Pregnancy Outcomes among Antenatal Women with Sickle Cell Anaemia: A Case Series
Sickle Cell Anaemia (SCA) is a common and severe form of an inherited blood disorder known as Sickle Cell Disease (SCD). SCD is a group of autosomal recessive disorders characterised by point mutation resulting in the formation of structurally defective haemoglobin (Hb), called haemoglobin S (HbS)....
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Published in | Journal of clinical and diagnostic research Vol. 18; no. 6; pp. 01 - 04 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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JCDR Research and Publications Private Limited
01.06.2024
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Abstract | Sickle Cell Anaemia (SCA) is a common and severe form of an inherited blood disorder known as Sickle Cell Disease (SCD). SCD is a group of autosomal recessive disorders characterised by point mutation resulting in the formation of structurally defective haemoglobin (Hb), called haemoglobin S (HbS). SCD is clinically heterogeneous, with variability in manifestation ranging from being asymptomatic to a severe crisis that can be fatal. Pregnancies complicated by SCA are high-risk due to the disease's heterogeneous manifestations and propensity for maternal and foetal complications. This case series aimed to understand associated maternal and foetal outcomes at a tertiary care hospital. Women presented with a spectrum of clinical presentations from uncomplicated deliveries to cases involving severe acute and chronic sequelae. Preterm birth before 37 weeks, low birth weight, and Neonatal Intensive Care Unit (NICU) admissions were common, reflecting known risks of growth restriction and prematurity. Previous adverse outcomes such as stillbirth and spontaneous abortion highlighted the threat to maternal and perinatal mortality. Acute sickle cell crises and splenic sequestration occurred. Advanced maternal age and comorbidities such as asthma exacerbated the disease burden. Most of the participants suffered from recurrent adverse outcomes with subsequent gestations. As most of the participants belonged to backward communities, targeted screening could help with earlier identification and counselling to reduce disease incidence in vulnerable populations. |
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AbstractList | Sickle Cell Anaemia (SCA) is a common and severe form of an inherited blood disorder known as Sickle Cell Disease (SCD). SCD is a group of autosomal recessive disorders characterised by point mutation resulting in the formation of structurally defective haemoglobin (Hb), called haemoglobin S (HbS). SCD is clinically heterogeneous, with variability in manifestation ranging from being asymptomatic to a severe crisis that can be fatal. Pregnancies complicated by SCA are high-risk due to the disease's heterogeneous manifestations and propensity for maternal and foetal complications. This case series aimed to understand associated maternal and foetal outcomes at a tertiary care hospital. Women presented with a spectrum of clinical presentations from uncomplicated deliveries to cases involving severe acute and chronic sequelae. Preterm birth before 37 weeks, low birth weight, and Neonatal Intensive Care Unit (NICU) admissions were common, reflecting known risks of growth restriction and prematurity. Previous adverse outcomes such as stillbirth and spontaneous abortion highlighted the threat to maternal and perinatal mortality. Acute sickle cell crises and splenic sequestration occurred. Advanced maternal age and comorbidities such as asthma exacerbated the disease burden. Most of the participants suffered from recurrent adverse outcomes with subsequent gestations. As most of the participants belonged to backward communities, targeted screening could help with earlier identification and counselling to reduce disease incidence in vulnerable populations. |
Author | RDN Swetha Jhansi Rani Kathari Srujana Palavalasa Rosemary Penumaka |
Author_xml | – sequence: 1 fullname: RDN Swetha organization: Assistant Professor, Department of Obstetrics and Gynaecology, Andhra Medical College, Visakhapatnam, Andhra Pradesh, India – sequence: 2 fullname: Srujana Palavalasa organization: Assistant Professor, Department of Obstetrics and Gynaecology, Andhra Medical College, Visakhapatnam, Andhra Pradesh, India – sequence: 3 fullname: Jhansi Rani Kathari organization: Assistant Professor, Department of Obstetrics and Gynaecology, Andhra Medical College, Visakhapatnam, Andhra Pradesh, India – sequence: 4 fullname: Rosemary Penumaka organization: Assistant Professor, Department of Obstetrics and Gynaecology, Andhra Medical College, Visakhapatnam, Andhra Pradesh, India |
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SubjectTerms | haematologic pregnancy complications low birth weight infant neonatal intensive care premature births |
Title | Pregnancy Outcomes among Antenatal Women with Sickle Cell Anaemia: A Case Series |
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