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      COVID-19 vaccine acceptance over time in patients with immune-mediated inflammatory rheumatic diseases

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          Abstract

          Before the global distribution of COVID-19 vaccines, we observed substantial concerns among non-immunocompromised people about the lack of long-term research or the occurrence of adverse events after vaccination, and concerns among patients with immune-mediated inflammatory rheumatic diseases about interactions with their underlying autoimmune disease or immunosuppressive treatment regimens. 1 Our findings have since been replicated,2, 3 but there is as yet no data on how patients' thoughts and behaviour have evolved as vaccines were distributed, or data that compare COVID-19 vaccine coverage between patients with rheumatic immune-mediated inflammatory diseases and healthy controls. In this Comment, we aim to describe the evolution of COVID-19 vaccination willingness over time in patients with immune-mediated inflammatory rheumatic diseases compared with controls, to evaluate motives for getting or not getting vaccinated against COVID-19, changes in psychosocial wellbeing after receiving a COVID-19 vaccination, and perspectives towards additional COVID-19 vaccinations. Questionnaires were sent to patients and controls included in an ongoing prospective cohort study (Netherlands Trial Register, trial ID NL8513) that was set up at the start of the COVID-19 pandemic to compare the severity of COVID-19 between patients with immune-mediated inflammatory rheumatic diseases and healthy controls. Between April 26, 2020, and March 1, 2021 all adult patients (aged ≥18 years) with an immune-mediated inflammatory rheumatic disease from the Amsterdam Rheumatology and Immunology Center (Amsterdam, Netherlands) were digitally invited to participate in the study. 4 Patients were asked, but not obliged, to recruit their own healthy control participant who was of the same sex and similar age (age difference <5 years). All participants provided written informed consent. Data were collected via online questionnaires distributed via email. 4 Demographic data, including age, sex, height, weight, smoking status, disease type, ethnicity, and educational level, were collected at baseline. Information on patients' perspectives on COVID-19 vaccinations were collected in some, but not all, follow-up questionnaires of the study: in December, 2020, before the start of the Dutch vaccination programme; in April and May, 2021, shortly before the application of the COVID-19 vaccination passport; and in August and September, 2021, when the whole Dutch population had been given the chance to get a COVID-19 vaccination. A complete overview of the study surveys, including the content, is presented in the appendix (pp 12–17). Participants who completed at least two questionnaires that assessed their perspective on COVID-19 vaccination were included in the analyses. In total, 1927 consecutive patients with immune-mediated inflammatory rheumatic diseases and 811 controls were included for analyses. The questionnaires sent in December, 2020, were completed by 1515 (79%) patients and 646 (80%) controls; those sent in April, 2021, were completed by 1804 (94%) and 790 (97%) controls; and those sent in August, 2021, were completed by 1489 (77%) patients and 575 (71%) controls. The mean age was 58 years (SD 13; appendix p 5). The majority of participants were female (1831 [67%] of 2738 participants) and of White ethnicity (2164 [89%] of 2435 participants; some data were missing for ethnicity). The prevalence of chronic pulmonary disease, cardiovascular diseases, diabetes, and obesity was higher in patients than in controls. The most common rheumatic diagnosis was rheumatoid arthritis (996 [52%] of 1927 patients), and 1506 (78%) of 1927 patients received immunosuppressive treatment. The proportion of participants who would be willing to get vaccinated against COVID-19 or who had already received a COVID-19 vaccination was similar between patients and controls, and increased with time: 936 (62%) of 1515 patients and 418 (65%) of 646 controls in December, 2020; 1649 (91%) of 1804 patients and 710 (90%) of 790 controls in April, 2021; and 1419 (95%) of 1489 patients and 551 (96%) of 575 controls in August, 2021 (appendix p 2). Patients and controls who were not willing to get a COVID-19 vaccination were younger than patients and controls who chose to get vaccinated (appendix p 6). A larger proportion of patients than controls consulted a physician before COVID-19 vaccination (540 [36%] of 1480 patients and 37 [6%] of 573 controls), mostly because of safety concerns (table ). In addition, a considerable proportion of patients indicated that they would not have taken a COVID-19 vaccination without the advice of their rheumatologist; 185 (34%) of 540 patients, which corresponds to 12% of all patients. This finding emphasises the importance of vaccination-specific counselling to improve vaccine coverage, which might not only be relevant for COVID-19 vaccinations, but also for influenza or pneumococcal vaccinations for which vaccine uptake has been shown to be low among patients with autoimmune diseases. 