Hemostasis after percutaneous transfemoral access : a protocol for systematic review

Detalhes bibliográficos
Autor(a) principal: Reich, Rejane
Data de Publicação: 2020
Outros Autores: Helal, Lucas Crescenti Abdalla Saad, Mantovani, Vanessa Monteiro, Silva, Eneida Rejane Rabelo da
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/231769
Resumo: Background: Access site hemostasis after percutaneous procedures done in the catheterization laboratory still needs to be better studied in relation to such aspects as the different results achieved with different hemostasis strategies, the impact of different introducer sheath sizes, and arterial versus venous access. The objective of this review is to synthesize the available scientific evidence regarding different techniques for hemostasis of femoral access sites after percutaneous diagnostic and therapeutic procedures. Methods: This review is being reported in accordance with the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols (PRISMA-P). The primary outcomes will include the following vascular complications: hematoma, pseudoaneurysm, bleeding, minor, and major vascular complications. The secondary outcomes will include the following: time to hemostasis, repetition of manual compression, and device failure. A structured strategy will be used to search the PubMed/ MEDLINE, Embase, CINAHL, and CENTRAL databases. In addition, a handsearch of the reference lists of selected studies will be conducted. The ERIC research database will be queried for the gray literature and ClinicalTrials.gov, for potential results not yet published in indexed journals. Two reviewers will independently screen citations and abstracts, identify full-text articles for inclusion, extract data, and appraise the quality and risk of bias of included studies. If possible, a meta-analysis will be carried out. All estimations will be made using Review Manager 5.3. Statistical heterogeneity will be assessed by considering the I 2 proxy, accompanied with qualitative indicators such as differences in procedures, interventions, and outcomes among the studies. If synthesis proves inappropriate, a narrative review will be undertaken. Results: This protocol adheres to the PRISMA-P guideline to ensure clarity and completeness of reporting at all phases of the systematic review. Conclusion: This study will provide synthesized information on different methods used to achieve hemostasis after femoral access. Ethics and dissemination: Ethical approval number CAAE 19713219700005327. The results of the systematic review will be disseminated via publication in a peer-reviewed journal and through conference presentations. Systematic review registration: PROSPERO CRD42019140794.
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spelling Reich, RejaneHelal, Lucas Crescenti Abdalla SaadMantovani, Vanessa MonteiroSilva, Eneida Rejane Rabelo da2021-11-13T04:46:09Z20200025-7974http://hdl.handle.net/10183/231769001132738Background: Access site hemostasis after percutaneous procedures done in the catheterization laboratory still needs to be better studied in relation to such aspects as the different results achieved with different hemostasis strategies, the impact of different introducer sheath sizes, and arterial versus venous access. The objective of this review is to synthesize the available scientific evidence regarding different techniques for hemostasis of femoral access sites after percutaneous diagnostic and therapeutic procedures. Methods: This review is being reported in accordance with the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols (PRISMA-P). The primary outcomes will include the following vascular complications: hematoma, pseudoaneurysm, bleeding, minor, and major vascular complications. The secondary outcomes will include the following: time to hemostasis, repetition of manual compression, and device failure. A structured strategy will be used to search the PubMed/ MEDLINE, Embase, CINAHL, and CENTRAL databases. In addition, a handsearch of the reference lists of selected studies will be conducted. The ERIC research database will be queried for the gray literature and ClinicalTrials.gov, for potential results not yet published in indexed journals. Two reviewers will independently screen citations and abstracts, identify full-text articles for inclusion, extract data, and appraise the quality and risk of bias of included studies. If possible, a meta-analysis will be carried out. All estimations will be made using Review Manager 5.3. Statistical heterogeneity will be assessed by considering the I 2 proxy, accompanied with qualitative indicators such as differences in procedures, interventions, and outcomes among the studies. If synthesis proves inappropriate, a narrative review will be undertaken. Results: This protocol adheres to the PRISMA-P guideline to ensure clarity and completeness of reporting at all phases of the systematic review. Conclusion: This study will provide synthesized information on different methods used to achieve hemostasis after femoral access. Ethics and dissemination: Ethical approval number CAAE 19713219700005327. The results of the systematic