Managing sickle cell disease and related complications in pregnancy: results of an international Delphi panel
•This international Delphi panel of 12 multidisciplinary experts explored 7 topics related to SCD management during pregnancy.•Based on consensus reached in several areas, recommendations were formulated to inform clinical care for pregnant patients with SCD. [Display omitted] Data to guide evidence...
Saved in:
Published in | Blood advances Vol. 8; no. 4; pp. 1018 - 1029 |
---|---|
Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
27.02.2024
The American Society of Hematology |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | •This international Delphi panel of 12 multidisciplinary experts explored 7 topics related to SCD management during pregnancy.•Based on consensus reached in several areas, recommendations were formulated to inform clinical care for pregnant patients with SCD.
[Display omitted]
Data to guide evidence-based management of pregnant people with sickle cell disease (SCD) are limited. This international Delphi panel aimed to identify consensus among multidisciplinary experts for SCD management during pregnancy. The 2-round Delphi process used questionnaires exploring 7 topics (antenatal care, hydroxyurea use, transfusion, prevention of complications, treatment of complications, delivery and follow-up, and bottlenecks and knowledge gaps) developed by a steering committee. Thirteen panelists (hematologists, physiologists, obstetricians, maternal fetal medicine, and transfusion medicine physicians) from the United States, the United Kingdom, Turkey, and France completed the first survey; 12 panelists completed the second round. Anonymized responses were collected and summarized by a contract research organization (Akkodis Belgium). Consensus and strong consensus were predefined as 75% to 90% (9-10 of 12) and >90% (≥11 of 12) of panelists, respectively, agreeing or disagreeing on a response to a predefined clinical scenario or statement. In several areas of SCD management, consensus was achieved: experts recommended performing at least monthly multidisciplinary antenatal follow-up, administering prophylactic aspirin for preeclampsia prevention between gestational weeks 12 and 36, initiating prophylactic transfusion therapy in certain cases, or choosing automated red blood cell exchange over other transfusion methods for patients with iron overload or severe acute chest syndrome. No consensus was reached on several topics including the prophylactic aspirin dose, indications for starting infection prophylaxis, routine use of prophylactic transfusions, or use of prophylactic transfusions for preventing fetal complications. These recommendations could inform clinical care for patients with SCD who are pregnant in the absence of large clinical trials involving this population; the identified knowledge gaps can orient future research. |
---|---|
AbstractList | ABSTRACTData to guide evidence-based management of pregnant people with sickle cell disease (SCD) are limited. This international Delphi panel aimed to identify consensus among multidisciplinary experts for SCD management during pregnancy. The 2-round Delphi process used questionnaires exploring 7 topics (antenatal care, hydroxyurea use, transfusion, prevention of complications, treatment of complications, delivery and follow-up, and bottlenecks and knowledge gaps) developed by a steering committee. Thirteen panelists (hematologists, physiologists, obstetricians, maternal fetal medicine, and transfusion medicine physicians) from the United States, the United Kingdom, Turkey, and France completed the first survey; 12 panelists completed the second round. Anonymized responses were collected and summarized by a contract research organization (Akkodis Belgium). Consensus and strong consensus were predefined as 75% to 90% (9-10 of 12) and >90% (≥11 of 12) of panelists, respectively, agreeing or disagreeing on a response to a predefined clinical scenario or statement. In several areas of SCD management, consensus was achieved: experts recommended performing at least monthly multidisciplinary antenatal follow-up, administering prophylactic aspirin for preeclampsia prevention between gestational weeks 12 and 36, initiating prophylactic transfusion therapy in certain cases, or choosing automated red blood cell exchange over other transfusion methods for patients with iron overload or severe acute chest syndrome. No consensus was reached on several topics including the prophylactic aspirin dose, indications for starting infection prophylaxis, routine use of prophylactic transfusions, or use of prophylactic transfusions for preventing fetal complications. These recommendations could inform clinical care for patients with SCD who are pregnant in the absence of large clinical trials involving this population; the identified knowledge gaps can orient future research. • This international Delphi panel of 12 multidisciplinary experts explored 7 topics related to SCD management during pregnancy. • Based on consensus reached in several areas, recommendations were formulated to inform clinical care for pregnant patients with SCD. Data to guide evidence-based management of pregnant people with sickle cell disease (SCD) are limited. This international Delphi panel aimed to identify consensus among multidisciplinary experts for SCD management during pregnancy. The 2-round Delphi process used questionnaires exploring 7 topics (antenatal care, hydroxyurea use, transfusion, prevention of complications, treatment of complications, delivery and follow-up, and bottlenecks and knowledge gaps) developed by a steering committee. Thirteen panelists (hematologists, physiologists, obstetricians, maternal fetal medicine, and transfusion medicine physicians) from the United States, the United