Neurally adjusted ventilatory assist (NAVA) mode as an adjunct diagnostic tool in congenital central hypoventilation syndrome

Journal of the College of Physicians and Surgeons Pakistan

Volumn 23, Issue 2, 2013, Pages 154-156

  Rahmani, Aiman ^a   Rehman, Naveed Ur ^a   Chedid, Fares ^a  

^a JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

Central apnea; Congenital hypoventilation syndrome; Neurally adjusted ventilatory assist (NAVA); PHOX2B gene

Indexed keywords

NALOXONE; PETHIDINE;

APNEA; ARTICLE; ARTIFICIAL VENTILATION; ASSISTED VENTILATION; CASE REPORT; CENTRAL SLEEP APNEA SYNDROME; CLINICAL OBSERVATION; CONGENITAL CENTRAL HYPOVENTILATION SYNDROME; DIAPHRAGM; ELECTROENCEPHALOGRAM; EPILEPTIC DISCHARGE; FEMALE; GENE; GENE MUTATION; GENETIC IDENTIFICATION; HOME CARE; HUMAN; INTUBATION; NEURALLY ADJUSTED VENTILATORY ASSIST MONITORING; NEWBORN; NEWBORN INTENSIVE CARE; NEWBORN MONITORING; PHOX2B GENE; RESUSCITATION; TRACHEOSTOMY; WAKEFULNESS;

DIAPHRAGM; ELECTROMYOGRAPHY; FEMALE; HOMEODOMAIN PROTEINS; HUMANS; HYPOVENTILATION; INFANT, NEWBORN; INTENSIVE CARE UNITS, NEONATAL; INTERACTIVE VENTILATORY SUPPORT; MONITORING, PHYSIOLOGIC; RESPIRATORY MECHANICS; SLEEP APNEA, CENTRAL; TRANSCRIPTION FACTORS;

EID: 84873132333     PISSN: 1022386X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. Spahija J, de Marchie M, Albert M, Bellemare P, Delisle S, Beck J. Patient-ventilator interaction during pressure support ventilation and neurally adjusted ventilatory assist. Crit Care Med 2010; 38:518-26.
2. Sassoon MD, Foster GT. Patient-ventilator asynchrony. Curr Opin Crit Care 2001; 7:28-33.
3. MacIntyre NR. Patient-ventilator interaction: optimizing conventional ventilation modes. Respir Care 2011; 56:73-84.
4. Becker K, Wallace JM. Central sleep apnea [Internet]. [cited 2010 Jul 31]. Available from: http://emedicine.medscape.com/article/304967-overview
5. AASM (2001). The international classification of sleep disorders. Westchester, Illinois: American Academy of Sleep Medicine; 2001.
6. Huang J, Colrain IM, Panitch HB, Tapia IE, Schwartz MS, Samuel J, et al. Effect of sleep stage on breathing in children with central hypoventilation. J Appl Physiol 2008; 105:44-53. Epub 2008 May 22.
7. Amiel J, Laudier B, Attie-Bitach T, Trang H, de Pontual L, Gener B, et al. Polyalanine expansion and frame shift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet 2003; 33:459-61.
8. Lee P, Su YN, Yu CJ, Yang PC, Wu HD. PHOX2B mutationconfirmed congenital central hypoventilation syndrome in a Chinese family: presentation from newborn to adulthood. Chest 2009; 135:537-44.
9. Repetto GM, Corrales RJ, Abara SG, Zhou L, Berry-Kravis EM, Rand CM, et al. Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B gene. Acta Paediatr 2009; 98:192-5. Epub 2008 Sep 16.
10. Weese-Mayer DE, Berry-Kravis EM, Ceccherini I, Keens TG, Loghmanee DA, Trang H, et al. An official ATS clinical policy statement: congenital central hypoventilation syndrome: genetic basis, diagnosis, and management. Am J Respir Crit Care Med 2010; 181:626-44.