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April 2, 2021
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Vaccine Hesitancy in Patients With Multiple Sclerosis
Preparing for the SARS-CoV-2 Vaccination Challenge

Abstract

Objective

Vaccine hesitancy is a complex public health issue referring to concerns about safety, efficacy, or need for vaccination. Using pneumococcal vaccination, which is recommend in anti-CD20–treated multiple sclerosis (MS) patients, as a model, we assessed vaccination behavior in patients with MS to prepare for the upcoming SARS-CoV-2 vaccination challenge.

Methods

By a medical chart review, we retrospectively identified patients with MS treated with ocrelizumab at the University Hospital Bern in 2018–2020. Pneumococcal vaccination was discussed with the patients during clinical visits and highlighted in the after-visit summary addressed to the general practitioner before ocrelizumab initiation as part of our clinical standard of care.

Results

Pneumococcal vaccination was performed in 71/121 (58.7%) of patients, and 50/121 (41.3%) patients were not vaccinated. Patients who did not get a pneumococcal vaccination were younger (no vaccination vs vaccination; mean [95% CI] 40.1 [36.1–44.1] vs 45.4 [41.9–48.8], p = 0.028) and had more frequently a relapsing remitting disease course (no vaccination vs vaccination, n [%]; 43/50 [86.0%] vs 49/71 [69.0%], p = 0.031). Furthermore, patients who did not get vaccination had more frequently a history of comorbid psychiatric disorder (no vaccination vs vaccination, n (%); 12/50 [24.0] vs 7/71 [9.8], p = 0.035).

Conclusion

Our study demonstrated that in our single-center cohort, 41.3% of patients with MS do not get the recommended pneumococcal vaccination. Future research should focus on vaccine hesitancy in the vulnerable cohort of patients with MS to improve the safety of MS immunotherapies.
Vaccine hesitancy is a complex public health issue referring to concerns about the safety, efficacy, or need for vaccination.1 Each year, Streptococcus pneumoniae is estimated to cause more than 1,000 serious infections in Switzerland.2 Patients with multiple sclerosis (MS) treated with ocrelizumab (OCR, Ocrevus, Roche, Basel, Switzerland) are at risk of S. pneumoniae infections. The Swiss Federal Office of Public Health (FOPH) recommends pneumococcal vaccination in patients treated with immunosuppressants including OCR.3 Using pneumococcal vaccination as a model, we aimed to assess vaccination behavior in patients with MS to prepare for the upcoming SARS-CoV-2 vaccination challenge.

Methods

By a medical chart review, we retrospectively identified patients with MS treated with OCR at the University Hospital Bern in 2018–2020 leading to a cohort of 166 patients. Of 166 patients, 45 patients were excluded because of missing clinical information regarding vaccination status because of the retrospective nature of our study, resulting in a cohort of 121 patients (table e-1, links.lww.com/NXI/A466). Pneumococcal vaccination was recommended as indicated per FOPH guidelines,3 discussed with the patients during clinical visits, and highlighted in the after-visit summary addressed to the general practitioner before OCR initiation as part of our clinical standard of care.
The following variables were extracted from medical records: age, sex, Expanded Disability Status Scale (EDSS), MS diagnosis, type of MS, disease modifying therapies before switching, time of vaccination, reason for missing vaccination, clinical relapse before OCR start, MRI activity—defined as gadolinium-enhancing lesion and/or new/enlarging T2 lesion—1 year before/after start of therapy/vaccination, and concomitant psychiatric disorders. Continuous variables are presented as mean and 95% CIs, whereas categorical variables are reported as frequencies. Continuous variables are compared using Mann-Whitney U and Wilcoxon signed rank tests and categorical variables with the χ2 test.

Standard Protocol Approvals, Registrations, and Patient Consents

The study was approved by the Cantonal Ethics Committee (KEK-BE #2017-01369).

Data Availability

Anonymized source data are available upon reasonable request via the corresponding author.

