Ventilation before Umbilical Cord Clamping Improves the Physiological Transition at Birth

Sasmira Bhatt, Graeme R Polglase, Euan M Wallace, Arjan B Te Pas, Stuart B Hooper, Sasmira Bhatt, Graeme R Polglase, Euan M Wallace, Arjan B Te Pas, Stuart B Hooper

Abstract

The transition from a fetus to a neonate at birth represents a critical phase in our life. Most infants make this transition without complications, but preterm infants usually require some form of assistance due to immature cardiopulmonary systems that predispose them to lifelong sequelae. As the incidence of preterm birth is increasing, there is now an urgent need for the development of management strategies that facilitate this transition, which will likely include improved strategies for the management of the maternal third stage of labor. For instance, recent studies on the physiological transition at birth have led to the discovery that establishing ventilation in the infant before the umbilical cord is clamped greatly stabilizes the cardiovascular transition at birth. While most benefits of delayed clamping previously have been attributed to an increase in placenta to infant blood transfusion, clearly there are other significant benefits for the infant, which are not well understood. Nevertheless, if ventilation can be established before cord clamping in a preterm infant, the large adverse changes in cardiac function that normally accompanies umbilical cord clamping can be avoided. As preterm infants have an immature cerebral vascular bed, large swings in cardiovascular function places them at high risk of cerebral vascular rupture and the associated increased risk of mortality and morbidity. In view of the impact that cord clamping has on the cardiovascular transition at birth, it is also time to re-examine some of the strategies used in the management of the third stage of labor. These include the appropriate timing of uterotonic administration in relation to delivery of the infant and placenta. As there is a lack of evidence on the effects these individual practices have on the infant, there is a necessity to improve our understanding of their impact in order to develop strategies that facilitate the transition to newborn life.

Keywords: delayed cord clamping; neonatal; preterm birth; transition; umbilical cord clamping.

Figures

Figure 1
Figure 1
Left Panel: The fetal circulation is unique due to the presence of the placenta, which provides the gas-exchange requirements of the fetus. The lungs are filled with fluid and, as a result, pulmonary vascular resistance (PVR) is high and the majority right ventricular output bypasses the pulmonary circulation through the ductus arteriosus (DA). Therefore, the placenta supplies both left and right ventricular output, with left ventricular output being support by blood flow through the foramen ovale (FO). Middle Panel: With clamping of the umbilical cord you immediately remove placental supply of right and left ventricular output, resulting in an instantaneous reduction to combined ventricular output (CVO) by ~50%. Since the lungs are still filled with fluid, PVR is high thus right ventricular output is still diverted away from the pulmonary circulation, through the DA. Right Panel: Removal of lung liquid and aeration of the lung results in a rapid fall in PVR and a subsequent increase in PBF, allowing 100% of right ventricular output to enter the lungs. This allows the pulmonary circulation to replace the placenta as the source of left ventricular output. There is also a reversal in pressure gradient and thus direction of blood flow across the ductus arteriosus (from left-to-right to right-to-left), allowing for up to 50% of left ventricular output to enter the pulmonary circulation, thus further stabilizing the upper body circulation.

