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Clinical significance of true umbilical cord knot: a propensity score matching study

Abstract

Objective

True umbilical cord knot (TUCK) is a rare finding that often leads to intensified surveillance and patient anxiety. This study sought to evaluate the incidence, risk factors, and obstetric and neonatal outcomes of TUCK.

Methods

A retrospective cohort study was conducted at a tertiary university medical center in 2007–2019. Patients with singleton pregnancies diagnosed postnatally with TUCK were identified and compared to women without TUCK for obstetric and neonatal outcomes using propensity score matching (PSM).

Results

TUCK was diagnosed in 780 of the 96,766 deliveries (0.8%). Women with TUCK were older than those without TUCK (32.57 vs. 31.06 years, P < 0.001) and had higher gravidity (3 vs. 2, P < 001) and a higher rate of prior stillbirth (1.76% vs. 0.43%, P < 0.01). Following covariate adjustment, 732 women with TUCK were compared to 7320 matched controls. TUCK was associated with emergency cesarean delivery due to non-reassuring fetal heart rate (2.54% vs. 4.35%, P = 0.008, OR 1.71, 95%CI 1.14–2.56) and intrapartum meconium-stained amniotic fluid (19.26% vs. 15.41%, P = 0.022, OR 1.31, 95%CI 1.04–1.65). Neonatal outcomes were comparable except for higher rates of 1-min Apgar score < 7 and neonatal seizures in the TUCK group. The stillbirth rate was higher in the TUCK group, but the difference was not statistically significant (1.23% vs 0.62%, P = 0.06, OR 1.96, 95%CI 0.96–4.03).

Conclusions

TUCK has several identifiable risk factors. Pregnant women with TUCK may cautiously be informed of the relatively low risks of major obstetric or perinatal complications. The lower occurrence of stillbirth in the TUCK group warrants further study.

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Synopsis

Using propensity score matching to avoid biases, this study showed that TUCK did not pose a drastic risk of major perinatal complications.

Introduction

A true umbilical cord knot (TUCK) occurs when the umbilical cord twists around itself, forming a tight knot [1]. TUCK is a rare occurrence during pregnancy, with a reported incidence of 0.3 to 2% [2, 3]. TUCK formation is assumed to take place between 9 and 12 gestational weeks [4], but its detection in-utero can be challenging, and it often goes unnoticed until delivery [1, 5, 6]. Risk factors include a long umbilical cord, polyhydramnios, male fetus, gestational diabetes, and multiparity [2, 7]. Although TUCK has no clinical significance in most cases [5], blood flow to the fetus may potentially be compromised as it moves and grows within the uterus [4, 8]. This can lead to fetal hypoxia, inadequate nutrient supply, impaired waste removal, and ultimately, fetal growth restriction, fetal distress, and even stillbirth [9].

Nevertheless, the association of TUCK with intrauterine complications has not been established [8,9,10,11]. Some studies reported an increased incidence of stillbirth in association with TUCK, and findings for other adverse fetal, neonatal, and maternal outcomes have been inconsistent. With advancements in ultrasound technology and the subsequent rise in the prenatal diagnosis of TUCK, understanding its causes and implicatons has become increasingly relevant [12, 13].

The aim of this study was to evaluate risk factors and perinatal outcomes of TUCK in women diagnosed postnatally. Given that traditional multivariable analyses yielded mixed conclusions in previous outcome studies of TUCK, in the present study, propensity score matching (PSM) was used to compare variables between patients with and without TUCK in order to avoid concerns about potential confounders.

Methods

Study population

A retrospective cohort study was conducted in a tertiary university medical center between January 2007 and October 2019. The cohort included all women who gave birth after 22 gestational weeks or with a neonatal birthweight of at least 500g. Women with multiple gestations and terminations of pregnancy were excluded.

In our delivery ward’s protocol, all placentas are reviewed following any delivery by a midwife or an obstetrician, in order to: i) ensure that the placenta is intact and whole; 2) quantify the number of umbilical vessels; and 3) describe any umbilical vessel abnormalities, such as velamentous insertion, TUCK, etc. These findings are documented in the medical chart. TUCK was defined according to the conventional definition used in the literature (1), regardless of the degree of tightness of the knot or the number of knots.

