Incidence and Risk Factors of Cholestasis in Newborns with Hemolytic Disease—A Case-Control Study
Background/Objectives: One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN). Methods: We retrospectively analyzed 88 medical records of HDFN newborns with cholestasis and 186 records of children with HDFN without cholestasis and conducted an observational, c...
Saved in:
Published in | Journal of clinical medicine Vol. 13; no. 11; p. 3190 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
01.06.2024
MDPI |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Background/Objectives: One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN). Methods: We retrospectively analyzed 88 medical records of HDFN newborns with cholestasis and 186 records of children with HDFN without cholestasis and conducted an observational, case-control, retrospective study. Results: Factors influencing the risk of cholestasis were lower gestational age at birth (36.83 ± 1.9 vs. 37.57 ± 1.8, p = 0.002), Rh or Kidd HDFN (80.7% vs. 53.2%), and the need for intrauterine transfusion (27.3 vs. 11.8%). The subjects had lower hemoglobin concentrations at birth (14.01 ± 3.8 vs. 16.39 ± 2.8 g/dL) and during whole hospital stay, higher cord blood total bilirubin concentration (4.26 ± 1.8 vs. 2.39 ± 1.4 mg/dL), higher maximum bilirubin concentration (15.27 ± 5.8 vs. 10.24 ± 3.4 mg/dL), and more frequent liver ultrasound abnormalities (19.9 vs. 6.3%). They also required more extended hospitalization due to higher rates of postnatal blood transfusion (33 vs. 3.8%), more frequent need for exchange transfusion (8.8% vs. 2.2%), more extended time and higher risk of phototherapy (94.3 vs. 59.1%), and higher usage of immunoglobulins (55.7 vs. 8.1%), parenteral nutrition (45.5 vs. 12.9%), and antibiotics (14.8 vs. 4.8%). Conclusions: The risk factors for cholestasis in children with HDFN are lower gestational age at delivery, Rh and Kidd serological type of HDFN, and the need for intrauterine transfusions. |
---|---|
AbstractList | : One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN).
: We retrospectively analyzed 88 medical records of HDFN newborns with cholestasis and 186 records of children with HDFN without cholestasis and conducted an observational, case-control, retrospective study.
: Factors influencing the risk of cholestasis were lower gestational age at birth (36.83 ± 1.9 vs. 37.57 ± 1.8,
= 0.002), Rh or Kidd HDFN (80.7% vs. 53.2%), and the need for intrauterine transfusion (27.3 vs. 11.8%). The subjects had lower hemoglobin concentrations at birth (14.01 ± 3.8 vs. 16.39 ± 2.8 g/dL) and during whole hospital stay, higher cord blood total bilirubin concentration (4.26 ± 1.8 vs. 2.39 ± 1.4 mg/dL), higher maximum bilirubin concentration (15.27 ± 5.8 vs. 10.24 ± 3.4 mg/dL), and more frequent liver ultrasound abnormalities (19.9 vs. 6.3%). They also required more extended hospitalization due to higher rates of postnatal blood transfusion (33 vs. 3.8%), more frequent need for exchange transfusion (8.8% vs. 2.2%), more extended time and higher risk of phototherapy (94.3 vs. 59.1%), and higher usage of immunoglobulins (55.7 vs. 8.1%), parenteral nutrition (45.5 vs. 12.9%), and antibiotics (14.8 vs. 4.8%).