Kingdom, Turkey, and France completed the first survey; 12 panelists completed the second round. Anonymized responses were collected and summarized by a contract research organization (Akkodis Belgium). Consensus and strong consensus were predefined as 75% to 90% (9-10 of 12) and >90% (≥11 of 12) of panelists, respectively, agreeing or disagreeing on a response to a predefined clinical scenario or statement. In several areas of SCD management, consensus was achieved: experts recommended performing at least monthly multidisciplinary antenatal follow-up, administering prophylactic aspirin for preeclampsia prevention between gestational weeks 12 and 36, initiating prophylactic transfusion therapy in certain cases, or choosing automated red blood cell exchange over other transfusion methods for patients with iron overload or severe acute chest syndrome. No consensus was reached on several topics including the prophylactic aspirin dose, indications for starting infection prophylaxis, routine use of prophylactic transfusions, or use of prophylactic transfusions for preventing fetal complications. These recommendations could inform clinical care for patients with SCD who are pregnant in the absence of large clinical trials involving this population; the identified knowledge gaps can orient future research. Abstract Data to guide evidence-based management of pregnant people with sickle cell disease (SCD) are limited. This international Delphi panel aimed to identify consensus among multidisciplinary experts for SCD management during pregnancy. The 2-round Delphi process used questionnaires exploring 7 topics (antenatal care, hydroxyurea use, transfusion, prevention of complications, treatment of complications, delivery and follow-up, and bottlenecks and knowledge gaps) developed by a steering committee. Thirteen panelists (hematologists, physiologists, obstetricians, maternal fetal medicine, and transfusion medicine physicians) from the United States, the United Kingdom, Turkey, and France completed the first survey; 12 panelists completed the second round. Anonymized responses were collected and summarized by a contract research organization (Akkodis Belgium). Consensus and strong consensus were predefined as 75% to 90% (9-10 of 12) and >90% (≥11 of 12) of panelists, respectively, agreeing or disagreeing on a response to a predefined clinical scenario or statement. In several areas of SCD management, consensus was achieved: experts recommended performing at least monthly multidisciplinary antenatal follow-up, administering prophylactic aspirin for preeclampsia prevention between gestational weeks 12 and 36, initiating prophylactic transfusion therapy in certain cases, or choosing automated red blood cell exchange over other transfusion methods for patients with iron overload or severe acute chest syndrome. No consensus was reached on several topics including the prophylactic aspirin dose, indications for starting infection prophylaxis, routine use of prophylactic transfusions, or use of prophylactic transfusions for preventing fetal complications. These recommendations could inform clinical care for patients with SCD who are pregnant in the absence of large clinical trials involving this population; the identified knowledge gaps can orient future research. Data to guide evidence-based management of pregnant people with sickle cell disease (SCD) are limited. This international Delphi panel aimed to identify consensus among multidisciplinary experts for SCD management during pregnancy. The 2-round Delphi process used questionnaires exploring 7 topics (antenatal care, hydroxyurea use, transfusion, prevention of complications, treatment of complications, delivery and follow-up, and bottlenecks and knowledge gaps) developed by a steering committee. Thirteen panelists (hematologists, physiologists, obstetricians, maternal fetal medicine, and transfusion medicine physicians) from the United States, the United Kingdom, Turkey, and France completed the first survey; 12 panelists completed the second round. Anonymized responses were collected and summarized by a contract research organization (Akkodis Belgium). Consensus and strong consensus were predefined as 75% to 90% (9-10 of 12) and >90% (≥11 of 12) of panelists, respectively, agreeing or disagreeing on a response to a predefined clinical scenario or statement. In several areas of SCD management, consensus was achieved: experts recommended performing at least monthly multidisciplinary antenatal follow-up, administering prophylactic aspirin for preeclampsia prevention between gestational weeks 12 and 36, initiating prophylactic transfusion therapy in certain cases, or choosing automated red blood cell exchange over other transfusion methods for patients with iron overload or severe acute chest syndrome. No consensus was reached on several topics including the prophylactic aspirin dose, indications for starting infection prophylaxis, routine use of prophylactic transfusions, or use of prophylactic transfusions for preventing fetal complications. These recommendations could inform clinical care for patients with SCD who are pregnant in the absence of large clinical trials involving this population; the identified knowledge gaps can orient future research. •This international Delphi panel of 12 multidisciplinary experts explored 7 topics related to SCD management during pregnancy.