Postnatal transition is a vast and complex physiological process whereby newborns must adapt from an environment of full placental support to complete self-maintenance. Dramatic respiratory and circulatory changes must occur rapidly and are crucial for survival. While these changes are well described, additional focus has now been brought to the critical timing of these events, with a greater understanding of the integral relationship between lung aeration, pulmonary blood flow and cardiac output. Placental transfusion via DCC is vital in supporting these processes to ensure a successful and stable transition to ex utero life15-19.
Full understanding of the physiology is fundamental in appreciating the processes during transition and the importance of placental transfusion. In utero, a large amount of fetal cardiac output lies within the placenta. Up to 50% of a preterm fetus’ circulating volume is within the placenta circulation, compared to up to 30% of a term fetus. As pulmonary blood flow is low, the placental circulation is the source of venous return to the heart. Placental venous return via the umbilical vein is predominantly shunted from the right atrium across the foramen ovale to the left atrium, and therefore provides preload to left ventricle. Placental blood flow is therefore the ultimate source of cardiac output, cerebral and systemic blood flow.
When babies are born, the umbilical arteries constrict to minimise forward flow to the placenta, while flow via the umbilical vein continues for several minutes. Aeration of the lungs at birth is then the key trigger that sets off the series of events, that combined with clamping of the cord, lead to the dramatic changes in the newborn cardiorespiratory system1,15-21. Lung aeration results in a rapid fall in pulmonary vascular resistance, and subsequent increase in pulmonary blood flow15-17. The baby can draw blood from the low resistance placental circulation, allowing redistribution of blood to the lungs, while maintaining venous return. This process preserves cardiac output which ensures no fall in cerebral or systemic blood flow15-17. The additional blood from the placenta during transition provides cardiovascular stability, by boosting circulating blood volume, maintaining organ perfusion, and facilitating a smoother transition from fetal to newborn circulation15,16.
Physiological based cord clamping (PBCC) is also an emerging practice, which brings additional focus to the timing of cord clamping in relation to lung aeration. PBCC allows generous placental transfusion through DCC, while supporting initiation of respiration and establishment of pulmonary blood flow20-29. In both animal and human studies, PBCC has been shown to allow a smoother transition, by supporting an increase in pulmonary blood flow, maintaining systemic blood flow and providing a more stable cerebral haemodynamic transition with less hypoxia and bradycardia24. Another study found PBCC stabilised core temperature at delivery when compared to those who had immediate cord clamping27. Further observational studies demonstrated increased mortality, increased risk of chronic lung disease and severe IVH if the cord is clamped prior to onset of breathing23-26.
Through these physiological processes, preterm babies who receive placental transfusion benefit from a significant reduction mortality of one third, as well as less brain haemorrhage, hypotension, anaemia, NEC and sepsis.
While most term infants can adapt without consequence without full DCC, immediate cord clamping (ICC) however, has now been clearly shown to cause harm in preterm babies18-21. Immediate or early clamping of the cord, particularly when performed prior to lung aeration, forces a baby to transition without the ability to draw from their innate circulation within the placenta. ICC cuts off umbilical venous flow leading to an abrupt drop in venous return by 30-50%15,17. The increase in systemic vascular resistance caused by removing the low resistance placental circulation, also leads to increased systemic arterial pressure. Combining a reduction in preload from reduced venous return, together with an increase in afterload due to increased arterial pressure, a sudden fall in cardiac output leads to hypotension and bradycardia13,22, reduced systemic blood flow and impaired organ perfusion.
The impact on cerebral blood flow here is also vital. Following the rapid increase in arterial pressure, cerebral blood flow initially increases, but then rapidly falls due to the reduction in cardiac output. These critical mechanisms contribute to the increased the risk of intraventricular haemorrhage and circulatory collapse in the preterm infant, as well as a greater need for inotropic support and need for blood transfusion16,17,20,30,34,38.
These negative effects can be mitigated by delaying the time at which the umbilical cord is clamped, allowing a much more physiological and safe transition. By keeping the baby attached to the cord while lung aeration and pulmonary blood flow is established, umbilical venous flow can maintain venous return, ventricular preload and therefore prevent the harm caused by the drop in cardiac output.
The evidence of benefit from DCC, underpinned by this increased physiological understanding, is now overwhelming and highlights the urgent need to update and improve our clinical practice. PBCC brings further focus to the importance of timing of cord clamping in relation to lung aeration. Perinatal teams should therefore ensure shared goals of clamping the cord after a minimum of 60 seconds and ideally after lung aeration has been achieved. Careful attention should be made to the assessment and understanding of an infant’s rapidly changing physiology at birth, to ensure they benefit from a stable postnatal transition.