References

    1. Sheldon WR, Durocher J, Winikoff B, Blum J, Trussell J. How effective are the components of active management of the third stage of labor? BMC Pregnancy Childbirth (2013) 13:46.10.1186/1471-2393-13-46
    1. Aflaifel N, Weeks AD. Active management of the third stage of labour. BMJ (2012) 345:e4546.10.1136/bmj.e4546
    1. Ononeze AB, Hutchon DJ. Attitude of obstetricians towards delayed cord clamping: a questionnaire-based study. J Obstet Gynaecol (2009) 29(3):223–4.10.1080/01443610802712918
    1. Sivaraman T, Arulkumaran S. Delayed umbilical cord clamping: potential for change in obstetric practice. BJOG (2011) 118(6):767.10.1111/j.1471-0528.2011.02899.x
    1. Niermeyer S, Velaphi S. Promoting physiologic transition at birth: re-examining resuscitation and the timing of cord clamping. Semin Fetal Neonatal Med (2013) 18(6):385–92.
    1. Bhatt S, Alison B, Wallace EM, Crossley KJ, Gill AW, Kluckow M, et al. Delaying cord clamping until ventilation onset improves cardiovascular function at birth in preterm lambs. J Physiol (2013) 591(8):2113–26.10.1113/jphysiol.2012.250084
    1. Darwin E. Zoonomia. London: T. Benfley; (1801).
    1. Dunn PM. The birth of perinatal medicine in the United Kingdom. Semin Fetal Neonatal Med (2007) 12(3):227–38.10.1016/j.siny.2007.02.001
    1. Downey CL, Bewley S. Historical perspectives on umbilical cord clamping and neonatal transition. J R Soc Med (2012) 105(8):325–9.10.1258/jrsm.2012.110316
    1. Hutchon DJ. Why do obstetricians and midwives still rush to clamp the cord? BMJ (2010) 341:c5447.10.1136/bmj.c5447
    1. Perlman JM, Wyllie J, Kattwinkel J, Atkins DL, Chameides L, Goldsmith JP, et al. Neonatal resuscitation: 2010 international consensus on cardiopulmonary resuscitation and emergency cardiovascular care science with treatment recommendations. Pediatrics (2010) 126(5):e1319–44.10.1542/peds.2010-2972B
    1. Roehr CC, Hansmann G, Hoehn T, Buhrer C. The 2010 guidelines on neonatal resuscitation (AHA, ERC, ILCOR): similarities and differences – what progress has been made since 2005? Klin Padiatr (2011) 223(5):299–307.10.1055/s-0031-1280750
    1. Hooper SB, Te Pas AB, Lewis RA, Morley CJ. Establishing functional residual capacity at birth. NeoReviews (2010) 11:474–83.10.1542/neo.11-9-e474
    1. Te Pas AB, Davis PG, Hooper SB, Morley CJ. From liquid to air: breathing after birth. J Pediatr (2008) 152(5):607–11.10.1016/j.jpeds.2007.10.041
    1. Kluckow M, Evans N. Low superior vena cava flow and intraventricular haemorrhage in preterm infants. Arch Dis Child Fetal Neonatal Ed (2000) 82(3):F188–94.10.1136/fn.82.3.F188
    1. Osborn DA, Evans N, Kluckow M. Left ventricular contractility in extremely premature infants in the first day and response to inotropes. Pediatr Res (2007) 61(3):335–40.10.1203/pdr.0b013e318030d1e1
    1. Hooper SB, Harding R. Fetal lung liquid: a major determinant of the growth and functional development of the fetal lung. Clin Exp Pharmacol Physiol (1995) 22:235–47.10.1111/j.1440-1681.1995.tb01988.x
    1. Harding R, Hooper SB. Regulation of lung expansion and lung growth before birth. J Appl Physiol (1996) 81(1):209–24.
    1. Hooper SB, Siew ML, Kitchen MJ, Te Pas AB. Establishing functional residual capacity in the non-breathing infant. Semin Fetal Neonatal Med (2013) 18(6):336–43.
    1. Gao Y, Raj JU. Regulation of the pulmonary circulation in the fetus and newborn. Physiol Rev (2010) 90(4):1291–335.10.1152/physrev.00032.2009
    1. Teitel DF, Iwamoto HS, Rudolph AM. Changes in the pulmonary circulation during birth-related events. Pediatr Res (1990) 27(4):372–8.10.1203/00006450-199004000-00010
    1. Sobotka KS, Hooper SB, Allison BJ, Te Pas AB, Davis PG, Morley CJ, et al. An initial sustained inflation improves the respiratory and cardiovascular transition at birth in preterm lambs. Pediatr Res (2011) 70(1):56–60.10.1038/pr.2011.281
    1. Hooper SB, Kitchen MJ, Wallace MJ, Yagi N, Uesugi K, Morgan MJ, et al. Imaging lung aeration and lung liquid clearance at birth. FASEB J (2007) 21:3329–37.10.1096/fj.07-8208com
