gms | German Medical Science

19th Annual Meeting of the German Drug Utilisation Research Group (GAA)

Gesellschaft für Arzneimittelforschung und Arzneimittelepidemiologie

22.11. - 23.11.2012, Jena

Medication persistence with Ginkgo biloba drugs of different dosage strengths

Persistenz bei Ginkgo biloba-Arzneimitteln unterschiedlicher Wirkstärke

Meeting Abstract

  • author Sittah Czeche - Deutsches Arzneiprüfungsinstitut e.V., Berlin, Germany
  • corresponding author Katrin Schuessel - Deutsches Arzneiprüfungsinstitut e.V., Berlin, Germany
  • Alexandra Franzmann - Deutsches Arzneiprüfungsinstitut e.V., Berlin, Germany
  • author Burkart Martin - Dr. Willmar Schwabe GmbH & Co. KG, Karlsruhe, Germany
  • author Schulz Martin - Deutsches Arzneiprüfungsinstitut e.V., Berlin, Germany

Gesellschaft für Arzneimittelanwendungsforschung und Arzneimittelepidemiologie e.V. (GAA). 19. Jahrestagung der Gesellschaft für Arzneimittelanwendungsforschung und Arzneimittelepidemiologie. Jena, 22.-23.11.2012. Düsseldorf: German Medical Science GMS Publishing House; 2012. Doc12gaa13

DOI: 10.3205/12gaa13, URN: urn:nbn:de:0183-12gaa135

Published: November 14, 2012

© 2012 Czeche et al.
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Outline

Text

Background: Ginkgo biloba drugs (Gb) are reimbursed within the German statutory health insurance (SHI) scheme for the treatment of dementia. In 2008, a novel Gb product with 240 mg tablets was introduced aiming to facilitate medication use and adherence by incorporating the recommended daily dose in one single tablet. The objective of this study was to investigate patients’ persistence with Gb therapy, with dosage strength as a hypothetically influential factor.

Materials and Methods: A retrospective cohort study was performed using claims data for outpatient prescriptions within the German SHI system. Persistence was defined as continuous treatment with an allowable gap of 20% between refills. Multivariate regression models were conducted to identify variables associated with persistence.

Results: Among 13,810 patients initiating treatment with Gb in 2008, 430 (3.1%) received a 240 mg dosage form, 7,070 (51.2%) a 120 mg dosage form and 6,310 (45.7%) a dosage form containing less than 120 mg Gb per single dose. After 6 months, persistence was highest for patients initially treated with the 240 mg dosage form (22.8% of patients), although persistence was very low in general (5.7% of patients treated with 120 mg). The risk for non-persistence was significantly reduced for patients receiving the 240 mg strength product compared to 120 mg strength products (HR=0.63; 95% CI 0.57–0.70).

Conclusion: Patients initially treated with Gb 240 mg were more persistent compared to those receiving lower strength dosage forms. Nevertheless, persistence with Gb therapy was generally low and should be improved in order to better realize therapeutic effects.