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Clinical symptoms related to anal sphincter defects and atrophy on external phased-array MR imaging

INTRODUCTION AND HYPOTHESIS: Defecatory complaints have a severe impact on quality of life. The additional value of pelvic floor MRI in patients with defecatory complaints is unclear. Our aim was to correlate the presence of defects and atrophy of the anal sphincter complex using pelvic floor MRI in...

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Autores principales: Kessels, Imke Maria Henricus, Fütterer, Jurgen Jacobus, Sultan, Abdul Hameed, Kluivers, Kirsten Birgit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611013/
https://www.ncbi.nlm.nih.gov/pubmed/26040812
http://dx.doi.org/10.1007/s00192-015-2743-4
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author Kessels, Imke Maria Henricus
Fütterer, Jurgen Jacobus
Sultan, Abdul Hameed
Kluivers, Kirsten Birgit
author_facet Kessels, Imke Maria Henricus
Fütterer, Jurgen Jacobus
Sultan, Abdul Hameed
Kluivers, Kirsten Birgit
author_sort Kessels, Imke Maria Henricus
collection PubMed
description INTRODUCTION AND HYPOTHESIS: Defecatory complaints have a severe impact on quality of life. The additional value of pelvic floor MRI in patients with defecatory complaints is unclear. Our aim was to correlate the presence of defects and atrophy of the anal sphincter complex using pelvic floor MRI in women with mixed pelvic floor symptoms and to establish patient characteristics and self reported complaints predictive of pathology. METHODS: This is a retrospective study among women with mixed pelvic floor symptoms who underwent external phased-array MRI and completed a questionnaire on bothersome defecatory complaints. Data on patient characteristics, including obstetrical history and questionnaire scores were correlated with the assessment of anal sphincter defects and atrophy on pelvic floor MRI. RESULTS: One hundred and fifty-eight women were included. A defect of the external anal sphincter (EAS) and internal anal sphincter (IAS) was found in 18 (11 %) and 5 (3 %) patients respectively. Atrophy of the EAS was present in 72 patients (46 %), with more cases of mild (n = 52, 33 %) than severe atrophy (n = 20, 13 %). The variable “previous third or fourth degree tear” had a significant positive association with an IAS defect on MRI, with an OR of 9.533 (1.425–63.776). Patients with EAS atrophy had higher scores for fecal incontinence (indicating more bother) than patients without EAS atrophy. Higher age and BMI were true predictors of the presence of more severe EAS atrophy. CONCLUSION: Atrophy of the EAS was highly prevalent in this population and was associated with bothersome symptoms of fecal incontinence.
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spelling pubmed-46110132015-10-22 Clinical symptoms related to anal sphincter defects and atrophy on external phased-array MR imaging Kessels, Imke Maria Henricus Fütterer, Jurgen Jacobus Sultan, Abdul Hameed Kluivers, Kirsten Birgit Int Urogynecol J Original Article INTRODUCTION AND HYPOTHESIS: Defecatory complaints have a severe impact on quality of life. The additional value of pelvic floor MRI in patients with defecatory complaints is unclear. Our aim was to correlate the presence of defects and atrophy of the anal sphincter complex using pelvic floor MRI in women with mixed pelvic floor symptoms and to establish patient characteristics and self reported complaints predictive of pathology. METHODS: This is a retrospective study among women with mixed pelvic floor symptoms who underwent external phased-array MRI and completed a questionnaire on bothersome defecatory complaints. Data on patient characteristics, including obstetrical history and questionnaire scores were correlated with the assessment of anal sphincter defects and atrophy on pelvic floor MRI. RESULTS: One hundred and fifty-eight women were included. A defect of the external anal sphincter (EAS) and internal anal sphincter (IAS) was found in 18 (11 %) and 5 (3 %) patients respectively. Atrophy of the EAS was present in 72 patients (46 %), with more cases of mild (n = 52, 33 %) than severe atrophy (n = 20, 13 %). The variable “previous third or fourth degree tear” had a significant positive association with an IAS defect on MRI, with an OR of 9.533 (1.425–63.776). Patients with EAS atrophy had higher scores for fecal incontinence (indicating more bother) than patients without EAS atrophy. Higher age and BMI were true predictors of the presence of more severe EAS atrophy. CONCLUSION: Atrophy of the EAS was highly prevalent in this population and was associated with bothersome symptoms of fecal incontinence. Springer London 2015-06-04 2015 /pmc/articles/PMC4611013/ /pubmed/26040812 http://dx.doi.org/10.1007/s00192-015-2743-4 Text en © The Author(s) 2015 Open Access This 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
Kessels, Imke Maria Henricus
Fütterer, Jurgen Jacobus
Sultan, Abdul Hameed
Kluivers, Kirsten Birgit
Clinical symptoms related to anal sphincter defects and atrophy on external phased-array MR imaging
title Clinical symptoms related to anal sphincter defects and atrophy on external phased-array MR imaging
title_full Clinical symptoms related to anal sphincter defects and atrophy on external phased-array MR imaging
title_fullStr Clinical symptoms related to anal sphincter defects and atrophy on external phased-array MR imaging
title_full_unstemmed Clinical symptoms related to anal sphincter defects and atrophy on external phased-array MR imaging
title_short Clinical symptoms related to anal sphincter defects and atrophy on external phased-array MR imaging
title_sort clinical symptoms related to anal sphincter defects and atrophy on external phased-array mr imaging
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611013/
https://www.ncbi.nlm.nih.gov/pubmed/26040812
http://dx.doi.org/10.1007/s00192-015-2743-4
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