Ignite Creation Date:
2024-05-05 @ 11:52 AM
Last Modification Date:
2024-10-26 @ 9:15 AM
Study NCT ID:
NCT00156455
Status:
WITHDRAWN
Last Update Posted:
2015-04-30
First Post:
2005-09-08
Brief Title:
Sleep Disordered Breathing in Children With Single Ventricle Physiology
Sponsor:
University of Rochester
Organization:
University of Rochester
Study Overview
Official Title:
Sleep Disordered Breathing in Children With Single Ventricle Physiology
Status:
WITHDRAWN
Status Verified Date:
2015-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
lack of study personel
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This is an exploratory study designed to evaluate the incidence of and to quantify sleep disordered breathing following stage I Norwood reconstructive surgery Sleep disordered breathing will be correlated with
1 Elevations in pulmonary vasculature resistance at the time of Stage II surgery
2 Risks of death
1 Elevations in pulmonary vasculature resistance at the time of Stage II surgery
2 Risks of death
Detailed Description:
This is an exploratory study designed to evaluate the incidence of and to quantify sleep disordered breathing following stage I Norwood reconstructive surgery Sleep disordered breathing will be correlated with
1 Elevations in pulmonary vasculature resistance at the time of Stage II surgery
2 Risks of death
Children with single ventricle physiology are exquisitely sensitive to alterations in pulmonary vascular resistance Following their first operative repair stage I Norwood performed in their first week of life pulmonary and systemic circulations are in parallel rather than series As such elevations in pulmonary vascular resistance can result in severe arterial desaturation Additionally elevated pre-operative pulmonary artery pressure is directly correlated with poor survival following the third and final operative repair stage III Norwood or Fontan
Periodic breathing is a normal breathing pattern in sleeping infants At the other end of the spectrum is sleep apnea In between lies a continuum of sleep disordered breathing Obstructive sleep apnea has an incidence of approximately 2 in children and is associated with pulmonary and systemic hypertension Specific studies of the incidence and effects of sleep disordered breathing in congenital heart disease are lacking Otherwise normal children have baseline oxygen saturation in the high 90s thereby placing them on the flat part of the oxyhemoglobin curve But children with cyanotic congenital heart disease live with baseline oxygen saturations in the mid 70s so that they exist on the steep part of the oxyhemoglobin dissociation curve We hypothesize therefore that these patients are at increased risk for the hemodynamic variations occurring during apneashypopneas even when they are more subtle namely during sleep disordered breathing
We hypothesize that children who have completed stage I Norwood will experience more significant arterial desaturations during sleep associated apneic events due to the concurrent elevation in pulmonary arterial pressure than their normal counterparts Additionally we hypothesize that children who experience more frequent apneic events during sleep will have elevated pre-operative pulmonary artery pressures and therefore worse outcome following stage II Norwood Thus we speculate that children who have completed stage I Norwood are more prone to the risks of sleep disordered breathing
Autonomic regulation mediated in part by aortic arch baroreceptors is undoubtedly disrupted by the extensive surgical reconstruction required at the aortic arch during stage I Norwood palliation Adults and children with severe sleep disordered breathing obstructive sleep apnea have impaired cardiac autonomic control and increased cardiac electrical instability with greater occurrence of ventricular arrhythmias Apneic events place a hypoxic mechanical and adrenergic load on the cardiovascular system thereby directly resulting in ventricular dysrhythmias Observed late deaths following stage I Norwood are usually postulated to be secondary to fatal arrhythmias Thus we hypothesize that children who experience more frequent apneic events during sleep will have an increased risk of interstage mortality
Sleep disordered breathing is a readily treatable condition in the pediatric population Non-invasive continuous positive airway pressure applied via a nasal mask is effective in treating sleep disordered breathing in infants Thus if sleep disordered breathing is identified effective treatment is available and may reduce the risk of inter-stage mortality and adverse hemodynamics in this medically fragile population
1 Elevations in pulmonary vasculature resistance at the time of Stage II surgery
2 Risks of death
Children with single ventricle physiology are exquisitely sensitive to alterations in pulmonary vascular resistance Following their first operative repair stage I Norwood performed in their first week of life pulmonary and systemic circulations are in parallel rather than series As such elevations in pulmonary vascular resistance can result in severe arterial desaturation Additionally elevated pre-operative pulmonary artery pressure is directly correlated with poor survival following the third and final operative repair stage III Norwood or Fontan
Periodic breathing is a normal breathing pattern in sleeping infants At the other end of the spectrum is sleep apnea In between lies a continuum of sleep disordered breathing Obstructive sleep apnea has an incidence of approximately 2 in children and is associated with pulmonary and systemic hypertension Specific studies of the incidence and effects of sleep disordered breathing in congenital heart disease are lacking Otherwise normal children have baseline oxygen saturation in the high 90s thereby placing them on the flat part of the oxyhemoglobin curve But children with cyanotic congenital heart disease live with baseline oxygen saturations in the mid 70s so that they exist on the steep part of the oxyhemoglobin dissociation curve We hypothesize therefore that these patients are at increased risk for the hemodynamic variations occurring during apneashypopneas even when they are more subtle namely during sleep disordered breathing
We hypothesize that children who have completed stage I Norwood will experience more significant arterial desaturations during sleep associated apneic events due to the concurrent elevation in pulmonary arterial pressure than their normal counterparts Additionally we hypothesize that children who experience more frequent apneic events during sleep will have elevated pre-operative pulmonary artery pressures and therefore worse outcome following stage II Norwood Thus we speculate that children who have completed stage I Norwood are more prone to the risks of sleep disordered breathing
Autonomic regulation mediated in part by aortic arch baroreceptors is undoubtedly disrupted by the extensive surgical reconstruction required at the aortic arch during stage I Norwood palliation Adults and children with severe sleep disordered breathing obstructive sleep apnea have impaired cardiac autonomic control and increased cardiac electrical instability with greater occurrence of ventricular arrhythmias Apneic events place a hypoxic mechanical and adrenergic load on the cardiovascular system thereby directly resulting in ventricular dysrhythmias Observed late deaths following stage I Norwood are usually postulated to be secondary to fatal arrhythmias Thus we hypothesize that children who experience more frequent apneic events during sleep will have an increased risk of interstage mortality
Sleep disordered breathing is a readily treatable condition in the pediatric population Non-invasive continuous positive airway pressure applied via a nasal mask is effective in treating sleep disordered breathing in infants Thus if sleep disordered breathing is identified effective treatment is available and may reduce the risk of inter-stage mortality and adverse hemodynamics in this medically fragile population
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None