Results

Patients were 43.2 years old (mean, 95% CI 40.6–45.8), predominantly female 75/121 (62.0%), and had a moderate degree of disability (mean EDSS (95% CI): 3.1 (2.8–3.4); table 1).
Table 1 Patient Characteristics Concerning Pneumococcal Vaccination Status
Pneumococcal vaccination was performed in 71/121 (58.7%) of patients in mean 4.0 weeks before first dose of OCR (95% CI 0.2–7.8) with a range of 46.44 weeks before and 68.53 weeks after first dose OCR. In total, 50/121 (41.3%) patients were not vaccinated. In these 50 patients, the reasons for lack of vaccination were as follows: lack of adherence to vaccination recommendations (n = 30), MS disease activity (n = 11), general vaccination recommendation (not specifically for pneumococcal vaccine) in after-visit summary addressed to the general practitioner (n = 8), and unexpected pregnancy (n = 1).
Patients who did not get a pneumococcal vaccination were younger (no vaccination vs vaccination; mean [95% CI] 40.1 [36.1–44.1] vs 45.4 [41.9–48.8], p = 0.028) and had more frequently a relapsing remitting (RR) disease course (no vaccination vs vaccination, n [%]; 43/50 [86.0%] vs 49/71 [69.0%], p = 0.031). Furthermore, patients who did not get a pneumococcal vaccination had more frequently a history of comorbid psychiatric disorder (no vaccination vs vaccination, n [%]; 12/50 [24.0] vs 7/71 [9.8], p = 0.035) including depression (n = 8), psychosis (n = 2), history of drug abuse (n = 1), and borderline personality disorder (n = 1) in those without vaccination.
MS immunotherapies before initiation of OCR had an impact on vaccination behavior: untreated patients with MS were vaccinated more frequently compared with treated patients with MS (14/50 [28.0%] vs 34/71 [47.8%], p = 0.028). Clinical and MRI disease activity within 12 months before OCR did not differ between patients with and without vaccination. Initiation of OCR resulted in a reduction of disease activity in both patient cohorts. Because date of vaccination differs from date of first OCR treatment, we also investigated in the subgroup of vaccinated MS patients for clinical and radiologic disease activity within 1 year before and after vaccination, which demonstrates a similar reduction of disease activity after OCR compared with the whole cohort (table 1).

Discussion

Our study demonstrated that in our single-center cohort, 41.3% of patients with MS do not get the recommended pneumococcal vaccination before initiation of OCR. Those patients were younger and had more frequently an RR disease course and a psychiatric comorbidity. This finding may be related to the behavior of young people toward vaccination. Often, young people argue that the corresponding diseases do not affect them and that the risk is mainly in older people.
Moreover, patients with use of disease-modifying treatments before initiation of OCR, which should not influence the decision to vaccinate against S. pneumoniae, did get vaccinations less frequently compared with untreated patients. MS disease activation after pneumococcal vaccination could not be observed neither in clinical relapses nor in MRI disease activity. These findings are crucial because the fear of disease activity is a main argument against vaccination in people with MS.4 This study showed that vaccine hesitancy remains a widespread problem in our monocentric cohort. Vaccine hesitancy is defined as the delay in acceptance or refusal of vaccination despite the availability of vaccination services.5 Vaccine hesitancy is an individual behavior influenced by a range of factors, such as knowledge or experiences in the past. The absence of awareness about “who and why” one should be vaccinated and self-estimated (in)sufficiency of information about vaccination is frequently associated with vaccination decisions.6 Perceived importance of vaccination is an individual determinant of vaccine adherence. Individuals who refuse or are hesitant regarding vaccination often have an own worldview regarding health (e.g., importance of natural immunity).7 Similarly, the increasing popularity of complementary and alternative medicine (CAM) plays an important role in the vaccination skepticism of the population. In fact, refusal of vaccination is significantly more frequent among CAM-users than among nonusers. Patients who consulted physicians practicing herbal medicine, anthroposophical medicine, or homeopathy reported the highest frequencies of vaccination refusal.8 In addition, experiences with vaccinations in the past can influence future decision-making regarding vaccination. Vaccine hesitancy can also be the result of broader influences and should always be looked at in the historical, political, and sociocultural context in which vaccination is discussed. The trust placed in the healthcare system, in the doctors who recommend and administer vaccines, and in the different types of vaccine information conveyed by the media plays an important role in the decision to be vaccinated.9 Unfortunately, vaccine misinformation on major social media companies is a common problem, and the companies are facing wide criticism for failing to deal with vaccine misinformation on their platforms. Especially in the light of the newly available COVID-19 vaccine, misinformation on social media is undoubtedly going to pose a serious barrier to uptake.10 The Strategic Advisory Group of Experts on Immunization Working Group discussed that poor communication of healthcare professionals plays an important role in the vaccine hesitancy. When communication of healthcare professionals is poor or inadequate, it can negatively influence vaccination uptake and contribute to vaccine hesitancy.5 Therefore, clear and targeted education, also taking into account social media, about vaccination is imperative. Obviously, we cannot extrapolate these data concerning pneumococcal vaccination without further ado on the now available COVID-19 vaccination. However, our short retrospective observation with all limitations inherent of the design highlights the fact that physicians caring for people with MS should proactively initiate vaccination discussions with their patients and follow up on the execution of the recommendation. Further studies of vaccination behavior in patients with MS are warranted, especially in the light of the current pandemic.

