免疫覆盖率和疫苗接种的及时性在年轻患者的先天性代谢错误:一项法国多中心研究。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Anne-Sophie Renous, Lena Damaj, Magali Gorce, Magalie Barth, Antoine Bedu, Elise Sacaze, Delphine Lamireau, Cécile Laroche-Raynaud, Laurent Pasquier, Zoha Maakaroun-Vermesse, Marine Tardieu, François Labarthe
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引用次数: 0

摘要

背景:先天性代谢错误(IEMs)是一种罕见的疾病,其严重程度和临床表现各不相同。IEMs患者应接受针对全体人群推荐的疫苗接种计划,并为最脆弱的人群接种特定疫苗,如季节性流感疫苗。本研究的目的是评估IEM年轻患者的疫苗接种覆盖率和及时性。患者和方法:我们在2021年2月至2022年5月期间进行了一项回顾性多中心(7个中心)研究,根据2002年以来公布的法国年度疫苗接种计划评估法国年轻IEM患者的疫苗接种覆盖率和延迟。分析结果时考虑患者健康状况为稳定或有危险(定义为心肺衰竭或有严重代谢危机风险的IEM)。结果:275名患者入组本研究。其中,只有164例(60%)接种了最新的法国标准疫苗接种计划,229例(83%)接种了至少一种疫苗。在dtap - ipvv - hib疫苗的主要初级和第一次加强剂以及第一次MMR注射中,危险组的延迟疫苗接种率明显高于稳定组。最后,在前三个冬季,只有30%至35%的高危患者接种了流感疫苗。结论:患有IEM的年轻患者疫苗接种覆盖率不足,严重延误,使他们暴露于疫苗可预防的疾病,特别是有心肺衰竭或严重代谢危机风险的高危患者。此外,只有少数最脆弱的病人接受了特定的疫苗接种,例如流感疫苗。因此,在推荐的时间表内优化疫苗接种对这群需要定期医院随访的脆弱儿童至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunization coverage and timeliness of vaccination in young patients with inborn errors of metabolism: a French multicentric study.

Background: Inborn errors of metabolism (IEMs) are rare disorders that are heterogeneous in severity and clinical presentation. Patients with IEMs should receive the vaccination schedule recommended for the whole population, and specific vaccinations, such as the seasonal influenza vaccine, for the most vulnerable. The aim of this study was to evaluate vaccination coverage and timeliness in young patients with an IEM.

Patients & methods: We conducted a retrospective multicentric (7 centers) study between February 2021 and May 2022 evaluating vaccination coverage and delays in French young patients with an IEM according to the yearly French vaccination schedules published since 2002. The results were analyzed considering patient health conditions as stable or at risk (defined as cardiorespiratory failure or by an IEM with a serious risk of metabolic crisis).

Results: Two hundred seventy-five patients were enrolled in this study. Among them, only 164 (60%) were up-to-date with the standard French vaccination schedule, and 229 (83%) had received at least one vaccine from this schedule late. The rate of delayed vaccination was significantly greater in the at-risk group than in the stable group for the main primaries and first booster doses of the DTaP-IPV-Hib vaccine and for the first MMR injection. Finally, only 30 to 35% of at-risk patients were vaccinated against influenza during the three previous winters.

Conclusion: Young patients with an IEM had insufficient vaccination coverage with significant delays, exposing them to vaccine-preventable diseases, particularly at-risk patients with cardiorespiratory failure or a serious risk of metabolic crisis. Furthermore, only a few of the most vulnerable patients had received specific vaccinations, such as the influenza vaccine. Therefore, optimizing vaccination within the recommended schedule is crucial for this population of vulnerable children who have regular hospital follow-up.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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