The impact of intrahepatic cholestasis on pregnancy outcomes: a retrospective cohort study
This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China. Cases of pregnant women monitored by antepartum testing at Hangzhou Women's Hospital from January 2018 to December 2020 were reviewed. Subjects were classified into two gr...
Saved in:
Published in | BMC gastroenterology Vol. 23; no. 1; pp. 16 - 11 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central Ltd
18.01.2023
BioMed Central BMC |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China.
Cases of pregnant women monitored by antepartum testing at Hangzhou Women's Hospital from January 2018 to December 2020 were reviewed. Subjects were classified into two groups according to whether they had ICP: 688 cases of ICP were assigned to an exposure group while 38,556 cases of non-ICP were assigned to a non-exposed group. Univariate analysis was performed on qualitative or quantitative data using the Chi-Squared test or Mann-Whitney U test, and the adjusted odds ratio (aOR) and 95% confidence interval (CI) of the two groups of related variables were calculated by multivariate binary logistic regression analysis.
The incidence rate of ICP was 1.75%. Pregnant women with hepatitis B virus were correlated with ICP. Hepatitis B carriers (aOR = 3.873), preeclampsia (PE, aOR = 3.712), thrombocytopenia (aOR = 1.992), gestational hypertension (GH, aOR = 1.627), hyperlipidemia (aOR = 1.602) and gestational diabetes mellitus (GDM, aOR = 1.265) were all risk factors for ICP. In contrast, Body Mass Index (BMI) ≥ 30 kg/m
(aOR = 0.446), 25 m
< maternal BMI < 29.9 kg/m
(aOR = 0.699) and parity ≥ 1 (aOR = 0.722) were protective factors for ICP. Pregnant women in the ICP group had an increased risk of gestation days < 259 days (aOR = 4.574) and cesarean delivery (aOR = 1.930) after ICP, and a decreased risk of longer gestational days (aOR = 0.105), premature rupture of membranes (aOR = 0.384) and fetal macrosomia (aOR = 0.551).
By analyzing a Chinese population with ICP, we identified that pregnant women who are hepatitis B carriers or with PE, thrombocytopenia, GH, hyperlipidemia, and GDM are at higher risk of ICP. Moreover, ICP is associated with adverse pregnancy outcomes; in particular, ICP may increase the incidence of shorter gestational days and non-vaginal delivery methods such as cesarean section but reduce the incidence of premature rupture of membranes and fetal macrosomia. |
---|---|
AbstractList | Abstract Background This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China. Methods Cases of pregnant women monitored by antepartum testing at Hangzhou Women’s Hospital from January 2018 to December 2020 were reviewed. Subjects were classified into two groups according to whether they had ICP: 688 cases of ICP were assigned to an exposure group while 38,556 cases of non-ICP were assigned to a non-exposed group. Univariate analysis was performed on qualitative or quantitative data using the Chi-Squared test or Mann–Whitney U test, and the adjusted odds ratio (aOR) and 95% confidence interval (CI) of the two groups of related variables were calculated by multivariate binary logistic regression analysis. Results The incidence rate of ICP was 1.75%. Pregnant women with hepatitis B virus were correlated with ICP. Hepatitis B carriers (aOR = 3.873), preeclampsia (PE, aOR = 3.712), thrombocytopenia (aOR = 1.992), gestational hypertension (GH, aOR = 1.627), hyperlipidemia (aOR = 1.602) and gestational diabetes mellitus (GDM, aOR = 1.265) were all risk factors for ICP. In contrast, Body Mass Index (BMI) ≥ 30 kg/m2 (aOR = 0.446), 25 m2 < maternal BMI < 29.9 kg/m2 (aOR = 0.699) and parity ≥ 1 (aOR = 0.722) were protective factors for ICP. Pregnant women in the ICP group had an increased risk of gestation days < 259 days (aOR = 4.574) and cesarean delivery (aOR = 1.930) after ICP, and a decreased