5 Table Perspectives on COVID-19 vaccination among patients with rheumatic immune-mediated inflammatory disease and healthy controls Patients with rheumatic immune-mediated inflammatory disease Healthy controls Vaccination status in August, 2021 n 1489 575 Vaccinated once 69 (5%) 50 (9%) Vaccinated twice 1350 (91%) 501 (87%) Not vaccinated 70 (5%) 24 (4%) Contact with physician before COVID-19 vaccination * n 1480 573 Yes 540 (36%) 37 (6%) No 940 (64%) 536 (94%) Reasons for contact with physician before vaccination * n 540 37 Concerned about safety of the vaccine 344 (64%) 20 (54%) Rheumatic treatment at the time of vaccination 195 (36%) NA Concerned about effectiveness of the vaccine 108 (20%) 3 (8%) To discuss whether there is a preference for a particular vaccine type 152 (28%) 7 (19%) Other 55 (10%) 10 (27%) Impact of contact with physician on vaccination willingness * n 540 37 No impact (vaccinated, but would have been vaccinated regardless of advice) 355 (66%) 24 (65%) Positive influence (vaccinated, and would not have been vaccinated without advice) 185 (34%) 13 (35%) Data are n or n (%). Percentages might not add to 100% due to rounding. NA=not applicable. * Data based on questionnaires sent in April and August, 2021 (responses were combined). A lack of long-term research remained the most important reason for doubting or refusing vaccination in both patients and controls over time (appendix p 3). However, concerns about interactions with immunosuppressive treatment regimens or the underlying immune-mediated inflammatory disease became a more prominent reason for doubt or refusal among patients over time, whereas a feeling of not being at risk for severe COVID-19 disease became more prominent for controls. The most important reasons to accept vaccination included concerns for personal health among patients, and wanting to contribute to herd immunity among controls (appendix p 4). Only a small proportion of patients and controls were vaccinated because of the advantages of a COVID-19 vaccination passport (44 [3%] of 1419 patients and 25 [5%] of 551 controls). Most patients and controls who had received two vaccinations by the end of August, 2021, indicated that they would be willing to get an additional vaccine dose (1085 [80%] of 1350 patients and 374 [75%] of 501 controls; appendix p 8), and ten patients had already received an additional dose. However, the majority of both groups agreed that all people in low-income countries should have had access to at least the first COVID-19 vaccine dose before the national rollout of additional doses, and also that there should be clear scientific evidence on the additional value of vaccine doses in reducing COVID-19 related morbidity and mortality. Similarly, these statements were the most frequently reported factors that would influence the decision to get an additional vaccination; 679 (50%) of 1350 patients and 296 (59%) of 501 controls indicated that the availability of scientific evidence about additional vaccinations would influence their decision, and 314 (23%) of 1350 patients and 182 (36%) of 501 controls indicated that a fair worldwide distribution of COVID-19 vaccines would influence their decision. In addition, 352 (26%) of 1350 patients and 14 (3%) of 501 controls indicated that the advice of a physician would be important for their decision regarding an additional COVID-19 vaccination. Adverse events of previous COVID-19 vaccinations were only relevant in a small proportion of participants (95 [7%] of 1350 patients and 15 [3%] of 501 controls), which is consistent with our previous observation that adverse events were mostly mild and self-limiting in both patients and controls. 6 Lastly, vaccination against COVID-19 had a favourable effect on the psychosocial wellbeing of both patients and controls; people felt safer, had more social contacts, and visited more public spaces. In addition, in a considerable number of patients and controls (546 [38%] of 1419 patients and 225 [41%] of 551 controls) experienced an increase in their quality of life after getting vaccinated (appendix p 7). These findings, combined with the focus in the scientific and public media reporting on waning of protective immunity against COVID-19, might explain the high willingness of patients and controls to get an additional COVID-19 vaccination. However, it is still unknown to what extent laboratory findings (eg, a diminished humoral or cellular immune response) are predictive of reduced protection against severe COVID-19 disease. Given the unknowns on the waning of actual protection, the emphasis on this topic going forward could therefore negatively affect patients' psychosocial wellbeing, because it might cause them to re-adhere to inappropriately strict social distancing measures for fear of severe illness.7, 8, 9 A limitation of this research is that clinical diagnoses and medication use were self-reported and not verified in health-care records. However, these data were only used to compare characteristics between study groups (eg, the prevalence of cardiovascular disease) rather than with other study cohorts, which minimises the bias introduced by this limitation. Moreover, a nationwide study showed concordance rates for self-reported diseases and medication use of over 90%. 