Data collection

Data were retrieved from the hospital’s computerized database. Women who had a postnatal diagnosis of TUCK were identified using the International Classification of Diseases, 10th Revision, (ICD-10-CM Diagnostic Code O69.2.) Maternal, neonatal, and outcome data were collected. Maternal parameters included age, gravidity, parity, history of abortions, history of a prior stillbirth, history of cesarean deliveries, use of assisted reproductive technology, body mass index (BMI), chronic hypertension, pregestational diabetes, polyhydramnios, and oligohydramnios. Neonatal parameters included gender, birthweight, 1-min and 5-min Apgar scores, umbilical artery pH, neonatal intensive care unit (NICU) admission, acidosis (umbilical cord pH < 7.2), asphyxia, seizures, and neonatal sepsis. Adverse pregnancy and delivery outcomes were defined as any hypertensive disorder of pregnancy (gestational hypertension, preeclampsia with or without severe features, or HELLP syndrome), gestational diabetes mellitus (GDM), low gestational age at delivery, mode of delivery (vaginal or cesarean delivery), the indication for cesarean delivery, meconium-stained amniotic fluid, and placental abruption.

Outcome measures

The primary outcome was the incidence of stillbirth in the current pregnancy. The secondary outcomes were pregnancy, delivery, and neonatal outcomes in both groups. We also defined a respiratory composite outcome that included any of the following: respiratory distress syndrome, transient tachypnea of the newborn, use of continuous positive airway pressure, need for mechanical ventilation, and meconium aspiration syndrome.

Ethics

The study was approved by the local Institutional Review Board (0132–22-RMC). Informed consent was waived due to the retrospective design.

Statistical analysis

Categorical variables were reported as frequency and percentage. Continuous variables were assessed for normal distribution using the Shapiro–Wilk test, histograms, and Q-Q plots. Normally distributed continuous variables were reported as mean and standard deviation, and skewed variables as median and interquartile range.

PSM was used to minimize confounding. The probability of having a TUCK was calculated using a multivariable logistic regression model based on relevant patient characteristics. The model included variables previously associated with the primary outcome and those showing an association on initial univariate analysis (P < 0.05). Variables entered into the multivariable analysis were maternal age, gestational age at delivery, BMI category, gravidity, parity, history of abortions, history of cesarean delivery, ART, chronic hypertension, any hypertensive disorder of pregnancy, diabetes mellitus (gestational or pregestational), polyhydramnios, oligohydramnios, history of stillbirth and fetal gender. Matching was performed without replacement using a caliper of 0.001 on the propensity score scale for nearest-neighbor matching [14]. Covariate balance was assessed using standardized mean differences (SMD) before and after matching [15], with SMD < 0.1 indicating negligible differences between groups [16]. After PSM, all model variables had an SMD < 0.1. There was still a significant difference in gravidity between the matched groups, but SMD indicated a good balance. The discrimination of the propensity model was measured using the concordance (C) statistic. Overlap between patients with and without TUCK was evaluated with mirrored histograms (Figure S1). Statistical analysis was performed with unpaired methods, as the groups were dissimilar, and not based on outcome selection. Continuous variables were compared using Student's t-test or Mann–Whitney U test, and categorical variables were compared using chi-squared or Fisher's exact tests, as appropriate.

All statistical tests were two-tailed, with a significance level of P < 0.05/n (Bonferroni correction for number of tests). Data were generated with SPSS, version 29.0 (IBM Corp., Armonk, NY, USA) and Python, version 3.10.4.

Results

A total of 103,917 deliveries were performed during the study period. After excluding patients with missing data, the number was reduced to 96,766 deliveries (Fig. 1). TUCK was diagnosed in 780 deliveries, for a prevalence of 0.8%.

