Evidence map›Paper›PMID 31495943›Full record

ArticleBritish journal of clinical pharmacology2019

A novel direct method to determine adherence to atorvastatin therapy in patients with coronary heart disease.

Oscar Kristiansen, Nils T Vethe, Morten W Fagerland, Stein Bergan, John Munkhaugen, Einar Husebye

Open access · hybridAbstract read
In one paragraph

Article in British journal of clinical pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 6% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

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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 3 institutions in 1 country.

Oscar KristiansenDepartment of Medicine, Vestre Viken Trust, Drammen Hospital, Drammen, Norway.ORCID 0000-0002-4539-0239
Nils T VetheDepartment of Pharmacology, Oslo University Hospital, Oslo, Norway.
Morten W FagerlandOslo Centre for Biostatistics and Epidemiology, Oslo University Hospital, Oslo, Norway.
Stein BerganDepartment of Pharmacology, Oslo University Hospital, Oslo, Norway.
John MunkhaugenDepartment of Medicine, Vestre Viken Trust, Drammen Hospital, Drammen, Norway.
Einar HusebyeDepartment of Medicine, Vestre Viken Trust, Drammen Hospital, Drammen, Norway.
Oslo University Hospital · NOUniversity of Oslo · NODrammen Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsObjective methods to monitor statin adherence are needed. We have established a liquid chromatography-tandem mass spectrometry assay for quantification of atorvastatin and its metabolites in blood. This study aimed to develop an objective drug exposure variable with cut-off values to discriminate among adherence, partial adherence and nonadherence to atorvastatin therapy in patients with coronary heart disease.

methodsTwenty-five patients treated with atorvastatin 10 mg (n = 5), 20 mg (n = 6), 40 mg (n = 7) and 80 mg (n = 7) participated in a directly observed atorvastatin therapy study to confirm baseline adherence. After the directly observed therapy, half of the patients (test group) were instructed to stop taking atorvastatin and return for blood sample collection the subsequent 3 days. Levels of atorvastatin and metabolites were compared between the test group and the adherent control group.

resultsThe sum of parent drug and all measured primary metabolites correlated well with the atorvastatin dose administered (Spearman's rho = 0.71, 95% CI 0.44-0.87). The dose-normalized atorvastatin plus metabolites concentrations completely separated the partially adherent test group from the controls at 0.18 nM/mg after 3 days without atorvastatin. To reduce the risk of misinterpreting adherent patients as partially adherent, a corresponding cut-off at 0.10 nM/mg is proposed. A metabolite level of 2-OH atorvastatin acid <0.014 nmol/L provided the optimal cut-off for nonadherence.

conclusionA direct method to discriminate among adherence, partial adherence and nonadherence to atorvastatin therapy in patients with coronary heart disease has been developed. This tool may be important for novel studies on adherence and potentially useful in clinical practice.

Indexed as

Medication AdherenceAgedAnticholesteremic AgentsAtorvastatinChromatography, LiquidCoronary DiseaseDirectly Observed TherapyDose-Response Relationship, DrugFemaleHumansMaleTandem Mass SpectrometryAnticholesteremic AgentsAtorvastatinadherenceatorvastatincoronary heart diseaseliquid chromatography tandem mass spectrometry

Identifiers

PMID31495943
PMCPMC6955401
OpenAlexW2972402980

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Registered trials

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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.