Evidence map›Paper›PMID 34767918›Full record

ArticleJournal of the American Academy of Child and Adolescent Psychiatry2022

Editorial: Beyond Red Light, Green Light: Examining the Role of Pharmacogenomics in Evidence-Based Care in Child and Adolescent Psychiatry.

Lisa B Namerow, Laura B Ramsey, Salma Malik, Samuele Cortese, Jeffrey R Strawn

Abstract readEditorialComment
In one paragraph

Article in Journal of the American Academy of Child and Adolescent Psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Pediatric Psychopharmacology for Depressive and Anxiety Disorders.Focus (American Psychiatric Publishing) · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Lisa B NamerowInstitute of Living/Hartford Healthcare, and the University of Connecticut School of Medicine, Hartford. Electronic address: lnamerow@connecticutchildrens.org.
Laura B RamseyCincinnati Children's Hospital Medical Cent and the College of Medicine at the University of Cincinnati, Ohio.
Salma MalikInstitute of Living/Hartford Healthcare, and the University of Connecticut School of Medicine, Hartford.
Samuele CorteseCentre for Innovation in Mental Health, Academic Unit of Psychology, and the Clinical and Experimental Sciences (CNS and Psychiatry), University of Southampton, UK; Solent National Health System Trust (NHS), Southampton, UK; Hassenfeld Children's Hospital at NYU Langone, New York University Child Study Center, New York; Division of Psychiatry and Applied Psychology, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
Jeffrey R StrawnCincinnati Children's Hospital Medical Cent and the College of Medicine at the University of Cincinnati, Ohio.

Funding

Improving the Effectiveness and Safety of Escitalopram in Pediatric Anxiety Disorders Using Pharmacogenetically-guided DosingR01HD099775 · NICHD · UNIVERSITY OF CINCINNATI · PI RAMSEY, LAURA B, STRAWN, JEFFREY ROBERT · 2020 to 2024
$2.9M
Estracellular Vesicles as Non-Invasive Predictors of Antidepressant Outcomes in Pediatric AnxietyR01HD098757 · NICHD · UNIVERSITY OF CINCINNATI · PI STRAWN, JEFFREY ROBERT · 2019 to 2024
$2.4M
NICHD NIH HHS R01 HD098757NICHD NIH HHS R01 HD099775
6 · The paper itself

Abstract

The role of pharmacogenetics in guiding psychopharmacologic treatment for children and adolescents remains elusive for many clinicians. In the absence of a solid and comprehensive evidence base, sufficient training, education, and consensus guidelines, commercial promotion of pharmacogenetic testing panels has the potential to become the main source of information for providers. Commonly, these tests include multigene panels and group medications into color-coded bins. These panels include both pharmacokinetic (PK) and pharmacodynamic (PD) genes and, using combinatorial algorithms, direct clinicians to use medications "as directed" or caution that "moderate gene-drug interaction(s)" or "significant gene-drug interaction(s)" may exist. Many industry-sponsored studies in adults have concluded that that when clinicians select medications based on pharmacogenomic guidance, patients have better outcomes,

Indexed as

Major Depressive DisorderPharmacogeneticsAdolescentAdolescent PsychiatryAdultAntidepressive AgentsChildDouble-Blind MethodEvidence-Based MedicineHumansProspective StudiesSelective Serotonin Reuptake InhibitorsAntidepressive AgentsSelective Serotonin Reuptake Inhibitors

Identifiers

PMID34767918
PMCPMC8994592

What OpenQuestion holds

Textmetadata
LicenceTDM
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.