: The risk factors for cholestasis in children with HDFN are lower gestational age at delivery, Rh and Kidd serological type of HDFN, and the need for intrauterine transfusions. Background/Objectives: One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN). Methods: We retrospectively analyzed 88 medical records of HDFN newborns with cholestasis and 186 records of children with HDFN without cholestasis and conducted an observational, case-control, retrospective study. Results: Factors influencing the risk of cholestasis were lower gestational age at birth (36.83 ± 1.9 vs. 37.57 ± 1.8, p = 0.002), Rh or Kidd HDFN (80.7% vs. 53.2%), and the need for intrauterine transfusion (27.3 vs. 11.8%). The subjects had lower hemoglobin concentrations at birth (14.01 ± 3.8 vs. 16.39 ± 2.8 g/dL) and during whole hospital stay, higher cord blood total bilirubin concentration (4.26 ± 1.8 vs. 2.39 ± 1.4 mg/dL), higher maximum bilirubin concentration (15.27 ± 5.8 vs. 10.24 ± 3.4 mg/dL), and more frequent liver ultrasound abnormalities (19.9 vs. 6.3%). They also required more extended hospitalization due to higher rates of postnatal blood transfusion (33 vs. 3.8%), more frequent need for exchange transfusion (8.8% vs. 2.2%), more extended time and higher risk of phototherapy (94.3 vs. 59.1%), and higher usage of immunoglobulins (55.7 vs. 8.1%), parenteral nutrition (45.5 vs. 12.9%), and antibiotics (14.8 vs. 4.8%). Conclusions: The risk factors for cholestasis in children with HDFN are lower gestational age at delivery, Rh and Kidd serological type of HDFN, and the need for intrauterine transfusions.Background/Objectives: One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN). Methods: We retrospectively analyzed 88 medical records of HDFN newborns with cholestasis and 186 records of children with HDFN without cholestasis and conducted an observational, case-control, retrospective study. Results: Factors influencing the risk of cholestasis were lower gestational age at birth (36.83 ± 1.9 vs. 37.57 ± 1.8, p = 0.002), Rh or Kidd HDFN (80.7% vs. 53.2%), and the need for intrauterine transfusion (27.3 vs. 11.8%). The subjects had lower hemoglobin concentrations at birth (14.01 ± 3.8 vs. 16.39 ± 2.8 g/dL) and during whole hospital stay, higher cord blood total bilirubin concentration (4.26 ± 1.8 vs. 2.39 ± 1.4 mg/dL), higher maximum bilirubin concentration (15.27 ± 5.8 vs. 10.24 ± 3.4 mg/dL), and more frequent liver ultrasound abnormalities (19.9 vs. 6.3%). They also required more extended hospitalization due to higher rates of postnatal blood transfusion (33 vs. 3.8%), more frequent need for exchange transfusion (8.8% vs. 2.2%), more extended time and higher risk of phototherapy (94.3 vs. 59.1%), and higher usage of immunoglobulins (55.7 vs. 8.1%), parenteral nutrition (45.5 vs. 12.9%), and antibiotics (14.8 vs. 4.8%). Conclusions: The risk factors for cholestasis in children with HDFN are lower gestational age at delivery, Rh and Kidd serological type of HDFN, and the need for intrauterine transfusions. Background/Objectives : One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN). Methods : We retrospectively analyzed 88 medical records of HDFN newborns with cholestasis and 186 records of children with HDFN without cholestasis and conducted an observational, case-control, retrospective study. Results : Factors influencing the risk of cholestasis were lower gestational age at birth (36.83 ± 1.9 vs. 37.57 ± 1.8, p = 0.002), Rh or Kidd HDFN (80.7% vs. 53.2%), and the need for intrauterine transfusion (27.3 vs. 11.8%). The subjects had lower hemoglobin concentrations