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      Initiation of Resuscitation with High Tidal Volumes Causes Cerebral Hemodynamic Disturbance, Brain Inflammation and Injury in Preterm Lambs

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          Abstract

          Aims

          Preterm infants can be inadvertently exposed to high tidal volumes (V T) in the delivery room, causing lung inflammation and injury, but little is known about their effects on the brain. The aim of this study was to compare an initial 15 min of high V T resuscitation strategy to a less injurious resuscitation strategy on cerebral haemodynamics, inflammation and injury.

          Methods

          Preterm lambs at 126 d gestation were surgically instrumented prior to receiving resuscitation with either: 1) High V T targeting 10–12 mL/kg for the first 15 min (n = 6) or 2) a protective resuscitation strategy (Prot V T), consisting of prophylactic surfactant, a 20 s sustained inflation and a lower initial V T (7 mL/kg; n = 6). Both groups were subsequently ventilated with a V T 7 mL/kg. Blood gases, arterial pressures and carotid blood flows were recorded. Cerebral blood volume and oxygenation were assessed using near infrared spectroscopy. The brain was collected for biochemical and histologic assessment of inflammation, injury, vascular extravasation, hemorrhage and oxidative injury. Unventilated controls (UVC; n = 6) were used for comparison.

          Results

          High V T lambs had worse oxygenation and required greater ventilatory support than Prot V T lambs. High V T resulted in cerebral haemodynamic instability during the initial 15 min, adverse cerebral tissue oxygenation index and cerebral vasoparalysis. While both resuscitation strategies increased lung and brain inflammation and oxidative stress, High V T resuscitation significantly amplified the effect (p = 0.014 and p<0.001). Vascular extravasation was evident in the brains of 60% of High V T lambs, but not in UVC or Prot V T lambs.

          Conclusion

          High V T resulted in greater cerebral haemodynamic instability, increased brain inflammation, oxidative stress and vascular extravasation than a Prot V T strategy. The initiation of resuscitation targeting Prot V T may reduce the severity of brain injury in preterm neonates.

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          Most cited references42

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          Late oligodendrocyte progenitors coincide with the developmental window of vulnerability for human perinatal white matter injury.

          Hypoxic-ischemic injury to the periventricular cerebral white matter [periventricular leukomalacia (PVL)] results in cerebral palsy and is the leading cause of brain injury in premature infants. The principal feature of PVL is a chronic disturbance of myelination and suggests that oligodendrocyte (OL) lineage progression is disrupted by ischemic injury. We determined the OL lineage stages at risk for injury during the developmental window of vulnerability for PVL (23-32 weeks, postconceptional age). In 26 normal control autopsy human brains, OL lineage progression was defined in parietal white matter, a region of predilection for PVL. Three successive OL stages, the late OL progenitor, the immature OL, and the mature OL, were characterized between 18 and 41 weeks with anti-NG2 proteoglycan, O4, O1, and anti-myelin basic protein (anti-MBP) antibodies. NG2+O4+ late OL progenitors were the predominant stage throughout the latter half of gestation. Between 18 and 27 weeks, O4+O1+ immature OLs were a minor population (9.9 +/- 2.1% of total OLs; n = 9). Between 28 and 41 weeks, an increase in immature OLs to 30.9 +/- 2.1% of total OLs (n = 9) was accompanied by a progressive increase in MBP+ myelin sheaths that were restricted to the periventricular white matter. The developmental window of high risk for PVL thus precedes the onset of myelination and identifies the late OL progenitor as the major potential target. Moreover, the decline in incidence of PVL at approximately 32 weeks coincides with the onset of myelination in the periventricular white matter and suggests that the risk for PVL is related to the presence of late OL progenitors in the periventricular white matter.
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            Pathogenesis of cerebral white matter injury of prematurity.