Fig. 1
figure 1

Flow diagram of patient selection. PSM, propensity score matching; TUCK, true umbilical cord knot

Maternal characteristics prior to PSM are presented in Table 1. Compared to the women without TUCK, the women with TUCK were older (median 32.56 vs. 31.05 years, P < 0.001), had higher median gravidity (3 vs. 2, P < 0.001) and parity (P < 0.001) and a higher rate of previous stillbirth (1.76% vs. 0.43%, P < 0.001), and were more likely to carry a male fetus (58.85% vs. 51.15%, P < 0.001).

Table 1 Maternal and obstetric characteristics before propensity score matching

Following co-variate adjustment, 732 of the 780 patients with TUCK were matched in a ratio of 1:10 with 7320 patients among the remaining cohort of patients (95,986) without TUCK (Table 2). On comparison of pregnancy and delivery outcomes, women with TUCK were at increased risk for intrapartum meconium-stained amniotic fluid (19.26% vs. 15.41%, P = 0.022) (Table 3). Gestational age at delivery, birthweight, and mode of delivery were not associated with TUCK. However, the incidence of emergency CD out of all women who attempted a vaginal birth (without elective CD) was also significant higher in the TUCK group (2.54% vs. 4.35%, P = 0.008, OR 1.71, 95%CI 1.14–2.56). Women with and without TUCK had similar rates of vacuum-assisted deliveries (21.85% vs. 21.09%, P = 0.314, respectively), and vacuum-assisted deliveries due to NRFHR (9.23% vs. 9.48%, P = 0.94).

Table 2 Maternal and obstetric characteristics after propensity score matching
Table 3 Pregnancy and delivery outcomes after propensity score matching

Neonatal outcomes are presented in Table 4. There were no differences between women with and without TUCK in rates of neonatal acidosis, NICU admission, infection, and composite respiratory outcome. Patients with TUCK had a higher rate of low Apgar score at 1 min (6.43% vs. 4.46%, P = 0.016, OR 1.47, 95% CI 1.07–2.02), as well as an increased rate of neonatal seizures (0.41% vs. 0.08%, P = 0.041, OR 5.01, 95% CI 1.25–20.10).

Table 4 Neonatal outcomes after propensity score matching

The rate of stillbirth was higher in the TUCK group, but the difference did not reach statistical significance (1.23% vs. 0.62%, P = 0.06, OR 1.96, 95% CI 0.96–4.03).

Discussion

This study sought to identify risk factors and evaluate perinatal outcomes among women with a postnatal diagnosis of TUCK. There were five key findings: 1) The incidence of TUCK in the research cohort was 0.8%, with the TUCK group demonstrating a non-significant increase in stillbirth rate compared to those without TUCK. 2) Women with TUCK were older than those without TUCK and had higher gravidity and a history of stillbirth. 3) Using PSM, we found that TUCK was associated with an increased risk of intrapartum meconium-stained amniotic fluid and a higher rate of emergency cesarean delivery due to NRFHR. 4) Neonates in the TUCK group had a higher rate of low 1-min Apgar score and neonatal seizures than neonates in the group without TUCK. 5) All other obstetric and neonatal outcomes were similar between the two groups.

The 0.8% incidence of TUCK in this study is similar to rates reported previously, with values ranging from 0.3 to 2.1% [2, 5, 17,18,19]. The identified risk factors of increased maternal age, increased gravidity and parity, and history of stillbirth have been reported previously, together with higher BMI [2, 17,18,19], multiparity, previous spontaneous abortion, polyhydramnios, and diabetes mellitus [2, 7]. Some authors hypothesized that a portion of these factors are associated with a relatively large uterine volume, enabling vigorous fetal movements with a subsequent increase in the rate of TUCK [17, 19]. Additionally, advanced maternal age and previous spontaneous abortion are likely to be associated with multiparity [2, 7]. As in our study, TUCK tended to occur more often with male than female fetuses [2, 7].

Several previous retrospective studies examined the association of TUCK with pregnancy, delivery, and neonatal outcomes, but results were inconsistent [3, 7, 19, 20]. None examined these outcomes in a large cohort using PSM, making the present study unique and more resilient to bias.