•Based on consensus reached in several areas, recommendations were formulated to inform clinical care for pregnant patients with SCD. [Display omitted] Data to guide evidence-based management of pregnant people with sickle cell disease (SCD) are limited. This international Delphi panel aimed to identify consensus among multidisciplinary experts for SCD management during pregnancy. The 2-round Delphi process used questionnaires exploring 7 topics (antenatal care, hydroxyurea use, transfusion, prevention of complications, treatment of complications, delivery and follow-up, and bottlenecks and knowledge gaps) developed by a steering committee. Thirteen panelists (hematologists, physiologists, obstetricians, maternal fetal medicine, and transfusion medicine physicians) from the United States, the United Kingdom, Turkey, and France completed the first survey; 12 panelists completed the second round. Anonymized responses were collected and summarized by a contract research organization (Akkodis Belgium). Consensus and strong consensus were predefined as 75% to 90% (9-10 of 12) and >90% (≥11 of 12) of panelists, respectively, agreeing or disagreeing on a response to a predefined clinical scenario or statement. In several areas of SCD management, consensus was achieved: experts recommended performing at least monthly multidisciplinary antenatal follow-up, administering prophylactic aspirin for preeclampsia prevention between gestational weeks 12 and 36, initiating prophylactic transfusion therapy in certain cases, or choosing automated red blood cell exchange over other transfusion methods for patients with iron overload or severe acute chest syndrome. No consensus was reached on several topics including the prophylactic aspirin dose, indications for starting infection prophylaxis, routine use of prophylactic transfusions, or use of prophylactic transfusions for preventing fetal complications. These recommendations could inform clinical care for patients with SCD who are pregnant in the absence of large clinical trials involving this population; the identified knowledge gaps can orient future research. |
Author | Pancham, Shivan Yilmaz Baran, Safak Howard, Jo Sharma, Deva Benachi, Alexandra Kozanoğlu, Ilknur Pecker, Lydia H. Ataga, Kenneth I. Büyükkurt, Selim Ozdogu, Hakan Robinson, Susan E. Lanzkron, Sophie |
Author_xml | – sequence: 1 givenname: Deva surname: Sharma fullname: Sharma, Deva email: deva.sharma@vumc.org organization: Vanderbilt University Medical Center, Nashville, TN – sequence: 2 givenname: Ilknur surname: Kozanoğlu fullname: Kozanoğlu, Ilknur organization: Department of Physiology, Faculty of Medicine, Başkent University, Ankara, Turkey – sequence: 3 givenname: Kenneth I. orcidid: 0000-0002-4501-9982 surname: Ataga fullname: Ataga, Kenneth I. organization: Center for Sickle Cell Disease, University of Tennessee Health Science Center, Memphis, TN – sequence: 4 givenname: Alexandra orcidid: 0000-0001-6045-0765 surname: Benachi fullname: Benachi, Alexandra organization: Division of Obstetrics and Gynecology, Department of Obstetrics and Gynecology, Antoine Béclère Hospital, Assistance Publique Hôpitaux de Paris, Paris Saclay University Hospitals, Clamart, France – sequence: 5 givenname: Selim orcidid: 0000-0003-0572-254X surname: Büyükkurt fullname: Büyükkurt, Selim organization: Department of Obstetrics and Gynecology, Faculty of Medicine, Çukurova University, Adana, Turkey – sequence: 6 givenname: Sophie surname: Lanzkron fullname: Lanzkron, Sophie organization: Division of Hematology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD – sequence: 7 givenname: Hakan orcidid: 0000-0002-8902-1283 surname: Ozdogu fullname: Ozdogu, Hakan organization: Department of Hematology, Faculty of Medicine, Başkent University, Ankara, Turkey – sequence: 8 givenname: Shivan surname: Pancham fullname: Pancham, Shivan organization: Department of Haematology, Sandwell and West Birmingham Hospitals National Health Service Trust, West Bromwich, United Kingdom – sequence: 9 givenname: Lydia H. orcidid: 0000-0002-8371-9752 surname: Pecker fullname: Pecker, Lydia H. organization: Division of Hematology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD – sequence: 10 givenname: Susan E. surname: Robinson fullname: Robinson, Susan E. organization: Department of Women's Health, Guy's and St Thomas' National Health Service Foundation Trust, London, United Kingdom – sequence: 11 givenname: Safak surname: Yilmaz Baran fullname: Yilmaz Baran, Safak organization: Department of Obstetrics and Gynecology, Başkent University, Dr. Turgut Noyan Application and Research Center, Adana, Turkey – sequence: 12 givenname: Jo surname: Howard fullname: Howard, Jo organization: Department of Clinical Haematology, Guy's and St Thomas' National Health Service Foundation Trust, London, United Kingdom |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38206762$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkctuFDEQRS0URELILyAv2Uzwo6fbZoMggYAUxAbWVtmunhjcdmP3jJS_x2GSgaxYWGWpTt163OfkKOWEhFDOzjlX4rWNOXvwO0gO67lgQjLO23tCTkQ3yJVey-Ho8Bf6mJzV-oMxxoderrV4Ro6lEqwfenFCpi-QYBPShtbgfkakDmOkPlSEihSSpwUjLOipy9Mcg4Ml5FRpSHQuuEltiNs3janbuFSax1bScguW9AeESC8xzjeBzpAwviBPR4gVz-7jKfn-8cO3i0-r669Xny_eXa9cp9iy0lZwQCuYBWk9F5b7gYMdfde1ZUfZgVboFfd8bRXate69Y8L1EqT3vbDylLzd685bO6F3mJYC0cwlTFBuTYZgHmdSuDGbvDOcqUH3g24Kr-4VSv61xbqYKdS727Q18rYaoYUSHVNKNFTtUVdyrQXHQx_OzJ1j5pFj5q9jrfTlv3MeCh_8acD7PYDtWruAxVQXsMn4UNAtxufw_y6_ASiXsgU |
CitedBy_id | crossref_primary_10_1080_17474086_2024_2372320 crossref_primary_10_1002_ajh_27315 |
Cites_doi | 10.1097/NCM.0000000000000260 10.1016/j.critrevonc.2015.11.018 10.1186/s13063-017-2402-9 10.1053/j.seminhematol.2018.04.010 10.4084/mjhid.2019.040 10.1111/j.1537-2995.2012.03659.x 10.1136/bmjopen-2020-047949 10.1002/ajh.25643 10.1002/ajh.24235 10.1046/j.1365-2648.2000.t01-1-01567.x 10.1097/HS9.0000000000000446 10.1182/bloodadvances.2019001143 10.3389/fphar.2021.770640 10.1182/hematology.2019000039 10.1186/s13063-023-07235-x 10.1056/NEJM198812013192204 10.1177/0269216317690685 10.1182/blood-2019-126529 10.1111/bjh.17671 10.1182/blood-2015-06-649319 10.3324/haematol.2018.207357 10.1016/j.ajog.2020.07.023 10.1016/S0248-8663(15)60002-9 10.1182/asheducation-2016.1.625 10.1002/(SICI)1096-8652(199902)60:2<148::AID-AJH12>3.0.CO;2-I 10.3390/pharmacy10050123 10.1002/ajh.26495 10.3390/biomedicines11020597 10.1002/bdrb.20123 10.1080/14767058.2022.2035713 10.1182/asheducation.V2015.1.436.3917688 10.1016/j.jclinepi.2013.12.002 10.1186/s13063-020-4212-8 |
