Particular features of labor activity at the presence of inflammation of the uterine layers and placental membranes
DOI:
https://doi.org/10.18370/2309-4117.2023.70.28-37Keywords:
abnormal labor activity, deciduitis, myometritis, chorioamnionitis, funisitisAbstract
Research objectives: to analyze the association between the various abnormalities of the labor activity and inflammatory changes of the placental, fetal membranes, and uterine layers.
Materials and methods. A prospective cohort study of 382 patients with singleton pregnancies at 28–42 weeks' gestation who underwent cesarean section for abnormal uterine contractions and other complications was conducted. The patients were divided into 3 observation groups: 168 women with hypotonic labor (HL), 70 women with hypertonic uterine dysfunction (HUD) and 144 women operated on for various indications (control group). The development of the inflammation of the decidua, myometrium, chorioamniotic membranes and umbilical cord in different types of labor activity abnormalities were studied. Statistical analyses included Mann-Whitney U test, Chi-squared test, and logistic regression.
Results. In the control group on the eve of the labor the lower uterine segments' polymorphonuclear leukocytes and macrophages infiltration of mild grade were detected in 73.6 and 59.7% cases accordingly.
The strength of the association of uterine layers, placental and fetal membranes inflammation with the HUD was: for the deciduitis – adjusted odds ratio (aOR): 2.6, 95% confidence interval (CI): 1.4–4.8; for the myometritis – aOR: 0.7, 95% CI: 0.3–2.4; for the histological chorioamnionitis (hCAM) – aOR: 4.5, 95% CI: 3.4–12.1; for the funisitis – aOR: 2.9, 95% CI: 1.3–10.6. The main clinical risk factors for hCAM, funisitis, and deciduitis in the HUD group, such as prematurity, nulliparity, group B streptococcus colonization, and duration of ruptured fetal membranes before the cesarean section, indicated the antenatal occurrence of inflammatory process.
А decrease of the uterine contractility іn the HL group was associated with grade 2+ deciduitis (aOR: 1.4, 95% CI: 0.6–3.6) and grade II+ myometritis (aOR: 3.9, 95% CI: 1.3–14.7), but no association was found with stage II+ hCAM (aOR: 0.8, 95% CI: 0.3–4.9) and stage 2+ funisitis (aOR: 0.3, 95% CI: 0.6–2.7). Decidual and myometrial inflammation was significantly connected with nulliparity and intrapartum factors such as protracted active first stage of labor with oxytocin augmentation, advanced cervical dilation, and number of vaginal examinations. Inflammation of the myometrium was accompanied by the deciduitis in all cases.
Conclusions. Mild inflammation of the decidua and myometrium of the lower segment of the uterus at term pregnancy is a physiological phenomenon that contributes to the initiation of labor. Inflammation of the chorioamniotic membranes and decidua against the background of intact myometrium plays a fundamental role in the occurrence of hypertensive uterine dysfunction, particularly in preterm birth. Marked myometrial inflammation that occurs in prolonged labor is an additional factor aggravating the hypotonic uterine activity.
References
- Friedman EA, Cohen WR. Dysfunctional labor and delivery: adverse effects on offspring. Am J Obstet Gynecol. 2023 May;228.5S:S1104–S1109. DOI: 10.1016/j.ajog.2022.10.011
- Hobson SR, Abdelmalek MZ, Farine D. Update on uterine tachysystole. J Perinat Med. 2018 Oct 20;1–9. DOI:10.1515/jpm-2018-0175
- Gimovsky A.C. Defining arrest in the first and second stages of labor. Minerva Obstet Gynecol. 2021 Feb;73.1: 6–18. DOI: 10.23736/S2724-606X.20.04644-4
- Harper LM, Caughey AB, Roehl KA, et al. Defining an abnormal first stage of labor based on maternal and neonatal outcomes. Am J Obstet Gynecol. 2014 Jun;210.6:536. e1–7. DOI: 10.1016/j.ajog.2013.12.027
- LeFevre NM, Krumm E, Cobb WJ. Labor dystocia in nulliparous women. Am Fam Physician. 2021 Jan 15;103.2: 90–6. PMID: 33448772.
