Division of Rheumatology, Department of Medicine, National University Hospital, Singapore, Singapore.
Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Int J Rheum Dis. 2021 Jun;24(6):746-757. doi: 10.1111/1756-185X.14107. Epub 2021 May 10.
People with rheumatic diseases (PRD) remain vulnerable in the era of the COVID-19 pandemic. We formulated recommendations to meet the urgent need for a consensus for vaccination against SARS-CoV-2 in PRD.
Systematic literature reviews were performed to evaluate: (a) outcomes in PRD with COVID-19; (b) efficacy, immunogenicity and safety of COVID-19 vaccination; and (c) published guidelines/recommendations for non-live, non-COVID-19 vaccinations in PRD. Recommendations were formulated based on the evidence and expert opinion according to the Grading of Recommendations Assessment, Development and Evaluation methodology.
The consensus comprises 2 overarching principles and 7 recommendations. Vaccination against SARS-CoV-2 in PRD should be aligned with prevailing national policy and should be individualized through shared decision between the healthcare provider and patient. We strongly recommend that eligible PRD and household contacts be vaccinated against SARS-CoV-2. We conditionally recommended that the COVID-19 vaccine be administered during quiescent disease if possible. Immunomodulatory drugs, other than rituximab, can be continued alongside vaccination. We conditionally recommend that the COVID-19 vaccine be administered prior to commencing rituximab if possible. For patients on rituximab, the vaccine should be administered a minimum of 6 months after the last dose and/or 4 weeks prior to the next dose of rituximab. Post-vaccination antibody titers against SARS-CoV-2 need not be measured. Any of the approved COVID-19 vaccines may be used, with no particular preference.
These recommendations provide guidance for COVID-19 vaccination in PRD. Most recommendations in this consensus are conditional, reflecting a lack of evidence or low-level evidence.
在 COVID-19 大流行时代,风湿性疾病患者仍然很脆弱。我们制定了建议,以满足风湿性疾病患者接种 SARS-CoV-2 疫苗的迫切共识需求。
系统地进行文献回顾,以评估:(a)COVID-19 中风湿性疾病患者的结局;(b)COVID-19 疫苗的疗效、免疫原性和安全性;以及(c)针对风湿性疾病患者的非活、非 COVID-19 疫苗的已发表指南/建议。根据推荐评估、制定与评价(Grading of Recommendations Assessment, Development and Evaluation)方法,根据证据和专家意见制定建议。
共识包括 2 项总体原则和 7 项建议。风湿性疾病患者接种 SARS-CoV-2 疫苗应与当前国家政策保持一致,并通过医疗保健提供者与患者之间的共同决策进行个体化。我们强烈建议符合条件的风湿性疾病患者及其家庭接触者接种 SARS-CoV-2 疫苗。如果可能,我们有条件地建议在疾病静止期接种 COVID-19 疫苗。除利妥昔单抗外,免疫调节剂药物可以与疫苗同时使用。如果可能,我们有条件地建议在开始利妥昔单抗治疗之前接种 COVID-19 疫苗。对于正在接受利妥昔单抗治疗的患者,疫苗应在最后一剂利妥昔单抗后至少 6 个月或在下一剂利妥昔单抗前 4 周进行接种。接种 SARS-CoV-2 疫苗后无需测量抗体滴度。可使用任何已批准的 COVID-19 疫苗,无特殊偏好。
这些建议为风湿性疾病患者接种 COVID-19 疫苗提供了指导。本共识中的大多数建议是有条件的,反映了证据不足或低水平证据。