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Article 2024 · 0 atıf

Cesarean Section Is a Risk Factor That Prevents Organ Transplantation by Increasing the Development of Anti-HLA Antibodies in Women

Akyuz, Gokhan, Dogan, Hasan

Özet

BackgroundIn this study, prenatal and postnatal blood samples were taken from pregnant women who had 35 or more gestational weeks and had not developed anti-HLA positivity yet. The aim of this study was to evaluate the factors that may be effective in the development of panel reactive antibody (PRA) positivity during pregnancy.MethodsPRA testing was studied by taking the blood of 86 pregnant women 1 month before birth. Blood was taken again 1 month after birth from these women with prenatal PRA negative and it was checked whether PRA positivity developed. As a control group, 40 women without pregnancy were selected for the study.ResultsOf the 86 pregnant, 42 (48.8%) had cesarean sections, 44 (51.2%) had normal births, and PRA positivity developed in 14 (32.5%) of cesarean deliveries and three (8.0%) of normal births. In the control group, there were three (7.5%) PRA positivity. A statistically significant difference was found between cesarean delivery, normal delivery, and control group. Moreover, when compared with the control group, it was found statistically significant that all deliveries increased the development of HLA Class II antibodies.DiscussionCesarean delivery was associated with increased PRA positivity compared to normal birth. The new information presented in this study will pave the way for further research and enable healthcare professionals to consider both the individual's potential future need for organ transplantation and the positive impact on public health and more effective management of healthcare costs when making decisions regarding cesarean section.

Anahtar Kelimeler
anti-HLA antibody cesarean HLA PRA pregnancy PREGNANCY IMMUNIZATION
WoS Kategorileri
Surgery Transplantation
Sürdürülebilir Kalkınma Amaçları
Künye
Dergi
CLINICAL TRANSPLANTATION
Yıl
2024
Cilt
38
Sayı
10
ISSN
0902-0063
eISSN
1399-0012
DOI
10.1111/ctr.70005
WoS UID
WOS:001337563100001
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