Cystic fibrosis and sleep

Clinics in Chest Medicine

Volumn 35, Issue 3, 2014, Pages 495-504

  Katz, Eliot S ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

Hypoventilation; Hypoxemia; Noninvasive ventilation; Respiratory insufficiency; Sleep disordered breathing

Indexed keywords

ANTIBIOTIC AGENT; CARBON DIOXIDE; OXYGEN;

ARTIFICIAL VENTILATION; BREATHING EXERCISE; CARDIOVASCULAR DISEASE; COGNITIVE DEFECT; COUGHING; CYSTIC FIBROSIS; EVIDENCE BASED MEDICINE; HUMAN; HYPERCAPNIA; HYPOXEMIA; LUNG GAS EXCHANGE; METABOLIC DISORDER; MORBIDITY; MORTALITY; NONINVASIVE VENTILATION; NUTRITIONAL COUNSELING; PATIENT CARE; PRIORITY JOURNAL; RESPIRATORY TRACT DISEASE; REVIEW; SCREENING TEST; SLEEP DISORDER; SLEEP DISORDERED BREATHING; SLEEP QUALITY; SLEEP TIME;

HYPOVENTILATION; HYPOXEMIA; NONINVASIVE VENTILATION; RESPIRATORY INSUFFICIENCY; SLEEP-DISORDERED BREATHING;

ANOXIA; CYSTIC FIBROSIS; HUMANS; HYPERCAPNIA; NONINVASIVE VENTILATION; OXYGEN INHALATION THERAPY; SLEEP; SLEEP APNEA, OBSTRUCTIVE; SLEEP DISORDERS;

EID: 84906791794     PISSN: 02725231     EISSN: 15578216     Source Type: Journal    
DOI: 10.1016/j.ccm.2014.06.005     Document Type: Review

References (82)

