Evidence map›Paper›PMID 37185428›Full record

ArticleCurrent oncology (Toronto, Ont.)2023

Active Pharmacovigilance Study: A Follow-Up Model of Oral Anti-Cancer Drugs under Additional Monitoring.

Sofia Pinto Carvalho da Silva, Mafalda Jesus, Fátima Roque, Maria Teresa Herdeiro, Rita Costa E Sousa, Ana Paula Duarte, Manuel Morgado

Abstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

7 authors.

Sofia Pinto Carvalho da SilvaPharmaceutical Services of Local Healthcare Unit of Matosinhos, 4464-513 Senhora da Hora, Portugal.
Mafalda JesusHealth Sciences Faculty, University of Beira Interior (FCS-UBI), 6200-506 Covilhã, Portugal.ORCID 0000-0003-3332-7280
Fátima RoqueHealth Sciences Research Centre, University of Beira Interior (CICS-UBI), 6200-506 Covilhã, Portugal.ORCID 0000-0003-0169-3788
Maria Teresa HerdeiroInstitute of Biomedicine, University of Aveiro (iBIMED-UA), 3810-193 Aveiro, Portugal.ORCID 0000-0002-0500-4049
Rita Costa E SousaHematology Service, University Hospital Center of Coimbra, 3004-561 Coimbra, Portugal.
Ana Paula DuarteHealth Sciences Faculty, University of Beira Interior (FCS-UBI), 6200-506 Covilhã, Portugal.ORCID 0000-0003-3333-5977
Manuel MorgadoHealth Sciences Faculty, University of Beira Interior (FCS-UBI), 6200-506 Covilhã, Portugal.ORCID 0000-0003-2112-2835

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adverse drug reactions (ADRs) are responsible for almost 5% of hospital admissions, making it necessary to implement different pharmacovigilance strategies. The additional monitoring (AM) concept has been highlighted and intended to increase the number of suspected ADRs reported, namely in medicines with limited safety data. A prospective, descriptive study of active pharmacovigilance (AP) was conducted between 2019 and 2021 in the Local Health Unit of Matosinhos (LHUM) (Porto, Portugal). A model of AP for medicines under AM, namely oral antineoplastic agents, was designed. Follow-up consultations were performed, and adverse events (AEs) data were collected. The overall response to the treatment was evaluated through the Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria. A total of 52 patients were included in the study, and 14 antineoplastic drugs under AM were analyzed. Of the total number of patients included, only 29 developed at least one type of toxicity. Hematological disorders were the most reported suspected ADR. However, only four patients interrupted their treatment due to toxicity. After 12 months of treatment, most patients had disease progression, which was the main reason for therapy discontinuation. This AP model played an important role in the early detection of AEs and, consequently, contributed to better management of them. Increasing the number of suspected ADR reports is crucial for drugs with limited safety data.

Indexed as

Antineoplastic AgentsDrug-Related Side Effects and Adverse ReactionsAdverse Drug Reaction Reporting SystemsFollow-Up StudiesHumansPharmacovigilanceProspective StudiesAntineoplastic Agentsadverse drug reactionsblack inverted trianglepatient safety and oral chemotherapypharmaceutical interventionrisk management

Identifiers

PMID37185428
PMCPMC10137106

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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.