    1. Siew ML, Wallace MJ, Allison BJ, Kitchen MJ, Te Pas AB, Islam MS, et al. The role of lung inflation and sodium transport in airway liquid clearance during lung aeration in newborn rabbits. Pediatr Res (2013) 73(4 Pt 1):443–9.10.1038/pr.2012.197
    1. Siew ML, Wallace MJ, Kitchen MJ, Lewis RA, Fouras A, Te Pas AB, et al. Inspiration regulates the rate and temporal pattern of lung liquid clearance and lung aeration at birth. J Appl Physiol (2009) 106(6):1888–95.10.1152/japplphysiol.91526.2008
    1. Harding R, Hooper SB, Dickson KA. A mechanism leading to reduced lung expansion and lung hypoplasia in fetal sheep during oligohydramnios. Am J Obstet Gynecol (1990) 163:1904–13.10.1016/0002-9378(90)90772-Y
    1. Olver RE, Walters DV, Wilson M. Developmental regulation of lung liquid transport. Annu Rev Physiol (2004) 66:77–101.10.1146/annurev.physiol.66.071702.145229
    1. Miserocchi G, Poskurica BH, Del Fabbro M. Pulmonary interstitial pressure in anesthetized paralyzed newborn rabbits. J Appl Physiol (1994) 77(5):2260–8.
    1. Siew ML, Te Pas AB, Wallace MJ, Kitchen MJ, Lewis RA, Fouras A, et al. Positive end expiratory pressure enhances development of a functional residual capacity in preterm rabbits ventilated from birth. J Appl Physiol (2009) 106:1487–93.10.1152/japplphysiol.91591.2008
    1. Rudolph AM. Fetal and neonatal pulmonary circulation. Annu Rev Physiol (1979) 41:383–95.10.1146/annurev.ph.41.030179.002123
    1. Rudolph AM. Distribution and regulation of blood flow in the fetal and neonatal lamb. Circ Res (1985) 57:811–21.10.1161/01.RES.57.6.811
    1. Crossley KJ, Allison BJ, Polglase GR, Morley CJ, Davis PG, Hooper SB. Dynamic changes in the direction of blood flow through the ductus arteriosus at birth. J Physiol (2009) 587(19):4695–704.
    1. Polglase GR, Wallace MJ, Grant DA, Hooper SB. Influence of fetal breathing movements on pulmonary hemodynamics in fetal sheep. Pediatr Res (2004) 56(6):932–8.10.1203/01.PDR.0000145254.66447.C0
    1. Seed M, van Amerom JF, Yoo SJ, Al Nafisi B, Grosse-Wortmann L, Jaeggi E, et al. Feasibility of quantification of the distribution of blood flow in the normal human fetal circulation using CMR: a cross-sectional study. J Cardiovasc Magn Reson (2012) 14:79.10.1186/1532-429X-14-79
    1. Dawson JA, Kamlin CO, Wong C, Te Pas AB, Vento M, Cole TJ, et al. Changes in heart rate in the first minutes after birth. Arch Dis Child Fetal Neonatal Ed (2010) 95(3):F177–81.10.1136/adc.2009.169102
    1. Dawes GS. Fetal and Neonatal Physiology. Chicago: Year Book Inc. (1968).
    1. van Vonderen JJ, Roest AA, Siew ML, Blom NA, van Lith JM, Walther FJ, et al. Noninvasive measurements of hemodynamic transition directly after birth. Pediatr Res (2014) 75(3):448–52.10.1038/pr.2013.241
    1. van Vonderen JJ, Roest AA, Siew ML, Walther FJ, Hooper SB, Te Pas AB. Measuring physiological changes during the transition to life after birth. Neonatology (2014) 105(3):230–42.10.1159/000356704
    1. Greisen G. Autoregulation of cerebral blood flow in newborn babies. Early Hum Dev (2005) 81(5):423–8.10.1016/j.earlhumdev.2005.03.005
    1. Stenson BJ, Boyle DW, Szyld EG. Initial ventilation strategies during newborn resuscitation. Clin Perinatol (2006) 33(1):65.10.1016/j.clp.2005.11.015
    1. O’Donnell CP, Kamlin CO, Davis PG, Morley CJ. Crying and breathing by extremely preterm infants immediately after birth. J Pediatr (2010) 156(5):846–7.10.1016/j.jpeds.2010.01.007
    1. Soltani H, Hutchon DR, Poulose TA. Timing of prophylactic uterotonics for the third stage of labour after vaginal birth. Cochrane Database Syst Rev (2010) (8):CD006173.10.1002/14651858.CD006173.pub2
    1. Begley CM, Gyte GML, Devane D, McGuire W, Weeks A. Active versus expectant management for women in the third stage of labour. Cochrane Database Syst Rev (2011) (11):CD007412.
    1. Rabe H. Cord clamping and neurodevelopmental outcome in very low birth weight infants. J Perinatol (2010) 30(1):1.10.1038/jp.2009.177