ContentType | Journal Article |
Copyright | 2024 The American Society of Hematology 2024 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. 2024 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. 2024 The American Society of Hematology |
Copyright_xml | – notice: 2024 The American Society of Hematology – notice: 2024 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. – notice: 2024 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. 2024 The American Society of Hematology |
DBID | 6I. AAFTH CGR CUY CVF ECM EIF NPM AAYXX CITATION 7X8 5PM |
DOI | 10.1182/bloodadvances.2023011301 |
DatabaseName | ScienceDirect Open Access Titles Elsevier:ScienceDirect:Open Access Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed CrossRef MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) CrossRef MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic CrossRef MEDLINE |
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: 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 |
EISSN | 2473-9537 |
EndPage | 1029 |
ExternalDocumentID | 10_1182_bloodadvances_2023011301 38206762 S247395292400017X |
Genre | Journal Article |
GroupedDBID | .1- .FO 53G 6I. AAFTH AAXUO AFCTW AFRHN AJUYK ALMA_UNASSIGNED_HOLDINGS AMRAJ EBS FDB HYE OK1 ROL RPM THE W2D Z5R 0R~ 0SF AALRI ADVLN AITUG AKRWK CGR CUY CVF ECM EIF GROUPED_DOAJ NPM AAYXX CITATION 7X8 5PM |
ID | FETCH-LOGICAL-c480t-9b21aeb20ba3bd12b1d71abfd44230f34a98ed81d15b8eb596dc02c63a3dd62b3 |
IEDL.DBID | RPM |
ISSN | 2473-9529 |
IngestDate | Tue Sep 17 21:29:28 EDT 2024 Fri Aug 16 03:52:15 EDT 2024 Fri Aug 23 01:19:01 EDT 2024 Sat Sep 28 08:11:22 EDT 2024 Sat Mar 02 15:59:53 EST 2024 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 4 |
Language | English |
License | This is an open access article under the CC BY-NC-ND license. 2024 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c480t-9b21aeb20ba3bd12b1d71abfd44230f34a98ed81d15b8eb596dc02c63a3dd62b3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ORCID | 0000-0002-4501-9982 0000-0001-6045-0765 0000-0002-8371-9752 0000-0003-0572-254X 0000-0002-8902-1283 |
OpenAccessLink | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10879679/ |
PMID | 38206762 |
PQID | 2928240882 |
PQPubID | 23479 |
PageCount | 12 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_10879679 proquest_miscellaneous_2928240882 crossref_primary_10_1182_bloodadvances_2023011301 pubmed_primary_38206762 elsevier_sciencedirect_doi_10_1182_bloodadvances_2023011301 |
PublicationCentury | 2000 |
PublicationDate | 2024-02-27 |
PublicationDateYYYYMMDD | 2024-02-27 |
PublicationDate_xml | – month: 02 year: 2024 text: 2024-02-27 day: 27 |
PublicationDecade | 2020 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | Blood advances |
PublicationTitleAlternate | Blood Adv |
PublicationYear | 2024 |
Publisher | Elsevier Inc The American Society of Hematology |
Publisher_xml | – name: Elsevier Inc – name: The American Society of Hematology |
References | Hasson, Keeney, McKenna (bib22) 2000; 32 Bailey, Shah, Boynewicz, Justice, Wood (bib11) 2022; 35 Diamond, Grant, Feldman (bib24) 2014; 67 Ware (bib9) 2015; 2015 Chaturvedi, DeBaun (bib2) 2016; 91 Habibi, Cannas, Bartolucci (bib25) 2023; 11 Taher, Iolascon, Matar (bib35) 2020; 4 Smart, Hernandez, Ware (bib18) 2018; 55 Migotsky, Beestrum, Badawy (bib12) 2022; 10 Carden, Little (bib1) 2019; 104 Diav-Citrin, Hunnisett, Sher, Koren (bib8) 1999; 60 Luzzatto, Makani (bib19) 2021; 12 Jain, Atmapoojya, Colah, Lodha (bib3) 2019; 11 Oakley, Awogbade, Brien (bib32) 2020; 21 Asare, Olayemi, Boafor (bib5) 2019; 94 Malinowski, Shehata, D’Souza (bib13) 2015; 126 Smith-Whitley (bib4) 2019; 2019 Gellen-Dautremer, Le Jeune, Receveur, Foïs (bib26) 2019; 134 Ballas, McCarthy, Guo (bib27) 2009; 101 van der Graaf, van der Zande, den Ruijter (bib21) 2018; 19 Boga, Ozdogu (bib6) 2016; 98 Kroner, Hankins, Pugh (bib10) 2022; 97 Afolabi, Babah, Adeyemo (bib30) 2021; 11 Oteng-Ntim, Pavord, Howard (bib7) 2021; 194 Habibi, Arlet, Stankovic (bib14) 2015; 36 Wahl, Garcia, Hagar, Gildengorin, Quirolo, Vichinsky (bib34) 2012; 52 Koshy, Burd, Wallace, Moawad, Baron (bib31) 1988; 319 Liebelt, Balk, Faber (bib28) 2007; 80 Jünger, Payne, Brine, Radbruch, Brearley (bib23) 2017; 31 Hastie, Tong, Wikström, Sandström, Hesselman, Bergman (bib29) 2021; 224 Seed, Brien, Oakley (bib33) 2023; 24 bib16 Howard (bib17) 2016; 2016 Chou, Alsawas, Fasano (bib15) 2020; 4 Brennan-Cook, Bonnabeau, Aponte, Augustin, Tanabe (bib20) 2018; 23 van der Graaf (2024022713560886700_bib21) 2018; 19 Luzzatto (2024022713560886700_bib19) 2021; 12 Smith-Whitley (2024022713560886700_bib4) 2019; 2019 2024022713560886700_bib16 Chaturvedi (2024022713560886700_bib2) 2016; 91 Oteng-Ntim (2024022713560886700_bib7) 2021; 194 Diav-Citrin (2024022713560886700_bib8) 1999; 60 Chou (2024022713560886700_bib15) 2020; 4 Smart (2024022713560886700_bib18) 2018; 55 Brennan-Cook (2024022713560886700_bib20) 2018; 23 Liebelt (2024022713560886700_bib28) 2007; 80 Jain (2024022713560886700_bib3) 2019; 11 Boga (2024022713560886700_bib6) 2016; 98 Hastie (2024022713560886700_bib29) 2021; 224 Asare (2024022713560886700_bib5) 2019; 94 Ballas (2024022713560886700_bib27) 2009; 101 Oakley (2024022713560886700_bib32) 2020; 21 Habibi (2024022713560886700_bib14) 2015; 36 Hasson (2024022713560886700_bib22) 2000; 32 Migotsky (2024022713560886700_bib12) 2022; 10 Taher (2024022713560886700_bib35) 2020; 4 Howard (2024022713560886700_bib17) 2016; 2016 Kroner (2024022713560886700_bib10) 2022; 97 Ware (2024022713560886700_bib9) 2015; 2015 Koshy (2024022713560886700_bib31) 1988; 319 Bailey (2024022713560886700_bib11) 2022; 35 Malinowski (2024022713560886700_bib13) 2015; 126 Afolabi (2024022713560886700_bib30) 2021; 11 Wahl (2024022713560886700_bib34) 2012; 52 Habibi (2024022713560886700_bib25) 2023; 11 Diamond (2024022713560886700_bib24) 2014; 67 Seed (2024022713560886700_bib33) 2023; 24 Carden (2024022713560886700_bib1) 2019; 104 Gellen-Dautremer (2024022713560886700_bib26) 2019; 134 Jünger (2024022713560886700_bib23) 2017; 31 |
