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Original Article

Delayed versus immediate cord clamping in dichorionic twins <32 weeks: a retrospective study

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Article: 2203300 | Received 24 Aug 2022, Accepted 11 Apr 2023, Published online: 26 Apr 2023

Abstract

Objectives

Strong evidence imply that delayed cord clamping (DCC) provides significant benefits for singleton neonates. However, there is little information about the safety or efficacy of DCC in twins to recommend for or against DCC in twins in guidelines. We aimed to determine the effect of DCC on dichorionic twins born at <32 weeks of gestation.

Study design

This is a retrospective cohort study comparing the neonatal and maternal outcomes of immediate cord clamping (ICC) [<15 second (s)] versus DCC (at 60 s). Generalized estimating equations models were performed accounting for twin correlation.

Results

A total of 82 pairs of twins (DCC: 41; ICC: 41) were included in analysis. The primary outcome of death before discharge occurred in 3.66% of twins in the DCC group and 7.32% in the ICC group, without a significant difference between the groups. Compared to ICC group, DCC was associated with increased hemoglobin levels [β1 coefficient 6.51; 95% confidence interval (CI) 0.69–12.32. β2 coefficient 5.80; 95% CI 0.07–11.54] at 12–24 h of life. There were no significant differences between the groups in neonatal death, neonatal major morbidities and maternal bleeding complications, although DCC was associated with higher estimated maternal blood loss in the cesarean section group (p = .005).

Conclusions

DCC for 60 s in dichorionic twins born at <32 weeks of gestation was associated with increased neonatal hemoglobin levels, when compared with ICC. The finding of a higher estimated maternal blood loss by cesarean section in the DCC group calls for further trials to assess maternal safety of this procedure in this patient population.

Introduction

Delaying umbilical cord clamping (DCC) at birth supports a smoother circulatory transition from fetal to neonatal life [Citation1] and increases infants’ blood volume [Citation2]. Strong evidence from multiple randomized controlled trials and meta-analyses imply that DCC provides significant benefits for neonates, especially preterm infants [Citation3–5]. Thus DCC for preterm infants is consistently recommended by the recent American College of Obstericians and Gynecologists (ACOG) [Citation6] and European Resuscitation Council Guidelines.

The rate of twining has increased largely in recent decades [Citation7]. As twins are at higher risk for prematurity and adverse perinatal outcome than singleton [Citation8], twins may particularly benefit from DCC. However, obstetricians and neonatologists may be hesitant about doing DCC in multiple pregnancies owing to concerns about fetus well-being, unfavorable hemodynamic changes in monochorionic placentation, and risk of maternal hemorrhage. Most studies of DCC usually either excluded multiples or included both multiples and singletons with no stratification analysis of outcomes [Citation9]. One meta-analysis found that none of the four published studies focusing on DCC in multiple gestations stratified outcomes by chorionicity [Citation5]. The conclusions regarding to the neonatal outcomes and maternal safety in preterm twins were varied [Citation10–14]. Statements or guidelines worldwide clearly endorsed DCC for uncompromised preterm infants but most of these guidelines are with no reference to multiple pregnancies [Citation15]. Italian recommendations for placental transfusion weakly recommended DCC for twin newborns from dichorionic pregnancy [Citation16]. No recommendations for or against DCC in multiple gestations were made in the most recent ACOG guidelines [Citation6], Society of Obstetrician and Gynecologists of Canada (SOGC) guidelines [Citation17] and the latest International Liaison Committee on Resuscitation (ILCOR) statement [Citation18] due to insufficient evidence. A further investigation on the safety and efficacy of DCC in multiple gestations is urgently required.

This retrospective cohort study aimed to evaluate the clinical outcomes of DCC in dichorionic twins, born at < 32 weeks of gestation. We hypothesized that DCC for 60 s would not be associated with any adverse neonatal effects or increased maternal hemorrhage risk.

Materials and methods

Study oversight

This retrospective cohort study was conducted in Women and Children’s Hospital of Chongqing Medical University, which is a tertiary class A hospital with a 126-bed Level 3 neonatal intensive care unit [Citation19]. We routinely admit very preterm infants (VPI) born between 24°/7 and 316/7 weeks gestation, which reaches about 220 admissions per year. Our hospital is a national pilot unit for twin pregnancy specialized clinic. We reported the study following the guidelines of Strengthening the Reporting of Observational Studies in Epidemiology (STROBE). This study was approved by the Ethics Committee of the Women and Children’s Hospital of Chongqing Medical University (no. 2021015).

