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Invasive dental treatment and acute vascular events: A systematic review and meta‐analysis
BACKGROUND: Acute infection/inflammation increases the risk of acute vascular events (AVEs). Invasive dental treatments (IDTs) trigger short‐term acute inflammation. PURPOSE: The aim of this work is to critically appraise the evidence linking IDTs and AVEs. DATA SOURCES: Six bibliographical database...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9311221/ https://www.ncbi.nlm.nih.gov/pubmed/35132650 http://dx.doi.org/10.1111/jcpe.13600 |
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author | Luthra, Shailly Orlandi, Marco Leira, Yago Bokre, Desta Marletta, Debora Rotundo, Roberto Harden, Simon D'Aiuto, Francesco |
author_facet | Luthra, Shailly Orlandi, Marco Leira, Yago Bokre, Desta Marletta, Debora Rotundo, Roberto Harden, Simon D'Aiuto, Francesco |
author_sort | Luthra, Shailly |
collection | PubMed |
description | BACKGROUND: Acute infection/inflammation increases the risk of acute vascular events (AVEs). Invasive dental treatments (IDTs) trigger short‐term acute inflammation. PURPOSE: The aim of this work is to critically appraise the evidence linking IDTs and AVEs. DATA SOURCES: Six bibliographical databases were searched up to 31 August 2021. A systematic review following PRISMA guidelines was performed. STUDY SELECTION: Intervention and observational studies reporting any AVEs following IDT were included. DATA EXTRACTION: Two reviewers independently extracted data and rated the quality of studies. Data were pooled using fixed‐effect, inverse variance weights analysis. RISK OF BIAS: Risk of bias was assessed by the Newcastle–Ottawa Quality Assessment Scale for observational studies and the Cochrane Handbook–Rob 2.0 for randomized controlled trials. DATA SYNTHESIS: In 3 out of 16 clinical studies, a total of 533,175 participants, 124,344 myocardial infarctions, and 327,804 ischaemic strokes were reported. Meta‐analysis confirmed that IDT did not increase incidence ratios (IR) for combined vascular events either at 1‐4 weeks (IR of 1.02, 95% CIs: 0.92 to 1.13) and at 5‐8 weeks (IR of 1.04, 95% CIs: 0.97 to1.10) after treatment. LIMITATIONS: A high level of heterogeneity (study designs and time point assessments) was found. CONCLUSION: Patients who received IDT exhibited no substantial increase in vascular risk over 8 weeks post treatment. |
format | Online Article Text |
id | pubmed-9311221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-93112212022-07-29 Invasive dental treatment and acute vascular events: A systematic review and meta‐analysis Luthra, Shailly Orlandi, Marco Leira, Yago Bokre, Desta Marletta, Debora Rotundo, Roberto Harden, Simon D'Aiuto, Francesco J Clin Periodontol Diagnosis, Epidemiology and Associated Co‐morbidities BACKGROUND: Acute infection/inflammation increases the risk of acute vascular events (AVEs). Invasive dental treatments (IDTs) trigger short‐term acute inflammation. PURPOSE: The aim of this work is to critically appraise the evidence linking IDTs and AVEs. DATA SOURCES: Six bibliographical databases were searched up to 31 August 2021. A systematic review following PRISMA guidelines was performed. STUDY SELECTION: Intervention and observational studies reporting any AVEs following IDT were included. DATA EXTRACTION: Two reviewers independently extracted data and rated the quality of studies. Data were pooled using fixed‐effect, inverse variance weights analysis. RISK OF BIAS: Risk of bias was assessed by the Newcastle–Ottawa Quality Assessment Scale for observational studies and the Cochrane Handbook–Rob 2.0 for randomized controlled trials. DATA SYNTHESIS: In 3 out of 16 clinical studies, a total of 533,175 participants, 124,344 myocardial infarctions, and 327,804 ischaemic strokes were reported. Meta‐analysis confirmed that IDT did not increase incidence ratios (IR) for combined vascular events either at 1‐4 weeks (IR of 1.02, 95% CIs: 0.92 to 1.13) and at 5‐8 weeks (IR of 1.04, 95% CIs: 0.97 to1.10) after treatment. LIMITATIONS: A high level of heterogeneity (study designs and time point assessments) was found. CONCLUSION: Patients who received IDT exhibited no substantial increase in vascular risk over 8 weeks post treatment. Blackwell Publishing Ltd 2022-03-16 2022-05 /pmc/articles/PMC9311221/ /pubmed/35132650 http://dx.doi.org/10.1111/jcpe.13600 Text en © 2022 The Authors. Journal of Clinical Periodontology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Diagnosis, Epidemiology and Associated Co‐morbidities Luthra, Shailly Orlandi, Marco Leira, Yago Bokre, Desta Marletta, Debora Rotundo, Roberto Harden, Simon D'Aiuto, Francesco Invasive dental treatment and acute vascular events: A systematic review and meta‐analysis |
title | Invasive dental treatment and acute vascular events: A systematic review and meta‐analysis |
title_full | Invasive dental treatment and acute vascular events: A systematic review and meta‐analysis |
title_fullStr | Invasive dental treatment and acute vascular events: A systematic review and meta‐analysis |
title_full_unstemmed | Invasive dental treatment and acute vascular events: A systematic review and meta‐analysis |
title_short | Invasive dental treatment and acute vascular events: A systematic review and meta‐analysis |
title_sort | invasive dental treatment and acute vascular events: a systematic review and meta‐analysis |
topic | Diagnosis, Epidemiology and Associated Co‐morbidities |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9311221/ https://www.ncbi.nlm.nih.gov/pubmed/35132650 http://dx.doi.org/10.1111/jcpe.13600 |
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