Evidence map›Paper›PMID 35057056›Full record

ArticlePharmaceutics2022

Ten Years of Experience Support Pharmacogenetic Testing to Guide Individualized Drug Therapy.

María Celsa Peña-Martín, Belén García-Berrocal, Almudena Sánchez-Martín, Elena Marcos-Vadillo, María Jesús García-Salgado, Santiago Sánchez, Carolina Lorenzo, David González-Parra, Francisco Sans, Manuel Franco and 4 more

Abstract read
In one paragraph

Article in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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

14 authors.

María Celsa Peña-MartínDepartment of Clinical Biochemistry, University Hospital of Salamanca, 37007 Salamanca, Spain.ORCID 0000-0002-3670-9228
Belén García-BerrocalDepartment of Clinical Biochemistry, University Hospital of Salamanca, 37007 Salamanca, Spain.
Almudena Sánchez-MartínDepartment of Pharmacy, University Hospital of Salamanca, 37007 Salamanca, Spain.
Elena Marcos-VadilloDepartment of Clinical Biochemistry, University Hospital of Salamanca, 37007 Salamanca, Spain.
María Jesús García-SalgadoDepartment of Clinical Biochemistry, University Hospital of Salamanca, 37007 Salamanca, Spain.
Santiago SánchezDepartment of Psychiatry, University Hospital of Salamanca, 37007 Salamanca, Spain.
Carolina LorenzoDepartment of Psychiatry, University Hospital of Salamanca, 37007 Salamanca, Spain.
David González-ParraDepartment of Psychiatry, University Hospital of Salamanca, 37007 Salamanca, Spain.
Francisco SansPsychiatry and Mental Health Department, Healthcare Complex of Zamora, 49022 Zamora, Spain.
Manuel FrancoPsychiatry and Mental Health Department, Healthcare Complex of Zamora, 49022 Zamora, Spain.
Andrea GaedigkDivision of Clinical Pharmacology, Toxicology & Therapeutic Innovation, Children's Mercy, Kansas City, MO 64108, USA.ORCID 0000-0001-6968-1893
María José Mateos-SexmeroPsychiatry and Mental Health Department, University Hospital of Valladolid, 47003 Valladolid, Spain.
Catalina SanzDepartment of Microbiology and Genetics, University of Salamanca, IBSAL, 37007 Salamanca, Spain.
María Isidoro-GarcíaDepartment of Clinical Biochemistry, University Hospital of Salamanca, 37007 Salamanca, Spain.

Funding

Instituto de Salud Carlos III through the project "IMP/00009" (Co-funded by European Regional Development Fund "A way to make Europe"). IMP/00009
6 · The paper itself

Abstract

Precision medicine utilizing the genetic information of genes involved in the metabolism and disposition of drugs can not only improve drug efficacy but also prevent or minimize adverse events. Polypharmacy is common among multimorbid patients and is associated with increased adverse events. One of the main objectives in health care is safe and efficacious drug therapy, which is directly correlated to the individual response to treatment. Precision medicine can increase drug safety in many scenarios, including polypharmacy. In this report, we share our experience utilizing precision medicine over the past ten years. Based on our experience using pharmacogenetic (PGx)-informed prescribing, we implemented a five-step precision medicine protocol (5SPM) that includes the assessment of the biological-clinical characteristics of the patient, current and past prescription history, and the patient's PGx test results. To illustrate our approach, we present cases highlighting the clinical relevance of precision medicine with a focus on patients with a complex history and polypharmacy.

Indexed as

pharmacogeneticspolypharmacyprecision medicine

Identifiers

PMID35057056
PMCPMC8779486

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Registered trials

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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.