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Maternal venous hemodynamics in gestational hypertension and preeclampsia
BACKGROUND: To evaluate characteristics of venous hemodynamics, together with cardiac and arterial function, in uncomplicated pregnancies (UP), non-proteinuric gestational hypertension (GH) and preeclampsia (PE). METHODS: In this observational cross-sectional study, venous hemodynamics was assessed...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090345/ https://www.ncbi.nlm.nih.gov/pubmed/24957330 http://dx.doi.org/10.1186/1471-2393-14-212 |
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author | Gyselaers, Wilfried Tomsin, Kathleen Staelens, Anneleen Mesens, Tinne Oben, Jolien Molenberghs, Geert |
author_facet | Gyselaers, Wilfried Tomsin, Kathleen Staelens, Anneleen Mesens, Tinne Oben, Jolien Molenberghs, Geert |
author_sort | Gyselaers, Wilfried |
collection | PubMed |
description | BACKGROUND: To evaluate characteristics of venous hemodynamics, together with cardiac and arterial function, in uncomplicated pregnancies (UP), non-proteinuric gestational hypertension (GH) and preeclampsia (PE). METHODS: In this observational cross-sectional study, venous hemodynamics was assessed using a standardised protocol for combined electrocardiogram (ECG)-Doppler ultrasonography, together with a non-invasive standardised cardiovascular assessment using impedance cardiography (ICG) in 13 women with UP, 21 with GH, 34 with late onset PE ≥ 34 w (LPE) and 22 with early onset PE < 34 w (EPE). ECG-Doppler parameters were impedance index at the level of hepatic veins (HVI) and renal interlobar veins (RIVI) together with venous pulse transit times (VPTT), as well as resistive and pulsatility index, and arterial pulse transit time (APTT) at the level of uterine arcuate arteries. ICG parameters were aortic flow velocity index (VI), acceleration index (ACI) and thoracic fluid content. Mann Whitney U-test, Kruskall-Wallis test and linear regression analysis with heteroskedastic variance was used for statistical analysis. RESULTS: RIVI in both kidneys was >15% higher (P ≤ .010) in LPE and EPE, as compared to GH and UP. Next to this, >30% lower values for VI and ACI (P ≤ .029), and > 15% lower values for APTT (P ≤ .012) were found in GH, LPE and EPE, as compared to GH. CONCLUSION: In comparison to UP, similar abnormalities of central arterial function and APTT were found in GH, EPE and LPE. Proteinuria of LPE and EPE was associated with increased RIVI, this was not observed in GH. |
format | Online Article Text |
id | pubmed-4090345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40903452014-07-11 Maternal venous hemodynamics in gestational hypertension and preeclampsia Gyselaers, Wilfried Tomsin, Kathleen Staelens, Anneleen Mesens, Tinne Oben, Jolien Molenberghs, Geert BMC Pregnancy Childbirth Research Article BACKGROUND: To evaluate characteristics of venous hemodynamics, together with cardiac and arterial function, in uncomplicated pregnancies (UP), non-proteinuric gestational hypertension (GH) and preeclampsia (PE). METHODS: In this observational cross-sectional study, venous hemodynamics was assessed using a standardised protocol for combined electrocardiogram (ECG)-Doppler ultrasonography, together with a non-invasive standardised cardiovascular assessment using impedance cardiography (ICG) in 13 women with UP, 21 with GH, 34 with late onset PE ≥ 34 w (LPE) and 22 with early onset PE < 34 w (EPE). ECG-Doppler parameters were impedance index at the level of hepatic veins (HVI) and renal interlobar veins (RIVI) together with venous pulse transit times (VPTT), as well as resistive and pulsatility index, and arterial pulse transit time (APTT) at the level of uterine arcuate arteries. ICG parameters were aortic flow velocity index (VI), acceleration index (ACI) and thoracic fluid content. Mann Whitney U-test, Kruskall-Wallis test and linear regression analysis with heteroskedastic variance was used for statistical analysis. RESULTS: RIVI in both kidneys was >15% higher (P ≤ .010) in LPE and EPE, as compared to GH and UP. Next to this, >30% lower values for VI and ACI (P ≤ .029), and > 15% lower values for APTT (P ≤ .012) were found in GH, LPE and EPE, as compared to GH. CONCLUSION: In comparison to UP, similar abnormalities of central arterial function and APTT were found in GH, EPE and LPE. Proteinuria of LPE and EPE was associated with increased RIVI, this was not observed in GH. BioMed Central 2014-06-23 /pmc/articles/PMC4090345/ /pubmed/24957330 http://dx.doi.org/10.1186/1471-2393-14-212 Text en Copyright © 2014 Gyselaers et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Gyselaers, Wilfried Tomsin, Kathleen Staelens, Anneleen Mesens, Tinne Oben, Jolien Molenberghs, Geert Maternal venous hemodynamics in gestational hypertension and preeclampsia |
title | Maternal venous hemodynamics in gestational hypertension and preeclampsia |
title_full | Maternal venous hemodynamics in gestational hypertension and preeclampsia |
title_fullStr | Maternal venous hemodynamics in gestational hypertension and preeclampsia |
title_full_unstemmed | Maternal venous hemodynamics in gestational hypertension and preeclampsia |
title_short | Maternal venous hemodynamics in gestational hypertension and preeclampsia |
title_sort | maternal venous hemodynamics in gestational hypertension and preeclampsia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090345/ https://www.ncbi.nlm.nih.gov/pubmed/24957330 http://dx.doi.org/10.1186/1471-2393-14-212 |
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