at birth (14.01 ± 3.8 vs. 16.39 ± 2.8 g/dL) and during whole hospital stay, higher cord blood total bilirubin concentration (4.26 ± 1.8 vs. 2.39 ± 1.4 mg/dL), higher maximum bilirubin concentration (15.27 ± 5.8 vs. 10.24 ± 3.4 mg/dL), and more frequent liver ultrasound abnormalities (19.9 vs. 6.3%). They also required more extended hospitalization due to higher rates of postnatal blood transfusion (33 vs. 3.8%), more frequent need for exchange transfusion (8.8% vs. 2.2%), more extended time and higher risk of phototherapy (94.3 vs. 59.1%), and higher usage of immunoglobulins (55.7 vs. 8.1%), parenteral nutrition (45.5 vs. 12.9%), and antibiotics (14.8 vs. 4.8%). Conclusions : The risk factors for cholestasis in children with HDFN are lower gestational age at delivery, Rh and Kidd serological type of HDFN, and the need for intrauterine transfusions. Background/Objectives : One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN). Methods : We retrospectively analyzed 88 medical records of HDFN newborns with cholestasis and 186 records of children with HDFN without cholestasis and conducted an observational, case-control, retrospective study. Results : Factors influencing the risk of cholestasis were lower gestational age at birth (36.83 ± 1.9 vs. 37.57 ± 1.8, p = 0.002), Rh or Kidd HDFN (80.7% vs. 53.2%), and the need for intrauterine transfusion (27.3 vs. 11.8%). The subjects had lower hemoglobin concentrations at birth (14.01 ± 3.8 vs. 16.39 ± 2.8 g/dL) and during whole hospital stay, higher cord blood total bilirubin concentration (4.26 ± 1.8 vs. 2.39 ± 1.4 mg/dL), higher maximum bilirubin concentration (15.27 ± 5.8 vs. 10.24 ± 3.4 mg/dL), and more frequent liver ultrasound abnormalities (19.9 vs. 6.3%). They also required more extended hospitalization due to higher rates of postnatal blood transfusion (33 vs. 3.8%), more frequent need for exchange transfusion (8.8% vs. 2.2%), more extended time and higher risk of phototherapy (94.3 vs. 59.1%), and higher usage of immunoglobulins (55.7 vs. 8.1%), parenteral nutrition (45.5 vs. 12.9%), and antibiotics (14.8 vs. 4.8%). Conclusions : The risk factors for cholestasis in children with HDFN are lower gestational age at delivery, Rh and Kidd serological type of HDFN, and the need for intrauterine transfusions. |
Audience | Academic |
Author | Ludwin, Artur Drozdowska-Szymczak, Agnieszka Mazanowska, Natalia Pomianek, Tomasz Krajewski, Paweł |
AuthorAffiliation | 1 Department of Neonatology and Neonatal Intensive Care, Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland; agnieszka.drozdowska@imid.med.pl (A.D.-S.); tomasz.pomianek@imid.med.pl (T.P.); pawel.krajewski@imid.med.pl (P.K.) 2 Department of Obstetrics and Gynecology, Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland 3 Department of Obstetrics and Gynecology, Medical University of Warsaw, Pl. Starynkiewicza 1/3, 02-015 Warsaw, Poland; ludwin@cm-uj.krakow.pl |
AuthorAffiliation_xml | – name: 3 Department of Obstetrics and Gynecology, Medical University of Warsaw, Pl. Starynkiewicza 1/3, 02-015 Warsaw, Poland; ludwin@cm-uj.krakow.pl – name: 1 Department of Neonatology and Neonatal Intensive Care, Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland; agnieszka.drozdowska@imid.med.pl (A.D.-S.); tomasz.pomianek@imid.med.pl (T.P.); pawel.krajewski@imid.med.pl (P.K.) – name: 2 Department of Obstetrics and Gynecology, Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland |
Author_xml | – sequence: 1 givenname: Agnieszka orcidid: 0009-0003-3503-6660 surname: Drozdowska-Szymczak fullname: Drozdowska-Szymczak, Agnieszka – sequence: 2 givenname: Natalia orcidid: 0000-0002-6970-5303 surname: Mazanowska fullname: Mazanowska, Natalia – sequence: 3 givenname: Tomasz surname: Pomianek fullname: Pomianek, Tomasz – sequence: 4 givenname: Artur surname: Ludwin fullname: Ludwin, Artur – sequence: 5 givenname: Paweł surname: Krajewski fullname: Krajewski, Paweł |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38892901$$D View this record in MEDLINE/PubMed |
BookMark | eNptkl1vFCEUhompsbX2yntD4o2JmcrH7MBcmc1obZNGEz-uCQOHLusM1IGx2Tt_hL_QXyKb1rptCiQQeM4LL-c8RXshBkDoOSXHnLfkzdqMlNMyWvIIHTAiREW45Hs76310lNKalCZlzah4gva5lC1rCT1A5iwYbyEYwDpY_Nmn7_hEmxynhKPD3SoOkLJOPmEf8Ee46uMUEr7yeYVPYYzDJnuD3_kEOsGfX7-XuCuLqoshT3HAX_JsN8_QY6eHBEc38yH6dvL-a3danX_6cNYtzytTC5Erad2CNHXfkHpBmbHWGc0Z0NoQI5umtT2VxrXWcakds8ItBOsp0ZJDD8y1_BC9vda9nPsRrIHyBj2oy8mPetqoqL26exL8Sl3En4pSKlhNtwqvbhSm-GMuxtXok4Fh0AHinBQngsjyj4IU9OU9dB3nKRR_hWpEUROy_k9d6AGUDy6Wi81WVC1FK1oiKReFOn6AKt3C6E1JuPNl_07Ai12ntxb_5bUAr68BM8WUJnC3CCVqWzhqp3AKTe_Rxmed_TaJ2g8PxvwFR_LFSQ |
CitedBy_id | crossref_primary_10_3390_jcm13237047 crossref_primary_10_3390_jcm13237048 |
Cites_doi | 10.3390/jcm13051272 10.1038/s41372-022-01330-8 10.1038/sj.jp.7200458 10.2147/PHMT.S327032 10.24953/turkjped.2018.03.018 10.1148/radiol.2017170305 10.1159/000343261 10.3390/jcm12247645 10.1182/asheducation-2015.1.146 10.1038/jp.2012.71 10.1097/01.mph.0000212906.07018.93 10.1542/peds.114.1.297 10.1159/000335333 10.1080/17474086.2017.1331124 10.1542/peds.2022-058859 10.1542/peds.2018-2859 10.1038/s41372-022-01345-1 10.1016/j.clp.2016.01.001 10.1159/000362812 10.1097/MPG.0000000000001334 10.1542/neo.14-2-e63 10.1016/j.jclinepi.2007.11.008 10.5152/tjh.2010.30 10.2147/IJCTM.S40019 10.1007/s00431-011-1521-7 |
ContentType | Journal Article |
Copyright | COPYRIGHT 2024 MDPI AG 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2024 by the authors. 2024 |
Copyright_xml | – notice: COPYRIGHT 2024 MDPI AG – notice: 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: 2024 by the authors. 2024 |
DBID | AAYXX CITATION NPM 3V. 7X7 7XB 8FI 8FJ 8FK ABUWG AFKRA AZQEC BENPR CCPQU DWQXO FYUFA GHDGH K9. M0S PHGZM PHGZT PIMPY PKEHL PQEST PQQKQ PQUKI PRINS 7X8 5PM |
DOI | 10.3390/jcm13113190 |
DatabaseName | CrossRef PubMed ProQuest Central (Corporate) Health & Medical Collection ProQuest Central (purchase pre-March 2016) Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials ProQuest Central ProQuest One Community College ProQuest Central Korea Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Health & Medical Complete (Alumni) ProQuest Health & Medical Collection ProQuest Central Premium ProQuest One Academic Publicly Available Content Database ProQuest One Academic Middle East (New) ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef PubMed Publicly Available Content Database ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest One Academic Eastern Edition ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Central China ProQuest Hospital Collection (Alumni) ProQuest Central ProQuest Health & Medical Complete Health Research Premium Collection ProQuest One Academic UKI Edition Health and Medicine Complete (Alumni Edition) ProQuest Central Korea ProQuest Central (New) ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | PubMed MEDLINE - Academic Publicly Available Content Database CrossRef |
Database_xml | – sequence: 1 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: 2 dbid: 7X7 name: Health & Medical Collection url: https://search.proquest.com/healthcomplete sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 2077-0383 |
