Cristiano Matos

Dr. Cristiano Matos

Escola Superior de Tecnologia da Saúde de Coimbra, Coimbra, Portugal
orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 August 2016 in Drug Safety
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Journal Article
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CMCristiano Matos
Cristiano Matos
LHLinda Härmark
Linda Härmark
FHFlorence van Hunsel
Florence van Hunsel

26 May 2015 in European Journal of Clinical Pharmacology
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Journal Article
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CMCristiano Matos
Cristiano Matos
FHFlorence van Hunsel
Florence van Hunsel
João José JoaquimJoão José Joaquim
João José Joaquim
New pharmacovigilance legislation allows consumers to report adverse drug reactions (ADRs) directly to competent authorities in all European Union countries. Consumer reporting is available in Portugal since July 2012. In 2013, the National Pharmacovigilance System (SNF) had received 3461 spontaneous ADR reports, of which only 1.4 % (n = 50) were from consumers. Consumer reporting could be one opportunity to reduce underreporting. The aim of this study was to describe the attitudes and knowledge of the general public regarding spontaneous reporting and the reasons and opinions that can influence consumers’ ADR underreporting. A descriptive-correlational study was performed looking for consumers’ attitudes and knowledge regarding spontaneous reporting. A 6-month survey was conducted from June to November 2013 in general adult consumers from a community pharmacy in Coimbra, Portugal, who used prescribed medicines or over-the-counter (OTC) drugs. Attitudes and opinions were surveyed by personal interview in a closed-answer questionnaire using a Likert scale. Questionnaires from healthcare professionals or incomplete ones were not considered. Data were analyzed using descriptive statistics, chi-square (χ 2) tests, and Spearman’s correlation coefficients. One thousand eighty-four questionnaires were collected (response rate of 81.1 %) and 948 completed were selected for analysis. Of the respondents, 44.1 % never heard about SNF. Younger people and those with a higher education were significantly more likely to be aware of SNF. Only one consumer had previously reported directly an ADR. Reporting ADRs indirectly through a healthcare professional (HCP) was preferred by 62.4 %. The main reasons for consumers reporting spontaneous ADR would be the severity of reactions (81.1 % agreed or strongly agreed) and worries about their situation (73.4 % agreed or strongly agreed). Only weak and moderate correlations were found between studied statements.. Consumers are more likely to do spontaneous report about severe reactions or if they are worried about the symptoms. Tailored and proactive information on ADR reporting and educational interventions on consumers could increase the number of reports from consumers in Portugal.

12 October 2023 in Drug Safety
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Journal Article
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MGMoa Gustafsson
Moa Gustafsson
CMCristiano Matos
Cristiano Matos
João José JoaquimJoão José Joaquim
João José Joaquim
JSJoep Scholl
Joep Scholl
FHFlorence van Hunsel
Florence van Hunsel

31 July 2024 in Pharmaceuticals
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Journal Article
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MGMoa Gustafsson
Moa Gustafsson
VSVitor Silva
Vitor Silva
CVCarolina Valeiro
Carolina Valeiro
João José JoaquimJoão José Joaquim
João José Joaquim
FHFlorence van Hunsel
Florence van Hunsel
CMCristiano Matos
Cristiano Matos
Opioids are the strongest analgesics available and are crucial in the treatment of acute and chronic pain. The line between these critical medications and how they are used beyond standard therapeutics in cases such as abuse, misuse, and medication errors needs to be understood, as it affects their safety, efficacy, and manner of use. The aim of this systematic review was to identify what is known about the adverse events resulting from the abuse, misuse, and medication errors associated with opioid use. A systematic search was conducted in the PubMed®, Scopus® and, EBSCO® databases to retrieve studies from the inception to December 2023 reporting abuse, misuse, and medication errors associated with medicinal opioid use. Two authors independently screened titles and abstracts and full text according to eligibility using Covidence® software. Full articles were examined by two independent reviewers, and disagreements were resolved by a third reviewer. The risk of bias was assessed by the JBI’s critical appraisal tools. A total of 934 articles were screened by their title and Then, 151 articles were selected for full text screening. Of these, 34 studies were eligible for inclusion in this review. The included studies varied significantly in their population sizes, ranging from 9 individuals to 298,433 patients, and encompassed a diverse demographic, including all ages and both sexes. The studies consistently reported a range of adverse events associated with opioid use. Fentanyl, morphine, oxycodone, tramadol, and hydrocodone were frequently implicated. The data heterogeneity in this field resulted in challenges in drawing conclusions. The review highlights that some opioids, particularly fentanyl, morphine, and oxycodone, are frequently associated with preventable adverse drug reactions, abuse, and medication errors, underscoring the need for robust preventative measures and ongoing research to mitigate opioid-related harm.

7 April 2022 in Drug Safety
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Journal Article
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CVCarolina Valeiro
Carolina Valeiro
CMCristiano Matos
Cristiano Matos
JSJoep Scholl
Joep Scholl
FHFlorence van Hunsel
Florence van Hunsel

25 August 2022 in Drug Safety
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Journal Article
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MHMonica van Hoof
Monica van Hoof
KCKatherine Chinchilla
Katherine Chinchilla
LHLinda Harmark
Linda Harmark
CMCristiano Matos
Cristiano Matos
PIPedro Inácio
Pedro Inácio
FHFlorence van Hunsel
Florence van Hunsel