Maternal and Fetal Outcomes of Pregnant Women With Sickle Cell Disease: A Single‐Center Canadian Study
- 1Division of Hematology and Hematologic Malignancies Department of Medicine University of Calgary Calgary Canada
- 2Division of Maternal‐Fetal Medicine Department of Obstetrics and Gynecology University of Calgary Calgary Canada
Abstract
Background: Sickle cell disease (SCD) increases the risk of complications during pregnancy. This study describes antenatal care patterns and maternal and fetal outcomes in pregnant women with SCD in a Canadian setting.
Methods: Women with SCD receiving antenatal/perinatal care through the Southern Alberta Rare Blood and Bleeding Disorders program (January 2010 to January 2025) were identified. Antenatal care, and maternal and fetal outcomes were assessed in periods before (2010–2019) and after (2020–2025) local multidisciplinary protocols for SCD pregnancy management were updated.
Results: 21 women (32 pregnancies; 31 neonates) were included. Most pregnancies were followed by maternal‐fetal medicine (81.3%), had regular fetal growth assessments (84.4%), and had high‐dose folic acid (90.6%) and acetylsalicylic acid (56.3%) supplementation; all were implemented more frequently following protocol update. Vaso‐occlusive crises occurred in 56.3% of pregnancies, infections requiring intravenous antibiotics occurred in 21.9%, preeclampsia occurred in 6.3%, and peripartum/postpartum hemorrhages occurred in 28.1%. Transfusions were required in 62.5% of pregnancies. There was one intensive care unit (ICU) admission and no maternal deaths. No neonates had fetal growth restriction and 16.1% required neonatal ICU admission. One stillbirth occurred at 23 weeks (mother had hyperhemolysis).
Conclusions: Multidisciplinary pregnancy management of women with SCD may improve antenatal care and maternal and fetal outcomes.
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BibTeX
@article{lam2026maternal,
title = {{Maternal and Fetal Outcomes of Pregnant Women With Sickle Cell Disease: A Single‐Center Canadian Study}},
author = {Wing Man (Joanne) Lam and Natalia Rydz and Nancy Soliman and Dawn Goodyear and Kelsey Uminski},
journal = {EJHaem},
year = {2026},
month = oct,
doi = {10.1002/jha2.70445},
url = {https://doi.org/10.1002/jha2.70445},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - Maternal and Fetal Outcomes of Pregnant Women With Sickle Cell Disease: A Single‐Center Canadian Study
AU - Wing Man (Joanne) Lam
AU - Natalia Rydz
AU - Nancy Soliman
AU - Dawn Goodyear
AU - Kelsey Uminski
PY - 2026
DA - 2026/10/26
JO - EJHaem
DO - 10.1002/jha2.70445
UR - https://doi.org/10.1002/jha2.70445
AB - Background: Sickle cell disease (SCD) increases the risk of complications during pregnancy. This study describes antenatal care patterns and maternal and fetal outcomes in pregnant women with SCD in a Canadian setting. Methods: Women with SCD receiving antenatal/perinatal care through the Southern Alberta Rare Blood and Bleeding Disorders program (January 2010 to January 2025) were identified. Antenatal care, and maternal and fetal outcomes were assessed in periods before (2010–2019) and after (2020–2025) local multidisciplinary protocols for SCD pregnancy management were updated. Results: 21 women (32 pregnancies; 31 neonates) were included. Most pregnancies were followed by maternal‐fetal medicine (81.3%), had regular fetal growth assessments (84.4%), and had high‐dose folic acid (90.6%) and acetylsalicylic acid (56.3%) supplementation; all were implemented more frequently following protocol update. Vaso‐occlusive crises occurred in 56.3% of pregnancies, infections requiring intravenous antibiotics occurred in 21.9%, preeclampsia occurred in 6.3%, and peripartum/postpartum hemorrhages occurred in 28.1%. Transfusions were required in 62.5% of pregnancies. There was one intensive care unit (ICU) admission and no maternal deaths. No neonates had fetal growth restriction and 16.1% required neonatal ICU admission. One stillbirth occurred at 23 weeks (mother had hyperhemolysis). Conclusions: Multidisciplinary pregnancy management of women with SCD may improve antenatal care and maternal and fetal outcomes.
SN - 2688-6146
ER -