    1. Yao AC, Hirvensalo M, Lind J. Placental transfusion-rate and uterine contraction. Lancet (1968) 1(7539):380–3.10.1016/S0140-6736(68)91352-4
    1. Yao AC, Lind J. Placental transfusion. Am J Dis Child (1974) 127(1):128–41
    1. Yao AC, Lind J. Blood flow in the umbilical vessels during the third stage of labor. Biol Neonate (1974) 25(3–4):186–93.10.1159/000240691
    1. Yao AC, Moinian M, Lind J. Distribution of blood between infant and placenta after birth. Lancet (1969) 2(7626):871–3.10.1016/S0140-6736(69)92328-9
    1. 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) 8:CD003248.10.1002/14651858.CD003248.pub3
    1. McDonald SJ, Middleton P, Dowswell T, Morris PS. Effect of timing of umbilical cord clamping of term infants on maternal and neonatal outcomes. Cochrane Database Syst Rev (2013) 7:CD004074.
    1. Mercer JS. Current best evidence: a review of the literature on umbilical cord clamping. J Midwifery Womens Health (2001) 46(6):402–14.10.1016/S1526-9523(01)00196-9
    1. Mercer JS, Vohr BR, McGrath MM, Padbury JF, Wallach M, Oh W. Delayed cord clamping in very preterm infants reduces the incidence of intraventricular hemorrhage and late-onset sepsis: a randomized, controlled trial. Pediatrics (2006) 117(4):1235–42.10.1542/peds.2005-1706
    1. Venancio SI, Levy RB, Saldiva SR, Mondini L, Alves MC, Leung SL. [Effects of delayed cord clamping on hemoglobin and ferritin levels in infants at three months of age]. Cadernos de saude publica (2008) 24(Suppl 2):S323–31.
    1. Andersson O, Hellstrom-Westas L, Andersson D, Domellof M. Effect of delayed versus early umbilical cord clamping on neonatal outcomes and iron status at 4 months: a randomised controlled trial. BMJ (2011) 343:d7157.10.1136/bmj.d7157
    1. Mathew JL. Timing of umbilical cord clamping in term and preterm deliveries and infant and maternal outcomes: a systematic review of randomized controlled trials. Indian Pediatr (2011) 48(2):123–9.10.1007/s13312-011-0031-z
    1. Hutton EK, Hassan ES. Late vs early clamping of the umbilical cord in full-term neonates – systematic review and meta-analysis of controlled trials. JAMA (2007) 297(11):1241–52.10.1001/jama.297.11.1241
    1. Westgate JA, Wibbens B, Bennet L, Wassink G, Parer JT, Gunn AJ. The intrapartum deceleration in center stage: a physiologic approach to the interpretation of fetal heart rate changes in labor. Am J Obstet Gynecol (2007) 197(3):e1–11.
    1. Yao AC, Lind J. Effect of gravity on placental transfusion. Lancet (1969) 2(7619):505–8.10.1016/S0140-6736(69)90213-X
    1. Vain NE, Satragno DS, Gorenstein AN, Gordillo JE, Berazategui JP, Alda MG, et al. Effect of gravity on volume of placental transfusion: a multicentre, randomised, non-inferiority trial. Lancet (2014) 384(9939):235–40.
    1. Rabe H, Jewison A, Alvarez RF, Crook D, Stilton D, Bradley R, et al. Milking compared with delayed cord clamping to increase placental transfusion in preterm neonates: a randomized controlled trial. Obstet Gynecol (2011) 117(2 Pt 1):205–11.10.1097/AOG.0b013e3181fe46ff
    1. Upadhyay A, Gothwal S, Parihar R, Garg A, Gupta A, Chawla D, et al. Effect of umbilical cord milking in term and near term infants: randomized control trial. Am J Obstet Gynecol (2013) 208(2):e1–6
    1. Erickson-Owens DA, Mercer JS, Oh W. Umbilical cord milking in term infants delivered by cesarean section: a randomized controlled trial. J Perinatol (2012) 32(8):580–4.10.1038/jp.2011.159
    1. Hosono S, Mugishima H, Fujita H, Hosono A, Minato M, Okada T, et al. Umbilical cord milking reduces the need for red cell transfusions and improves neonatal adaptation in infants born at less than 29 weeks’ gestation: a randomised controlled trial. Arch Dis Child Fetal Neonatal Ed (2008) 93(1):F14–9.10.1136/adc.2006.108902
    1. Hosono S, Mugishima H, Fujita H, Hosono A, Okada T, Takahashi S, et al. Blood pressure and urine output during the first 120 h of life in infants born at less than 29 weeks’ gestation related to umbilical cord milking. Arch Dis Child Fetal Neonatal Ed (2009) 94(5):F328–31.10.1136/adc.2008.142935

Source: PubMed

3
구독하다