risk of longer gestational days (aOR = 0.105), premature rupture of membranes (aOR = 0.384) and fetal macrosomia (aOR = 0.551). Conclusions By analyzing a Chinese population with ICP, we identified that pregnant women who are hepatitis B carriers or with PE, thrombocytopenia, GH, hyperlipidemia, and GDM are at higher risk of ICP. Moreover, ICP is associated with adverse pregnancy outcomes; in particular, ICP may increase the incidence of shorter gestational days and non-vaginal delivery methods such as cesarean section but reduce the incidence of premature rupture of membranes and fetal macrosomia. This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China. Cases of pregnant women monitored by antepartum testing at Hangzhou Women's Hospital from January 2018 to December 2020 were reviewed. Subjects were classified into two groups according to whether they had ICP: 688 cases of ICP were assigned to an exposure group while 38,556 cases of non-ICP were assigned to a non-exposed group. Univariate analysis was performed on qualitative or quantitative data using the Chi-Squared test or Mann-Whitney U test, and the adjusted odds ratio (aOR) and 95% confidence interval (CI) of the two groups of related variables were calculated by multivariate binary logistic regression analysis. The incidence rate of ICP was 1.75%. Pregnant women with hepatitis B virus were correlated with ICP. Hepatitis B carriers (aOR = 3.873), preeclampsia (PE, aOR = 3.712), thrombocytopenia (aOR = 1.992), gestational hypertension (GH, aOR = 1.627), hyperlipidemia (aOR = 1.602) and gestational diabetes mellitus (GDM, aOR = 1.265) were all risk factors for ICP. In contrast, Body Mass Index (BMI) [greater than or equal to] 30 kg/m.sup.2 (aOR = 0.446), 25 m.sup.2 < maternal BMI < 29.9 kg/m.sup.2 (aOR = 0.699) and parity [greater than or equal to] 1 (aOR = 0.722) were protective factors for ICP. Pregnant women in the ICP group had an increased risk of gestation days < 259 days (aOR = 4.574) and cesarean delivery (aOR = 1.930) after ICP, and a decreased risk of longer gestational days (aOR = 0.105), premature rupture of membranes (aOR = 0.384) and fetal macrosomia (aOR = 0.551). By analyzing a Chinese population with ICP, we identified that pregnant women who are hepatitis B carriers or with PE, thrombocytopenia, GH, hyperlipidemia, and GDM are at higher risk of ICP. Moreover, ICP is associated with adverse pregnancy outcomes; in particular, ICP may increase the incidence of shorter gestational days and non-vaginal delivery methods such as cesarean section but reduce the incidence of premature rupture of membranes and fetal macrosomia. This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China. Cases of pregnant women monitored by antepartum testing at Hangzhou Women's Hospital from January 2018 to December 2020 were reviewed. Subjects were classified into two groups according to whether they had ICP: 688 cases of ICP were assigned to an exposure group while 38,556 cases of non-ICP were assigned to a non-exposed group. Univariate analysis was performed on qualitative or quantitative data using the Chi-Squared test or Mann-Whitney U test, and the adjusted odds ratio (aOR) and 95% confidence interval (CI) of the two groups of related variables were calculated by multivariate binary logistic regression analysis. The incidence rate of ICP was 1.75%. Pregnant women with hepatitis B virus were correlated with ICP. Hepatitis B carriers (aOR = 3.873), preeclampsia (PE, aOR = 3.712), thrombocytopenia (aOR = 1.992), gestational hypertension (GH, aOR = 1.627), hyperlipidemia (aOR = 1.602) and gestational diabetes mellitus (GDM, aOR = 1.265) were all risk factors for ICP. In contrast, Body Mass Index (BMI) ≥ 30 kg/m (aOR = 0.446), 25 m < maternal BMI < 29.9 kg/m (aOR = 0.699) and parity ≥ 1 (aOR = 0.722) were protective factors for ICP. Pregnant women in the ICP group had an