Lazurenko V. V., Ovcharenko O. B., Zhelezniakov O. Yu., Tertyshnyk D. Yu., Kudin I. D., Komova V. O.
PREMATURE PLACENTAL ABRUPTION IN A PREGNANT WOMAN WITH TETRAPARESIS AND INTRAUTERINE INFECTION (A CLINICAL CASE)
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About the author:
Lazurenko V. V., Ovcharenko O. B., Zhelezniakov O. Yu., Tertyshnyk D. Yu., Kudin I. D., Komova V. O.
Heading:
CLINICAL AND EXPERIMENTAL MEDICINE
Type of article:
Scientific article
Annotation:
According to the literature, 30–35% of bleeding episodes during the gestational process are associated with premature placental abruption (PPA), which complicates 0.6–1.2% of pregnancies. In most cases, PPA results from an acute or chronic inflammatory process in the maternal and fetal organisms. The aim of the study was to clarify the pathogenesis of PPA considering the data on maternal and fetal infection through a detailed analysis of a clinical case of preterm delivery in a pregnant woman with tetraparesis and subsequent observation of the newborn’s condition. The presented clinical case describes PPA in a 41-year-old pregnant woman M. with tetraparesis, sphincter dysfunction, cervical spinal stenosis after total removal of an extramedullary spinal cord tumor (C6) at the age of 16 years, and class II obesity. During inpatient examination, urine bacterial culture revealed Escherichia coli 10⁴; IgG antibodies to cytomegalovirus infection were positive. A decreased VEGF level (59.4±4.2 pg/mL) and increased ET-1 level (1.77±0.12 pg/mL) in the pregnant woman’s blood indicated alterations in endothelial status. Hyperexpression of proinflammatory cytokines was also detected (IL-1β – 19.2±2.8 pg/mL, IL-6 – 9.7±0.8 pg/mL, TNFα – 13.1±1.4 pg/ mL), indicating the presence of an inflammatory or infectious process in the maternal organism. Due to hemorrhage resulting from PPA, a cesarean section was performed, and a live premature female infant was delivered with an Apgar score of 3–4 points. The early postpartum period was complicated by hypotonic hemorrhage with the development of DIC syndrome, requiring relaparotomy, hysterectomy with adnexa, bilateral ligation of the internal iliac arteries, and drainage of the abdominal cavity. Bacteriological examination of the uterus and placenta revealed chronic purulent endomyometritis (Enterococcus faecalis 10⁵, Escherichia coli 10⁷), chronic cervicitis (Enterococcus faecalis 10⁶, Escherichia coli 10⁴), chronic purulent placentitis (Enterococcus faecalis 10⁵, Escherichia coli 10⁷), and chronic purulent salpingo-oophoritis. In the newborn, blood bacterial culture, CRP assessment, and complete blood count were also performed (CRP – 11.6 mg/dL (normal <5.0 mg/dL); leukopenia in the complete blood count (leukocytes – 8.4×10⁹/L, normal range 9.4–32.2×10⁹/L); blood culture positive for E. coli). The obtained clinical and laboratory data indicated signs of early neonatal sepsis of escherichial etiology, and antibacterial therapy was prescribed according to the antibiotic sensitivity of the identified flora. The presented case of PPA in a pregnant woman with tetraparesis who had been bedridden or wheelchairbound for 25 years demonstrates the combined influence of multiple factors on the development of complications, particularly chronic infectious lesions of the female reproductive system (purulent placentitis, endomyometritis, intrauterine infection), reduced mobility caused by neurological pathology with impaired autonomic innervation, which resulted in decreased uterine contractility after delivery and the development of hypotonic hemorrhage, as well as the presence of cytokine imbalance, endothelial dysfunction, and impaired eryptosis processes.
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Bibliography:
- Brandt JS, Ananth CV. Placental abruption at near-term and term gestations: pathophysiology, epidemiology, diagnosis, and management. Am J Obstet Gynecol. 2023;228(5S):1313-29. DOI: https://doi.org/10.1016/j.ajog.2022.06.059
- Tkachenko RO, Kaminskyi VV. Peripartalna krovotecha: suchasna diahnostyka ta likuvannia (dokazovi pryntsypy). Kyiv; 2025. 272 s. [in Ukrainian].
