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Consequences of cervical pessary for subsequent pregnancy: follow‐up of randomized clinical trial (ProTWIN)

OBJECTIVE: To evaluate the effect of cervical pessary, as a strategy to prevent preterm birth (PTB), on the outcome of subsequent pregnancy and maternal quality of life 4 years after the index twin pregnancy. METHODS: Between 2009 and 2012, the ProTWIN trial randomized women with a multiple pregnanc...

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Autores principales: van Limburg Stirum, E. V. J., Zegveld, S. J., Simons, N. E., de Boer, M. A., Pajkrt, E., Mol, B. W. J., Oudijk, M. A., van 't Hooft, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328140/
https://www.ncbi.nlm.nih.gov/pubmed/34826166
http://dx.doi.org/10.1002/uog.24821
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author van Limburg Stirum, E. V. J.
Zegveld, S. J.
Simons, N. E.
de Boer, M. A.
Pajkrt, E.
Mol, B. W. J.
Oudijk, M. A.
van 't Hooft, J.
author_facet van Limburg Stirum, E. V. J.
Zegveld, S. J.
Simons, N. E.
de Boer, M. A.
Pajkrt, E.
Mol, B. W. J.
Oudijk, M. A.
van 't Hooft, J.
author_sort van Limburg Stirum, E. V. J.
collection PubMed
description OBJECTIVE: To evaluate the effect of cervical pessary, as a strategy to prevent preterm birth (PTB), on the outcome of subsequent pregnancy and maternal quality of life 4 years after the index twin pregnancy. METHODS: Between 2009 and 2012, the ProTWIN trial randomized women with a multiple pregnancy to pessary use vs standard care for the prevention of PTB. The trial showed no benefit in unselected women with a twin pregnancy, but showed a 60% reduction in poor perinatal outcomes in favor of the pessary group in the subgroup of women with a mid‐trimester short cervix (cervical length < 38 mm). All women were invited to participate in a follow‐up study 4 years after their participation in the ProTWIN trial. In this follow‐up study, maternal quality of life was assessed using the EQ‐5D‐3L questionnaire and women were asked separate questions about subsequent pregnancies. Results were compared between women who were randomized to the pessary vs the control group in the ProTWIN trial by calculating relative risk (RR) and 95% CI. Subgroup analysis was performed for women with a mid‐trimester short cervix (cervical length < 38 mm). RESULTS: Of the 813 women included in the ProTWIN trial, 408 (50.2%) participated in this follow‐up study, comprising 228 randomized to the pessary group and 180 to the control group in the original trial. The median interval between participation in the ProTWIN trial and participation in this follow‐up study was 4.1 (interquartile range (IQR), 3.9–7.1) years. Ninety‐eight (24.0%) participants tried to conceive after their participation in the ProTWIN trial. Of those, 22 (22.4%) women did not have a subsequent pregnancy (no difference between pessary and control groups), seven (7.1%) women had at least one miscarriage but no live birth, and 67 (68.4%) women had at least one live birth (35 in the pessary vs 32 in the control group; RR, 0.93 (95% CI, 0.8–1.07)). In two women, the pregnancy outcome was unknown. Preterm delivery (< 37 weeks of gestation) of the first live birth occurred in three women in the pessary vs one woman in the control group (all singleton; RR, 2.57 (95% CI, 0.28–23.44)). No differences were found between the pessary and control groups in the subgroup of women with mid‐trimester short cervix, but the numbers analyzed were small. The median health state index score was 0.95 (IQR, 0.82–0.95), with no difference between the pessary and control groups. CONCLUSION: Our findings suggest that there are no long‐term effects of pessary use on the outcome of subsequent pregnancies and maternal quality of life. Data on obstetric outcome were limited due to the small numbers. © 2021 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