Procedures

The umbilical cord was cut within 15 second (s) in the immediate cord clamping (ICC) group and at 60 s after birth in the delayed cord clamping (DCC) group. In 6/2018, a DCC protocol targeted on singleton preterm infants was introduced in this perinatal center. In 1/2019, the DCC protocol was extended to include preterm dichorionic-diamniotic twins based on the Italian guideline with some modifications [Citation16]. The temperature of the delivery room or operating room was pre-adjusted to 28–30 °C. Preheated sterile towels were used to dry the newborn infant as quickly as possible and were replaced to prevent heat loss during the intervention. Time was elapsed from birth and called every 15 s by the timer person, who was not part of the resuscitation team. Once the first twin was delivered, he was placed on his mother’s perineum in a vaginal delivery (VD) or on his mother’s abdomen in a cesarean section (CS). In the DCC group, the attending neonatologist at mother’s bedside, initiated the initial resuscitation steps during the first 30 s. At 30 s of life, the neonatologist evaluated heart rate, tone and breathing activity. DCC was discontinued if any of the twins was bradycardic, apneic or gasping at 30 s of life. If the heart rate was >100 bpm and active breathing or efforts to breath were present, the cord was clamped at 60 s. After the cord was cut, the first twin received further resuscitation if necessary following the 2015 American Heart Association Neonatal Resuscitation Guidelines. Giraffe incubator (Giraffe Incubator Carestation SC1,Ohmeda Medical, United states) and Giraffe shuttle(Giraffe shuttle, Ohmeda Medical, United States) were used for resuscitation/transition and intra-hospital transfers.

Inclusion and exclusion criteria

We included all liveborn dichorionic-diamniotic twins born at <32 weeks of gestation and excluded infants with (1) severe placental abruption, (2) major congenital anomalies, (3) general anesthesia, and (4) severe maternal illness that prompted immediate delivery. Twins were excluded from analyses if one of them in the DCC group (1) received less than 60s DCC or (2) had no recorded DCC details.

Outcomes

Neonatal outcomes data included hemoglobin analysis of infants at 12–24 h of life, death before discharge, necrotizing enterocolitis (NEC) stage ≫2 [Citation20], intraventricular hemorrhage (IVH) [Citation21], periventricular leukomalacia (PVL) [Citation22], respiratory distress syndrome (RDS), patent ductus arteriosus (PDA) requiring medical or surgical treatment, bronchopulmonary dysplasia (BPD) [Citation23], early onset sepsis (EOS) and late onset sepsis (LOS), need for packed red blood cell transfusions within the first week of life, total number of blood transfusions before discharge and duration of mechanical ventation.

Maternal outcomes data included estimated blood loss (EBL), postpartum hemorrhage (PPH) defined as EBL >500 ml for vaginal delivery or EBL >1000 ml for cesarean delivery [Citation13], post-delivery decrease in maternal hemoglobin, postpartum infection, blood transfusion and hysterectomy.

Statistical analyses

Maternal and neonatal characteristics and outcomes were compared between the groups. For continuous variables, the Student t test or Mann–Whitney U test where applicable was used. For categorical variables, χ2 or Fisher exact test where applicable was used. Generalized estimating equations models were performed to account for the correlation between twins. Biologically plausible confounding variables including gestational age and birth weight were selected for the statistical model 1. Gestational age, birth weight, mode of delivery, administration of antenatal corticosteriods and maternal diabetes (pre-gestational or gestational diabetes) were selected for the statistical model 2. β coefficients for continuous variables and crude and aOR for categorical variables, along with 95% CIs, were calculated. To determine whether the neonatal outcomes varied by gestational age, planned subgroup analysis was performed among infants born at ≪29+6 weeks vs. those born between 30+0 and 31+6 weeks. p < .05 or a 95% CI that does not include 1 for ORs and 0 for β coefficients denoted significance, and all tests were 2-tailed. Statistical analyses were performed with SPSS (version 22, IBM, Chicago, IL) and SAS Enterprise Guide software (version 9.21, SAS Institute Inc., Cary, NC) (SAS for GEE model).

Results

Maternal and neonatal demographics

From 2017 to 2020, 105 dichorionic twins pairs were born at <32weeks of gestation and 82 twins pairs were included in our analysis, of whom 41 received DCC for 60 s and 41 received ICC <15 s ().

