Evidence map›Paper›PMID 16307209›Full record

ArticleJournal of pharmacokinetics and pharmacodynamics2005

The population pharmacokinetics of citalopram after deliberate self-poisoning: a Bayesian approach.

Lena E Friberg, Geoffrey K Isbister, L Peter Hackett, Stephen B Duffull

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of pharmacokinetics and pharmacodynamics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.1field-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

27 citing papers in PubMed, 69 citations in OpenAlex.

  1. Effect of activated charcoal on apixaban pharmacokinetics in healthy subjects.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2014
    Trial
  2. Article
  3. Challenges faced when modeling clinical toxicology and toxinology events.CPT: pharmacometrics & systems pharmacology · 2022
    Article
  4. Reply to "Reflections on Aspirin Toxicity: Interpreting Effects of Sodium Bicarbonate and Activated Charcoal".Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2022
    Article
  5. Article
  6. Review
  7. The Use of Activated Charcoal to Treat Intoxications.Deutsches Arzteblatt international · 2019
    Review
  8. Review
  9. Fatal intoxication with antidepressants: a case with many culprits.Forensic science, medicine, and pathology · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Activated charcoal for acute overdose: a reappraisal.British journal of clinical pharmacology · 2016
    Review
  14. Article
  15. Mirtazapine overdose is unlikely to cause major toxicity.Clinical toxicology (Philadelphia, Pa.) · 2014
    Observational
  16. Article
  17. Article
  18. Mechanism-based pharmacodynamic modeling.Methods in molecular biology (Clifton, N.J.) · 2012
    Article
  19. Activated charcoal for acute poisoning: one toxicologist's journey.Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2010
    Review
  20. Electrocardiogram changes and arrhythmias in venlafaxine overdose.British journal of clinical pharmacology · 2009
    Article
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.

Lena E FribergSchool of Pharmacy, University of Queensland, Brishane, Australia.
Geoffrey K Isbister
L Peter Hackett
Stephen B Duffull
University of Queensland · AUCharles Darwin University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defining the pharmacokinetics of drugs in overdose is complicated. Deliberate self-poisoning is generally impulsive and associated with poor accuracy in dose history. In addition, early blood samples are rarely collected to characterize the whole plasma-concentration time profile and the effect of decontamination on the pharmacokinetics is uncertain. The aim of this study was to explore a fully Bayesian methodology for population pharmacokinetic analysis of data that arose from deliberate self-poisoning with citalopram. Prior information on the pharmacokinetic parameters was elicited from 14 published studies on citalopram when taken in therapeutic doses. The data set included concentration-time data from 53 patients studied after 63 citalopram overdose events (dose range: 20-1700 mg). Activated charcoal was administered between 0.5 and 4 h after 17 overdose events. The clinical investigator graded the veracity of the patients' dosing history on a 5-point ordinal scale. Inclusion of informative priors stabilised the pharmacokinetic model and the population mean values could be estimated well. There were no indications of non-linear clearance after excessive doses. The final model included an estimated uncertainty of the dose amount which in a simulation study was shown to not affect the model's ability to characterise the effects of activated charcoal. The effect of activated charcoal on clearance and bioavailability was pronounced and resulted in a 72% increase and 22% decrease, respectively. These findings suggest charcoal administration is potentially beneficial after citalopram overdose. The methodology explored seems promising for exploring the dose-exposure relationship in the toxicological settings.

Indexed as

AdolescentAdultAgedAntidepressive Agents, Second-GenerationBayes TheoremBiological AvailabilityCharcoalCitalopramClinical Trials as TopicFemaleHumansLong QT SyndromeMaleMiddle AgedModels, BiologicalPoisoningAntidepressive Agents, Second-GenerationCharcoalCitalopram

Identifiers

PMID16307209
OpenAlexW2070876075

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.