increased risk of gestation days < 259 days (aOR = 4.574) and cesarean delivery (aOR = 1.930) after ICP, and a decreased risk of longer gestational days (aOR = 0.105), premature rupture of membranes (aOR = 0.384) and fetal macrosomia (aOR = 0.551). By analyzing a Chinese population with ICP, we identified that pregnant women who are hepatitis B carriers or with PE, thrombocytopenia, GH, hyperlipidemia, and GDM are at higher risk of ICP. Moreover, ICP is associated with adverse pregnancy outcomes; in particular, ICP may increase the incidence of shorter gestational days and non-vaginal delivery methods such as cesarean section but reduce the incidence of premature rupture of membranes and fetal macrosomia. This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China.BACKGROUNDThis study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China.Cases of pregnant women monitored by antepartum testing at Hangzhou Women's Hospital from January 2018 to December 2020 were reviewed. Subjects were classified into two groups according to whether they had ICP: 688 cases of ICP were assigned to an exposure group while 38,556 cases of non-ICP were assigned to a non-exposed group. Univariate analysis was performed on qualitative or quantitative data using the Chi-Squared test or Mann-Whitney U test, and the adjusted odds ratio (aOR) and 95% confidence interval (CI) of the two groups of related variables were calculated by multivariate binary logistic regression analysis.METHODSCases of pregnant women monitored by antepartum testing at Hangzhou Women's Hospital from January 2018 to December 2020 were reviewed. Subjects were classified into two groups according to whether they had ICP: 688 cases of ICP were assigned to an exposure group while 38,556 cases of non-ICP were assigned to a non-exposed group. Univariate analysis was performed on qualitative or quantitative data using the Chi-Squared test or Mann-Whitney U test, and the adjusted odds ratio (aOR) and 95% confidence interval (CI) of the two groups of related variables were calculated by multivariate binary logistic regression analysis.The incidence rate of ICP was 1.75%. Pregnant women with hepatitis B virus were correlated with ICP. Hepatitis B carriers (aOR = 3.873), preeclampsia (PE, aOR = 3.712), thrombocytopenia (aOR = 1.992), gestational hypertension (GH, aOR = 1.627), hyperlipidemia (aOR = 1.602) and gestational diabetes mellitus (GDM, aOR = 1.265) were all risk factors for ICP. In contrast, Body Mass Index (BMI) ≥ 30 kg/m2 (aOR = 0.446), 25 m2 < maternal BMI < 29.9 kg/m2 (aOR = 0.699) and parity ≥ 1 (aOR = 0.722) were protective factors for ICP. Pregnant women in the ICP group had an increased risk of gestation days < 259 days (aOR = 4.574) and cesarean delivery (aOR = 1.930) after ICP, and a decreased risk of longer gestational days (aOR = 0.105), premature rupture of membranes (aOR = 0.384) and fetal macrosomia (aOR = 0.551).RESULTSThe incidence rate of ICP was 1.75%. Pregnant women with hepatitis B virus were correlated with ICP. Hepatitis B carriers (aOR = 3.873), preeclampsia (PE, aOR = 3.712), thrombocytopenia (aOR = 1.992), gestational hypertension (GH, aOR = 1.627), hyperlipidemia (aOR = 1.602) and gestational diabetes mellitus (GDM, aOR = 1.265) were all risk factors for ICP. In contrast, Body Mass Index (BMI) ≥ 30 kg/m2 (aOR = 0.446), 25 m2 < maternal BMI < 29.9 kg/m2 (aOR = 0.699) and parity ≥ 1 (aOR = 0.722) were protective factors for ICP. Pregnant women in the ICP group had an increased risk of gestation days < 259 days (aOR = 4.574) and cesarean delivery (aOR = 1.930) after ICP, and a decreased risk of longer gestational days (aOR = 0.105), premature rupture of membranes (aOR = 0.384) and fetal macrosomia (aOR = 0.551).By analyzing a Chinese population with ICP, we identified that pregnant women who are hepatitis B carriers or with PE, thrombocytopenia, GH, hyperlipidemia, and