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Hospital admission for hyperemesis gravidarum in women at increased risk of spontaneous preterm birth
BACKGROUND: Progesterone administration prevents spontaneous preterm birth (sPTB) in women at increased risk. Progesterone concentration is lower in women with subsequent sPTB. Conversely, high concentrations of progesterone are implicated in the pathogenesis of hyperemesis gravidarum (HG). We hypot...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697573/ https://www.ncbi.nlm.nih.gov/pubmed/28857251 http://dx.doi.org/10.1111/birt.12303 |
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author | Kleine, Ira Da Silva, Ana Ahmed, Wafaa Forya, Frida Whitten, Sara M. David, Anna L. James, Catherine P. |
author_facet | Kleine, Ira Da Silva, Ana Ahmed, Wafaa Forya, Frida Whitten, Sara M. David, Anna L. James, Catherine P. |
author_sort | Kleine, Ira |
collection | PubMed |
description | BACKGROUND: Progesterone administration prevents spontaneous preterm birth (sPTB) in women at increased risk. Progesterone concentration is lower in women with subsequent sPTB. Conversely, high concentrations of progesterone are implicated in the pathogenesis of hyperemesis gravidarum (HG). We hypothesized that women at increased risk of sPTB or spontaneous late miscarriage would be less likely to have a diagnosis of HG. To explore this hypothesis, we compared the incidence of HG in women at increased risk of sPTB and women with no identifiable risk factors. METHODS: Women at increased risk of sPTB were identified from a specialist Preterm Birth Clinic (PTBC) database where criteria for PTBC attendance are previous cervical surgery, previous sPTB <34 weeks, previous spontaneous late miscarriage, incidental sonographic cervical shortening, and uterine anomaly. Hospital antenatal booking and coding records for the same time period were examined to identify HG admissions. Women with multiple gestations, trophoblastic disease, or pre‐existing abnormal thyroid function were excluded. The incidence of HG among PTBC (n=394) and non‐PTBC attendees (n=4762) was calculated. RESULTS: The incidence of HG was lower in women at increased risk of sPTB (1.52%, n=6) compared with women with no identifiable risk factor for sPTB (3.33%, n=159; P=.049). CONCLUSION: Hospital admission for HG is reduced in women with risk factors for sPTB compared with those without risk factors. Exploration of the pathogenesis of HG may improve understanding of the mechanisms underlying sPTB. |
format | Online Article Text |
id | pubmed-5697573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56975732017-11-28 Hospital admission for hyperemesis gravidarum in women at increased risk of spontaneous preterm birth Kleine, Ira Da Silva, Ana Ahmed, Wafaa Forya, Frida Whitten, Sara M. David, Anna L. James, Catherine P. Birth Original Articles BACKGROUND: Progesterone administration prevents spontaneous preterm birth (sPTB) in women at increased risk. Progesterone concentration is lower in women with subsequent sPTB. Conversely, high concentrations of progesterone are implicated in the pathogenesis of hyperemesis gravidarum (HG). We hypothesized that women at increased risk of sPTB or spontaneous late miscarriage would be less likely to have a diagnosis of HG. To explore this hypothesis, we compared the incidence of HG in women at increased risk of sPTB and women with no identifiable risk factors. METHODS: Women at increased risk of sPTB were identified from a specialist Preterm Birth Clinic (PTBC) database where criteria for PTBC attendance are previous cervical surgery, previous sPTB <34 weeks, previous spontaneous late miscarriage, incidental sonographic cervical shortening, and uterine anomaly. Hospital antenatal booking and coding records for the same time period were examined to identify HG admissions. Women with multiple gestations, trophoblastic disease, or pre‐existing abnormal thyroid function were excluded. The incidence of HG among PTBC (n=394) and non‐PTBC attendees (n=4762) was calculated. RESULTS: The incidence of HG was lower in women at increased risk of sPTB (1.52%, n=6) compared with women with no identifiable risk factor for sPTB (3.33%, n=159; P=.049). CONCLUSION: Hospital admission for HG is reduced in women with risk factors for sPTB compared with those without risk factors. Exploration of the pathogenesis of HG may improve understanding of the mechanisms underlying sPTB. John Wiley and Sons Inc. 2017-08-30 2017-12 /pmc/articles/PMC5697573/ /pubmed/28857251 http://dx.doi.org/10.1111/birt.12303 Text en © 2017 the Authors. Birth published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://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 Articles Kleine, Ira Da Silva, Ana Ahmed, Wafaa Forya, Frida Whitten, Sara M. David, Anna L. James, Catherine P. Hospital admission for hyperemesis gravidarum in women at increased risk of spontaneous preterm birth |
title | Hospital admission for hyperemesis gravidarum in women at increased risk of spontaneous preterm birth |
title_full | Hospital admission for hyperemesis gravidarum in women at increased risk of spontaneous preterm birth |
title_fullStr | Hospital admission for hyperemesis gravidarum in women at increased risk of spontaneous preterm birth |
title_full_unstemmed | Hospital admission for hyperemesis gravidarum in women at increased risk of spontaneous preterm birth |
title_short | Hospital admission for hyperemesis gravidarum in women at increased risk of spontaneous preterm birth |
title_sort | hospital admission for hyperemesis gravidarum in women at increased risk of spontaneous preterm birth |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697573/ https://www.ncbi.nlm.nih.gov/pubmed/28857251 http://dx.doi.org/10.1111/birt.12303 |
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