Glossary

CAM
complementary and alternative medicine
EDSS
Expanded Disability Status Scale
FOPH
Federal Office of Public Health
MS
multiple sclerosis
OCR
ocrelizumab

Appendix Authors

References

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Deml MJ, Jafflin K, Merten S, et al. Determinants of vaccine hesitancy in Switzerland: study protocol of a mixed-methods national research programme. BMJ Open. 2019;9:e032218.
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McDonald N; the SAGE Working Group on Vaccine Hesitancy. Vaccine hesitancy: definition, scope and determinants. Vaccine. 2015;33:4161–4164.
6.
Streefland P, Chowdhury AM, Ramos-Jimenez P. Patterns of vaccination acceptance. Soc Sci Med. 1999;49:1705–1716.
7.
Guay M, Gallagher F, Petit G, Ménard S, Clément P, Boyer G. Pourquoi les couvertures vaccinales chez les nourrissons de l'Estrie sont-elles sous-optimales? Sherbrooke, QC: Centre de santé et de services sociaux - Institut universitaire de gériatrie de Sherbrooke, Direction de la coordination et des affaires académiques; 2009.
8.
Zuzak T, Zuzak-Siegrist I, Rist L, Staubli G, Simoes-Wüst AP. Attitudes towards vaccination: users of complementary and alternative medicine versus non-users. Swiss Med Wkly. 2008;138:713–718.
9.
Larson HJ, Cooper LZ, Eskola J, Katz SL, Ratzan S. Addressing the vaccine confidence gap. Lancet. 2011;378:526–535.
10.
Wardle C, Singerman E. Too little, too late: social media companies' failure to tackle vaccine misinformation poses a real threat. BMJ. 2021;372:n26.

Information & Authors

Information

Published In

Neurology® Neuroimmunology & Neuroinflammation
Volume 8Number 3May 2021
PubMed: 33811158

Publication History

Received: December 23, 2020
Accepted: March 3, 2021
Published online: April 2, 2021
Published in print: May 2021

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Disclosure

All authors report no disclosures relevant to the article. Go to Neurology.org/NN for full disclosures.

Study Funding

The authors report no targeted funding.