GDM are at higher risk of ICP. Moreover, ICP is associated with adverse pregnancy outcomes; in particular, ICP may increase the incidence of shorter gestational days and non-vaginal delivery methods such as cesarean section but reduce the incidence of premature rupture of membranes and fetal macrosomia.CONCLUSIONSBy analyzing a Chinese population with ICP, we identified that pregnant women who are hepatitis B carriers or with PE, thrombocytopenia, GH, hyperlipidemia, and GDM are at higher risk of ICP. Moreover, ICP is associated with adverse pregnancy outcomes; in particular, ICP may increase the incidence of shorter gestational days and non-vaginal delivery methods such as cesarean section but reduce the incidence of premature rupture of membranes and fetal macrosomia. Background This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China. Methods Cases of pregnant women monitored by antepartum testing at Hangzhou Women's Hospital from January 2018 to December 2020 were reviewed. Subjects were classified into two groups according to whether they had ICP: 688 cases of ICP were assigned to an exposure group while 38,556 cases of non-ICP were assigned to a non-exposed group. Univariate analysis was performed on qualitative or quantitative data using the Chi-Squared test or Mann-Whitney U test, and the adjusted odds ratio (aOR) and 95% confidence interval (CI) of the two groups of related variables were calculated by multivariate binary logistic regression analysis. Results The incidence rate of ICP was 1.75%. Pregnant women with hepatitis B virus were correlated with ICP. Hepatitis B carriers (aOR = 3.873), preeclampsia (PE, aOR = 3.712), thrombocytopenia (aOR = 1.992), gestational hypertension (GH, aOR = 1.627), hyperlipidemia (aOR = 1.602) and gestational diabetes mellitus (GDM, aOR = 1.265) were all risk factors for ICP. In contrast, Body Mass Index (BMI) [greater than or equal to] 30 kg/m.sup.2 (aOR = 0.446), 25 m.sup.2 < maternal BMI < 29.9 kg/m.sup.2 (aOR = 0.699) and parity [greater than or equal to] 1 (aOR = 0.722) were protective factors for ICP. Pregnant women in the ICP group had an increased risk of gestation days < 259 days (aOR = 4.574) and cesarean delivery (aOR = 1.930) after ICP, and a decreased risk of longer gestational days (aOR = 0.105), premature rupture of membranes (aOR = 0.384) and fetal macrosomia (aOR = 0.551). Conclusions By analyzing a Chinese population with ICP, we identified that pregnant women who are hepatitis B carriers or with PE, thrombocytopenia, GH, hyperlipidemia, and GDM are at higher risk of ICP. Moreover, ICP is associated with adverse pregnancy outcomes; in particular, ICP may increase the incidence of shorter gestational days and non-vaginal delivery methods such as cesarean section but reduce the incidence of premature rupture of membranes and fetal macrosomia. Keywords: Intrahepatic cholestasis of pregnancy, Fetal intrauterine growth restriction, Thrombocytopenia, Hyperlipidemia, Premature rupture of membranes, Low birth weight infants, Odds ratio, Pregnancy outcomes |
ArticleNumber | 16 |
Audience | Academic |
Author | Ning, Wenwen Zhang, Huimin Chen, Yijie Chen, Yiming Wen, Caihe |
Author_xml | – sequence: 1 givenname: Yiming surname: Chen fullname: Chen, Yiming – sequence: 2 givenname: Huimin surname: Zhang fullname: Zhang, Huimin – sequence: 3 givenname: Wenwen surname: Ning fullname: Ning, Wenwen – sequence: 4 givenname: Yijie surname: Chen fullname: Chen, Yijie – sequence: 5 givenname: Caihe surname: Wen fullname: Wen, Caihe |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36653757$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kstq3TAQhk1JaS7tC3RRBN1041Q3S3IXhRB6CQS6SaF0I2R5dI6CbbmSTuC8feU4DTmlFCEkRt_8zIz-0-poChNU1WuCzwlR4n0iVElRY8rKFg2t2bPqhHBJasrwj6Mn9-PqNKVbjIlUlL2ojpkQDZONPKl-3mwB-XE2NqPgkJ9yNFuYTfYW2W0YIGWTfEJhQnOEzWQmu0dhl20YIX1ABkXIMaQZbPZ3gGzYhphRyrt-_7J67syQ4NXDeVZ9__zp5vJrff3ty9XlxXVtuWhyzY1x3LS4b7ljLcNdyzrJDGVkiTPpMEjRW44tl93SUSsU6QkDwmnHLWVn1dWq2wdzq-foRxP3Ohiv7wMhbrSJpZ8BNG-saVTfg1OKO6xM54gUQEA0SlDGitbHVWvedSP0FpZ5DAeihy-T3-pNuNOtKpUJUgTePQjE8GtXpqdHnywMg5kg7JKmUhROMSoK-nZFN6aU5icXiqJdcH0hGZO8LbUV6vwfVFk9jN4WQzhf4gcJb5628Fj7nz8vAF0BWz4uRXCPCMF6MZZejaWLsfS9sfQyGPVXkvW5uCQsY_DD_1J_A-fT0i0 |