ExternalDocumentID | PMC11172419 A797908137 38892901 10_3390_jcm13113190 |
Genre | Journal Article |
GeographicLocations | Poland |
GeographicLocations_xml | – name: Poland |
GroupedDBID | 53G 5VS 7X7 8FI 8FJ AADQD AAFWJ AAYXX ABDBF ABUWG ACUHS ADBBV AFKRA AFZYC ALIPV ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BCNDV BENPR CCPQU CITATION DIK FYUFA HMCUK HYE IAO IHR ITC KQ8 M48 MODMG M~E OK1 PGMZT PHGZM PHGZT PIMPY RPM UKHRP NPM PMFND 3V. 7XB 8FK AZQEC DWQXO K9. PKEHL PQEST PQQKQ PQUKI PRINS 7X8 5PM |
ID | FETCH-LOGICAL-c477t-8df5064b604512cddfca32e14c0c8669db18cf9df38af2d7f572b10a83ebe2f93 |
IEDL.DBID | M48 |
ISSN | 2077-0383 |
IngestDate | Thu Aug 21 18:33:41 EDT 2025 Fri Jul 11 03:47:14 EDT 2025 Mon Jun 30 12:11:52 EDT 2025 Tue Jun 17 22:09:14 EDT 2025 Tue Jun 10 21:08:39 EDT 2025 Mon Jul 21 05:49:48 EDT 2025 Tue Jul 01 01:38:14 EDT 2025 Thu Apr 24 23:01:32 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 11 |
Keywords | direct bilirubin HDN hemolytic disease of the newborn HDFN cholestasis IUT newborn |
Language | English |
License | https://creativecommons.org/licenses/by/4.0 Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c477t-8df5064b604512cddfca32e14c0c8669db18cf9df38af2d7f572b10a83ebe2f93 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0009-0003-3503-6660 0000-0002-6970-5303 |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.3390/jcm13113190 |
PMID | 38892901 |
PQID | 3067419784 |
PQPubID | 5046890 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_11172419 proquest_miscellaneous_3070800870 proquest_journals_3067419784 gale_infotracmisc_A797908137 gale_infotracacademiconefile_A797908137 pubmed_primary_38892901 crossref_primary_10_3390_jcm13113190 crossref_citationtrail_10_3390_jcm13113190 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2024-06-01 |
PublicationDateYYYYMMDD | 2024-06-01 |
PublicationDate_xml | – month: 06 year: 2024 text: 2024-06-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | Switzerland |
PublicationPlace_xml | – name: Switzerland – name: Basel |
PublicationTitle | Journal of clinical medicine |
PublicationTitleAlternate | J Clin Med |
PublicationYear | 2024 |
Publisher | MDPI AG MDPI |
Publisher_xml | – name: MDPI AG – name: MDPI |
References | Teng (ref_20) 2022; 42 Kemper (ref_14) 2022; 150 Altman (ref_16) 2008; 61 Zonneveld (ref_25) 2019; 143 Aladily (ref_24) 2018; 60 Grobler (ref_26) 1997; 87 Maisels (ref_11) 2012; 32 Feldman (ref_21) 2013; 14 Fawaz (ref_3) 2017; 64 ref_19 Rath (ref_4) 2012; 101 Jankowska (ref_1) 2017; 14 Myle (ref_10) 2021; 12 Mundy (ref_12) 2015; 3 Sreenan (ref_29) 2000; 20 Delaney (ref_8) 2015; 2015 Yilmaz (ref_28) 2006; 28 Ree (ref_5) 2017; 10 Jankowska (ref_22) 2013; 1 Yalaz (ref_30) 2011; 170 Shamir (ref_2) 2017; 285 Rath (ref_9) 2013; 103 Lindenburg (ref_18) 2014; 36 Arslan (ref_23) 2010; 27 Bhutani (ref_13) 2016; 43 Zwiers (ref_15) 2018; 3 Watchko (ref_27) 2022; 42 Andrei (ref_17) 2012; 7 ref_7 ref_6 |
References_xml | – volume: 87 start-page: 1146 year: 1997 ident: ref_26 article-title: Kernicterus associated with elevated predominantly direct-reacting bilirubin publication-title: S. Afr. Med. J. – ident: ref_6 doi: 10.3390/jcm13051272 – volume: 42 start-page: 695 year: 2022 ident: ref_27 article-title: Management of severe hyperbilirubinemia in the cholestatic neonate: A review and an approach publication-title: J. Perinatol. doi: 10.1038/s41372-022-01330-8 – volume: 20 start-page: 509 year: 2000 ident: ref_29 article-title: Successful chelation therapy in a case of neonatal iron overload following intravascular intrauterine transfusion publication-title: J. Perinatol. doi: 