Abstract
Objective
Methods
Results
Conclusion
Notes
FUNDING
This work was supported by the New Faculty Startup Fund from Seoul National University and grant from the Korea Health Technology R&D Project through the Ministry of Science, ICT and Future Planning (NRF-2020M3E5E203743011, 2019M3A9A8065574).
AUTHOR CONTRIBUTIONS
JKP conceived of the study. PS, KW, EBL, and JKP participated in its design and coordination. PS, KW, AHS, SC, WH, HAP, EBL, and JKP contributed to the collection, analysis and interpretation of the data. All authors participated in preparation of the manuscript. All authors read and approved the final manuscript.
REFERENCES
Table 1
Variables | Number (%) | |
---|---|---|
Continent of practice* | Asia (East, Southeast, Central, South Asia) | 156 (42.2) |
North America (e.g., Canada, Mexico, USA) | 154 (41.6) | |
Europe | 51 (13.8) | |
South America | 7 (1.9) | |
Other | 2 (0.5) | |
Age group | 20~30 years | 13 (3.5) |
31~40 years | 95 (25.6) | |
41~50 years | 115 (31.0) | |
51~60 years | 78 (21.0) | |
61~70 years | 54 (14.6) | |
>70 years | 16 (4.3) | |
Sex | Female | 147 (39.6) |
Male | 224 (60.4) | |
Work experience | 1~5 years | 28 (7.5) |
6~10 years | 49 (13.2) | |
11~15 years | 53 (14.3) | |
16~20 years | 64 (17.3) | |
21~25 years | 50 (13.5) | |
26~30 years | 40 (10.8) | |
>30 years | 87 (23.5) | |
Level of training | Resident-in-training | 11 (3) |
Fellow-in-training | 34 (9.2) | |
Board-certified/eligible | 312 (84.1) | |
Others | 14 (3.8) | |
Medical specialty | Rheumatology | 330 (88.9) |
Internal medicine | 13 (3.5) | |
Orthopedic surgery | 8 (2.2) | |
Family medicine | 4 (1.1) | |
Infectious disease | 1 (0.3) | |
Others | 15 (4.0) | |
Practice setting | Primary care/Private practice | 79 (21.3) |
Secondary care/General hospital (not university-affiliated) | 47 (12.7) | |
Tertiary care/Academic medical center (University-based or university-affiliated) | 245 (66) | |
Number of patients† | <10 patients | 141 (38) |
11~20 patients | 127 (34.2) | |
21~30 patients | 50 (13.5) | |
31~40 patients | 28 (7.5) | |
41~50 patients | 12 (3.2) | |
>50 patients | 13 (3.5) |
Table 2
Agreement | Implementation | Difference* | |
---|---|---|---|
Overarching principles | |||
1. The vaccination status and indications for further vaccination in patients with AIIRD should be assessed yearly by the rheumatology team | 4.2±0.9 | 3.5±1.2 | 0.7±0.9 |
2. The individualised vaccination programme should be explained to the patient by the rheumatology team, providing a basis for shared decision-making, and be jointly implemented by the primary care physician, the rheumatology team and the patient | 4.2±0.9 | 3.5±1.2 | 0.7±0.9 |
3. Vaccination in patients with AIIRD should preferably be administered during quiescent disease | 4.0±1.0 | 3.6±1.1 | 0.3±0.7 |
4. Vaccines should preferably be administered prior to planned immunosuppression, in particular B cell depleting therapy | 4.5±0.7 | 3.9±1.0 | 0.6±0.9 |
5. Non-live vaccines can be administered to patients with AIIRD also while treated with systemic glucocorticoids and DMARDs | 4.4±0.8 | 4.3±0.9 | 0.1±0.5 |
6. Live-attenuated vaccines may be considered with caution in patients with AIIRD | 3.6±1.2 | 3.3±1.4 | 0.3±0.7 |
Recommendations | |||
1. Influenza vaccination should be strongly considered for the majority of patients with AIIRD | 4.7±0.6 | 4.6±0.8 | 0.2±0.5 |
2. Pneumococcal vaccination should be strongly considered for the majority of patients with AIIRD | 4.6±0.7 | 4.2±1.0 | 0.4±0.7 |
3a. Patients with AIIRD should receive toxoid tetanus vaccination in accordance with recommendations for the general population | 4.2±1.0 | 3.4±1.4 | 0.8±1.1 |
3b. Passive immunisation should be considered for patients treated with B cell depleting therapy | 3.3±1.1 | 2.8±1.2 | 0.6±0.9 |
4a. Hepatitis A and hepatitis B vaccination should be administrated to patients with AIIRD at risk | 3.9±1.0 | 3.2±1.4 | 0.8±1.1 |
4b. In specific situations booster or passive immunisation of hepatitis A or hepatitis B is indicated | 3.6±1.0 | 2.8±1.3 | 0.8±1.1 |
5. Herpes zoster vaccination may be considered in high-risk patients with AIIRD | 4.3±0.9 | 3.5±1.4 | 0.8±1.1 |
6. Vaccination against yellow fever should be generally avoided in patients with AIIRD | 3.6±1.3 | 3.2±1.5 | 0.4±0.9 |
7. Patients with AIIRD, in particular patients with SLE, should receive vaccinations against HPV in accordance with recommendations for the general population | 4.1±1.0 | 3.1±1.4 | 1.0±1.2 |
8. Immunocompetent household members of patients with AIIRD should be encouraged to receive vaccines according to national guidelines with the exception of the oral polio vaccines | 4.2±0.9 | 3.2±1.4 | 1.0±1.2 |
9. Live-attenuated vaccines should be avoided during the first 6 months of life in newborns of mothers treated with biologics during the second half of pregnancy | 4.0±1.1 | 3.5±1.4 | 0.5±1.0 |
9a. Bacillus Calmette–Guérin should be avoided during the first 6 months of life in newborns of mothers treated with biologics during the second half of pregnancy | 3.9±1.1 | 3.4±1.4 | 0.5±1.0 |
Values are presented as mean±standard deviation. Agreement: 1=strongly disagree; 5=strongly agree. Practice: 1=not at all; 5=all the time. EULAR: European Alliance of Associations for Rheumatology, AIIRD: autoimmune inflammatory rheumatic diseases, DMARDs: disease modifying antirheumatic drugs, SLE: systemic lupus erythematosus. *Difference between agreement and implementation.