Figure 1. Flow chart of participants. 

Figure 1. Flow chart of participants. 

and show maternal and neonatal characteristics. There were significant differences in maternal characteristics including steroids given before delivery (p = .026) and maternal diabetes (p = .003), both of which were included in the adjusted analysis model 2. There were no significant differences in neonatal characteristics except in mode of delivery (p = .001), which was also included in the adjusted analysis model 2.

Table 1. Maternal characteristics.

Table 2. Neonatal demographics by treatment group.

Maternal outcomes

There were no statistically significant differences in postpartum hemorrhage, postpartum infection and incidence of blood transfusion (). In the CS group, there was higher estimated maternal blood loss with delayed (p = .005), compared with immediate, cord clamping. 2 women in the DCC group and 6 women in the ICC group, all of whom suffered prenatal anemia, 1 woman with unanticipated placenta accreta in the ICC group, required blood transfusion for symptomatic anemia on postoperative day 1. One woman in the ICC group underwent unplanned hysterectomy.

Table 3. Maternal outcomes.

Neonatal outcomes

As shown in , the primary outcome of death before discharge occurred in 3.66% of twins in the DCC group and 7.32% in the ICC group, without a significant difference between the groups (aOR1 0.48; 95% CI, 0.08–2.78. aOR2 0.44; 95% CI, 0.05–4.03). The incidence of major neonatal morbidities (NEC, any IVH, RDS, PDA requiring medical or surgical treatment, BPD, EOS and LOS), blood transfusions and duration of mechanical ventilation were similar between the groups. DCC was associated with increased hemoglobin levels (β1 coefficient 6.51; 95% CI 0.69–12.32. β2 coefficient 5.80; 95%CI 0.07–11.54) at 12-24 h in the adjusted analyses compared with ICC. The incidence of PVL was low, which can’t be calculated using the adjusted GEE model.

Table 4. Neonatal outcomes.

In our a priori planned analyses to determine whether the neonatal outcomes varied by gestational age (Table S1), there were no significant differences in the neonatal death and major morbidities in infants either <30 weeks or ≥ 30 weeks between the groups (Table S2 and Table S3).

Discussion

There is little information about the safety or efficacy of DCC in twins to recommend for or against DCC in multiple gestations[Citation6]. The current retrospective study of DCC in twins of dichorionic-diamniotic born at <32 weeks of gestation showed no significant difference in the primary neonatal outcome of death before discharge, major neonatal morbidity and maternal hemorrhage, although DCC was associated with increased hemoglobin levels of the infants and higher estimated maternal blood loss in the CS group.

A previous systematic review of preterm singletons showed lower mortality [Citation4,Citation5] and reduced incidence of intraventricular hemorrhage and necrotizing enterocolitis [Citation3] with DCC than ICC. However, the neonatal outcomes of mortality and major morbidity in our study was consistent with existing studies on DCC in twins. An RCT of preterm (28–36 weeks) comparing DCC (24 pregnancies, 51 infants, 30–60 s) to ICC (23 pregnancies, 50 infants, <3–5 s) found no significant differences between the groups in neonatal outcomes, however DCC was associated with a higher PPH rate compared with ICC[12]. A retrospective study of 31 pairs of twins (23+0–31+6 weeks) comparing DCC (60 s) to ICC (not defined) found a reduction in RBC transfusions in first week in the DCC group and no differences in neonatal outcomes [Citation10]. Another large retrospective cohort study of 1597 pairs of twins (<30 weeks) comparing DCC ≥30 s versus <30 s found a reduction of blood transfusions and no difference in neonatal death and/or severe neurological injury [Citation14]. These three prior studies involved monochorionic and dichorionic twins without stratifying by chorionicity. A retrospective study involving 58 pairs of dichorionic twins (23–32 weeks) comparing DCC (30 s; N = 8) to ICC (not defined; N = 50) also did not find significant differences in neonatal outcomes between the two groups. In addition, the Australian Placental Transfusion Study (APTS) including 1566 infants born before 30 weeks of gestation, of which 24.9% were of multiple births, found no significant differences in the incidence of death or major morbidity [Citation9]. Whether DCC in twins reduces mortality or major morbidity requires verification in large randomized trial.