10.1038/sj.jp.7200458 – volume: 12 start-page: 491 year: 2021 ident: ref_10 article-title: Hemolytic Disease of the Newborn: A Review of Current Trends and Prospects publication-title: Pediatr. Health Med. Ther. doi: 10.2147/PHMT.S327032 – volume: 60 start-page: 335 year: 2018 ident: ref_24 article-title: Chelation therapy for secondary neonatal iron overload: Lessons learned from rhesus hemolytic disease publication-title: Turk. J. Pediatr. doi: 10.24953/turkjped.2018.03.018 – volume: 285 start-page: 763 year: 2017 ident: ref_2 article-title: Hepatic Imaging in Neonates and Young Infants: State of the Art publication-title: Radiology doi: 10.1148/radiol.2017170305 – volume: 3 start-page: CD003313 year: 2018 ident: ref_15 article-title: Immunoglobulin for alloimmune hemolytic disease in neonates publication-title: Cochrane Database Syst. Rev. – volume: 1 start-page: 41 year: 2013 ident: ref_22 article-title: Management of cholestasis in infants publication-title: Stand. Med. Pediatr. – volume: 103 start-page: 141 year: 2013 ident: ref_9 article-title: Neonatal morbidity after Exchange transfusion for cell alloimmune hemolytic disease publication-title: Neonatology doi: 10.1159/000343261 – ident: ref_7 doi: 10.3390/jcm12247645 – volume: 2015 start-page: 146 year: 2015 ident: ref_8 article-title: Hematology Hemolytic disease of the fetus and newborn: Managing the mother, fetus, and newborn publication-title: Am. Soc. Hematol. Educ. Program doi: 10.1182/asheducation-2015.1.146 – volume: 32 start-page: 660 year: 2012 ident: ref_11 article-title: An approach to the management of hiperbilirubinemia in the preterm infant less than 35 weeks of gestation publication-title: J. Perinatol. doi: 10.1038/jp.2012.71 – volume: 28 start-page: 290 year: 2006 ident: ref_28 article-title: A case of rhesus hemolytic disease with hemophagocytosis and severe iron overload due to multiple transfusions publication-title: J. Pediatr. Hematol. Oncol. doi: 10.1097/01.mph.0000212906.07018.93 – ident: ref_19 doi: 10.1542/peds.114.1.297 – volume: 101 start-page: 306 year: 2012 ident: ref_4 article-title: Cholestasis in neonates with red cell alloimmune hemolytic disease: Incidence, risk factors and outcome publication-title: Neonatology doi: 10.1159/000335333 – volume: 10 start-page: 607 year: 2017 ident: ref_5 article-title: Neonatal management and outcome in alloimmune hemolytic disease publication-title: Expert Rev. Hematol. doi: 10.1080/17474086.2017.1331124 – volume: 150 start-page: e2022058859 year: 2022 ident: ref_14 article-title: Clinical Practice Guideline Revision: Management of Hyperbilirubinemia in the Newborn Infant 35 or More Weeks of Gestation publication-title: Pediatrics doi: 10.1542/peds.2022-058859 – volume: 143 start-page: e20182859 year: 2019 ident: ref_25 article-title: Severe Fetal Hemolysis and Cholestasis Due to High-Titer Maternal IgG Anti-A Antibodies publication-title: Pediatrics doi: 10.1542/peds.2018-2859 – volume: 42 start-page: 702 year: 2022 ident: ref_20 article-title: Population-based incidence and risk factors for cholestasis in hemolytic disease of the fetus and newborn publication-title: J. Perinatol. doi: 10.1038/s41372-022-01345-1 – volume: 43 start-page: 215 year: 2016 ident: ref_13 article-title: Hyperbilirubinemia in preterm neonates publication-title: Clin. Perinatol. doi: 10.1016/j.clp.2016.01.001 – volume: 36 start-page: 263 year: 2014 ident: ref_18 article-title: Intrauterine blood transfusion: Current indications and associated risks publication-title: Fetal Diagn. Ther. doi: 10.1159/000362812 – volume: 64 start-page: 154 year: 2017 ident: ref_3 article-title: Guideline for the Evaluation of Cholestatic Jaundice in Infants: Joint Recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition publication-title: J. Pediatr. Gastroenterol. Nutr. doi: 10.1097/MPG.0000000000001334 – volume: 14 start-page: e63 year: 2013 ident: ref_21 article-title: Neonatal Cholestasis publication-title: Neoreviews doi: 10.1542/neo.14-2-e63 – volume: 7 start-page: 14 year: 2012 ident: ref_17 article-title: The value of reference ranges for middle cerebral artery peak systolic velocity in the management of rhesus alloimmunized pregnancies publication-title: Maedica – volume: 14 start-page: 7 year: 2017 ident: ref_1 article-title: Zalecenia dotyczące wczesnego rozpoznawania cholestazy u niemowląt publication-title: Stand. Med./Pediatr. – volume: 61 start-page: 344 year: 2008 ident: ref_16 article-title: The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: Guidelines for reporting observational studies publication-title: J. Clin. Epidemiol. doi: 10.1016/j.jclinepi.2007.11.008 – volume: 27 start-page: 204 year: 2010 ident: ref_23 article-title: Severe iron overload and hyporegenerative anemia in a case with rhesus hemolytic disease: Therapeutic approach to rare complications publication-title: Turk. J. Haematol. doi: 10.5152/tjh.2010.30 – volume: 3 start-page: 41 year: 2015 ident: ref_12 article-title: Immunoglobulin transfusion in hemolytic disease of the newborn: Place in therapy publication-title: Int. J. Clin. Transfus. Med. doi: 10.2147/IJCTM.S40019 – volume: 170 start-page: 1457 year: 2011 ident: ref_30 article-title: Desferrioxamine treatment of iron overload secondary to RH isoimmunization and intrauterine transfusion in a newborn infant publication-title: Eur. J. Pediatr. doi: 10.1007/s00431-011-1521-7 |
SSID | ssj0000884217 |
Score | 2.2859159 |
Snippet | Background/Objectives: One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN). Methods: We retrospectively analyzed 88... : One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN). : We retrospectively analyzed 88 medical records of HDFN... Background/Objectives : One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN). Methods : We retrospectively analyzed... Background/Objectives : One of the rare causes of cholestasis may be hemolytic disease of the fetus and newborn (HDFN). Methods : We retrospectively analyzed... |
SourceID | pubmedcentral proquest gale pubmed crossref |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 3190 |
SubjectTerms | Antibiotics Bile Birth weight Blood-brain barrier Cholestasis Complications and side effects Erythroblastosis fetalis Fetuses Flow velocity Gallbladder diseases Gestational age Gynecology Health aspects Hemoglobin Hospitals Immunization Immunoglobulins Infants (Newborn) Jaundice, Obstructive Light therapy Liver Neonatology Normal distribution Nutrition Obstetrics Placenta Pregnancy Risk factors Ultrasonic imaging Variables |
SummonAdditionalLinks | – databaseName: Health & Medical Collection dbid: 7X7 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3NihQxEC50BfEi_tu6SoQFQQg73cl0kpMMo8MgrAdxYW5NJ-nguLvdqz172JsP4RP6JFZNMu20iLeB1DQh9ZMvlcpXAEeeWMG88JxevHLpcs2ttoLnNijhfWl8TamBk4_l8lR-WE1XKeHWp7LKXUzcBmrfOcqRHxO0lTmeeeTby2-cukbR7WpqoXETbhF1GVm1Wqkhx4IeJBFyx2d5Ak_3x1_dBfHLoN1NRhvR3-F4bz8a10rubT6Le3A3oUY2i2q-Dzea9gHcPkn34g_BoZvH7qCsbj37tO7P2CJ20mFdYHNqgoswsF_3bN0yDGyo-bZnlIRly-aiO7_GD7N38bLm14-fMzbHH3we69gZFRteP4LTxfvP8yVP7RO4k0ptuPaB2OhsSRQyhfM-uFoUTS7dxOkStWBz7YLxQeg6FF6FqSpsPqm1QMUWwYjHcNB2bfMUWGmId07UJkykDGZqS-_zumzwKIt4prAZvNmtZeUStzi1uDiv8IxBC1_tLXwGR4PwZaTU-LfYa1JKRY6G33J1ei-AMyLKqmqmjDIIaITK4HAkiQ7ixsM7tVbJQfvqjzll8GoYpn9S0VnbdFckowhPY0TL4Em0gmHCQmtDV9AZ6JF9DAJE2z0eaddftvTduLsoxE3m2f_n9RzuFAigYlnaIRxsvl81LxAAbezLrZX_BgNoBs8 priority: 102 providerName: ProQuest |
