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Intravenous immunoglobulin for the treatment of severe maternal alloimmunization: individual patient data meta-analysis.
Mustafa, Hiba J; Sambatur, Enaja V; Pagani, Giorgio; D'Antonio, Francesco; Maisonneuve, Emeline; Maurice, Paul; Zwiers, Carolien; Verweij, Joanne E J T; Flood, Anna; Shamshirsaz, Alireza A; Jouannic, Jean-Marie; Khalil, Asma.
Afiliação
  • Mustafa HJ; Division of Maternal-Fetal Medicine, Indiana University School of Medicine, Indianapolis, IN; Fetal Center at Riley Children's and Indiana University Health, Indianapolis, IN. Electronic address: hmustafa@iu.edu.
  • Sambatur EV; Division of Fetal Medicine and Surgery, Maternal Fetal Care Center, Boston Children's Hospital and Harvard School of Medicine, Boston, MA.
  • Pagani G; Maternal-Fetal Medicine Unit, Department of Obstetrics and Gynecology, Azienda Socio-Sanitaria Territoriale-Papa Giovanni XXIII, Bergamo, Italy.
  • D'Antonio F; Department of Obstetrics and Gynecology, Center for Fetal Care and High-Risk Pregnancy, University Hospital of Chieti, Chieti, Italy.
  • Maisonneuve E; Materno-Fetal and Obstetrics Research Unit, Woman-Mother-Child Department, Lausanne University Hospital, Lausanne, Switzerland; Fetal Medicine Department and French Referral National Centre for Perinatal Hemobiology, Armand Trousseau Hospital, Assistance Publique-Hôpitaux de Paris Sorbonne Universit
  • Maurice P; Fetal Medicine Department and French Referral National Centre for Perinatal Hemobiology, Armand Trousseau Hospital, Assistance Publique-Hôpitaux de Paris Sorbonne Université, Paris, France.
  • Zwiers C; Division of Fetal Therapy, Department of Obstetrics, Leiden University Medical Center, Leiden, The Netherlands.
  • Verweij JEJT; Division of Fetal Therapy, Department of Obstetrics, Leiden University Medical Center, Leiden, The Netherlands.
  • Flood A; Division of Maternal-Fetal Medicine, Indiana University School of Medicine, Indianapolis, IN.
  • Shamshirsaz AA; Division of Fetal Medicine and Surgery, Maternal Fetal Care Center, Boston Children's Hospital and Harvard School of Medicine, Boston, MA.
  • Jouannic JM; Fetal Medicine Department and French Referral National Centre for Perinatal Hemobiology, Armand Trousseau Hospital, Assistance Publique-Hôpitaux de Paris Sorbonne Université, Paris, France.
  • Khalil A; Fetal Medicine Unit, St George's Hospital, St George's University of London, London, United Kingdom; Vascular Biology Research Centre, Molecular and Clinical Sciences Research Institute, St George's University of London, London, United Kingdom.
Am J Obstet Gynecol ; 231(4): 417-429.e21, 2024 Oct.
Article em En | MEDLINE | ID: mdl-38588966
ABSTRACT

OBJECTIVE:

This study aimed to investigate the outcomes associated with the administration of maternal intravenous immunoglobulin in high-risk red blood cell-alloimmunized pregnancies. DATA SOURCES Medline, Embase, and Cochrane Library were systematically searched until June 2023. STUDY ELIGIBILITY CRITERIA This review included studies reporting on pregnancies with severe red blood cell alloimmunization, defined as either a previous fetal or neonatal death or the need for intrauterine transfusion before 24 weeks of gestation in the previous pregnancy as a result of hemolytic disease of the fetus and newborn.

METHODS:

Cases were pregnancies that received intravenous immunoglobulin, whereas controls did not. Individual patient data meta-analysis was performed using the Bayesian framework.

RESULTS:

Individual patient data analysis included 8 studies consisting of 97 cases and 97 controls. Intravenous immunoglobulin was associated with prolonged delta gestational age at the first intrauterine transfusion (gestational age of current pregnancy - gestational age at previous pregnancy) (mean difference, 3.19 weeks; 95% credible interval, 1.28-5.05), prolonged gestational age at the first intrauterine transfusion (mean difference, 1.32 weeks; 95% credible interval, 0.08-2.50), reduced risk of fetal hydrops at the time of first intrauterine transfusion (incidence rate ratio, 0.19; 95% credible interval, 0.07-0.45), reduced risk of fetal demise (incidence rate ratio, 0.23; 95% credible interval, 0.10-0.47), higher chances of live birth at ≥28 weeks (incidence rate ratio, 1.88; 95% credible interval, 1.31-2.69;), higher chances of live birth at ≥32 weeks (incidence rate ratio, 1.93; 95% credible interval, 1.32-2.83), and higher chances of survival at birth (incidence rate ratio, 1.82; 95% credible interval, 1.30-2.61). There was no substantial difference in the number of intrauterine transfusions, hemoglobin level at birth, bilirubin level at birth, or survival at hospital discharge for live births.

CONCLUSION:

Intravenous immunoglobulin treatment in pregnancies at risk of severe early hemolytic disease of the fetus and newborn seems to have a clinically relevant beneficial effect on the course and severity of the disease.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Transfusão de Sangue Intrauterina / Imunoglobulinas Intravenosas Limite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Am J Obstet Gynecol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Transfusão de Sangue Intrauterina / Imunoglobulinas Intravenosas Limite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Am J Obstet Gynecol Ano de publicação: 2024 Tipo de documento: Article