References_xml | – volume: 2016 start-page: 625 year: 2016 end-page: 631 ident: bib17 article-title: Sickle cell disease: when and how to transfuse publication-title: Hematology Am Soc Hematol Educ Program contributor: fullname: Howard – volume: 98 start-page: 364 year: 2016 end-page: 374 ident: bib6 article-title: Pregnancy and sickle cell disease: a review of the current literature publication-title: Crit Rev Oncol Hematol contributor: fullname: Ozdogu – volume: 52 start-page: 2671 year: 2012 end-page: 2676 ident: bib34 article-title: Lower alloimmunization rates in pediatric sickle cell patients on chronic erythrocytapheresis compared to chronic simple transfusions publication-title: Transfusion contributor: fullname: Vichinsky – volume: 97 start-page: 603 year: 2022 end-page: 612 ident: bib10 article-title: Pregnancy outcomes with hydroxyurea use in women with sickle cell disease publication-title: Am J Hematol contributor: fullname: Pugh – volume: 31 start-page: 684 year: 2017 end-page: 706 ident: bib23 article-title: Guidance on Conducting and REporting DElphi Studies (CREDES) in palliative care: recommendations based on a methodological systematic review publication-title: Palliat Med contributor: fullname: Brearley – volume: 11 year: 2021 ident: bib30 article-title: Low-dose aspirin for preventing intrauterine growth restriction and pre-eclampsia in sickle cell pregnancy (PIPSICKLE): a randomised controlled trial (study protocol) publication-title: BMJ Open contributor: fullname: Adeyemo – volume: 94 start-page: E328 year: 2019 end-page: E331 ident: bib5 article-title: Third trimester and early postpartum period of pregnancy have the greatest risk for ACS in women with SCD publication-title: Am J Hematol contributor: fullname: Boafor – volume: 11 year: 2019 ident: bib3 article-title: Sickle cell disease and pregnancy publication-title: Mediterr J Hematol Infect Dis contributor: fullname: Lodha – volume: 2015 start-page: 436 year: 2015 end-page: 443 ident: bib9 article-title: Optimizing hydroxyurea therapy for sickle cell anemia publication-title: Hematology Am Soc Hematol Educ Program contributor: fullname: Ware – volume: 4 start-page: 327 year: 2020 end-page: 355 ident: bib15 article-title: American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support publication-title: Blood Adv contributor: fullname: Fasano – volume: 55 start-page: 102 year: 2018 end-page: 112 ident: bib18 article-title: Sickle cell disease: translating clinical care to low-resource countries through international research collaborations publication-title: Semin Hematol contributor: fullname: Ware – volume: 23 start-page: 213 year: 2018 end-page: 219 ident: bib20 article-title: Barriers to care for persons with sickle cell disease: the case manager's opportunity to improve patient outcomes publication-title: Prof Case Manag contributor: fullname: Tanabe – volume: 80 start-page: 259 year: 2007 end-page: 366 ident: bib28 article-title: NTP-CERHR expert panel report on the reproductive and developmental toxicity of hydroxyurea publication-title: Birth Defects Res B Dev Reprod Toxicol contributor: fullname: Faber – volume: 134 start-page: 1027 year: 2019 ident: bib26 article-title: Hydroxyurea exposure throughout pregnancy in patients with sickle-cell disease: 4 case reports from European non-interventional, multicentric, prospective Escort-HU study publication-title: Blood contributor: fullname: Foïs – volume: 24 start-page: 225 year: 2023 ident: bib33 article-title: Serial prophylactic exchange blood transfusion in pregnant women with sickle cell disease (TAPS-2): statistical and qualitative analysis plan for a randomised controlled feasibility trial publication-title: Trials contributor: fullname: Oakley – volume: 2019 start-page: 359 year: 2019 end-page: 366 ident: bib4 article-title: Complications in pregnant women with sickle cell disease publication-title: Hematology Am Soc Hematol Educ Program contributor: fullname: Smith-Whitley – volume: 126 start-page: 2424 year: 2015 end-page: 2435 ident: bib13 article-title: Prophylactic transfusion for pregnant women with sickle cell disease: a systematic review and meta-analysis publication-title: Blood contributor: fullname: D’Souza – volume: 32 start-page: 1008 year: 2000 end-page: 1015 ident: bib22 article-title: Research guidelines for the Delphi survey technique publication-title: J Adv Nurs contributor: fullname: McKenna – volume: 319 start-page: 1447 year: 1988 end-page: 1452 ident: bib31 article-title: Prophylactic red-cell transfusions in pregnant patients with sickle cell disease. A randomized cooperative study publication-title: N Engl J Med contributor: fullname: Baron – volume: 4 start-page: e446 year: 2020 ident: bib35 article-title: Recommendations for pregnancy in rare inherited anemias publication-title: Hemasphere contributor: fullname: Matar – volume: 36 start-page: 5S3 year: 2015 end-page: 5S84 ident: bib14 article-title: Recommandations françaises de prise en charge de la drépanocytose de l’adulte: actualisation 2015 [French guidelines for the management of adult sickle cell disease: 2015 update] publication-title: Rev Med Interne contributor: fullname: Stankovic – volume: 21 start-page: 347 year: 2020 ident: bib32 article-title: Serial prophylactic exchange blood transfusion in pregnant women with sickle cell disease (TAPS-2): study protocol for a randomised controlled