Evidence map›Paper›PMID 33185773›Full record

ArticleEuropean child & adolescent psychiatry2022

Metabolic events associated with the use of antipsychotics in children, adolescents and young adults: a multinational sequence symmetry study.

Kenneth K C Man, Shih-Chieh Shao, Nathorn Chaiyakunapruk, Piyameth Dilokthornsakul, Kiyoshi Kubota, Junqing Li, Nobuhiro Ooba, Nicole Pratt, Anton Pottegård, Lotte Rasmussen and 6 more

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In one paragraph

Article in European child & adolescent psychiatry, 2022. 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
1.1field-weighted citation impact, top 23% 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, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. 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

16 authors at 11 institutions in 10 countries.

Kenneth K C ManResearch Department of Practice and Policy, UCL School of Pharmacy, London, UK.ORCID http://orcid.org/0000-0001-8645-1942
Shih-Chieh ShaoSchool of Pharmacy, Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University, No.1, University Road, Tainan, 701, Taiwan.
Nathorn ChaiyakunaprukDepartment of Pharmacotherapy, College of Pharmacy, University of Utah, 30 2000 E, Salt Lake City, UT, 84112, USA.
Piyameth DilokthornsakulCenter of Pharmaceutical Outcomes Research, Department of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Naresuan University, Phitsanulok, Thailand.
Kiyoshi KubotaNPO Drug Safety Research Unit Japan, Tokyo, Japan.
Junqing LiSchool of Pharmacy, Sungkyunkwan University, Seoul, South Korea.
Nobuhiro OobaDepartment of Clinical Pharmacy, Nihon University School of Pharmacy, Chiba, Japan.
Nicole PrattQuality Use of Medicines and Pharmacy Research Centre, Clinical and Health Sciences, University of South Australia, Adelaide, Australia.
Anton PottegårdClinical Pharmacology and Pharmacy, Department of Public Health, University of Southern Denmark, Odense, Denmark.
Lotte RasmussenDepartment of Pharmacy, National Cheng Kung University Hospital, Tainan, Taiwan.
Elizabeth E RougheadQuality Use of Medicines and Pharmacy Research Centre, Clinical and Health Sciences, University of South Australia, Adelaide, Australia.
Ju-Young ShinSchool of Pharmacy, Sungkyunkwan University, Seoul, South Korea.
Chien-Chou SuSchool of Pharmacy, Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University, No.1, University Road, Tainan, 701, Taiwan.
Ian C K WongResearch Department of Practice and Policy, UCL School of Pharmacy, London, UK.
Yea-Huei Kao YangSchool of Pharmacy, Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University, No.1, University Road, Tainan, 701, Taiwan.
Edward Chia-Cheng LaiSchool of Pharmacy, Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University, No.1, University Road, Tainan, 701, Taiwan. edward_lai@mail.ncku.edu.tw.ORCID http://orcid.org/0000-0002-5852-7652
National Cheng Kung University Hospital · TWSungkyunkwan University · KRUniversity College London · GBUniversity of South Australia · AUFood and Drug Safety Center · JPKeelung Chang Gung Memorial Hospital · TWMonash University Malaysia · MYNaresuan University · THNational Cheng Kung University · TWNihon University · JPUniversity of Southern Denmark · DK

Funding

Ministry of Science and Technology of Taiwan 106-2320-B-006-025-MY2
6 · The paper itself

Abstract

It is known that younger patients treated with antipsychotics are at increased risk of metabolic events; however, it is unknown how this risk varies according to ethnicity, the class of antipsychotic and the specific product used, and by age group. We conducted a multinational sequence symmetry study in Asian populations (Hong Kong, Japan, Korea, Taiwan and Thailand) and non-Asian populations (Australia and Denmark) to evaluate the metabolic events associated with antipsychotics in both Asian and non-Asian populations, for typical and atypical antipsychotics, and by the subgroups of children and adolescents, and young adults. Patients aged 6-30 years newly initiating oral antipsychotic drugs were included. We defined a composite outcome for metabolic events which included dyslipidemia, hypertension and hyperglycemia. We calculated the sequence ratio (SR) by dividing the number of people for whom a medicine for one of the outcome events was initiated within a 12-month period after antipsychotic initiation by the number before antipsychotic initiation. This study included 346,904 antipsychotic initiators across seven countries. Antipsychotic use was associated with an increased risk of composite metabolic events with a pooled adjusted SR (ASR) of 1.22 (95% CI 1.00-1.50). Pooled ASRs were similar between Asian (ASR, 1.22; 95% CI 0.88-1.70) and non-Asian populations (ASR, 1.22; 95% CI 1.04-1.43). The pooled ASR for typical and atypical antipsychotics was 0.98 (95% CI 0.85-1.12) and 1.24 (95% CI 0.97-1.59), respectively. No difference was observed in the relative effect in children and adolescents compared to young adults. The risk of metabolic events associated with antipsychotics use was similar in magnitude in Asian and non-Asian populations despite the marked difference in drug utilization patterns.

Indexed as

Antipsychotic AgentsAdolescentAdultAustraliaChildEthnicityHumansRepublic of KoreaTaiwanYoung AdultAntipsychotic AgentsAntipsychoticsMetabolic eventsMulti-national dataPediatricsSequence symmetry analysis

Identifiers

PMID33185773
OpenAlexW3099400008

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.