The higher hemoglobin level at 12–24 h after adjusting for confounding factors in the DCC group suggest an effective placental transfusion. However, there was no difference in the total number of blood transfusions before discharge. Two previous studies found no differences in hematocrit at birth or in admission [Citation10,Citation12], while the other two previous studies defined no details about the hemoglobin or hematocrit levels [Citation11,Citation14]. As in our study, there seems to be higher hematocrit levels at 12–24 h of life in the DCC group (52.58 ± 5.55) than in the ICC group (50.97 ± 5.86) although with no significant difference. Previous study involving 1566 preterm infants found only a 2.7% difference in peak hematocrit in the first week between DCC and ICC group[Citation9]. Our study was not powered to detect a similar finding due to the small size. Besides, the infant-placental blood volume distribution of normal term infants was 67%–33% at less than 5 s after birth, 73%–27% at 15 s and 80%–20% at 1 min[Citation2]. Infants included in our study were all less than 32 weeks of gestation and the blood volume of these infants may be fewer than that of the term. The cord was clamped at less than 15 s in the ICC group and at 60 s in the DCC group in our study. It is possible that cord clamped at less than 5 s in the ICC group could have resulted more profound significant difference between the two groups. Since onset of infants’ ventilation, which was not collected in our study, affect placental transfusion and the inadequacy of ventilation during the delaying procedure in the DCC group could partially explain our negative results.

In our study, there was higher estimated maternal blood loss in the CS group with delayed, compared with immediate, cord clamping, which was contrasted to the previous study [Citation13]. One explanation of the discrepancy may be that the patients received umbilical cord clamping before 30 s in early cord clamping group and at least after 30 s in DCC group in the previous study [Citation13], however we defined DCC as cord clamping at 60 s and ICC as less than 15 s. DCC was not associated with maternal bleeding complications in our study, consistent with previous studies [Citation10,Citation13]. A higher rate of maternal PPH was found in the DCC group, however 3/7 PPH cases were triplets [Citation12]. Therefore, further larger sample size of trials targeted to assess the effect of DCC on maternal safety are needed.

Our study has limitations as a single-center retrospective study and a subsequent randomized controlled trial is planned. There were significant differences in mode of delivery, administration of antenatal corticosteriods and maternal diabetes, which has impacts on the prognosis of the infants. Although we stratified by these potential confounding factors, there may still be some bias in our study. Also there may be selection bias related to implementing DCC. Our study was limited by its small sample size and low numbers of extremely low birth weight infants. Our study was not powered to demonstrate differences in neonatal benefits previous detected in singletons. As there is potential risks of acute twin to twin transfusion syndrome during DCC in monochorionic multiple gestations [Citation6,Citation24], our DCC protocol only includes dichorionic twins but excludes monochorionic twins, which partly contribute to the small sample size of our study. Despite these limitations, we believe it is important to share our findings, as an important gap in the practice of DCC in preterm twins need to be addressed.

In conclusion, DCC for 60 s in very preterm dichorionic twins was associated with increased neonatal hemoglobin levels, when compared with ICC. The finding of a higher estimated maternal blood loss by cesarean section in the DCC group was unexpected. Further larger clinical trials are urgent needed to confirm the observed findings and long term neurodevelopmental outcomes.

Author contributions

Conceived and designed the study: LW, XY Z, HG, WC, and LG Z. Performed data collection and data analysis: LW, JF O, and GY X. Drafted the original manuscript: LW and XY Z. Revised the final manuscript: LW, YW, HG, WC, LG Z and XY Z. All authors read and approved the final manuscript.

Supplemental material

Supplementary Material

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Acknowledgements

Gratitude is expressed to our patients and families. We thank the obstetricians and midwives participating in this study. We thank Dr Dingmei Wang of Fudan university for her valuable suggestions.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Availability of data and materials

The data are included in the article and supplementary materials.

Additional information

Funding

This study was supported by the [Chongqing Health Commission] under Grant [2021MSXM239]; [Joint Scientific Research Grants of Chongqing Health Commission and Science and Technology Bureau] under Grant [2023QNXM037] and [Scientific Research Grants of Women and Children’s Hospital of Chongqing Medical University] under Grant [2020YJQN01].

