Delaying Umbilical Cord Clamping at birth can be very important for your baby. I will share more information as time goes on. For now I am sharing an excerpt from an assignment I wrote for my Masters in 2015. Obviously, since 2015 there has been more literature released, and so as time goes by I will put together some more updated information. There is also a link to a website (Wait for White) in the resources page that shares lots of information on this subject.
The timing of the clamping of the umbilical cord after birth has potential impacts on the well-being and development of the baby. In recent decades the practice of immediate cord clamping became routine as part of the active management of third stage of labour, as it was thought it would reduce bleeding post birth (Raju, 2013). More recent evidence has shown that there is no difference in post birth bleeding with early or delayed cord clamping (DCC) (McDonald et al., 2013). By waiting for a period of time after the baby is born before clamping the cord, blood can flow from the placenta to the baby, which is referred to as a placental transfusion (Farrar, 2010). The benefits of this practice have been the subject of multiple research studies which will be investigated in this assignment.
DCC provides the benefit of an increased haemoglobin in the infant period, with potential for associated long term neurological benefits. There is a smoother transition to life, both by stabilising the baby’s heartbeat and increasing blood volume, which may help prepare the lungs for extra-uterine life. There is debate about the ideal time to clamp the cord, and further research needs to be performed to establish the optimal time (Boere et al., 2015).
The relevance of iron deficiency in infants has been demonstrated in studies where both motor and social function deficits have been found to be associated with iron deficiency in the infant period, with or without anaemia (Lozoff et al., 2006; Lozoff, 2011; Congdon et al., 2012; Algarin et al., 2013). The gains from increased iron levels are thought to relate to the increased need for iron in the development of myelin sheaths during the early phase of accelerated neurological development (Shafir et al., 2008). Congdon et al. (2012) highlight that even after treatment with oral iron, the individuals identified as iron deficient as infants in their study showed neurological deficits at 10 years of age. However, Shirvani et al. (2010) suggest that treating infants with oral iron may cause competition with other nutrients during the absorption process in the gut. They suggest that reducing the risk of iron deficiency can be best achieved by DCC and they showed an increase in haemoglobin 48 hours after birth for DCC neonates (Shrivani et al., 2010). Chaparro, et al. (2006) demonstrated that with DCC of two minutes there was a higher haemoglobin at two months of age, and improved iron status at six months of age. In contrast, Tiemermsa et al. (2014) found haemoglobin levels were similar at two months of age. The discrepancies in these findings brings controversy to the argument that DCC may be an effective way to improve iron status and allow for optimal neurological development.
The work of Andersson and his team adds to the knowledge around how delayed cord clamping, and resultant increased iron stores, can have long term effects on infants (Andersson et al. 2013; Andersson et al., 2014; Andersson et al., 2015). Andersson et al. (2015) found that at four years of age, children who had experienced delayed cord clamping, were found to have improved fine motor skills and improved prosocial behaviour. These findings displayed differences which were not as marked as expected, but the trials were carried out in a high income country where dietary deficiencies were not common (Andersson et al., 2015). Repeating this research in low resource settings may give a better idea of the effect of DCC on iron status and associated neurological development.
Diaz-Castro et al. (2014) discovered that neonates who had experienced DCC were likely to demonstrate higher superoxide dismulase activity. They surmise that this may help protect neonates against the oxidative stress that is caused by labour. Bhatt et al.’s (2013) work has demonstrated that there is a smoother transition to life for premature lambs who have delayed cord clamping and Langli Ersdal et al.’s (2014) work supports this hypothesis in human neonates. They surmise that this is because the pulmonary blood flow is improved with improved cardiac function. Langli Erdal et al. (2014) report, after their large observational study, that if the cord is clamped after spontaneous respiration, then the baby is at less risk of dying during transition to life. Hooper et al. (2015) explain that this may be because establishing respiration before clamping the cord reduces pulmonary resistance and increases preload to increase cardiac output.
