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Maternal HCV infection is associated with intrauterine fetal growth disturbance: A meta-analysis of observational studies
Since the evidence regarding the association between maternal hepatitis C virus (HCV) infection and impaired intrauterine fetal growth had not been conclusive, the aim of the present study was to evaluate the risk of maternal HCV infection in association with intrauterine fetal growth restriction (I...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008616/ https://www.ncbi.nlm.nih.gov/pubmed/27583932 http://dx.doi.org/10.1097/MD.0000000000004777 |
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author | Huang, Qi-tao Hang, Li-lin Zhong, Mei Gao, Yun-fei Luo, Man-ling Yu, Yan-hong |
author_facet | Huang, Qi-tao Hang, Li-lin Zhong, Mei Gao, Yun-fei Luo, Man-ling Yu, Yan-hong |
author_sort | Huang, Qi-tao |
collection | PubMed |
description | Since the evidence regarding the association between maternal hepatitis C virus (HCV) infection and impaired intrauterine fetal growth had not been conclusive, the aim of the present study was to evaluate the risk of maternal HCV infection in association with intrauterine fetal growth restriction (IUGR) and/or low birth weight infants (LBW). We performed an extensive literature search of PubMed, MEDLINE, and EMBASE through December 1, 2015. The odds ratios (ORs) of HCV infection and IUGR/LBW were calculated and reported with 95% confidence intervals (95% CIs). Statistical analysis was performed using RevMen 5.3 and Stata 10.0. Seven studies involving 4,185,414 participants and 5094 HCV infection cases were included. Significant associations between HCV infection and IUGR (OR = 1.53, 95% CI: 1.40–1.68, fixed effect model) as well as LBW were observed (OR = 1.97, 95% CI: 1.43–2.71, random effect model). The results still indicated consistencies after adjusting for multiple risk factors which could affect fetal growth, including maternal age, parity, maternal smoking, alcohol abuse, drugs abuse, coinfected with HBV/HIV and preeclampsia. Our findings suggested that maternal HCV infection was significantly associated with an increased risk of impaired intrauterine fetal growth. In clinical practice, a closer monitoring of intrauterine fetal growth by a series of ultrasound might be necessary for HCV-infected pregnant population. |
format | Online Article Text |
id | pubmed-5008616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-50086162016-09-10 Maternal HCV infection is associated with intrauterine fetal growth disturbance: A meta-analysis of observational studies Huang, Qi-tao Hang, Li-lin Zhong, Mei Gao, Yun-fei Luo, Man-ling Yu, Yan-hong Medicine (Baltimore) 5600 Since the evidence regarding the association between maternal hepatitis C virus (HCV) infection and impaired intrauterine fetal growth had not been conclusive, the aim of the present study was to evaluate the risk of maternal HCV infection in association with intrauterine fetal growth restriction (IUGR) and/or low birth weight infants (LBW). We performed an extensive literature search of PubMed, MEDLINE, and EMBASE through December 1, 2015. The odds ratios (ORs) of HCV infection and IUGR/LBW were calculated and reported with 95% confidence intervals (95% CIs). Statistical analysis was performed using RevMen 5.3 and Stata 10.0. Seven studies involving 4,185,414 participants and 5094 HCV infection cases were included. Significant associations between HCV infection and IUGR (OR = 1.53, 95% CI: 1.40–1.68, fixed effect model) as well as LBW were observed (OR = 1.97, 95% CI: 1.43–2.71, random effect model). The results still indicated consistencies after adjusting for multiple risk factors which could affect fetal growth, including maternal age, parity, maternal smoking, alcohol abuse, drugs abuse, coinfected with HBV/HIV and preeclampsia. Our findings suggested that maternal HCV infection was significantly associated with an increased risk of impaired intrauterine fetal growth. In clinical practice, a closer monitoring of intrauterine fetal growth by a series of ultrasound might be necessary for HCV-infected pregnant population. Wolters Kluwer Health 2016-09-02 /pmc/articles/PMC5008616/ /pubmed/27583932 http://dx.doi.org/10.1097/MD.0000000000004777 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-nc-sa/4.0 |
spellingShingle | 5600 Huang, Qi-tao Hang, Li-lin Zhong, Mei Gao, Yun-fei Luo, Man-ling Yu, Yan-hong Maternal HCV infection is associated with intrauterine fetal growth disturbance: A meta-analysis of observational studies |
title | Maternal HCV infection is associated with intrauterine fetal growth disturbance: A meta-analysis of observational studies |
title_full | Maternal HCV infection is associated with intrauterine fetal growth disturbance: A meta-analysis of observational studies |
title_fullStr | Maternal HCV infection is associated with intrauterine fetal growth disturbance: A meta-analysis of observational studies |
title_full_unstemmed | Maternal HCV infection is associated with intrauterine fetal growth disturbance: A meta-analysis of observational studies |
title_short | Maternal HCV infection is associated with intrauterine fetal growth disturbance: A meta-analysis of observational studies |
title_sort | maternal hcv infection is associated with intrauterine fetal growth disturbance: a meta-analysis of observational studies |
topic | 5600 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008616/ https://www.ncbi.nlm.nih.gov/pubmed/27583932 http://dx.doi.org/10.1097/MD.0000000000004777 |
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