CitedBy_id | crossref_primary_10_1177_1753495X241265772 crossref_primary_10_1371_journal_pone_0304604 crossref_primary_10_1007_s43032_023_01329_2 crossref_primary_10_1177_1753495X241258385 crossref_primary_10_1002_ijgo_15016 crossref_primary_10_3389_fcvm_2024_1401010 crossref_primary_10_1371_journal_pone_0300076 crossref_primary_10_1097_FM9_0000000000000207 crossref_primary_10_31083_j_ceog5102036 crossref_primary_10_1186_s12916_025_03935_0 crossref_primary_10_1016_j_iliver_2023_11_001 crossref_primary_10_1590_1806_9282_20240860 crossref_primary_10_1111_jmwh_13640 |
Cites_doi | 10.1586/17474124.2015.1083857 10.4103/0019-5154.113971 10.1016/S2468-1253(21)00074-1 10.1097/01.AOG.0000435415.21944.8f 10.1111/1471-0528.12174 10.1016/j.ajog.2012.05.011 10.1097/AOG.0000000000000346 10.1016/j.ajog.2015.10.931 10.1287/isre.2013.0480 10.1097/MD.0000000000021416 10.3748/wjg.15.2049 10.1016/j.placenta.2021.09.014 10.1177/1753495X18797749 10.1016/S0140-6736(03)14896-9 10.1080/14767058.2017.1332036 10.1055/s-0039-3402724 10.1111/jvh.13105 10.1007/s00404-016-4019-8 10.1097/OGX.0000000000000524 10.1016/j.ijgo.2010.11.002 10.2337/dc14-2143 10.1016/j.ejogrb.2013.12.037 10.1017/S0950268822001388 10.1542/peds.2005-1801 10.1016/S0002-9378(96)80031-7 10.1371/journal.pone.0228213 10.1016/j.srhc.2012.11.005 10.1016/j.ejogrb.2017.09.012 10.3109/14767058.2014.984605 10.1038/s41598-018-22387-6 10.1016/j.ajog.2015.05.011 10.1007/s00404-020-05456-y 10.3109/01443615.2014.968102 10.1111/jog.13681 10.1111/jvh.13472 |
ContentType | Journal Article |
Copyright | 2023. The Author(s). COPYRIGHT 2023 BioMed Central Ltd. The Author(s) 2023 |
Copyright_xml | – notice: 2023. The Author(s). – notice: COPYRIGHT 2023 BioMed Central Ltd. – notice: The Author(s) 2023 |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 5PM DOA |
DOI | 10.1186/s12876-023-02652-3 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 3 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1471-230X |
EndPage | 11 |
ExternalDocumentID | oai_doaj_org_article_45ca58ddef884f08abf176e1e6586233 PMC9847161 A733749176 36653757 10_1186_s12876_023_02652_3 |
Genre | Journal Article |
GeographicLocations | China |
GeographicLocations_xml | – name: China |
GrantInformation_xml | – fundername: Zhejiang Medicine and Health Scientific Research Project grantid: 2021KY258 – fundername: ; grantid: 2021KY258; 2021KY258 |
GroupedDBID | --- 0R~ 23N 2WC 53G 5VS 6J9 6PF 7X7 88E 8FI 8FJ AAFWJ AAJSJ AASML AAWTL AAYXX ABDBF ABUWG ACGFO ACGFS ACIHN ACIWK ACPRK ACUHS ADBBV ADRAZ ADUKV AEAQA AENEX AFKRA AFPKN AHBYD AHMBA AHYZX ALIPV ALMA_UNASSIGNED_HOLDINGS AMKLP AMTXH AOIJS BAPOH BAWUL BCNDV BENPR BFQNJ BMC BPHCQ BVXVI C6C CCPQU CITATION CS3 DIK E3Z EAD EAP EAS EBD EBLON EBS EMB EMK EMOBN ESX F5P FYUFA GROUPED_DOAJ GX1 HMCUK HYE IAO IHR INH INR ITC KQ8 M1P M48 M~E O5R O5S OK1 OVT P2P PHGZM PHGZT PIMPY PQQKQ PROAC PSQYO RBZ RNS ROL RPM RSV SMD SOJ SV3 TR2 TUS UKHRP W2D WOQ WOW XSB -A0 3V. ACRMQ ADINQ C24 CGR CUY CVF ECM EIF NPM PMFND 7X8 PPXIY 5PM PJZUB PUEGO |
ID | FETCH-LOGICAL-c465t-4aaf4a90d94f3930b93b73a231af4a37f0e76dc40c47b14719681d13e142b4c23 |
IEDL.DBID | M48 |
ISSN | 1471-230X |
IngestDate | Wed Aug 27 01:21:42 EDT 2025 Thu Aug 21 18:39:10 EDT 2025 Fri Jul 11 13:41:56 EDT 2025 Tue Jun 17 21:29:46 EDT 2025 Tue Jun 10 20:40:50 EDT 2025 Thu Jan 02 22:52:48 EST 2025 Tue Jul 01 04:12:10 EDT 2025 Thu Apr 24 23:00:13 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Keywords | Thrombocytopenia Intrahepatic cholestasis of pregnancy Premature rupture of membranes Hyperlipidemia Pregnancy outcomes Odds ratio Fetal intrauterine growth restriction Low birth weight infants |