- Khong TY, Mooney EE, Ariel I, Balmus NC, Boyd TK, Brundler MA, et al. Sampling and Definitions of Placental Lesions: Amsterdam Placental Workshop Group Consensus Statement. Arch Pathol Lab Med. 2016;140(7):698-713. DOI: https://doi.org/10.5858/arpa.2015-0225-CC
- Zheng D, Liwinski T, Elinav E. Inflammasome activation and regulation: toward a better understanding of complex mechanisms. Cell Discov. 2020;6:36. DOI: https://doi.org/10.1038/s41421-020-0167-x
- Workalemahu T, Enquobahrie DA, Gelaye B, Sanchez SE, Garcia PJ, Tekola-Ayele F, et al. Genetic variations and risk of placental abruption: A genome-wide association study and meta-analysis of genome-wide association studies. Placenta. 2018;66:8-16. DOI: https://doi.org/10.1016/j.placenta.2018.04.008
- Workalemahu T, Enquobahrie DA, Gelaye B, Thornton TA, Tekola-Ayele F, Sanchez SE, et al. Abruptio placentae risk and genetic variations in mitochondrial biogenesis and oxidative phosphorylation: replication of a candidate gene association study. Am J Obstet Gynecol. 2018;219(6):617.e1-17. DOI: https://doi.org/10.1016/j.ajog.2018.08.042
- Downes KL, Grantz KL, Shenassa ED. Maternal, Labor, Delivery, and Perinatal Outcomes Associated with Placental Abruption: A Systematic Review. Am J Perinatol. 2017;34(10):935-57. DOI: https://doi.org/10.1055/s-0037-1599149
- Morgan TK. Role of the Placenta in Preterm Birth: A Review. Am J Perinatol. 2016;33(3):258-66. DOI: https://doi.org/10.1055/s-0035-1570379
- Brosens I, Puttemans P, Benagiano G. Placental bed research: I. The placental bed: from spiral arteries remodeling to the great obstetrical syndromes. Am J Obstet Gynecol. 2019;221(5):437-56. DOI: https://doi.org/10.1016/j.ajog.2019.05.044
- Goldstein JA, Gallagher K, Beck C, Kumar R, Gernand AD. Maternal-Fetal Inflammation in the Placenta and the Developmental Origins of Health and Disease. Front Immunol. 2020;11:531543. DOI: https://doi.org/10.3389/fimmu.2020.531543
- Mhatre MV, Potter JA, Lockwood CJ, Krikun G, Abrahams VM. Thrombin Augments LPS-Induced Human Endometrial Endothelial Cell Inflammation via PAR1 Activation. Am J Reprod Immunol. 2016;76(1):29-37. DOI: https://doi.org/10.1111/aji.12517
- Singh N, Herbert B, Sooranna G, Das A, Sooranna SR, Yellon SM, et al. Distinct preterm labor phenotypes have unique inflammatory signatures and contraction associated protein profiles†. Biol Reprod. 2019;101(5):1031-45. DOI: https://doi.org/10.1093/biolre/ioz144
- Feng L, Allen TK, Marinello WP, Murtha AP. Infection-induced thrombin production: a potential novel mechanism for preterm premature rupture of membranes (PPROM). Am J Obstet Gynecol. 2018;219(1):101.e1-12. DOI: https://doi.org/10.1016/j.ajog.2018.04.014
- Kudin ID, Lazurenko VV. Problema infektsiinykh urazhen vahitnoi ta yikh vplyv na stan ploda ta novonarodzhenoho. Visnyk morskoi medytsyny. 2024;3(103):160-70. [in Ukrainian].
- Kudin I, Lazurenko V, Prokopiuk V, Zhelezniakov O, Panasovskyi M. Eryptosis as a link between bacterial reproductive tract infection and anemia in pregnant women. Neonatology, Surgery and Perinatal Medicine. 2024;2(52):70-7. DOI: https://doi.org/10.24061/2413-4260.XIV.2.52.2024.11
- Kyozuka H, Murata T, Fukusda T, Yamaguchi A, Kanno A, Yasuda S, et al. Teenage pregnancy as a risk factor for placental abruption: Findings from the prospective Japan environment and children’s study. PLoS One. 2021;16(5):e0251428. DOI: https://doi.org/10.1371/journal.pone.0251428
Publication of the article:
«Bulletin of problems biology and medicine», 2026 Issue 2, 181, 178-183 pages, index UDC 618.36-007.281-027.15-06:[616.831-009.12-031.37/38+618.33-022.6/9]