1. Fauroux B., Pepin J.L., Boelle P.Y., et al. Sleep quality and nocturnal hypoxaemia and hypercapnia in children and young adults with cystic fibrosis. Arch Dis Child 2012, 97:960-966.
2. Perin C., Fagondes S.C., Casarotto F.C., et al. Sleep findings and predictors of sleep desaturation in adult cystic fibrosis patients. Sleep Breath 2012, 16(4):1041-1048.
3. Sawicki G.S., Sellers D.E., Robinson W.M. Self-reported physical and psychological symptom burden in adults with cystic fibrosis. JPain Symptom Manage 2008, 35:372-380.
4. Amin R., Bean J., Burklow K., et al. The relationship between sleep disturbance and pulmonary function in stable pediatric cystic fibrosis patients. Chest 2005, 128:1357-1363.
5. Flume P.A., Ciolino J., Gray S., et al. Patient-reported pain and impaired sleep quality in adult patients with cystic fibrosis. JCyst Fibros 2009, 8:321-325.
6. Sheehan J., Massie J., Hay M., et al. The natural history and predictors of persistent problem behaviours in cystic fibrosis: a multicentre, prospective study. Arch Dis Child 2012, 97:625-631.
7. Ward C., Massie J., Glazner J., et al. Problem behaviours and parenting in preschool children with cystic fibrosis. Arch Dis Child 2009, 94:341-347.
8. Naqvi S.K., Sotelo C., Murry L., et al. Sleep architecture in children and adolescents with cystic fibrosis and the association with severity of lung disease. Sleep Breath 2008, 12:77-83.
9. Bouka A., Tiede H., Liebich L., et al. Quality of life in clinically stable adult cystic fibrosis out-patients: associations with daytime sleepiness and sleep quality. Respir Med 2012, 106:1244-1249.
10. Burker E.J., Carels R.A., Thompson L.F., et al. Quality of life in patients awaiting lung transplant: cystic fibrosis versus other end-stage lung diseases. Pediatr Pulmonol 2000, 30:453-460.
11. Abbott J., Holt A., Morton A.M., et al. Patient indicators of a pulmonary exacerbation: preliminary reports from school aged children map onto those of adults. JCyst Fibros 2012, 11:180-186.
12. Abbott J., Holt A., Hart A., et al. What defines a pulmonary exacerbation? The perceptions of adults with cystic fibrosis. JCyst Fibros 2009, 8:356-359.
13. Bramwell E.C., Halpin D.M., Duncan-Skingle F., et al. Home treatment of patients with cystic fibrosis using the 'Intermate': the first year's experience. JAdv Nurs 1995, 22:1063-1067.
14. Dobbin C.J., Bartlett D., Melehan K., et al. The effect of infective exacerbations on sleep and neurobehavioral function in cystic fibrosis. Am J Respir Crit Care Med 2005, 172:99-104.
15. Smith J.A., Owen E.C., Jones A.M., et al. Objective measurement of cough during pulmonary exacerbations in adults with cystic fibrosis. Thorax 2006, 61:425-429.
16. Hamutcu R., Francis J., Karakoc F., et al. Objective monitoring of cough in children with cystic fibrosis. Pediatr Pulmonol 2002, 34:331-335.
17. Munyard P., Bush A. How much coughing is normal?. Arch Dis Child 1996, 74:531-534.
18. Power J.T., Stewart I.C., Connaughton J.J., et al. Nocturnal cough in patients with chronic bronchitis and emphysema. Am Rev Respir Dis 1984, 130:999-1001.
19. van der Giessen L., Loeve M., de Jongste J., et al. Nocturnal cough in children with stable cystic fibrosis. Pediatr Pulmonol 2009, 44:859-865.
20. Stenekes S.J., Hughes A., Grégoire M.C., et al. Frequency and self-management of pain, dyspnea, and cough in cystic fibrosis. JPain Symptom Manage 2009, 38:837-848.
21. Kerem E., Wilschanski M., Miller N.L., et al. Ambulatory quantitative waking and sleeping cough assessment in patients with cystic fibrosis. JCyst Fibros 2011, 10:193-200.
22. Chang B., Newman G., Carlin B., et al. Subjective scoring of cough in children: parent-completed vs child-completed diary cards vs an objective method. Eur Respir J 1998, 11:462-466.
23. Stokes D.C., McBride J.T., Wall M.A., et al. Sleep hypoxemia in young adults with cystic fibrosis. Am J Dis Child 1980, 134:741-743.
24. Ravilly S., Robinson W., Suresh S., et al. Chronic pain in cystic fibrosis. Pediatrics 1996, 98:741-747.
25. Hayes D. Restless leg syndrome manifested by iron deficiency from chronic hemoptysis in cystic fibrosis. JCyst Fibros 2007, 6:234-236.
26. Spier S., Rivlin J., Hughes D., et al. The effect of oxygen on sleep, blood gases, and ventilation in cystic fibrosis. Am Rev Respir Dis 1984, 129:712-718.
27. Suratwala D., Chan J.S., Kelly A., et al. Nocturnal saturation and glucose tolerance in children with cystic fibrosis. Thorax 2011, 66:574-578.
28. Spicuzza L., Sciuto C., Leonardi S., et al. Early occurrence of obstructive sleep apnea in infants and children with cystic fibrosis. Arch Pediatr Adolesc Med 2012, 166:1165-1169.
29. Villa M.P., Pagani J., Lucidi V., et al. Nocturnal oximetry in infants with cystic fibrosis. Arch Dis Child 2001, 84:50.
30. Bradley S., Solin P., Wilson J., et al. Hypoxemia and hypercapnia during exercise and sleep in patients with cystic fibrosis. Chest 1999, 116:647-654.
31. de Castro-Silva C., de Bruin V.M., Cavalcante A.G., et al. Nocturnal hypoxia and sleep disturbances in cystic fibrosis. Pediatr Pulmonol 2009, 44:1143-1150.
32. Francis P.W., Muller N.L., Gurwitz D., et al. Hemoglobin desaturation: its occurrence during sleep in patients with cystic fibrosis. Am J Dis Child 1980, 134:734-740.
33. Jankelowitz L., Reid K.J., Wolfe L., et al. Cystic fibrosis patients have poor sleep quality despite normal sleep latency and efficiency. Chest 2005, 127:1593-1599.
34. Dancey R., Tullis D., Heslegrave R., et al. Sleep quality and daytime function in adults with cystic fibrosis and severe lung disease. Eur Respir J 2002, 19:504-510.