- Blankenship SA, Raghuraman N, Delhi A, et al. Association of abnormal first stage of labor duration and maternal and neonatal morbidity. Am J Obstet Gynecol. 2020 Sep;223.3:445.e1–445.e15. DOI: 10.1016/j.ajog.2020.06.053
- Ragusa A, Gizzo S, Noventa M, et al. Prevention of primary caesarean delivery: comprehensive management of dystocia in nulliparous patients at term. Arch Gynecol Obstet. 2016 Oct;294.4:753–61. DOI:10.1007/s00404-016-4046-5
- Ende HB, Lozada MJ, Chestnut DH, et al. Risk factors for atonic postpartum hemorrhage: a systematic review and meta-analysis. Obstet Gynecol. 2021 Feb 1;137.2:305–323. DOI: 10.1097/AOG.0000000000004228
- Heuser CC, Knight S, Esplin MS, et al. Tachysystole in term labor: incidence, risk factors, outcomes, and effect on fetal heart tracings. Am J Obstet Gynecol. 2013 Jul;209.1:32.e1–6. DOI:10.1016/j.ajog.2013.04.004
- Smith S, Zacharias J, Lucas V, et al. Clinical associations with uterine tachysystole. J Matern Fetal Neonatal Med. 2014 May;27:709–13. DOI:10.3109/14767058.2013.836484
- Sims ME Legal briefs: tachysystole, uterine rupture, and a bad outcome. Neoreviews. 2019 Feb;20.2:e110–e112. DOI: 10.1542/neo.20-2-e110
- Leathersich SJ, Vogel JP, Tran TS, Hofmeyr GJ. Acute tocolysis for uterine tachysystole or suspected fetal distress. Cochrane Database Syst Rev. 2018 Jul 4;7.7:CD009770. DOI: 10.1002/14651858.CD009770.pub2
- Reynolds AJ, Geary MP, Hayes BC. Intrapartum uterine activity and neonatal outcomes: a systematic review. BMC Pregnancy Childbirth. 2020 Sep 12;20.1:532. DOI: 10.1186/s12884–020–03219–w
- Higgins RD, Saade G, Polin RA, et al. Evaluation and management of women and newborns with a maternal diagnosis of chorioamnionitis: summary of a workshop. Obstet Gynecol. 2016 Mar;127: 426–36. DOI: 10.1097/AOG.0000000000001246
- Kim CJ, Romero R, Chaemsaithong P, et al. Acute chorioamnionitis and funisitis: definition, pathologic features, and clinical significance. Am J Obstet Gynecol. 2015 Oct;213:S29–52. DOI: 10.1016/j.ajog.2015.08.040
- Tita ATN, Andrews WW. Diagnosis and management of clinical chorioamnionitis. Clin Perinatol. 2010 Jun;37.2:339–354. DOI:10.1016/j.clp.2010.02.003
- Romero R, Chaemsaithong P, Korzeniewski SJ, et al. Clinical chorioamnionitis at term III: how well do clinical criteria perform in the identification of proven intra–amniotic infection? J Perinat Med. 2016 Jan;44(1):23–32. DOI:10.1515/jpm–2015–0044
- Chaiyasit N, Romero R, Chaemsaithong P, et al. Clinical chorioamnionitis at term VIII: a rapid MMP–8 test for the identification of intra–amniotic inflammation. J Perinat Med. 2017 Jul 26;45.5:539-550. DOI:10.1515/jpm–2016–0344
- Horvath B, Lakatos F, Tóth C, et al. Silent chorioamnionitis and associated pregnancy outcomes: a review of clinical data gathered over a 16–year period. J Perinat Med. 2014 Jul;42.4: :441-7. DOI:10.1515/jpm–2013–0186
- Slutsky R, Romero R, Xu Y, et al. Exhausted and senescent T cells at the maternal–fetal interface in preterm and term labor. J Immunol Res. 2019 May 23:2019:3128010. DOI:10.1155/2019/3128010
- Than NG, Hahn S, Rossi SW, et al. Editorial: fetal–maternal immune interactions in pregnancy. Front Immunol. 2019 Nov 27:10:2729. DOI: 10.3389/fimmu.2019.02729
- Gomez–Lopez N, StLouis D, Lehr MA, et al. Immune cells in term and preterm labor. Cell Molecul Immunol. 2014 Nov;11(6):571–581. DOI:10.1038/cmi.2014.46
- Romero R, Chaemsaithong P, Korzeniewski SJ, et al. Clinical chorioamnionitis at term II: the intra–amniotic inflammatory response. J Perinat Med. 2016 Jan;44(1):5–22. DOI:10.1515/jpm–2015–0045