feasibility trial publication-title: Trials contributor: fullname: Brien – volume: 12 year: 2021 ident: bib19 article-title: Treating rare diseases in Africa: the drugs exist but the need is unmet publication-title: Front Pharmacol contributor: fullname: Makani – volume: 101 start-page: 1046 year: 2009 end-page: 1051 ident: bib27 article-title: Exposure to hydroxyurea and pregnancy outcomes in patients with sickle cell anemia publication-title: J Natl Med Assoc contributor: fullname: Guo – volume: 104 start-page: 1710 year: 2019 end-page: 1719 ident: bib1 article-title: Emerging disease-modifying therapies for sickle cell disease publication-title: Haematologica contributor: fullname: Little – volume: 194 start-page: 980 year: 2021 end-page: 995 ident: bib7 article-title: Management of sickle cell disease in pregnancy. A British Society for Haematology guideline publication-title: Br J Haematol contributor: fullname: Howard – volume: 60 start-page: 148 year: 1999 end-page: 150 ident: bib8 article-title: Hydroxyurea use during pregnancy: a case report in sickle cell disease and review of the literature publication-title: Am J Hematol contributor: fullname: Koren – ident: bib16 article-title: Hemoglobinopathies in pregnancy – volume: 91 start-page: 5 year: 2016 end-page: 14 ident: bib2 article-title: Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: the last 40 years publication-title: Am J Hematol contributor: fullname: DeBaun – volume: 11 year: 2023 ident: bib25 article-title: Outcomes of pregnancy in sickle cell disease patients: results from the prospective ESCORT-HU cohort study publication-title: Biomedicines contributor: fullname: Bartolucci – volume: 19 start-page: 78 year: 2018 ident: bib21 article-title: Fair inclusion of pregnant women in clinical trials: an integrated scientific and ethical approach publication-title: Trials contributor: fullname: den Ruijter – volume: 10 start-page: 123 year: 2022 ident: bib12 article-title: Recent advances in sickle-cell disease therapies: a review of voxelotor, crizanlizumab, and L-glutamine publication-title: Pharmacy (Basel) contributor: fullname: Badawy – volume: 224 start-page: 95.e1 year: 2021 end-page: 95.e12 ident: bib29 article-title: Aspirin use during pregnancy and the risk of bleeding complications: a Swedish population-based cohort study publication-title: Am J Obstet Gynecol contributor: fullname: Bergman – volume: 35 start-page: 9383 year: 2022 end-page: 9390 ident: bib11 article-title: Impact of publication-title: J Matern Fetal Neonatal Med contributor: fullname: Wood – volume: 67 start-page: 401 year: 2014 end-page: 409 ident: bib24 article-title: Defining consensus: a systematic review recommends methodologic criteria for reporting of Delphi studies publication-title: J Clin Epidemiol contributor: fullname: Feldman – volume: 23 start-page: 213 issue: 4 year: 2018 ident: 2024022713560886700_bib20 article-title: Barriers to care for persons with sickle cell disease: the case manager's opportunity to improve patient outcomes publication-title: Prof Case Manag doi: 10.1097/NCM.0000000000000260 contributor: fullname: Brennan-Cook – volume: 98 start-page: 364 year: 2016 ident: 2024022713560886700_bib6 article-title: Pregnancy and sickle cell disease: a review of the current literature publication-title: Crit Rev Oncol Hematol doi: 10.1016/j.critrevonc.2015.11.018 contributor: fullname: Boga – volume: 19 start-page: 78 issue: 1 year: 2018 ident: 2024022713560886700_bib21 article-title: Fair inclusion of pregnant women in clinical trials: an integrated scientific and ethical approach publication-title: Trials doi: 10.1186/s13063-017-2402-9 contributor: fullname: van der Graaf – volume: 55 start-page: 102 issue: 2 year: 2018 ident: 2024022713560886700_bib18 article-title: Sickle cell disease: translating clinical care to low-resource countries through international research collaborations publication-title: Semin Hematol doi: 10.1053/j.seminhematol.2018.04.010 contributor: fullname: Smart – volume: 11 start-page: e2019040 issue: 1 year: 2019 ident: 2024022713560886700_bib3 article-title: Sickle cell disease and pregnancy publication-title: Mediterr J Hematol Infect Dis doi: 10.4084/mjhid.2019.040 contributor: fullname: Jain – volume: 52 start-page: 2671 issue: 12 year: 2012 ident: 2024022713560886700_bib34 article-title: Lower alloimmunization rates in pediatric sickle cell patients on chronic erythrocytapheresis compared to chronic simple transfusions publication-title: Transfusion doi: 10.1111/j.1537-2995.2012.03659.x contributor: fullname: Wahl – volume: 11 start-page: e047949 issue: 8 year: 2021 ident: 2024022713560886700_bib30 article-title: Low-dose aspirin for preventing intrauterine growth restriction and pre-eclampsia in sickle cell pregnancy (PIPSICKLE): a randomised controlled trial (study protocol) publication-title: BMJ Open doi: 10.1136/bmjopen-2020-047949 contributor: fullname: Afolabi – volume: 94 start-page: E328 issue: 12 year: 2019 ident: 2024022713560886700_bib5 article-title: Third trimester and early postpartum period of pregnancy have the greatest risk for ACS in women with SCD publication-title: Am J Hematol doi: 10.1002/ajh.25643 contributor: fullname: Asare – volume: 91 start-page: 5 issue: 1 year: 2016 ident: 2024022713560886700_bib2 article-title: Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: the last 40 years publication-title: Am J Hematol doi: 10.1002/ajh.24235 contributor: fullname: Chaturvedi – volume: 32 start-page: 1008 issue: 4 year: 2000 ident: 2024022713560886700_bib22 article-title: Research guidelines for the Delphi survey technique publication-title: J Adv Nurs doi: 10.1046/j.1365-2648.2000.t01-1-01567.x contributor: fullname: Hasson – volume: 4 start-page: e446 issue: 4 year: 2020 ident: 2024022713560886700_bib35 article-title: Recommendations