Authors

Affiliations & Disclosures

Lara Diem, MD
From the Department of Neurology, Inselspital, Bern University Hospital and University of Bern, Freiburgstrasse, Bern, Switzerland.
Disclosure
Scientific Advisory Boards:
1.
NONE
Gifts:
1.
NONE
Funding for Travel or Speaker Honoraria:
1.
NONE
Editorial Boards:
1.
NONE
Patents:
1.
NONE
Publishing Royalties:
1.
NONE
Employment, Commercial Entity:
1.
NONE
Consultancies:
1.
NONE
Speakers' Bureaus:
1.
NONE
Other Activities:
1.
NONE
Clinical Procedures or Imaging Studies:
1.
NONE
Research Support, Commercial Entities:
1.
NONE
Research Support, Government Entities:
1.
NONE
Research Support, Academic Entities:
1.
NONE
Research Support, Foundations and Societies:
1.
NONE
Stock/stock Options/board of Directors Compensation:
1.
NONE
License Fee Payments, Technology or Inventions:
1.
NONE
Royalty Payments, Technology or Inventions:
1.
NONE
Stock/stock Options, Research Sponsor:
1.
NONE
Stock/stock Options, Medical Equipment & Materials:
1.
NONE
Legal Proceedings:
1.
NONE
Christoph Friedli, MD
From the Department of Neurology, Inselspital, Bern University Hospital and University of Bern, Freiburgstrasse, Bern, Switzerland.
Disclosure
Scientific Advisory Boards:
1.
I served on scientific advisory boards for Biogen and Merck, not related to this work.
Gifts:
1.
NONE
Funding for Travel or Speaker Honoraria:
1.
I received travel grants from Biogen and Sanofi Genzyme, as well as speaker honoraria from Biogen and Merck, not related to this work.
Editorial Boards:
1.
NONE
Patents:
1.
NONE
Publishing Royalties:
1.
NONE
Employment, Commercial Entity:
1.
NONE
Consultancies:
1.
NONE
Speakers' Bureaus:
1.
NONE
Other Activities:
1.
NONE
Clinical Procedures or Imaging Studies:
1.
NONE
Research Support, Commercial Entities:
1.
NONE
Research Support, Government Entities:
1.
NONE
Research Support, Academic Entities:
1.
NONE
Research Support, Foundations and Societies:
1.
NONE
Stock/stock Options/board of Directors Compensation:
1.
NONE
License Fee Payments, Technology or Inventions:
1.
NONE
Royalty Payments, Technology or Inventions:
1.
NONE
Stock/stock Options, Research Sponsor:
1.
NONE
Stock/stock Options, Medical Equipment & Materials:
1.
NONE
Legal Proceedings:
1.
NONE
Andrew Chan, MD
From the Department of Neurology, Inselspital, Bern University Hospital and University of Bern, Freiburgstrasse, Bern, Switzerland.
Disclosure
Scientific Advisory Boards:
1.
(1) Almirall (2) Actelion-Janssen (3) Bayer (4) Biogen (5) Celgene (6) Genzyme (7) Merck (8) Novartis (8) Roche (9) Teva, all for Hospital Research funds
Gifts:
1.
NONE
Funding for Travel or Speaker Honoraria:
1.
(1) Almirall (2) Actelion-Janssen (3) Bayer (4) Biogen (5) Celgene (6) Genzyme (7) Merck (8) Novartis (8) Roche (9) Teva; travel and speaker honoraria, all for Hospital Research funds
Editorial Boards:
1.
Clinical and Translational Neuroscience (Editorial board) Topic editor, Journal of International medical Research, European Journal of Neurology (Associate Editor)
Patents:
1.
NONE
Publishing Royalties:
1.
NONE
Employment, Commercial Entity:
1.
NONE
Consultancies:
1.
NONE
Speakers' Bureaus:
1.
NONE
Other Activities:
1.
NONE
Clinical Procedures or Imaging Studies:
1.
NONE
Research Support, Commercial Entities:
1.
Research support from Biogen, Genzyme, UCB
Research Support, Government Entities:
1.
(1) Schweizer Nationalfonds, Principle investigator, 2 years, (2) EU Horizon 2020, Principle Investigator 2 years, (3) EU Marie Curie Network, Principle Investigator 2 years
Research Support, Academic Entities:
1.
NONE
Research Support, Foundations and Societies:
1.
Swiss multiple sclerosis society, Co-PI, 2 years
Stock/stock Options/board of Directors Compensation:
1.
NONE
License Fee Payments, Technology or Inventions:
1.
NONE
Royalty Payments, Technology or Inventions:
1.
NONE
Stock/stock Options, Research Sponsor:
1.
NONE
Stock/stock Options, Medical Equipment & Materials:
1.
NONE
Legal Proceedings:
1.
NONE
Anke Salmen, PD, MD
From the Department of Neurology, Inselspital, Bern University Hospital and University of Bern, Freiburgstrasse, Bern, Switzerland.
Disclosure
Scientific Advisory Boards:
1.
NONE
Gifts:
1.
NONE
Funding for Travel or Speaker Honoraria:
1.
speaker honoraria and/or travel compensation for activities with Almirall Hermal GmbH, Biogen, Merck, Novartis, Roche, and Sanofi Genzyme, not related to this work.
Editorial Boards:
1.
NONE
Patents:
1.
NONE
Publishing Royalties:
1.
NONE
Employment, Commercial Entity:
1.
NONE
Consultancies:
1.
NONE
Speakers' Bureaus:
1.
NONE
Other Activities:
1.
NONE
Clinical Procedures or Imaging Studies:
1.
NONE
Research Support, Commercial Entities:
1.
NONE
Research Support, Government Entities:
1.
NONE
Research Support, Academic Entities:
1.
NONE
Research Support, Foundations and Societies:
1.
Swiss MS Society
Stock/stock Options/board of Directors Compensation:
1.
NONE
License Fee Payments, Technology or Inventions:
1.
NONE
Royalty Payments, Technology or Inventions:
1.
NONE
Stock/stock Options, Research Sponsor:
1.
NONE
Stock/stock Options, Medical Equipment & Materials:
1.
NONE
Legal Proceedings:
1.
NONE
Robert Hoepner, PD, MD
From the Department of Neurology, Inselspital, Bern University Hospital and University of Bern, Freiburgstrasse, Bern, Switzerland.
Disclosure
Scientific Advisory Boards:
1.
NONE
Gifts:
1.
NONE
Funding for Travel or Speaker Honoraria:
1.
NONE
Editorial Boards:
1.
NONE
Patents:
1.
NONE
Publishing Royalties:
1.
NONE
Employment, Commercial Entity:
1.
NONE
Consultancies:
1.
NONE
Speakers' Bureaus:
1.
NONE
Other Activities:
1.
R Hoepner received research and travel grants from Novartis and Biogen Idec. He also received speaker’s honoraria from Biogen, Novartis, Roche, Merk, Alexion, Bristol-Myers-Squibb and Almirall.
Clinical Procedures or Imaging Studies:
1.
NONE
Research Support, Commercial Entities:
1.
Roche IIT not related to the sudy
Research Support, Government Entities:
1.
NONE
Research Support, Academic Entities:
1.
NONE
Research Support, Foundations and Societies:
1.
NONE
Stock/stock Options/board of Directors Compensation:
1.
NONE
License Fee Payments, Technology or Inventions:
1.
NONE
Royalty Payments, Technology or Inventions:
1.
NONE
Stock/stock Options, Research Sponsor:
1.
NONE
Stock/stock Options, Medical Equipment & Materials:
1.
NONE
Legal Proceedings:
1.
NONE

