Evidence map›Paper›PMID 38407283›Full record

ArticleJournal of analytical toxicology2024

Distribution of quetiapine between serum and whole blood in therapeutic drug-monitoring specimens.

Håvard Breivik, Mette Elise Tunset, Morten Brix Schou, Joachim Frost

Open access · hybridAbstract read
In one paragraph

Article in Journal of analytical toxicology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
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

4 authors at 2 institutions in 1 country.

Håvard BreivikInstitute of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Erling Skjalgssons gate 1, Trondheim 7491, Norway.ORCID 0000-0002-9760-6986
Mette Elise TunsetDepartment of Psychosis and Rehabilitation, Psychiatry Clinic, St. Olavs University Hospital, Østmarkveien 29A 7040, Norway.
Morten Brix SchouDepartment of Psychosis and Rehabilitation, Psychiatry Clinic, St. Olavs University Hospital, Østmarkveien 29A 7040, Norway.
Joachim FrostInstitute of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Erling Skjalgssons gate 1, Trondheim 7491, Norway.
Norwegian University of Science and Technology · NOSt Olav's University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quetiapine use is on the rise, leading to a corresponding increase in acute intoxications, some of which have fatal outcomes. When assessing whole-blood quetiapine concentrations during forensic autopsies, interpretations are primarily based on toxicity data from studies of serum concentrations. To our knowledge, there are only two previous studies that have attempted to establish the ratio between whole blood and serum quetiapine concentrations with limited populations and high variability of results. Paired specimens of whole blood and serum from 16 quetiapine users recruited from the Psychiatric Clinic, St. Olav University Hospital were analyzed using LC-MS-MS. Quetiapine concentrations in both matrices were determined and compared. The mean blood:serum ratio of quetiapine was 0.74 (standard deviation (SD) = 0.05, 95% confidence interval (CI) 0.71-0.76, P < 0.001), range 0.66-0.85. Simple linear regression showed strong linear correlation between quetiapine concentrations in the two matrices (B = 0.774, P > 0.001, r = 0.999). Our results imply that quetiapine occurs at lower concentrations within erythrocytes than in plasma. This is most likely due to a high degree of plasma protein binding. Other factors which may influence the distribution of quetiapine between these compartments are solubility, metabolism and passive or active efflux mechanisms. We did not observe any covariation between blood:serum ratios and serum concentrations. Quetiapine was consistently present at lower concentrations in whole blood than in serum. If so inclined to, a conversion factor of ∼0.7 may be considered for extrapolation of concentrations from serum to whole blood, at least in cases with therapeutic quetiapine concentration levels.

Indexed as

Antipsychotic AgentsAutopsyDibenzothiazepinesDrug MonitoringHumansPlasmaQuetiapine FumarateAntipsychotic AgentsDibenzothiazepinesQuetiapine Fumarate

Identifiers

PMID38407283
PMCPMC10977622
OpenAlexW4392167849

What OpenQuestion holds

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LicenceCC BY-NC
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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.