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Pain evaluation during gynaecological surveillance in women with Lynch syndrome
To evaluate perceived pain during repetitive annual endometrial sampling at gynaecologic surveillance in asymptomatic women with Lynch syndrome (LS) over time and in addition to symptomatic women without LS, undergoing single endometrial sampling. In this prospective study, 52 women with LS or first...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357504/ https://www.ncbi.nlm.nih.gov/pubmed/27787750 http://dx.doi.org/10.1007/s10689-016-9937-x |
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author | Helder-Woolderink, Jorien de Bock, Geertruida Hollema, Harry van Oven, Magda Mourits, Marian |
author_facet | Helder-Woolderink, Jorien de Bock, Geertruida Hollema, Harry van Oven, Magda Mourits, Marian |
author_sort | Helder-Woolderink, Jorien |
collection | PubMed |
description | To evaluate perceived pain during repetitive annual endometrial sampling at gynaecologic surveillance in asymptomatic women with Lynch syndrome (LS) over time and in addition to symptomatic women without LS, undergoing single endometrial sampling. In this prospective study, 52 women with LS or first degree relatives who underwent repetitive annual gynaecological surveillance including endometrial sampling of which 33 were evaluated twice or more and 50 symptomatic women without LS who had single endometrial sampling, were included. Pain intensity was registered with VAS scores. Differences in pain intensities between subsequent visits (in LS) and between the two groups were evaluated. The use of painkillers before endometrial sampling was registered. If women with LS decided for preventive surgery, the reason was recorded. The LS group reported a median VAS score of 5.0 (range 0–10) at the first surveillance (n = 52) and at the second visit (n = 24). Women who repeatedly underwent endometrial sampling more often used painkillers for this procedure. During the study period 7/52 (13 %) women with LS choose for preventive surgery, another 4/52 (8 %) refused further endometrial sampling. Painful endometrial sampling was mentioned as main reason to quit screening. The median VAS score of the 50 symptomatic women was 5.0 (range 1–9). Endometrial sampling, irrespective of indication, is a painful procedure, with a median VAS score of 5.0. During subsequent procedures in women with LS, the median pain score does not aggravate although one in five women chose an alternative for endometrial sampling. |
format | Online Article Text |
id | pubmed-5357504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-53575042017-03-30 Pain evaluation during gynaecological surveillance in women with Lynch syndrome Helder-Woolderink, Jorien de Bock, Geertruida Hollema, Harry van Oven, Magda Mourits, Marian Fam Cancer Original Article To evaluate perceived pain during repetitive annual endometrial sampling at gynaecologic surveillance in asymptomatic women with Lynch syndrome (LS) over time and in addition to symptomatic women without LS, undergoing single endometrial sampling. In this prospective study, 52 women with LS or first degree relatives who underwent repetitive annual gynaecological surveillance including endometrial sampling of which 33 were evaluated twice or more and 50 symptomatic women without LS who had single endometrial sampling, were included. Pain intensity was registered with VAS scores. Differences in pain intensities between subsequent visits (in LS) and between the two groups were evaluated. The use of painkillers before endometrial sampling was registered. If women with LS decided for preventive surgery, the reason was recorded. The LS group reported a median VAS score of 5.0 (range 0–10) at the first surveillance (n = 52) and at the second visit (n = 24). Women who repeatedly underwent endometrial sampling more often used painkillers for this procedure. During the study period 7/52 (13 %) women with LS choose for preventive surgery, another 4/52 (8 %) refused further endometrial sampling. Painful endometrial sampling was mentioned as main reason to quit screening. The median VAS score of the 50 symptomatic women was 5.0 (range 1–9). Endometrial sampling, irrespective of indication, is a painful procedure, with a median VAS score of 5.0. During subsequent procedures in women with LS, the median pain score does not aggravate although one in five women chose an alternative for endometrial sampling. Springer Netherlands 2016-10-27 2017 /pmc/articles/PMC5357504/ /pubmed/27787750 http://dx.doi.org/10.1007/s10689-016-9937-x Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Helder-Woolderink, Jorien de Bock, Geertruida Hollema, Harry van Oven, Magda Mourits, Marian Pain evaluation during gynaecological surveillance in women with Lynch syndrome |
title | Pain evaluation during gynaecological surveillance in women with Lynch syndrome |
title_full | Pain evaluation during gynaecological surveillance in women with Lynch syndrome |
title_fullStr | Pain evaluation during gynaecological surveillance in women with Lynch syndrome |
title_full_unstemmed | Pain evaluation during gynaecological surveillance in women with Lynch syndrome |
title_short | Pain evaluation during gynaecological surveillance in women with Lynch syndrome |
title_sort | pain evaluation during gynaecological surveillance in women with lynch syndrome |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357504/ https://www.ncbi.nlm.nih.gov/pubmed/27787750 http://dx.doi.org/10.1007/s10689-016-9937-x |
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