Evaluation of a prophylactic transfusion program on obstetric outcomes in pregnant women with sickle cell disease: A single centre retrospective cohort study.


Journal

European journal of obstetrics, gynecology, and reproductive biology
ISSN: 1872-7654
Titre abrégé: Eur J Obstet Gynecol Reprod Biol
Pays: Ireland
ID NLM: 0375672

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 14 03 2023
revised: 04 08 2023
accepted: 30 08 2023
medline: 13 11 2023
pubmed: 1 10 2023
entrez: 30 9 2023
Statut: ppublish

Résumé

To evaluate the effects of a prophylactic transfusion program (TP) on obstetric and perinatal outcomes in pregnant women with sickle cell disease (SCD). This retrospective cohort study included all singleton pregnancies among women with SCD in a French university tertiary care center between 1 January 2004 and 31 December 2017. The TP group included patients selected according to the French guidelines who received regular red blood cell transfusions during pregnancy until delivery. The factors associated with TP indication [year of birth, SCD genotype, history of acute chest syndrome and delayed hemolysis transfusion reaction (DHTR) risk score] were taken into account in a propensity score. A composite obstetric adverse outcome was defined associating birth before 34 gestational weeks and/or pre-eclampsia and/or small for gestational age and/or abruption and/or stillbirth and/or maternal death and/or neonatal death. In total, 246 pregnancies in 173 patients were analyzed. Twenty-two pregnancies with a history of DHTR were excluded. A higher frequency of TP was found before 2013 [119/148 (80.4%) vs 38/76 (50%); p < 0.001]. Rates of preterm birth before 34 gestational weeks (5.6% vs 19.7%; p = 0.001), vaso-occlusive crisis (36.5% vs. 61.8%; p < 0.001), and acute chest syndrome (6.1% vs. 14.5%; p = 0.04) during pregnancy were decreased significantly in the TP group. Among the groups with and without composite obstetric adverse outcomes, the frequency of TP was 52.6% and 74.7%, respectively [odds ratio (OR) 0.30, 95% confidence interval (CI) 0.09-1.02]. The multivariate analysis shows that the TP was associated with a significant reduction in the risk of composite obstetric adverse outcomes (OR 0.28, 95% CI 0.08-0.97; p = 0.04). A red blood cell TP may have an independent protective effect on maternal and perinatal adverse outcomes during pregnancy in women with SCD.

Identifiants

pubmed: 37776703
pii: S0301-2115(23)00696-6
doi: 10.1016/j.ejogrb.2023.08.390
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103-108

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

O Sobczyk (O)

Service de Gynécologie Obstétrique, Centre Hospitalier Intercommunal de Créteil, France; Univ Paris Est Créteil, France.

E Gottardi (E)

Service de Gynécologie Obstétrique, Centre Hospitalier Intercommunal de Créteil, France; Univ Paris Est Créteil, France.

M Lefebvre (M)

Service de Gynécologie Obstétrique, Centre Hospitalier Intercommunal de Créteil, France; Univ Paris Est Créteil, France.

F Canouï-Poitrine (F)

Univ Paris Est Créteil, France; Département de Santé Publique et de Biostatistiques de l'Hôpital Henri Mondo, France; Unité de Recherche Clinique de l'Hôpital Henri Mondor, France.

A Jebali (A)

Sickle Cell Referral Center, Henri Mondor Hospital, AP-HP, Creteil, France.

G De Luna (G)

Sickle Cell Referral Center, Henri Mondor Hospital, AP-HP, Creteil, France.

F Pirenne (F)

Univ Paris Est Créteil, France; Laboratory of Excellence GR-Ex, INSERM Unit 955, Mondor Institute of Biomedical Research, Paris-Est Creteil University, Creteil, France; Établissement Français du Sang Ile de France, Créteil, France.

D Redel (D)

Service de Gynécologie Obstétrique, Centre Hospitalier Intercommunal de Créteil, France; Centre de recherche clinique du CHI Créteil, France.

F Galacteros (F)

Sickle Cell Referral Center, Henri Mondor Hospital, AP-HP, Creteil, France; Laboratory of Excellence GR-Ex, INSERM Unit 955, Mondor Institute of Biomedical Research, Paris-Est Creteil University, Creteil, France.

E Boutin (E)

Département de Santé Publique et de Biostatistiques de l'Hôpital Henri Mondo, France; Unité de Recherche Clinique de l'Hôpital Henri Mondor, France.

P Bartolucci (P)

Univ Paris Est Créteil, France; Sickle Cell Referral Center, Henri Mondor Hospital, AP-HP, Creteil, France; Laboratory of Excellence GR-Ex, INSERM Unit 955, Mondor Institute of Biomedical Research, Paris-Est Creteil University, Creteil, France.

B Haddad (B)

Service de Gynécologie Obstétrique, Centre Hospitalier Intercommunal de Créteil, France; Univ Paris Est Créteil, France; INSERM, IMRB U955 I-BIOT, 94010 Créteil, France.

A Habibi (A)

Univ Paris Est Créteil, France; Sickle Cell Referral Center, Henri Mondor Hospital, AP-HP, Creteil, France; Laboratory of Excellence GR-Ex, INSERM Unit 955, Mondor Institute of Biomedical Research, Paris-Est Creteil University, Creteil, France.

E Lecarpentier (E)

Service de Gynécologie Obstétrique, Centre Hospitalier Intercommunal de Créteil, France; Univ Paris Est Créteil, France; INSERM, IMRB U955 I-BIOT, 94010 Créteil, France. Electronic address: edouard.lecarpentier@chicreteil.fr.

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