Notes

Correspondence Dr. Diem [email protected]
Go to Neurology.org/NN for full disclosures. Funding information is provided at the end of the article.
The Article Processing Charge was funded by the authors.

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  2. Frequency and Predictors of Relapses following SARS-CoV-2 Vaccination in Patients with Multiple Sclerosis: Interim Results from a Longitudinal Observational Study, Journal of Clinical Medicine, 12, 11, (3640), (2023).https://doi.org/10.3390/jcm12113640
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  3. Effects of the COVID-19 Pandemic on Patients With NMO Spectrum Disorders and MOG-Antibody–Associated Diseases, Neurology Neuroimmunology & Neuroinflammation, 10, 2, (2023)./doi/10.1212/NXI.0000000000200082
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  4. Incidence of multiple sclerosis relapses and pseudo-relapses following COVID-19 vaccination, Multiple Sclerosis and Related Disorders, 77, (104865), (2023).https://doi.org/10.1016/j.msard.2023.104865
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  5. Multiple Sclerosis Relapse Following COVID-19 Vaccination: A Case Report and Literature Review, Cureus, (2022).https://doi.org/10.7759/cureus.21374
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  6. COVID-19 in a Neuroimmunological Outpatient Cohort: The Bernese Experience, Clinical and Translational Neuroscience, 6, 1, (6), (2022).https://doi.org/10.3390/ctn6010006
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  7. The Disease Influenced Vaccine Acceptance Scale-Six (DIVAS-6): Validation of a Measure to Assess Disease-Related COVID-19 Vaccine Attitudes and Concerns, Behavioral Medicine, 49, 4, (402-411), (2022).https://doi.org/10.1080/08964289.2022.2082358
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  8. Implementing education: Personal communication with a healthcare professional is a critical step to address vaccine hesitancy for people with multiple sclerosis, Multiple Sclerosis and Related Disorders, 63, (103933), (2022).https://doi.org/10.1016/j.msard.2022.103933
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  9. COVID-19 vaccine hesitancy in Iranian patients with multiple sclerosis, Multiple Sclerosis and Related Disorders, 60, (103723), (2022).https://doi.org/10.1016/j.msard.2022.103723
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  10. Derisking CD20-therapies for long-term use, Multiple Sclerosis and Related Disorders, 57, (103418), (2022).https://doi.org/10.1016/j.msard.2021.103418
    Crossref
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