dc.contributor.author
Katzmann, Julius L.
dc.contributor.author
Grellmann, Claudia
dc.contributor.author
Leppert, Beate
dc.contributor.author
Müller-Kozarez, Irina
dc.contributor.author
Schulz, Martin
dc.contributor.author
Laufs, Ulrich
dc.date.accessioned
2026-01-26T09:23:09Z
dc.date.available
2026-01-26T09:23:09Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/48835
dc.description.abstract
Background
Despite the availability of effective LDL cholesterol (LDL-C)-lowering drugs, only a minority of patients achieves the guideline-recommended treatment targets. This analysis describes treatment pathways of lipid-lowering therapy (LLT) in Germany.
Methods
Health claims data were used to identify patients at high or very-high cardiovascular risk who received a LLT prescription 2016–2022. Treatment pathways and the time to switch or discontinue LLT were analysed for statins, ezetimibe, bempedoic acid (BA), and PCSK9 inhibitors (PCSK9i).
Results
Out of 3,487,827 insured persons, 247,529 met the inclusion criteria. The most frequent first-line LLT were statins in 96.3%. Ezetimibe, BA, and PCSK9i were first-line LLT in only 0.9%, 0.061%, and 0.046%, respectively. Only few patients experienced a change in their treatment regimen following LLT initiation. Prescriptions of BA and PCSK9i were mainly second-, third-, or fourth-line add-on treatment. Termination of treatment with BA and PCSK9i was less frequent compared to statins and ezetimibe. The median time to treatment discontinuation was 1.45, 1.04, 0.60, and 2.45 years for statins, ezetimibe, BA, and PCSK9i, respectively, and the median time to switch therapy was 4.81 and 4.87 years for ezetimibe and PCSK9i, respectively (median not reached for statins and BA).
Conclusions
Changes in LLT were only observed in a minority of patients. BA and PCSK9i were switched more frequently than statins and ezetimibe. BA was discontinued earlier, and PCSK9i later than the other agents. Continued efforts to maintain long-term adherence and overcome therapeutic inertia are needed to realise the potential of available LLT with proven cardiovascular benefit.
en
dc.format.extent
11 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Bempedoic acid
en
dc.subject
PCSK9 inhibitor
en
dc.subject
Therapeutic inertia
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::615 Pharmakologie, Therapeutik
dc.title
Treatment pathways of lipid-lowering therapies in Germany 2016–2022
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1007/s00392-025-02686-5
dcterms.bibliographicCitation.journaltitle
Clinical Research in Cardiology
dcterms.bibliographicCitation.number
2
dcterms.bibliographicCitation.pagestart
266
dcterms.bibliographicCitation.pageend
276
dcterms.bibliographicCitation.volume
115
dcterms.bibliographicCitation.url
https://doi.org/10.1007/s00392-025-02686-5
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Pharmazie

refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1861-0692
refubium.resourceType.provider
WoS-Alert