Bhatt et al. (2013) conclude that blood flow is reduced to the left atrium when the cord is clamped, which effectively reduces cardiac output at a critical time in transition. The increased blood flow in the superior vena cava when DCC occurs may decrease rates of intra-ventricular haemorrhage, which is associated with decreased cerebral blood flow (Meyer & Mildenhall, 2012). Later research has confirmed the thought that the stabilising of cerebral blood flow may decrease the risk of cerebral injury during transition to extra-uterine life (Bhatt et al., 2013; Nevill & Meyer, 2015). Mercer et al. (2008) suggest that it could be an inflammatory response to hypovolaemia which was causative for some cases of cerebral palsy. Diaz-Castro et al. (2014) mention moderation of inflammatory effects with DCC, but do not link it to a particular pathology.
Mercer et al. (2008) suggest babies who have DCC will have 30 percent more blood volume. Farrar et al.’s (2011) research suggests that DCC allows a placental transfusion, which comprises between one quarter to one third of the neonate’s blood volume. Mercer et al. (2010) suggest that the lungs receive about eight percent of cardiac output before birth, increasing to 45 percent after birth. The extra blood volume may be needed to service organs that have not been fully functioning in-utero (Mercer et al., 2010).
The increase in blood volume available to the baby after DCC, gives the expectation that neonates receiving this care would be less likely to need a blood transfusion, as was confirmed by Rabe et al. (2012). However, Elimian et al. (2014) demonstrated that there was no difference in the need for blood transfusions between 200 randomised preterm infants who experienced DCC and those who did not. As Elimian et al. (2014) acknowledges, the delay in their study was only 30 seconds, which may be inadequate to allow for sufficient blood transfer, whereas Rabe et al.’s (2012) studies DCC for 30 to 120 seconds. To allow for longer DCC without the concern of needing to remove the baby for resuscitation, this work could be repeated using bedside resuscitation trolleys (Hutchon, 2012). This would enable resuscitation, where needed, with an intact cord.
Smit et al. (2014) have identified an increase in oxygen saturation in the first few minutes of life where DCC occurred. Although heart rates were observed to be lower in this period with DCC, it was theorised that with increased blood volume the heart would not have to work as hard to circulate blood effectively (Smit et al., 2014). In other research Tiemermsa et al. (2015) found increased weight gain at two months of age for low birth weight babies who had DCC. McDonald et al. (2013) only mentions increased weights at birth with DCC, which may be expected with increased blood passing the baby, but no mention is made as to how long this increase in weight lasted.
Some articles express concerns about polycythaemia and jaundice needing phototherapy when babies have DCC (Rabe et al., 2012). McDonald et al. (2013) suggest that increased levels of jaundice, needing phototherapy, are two percent more likely to occur in babies that have had DCC. Ranjit et al. (2015) claim that preterm babies that needed phototherapy, had it for a longer duration if they experienced DCC. However, Andersson et al. (2011) and Diaz-Castro et al. (2014) found that there were no infants in their cohort who had DCC and experienced jaundice requiring phototherapy. Polycythaemia was not found by Shirvani et al. (2010) and Tiemersma et al. (2015); and Hutchon (2013) states that polycythaemia is not a risk factor for DCC. Concerns about polycythaemia and jaundice, which can be treated with phototherapy, need to be weighed up against the potential negative physiological effects for babies who do not receive DCC.
The benefits of DCC have been established in many studies. There is sometimes disagreement about aspects of the benefits and the optimal timing of cord clamping. However, most researchers agree that DCC is useful to the baby as it transitions to life, as well as in the long term through the increased iron stores. There is limited research on how often it is practiced and reasons individuals do not practice DCC. It is of interest to know whether the impediments to the adoption of DCC at a more global level are perhaps due to either lack of knowledge of the procedure, lack of acceptance of the evidence, or some doubts regarding the validity of the evidence that is in existence.