Title | Incidence and Risk Factors of Cholestasis in Newborns with Hemolytic Disease—A Case-Control Study |
URI | https://www.ncbi.nlm.nih.gov/pubmed/38892901 https://www.proquest.com/docview/3067419784 https://www.proquest.com/docview/3070800870 https://pubmed.ncbi.nlm.nih.gov/PMC11172419 |
Volume | 13 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwdV3da9swED-6FkpfxrpPb13QoDAYaLMtx5IexkjThjBIGWWBvBlZsmi21NnqFJb_fnexHeLSPvlBJ2F8p_uwTr8fwKkjVDAnHKcbrzyxkeK5ygWPci-Fc6l2hn4NTC7T8TT5PuvP9qAl42w-YPVgaUd8UtPbxed_f9ffcMN_pYoTS_Yvv-wNgcagMWHtfoAhSRKVwaTJ8zcuWakk3rDvxqGUPMSyrL6rd3_-ERwKpTQdLnYC1X13vROvur2UO8Fp9AyeNlklG9RmcAx7RfkcDifNufkLMOgGavZQZkrHrubVbzaqmXbY0rMhkeRimljNKzYvGTo-tIyyYvSTlo2Lm-VijQuz8_owhw_YkB7DusudUSvi-iVMRxc_h2PekCtwm0i54sp5wqrLUwKYia1z3hoRF1FiQ6tS1FEeKeu180IZHzvp-zLOo9AogWqPvRavYL9clsUbYKkmVDphtA-TxOt-njoXmbTAQheznTgP4FP7JTPbII8TAcYiwwqENJDtaCCA063wnxpw42Gxj6SSjAwD17KmuU2Ab0SAVtlAaqkx3REygJOOJG4f2x1ulZq11pdRHZVEWGAnAXzYDtNMakkri-UdyUjKttHfBfC6toHtC7c2FIDqWMdWgEC9uyPl_HoD7o2xR6IJ67ePLvoOjmLMrOp-tRPYX93eFe8xM1rlPXgiZ7IHB2cXlz-ueps98B-4ugtZ |
linkProvider | Scholars Portal |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3NbtQwEB5VRQIuiP-GFjBSERJS1CTOxvYBodWW1ZZ2e0CttLeQ2LFYaJPSbIX2xkPwHDwUT8LMOgkbhLj1FsmTyLHHM9_Y428Adg2xghlufLrx6sc6lH4uc-6HuRXcmESZjLYGpsfJ5DR-PxvMNuBnexeG0ipbm7gy1KbStEe-R9A2DjHmid9efPWpahSdrrYlNJxaHBbLbxiy1W8O9nF-X0bR-N3JaOI3VQV8HQux8KWxRNKWJ8SsEmljrM54VISxDrRMsHN5KLVVxnKZ2cgIOxBRHgaZ5Pi_kSXyJTT5N9DxBhTsiZno9nRwxcYI8d01QM5VsPdZnxOfDep50HN8f5v_Nf_Xz81cc3bju3CnQals6NTqHmwU5X24OW3O4R-ARrPiqpGyrDTsw7z-wsaucg-rLBtR0V2EnfW8ZvOSoSFFTStrRpu-bFKcV2dL_DDbd4dDv77_GLIRPvgjlzfPKLlx-RBOr2VgH8FmWZXFFrBEEc8dz5QN4tiqQZ4YE2ZJgaEz4qco9-B1O5apbrjMqaTGWYoxDQ18ujbwHux2wheOwuPfYq9oUlJa2PgtnTX3E7BHRJGVDoUSCgEUFx7s9CRxQep-czutaWMQ6vSP-nrwomumNynJrSyqK5IRhN_Rgnrw2GlB12EupaIjbw9kTz86AaIJ77eU808runD0ZgJxmnry_349h1uTk-lRenRwfLgNtyMEby4lbgc2F5dXxVMEX4v82UrjGXy87iX2G-dCRPw |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3dbtMwFD6aOmniBvFPYICRhpCQojZxGtsXCJV2VcdYNU1M2l1I7FgrbMkgnVDveAiehsfhSThnTkKDEHe7i2Qncuzz8x37-DsAO4ZYwQw3Pt149SMdSD-TGfeDzApuTKxMSlsDB_N4dhy9OxmebMDP5i4MpVU2NvHKUJtS0x55n6BtFGDME_VtnRZxOJm-ufjiUwUpOmltymk4EdnPV98wfKte701wrV-E4XT3w3jm1xUGfB0JsfSlsUTYlsXEshJqY6xOeZgHkR5oGeNAs0Bqq4zlMrWhEXYowiwYpJLjv4eWiJjQ_G8Kiop6sPl2d3541O7woP5GCPjdpUDO1aD_SZ8Tuw1K_aDjBv92BmvesJupueb6prfgZo1Z2cgJ2W3YyIs7sHVQn8rfBY1GxtUmZWlh2NGi-symro4PKy0bUwleBKHVomKLgqFZRbkrKkZbwGyWn5dnK_wwm7ijol_ff4zYGB_8scuiZ5TquLoHx9cytfehV5RF_hBYrIj1jqfKDqLIqmEWGxOkcY6BNKKpMPPgVTOXia6ZzanAxlmCEQ5NfLI28R7stJ0vHKHHv7u9pEVJSM3xWzqtbyvgiIgwKxkJJRTCKS482O70RPXU3eZmWZPaPFTJH2H24HnbTG9SyluRl5fURxCaR3vqwQMnBe2AuZSKDsA9kB35aDsQaXi3pVicXpGHo28TiNrUo_-P6xlsoXol7_fm-4_hRohIzuXHbUNv-fUyf4JIbJk9rUWewcfr1rLfV-VKlw |
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=Incidence+and+Risk+Factors+of+Cholestasis+in+Newborns+with+Hemolytic+Disease-A+Case-Control+Study&rft.jtitle=Journal+of+clinical+medicine&rft.au=Drozdowska-Szymczak%2C+Agnieszka&rft.au=Mazanowska%2C+Natalia&rft.au=Pomianek%2C+Tomasz&rft.au=Ludwin%2C+Artur&rft.date=2024-06-01&rft.issn=2077-0383&rft.eissn=2077-0383&rft.volume=13&rft.issue=11&rft_id=info:doi/10.3390%2Fjcm13113190&rft_id=info%3Apmid%2F38892901&rft.externalDocID=38892901 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2077-0383&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2077-0383&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2077-0383&client=summon |