Evidence map›Paper›PMID 9803978›Full record

ReviewBritish journal of clinical pharmacology1998

Therapeutic drug monitoring: antiarrhythmic drugs.

T J Campbell, K M Williams

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of clinical pharmacology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 114 citations in OpenAlex.

  1. Trial
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  3. Treatment of ventricular arrhythmias with oral sotalol in four horses.Journal of veterinary internal medicine · 2026
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  9. Iatrogenic hypertension: a bioinformatic analysis.The pharmacogenomics journal · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

T J CampbellDepartment of Clinical Pharmacology, St Vincent's Hospital, Darlinghurst, NSW, Australia.
K M Williams
St Vincent's Hospital Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antiarrhythmic agents are traditionally classified according to Vaughan Williams into four classes of action. Class I antiarrhythmic agents include most of the drugs traditionally thought of as antiarrhythmics, and have as a common action, blockade of the fast-inward sodium channel on myocardium. These agents have a very significant toxicity, and while they are being used less, therapeutic drug monitoring (TDM) does significantly increase the safety with which they can be administered. Class II agents are antisympathetic drugs, particularly the beta-adrenoceptor blockers. These are generally safe agents which do not normally require TDM. Class III antiarrhythmic agents include sotalol and amiodarone. TDM can be useful in the case of amiodarone to monitor compliance and toxicity but is generally of little value for sotalol. Class IV antiarrhythmic drugs are the calcium channel blockers verapamil and diltiazem. These are normally monitored by haemodynamic effects, rather than using TDM. Other agents which do not fall neatly into the Vaughan Williams classification include digoxin and perhexiline. TDM is very useful for monitoring the administration (and particularly the safety) of both of these agents.

Indexed as

Drug MonitoringAdrenergic beta-AntagonistsAnti-Arrhythmia AgentsCalcium Channel BlockersCatecholaminesHumansPotassium Channel BlockersSodium Channel BlockersAdrenergic beta-AntagonistsAnti-Arrhythmia AgentsCalcium Channel BlockersCatecholaminesPotassium Channel BlockersSodium Channel Blockers

Identifiers

PMID9803978
PMCPMC1874159
OpenAlexW1978313067

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.