Jeffrey R. Kaiser, M.D., MA
Physiological Disturbances Associated with Neonatal Intraventricular Hemorrhage: Annually, nearly 5,000 extremely low birth weight (ELBW, birth weight ≤1000 g) infants in the US develop severe intraventricular hemorrhage (IVH, grades III and IV); this devastating complication of prematurity is associated with long-term adverse neurodevelopmental sequelae, such as cognitive, behavioral, and learning disabilities, as well as cerebral palsy. Unfortunately, identifying the ELBW infants who are at highest risk for developing IVH and who could benefit most from specific interventions has been difficult and based on retrospective studies. Our overall goal is to prospectively evaluate and understand disturbed physiological phenomena associated with IVH in order to predict those infants most at risk and to develop best care clinical practices that may subsequently limit severe brain injury in ELBW infants. While the etiology of IVH is multifactorial, disturbances of cerebral blood flow (CBF) and cerebral autoregulation play important roles; both are influenced by alterations of gas exchange and systemic hemodynamics associated with routine intensive care procedures. Extremes of CO2 may have deleterious effects on infants’ CBF because the arterial CO2 tension (PaCO2) is a potent mediator of cerebral vascular tone and influences cerebral blood supply. Hypotension or hypertension may cause cerebral hypo- or hyperperfusion, respectively, leading to IVH in infants with impaired cerebral autoregulation by an ischemia/reperfusion mechanism. Because disturbances of PaCO2, blood pressure (BP), and heart rhythm are common in ELBW infants undergoing intensive care, our central hypothesis is that alterations and extremes of these physiological factors that influence CBF and cerebral autoregulation in ELBW infants may initiate IVH and serve as important predictors of ELBW infants most at risk of IVH, thereby allowing identification of a high-risk subgroup of infants who may benefit most from intervention.
1. Kaiser JR, Gauss CH, Williams DK. Surfactant administration acutely affects cerebral and systemic hemodynamics and gas exchange in very low birth weight infants. J Pediatr 2004; 144: 809-814.
2. Hall RW, Kronsberg SS, Barton BA, Kaiser JR, Anand KJS. Morphine, hypotension, and adverse outcomes in premature neonates: Who’s to blame? Secondary results from the NEOPAIN trial. Pediatrics 2005; 115: 1351-1359.
3. Kaiser JR, Gauss CH, Williams DK. The Effects of hypercapnia on cerebral autoregulation in ventilated very low birth weight infants. Pediatr Res 58 (5):931-935, 2005.
4. Gluckman PD, Wyatt JS, Azzopardi D, Ballard R, Edwards AD, Ferriero DM, Polin RA, Robertson CM, Thoresen M, Whitelaw A, Gunn AJ, on behalf of the CoolCap Study Group. Selective head cooling with mild systemic hypothermia after neonatal encephalopathy: multicenter randomised trial. The Lancet, 2005; 365: 663-670.
5. Kaiser JR, Gauss CH, Pont MK, Williams DK. Hypercapnia during the first three days of life is associated with severe intraventricular hemorrhage in very low birth weight infants. J Perinatol, 2006; 26:279-285.
6. May-Wewers J, Kaiser JR, Moore EK, Blackall DP. Severe neonatal hemolysis due to a maternal antibody to the low-frequency Rh Antigen Cw. Am J Perinatol, 2006; 23: 1-5
7. Chalak LF, Kaiser JR, Arrington RW. Resolution of pulmonary interstitial emphysema following selective left main stem intubation in a premature newborn: an old procedure revisited. Pediatric Anesthesia, 2007; 17: 183-186.
Kaiser JR. Neurologic Sequelae following Mechanical Ventilation. In Hot Topics in Neonatal Neurology, Michael Schimmel (ed), Nova Scientific Publishing, 2007.