Weissmann-Brenner et al. [19] examined perinatal outcomes (867 pregnancies with TUCK compared to 85,541 without) and found that women with TUCK were older, had a higher BMI, gravidity, and parity, and had a higher rate of induction of labor, meconium-stained amniotic fluid, and preterm delivery. Similar to our findings, in their study, pregnancies with TUCK were associated with a significantly higher rate of cesarean delivery due to NRFHR. However, unlike our findings, the overall rate of stillbirth in their study was significantly higher in the TUCK group (2.5% vs. 1%, P < 0.001), with pregnancies extending beyond 37 gestational weeks accounting for most of the (tenfold) difference (0.9% vs. 0.08% P < 0.001). Neonatal outcomes were also worse with TUCK, including hypoglycemia and need for phototherapy, with no differences compared to pregnancies without TUCK in 5-min Apgar score, NICU admissions, and number of hospitalization days [19].

Notably, although we found a higher rate of emergency cesarean delivery for NRFHR in the TUCK group compared to the non-TUCK group, the rates of vacuum-assisted deliveries for NRFHR were comparable between groups. This may possibly be due to the smaller number of cases, or due to some of these patients having an antenatally diagnosed TUCK, leading to an increased tendency for cesarean delivery which was clinician driven.

Using PSM, we found that neonates in the TUCK group had a higher rate of 1-min Apgar score < 7 and of seizures than neonates in the control group. There were no significant differences in any of the other pregnancy, delivery, and neonatal outcomes between the two groups.

Similar to our study, Linde et al. [3] (288 singleton pregnancies with TUCK vs 23,027 without) reported higher rates of low 1-min Apgar score in the TUCK group (aOR 3.93,95% CI 1.41–11.0). However, and in contrast to our findings, that study reported a fourfold higher risk of stillbirth. Joura et al. [7] (216 pregnancies with TUCK vs 21796 without) found TUCK to be associated with large-for-gestational age newborn, a longer umbilical cord, and a tenfold higher risk of stillbirth. Sørnes et al. [20] (286 pregnancies with TUCK vs 22,531 without) found a higher rate of stillbirth (1.7% vs. 0.6%, P < 0.05) and fetal acidosis (pH < 7.1) (8.33% vs. 4.03%, P < 0.01) in the TUCK group, but no difference compared to controls in Apgar scores and NICU admission. A possible explanation for the discrepancy between the nonsignificant increase in stillbirths in our present study (p = 0.06) and the significant findings in earlier ones might be our exclusion of some TUCK cases in which stillbirth may have occurred from the PSM model. Additionally, we examined perinatal outcomes in postnatally detected TUCK. We lacked data on the proportion of patients in the whole cohort who had antenatally detected TUCK, which could have altered pregnancy management and outcomes. Therefore, we believe the comparable stillbirth rates in the two groups in our cohort should be interpreted with caution.

Furthermore, although the neonatal seizure rate was increased in the TUCK group, it was still very low in both groups (3 cases in the TUCK group and 6 in the control group), limiting the robustness of this finding. Prenatal sonographic detection of TUCK has become easier and more common [21], but the management of nuchal or true knots of the umbilical cord has not been addressed to date by the International Society of Ultrasound in Obstetrics and Gynecology (ISUOG) and other expert groups [22, 23]. Some studies suggested that detection during pregnancy is important and that intensive follow-up, including induction of labor at 37 gestational weeks [20, 21, 24], may be helpful. Our results suggest that the association between TUCK and stillbirth remains uncertain, and therefore unnecessary intervention should be avoided. Continued expectant management with interval fetal testing while awaiting the onset of spontaneous labor is a viable clinical option. A prenatal sonographic diagnosis of TUCK should not serve as the sole indication for cesarean delivery.

The main strengths of our study are the large sample size, single-center setting, and uniform treatment and follow-up during pregnancy and delivery. The large sample permitted the utilization of PSM, which is a statistically robust means of using observational data to simulate a controlled experiment and isolate the predictor of interest, thereby increasing the validity of our results.