Language | English |
License | 2023. The Author(s). Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c465t-4aaf4a90d94f3930b93b73a231af4a37f0e76dc40c47b14719681d13e142b4c23 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.1186/s12876-023-02652-3 |
PMID | 36653757 |
PQID | 2767168326 |
PQPubID | 23479 |
PageCount | 11 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_45ca58ddef884f08abf176e1e6586233 pubmedcentral_primary_oai_pubmedcentral_nih_gov_9847161 proquest_miscellaneous_2767168326 gale_infotracmisc_A733749176 gale_infotracacademiconefile_A733749176 pubmed_primary_36653757 crossref_primary_10_1186_s12876_023_02652_3 crossref_citationtrail_10_1186_s12876_023_02652_3 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2023-01-18 |
PublicationDateYYYYMMDD | 2023-01-18 |
PublicationDate_xml | – month: 01 year: 2023 text: 2023-01-18 day: 18 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: London |
PublicationTitle | BMC gastroenterology |
PublicationTitleAlternate | BMC Gastroenterol |
PublicationYear | 2023 |
Publisher | BioMed Central Ltd BioMed Central BMC |
Publisher_xml | – name: BioMed Central Ltd – name: BioMed Central – name: BMC |
References | EA Wikström Shemer (2652_CR28) 2013; 4 2652_CR14 Y Chen (2652_CR19) 2022; 150 2652_CR16 2652_CR38 NH Anderson (2652_CR17) 2016; 214 R Madazli (2652_CR29) 2015; 35 D Sitaula (2652_CR21) 2021; 19 C Williamson (2652_CR1) 2014; 124 V Geenes (2652_CR8) 2009; 15 C Haitian (2652_CR13) 2020; 36 FW Gardiner (2652_CR22) 2019; 12 AK Friberg (2652_CR27) 2016; 294 AM Wood (2652_CR6) 2018; 73 D Shan (2652_CR5) 2021; 115 Y Raz (2652_CR35) 2015; 213 M Martineau (2652_CR42) 2014; 176 Y Yue (2652_CR4) 2018; 44 Q Cai (2652_CR26) 2019; 26 2652_CR12 L Jacob (2652_CR32) 2016; 14 D Baliutavičiene (2652_CR37) 2011; 112 C Ovadia (2652_CR2) 2021; 6 R Ehsanipoor (2652_CR15) 2013; 122 2652_CR30 MG Martineau (2652_CR41) 2015; 38 C Arthuis (2652_CR7) 2020; 15 M Lin (2652_CR44) 2013; 24 OM Alsulyman (2652_CR9) 1996; 175 S Heinonen (2652_CR31) 1999; 94 C Feng (2652_CR43) 2018; 8 CA Herrera (2652_CR10) 2018; 31 M Mor (2652_CR34) 2020; 301 E Zecca (2652_CR39) 2006; 117 2652_CR3 O Subgroup (2652_CR11) 2015; 50 F Crispi (2652_CR18) 2012; 207 R Jiang (2652_CR24) 2020; 99 E Wikström Shemer (2652_CR36) 2013; 120 S Ghosh (2652_CR20) 2013; 58 Y Xiong (2652_CR25) 2021; 28 GC Smith (2652_CR33) 2003; 362 JA Marathe (2652_CR23) 2017; 218 Y Zhang (2652_CR40) 2021; 38 |
References_xml | – ident: 2652_CR3 doi: 10.1586/17474124.2015.1083857 – volume: 58 start-page: 327 issue: 4 year: 2013 ident: 2652_CR20 publication-title: Indian J Dermatol doi: 10.4103/0019-5154.113971 – volume: 36 start-page: 1003 issue: 12 year: 2020 ident: 2652_CR13 publication-title: Chin J Endocrinol Metab – volume: 6 start-page: 547 issue: 7 year: 2021 ident: 2652_CR2 publication-title: Lancet Gastroenterol Hepatol doi: 10.1016/S2468-1253(21)00074-1 – volume: 122 start-page: 918 issue: 4 year: 2013 ident: 2652_CR15 publication-title: Obs Gynecol doi: 10.1097/01.AOG.0000435415.21944.8f – volume: 120 start-page: 717 issue: 6 year: 2013 ident: 2652_CR36 publication-title: BJOG An Int J Obstet Gynaecol doi: 10.1111/1471-0528.12174 – ident: 2652_CR12 – volume: 207 start-page: 121.e1 issue: 2 year: 2012 ident: 2652_CR18 publication-title: Am J Obstet Gynecol doi: 10.1016/j.ajog.2012.05.011 – volume: 124 start-page: 120 issue: 1 year: 2014 ident: 2652_CR1 publication-title: Obstet Gynecol doi: 10.1097/AOG.0000000000000346 – volume: 19 start-page: 321 issue: 2 year: 2021 ident: 2652_CR21 publication-title: J Nepal Health Res Counc – volume: 214 start-page: 509.e1 issue: 4 year: 2016 ident: 2652_CR17 publication-title: Am J Obstet Gynecol doi: 10.1016/j.ajog.2015.10.931 – volume: 24 start-page: 906 issue: 4 year: 2013 ident: 2652_CR44 publication-title: