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Acute Tocolysis – a Critical Analysis of Evidence-Based Data
Tocolysis is among the most common obstetric measures. The objective is to prolong the pregnancy by at least 48 hours to complete foetal lung maturation and for the in-utero transfer of the pregnant woman to a perinatal centre. The indication for tocolysis is regular, premature contractions (≥ 4/20 ...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Georg Thieme Verlag KG
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294642/ https://www.ncbi.nlm.nih.gov/pubmed/30655648 http://dx.doi.org/10.1055/a-0717-5329 |
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author | Rath, Werner Kehl, Sven |
author_facet | Rath, Werner Kehl, Sven |
author_sort | Rath, Werner |
collection | PubMed |
description | Tocolysis is among the most common obstetric measures. The objective is to prolong the pregnancy by at least 48 hours to complete foetal lung maturation and for the in-utero transfer of the pregnant woman to a perinatal centre. The indication for tocolysis is regular, premature contractions (≥ 4/20 min) and a dynamic shortening of the cervical length/cervical opening between 22 + 0 to 33 + 6 weeks of pregnancy. In this connection, the cervical length measured on ultrasound and the determination of biomarkers in the cervicovaginal secretions can be important decision-making aids. Beta sympathomimetics should no longer be used due to the high rate of severe maternal adverse effects. Given controversial data, magnesium sulphate is no longer recommended for tocolysis in current guidelines. Atosiban is as effective for prolonging pregnancy as beta sympathomimetics and nifedipine, has the lowest rate of maternal adverse effects, but also the highest drug costs. Nifedipine and indomethacin are recommended in international guidelines for acute tocolysis, however there are indications of increased neonatal morbidity following indomethacin. Current problems are, above all, the lack of randomised, controlled comparative and placebo-controlled studies, the data which are controversial to some extent, and the insufficient evidence of tocolytics to significantly improve the neonatal outcome. |
format | Online Article Text |
id | pubmed-6294642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Georg Thieme Verlag KG |
record_format | MEDLINE/PubMed |
spelling | pubmed-62946422019-01-15 Acute Tocolysis – a Critical Analysis of Evidence-Based Data Rath, Werner Kehl, Sven Geburtshilfe Frauenheilkd Tocolysis is among the most common obstetric measures. The objective is to prolong the pregnancy by at least 48 hours to complete foetal lung maturation and for the in-utero transfer of the pregnant woman to a perinatal centre. The indication for tocolysis is regular, premature contractions (≥ 4/20 min) and a dynamic shortening of the cervical length/cervical opening between 22 + 0 to 33 + 6 weeks of pregnancy. In this connection, the cervical length measured on ultrasound and the determination of biomarkers in the cervicovaginal secretions can be important decision-making aids. Beta sympathomimetics should no longer be used due to the high rate of severe maternal adverse effects. Given controversial data, magnesium sulphate is no longer recommended for tocolysis in current guidelines. Atosiban is as effective for prolonging pregnancy as beta sympathomimetics and nifedipine, has the lowest rate of maternal adverse effects, but also the highest drug costs. Nifedipine and indomethacin are recommended in international guidelines for acute tocolysis, however there are indications of increased neonatal morbidity following indomethacin. Current problems are, above all, the lack of randomised, controlled comparative and placebo-controlled studies, the data which are controversial to some extent, and the insufficient evidence of tocolytics to significantly improve the neonatal outcome. Georg Thieme Verlag KG 2018-12 2018-12-14 /pmc/articles/PMC6294642/ /pubmed/30655648 http://dx.doi.org/10.1055/a-0717-5329 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Rath, Werner Kehl, Sven Acute Tocolysis – a Critical Analysis of Evidence-Based Data |
title | Acute Tocolysis – a Critical Analysis of Evidence-Based Data |
title_full | Acute Tocolysis – a Critical Analysis of Evidence-Based Data |
title_fullStr | Acute Tocolysis – a Critical Analysis of Evidence-Based Data |
title_full_unstemmed | Acute Tocolysis – a Critical Analysis of Evidence-Based Data |
title_short | Acute Tocolysis – a Critical Analysis of Evidence-Based Data |
title_sort | acute tocolysis – a critical analysis of evidence-based data |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294642/ https://www.ncbi.nlm.nih.gov/pubmed/30655648 http://dx.doi.org/10.1055/a-0717-5329 |
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