for pregnancy in rare inherited anemias publication-title: Hemasphere doi: 10.1097/HS9.0000000000000446 contributor: fullname: Taher – volume: 4 start-page: 327 issue: 2 year: 2020 ident: 2024022713560886700_bib15 article-title: American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support publication-title: Blood Adv doi: 10.1182/bloodadvances.2019001143 contributor: fullname: Chou – volume: 12 start-page: 770640 year: 2021 ident: 2024022713560886700_bib19 article-title: Treating rare diseases in Africa: the drugs exist but the need is unmet publication-title: Front Pharmacol doi: 10.3389/fphar.2021.770640 contributor: fullname: Luzzatto – ident: 2024022713560886700_bib16 – volume: 2019 start-page: 359 issue: 1 year: 2019 ident: 2024022713560886700_bib4 article-title: Complications in pregnant women with sickle cell disease publication-title: Hematology Am Soc Hematol Educ Program doi: 10.1182/hematology.2019000039 contributor: fullname: Smith-Whitley – volume: 24 start-page: 225 issue: 1 year: 2023 ident: 2024022713560886700_bib33 article-title: Serial prophylactic exchange blood transfusion in pregnant women with sickle cell disease (TAPS-2): statistical and qualitative analysis plan for a randomised controlled feasibility trial publication-title: Trials doi: 10.1186/s13063-023-07235-x contributor: fullname: Seed – volume: 319 start-page: 1447 issue: 22 year: 1988 ident: 2024022713560886700_bib31 article-title: Prophylactic red-cell transfusions in pregnant patients with sickle cell disease. A randomized cooperative study publication-title: N Engl J Med doi: 10.1056/NEJM198812013192204 contributor: fullname: Koshy – volume: 31 start-page: 684 issue: 8 year: 2017 ident: 2024022713560886700_bib23 article-title: Guidance on Conducting and REporting DElphi Studies (CREDES) in palliative care: recommendations based on a methodological systematic review publication-title: Palliat Med doi: 10.1177/0269216317690685 contributor: fullname: Jünger – volume: 134 start-page: 1027 issue: suppl 1 year: 2019 ident: 2024022713560886700_bib26 article-title: Hydroxyurea exposure throughout pregnancy in patients with sickle-cell disease: 4 case reports from European non-interventional, multicentric, prospective Escort-HU study publication-title: Blood doi: 10.1182/blood-2019-126529 contributor: fullname: Gellen-Dautremer – volume: 194 start-page: 980 issue: 6 year: 2021 ident: 2024022713560886700_bib7 article-title: Management of sickle cell disease in pregnancy. A British Society for Haematology guideline publication-title: Br J Haematol doi: 10.1111/bjh.17671 contributor: fullname: Oteng-Ntim – volume: 126 start-page: 2424 issue: 21 year: 2015 ident: 2024022713560886700_bib13 article-title: Prophylactic transfusion for pregnant women with sickle cell disease: a systematic review and meta-analysis publication-title: Blood doi: 10.1182/blood-2015-06-649319 contributor: fullname: Malinowski – volume: 104 start-page: 1710 issue: 9 year: 2019 ident: 2024022713560886700_bib1 article-title: Emerging disease-modifying therapies for sickle cell disease publication-title: Haematologica doi: 10.3324/haematol.2018.207357 contributor: fullname: Carden – volume: 224 start-page: 95.e1 issue: 1 year: 2021 ident: 2024022713560886700_bib29 article-title: Aspirin use during pregnancy and the risk of bleeding complications: a Swedish population-based cohort study publication-title: Am J Obstet Gynecol doi: 10.1016/j.ajog.2020.07.023 contributor: fullname: Hastie – volume: 36 start-page: 5S3 issue: 5 year: 2015 ident: 2024022713560886700_bib14 article-title: Recommandations françaises de prise en charge de la drépanocytose de l’adulte: actualisation 2015 [French guidelines for the management of adult sickle cell disease: 2015 update] publication-title: Rev Med Interne doi: 10.1016/S0248-8663(15)60002-9 contributor: fullname: Habibi – volume: 2016 start-page: 625 issue: 1 year: 2016 ident: 2024022713560886700_bib17 article-title: Sickle cell disease: when and how to transfuse publication-title: Hematology Am Soc Hematol Educ Program doi: 10.1182/asheducation-2016.1.625 contributor: fullname: Howard – volume: 60 start-page: 148 issue: 2 year: 1999 ident: 2024022713560886700_bib8 article-title: Hydroxyurea use during pregnancy: a case report in sickle cell disease and review of the literature publication-title: Am J Hematol doi: 10.1002/(SICI)1096-8652(199902)60:2<148::AID-AJH12>3.0.CO;2-I contributor: fullname: Diav-Citrin – volume: 10 start-page: 123 issue: 5 year: 2022 ident: 2024022713560886700_bib12 article-title: Recent advances in sickle-cell disease therapies: a review of voxelotor, crizanlizumab, and L-glutamine publication-title: Pharmacy (Basel) doi: 10.3390/pharmacy10050123 contributor: fullname: Migotsky – volume: 97 start-page: 603 issue: 5 year: 2022 ident: 2024022713560886700_bib10 article-title: Pregnancy outcomes with hydroxyurea use in women with sickle cell disease publication-title: Am J Hematol doi: 10.1002/ajh.26495 contributor: fullname: Kroner – volume: 11 start-page: 597 issue: 2 year: 2023 ident: 2024022713560886700_bib25 article-title: Outcomes of pregnancy in sickle cell disease patients: results from the prospective ESCORT-HU cohort study publication-title: Biomedicines doi: 10.3390/biomedicines11020597 contributor: fullname: Habibi – volume: 80 start-page: 259 issue: 4 year: 2007 ident: 2024022713560886700_bib28 article-title: NTP-CERHR expert panel report on the reproductive and developmental toxicity of hydroxyurea publication-title: Birth Defects Res B Dev Reprod Toxicol doi: 10.1002/bdrb.20123 contributor: fullname: Liebelt – volume: 35 start-page: 9383 issue: 25 year: 2022 ident: 2024022713560886700_bib11 article-title: Impact of in utero opioid exposure on newborn outcomes: beyond neonatal opioid withdrawal syndrome publication-title: J