The study has several limitations. First, owing to the retrospective design and use of hospital databases, some data were missing, which could have impacted the results. These also include the percentage of pregnancies with an antepartum diagnosis of TUCK, and pregnancy follow-up in those cases versus cases with an overlooked diagnosis. Second, clinical follow-up was limited to early neonatal complications. Third, stillbirth is a rare event; therefore, a very large cohort is needed in order to determine statistically significant differences between groups. Thus, this finding of a comparable stillbirth rate between groups should be interpreted with caution, especially in a single-center setting, which may restrict generalizability to other medical practices. Finally, TUCK in our study was based on a macroscopic diagnosis made by a midwife or physician, and therefore, might have been under-reported. The degree of tightness of the knot, a hard-to-quantify parameter, and the number of knots, were not recorded or described, which could have had an unknown impact on outcomes.

In conclusion, based on a large cohort of patients and using a robust statistical design, this study suggests a comparable stillbirth rate in TUCK pregnancies as compared to pregnancies without TUCK. This finding may cautiously reassure both physicians and parturient patients and attenuate the need for intense fetal surveillance with its resultant maternal stress in cases of TUCK. Nevertheless, given the rarity of stillbirth, our findings should be interpreted with caution and be examined further in larger studies.

Availability of data and materials

The data that support the findings of this study are available on request from the corresponding author [O.H]. Restrictions apply to the availability of these data, which were used under license for this study. Data are available from the author [O.H] with the permission of the local institutional review board -Beilinson hospital.

References

  1. Guzikowski W, Kowalczyk D, Więcek J. Diagnosis of true umbilical cord knot. Arch Med Sci. 2014;10:91–5.

    Article  PubMed  Google Scholar 

  2. Hershkovitz R, Silberstein T, Sheiner E, et al. Risk factors associated with true knots of the umbilical cord. Eur J Obstet Gynecol Reprod Biol. 2001;98:36–9.

    Article  CAS  PubMed  Google Scholar 

  3. Linde LE, Rasmussen S, Kessler J, Ebbing C. Extreme umbilical cord lengths, cord knot and entanglement: risk factors and risk of adverse outcomes, a population-based study. PLoS ONE. 2018;13:e0194814.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Chan JS, Baergen RN. Gross umbilical cord complications are associated with placental lesions of circulatory stasis and fetal hypoxia. Pediatr Dev Pathol. 2012;15:487–94.

    Article  PubMed  Google Scholar 

  5. Airas U, Heinonen S. Clinical significance of true umbilical knots: a population-based analysis. Am J Perinatol. 2002;19:127–32.

    Article  PubMed  Google Scholar 

  6. Sepulveda W, Shennan AH, Bower S, Nicolaidis P, Fisk NM. True knot of the umbilical cord: a difficult prenatal ultrasonographic diagnosis. Ultrasound Obstet Gynecol. 1995;5:106–8.

    Article  CAS  PubMed  Google Scholar 

  7. Joura EA, Zeisler H, Sator MO. Epidemiology and clinical value of true umbilical cord knots. Wien Klin Wochenschr. 1998;110:232–5 German.

    CAS  PubMed  Google Scholar 

  8. da Cunha AC, da Silveira BR, Dal Pai TK, et al. Prenatal diagnosis of a true umbilical cord knot in a fetus with intrauterine growth restriction and placenta accreta. Taiwan J Obstet Gynecol. 2016;55:616–7.

    Article  PubMed  Google Scholar 

  9. Bakas P, Papadakis E, Hassiakos D, Liapis A. Second-trimester miscarriage and umbilical cord knot. Case report and review of the literature. Clin Exp Obstet Gynecol. 2013;40:448–51.

    CAS  PubMed  Google Scholar 

  10. Ikechebelu J, Eleje G, Ofojebe C. True umbilical cord knot leading to fetal demise. Ann Med Health Sci Res. 2014;4(Suppl 2):S155–S118.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Pinar H, Carpenter M. Placenta and umbilical cord abnormalities seen with stillbirth. Clin Obstet Gynecol. 2010;53:656–72.