10 In conclusion, our data show that COVID-19 vaccine hesitancy largely subsided during the first 6 months after the start of global distribution of COVID-19 vaccinations in both patients with immune-mediated inflammatory rheumatic diseases and healthy controls, due to increased confidence in the safety and efficacy of COVID-19 vaccinations. Rheumatologists played an important role in this process, highlighting the relevance of vaccination-specific counselling in patients with rheumatic immune-mediated inflammatory diseases, which might also go beyond COVID-19 vaccination. Trial ID NL8513 received funding from ZonMw and the Reade Foundation. TR and GW received funding from ZonMw during the conduct of the study. WHB reports grants and personal fees from Abbvie, Eli Lilly, and Sanofi; personal fees from Galapagos; and grants from Gelgene, Pfizer, Roche, and UCB, outside the submitted work. All other authors declare no competing interests.

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          Considerations in boosting COVID-19 vaccine immune responses

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            Concordance between Patient Self-Reports and Claims Data on Clinical Diagnoses, Medication Use, and Health System Utilization in Taiwan

            Purpose The aim of this study was to evaluate the concordance between claims records in the National Health Insurance Research Database and patient self-reports on clinical diagnoses, medication use, and health system utilization. Methods In this study, we used the data of 15,574 participants collected from the 2005 Taiwan National Health Interview Survey. We assessed positive agreement, negative agreement, and Cohen's kappa statistics to examine the concordance between claims records and patient self-reports. Results Kappa values were 0.43, 0.64, and 0.61 for clinical diagnoses, medication use, and health system utilization, respectively. Using a strict algorithm to identify the clinical diagnoses recorded in claims records could improve the negative agreement; however, the effect on positive agreement and kappa was diverse across various conditions. Conclusion We found that the overall concordance between claims records in the National Health Insurance Research Database and patient self-reports in the Taiwan National Health Interview Survey was moderate for clinical diagnosis and substantial for both medication use and health system utilization.
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              Perspective of patients with autoimmune diseases on COVID-19 vaccination

              The socioeconomic burden of COVID-19 and pressure on health-care systems can only be reduced by achieving herd immunity against SARS-CoV-2. For herd immunity to be achieved, it has been estimated that, depending on the efficacy of the vaccines employed, approximately 60–100% of the global population needs to be vaccinated. 1 Countries all over the world are developing vaccination strategies, and many have already started vaccinating their populations. However, the rapid development, approval, and release of vaccines against SARS-CoV-2 has led to uncertainties in the population, which might reduce willingness to get vaccinated. 2 These reservations might be especially apparent for patients with autoimmune diseases, such as rheumatic or neuroinflammatory diseases, because there is no data available about the balance between benefits and risks of the newly developed COVID-19 vaccines in this population. It is therefore relevant to evaluate considerations and concerns regarding vaccination of patients with autoimmune diseases and to identify if and how physicians can influence their patients' decision to get vaccinated. This Comment reports the results of a questionnaire assessing the perspective of patients with autoimmune diseases on vaccination against SARS-CoV-2. We sent a questionnaire to patients with various rheumatic diseases or multiple sclerosis and controls who were enrolled in two ongoing prospective cohort studies (Netherlands Trial Register, trial ID NL8513 and NCT04498286). Between April 26 and Dec 1, 2020, all adult patients (18 years and older) with systemic autoimmune diseases from the Amsterdam Rheumatology & Immunology Center, Amsterdam, Netherlands; all adult patients with vasculitis from the Amsterdam UMC, Amsterdam, Netherlands; and all adult patients with multiple sclerosis from the Amsterdam Multiple Sclerosis Center of Amsterdam UMC, Amsterdam, Netherlands were