庭状况相似。与JIA和健康对照组相比,JIA和IBD患者的疫苗覆盖率较低,没有父母对IBD疫苗接种的排斥反应。接种不完全的主要原因是IBD和JIA的医疗条件。与JIA和HC相比,IBD患者的正常疫苗相关反应率较低。医生对疫苗接种的鼓励作用在JIA患者中最低。与JIA和HC相比,IBD患者在免疫抑制治疗前检查抗体的可能性更大,并且补充接种疫苗的次数更多。结论:JIA和IBD患者疫苗接种率低于HC。医生鼓励接种疫苗和不可能讨论未来接种疫苗及其结果似乎是影响免疫介导性疾病患者疫苗覆盖率的主要因素。需要进一步调查,以了解疫苗接种不完全的原因,并提高两组的疫苗覆盖率,特别是在风湿病患者中。刺激健康儿童接种疫苗的方法对于患有免疫介导性疾病的儿童并不总是最佳的。有必要为慢性病儿童的父母提供个性化的疫苗鼓励策略,并对这些技术进行以下验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Vaccination coverage in children with juvenile idiopathic arthritis, inflammatory bowel diseases, and healthy peers: Cross-sectional electronic survey data.

Background: Patients with immune-mediated diseases, such as juvenile idiopathic arthritis (JIA) and inflammatory bowel disease (IBD) are at increased risk of developing infections, due to disease-related immune dysfunction and applying of immunosuppressive drugs.

Aim: To evaluate vaccine coverage in patients with IBD and JIA, and compare it with healthy children.

Methods: In the cross-sectional study we included the data from a questionnaire survey of 190 Legal representatives of children with JIA (n = 81), IBD (n = 51), and healthy children (HC, n = 58). An electronic online questionnaire was created for the survey.

Results: There were female predominance in JIA patients and younger onset age. Parents of JIA had higher education levels. Employment level and family status were similar in the three studied groups. Patients with JIA and IBD had lower vaccine coverage, without parental rejection of vaccinations in IBD, compare to JIA and healthy controls. The main reason for incomplete vaccination was medical conditions in IBD and JIA. IBD patients had a lower rate of normal vaccine-associated reactions compared to JIA and HC. The encouraging role of physicians for vaccinations was the lowest in JIA patients. IBD patients had more possibilities to check antibodies before immune-suppressive therapy and had more supplementary vaccinations compared to JIA and HC.

Conclusion: JIA and IBD patients had lower vaccine coverage compared to HC. Physicians' encouragement of vaccination and the impossibility of discus about future vaccinations and their outcomes seemed the main factors for patients with immune-mediated diseases, influencing vaccine coverage. Further investigations are required to understand the reasons for incomplete vaccinations and improve vaccine coverage in both groups, especially in rheumatic disease patients. The approaches that stimulate vaccination in healthy children are not always optimal in children with immune-mediated diseases. It is necessary to provide personalized vaccine-encouraging strategies for parents of chronically ill children with the following validation of these technics.

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