Inf Syst Res doi: 10.1287/isre.2013.0480 – volume: 99 start-page: E21416 issue: 31 year: 2020 ident: 2652_CR24 publication-title: Medicine (Baltimore) doi: 10.1097/MD.0000000000021416 – volume: 15 start-page: 2049 issue: 17 year: 2009 ident: 2652_CR8 publication-title: World J Gastroenterol doi: 10.3748/wjg.15.2049 – volume: 14 start-page: Doc06 year: 2016 ident: 2652_CR32 publication-title: GMS Ger Med Sci – volume: 115 start-page: 53 year: 2021 ident: 2652_CR5 publication-title: Placenta doi: 10.1016/j.placenta.2021.09.014 – ident: 2652_CR16 – volume: 12 start-page: 123 issue: 3 year: 2019 ident: 2652_CR22 publication-title: Obstet Med doi: 10.1177/1753495X18797749 – ident: 2652_CR14 – volume: 362 start-page: 1779 issue: 9398 year: 2003 ident: 2652_CR33 publication-title: Lancet doi: 10.1016/S0140-6736(03)14896-9 – volume: 31 start-page: 1913 issue: 14 year: 2018 ident: 2652_CR10 publication-title: J Matern Fetal Neonatal Med doi: 10.1080/14767058.2017.1332036 – volume: 38 start-page: 834 issue: 8 year: 2021 ident: 2652_CR40 publication-title: Am J Perinatol doi: 10.1055/s-0039-3402724 – volume: 26 start-page: 1011 issue: 8 year: 2019 ident: 2652_CR26 publication-title: J Viral Hepat doi: 10.1111/jvh.13105 – volume: 294 start-page: 709 issue: 4 year: 2016 ident: 2652_CR27 publication-title: Arch Gynecol Obstet doi: 10.1007/s00404-016-4019-8 – volume: 73 start-page: 103 issue: 2 year: 2018 ident: 2652_CR6 publication-title: Obstet Gynecol Surv doi: 10.1097/OGX.0000000000000524 – volume: 112 start-page: 250 issue: 3 year: 2011 ident: 2652_CR37 publication-title: Int J Gynecol Obstet doi: 10.1016/j.ijgo.2010.11.002 – volume: 38 start-page: 243 issue: 2 year: 2015 ident: 2652_CR41 publication-title: Diabetes Care doi: 10.2337/dc14-2143 – volume: 176 start-page: 80 year: 2014 ident: 2652_CR42 publication-title: Eur J Obs Gynecol Reprod Biol doi: 10.1016/j.ejogrb.2013.12.037 – volume: 150 start-page: 1 issue: e89 year: 2022 ident: 2652_CR19 publication-title: Epidemiol Infect doi: 10.1017/S0950268822001388 – volume: 117 start-page: 1669 issue: 5 year: 2006 ident: 2652_CR39 publication-title: Pediatrics doi: 10.1542/peds.2005-1801 – ident: 2652_CR38 – volume: 175 start-page: 957 issue: 4 year: 1996 ident: 2652_CR9 publication-title: Am J Obstet Gynecol doi: 10.1016/S0002-9378(96)80031-7 – volume: 94 start-page: 189 issue: 2 year: 1999 ident: 2652_CR31 publication-title: Obstet Gynecol – volume: 15 start-page: e0228213 issue: 2 year: 2020 ident: 2652_CR7 publication-title: PLOS ONE doi: 10.1371/journal.pone.0228213 – volume: 4 start-page: 17 issue: 1 year: 2013 ident: 2652_CR28 publication-title: Sex Reprod Healthc doi: 10.1016/j.srhc.2012.11.005 – volume: 218 start-page: 33 year: 2017 ident: 2652_CR23 publication-title: Eur J Obstet Gynecol Reprod Biol doi: 10.1016/j.ejogrb.2017.09.012 – ident: 2652_CR30 doi: 10.3109/14767058.2014.984605 – volume: 8 start-page: 3985 issue: 1 year: 2018 ident: 2652_CR43 publication-title: Sci Rep doi: 10.1038/s41598-018-22387-6 – volume: 213 start-page: 395.e1 issue: 3 year: 2015 ident: 2652_CR35 publication-title: Am J Obstet Gynecol doi: 10.1016/j.ajog.2015.05.011 – volume: 301 start-page: 655 issue: 3 year: 2020 ident: 2652_CR34 publication-title: Arch Gynecol Obstet doi: 10.1007/s00404-020-05456-y – volume: 50 start-page: 481 issue: 7 year: 2015 ident: 2652_CR11 publication-title: Zhonghua Fu Chan Ke Za Zhi – volume: 35 start-page: 358 issue: 4 year: 2015 ident: 2652_CR29 publication-title: J Obstet Gynaecol doi: 10.3109/01443615.2014.968102 – volume: 44 start-page: 1377 issue: 8 year: 2018 ident: 2652_CR4 publication-title: J Obstet Gynaecol Res doi: 10.1111/jog.13681 – volume: 28 start-page: 613 issue: 4 year: 2021 ident: 2652_CR25 publication-title: J Viral Hepat doi: 10.1111/jvh.13472 |
SSID | ssj0017823 |
Score | 2.4270892 |
Snippet | This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China.