References

  • Manley BJ, Owen LS, Hooper SB, et al. Towards evidence-based resuscitation of the newborn infant. Lancet. 2017;389(10079):1639–1648.
  • Ac Y. Distribution of blood between infant and placenta after birth. Lancet. 1969;2(7626):871–873.
  • Rabe H, Diaz-Rossello JL, Duley L, Dowswell T. Effect of timing of umbilical cord clamping and other strategies to influence placental transfusion at preterm birth on maternal and infant outcomes. Cochrane Database Syst Rev. 2012;15(8):CD003248.
  • Rabe H, Gyte GM, Díaz-Rossello JL, et al. Effect of timing of umbilical cord clamping and other strategies to influence placental transfusion at preterm birth on maternal and infant outcomes. Cochrane Database Syst Rev. 2019;9(9).
  • Fogarty M, Osborn DA, Askie L, et al. Delayed vs early umbilical cord clamping for preterm infants: a systematic review and meta-analysis. Am J Obstet Gynecol. 2018;218(1):1–18.
  • Delayed umbilical cord clamping after birth: ACOG committee opinion, number 814. Obstet Gynecol. 2020;136(6):e100–e106.
  • Ananth CV, Chauhan SP. Epidemiology of twinning in developed countries. Semin Perinatol. 2012;36(3):156–161.
  • Gupta P, Faridi MM, Goel N, et al. Reappraisal of twinning: epidemiology and outcome in the early neonatal period. Singapore Med J. 2014;55(6):310–317.
  • Tarnow-Mordi W, Morris J, Kirby A, et al. Delayed versus immediate cord clamping in preterm infants. N Engl J Med. 2017;377(25):2445–2455.
  • Chiruvolu A, Daoud Y, Inzer RW. Effect of delayed cord clamping on very preterm twins. Early Hum Dev. 2018;124:22–25.
  • Liu LY, Yee LM. Delayed cord clamping in preterm dichorionic twin gestations. J Matern Fetal Neonatal Med. 2020;33(23):3949–3953.
  • Ruangkit C, Bumrungphuet S, Panburana P, et al. A randomized controlled trial of immediate versus delayed umbilical cord clamping in multiple-birth infants born preterm. Neonatology. 2019;115(2):156–163.
  • Ruangkit C, Leon M, Hassen K, et al. Maternal bleeding complications following early versus delayed umbilical cord clamping in multiple pregnancies. BMC Pregnancy Childbirth. 2018;18(1):131.
  • Grabovac M, Beltempo M, Lodha A, et al. Impact of deferred cord clamping on mortality and severe neurologic injury in twins born at <30 weeks of gestation. J Pediatr. 2021;238:118–123.e3.
  • Liyanage SK, Ninan K, McDonald SD. Guidelines on deferred cord clamping and cord milking: a systematic review. Pediatrics. 2020;146(5):e20201429.
  • Ghirardello S, Di Tommaso M, Fiocchi S, et al. Italian recommendations for placental transfusion strategies. Front Pediatr. 2018;6:372.
  • McDonald SD, Narvey M, Ehman W, et al. Guideline no. 424: umbilical cord management in preterm and term infants. J Obstet Gynaecol Can. 2022;44(3):313–322 e1.
  • Wyckoff MH, Singletary EM, Soar J, et al. International consensus on cardiopulmonary resuscitation and emergency cardiovascular care science with treatment recommendations: summary from the basic life support; advanced life support; neonatal life support; education, implementation, and teams; first aid task forces; and the COVID-19 working group. Circulation. 2021;145(9):e645–e721.
  • Zhang H, Ma H, Ye JY, et al. Practical experience of establishing German standard level 1 perinatal center in Chongqing health care for women and children. Curr Med Sci. 2020;40(5):829–834.
  • Bell MJ, Ternberg JL, Feigin RD, et al. Neonatal necrotizing enterocolitis. Therapeutic decisions based upon clinical staging. Ann Surg. 1978;187(1):1–7.
  • Papile LA, Burstein J, Burstein R, et al. Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birth weights less than 1,500 gm. J Pediatr. 1978;92(4):529–534.
  • Volpe JJ. Neurology of the newborn. 5th ed. Philadelphia, PA: Saunders Elsevier; 2008.
  • Higgins RD, Jobe AH, Koso-Thomas M, et al. Bronchopulmonary dysplasia: executive summary of a workshop. J Pediatr. 2018;197:300–308.
  • Lewi L, Cannie M, Blickstein I, et al. Placental sharing, birthweight discordance, and vascular anastomoses in monochorionic diamniotic twin placentas. Am J Obstet Gynecol. 2007;197(6):587.e1-587–e8.