Evidence map›Paper›PMID 31504560›Full record

Observational studyThe international journal of neuropsychopharmacology2020

Cardiovascular Adverse Reactions During Antipsychotic Treatment: Results of AMSP, A Drug Surveillance Program Between 1993 and 2013.

Michaela-Elena Friedrich, Dietmar Winkler, Anastasios Konstantinidis, Wolfgang Huf, Rolf Engel, Sermin Toto, Renate Grohmann, Siegfried Kasper

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in The international journal of neuropsychopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.6field-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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Clozapine-induced Myocarditis in Korea: Analysis of a Nationwide Database and Comparison to Other Countries.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2026
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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

8 authors at 4 institutions in 2 countries.

Michaela-Elena FriedrichDepartment of Psychiatry and Psychotherapy, Division of General Psychiatry, Medical University of Vienna, Austria.
Dietmar WinklerDepartment of Psychiatry and Psychotherapy, Division of General Psychiatry, Medical University of Vienna, Austria.
Anastasios KonstantinidisDepartment of Psychiatry and Psychotherapy, Division of General Psychiatry, Medical University of Vienna, Austria.
Wolfgang HufKarl Landsteiner Institute for Clinical Risk Management, Vienna, Austria.
Rolf Engel
Sermin TotoDepartment of Psychiatry, Social Psychiatry and Psychotherapy, Hannover Medical School, Germany.
Renate GrohmannDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilian-University, Munich, Germany.
Siegfried KasperDepartment of Psychiatry and Psychotherapy, Division of General Psychiatry, Medical University of Vienna, Austria.
Medical University of Vienna · ATKarl Landsteiner Society · ATLudwig-Maximilians-Universität München · DEMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiovascular diseases are still the leading cause of global mortality. Some antipsychotic agents can show severe cardiovascular side effects and are also associated with metabolic syndrome.

methodsThis observational study was based on data of AMSP (Arzneimittelsicherheit in der Psychiatrie), a multicenter drug surveillance program in Austria, Germany and Switzerland, that recorded severe drug reactions in psychiatric inpatients.

resultsA total of 404 009 inpatients were monitored between 1993 and 2013, whereas 291 510 were treated with antipsychotics either in combination or alone. There were 376 cases of severe cardiovascular adverse reactions reported in the given timespan, yielding a relative frequency of 0.13%. The study revealed that incidence rates of cardiovascular adverse reactions were highest during treatment with ziprasidone (0.35%), prothipendyl (0.32%), and clozapine (0.23%). The lowest rate of cardiovascular symptoms occurred during treatment with promethazine (0.03%) as well as with aripiprazole (0.06%). The most common clinical symptoms were orthostatic collapse and severe hypotonia, sinustachycardia, QTc prolongation, myocarditis, and different forms of arrhythmia. The dosage at the timepoint when severe cardiovascular events occurred was not higher in any of the given antipsychotics than in everyday clinical practice and was in average therapeutic ranges. In terms of subclasses of antipsychotics, no significant statistical difference was seen in the overall frequencies of adverse reactions cases, when first-generation high potency, first-generation low potency, and second-generation antipsychotics were compared. Thirty percent of adverse events among second-generation antipsychotics were induced by clozapine.

conclusionsOur findings on cardiovascular adverse reactions contribute to a better understanding of cardiovascular risk profiles of antipsychotic agents in inpatients.

Indexed as

AdolescentAdultAgedAged, 80 and overAntipsychotic AgentsAustriaCardiovascular DiseasesDrug-Related Side Effects and Adverse ReactionsFemaleGermanyHumansMaleMiddle AgedProduct Surveillance, PostmarketingProgram DevelopmentSwitzerlandAntipsychotic Agentsadverse drug reactionantipsychoticscardiovasculardrug surveillance

Identifiers

PMID31504560
PMCPMC7093998
OpenAlexW2971134052

What OpenQuestion holds

Textmetadata
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.