invited to participate in these studies. In the first study (NL8513), patients needed to be diagnosed by their treating physician with a systemic autoimmune disease. In the second study (NCT04498286), patients needed to be diagnosed by their treating physician with multiple sclerosis. Our study did not have any exclusion criteria. Patients with rheumatic disease were asked (but not obliged) to register a control subject from their family or close network who did not have a rheumatic disease, were the same sex, and were a comparable age (an age difference of <5 years). Information on demographic data and medication use was collected at baseline (when patients were included into the study, rather than only at the start of the study) and information on patients' perspective on vaccination was collected between Dec 1 and Dec 24, 2020. At both timepoints, data were collected via online questionnaires, which were distributed via email. In the vaccination questionnaire, participants were asked to indicate which scenarios were most applicable, considering their behaviour, thoughts, and concerns regarding COVID-19 vaccination and COVID-19 in general. We included questions regarding a history of COVID-19, and participants were asked about their willingness to get vaccinated if they were to be invited in the first few months of the vaccination programme. There were additional disease related questions for patients with rheumatic diseases or multiple sclerosis. All participants who completed the vaccination questionnaire before Dec 24, 2020, were included in the analyses. Multivariable logistic regression analyses were used to compare willingness to get a COVID-19 vaccine between patients and controls, patients treated with and without biological agents, all participants younger than and older than 60 years, and all male and female participants. When applicable, associations were adjusted for age, gender, presence of comorbidities, and presence of autoimmune diseases. To identify effect modifiers, a threshold of p<0·05 was used for interaction terms. Exploratory subgroup analyses within patients with rheumatoid arthritis, vasculitis or systemic lupus erythematosus (SLE), and multiple sclerosis were done. Data on the patient perspective on COVID-19 vaccinations were compared between patients with autoimmune diseases who were willing to, not willing to, and unsure about getting vaccinated. SPSS (version 23.0) was used for the analyses. The research protocols were approved by the medical ethical committee of the VU University medical center (registration number 2020·169 and 2020·370). All participants gave informed consent. Between April 26 and Dec 1, 2020, 2887 patients with rheumatic disease, 530 patients with multiple sclerosis, and 1050 controls were included in this study. The vaccination questionnaire was completed by 1727 patients (1361 patients with rheumatic disease and 366 patients with multiple sclerosis) and 682 controls, who were all included in the analyses. Individuals in the patient group had a mean age of 56 years (SD 13) and individuals in the control group had a mean age of 55 years (SD 13); the majority of participants were female (1113 [64%] of 1727 female vs 614 [36%] male in the patient group and 479 [70%] of 682 female vs 203 [30%] male in the control group; appendix p 1). Patients with rheumatoid arthritis, and patients with vasculitis or SLE, were older than were patients with multiple sclerosis (mean age 60 years [12] and 56 [13] years vs 48 [12] years; appendix p 1). Most patients received immunosuppressive treatment: 1325 (77%) of 1727 patients, 813 (99%) of 823 patients with rheumatoid arthritis, 45 (98%) of 46 patients with vasculitis or SLE, 184 (37%) of 492 patients with other rheumatic diseases, and 283 (77%) of 366 patients with multiple sclerosis. 710 (41%) of 1727 patients received biological agents, which predominantly consisted of tumour necrosis factor inhibitors in patients with rheumatoid arthritis (257 [73%] of 354 patients receiving biologics) and anti-CD20 therapies in patients with vasculitis or SLE (8 [40%] of 20 patients receiving biologics) and patients with multiple sclerosis (64 [55%] of 117 patients receiving biologics). The proportion of patients and controls who would be willing to get vaccinated against SARS-CoV-2 was similar; 1060 (61%) individuals in the patient group and 441 (65%) in the control group (appendix p 2). Accordingly, multivariable regression analyses showed no significant difference between patients and controls. Odds ratios (ORs) for individuals in the rheumatoid arthritis group, vasculitis or SLE group, and multiple sclerosis group compared with individuals in the control group were similar, and they remained similar after adjusting for confounders (appendix p 3). Use of biological agents was not associated with willingness to get vaccinated in all patients or in the patient subgroups. Overall, male participants and individuals older than 60 years were both approximately twice as likely to be