Development of a pelvic floor evaluation device

© 2015, Medical Association of Thailand. All rights reserved. Objective: To validate the device and investigate the effect of this device on symptoms, quality of life, and pelvic floor muscle strength. Material and Method: The device was designed to measure vaginal pressure changes using air-pressur...

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Main Authors: Jittima Manonai, Sakuntala Kamthaworn, Kuson Petsarb, Rujira Wattanayingcharoenchai
Other Authors: Mahidol University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/36734
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spelling th-mahidol.367342018-11-23T18:00:14Z Development of a pelvic floor evaluation device Jittima Manonai Sakuntala Kamthaworn Kuson Petsarb Rujira Wattanayingcharoenchai Mahidol University Medicine © 2015, Medical Association of Thailand. All rights reserved. Objective: To validate the device and investigate the effect of this device on symptoms, quality of life, and pelvic floor muscle strength. Material and Method: The device was designed to measure vaginal pressure changes using air-pressure balloon and abdominal wall muscle activities using surface electromyography. To test the accuracy of the device, for vaginal pressure measurement, a Mercury sphygmomanometer was used as a gold standard, and for abdominal wall muscle activity, a standard biofeedback machine was used as a reference device. A randomized, controlled trial was conducted in sixty-one women with stress urinary incontinence. They were randomly divided into two groups undergoing PFMT with a single 15-minute biofeedback session (BF + PFMT group) or without biofeedback (PFMT group). The pelvic floor muscle strength, abdominal wall muscle activity and incontinence-specific quality of life questionnaire (I-QOL), measurements were evaluated at baseline and at 8- and 16-week after treatment. Results: The accuracy of vaginal probe pressure perineometry was 98% compared to a standard sphygmomanometer. The device could detect abdominal wall muscles activities at 10 milliseconds (100 Hz), 20 milliseconds (50 Hz), and 50 milliseconds (20 Hz). After 8 and 16 weeks of treatment, there were statistically significant intra-group differences in the maximum vaginal squeeze pressure in both groups. However, the inter-group differences were not demonstrated. The proportion of women who performed pelvic floor muscle exercise correctly was significantly higher in the BF + PFMT group (72.41%) compared to the PFMT group (21.88%) at week 16 (p<0.05). Conclusion: The simple pelvic floor muscle strength evaluation device might be helpful in pelvic floor muscle training in a low resource setting. 2018-11-23T11:00:14Z 2018-11-23T11:00:14Z 2015-01-01 Article Journal of the Medical Association of Thailand. Vol.98, No.3 (2015), 219-225 01252208 01252208 2-s2.0-84929509091 https://repository.li.mahidol.ac.th/handle/123456789/36734 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84929509091&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Jittima Manonai
Sakuntala Kamthaworn
Kuson Petsarb
Rujira Wattanayingcharoenchai
Development of a pelvic floor evaluation device
description © 2015, Medical Association of Thailand. All rights reserved. Objective: To validate the device and investigate the effect of this device on symptoms, quality of life, and pelvic floor muscle strength. Material and Method: The device was designed to measure vaginal pressure changes using air-pressure balloon and abdominal wall muscle activities using surface electromyography. To test the accuracy of the device, for vaginal pressure measurement, a Mercury sphygmomanometer was used as a gold standard, and for abdominal wall muscle activity, a standard biofeedback machine was used as a reference device. A randomized, controlled trial was conducted in sixty-one women with stress urinary incontinence. They were randomly divided into two groups undergoing PFMT with a single 15-minute biofeedback session (BF + PFMT group) or without biofeedback (PFMT group). The pelvic floor muscle strength, abdominal wall muscle activity and incontinence-specific quality of life questionnaire (I-QOL), measurements were evaluated at baseline and at 8- and 16-week after treatment. Results: The accuracy of vaginal probe pressure perineometry was 98% compared to a standard sphygmomanometer. The device could detect abdominal wall muscles activities at 10 milliseconds (100 Hz), 20 milliseconds (50 Hz), and 50 milliseconds (20 Hz). After 8 and 16 weeks of treatment, there were statistically significant intra-group differences in the maximum vaginal squeeze pressure in both groups. However, the inter-group differences were not demonstrated. The proportion of women who performed pelvic floor muscle exercise correctly was significantly higher in the BF + PFMT group (72.41%) compared to the PFMT group (21.88%) at week 16 (p<0.05). Conclusion: The simple pelvic floor muscle strength evaluation device might be helpful in pelvic floor muscle training in a low resource setting.
author2 Mahidol University
author_facet Mahidol University
Jittima Manonai
Sakuntala Kamthaworn
Kuson Petsarb
Rujira Wattanayingcharoenchai
format Article
author Jittima Manonai
Sakuntala Kamthaworn
Kuson Petsarb
Rujira Wattanayingcharoenchai
author_sort Jittima Manonai
title Development of a pelvic floor evaluation device
title_short Development of a pelvic floor evaluation device
title_full Development of a pelvic floor evaluation device
title_fullStr Development of a pelvic floor evaluation device
title_full_unstemmed Development of a pelvic floor evaluation device
title_sort development of a pelvic floor evaluation device
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/36734
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