Prophylaxis of TBE in adult persons over fifty years A84.1 A84.1
Conditions
Interventions
Group 1: Each participating site documents once at the start of participation whether and how it
motivates patients to have the TBE vaccination.
Once the patients consent to disclosure of his or
her p
Sponsors
Baxter Deutschland GmbH
Eligibility
Sex/Gender
All
Age
50 Years to No maximum
Inclusion criteria
Inclusion criteria: All patients 50 years and older who receive the basic immunization with FSME-IMMUN Adults can be considered for the target population. The patients must not have received any TBE vaccination in the past and must not have ever been infected with TBE. They must have given their written consent to participate in this noninterventional study.
Exclusion criteria
Exclusion criteria: no exclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identify methods for motivating patients for TBE vaccination in practices: Documentation once per site on a separate questionnaire. Collect patients' motivation and indication for TBE vaccination: Documentation once in the CRF. Identify vaccinations with FSME-IMMUN Adults: Documentation in the CRF. Documentation in the CRF whether the antibody concentration is determined after the 2nd vaccination - If performed: Identify antibody concentration - If performed: Identify whether the antibody measurement leads to administration of an additional vaccine dose. - If yes: Documentation of the additional vaccination | — |
Countries
Germany
Contacts
Public ContactAnja Reichert
Baxter Deutschland GmbH
Outcome results
None listed