willing to get vaccinated than were female participants (930 [58%] of 1592 female participants vs 572 [70%] of 817 male participants; OR 1·7 [95% CI 1·4–2·0]) and individuals younger than 60 years (767 (55%) of 1391 people younger than 60 years vs 734 (72%) of 1018 people aged 60 years or older years; OR 2·0 [1·7–2·4]; appendix p 3). The most common reasons for refusing or doubting vaccination in both patients and controls were concerns for adverse events and no long-term research (appendix p 4). Patients who were unsure about vaccination or who were not willing to get vaccinated were more concerned that the vaccine might aggravate their autoimmune disease than were patients who were willing to get vaccinated (164 [32%] of 515 patients and 53 [45%] of 118 patients vs 119 [11%] of 1060 patients; appendix p 4). Lastly, 392 (23%) of 1727 patients with autoimmune diseases indicated that a physicians' advice to get vaccinated would lead to a change in their preference regarding vaccination willingness; 356 [69%] of 515 patients who were uncertain about vaccination and 36 (31%) of 118 patients who would be unwilling to get vaccinated would change their minds following physicians' advice (appendix p 4). A limitation of this study was that control participants were not a random sample of the general population, but often people with close ties to patients with autoimmune diseases (eg, friends or family). This limitation could contribute to an absence of differences between patients and controls regarding vaccination willingness, because people close to patients with autoimmune diseases might be more health conscious than people without close ties to these patients. However, a US study 2 reported similar proportions of vaccination willingness in the general population as compared with our own findings in the control group (60% vs 441 [65%] of 682). The effect of our method for recruiting healthy controls on our final results is therefore probably limited. Altogether, our results indicate that willingness to get vaccinated against SARS-CoV-2 does not differ between patients with autoimmune diseases and controls, and that it is not influenced by autoimmune disease type or medication use. Additionally, we showed that approximately 1060 (61%) of 1727 patients with autoimmune diseases were willing to get vaccinated against SARS-CoV-2, and that physicians have the potential to increase this number by more than 20% (392/1727 patients). Important causes of vaccine hesitancy in patients with autoimmune diseases are concerns about adverse events and aggravation of the underlying autoimmune disease, which has been reported by others as well. 3 However, although data are still scarce, results of previous studies on vaccines against other viruses are reassuring; few adverse events and disease flares in patients with autoimmune diseases have been described. 4 The possibility of the occurrence of adverse events should therefore not be a reason to not recommend vaccination against SARS-CoV-2 in patients with autoimmune diseases, especially because results of previous studies suggest that these patients can be at increased risk of severe COVID-19 disease. 5 Therefore, physicians of patients with autoimmune diseases should actively encourage their patients to get vaccinated against SARS-CoV-2, because this can contribute considerably to a reduction in COVID-19 related morbidity and mortality.
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                Author and article information

                Journal
                Lancet Rheumatol
                Lancet Rheumatol
                The Lancet. Rheumatology
                Published by Elsevier Ltd.
                2665-9913
                8 February 2022
                8 February 2022
                Affiliations
                [a ]Amsterdam Rheumatology and Immunology Center, Location Reade, Department of Rheumatology, Amsterdam 1056 AB, Netherlands
                [b ]Department of Medical Microbiology and Infection Control, Amsterdam UMC, Location AMC, Amsterdam, Netherlands
                [c ]Department of Immunopathology, Sanquin Research, Amsterdam, Netherlands
                [d ]Landsteiner Laboratory Academic Medical Center, Amsterdam, Netherlands
                [e ]Department of Rheumatology and Clinical Immunology, Amsterdam Rheumatology and Immunology Center, University of Amsterdam, Amsterdam UMC, Netherlands
                [f ]Department of Rheumatology and Clinical Immunology, Amsterdam Rheumatology and Immunology Center, Vrije Universiteit, Amsterdam UMC, Netherlands
                [g ]Department of Epidemiology and Data Science, Vrije Universiteit, Amsterdam UMC, Amsterdam, Netherlands
                Article
                S2665-9913(22)00009-1
                10.1016/S2665-9913(22)00009-1
                8824534
                35156061
                ddfe1dae-3ce6-45f3-9600-95c95aaa2a98
                © 2022 Published by Elsevier Ltd.

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