- Gonzalez JM, Franzke CW, Yang F, et al. Complement activation triggers metalloproteinases release inducing cervical remodeling and preterm birth in mice. Amer J Pathol. 2011 Aug;179(2):838–849. DOI:10.1016/j.ajpath.2011.04.024
- Hamilton S, Oomomian Y, Stephen G, et al. Macrophages infiltrate the human and rat decidua during term and preterm labor:evidence that decidual inflammation precedes labor. Biol Reprod. 2012 Feb 14 86(2):39. DOI:10.1095/biolreprod.111.095505
- Hamilton SA, Tower CL, Jones RL. Identification of chemokines associated with the recruitment of decidual leukocytes in human labour:potential novel targets for preterm labour. PLoS One. 2013;8(2):e56946. DOI:10.1371/journal.pone.0056946
- Keelan JA. Intrauterine inflammatory activation, functional progesterone withdrawal, and the timing of term and preterm birth. J Reprod Immunol. 2018 Feb:125:89–99. DOI:10.1016/j.jri.2017.12.004
- Shynlova O, Nadeem L, Zhang J, et al. Myometrial activation:Novel concepts underlying labor. Placenta. 2020. 92;5:28–36. DOI:10.1016/j.placenta.2020.02.005
- Zackler A, Flood P, Dajao R, et al. Suspected chorioamnionitis and myometrial contractility:mechanisms for increased risk of cesarean delivery and postpartum hemorrhage. Reprod Sci. 2019;26(2):178–183. DOI:10.1177/1933719118778819
- Wetta LA, Szychowski JM, Seals S, et al. Risk factors for uterine atony/postpartum hemorrhage requiring treatment after vaginal delivery. Am J Obstet Gynecol. 2013 Jul;209(1):51.e1–e6. DOI:10.1016/j.ajog.2013.03.011
- Lavesson T, Akerman F, Källén K, Olofsson P. Effects on fetal and maternal temperatures of paracetamol administration during labour:a case–control study. Eur J Obstet Gynecol Reprod Biol. 2013 Jun;168(2):138–144. DOI:10.1016/j.ejogrb.2012.12.033
- Venkatesh KK, Glover AV, Vladutiu CJ, Stamilio DM. Association of chorioamnionitis and its duration with adverse maternal outcomes by mode of delivery: a cohort study. BJOG. 2019;126:719–27. DOI:10.1111/1471–0528.15565
- Wiley RL, Racusin D, Chen HY, Chauhan SP. Chorioamnionitis and adverse outcomes in low–risk pregnancies: a population-based study. Am J Obstet Gynecol. 2020;222:S244–S245 DOI:10.1080/14767058.2021.1887126
- Conde-Agudelo A, Romero R, Jung EJ, et al. Management of clinical chorioamnionitis:an evidence-based approach. Am J Obstet Gynecol. 2020 Dec;223(6):848–869. DOI:10.1016/j.ajog.2020.09.044
- Wisner K. Intrapartum management of chorioamnionitis. MCN Am J Matern Child Nurs. 2018 Jan/Feb;43(1):52. DOI:10.1097/NMC.0000000000000396
- Lee J, Romero R, Kim SM, et al. A new anti-microbial combination prolongs the latency period, reduces acute histologic chorioamnionitis as well as funisitis, and improves neonatal outcomes in preterm PROM. J Matern Fetal Neonatal Med. 2016 Mar;29(5):707–20. DOI:10.3109/14767058.2015.1020293
- Burgess APH, Katz JE, Moretti M, Lakhi N. Risk factors for intrapartum fever in term gestations and associated maternal and neonatal sequelae. Gynecol Obstet Invest. 2017;82(5):508–16. DOI:10.1159/000453611
- Wang C, Sirluck-Schroeder I, Cazales AСS, et al. Management of fever in labor after institution of a standardized order set at a maternity quaternary care center. Am J Obstet Gynecol 221.6 (2019):687. DOI:10.1016/j.ajog.2019.10.041
- Dior UP, Kogan L, Eventov-Friedman S, et al. Very high intrapartum fever in term pregnancies and adverse obstetric and neonatal outcomes. Neonatology. 2022 Jan;44(1):62–8. DOI: 10.1159/000440938
