Pregnancy Outcomes among Patients with Sickle Cell Disease in Brazzaville

Introduction. Sickle cell disease (SCD) is one of the most common genetic diseases in the world. It combines, in its homozygous form, chronic hemolytic anemia, vasoocclusive complications, and susceptibility to infections. It is well known that the combination of pregnancy and sickle cell disease pr...

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Main Authors: F. O. Galiba Atipo Tsiba, C. Itoua, C. Ehourossika, N. Y. Ngakegni, G. Buambo, N. S. B. Potokoue Mpia, A. Elira Dokekias
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Anemia
Online Access:http://dx.doi.org/10.1155/2020/1989134
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author F. O. Galiba Atipo Tsiba
C. Itoua
C. Ehourossika
N. Y. Ngakegni
G. Buambo
N. S. B. Potokoue Mpia
A. Elira Dokekias
author_facet F. O. Galiba Atipo Tsiba
C. Itoua
C. Ehourossika
N. Y. Ngakegni
G. Buambo
N. S. B. Potokoue Mpia
A. Elira Dokekias
author_sort F. O. Galiba Atipo Tsiba
collection DOAJ
description Introduction. Sickle cell disease (SCD) is one of the most common genetic diseases in the world. It combines, in its homozygous form, chronic hemolytic anemia, vasoocclusive complications, and susceptibility to infections. It is well known that the combination of pregnancy and sickle cell disease promotes the occurrence of complications that are sometimes fatal for the mother and/or the fetus. Objective. The objective of the current study was to compare pregnancy outcomes among women with SCD with those of women without the diagnosis of SCD. Materials and methods. It was a case-control study carried out in four maternity hospitals in Brazzaville in 2 years (July 2017–June 2019). It concerned 65 parturients with SS homozygous SCD. The mode of childbirth and maternal and perinatal morbidity and mortality were compared with those of 130 non-sickle cell pregnant women. Results. The average age was 27 years for SCD women and 31 years for non-SCD women. The average gestational age at delivery was 35 weeks for SCD women and 38 weeks for non-SCD women. From the logistic regression analysis using the comparison group as the reference group, there was excessive risk in SCD compared to non-SCD of infection (29.3% vs. 4.6%, OR = 21.7, 95% CI [7.6–62.7]; p=0.001), cesarean (63% vs. 35.4%, OR = 3.1, 95% CI [1.6–5.7]; p=0.001), prematurity (75.4% vs. 30.8%, OR = 8, 95% CI [3.0–23.2]; p=0.001), low birth weight (52.3% vs. 16.1%, OR = 4.7, 95% CI [2.4–9.4]; p=0.001), neonatal requiring admission to the intensive care unit (40.3% vs. 17.5%, OR = 3.2, 95% CI [1.6–6.3]; p=0.01), and neonatal death (21.5% vs. 4.8%, OR = 4.3, 95% CI [1.5–12.2]; p=0.01). Conclusion. The risk of pregnancy in patients with homozygous sickle cell anemia remains high, on both the maternal and fetal sides.
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spelling doaj-art-c8727b7ac7f34b1aa3579aac2abe38cf2025-02-03T06:46:55ZengWileyAnemia2090-12672090-12752020-01-01202010.1155/2020/19891341989134Pregnancy Outcomes among Patients with Sickle Cell Disease in BrazzavilleF. O. Galiba Atipo Tsiba0C. Itoua1C. Ehourossika2N. Y. Ngakegni3G. Buambo4N. S. B. Potokoue Mpia5A. Elira Dokekias6Hematology Department, University Hospital of Brazzaville (Congo), Brazzaville, CongoFaculty of Health Sciences, Marien Ngouabi University of Brazzaville (Congo), Brazzaville, CongoGynecology-Obstetrics Department, University Hospital of Brazzaville (Congo), Brazzaville, CongoFaculty of Health Sciences, Marien Ngouabi University of Brazzaville (Congo), Brazzaville, CongoGynecology-Obstetrics Department, University Hospital of Brazzaville (Congo), Brazzaville, CongoFaculty of Health Sciences, Marien Ngouabi University of Brazzaville (Congo), Brazzaville, CongoHematology Department, University Hospital of Brazzaville (Congo), Brazzaville, CongoIntroduction. Sickle cell disease (SCD) is one of the most common genetic diseases in the world. It combines, in its homozygous form, chronic hemolytic anemia, vasoocclusive complications, and susceptibility to infections. It is well known that the combination of pregnancy and sickle cell disease promotes the occurrence of complications that are sometimes fatal for the mother and/or the fetus. Objective. The objective of the current study was to compare pregnancy outcomes among women with SCD with those of women without the diagnosis of SCD. Materials and methods. It was a case-control study carried out in four maternity hospitals in Brazzaville in 2 years (July 2017–June 2019). It concerned 65 parturients with SS homozygous SCD. The mode of childbirth and maternal and perinatal morbidity and mortality were compared with those of 130 non-sickle cell pregnant women. Results. The average age was 27 years for SCD women and 31 years for non-SCD women. The average gestational age at delivery was 35 weeks for SCD women and 38 weeks for non-SCD women. From the logistic regression analysis using the comparison group as the reference group, there was excessive risk in SCD compared to non-SCD of infection (29.3% vs. 4.6%, OR = 21.7, 95% CI [7.6–62.7]; p=0.001), cesarean (63% vs. 35.4%, OR = 3.1, 95% CI [1.6–5.7]; p=0.001), prematurity (75.4% vs. 30.8%, OR = 8, 95% CI [3.0–23.2]; p=0.001), low birth weight (52.3% vs. 16.1%, OR = 4.7, 95% CI [2.4–9.4]; p=0.001), neonatal requiring admission to the intensive care unit (40.3% vs. 17.5%, OR = 3.2, 95% CI [1.6–6.3]; p=0.01), and neonatal death (21.5% vs. 4.8%, OR = 4.3, 95% CI [1.5–12.2]; p=0.01). Conclusion. The risk of pregnancy in patients with homozygous sickle cell anemia remains high, on both the maternal and fetal sides.http://dx.doi.org/10.1155/2020/1989134
spellingShingle F. O. Galiba Atipo Tsiba
C. Itoua
C. Ehourossika
N. Y. Ngakegni
G. Buambo
N. S. B. Potokoue Mpia
A. Elira Dokekias
Pregnancy Outcomes among Patients with Sickle Cell Disease in Brazzaville
Anemia
title Pregnancy Outcomes among Patients with Sickle Cell Disease in Brazzaville
title_full Pregnancy Outcomes among Patients with Sickle Cell Disease in Brazzaville
title_fullStr Pregnancy Outcomes among Patients with Sickle Cell Disease in Brazzaville
title_full_unstemmed Pregnancy Outcomes among Patients with Sickle Cell Disease in Brazzaville
title_short Pregnancy Outcomes among Patients with Sickle Cell Disease in Brazzaville
title_sort pregnancy outcomes among patients with sickle cell disease in brazzaville
url http://dx.doi.org/10.1155/2020/1989134
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