Xu Chuanhui, Lahiri Manjari, Santosa Amelia, Chew Li-Ching, Angkodjojo Stanley, Sriranganathan Melonie, Fong Warren, Arkachaisri Thaschawee, Suresh Ernest, Kong Kok Ooi, Lateef Aisha, Lee Tau Hong, Leong Keng Hong, Low Andrea, Tan Teck Choon, Leung Ying-Ying
Department of Rheumatology, Allergy and Immunology, Tan Tock Seng Hospital, Singapore.
Division of Rheumatology, Department of Medicine, National University Hospital; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Singapore Med J. 2023 Jul 27. doi: 10.4103/singaporemedj.SMJ-2022-070.
This review aims to provide evidence-based recommendations for an enhanced primary series (third dose) coronavirus disease 2019 (COVID-19) vaccination in people with rheumatic diseases (PRDs) in the local and regional context.
Literature reviews were performed regarding the necessity, efficacy, safety and strategies for enhanced primary series COVID-19 vaccination in PRDs. Recommendations were developed based on evidence according to the Grading of Recommendations Assessment, Development and Evaluation (GRADE) methodology. Evidence was synthesised by eight working group members, and the consensus was achieved by a Delphi method with nine members of an expert task force panel.
Two graded recommendations and one ungraded position statement were developed. PRDs have impaired immunogenicity from the COVID-19 vaccine and are at an increased risk of postvaccine breakthrough severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and poor clinical outcomes, compared to the general population. We strongly recommend that PRDs on immunomodulatory drugs be offered a third dose of the messenger RNA (mRNA) vaccine as part of an enhanced primary series, after the standard two-dose regimen. We conditionally recommend that the third dose of mRNA vaccine against SARS-CoV-2 be given at least 4 weeks after the second dose or as soon as possible thereafter. There is insufficient data to inform whether the third mRNA vaccine should be homologous or heterologous in PRDs.
These recommendations that were developed through evidence synthesis and formal consensus process provide guidance for an enhanced primary series COVID-19 vaccination in PRDs.
本综述旨在针对当地和区域范围内的风湿性疾病患者(PRD)加强2019冠状病毒病(COVID-19)基础免疫系列(第三剂)疫苗接种提供循证建议。
针对PRD加强基础免疫系列COVID-19疫苗接种的必要性、有效性、安全性及策略进行了文献综述。根据推荐分级评估、制定与评价(GRADE)方法,基于证据制定了建议。由八名工作组成员综合证据,并通过专家工作组小组的九名成员采用德尔菲法达成共识。
制定了两项分级建议和一项未分级立场声明。与普通人群相比,PRD对COVID-19疫苗的免疫原性受损,疫苗接种后出现严重急性呼吸综合征冠状病毒2(SARS-CoV-2)突破性感染及不良临床结局的风险增加。我们强烈建议,在完成标准两剂接种方案后,为正在使用免疫调节药物的PRD提供第三剂信使核糖核酸(mRNA)疫苗,作为加强基础免疫系列的一部分。我们有条件地建议,第三剂针对SARS-CoV-2的mRNA疫苗应在第二剂接种后至少4周接种,或此后尽快接种。尚无足够数据说明PRD接种第三剂mRNA疫苗时应采用同源还是异源接种。
这些通过证据综合和正式共识过程制定的建议,为PRD加强基础免疫系列COVID-19疫苗接种提供了指导。