- Kissler K, Hurt KJ. The pathophysiology of labor dystocia:theme with variations. Reprod Sci. 2023 Mar;30(3):729–42. DOI:10.1007/s43032-022-01018-6
- Friedman EA, Cohen WR. The active phase of labor. Am J Obstet Gynecol. 2023 May;228(5S):S1037–S1049. DOI:10.1016/j.ajog.2021.12.269
- Kissler KJ, Hernandez TL, Carlson N. The relationship between uterine activity, oxytocin dosing, labor progress, and mode of birth in nulliparas with obesity: minimal usefulness of Montevideo unit measurement. Biol Res Nurs. 2023 Jul;25(3):426–35. DOI:10.1177/10998004221150798
- Brüggemann C, Carlhäll S, Grundström H, Blomberg M. Labor dystocia and oxytocin augmentation before or after six centimeters cervical dilatation, in nulliparous women with spontaneous labor, in relation to mode of birth. BMC Pregnancy Childbirth. 2022 May 13;22(1):408. DOI:10.1186/s12884-022-04710-2
- WHO recommendations for augmentation of labor. Executive summary. [Internet]. Geneva:World Health Organization. 2014. Available from: https://www.ncbi.nlm.nih. gov/books/NBK258881/
- Dike NO, Ibine R. Hypotonic Labor. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing. 2023. Available from: https://www.ncbi. nlm.nih.gov/books/NBK564403/
- Prevention of Group B Streptococcal Early–Onset Disease in Newborns: ACOG Committee Opinion, Number 797. Obstet Gynecol. 2020 Feb;135(2):e51–e72. DOI:10.1097/AOG.0000000000003668
- Committee Opinion No. 797: Prevention of Group B Streptococcal Early–Onset Disease in Newborns:Correction. Obstet Gynecol. 2020 Apr;135(4):978–979. DOI:10.1097/AOG.0000000000003824
- Order of the Ministry of Health of Ukraine No. 1533 On approval of the Standard of medical care Premature rupture of amniotic membranes. Standard of medical care Premature rupture of membranes. [Internet]. 2023:19 p. Available at: https://www.dec.gov.ua/wp-content/uploads/2023/08/smd_1533_25082023.pdf
- Ayres-de-Campos D, Arulkumaran S. FIGO intrapartum fetal monitoring expert consensus panel. FIGO consensus guidelines on intrapartum fetal monitoring: Introduction. Int J Gynaecol Obstet. 2015 Oct;131(1):3–4. DOI:10.1016/j.ijgo.2015.06.017
- Altemani A, Gonzatti A, Metze K. How many paraffin blocks are necessary to detect villitis? Placenta. 2003 Jan;24(1):116–117. DOI:10.1053/plac.2002.0875
- Vareniuk IM, Dzerzhynskyi ME. Methods of cyto-histological diagnosis:an educational textbook. [Internet]. Kyiv: Interservice; 2019:256 p. Available at: https://biology.univ.kiev.ua/images/stories/Kafedry/Cytologiya/Biblioteca/Metody_cytohistologicnoi_diagnostiki.pdf
- Keski-Nisula LT, Aalto M-L, Kirkinen PP. Myometrial inflammation in human delivery and its association with labor and infection. Am J Clin Pathol. 2003 Aug;120(2):217–224. DOI:10.1309/KC6KDTX98LFYB3J7
- Nath CA, Ananth CV, Smulian JC, et al. Histologic evidence of inflammation and risk of placental abruption. Am J Obstet Gynecol. 2007 Sep;197(3):319e1–319e6. DOI:10.1016/j.ajog.2007.06.012.
- Keski-Nisula L, Aalto ML, Katila ML, Kirkinen P. Intrauterine inflammation at term:a histopathologic study. Hum Pathol. 2000 Jul;31(7):841–6. DOI:10.1053/hupa.2000.8449.
- Redline RW. Placental pathology:a systematic approach with clinical correlations. Placenta. 2008 Mar:29 Suppl A:S86–91. DOI:10.1016/j.placenta.2007.09.003.
- Khong TY, Mooney EE, Ariel I. Sampling and definitions of placental lesions Amsterdam placental workshop group consensus statement. Arch Pathol Lab Med. 2016 Jul;140(7):698–713. DOI:10.5858/arpa.2015-0225-CC.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 К.Л. Шатилович, Л.Б. Маркін
This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.