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How to write an ICS/IUGA conference abstract

INTRODUCTION: This article aims to condense the lectures and discussions from workshops on good reporting at IUGA Como 2009 and ICS San Francisco 2009, providing practical advice for the novice researcher summarising their data for the first time. CONCLUSIONS: Drafting an abstract can be a time cons...

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Detalles Bibliográficos
Autores principales: Cartwright, Rufus, Tikkinen, Kari A. O., Vierhout, Mark E., Koelbl, Heinz
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845882/
https://www.ncbi.nlm.nih.gov/pubmed/20179902
http://dx.doi.org/10.1007/s00192-010-1117-1
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author Cartwright, Rufus
Tikkinen, Kari A. O.
Vierhout, Mark E.
Koelbl, Heinz
author_facet Cartwright, Rufus
Tikkinen, Kari A. O.
Vierhout, Mark E.
Koelbl, Heinz
author_sort Cartwright, Rufus
collection PubMed
description INTRODUCTION: This article aims to condense the lectures and discussions from workshops on good reporting at IUGA Como 2009 and ICS San Francisco 2009, providing practical advice for the novice researcher summarising their data for the first time. CONCLUSIONS: Drafting an abstract can be a time consuming process. Formal guidance, such as CONSORT and STROBE, exists for the kinds of information that should be included regarding almost all designs of clinical trials. Follow the abstract submission rules closely to avoid outright rejection. Plan to highlight the novelty, scientific merit and clinical impact of the work. Try not to overstate the importance of the findings. Do not forget to publish the work in a peer reviewed journal.
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spelling pubmed-28458822010-04-05 How to write an ICS/IUGA conference abstract Cartwright, Rufus Tikkinen, Kari A. O. Vierhout, Mark E. Koelbl, Heinz Int Urogynecol J Current Opinion/Update INTRODUCTION: This article aims to condense the lectures and discussions from workshops on good reporting at IUGA Como 2009 and ICS San Francisco 2009, providing practical advice for the novice researcher summarising their data for the first time. CONCLUSIONS: Drafting an abstract can be a time consuming process. Formal guidance, such as CONSORT and STROBE, exists for the kinds of information that should be included regarding almost all designs of clinical trials. Follow the abstract submission rules closely to avoid outright rejection. Plan to highlight the novelty, scientific merit and clinical impact of the work. Try not to overstate the importance of the findings. Do not forget to publish the work in a peer reviewed journal. Springer-Verlag 2010-02-24 2010 /pmc/articles/PMC2845882/ /pubmed/20179902 http://dx.doi.org/10.1007/s00192-010-1117-1 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Current Opinion/Update
Cartwright, Rufus
Tikkinen, Kari A. O.
Vierhout, Mark E.
Koelbl, Heinz
How to write an ICS/IUGA conference abstract
title How to write an ICS/IUGA conference abstract
title_full How to write an ICS/IUGA conference abstract
title_fullStr How to write an ICS/IUGA conference abstract
title_full_unstemmed How to write an ICS/IUGA conference abstract
title_short How to write an ICS/IUGA conference abstract
title_sort how to write an ics/iuga conference abstract
topic Current Opinion/Update
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845882/
https://www.ncbi.nlm.nih.gov/pubmed/20179902
http://dx.doi.org/10.1007/s00192-010-1117-1
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