Evidence map›Paper›PMID 36808306›Full record

ArticleWiener klinische Wochenschrift2023

Patient adherence to fully reimbursed proprotein convertase subtilisin/kexin type 9 inhibitor (PCSK9i) treatment.

Alissia Stummer, Robin Ristl, Bernhard Kogler, Melanie Muskovich, Michael Kossmeier, Thomas M Stulnig

Abstract read
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In one paragraph

Article in Wiener klinische Wochenschrift, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Observational
  3. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Alissia StummerMedical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria.
Robin RistlCenter for Medical Statistics, Informatics and Intelligent Systems, Medical University of Vienna, Spitalgasse 23 BT88/E 03, 1090, Vienna, Austria.
Bernhard KoglerFederation of Social Insurances, Kundmanngasse 21, 1030, Vienna, Austria.
Melanie MuskovichFederation of Social Insurances, Kundmanngasse 21, 1030, Vienna, Austria.
Michael KossmeierFederation of Social Insurances, Kundmanngasse 21, 1030, Vienna, Austria.
Thomas M StulnigDepartment of Medicine III and Karl Landsteiner Institute for Metabolic Diseases and Nephrology, Clinic Hietzing, Wolkersbergenstr. 1, 1130, Vienna, Austria. thomas.stulnig@gesundheitsverbund.at.ORCID http://orcid.org/0000-0003-3300-6161
Klinik Hietzing · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsProprotein convertase subtilisin/kexin-type 9 inhibitor (PCSK9i) treatment reduces cardiovascular events when taken over a long time for secondary prevention. Data on treatment adherence are scarce and maybe affected by co-payment of patients. The aim of this study was to elucidate PCSK9i treatment adherence in a setting of full cost coverage as it is the case in a number of European countries. METHODS AND

resultsBaseline data and prescription patterns of all 7302 patients with PCSK9i prescriptions dispensed on the account of Austrian Social Insurances between September 2015 and December 2020 were retrieved and analyzed. A gap of ≥ 60 days between prescriptions was defined as treatment discontinuation. Patient adherence was evaluated as the proportion of days covered (PDC) over the observation period and treatment discontinuation rates were investigated by the Kaplan-Meier method. The mean PDC was 81.8% and was significantly lower in female patients. A PDC of ≥ 80% indicating adequate adherence was found in 73.8%. Of the study population 27.4% discontinued PCSK9i treatment and 49.2% thereof re-initiated treatment during the observation period. Most of the patients who discontinued treatment did so within the first year. Male patients and patients under 64 years showed significantly lower discontinuation and higher re-initiation rates.

conclusionConsidering the high PDC and low discontinuation rates, the majority of patients adhere to PCSK9i treatment. Hence, in a system where PCSK9i treatment is made available at virtually no costs for patients this highly effective treatment is well-accepted as a long-term treatment.

Indexed as

Patient CompliancePCSK9 InhibitorsCholesterol, LDLFemaleHumansMaleProprotein Convertase 9Proprotein ConvertasesSubtilisinsCholesterol, LDLPCSK9 InhibitorsProprotein Convertase 9Proprotein ConvertasesSubtilisinsCardiovascular riskLipid-lowering therapyLow-density lipoproteinMonoclonal antibodiesSecondary prevention

Identifiers

PMID36808306
OpenAlexW4321478512

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.