    Article  PubMed  Google Scholar 

  12. Bosselmann S, Mielke G. Sonographic assessment of the umbilical cord. Geburtshilfe Frauenheilkd. 2015;75:808–18.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Bohîlțea RE, Turcan N, Cîrstoiu M. Prenatal ultrasound diagnosis and pregnancy outcome of umbilical cord knot - debate regarding ethical aspects of a series of cases. J Med Life. 2016;9:297–301.

    PubMed  PubMed Central  Google Scholar 

  14. Austin PC. A comparison of 12 algorithms for matching on the propensity score. Stat Med. 2014;33:1057–69.

    Article  PubMed  Google Scholar 

  15. Flury BK, Riedwyl H. Standard distance in univariate and multivariate analysis. Am Stat. 1986;40:249–51.

    Google Scholar 

  16. Austin PC. Balance diagnostics for comparing the distribution of baseline covariates between treatment groups in propensity-score matched samples. Stat Med. 2009;28:3083–107.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Räisänen S, Georgiadis L, Harju M, Keski-Nisula L, Heinonen S. True umbilical cord knot and obstetric outcome. Int J Gynaecol Obstet. 2013;122:18–21.

    Article  PubMed  Google Scholar 

  18. Stempel LE. Beyond the pretty pictures: giving obstetricians just enough (umbilical) cord to hang themselves. Am J Obstet Gynecol. 2006;195:888–90.

    Article  PubMed  Google Scholar 

  19. Weissmann-Brenner A, Meyer R, Domniz N, et al. The perils of true knot of the umbilical cord: antepartum, intrapartum and postpartum complications and clinical implications. Arch Gynecol Obstet. 2022;305:573–9.

    Article  PubMed  Google Scholar 

  20. Sørnes T. Umbilical cord knots. Acta Obstet Gynecol Scand. 2000;79:157–9.

    Article  PubMed  Google Scholar 

  21. Weissmann-Brenner A, Domniz N, Weissbach T, et al. Antenatal detection of true knot in the umbilical cord - how accurate can we be? Ultraschall Med. 2022;43:298–303.

    Article  PubMed  Google Scholar 

  22. AIUM-ACR-ACOG-SMFM-SRU practice parameter for the performance of standard diagnostic obstetric ultrasound examinations. J Ultrasound Med 2018;37:E13-E24.

  23. Salomon LJ, Alfirevic Z, Berghella V, ISUOG Clinical Standards Committee, et al. Practice guidelines for performance of the routine mid-trimester fetal ultrasound scan. Ultrasound Obstet Gynecol. 2011;37:116–26.

    Article  CAS  PubMed  Google Scholar 

  24. Sherer DM, Amoabeng O, Dryer AM, Dalloul M. Current perspectives of prenatal sonographic diagnosis and clinical management challenges of true knot of the umbilical cord. Int J Womens Health. 2020;12:221–33.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Authors and Affiliations

Authors

Contributions

All authors contributed to the study conception and design. The first draft of the manuscript was written by OH and AH, and all authors commented on previous versions of the manuscript. Material preparation, data collection were performed by OH, AH, AB, AP and EH. Data analysis was done by OB and AW. All authors read and approved the final manuscript.  Except for the substantial contribution to the conception of this work mentioned above, all authors read, revised and approved the draft and this final manuscript.

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Correspondence to Ohad Houri.

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Ethics approval and consent to participate

All procedures performed in studies involving human participants were approved and in accordance with the ethical standards of the institutional research review board at Rabin Medical Center and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. For this type of study formal consent is not required.

This article does not contain any studies with animals performed by any of the authors. The Rabin Medical Center institutional review board approved the study (Approval No, 0132–22-RMC), with waiver of informed consent due to the retrospective, observational design of the study.

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The authors declare no competing interests.

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Supplementary Information

Additional file 1

: Fig. S1. Mirrored histograms showing overlap of patients with and without TUCK.

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Houri, O., Bercovich, O., Wertheimer, A. et al. Clinical significance of true umbilical cord knot: a propensity score matching study. BMC Pregnancy Childbirth 24, 59 (2024). https://doi.org/10.1186/s12884-024-06249-w

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