Cases of pregnant women monitored... Background This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China. Methods Cases of... This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China. Cases of pregnant women monitored... This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China.BACKGROUNDThis study analyzed the... Abstract Background This study analyzed the pregnancy outcomes of patients with intrahepatic cholestasis of pregnancy (ICP) in Hangzhou, China. Methods Cases... |
SourceID | doaj pubmedcentral proquest gale pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 16 |
SubjectTerms | Amniotic fluid Care and treatment Cesarean Section - adverse effects Childbirth Cholestasis Cholestasis, Intrahepatic - complications Cholestasis, Intrahepatic - epidemiology Complications and side effects Contamination Diabetes, Gestational - epidemiology Diagnosis Diseases Female Fetal intrauterine growth restriction Fetal Macrosomia - complications Health aspects Hepatitis B - complications Humans Hyperlipidemia Infants (Newborn) Intrahepatic cholestasis of pregnancy Jaundice, Obstructive Low birth weight infants Patient outcomes Pregnancy Pregnancy Complications - epidemiology Pregnancy Outcome - epidemiology Pregnancy, Complications of Pregnant women Premature Birth - epidemiology Premature Birth - etiology Premature rupture of membranes Retrospective Studies Thrombocytopenia |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3Na90wDDejh7LL2PeytcWDwQ4jNI5t2emtLStl0J1WKLsYx7HXByMpSd5h__1kJ3m8MNguu_ojsWXJkrD0EyEfbCiaspYu9yzoXFSe57XQMi8cr4WzEqqU4X3zFa5vxZc7ebdX6ivGhE3wwBPhToXEGRqFMGgtQqFtHZgCzzyqTlTdCecTdd7iTM3vB6j3-JIio-F0wFtYxWDb-GYJssz5Sg0ltP4_7-Q9pbQOmNzTQFdPyZPZdKTn05KfkUe-fU4Ob-bH8RfkOx45nbIeaRfoJn7k3seIaUfjJYf_ssNmoF1LH3r_IyJt_KLddkSe88MZtbT3Y98tqZc0ls7tR5rwZ1-S26vP3y6v87l0Qu4EyDEX1gZhq6KpROAVL-qK14pbNOZiO1eh8AoaJwonVM1QQVWAhivjnokSz6jkr8hB27X-DaEKoPBeWscFuo6isk4FDyAgSGiaUmSELZQ0bsYVj-UtfprkX2gwE_UNUt8k6huekU-7OQ8TqsZfR1_EA9qNjIjYqQH5xMx8Yv7FJxn5GI_XRLnF5Tk7px_gJiMCljlXnCuBzitk5Gg1EuXNrbrfLwxiYlcMUmt9tx1MqQC9T7wicczriWF2a-YAkiupMqJWrLTa1Lqn3dwnuO8qGhDA3v4PKrwjj8skBSxn-ogcjP3WH6NVNdYnSYB-A8MTHm4 priority: 102 providerName: Directory of Open Access Journals |
Title | The impact of intrahepatic cholestasis on pregnancy outcomes: a retrospective cohort study |
URI | https://www.ncbi.nlm.nih.gov/pubmed/36653757 https://www.proquest.com/docview/2767168326 https://pubmed.ncbi.nlm.nih.gov/PMC9847161 https://doaj.org/article/45ca58ddef884f08abf176e1e6586233 |
Volume | 23 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1ba9RAFB56AfFFvLtalxEEHySaZG6JINKVliJskeLC0pdhMjvTLpSkJlmw_95zJsnaYBFf9iEzO0nOfOeWORdC3hofr9JC2MglPot47lhU8ExEsWUFt0bIPGR4z0_lyYJ_W4rlDhnaHfUEbO507bCf1KK--vDr580XYPjPgeEz-bEBGaswlBZPJKVII7ZL9kEzKWTUOf9zqgDaMATcg0COwPReDkk0d64xUlShnv_fUvuW2hqHVN7SUccPyYPeuKSHHRoekR1XPib35v3x-RNyDqCgXV4krTxd4yKXDmOqLUVKwL1Ms25oVdLr2l1gLY4bWm1aQKVrPlFDa9fW1ZCcSbG5bt3SUKH2KVkcH_34ehL1zRUiy6VoI26M5yaPVzn3LGdxkbNCMQPmHl5nysdOyZXlseWqQIrlEkzbhLmEp7CLKXtG9sqqdC8IVVLGzgljGQfnkufGKu-k5NILuVqlfEKSgZLa9pXHsQHGlQ4eSCZ1R30N1NeB-ppNyPvtf667uhv_nD3DDdrOxJrZ4UJVX-ieBTUXgL0MxLnPMu7jzBQ-UdIlDowwMAJhkXe4vRqxBo9nTZ-gAC-JNbL0oWJMcXBv5YQcjGYCR9rR8JsBIBqHMIytdNWm0amS4J-CEIU5zzvAbJ-ZSSmYEmpC1AhKo5caj5Try1AQPEcTQyYv_-O-r8j9NIA8iZLsgOy19ca9BrOqLaZkVy3VlOzPjk6_n03Dx4lp4B_4PZud_wbaGiFu |
linkProvider | Scholars Portal |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=The+impact+of+intrahepatic+cholestasis+on+pregnancy+outcomes%3A+a+retrospective+cohort+study&rft.jtitle=BMC+gastroenterology&rft.au=Chen%2C+Yiming&rft.au=Zhang%2C+Huimin&rft.au=Ning%2C+Wenwen&rft.au=Chen%2C+Yijie&rft.date=2023-01-18&rft.issn=1471-230X&rft.eissn=1471-230X&rft.volume=23&rft.issue=1&rft.spage=16&rft_id=info:doi/10.1186%2Fs12876-023-02652-3&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1471-230X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1471-230X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1471-230X&client=summon |