            Cerebral white matter injury, characterised by loss of premyelinating oligodendrocytes (pre-OLs), is the most common form of injury to the preterm brain and is associated with a high risk of neurodevelopmental impairment. The unique cerebrovascular anatomy and physiology of the premature baby underlies the exquisite sensitivity of white matter to the abnormal milieu of preterm extrauterine life, in particular ischaemia and inflammation. These two upstream mechanisms can coexist and amplify their effects, leading to activation of two principal downstream mechanisms: excitotoxicity and free radical attack. Upstream mechanisms trigger generation of reactive oxygen and nitrogen species. The pre-OL is intrinsically vulnerable to free radical attack due to immaturity of antioxidant enzyme systems and iron accumulation. Ischaemia and inflammation trigger glutamate receptor-mediated injury leading to maturation-dependent cell death and loss of cellular processes. This review looks at recent evidence for pathogenetic mechanisms in white matter injury with emphasis on targets for prevention and treatment of injury.
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              Manual ventilation with a few large breaths at birth compromises the therapeutic effect of subsequent surfactant replacement in immature lambs.

              The reason why some infants with respiratory distress syndrome fail to respond to surfactant, or respond only transiently, is incompletely understood. We hypothesized that resuscitation with large breaths at birth might damage the lungs and blunt the effect of surfactant. Five pairs of lamb siblings were delivered by cesarean section at 127-128 d of gestation. One lamb in each pair was randomly selected to receive six manual inflations of 35-40 mL/kg ("bagging") before the start of mechanical ventilation, a volume roughly corresponding to the inspiratory capacity of lamb lungs after prophylactic surfactant supplementation. Both siblings were given rescue porcine surfactant, 200 mg/kg, at 30 min of age. Blood gases and deflation pressure-volume (P-V) curves of the respiratory system were recorded until the lambs were killed at 4 h. The P-V curves became steeper after surfactant in the control group, but no such effect was seen in those subjected to bagging. At 4 h, inspiratory capacity and maximal deflation compliance were almost three times higher (p < 0.01) in the controls than in the bagged lambs. The latter were also more difficult to ventilate and tended to have less well expanded alveoli and more widespread lung injury in histologic sections. We conclude that a few inflations with volumes that are probably harmless in other circumstances might, when forced into the surfactant-deficient lung immediately at birth, compromise the effect of subsequent surfactant rescue treatment. Our findings challenge current neonatal resuscitation practice of rapidly establishing a normal lung volume by vigorous manual ventilation.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2012
                22 June 2012
                : 7
                : 6
                : e39535
                Affiliations
                [1 ]The Ritchie Centre, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia
                [2 ]Department of Obstetrics and Gynecology, Monash University, Clayton, Victoria, Australia
                [3 ]Centre for Neonatal Research and Education, School of Women’s and Infants’ Health, The University of Western Australia, Crawley, Western Australia, Australia
                [4 ]Department of Neonatal Medicine, Royal North Shore Hospital and University of Sydney, Sydney, New South Wales, Australia
                Erasmus University Rotterdam, The Netherlands
                Author notes

                Conceived and designed the experiments: GP SM FW AG TM MK SH. Performed the experiments: GP SM SB AB FW JA AG TM MT MK SH. Analyzed the data: GP SM SB AB FW JA MT. Contributed reagents/materials/analysis tools: GP SM SB AB FW JA MT. Wrote the paper: GP SM SB AB FW JA AG TM MT MK SH.

                Article
                PONE-D-12-06915
                10.1371/journal.pone.0039535
                3382197
                22761816
                e8c68262-8735-48f5-b939-ba0e92781126
                Polglase et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 29 February 2012
                : 23 May 2012
                Page count
                Pages: 8
                Categories
                Research Article
                Medicine
                Anatomy and Physiology
                Cardiovascular System
                Circulatory Physiology
                Respiratory System
                Respiratory Physiology
                Neurology
                Cerebrovascular Diseases
                Ischemic Stroke
                Cerebral Palsy
                Pediatrics
                Neonatology
                Pediatric Pulmonology

                Uncategorized
                Uncategorized

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