review will be disseminated via publication in a peer-reviewed journal and through conference presentations. Systematic review registration: PROSPERO CRD42019140794.application/pdfengMedicine (Baltimore). Vol. 99, no.52 (2020), e23731,5 p.Revisão sistemáticaEnsaios clínicos controlados aleatórios como assuntorandomized controlled trialssystematic reviewtransfemoral accessHemostasis after percutaneous transfemoral access : a protocol for systematic reviewEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001132738.pdf.txt001132738.pdf.txtExtracted Texttext/plain26165http://www.lume.ufrgs.br/bitstream/10183/231769/2/001132738.pdf.txta97c689ab4ba867e6a87e7f3c4137e51MD52ORIGINAL001132738.pdfTexto completo (inglês)application/pdf214147http://www.lume.ufrgs.br/bitstream/10183/231769/1/001132738.pdf39d3eb16bf197c4a5bbe9acfcd5bef68MD5110183/2317692021-11-20 06:14:20.807249oai:www.lume.ufrgs.br:10183/231769Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-11-20T08:14:20Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Hemostasis after percutaneous transfemoral access : a protocol for systematic review
title Hemostasis after percutaneous transfemoral access : a protocol for systematic review
spellingShingle Hemostasis after percutaneous transfemoral access : a protocol for systematic review
Reich, Rejane
Revisão sistemática
Ensaios clínicos controlados aleatórios como assunto
randomized controlled trials
systematic review
transfemoral access
title_short Hemostasis after percutaneous transfemoral access : a protocol for systematic review
title_full Hemostasis after percutaneous transfemoral access : a protocol for systematic review
title_fullStr Hemostasis after percutaneous transfemoral access : a protocol for systematic review
title_full_unstemmed Hemostasis after percutaneous transfemoral access : a protocol for systematic review
title_sort Hemostasis after percutaneous transfemoral access : a protocol for systematic review
author Reich, Rejane
author_facet Reich, Rejane
Helal, Lucas Crescenti Abdalla Saad
Mantovani, Vanessa Monteiro
Silva, Eneida Rejane Rabelo da
author_role author
author2 Helal, Lucas Crescenti Abdalla Saad
Mantovani, Vanessa Monteiro
Silva, Eneida Rejane Rabelo da
author2_role author
author
author
dc.contributor.author.fl_str_mv Reich, Rejane
Helal, Lucas Crescenti Abdalla Saad
Mantovani, Vanessa Monteiro
Silva, Eneida Rejane Rabelo da
dc.subject.por.fl_str_mv Revisão sistemática
Ensaios clínicos controlados aleatórios como assunto
topic Revisão sistemática
Ensaios clínicos controlados aleatórios como assunto
randomized controlled trials
systematic review
transfemoral access
dc.subject.eng.fl_str_mv randomized controlled trials
systematic review
transfemoral access
description Background: Access site hemostasis after percutaneous procedures done in the catheterization laboratory still needs to be better studied in relation to such aspects as the different results achieved with different hemostasis strategies, the impact of different introducer sheath sizes, and arterial versus venous access. The objective of this review is to synthesize the available scientific evidence regarding different techniques for hemostasis of femoral access sites after percutaneous diagnostic and therapeutic procedures. Methods: This review is being reported in accordance with the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols (PRISMA-P). The primary outcomes will include the following vascular complications: hematoma, pseudoaneurysm, bleeding, minor, and major vascular complications. The secondary outcomes will include the following: time to hemostasis, repetition of manual compression, and device failure. A structured strategy will be used to search the PubMed/ MEDLINE, Embase, CINAHL, and CENTRAL databases. In addition, a handsearch of the reference lists of selected studies will be conducted. The ERIC research database will be queried for the gray literature and ClinicalTrials.gov, for potential results not yet published in indexed journals. Two reviewers will independently screen citations and abstracts, identify full-text articles for inclusion, extract data, and appraise the quality and risk of bias of included studies. If possible, a meta-analysis will be carried out. All estimations will be made using Review Manager 5.3. Statistical heterogeneity will be assessed by considering the I 2 proxy, accompanied with qualitative indicators such as differences in procedures, interventions, and outcomes among the studies. If synthesis proves inappropriate, a narrative review will be undertaken. Results: This protocol adheres to the PRISMA-P guideline to ensure clarity and completeness of reporting at all phases of the systematic review. Conclusion: This study will provide synthesized information on different methods used to achieve hemostasis after femoral access. Ethics and dissemination: Ethical approval number CAAE 19713219700005327. The results of the systematic review will be disseminated via publication in a peer-reviewed journal and through conference presentations. Systematic review registration: PROSPERO CRD42019140794.
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