Matern Fetal Neonatal Med doi: 10.1080/14767058.2022.2035713 contributor: fullname: Bailey – volume: 2015 start-page: 436 issue: 1 year: 2015 ident: 2024022713560886700_bib9 article-title: Optimizing hydroxyurea therapy for sickle cell anemia publication-title: Hematology Am Soc Hematol Educ Program doi: 10.1182/asheducation.V2015.1.436.3917688 contributor: fullname: Ware – volume: 67 start-page: 401 issue: 4 year: 2014 ident: 2024022713560886700_bib24 article-title: Defining consensus: a systematic review recommends methodologic criteria for reporting of Delphi studies publication-title: J Clin Epidemiol doi: 10.1016/j.jclinepi.2013.12.002 contributor: fullname: Diamond – volume: 101 start-page: 1046 issue: 10 year: 2009 ident: 2024022713560886700_bib27 article-title: Exposure to hydroxyurea and pregnancy outcomes in patients with sickle cell anemia publication-title: J Natl Med Assoc contributor: fullname: Ballas – volume: 21 start-page: 347 issue: 1 year: 2020 ident: 2024022713560886700_bib32 article-title: Serial prophylactic exchange blood transfusion in pregnant women with sickle cell disease (TAPS-2): study protocol for a randomised controlled feasibility trial publication-title: Trials doi: 10.1186/s13063-020-4212-8 contributor: fullname: Oakley |
SSID | ssj0001763592 |
Score | 2.3181572 |
Snippet | •This international Delphi panel of 12 multidisciplinary experts explored 7 topics related to SCD management during pregnancy.•Based on consensus reached in... Data to guide evidence-based management of pregnant people with sickle cell disease (SCD) are limited. This international Delphi panel aimed to identify... Abstract Data to guide evidence-based management of pregnant people with sickle cell disease (SCD) are limited. This international Delphi panel aimed to... ABSTRACTData to guide evidence-based management of pregnant people with sickle cell disease (SCD) are limited. This international Delphi panel aimed to... • This international Delphi panel of 12 multidisciplinary experts explored 7 topics related to SCD management during pregnancy. • Based on consensus reached in... |
SourceID | pubmedcentral proquest crossref pubmed elsevier |
SourceType | Open Access Repository Aggregation Database Index Database Publisher |
StartPage | 1018 |
SubjectTerms | Acute Chest Syndrome - complications Acute Chest Syndrome - therapy Anemia, Sickle Cell - complications Anemia, Sickle Cell - therapy Aspirin Blood Transfusion - methods Female Humans Hydroxyurea - therapeutic use Pregnancy Red Cells, Iron, and Erythropoiesis |
Title | Managing sickle cell disease and related complications in pregnancy: results of an international Delphi panel |
URI | https://dx.doi.org/10.1182/bloodadvances.2023011301 https://www.ncbi.nlm.nih.gov/pubmed/38206762 https://search.proquest.com/docview/2928240882 https://pubmed.ncbi.nlm.nih.gov/PMC10879679 |
Volume | 8 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV07T8MwELagEwsC8SovGYk1NPErNkyogBASiAEktih-BCLStCrtwL_n7CbQAgNi9lly7i738vk7hI49ZJYpNI8SY3XEuBORlHkRaSsEp8xZsMu-2-JOXD-ymyf-tIRE-xYmNO0bXZ7U1eCkLl9Cb-VoYHptn1jv_rafxDJVIlW9ZbScUjqXo4fKisdYC9OQCUtppDhRbQuPJL3QD97cr3u4buI1nDYzYX7xSz_jzu_tk3P-6GoNrTaBJD6fHXgdLbl6Aw3asUMYmP9aOezr8ri5hMF5bXF4u-IsXmglx2WNR2P37ME33k-B5m1aTd7wsIAtuJyvGeILV41eSgw2xFWb6PHq8qF_HTUDFSLDZDyJlCZJDql0rHOqbUJ0YtMk14VlEFTFBWW5ks5CBJtwLZ3mSlgTEyNoTq0VRNMt1KmHtdtB2AmiIHYyghvDwNpqoNS8SJ1QBlJA2UVJy85sNMPNyEK-IUm2IILsSwRddNbyPWv8_8yvZ2De_7D7qBVVBr-I5y-wYjgFGgV5JfO5RBdtz0T3eSYa8OsFrMgFoX4SePjtxRXQygDD3Wrh7v-37qEV-AAWnsin-6gzGU_dAQQ5E30YigOHQbM_AJkAAyA |
link.rule.ids | 230,315,733,786,790,870,891,27957,27958,53827,53829 |
linkProvider | National Library of Medicine |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELZKOcCFFvFaSsFIXLOb-BUbTqgPLdBWHFrRWxQ_0kbNZldt9gC_nrETl93CATh7LMWesf2N8_kbhN55ySxTaZ5kxuqEcScSKcsq0VYITpmzsC97tsWJmJ6xz-f8fAOJ-BYmkPaNrsdtMxu39WXgVi5mZhJ5YpOvx3tZKnMlcjW5h-7DgiX5SpYe7la8ylqoh0xYThPFiYokHkkmgRE-_GH3gt3ExzgdqsL84WT6HXneJVCunEiHW-hbHEtPRLkaLzs9Nj_uyDz--2C30aMBpOKPfftjtOHaJ2gWSxphcOxV47C_88fDDx5cthaHdzHO4jWaOq5bvLh2F17Y4_t7sLlZNt0NnlfQBder95F43zWLyxrD_uSap-js8OB0b5oMxRoSw2TaJUqTrIQ0PdUl1TYjOrN5VurKMgBsaUVZqaSzgI4zrqXTXAlrUmIELam1gmj6DG2289a9QNgJogCXGcGNYbCTa7DUvMqdUAbSSzlCWXRUseg1OYqQy0hSrDm3-OXcEfoQPVoM2KLHDAUcHX_R-20MggKWn59fmIr5EmwU5KzM5ykj9LwPittvokEbX0CLXAuXWwMv7b3eAkEQJL6j01_-f9c36MH09PioOPp08mUHPYTBsPAUP3-FNrvrpdsFMNXp12Hl_ARnFyRj |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELagSIgLLeK1lIKRuGaT-BUbTqjtqryqHqhUiUMUP9JGzWajbvYAv56xk7S7hQPq2WMp9oztb5zP3yD03ktmmVLzKDVWR4w7EUlZlJG2QnDKnIV92bMtjsXRKftyxs8GVuVyoFU2RlfTpp5Pm-oicCvbuYlHnlh88n0_TWSmRKbi1pbxffQAFi1Ra5l6uF_xSmuhJjJhGY0UJ2ok8kgSB1b48Jfdi3YTH-d0qAzzj9Ppb_R5m0S5dirNttHPcTw9GeVyuur01Py-JfV4twHvoMcDWMWfepsn6J5rnqL5WNoIg4Mva4f93T8efvTgorE4vI9xFm_Q1XHV4PbKnXuBj18fwGa5qrslXpTQBVfr95L4wNXtRYVhn3L1M3Q6O_yxfxQNRRsiw2TSRUqTtIB0PdEF1TYlOrVZWujSMgBuSUlZoaSzgJJTrqXTXAlrEmIELai1gmj6HG01i8a9RNgJogCfGcGNYbCja7DUvMycUAbSTDlB6eisvO21OfKQ00iSbzg4v3HwBH0cvZoPGKPHDjkcIf_R-90YCDksQz-_MBWLFdgoyF2Zz1cm6EUfGNffRINGvoAWuREy1wZe4nuzBQIhSH2Pjn91965v0cOTg1n-7fPx1130CMbCwov87DXa6q5Wbg8wVaffhMXzB2NwJuM |
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=Managing+sickle+cell+disease+and+related+complications+in+pregnancy%3A+results+of+an+international+Delphi+panel&rft.jtitle=Blood+advances&rft.au=Sharma%2C+Deva&rft.au=Kozano%C4%9Flu%2C+Ilknur&rft.au=Ataga%2C+Kenneth+I.&rft.au=Benachi%2C+Alexandra&rft.date=2024-02-27&rft.issn=2473-9529&rft.eissn=2473-9537&rft.volume=8&rft.issue=4&rft.spage=1018&rft.epage=1029&rft_id=info:doi/10.1182%2Fbloodadvances.2023011301&rft.externalDBID=n%2Fa&rft.externalDocID=10_1182_bloodadvances_2023011301 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2473-9529&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2473-9529&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2473-9529&client=summon |