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spelling pubmed-93281402022-07-30 Consequences of cervical pessary for subsequent pregnancy: follow‐up of randomized clinical trial (ProTWIN) van Limburg Stirum, E. V. J. Zegveld, S. J. Simons, N. E. de Boer, M. A. Pajkrt, E. Mol, B. W. J. Oudijk, M. A. van 't Hooft, J. Ultrasound Obstet Gynecol Original Papers OBJECTIVE: To evaluate the effect of cervical pessary, as a strategy to prevent preterm birth (PTB), on the outcome of subsequent pregnancy and maternal quality of life 4 years after the index twin pregnancy. METHODS: Between 2009 and 2012, the ProTWIN trial randomized women with a multiple pregnancy to pessary use vs standard care for the prevention of PTB. The trial showed no benefit in unselected women with a twin pregnancy, but showed a 60% reduction in poor perinatal outcomes in favor of the pessary group in the subgroup of women with a mid‐trimester short cervix (cervical length < 38 mm). All women were invited to participate in a follow‐up study 4 years after their participation in the ProTWIN trial. In this follow‐up study, maternal quality of life was assessed using the EQ‐5D‐3L questionnaire and women were asked separate questions about subsequent pregnancies. Results were compared between women who were randomized to the pessary vs the control group in the ProTWIN trial by calculating relative risk (RR) and 95% CI. Subgroup analysis was performed for women with a mid‐trimester short cervix (cervical length < 38 mm). RESULTS: Of the 813 women included in the ProTWIN trial, 408 (50.2%) participated in this follow‐up study, comprising 228 randomized to the pessary group and 180 to the control group in the original trial. The median interval between participation in the ProTWIN trial and participation in this follow‐up study was 4.1 (interquartile range (IQR), 3.9–7.1) years. Ninety‐eight (24.0%) participants tried to conceive after their participation in the ProTWIN trial. Of those, 22 (22.4%) women did not have a subsequent pregnancy (no difference between pessary and control groups), seven (7.1%) women had at least one miscarriage but no live birth, and 67 (68.4%) women had at least one live birth (35 in the pessary vs 32 in the control group; RR, 0.93 (95% CI, 0.8–1.07)). In two women, the pregnancy outcome was unknown. Preterm delivery (< 37 weeks of gestation) of the first live birth occurred in three women in the pessary vs one woman in the control group (all singleton; RR, 2.57 (95% CI, 0.28–23.44)). No differences were found between the pessary and control groups in the subgroup of women with mid‐trimester short cervix, but the numbers analyzed were small. The median health state index score was 0.95 (IQR, 0.82–0.95), with no difference between the pessary and control groups. CONCLUSION: Our findings suggest that there are no long‐term effects of pessary use on the outcome of subsequent pregnancies and maternal quality of life. Data on obstetric outcome were limited due to the small numbers. © 2021 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology. John Wiley & Sons, Ltd. 2022-06-01 2022-06 /pmc/articles/PMC9328140/ /pubmed/34826166 http://dx.doi.org/10.1002/uog.24821 Text en © 2021 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
van Limburg Stirum, E. V. J.
Zegveld, S. J.
Simons, N. E.
de Boer, M. A.
Pajkrt, E.
Mol, B. W. J.
Oudijk, M. A.
van 't Hooft, J.
Consequences of cervical pessary for subsequent pregnancy: follow‐up of randomized clinical trial (ProTWIN)
title Consequences of cervical pessary for subsequent pregnancy: follow‐up of randomized clinical trial (ProTWIN)
title_full Consequences of cervical pessary for subsequent pregnancy: follow‐up of randomized clinical trial (ProTWIN)
title_fullStr Consequences of cervical pessary for subsequent pregnancy: follow‐up of randomized clinical trial (ProTWIN)
title_full_unstemmed Consequences of cervical pessary for subsequent pregnancy: follow‐up of randomized clinical trial (ProTWIN)
title_short Consequences of cervical pessary for subsequent pregnancy: follow‐up of randomized clinical trial (ProTWIN)
title_sort consequences of cervical pessary for subsequent pregnancy: follow‐up of randomized clinical trial (protwin)
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328140/
https://www.ncbi.nlm.nih.gov/pubmed/34826166
http://dx.doi.org/10.1002/uog.24821
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