35. Zinman R., Corey M., Coates A.L., et al. Nocturnal home oxygen in the treatment of hypoxemic cystic fibrosis patients. JPediatr 1989, 114:368-377.
36. Gozal D. Nocturnal ventilatory support in patients with cystic fibrosis: comparison with supplemental oxygen. Eur Respir J 1997, 10:1999-2003.
37. Regnis J.A., Piper A.J., Henke K.G., et al. Benefits of nocturnal nasal CPAP in patients with cystic fibrosis. Chest 1994, 106:1717-1724.
38. Milross M.A., Piper A.J., Norman M., et al. Night-to-night variability in sleep in cystic fibrosis. Sleep Med 2002, 3:213-219.
39. Versteegh F.G., Bogaard J.M., Raatgever J.W., et al. Relationship between airway obstruction, desaturation during exercise and nocturnal hypoxaemia in cystic fibrosis patients. Eur Respir J 1990, 3:68-73.
40. Coffey M.J., FitzGerald M.X., McNicholas W.T. Comparison of oxygen desaturation during sleep and exercise in patients with cystic fibrosis. Chest 1991, 100:659-662.
41. Montgomery M., Wiebicke W., Bibi H., et al. Home measurement of oxygen saturation during sleep in patients with cystic fibrosis. Pediatr Pulmonol 1989, 7:29-34.
42. Darracott C., McNamara P.S., Pipon M., et al. Towards the development of cumulative overnight oximetry curves for children with cystic fibrosis. JCyst Fibros 2004, 3:S53.
43. Uyan Z.S., Ozdemir N., Ersu R., et al. Factors that correlate with sleep oxygenation in children with cystic fibrosis. Pediatr Pulmonol 2007, 42:716-722.
44. Ryland D., Reid L. The pulmonary circulation in cystic fibrosis. Thorax 1975, 30:285-292.
45. Tabachnik E., Muller N.L., Bryan A.C., et al. Changes in ventilation and chest wall mechanics during sleep in normal adolescents. JAppl Physiol Respir Environ Exerc Physiol 1981, 51:557.
46. Hudgel D.W., Devadatta P. Decrease in functional residual capacity during sleep in normal humans. JAppl Physiol Respir Environ Exerc Physiol 1984, 57:1319-1322.
47. Douglas J., White P., Pickett K., et al. Respiration during sleep in normal man. Thorax 1982, 37:840-844.
48. Ballard R.D., Sutarik J.M., Clover C.W., et al. Effects of non-REM sleep on ventilation and respiratory mechanics in adults with cystic fibrosis. Am J Respir Crit Care Med 1996, 153:266-271.
49. Henderson-Smart D.J., Read D.J. Reduced lung volume during behavioral active sleep in the newborn. JAppl Physiol Respir Environ Exerc Physiol 1979, 46:1081.
50. Milross M.A., Piper A.J., Norman M., et al. Low-flow oxygen and bilevel ventilatory support: effects on ventilation during sleep in cystic fibrosis. Am J Respir Crit Care Med 2001, 163:129-134.
51. Tepper R.S., Skatrud J.B., Dempsey J.A. Ventilation and oxygenation changes during sleep in cystic fibrosis. Chest 1983, 84:388-393.
52. Muller N.L., Francis P.W., Gurwitz D., et al. Mechanism of hemoglobin desaturation during rapid-eye-movement sleep in normal subjects and in patients with cystic fibrosis. Am Rev Respir Dis 1980, 121:463-469.
53. Soni R., Dobbin C.J., Milross M.A., et al. Gas exchange in stable patients with moderate-to-severe lung disease from cystic fibrosis. JCyst Fibros 2008, 7:285-291.
54. Smith D.L., Freeman W., Cayton R.M., et al. Nocturnal hypoxaemia in cystic fibrosis: relationship to pulmonary function tests. Respir Med 1994, 88:537-539.
55. Milross M.A., Piper A.J., Norman M., et al. Predicting sleep-disordered breathing in patients with cystic fibrosis. Chest 2001, 120:1239-1245.
56. Frangolias D.D., Wilcox P.G. Predictability of oxygen desaturation during sleep in patients with cystic fibrosis: clinical, spirometric, and exercise parameters. Chest 2001, 119:434-441.
57. Allen B., Mellon F., Simmonds J., et al. Changes in nocturnal oximetry after treatment of exacerbations in cystic fibrosis. Arch Dis Child 1993, 69:197-201.
58. Paiva R., Krivec U., Aubertin G., et al. Carbon dioxide monitoring during long-term noninvasive respiratory support in children. Intensive Care Med 2009, 35:1068-1074.
59. Pradal U., Braggion C., Mastella G. Transcutaneous blood gas analysis during sleep and exercise in cystic fibrosis. Pediatr Pulmonol 1990, 8:162-167.
60. Dobbin C.J., Milross M.A., Piper A.J., et al. Sequential use of oxygen and bi-level ventilation for respiratory failure in cystic fibrosis. JCyst Fibros 2004, 3:237-242.
61. Hadfield P.J., Rowe-Jones J.M., Mackay I.S. The prevalence of nasal polyps in adults with cystic fibrosis. Clin Otolaryngol Allied Sci 2000, 25:19-22.
62. Eggesbø B., Søvik S., Dølvik S., et al. CT characterization of inflammatory paranasal sinus disease in cystic fibrosis. Acta Radiol 2002, 43:21-28.
63. Franco L.P., Camargos P.A., Becker H.M., et al. Nasal endoscopic evaluation of children and adolescents with cystic fibrosis. Braz J Otorhinolaryngol 2009, 75:806-813.
64. Macdonald K.D., McGinley B.M., Brown D.J., et al. Primary snoring and growth failure in a patient with cystic fibrosis. Respir Care 2009, 54:1727-1731.
65. Hayes D. Obstructive sleep apnea syndrome: a potential cause of lower airway obstruction in cystic fibrosis. Sleep Med 2006, 7:73-75.
66. Ramos R.T., Salles C., Gregório P.B., et al. Evaluation of the upper airway in children and adolescents with cystic fibrosis and obstructive sleep apnea syndrome. Int J Pediatr Otorhinolaryngol 2009, 73:1780-1785.
67. Yankaskas J.R., Marshall B.C., Sufian B., et al. Cystic fibrosis adult care: consensus conference report. Chest 2004, 125:1S-39S.
68. Davidson A., Bossuyt A., Dab I. Acute effects of oxygen, nifedipine, and diltiazem in patients with cystic fibrosis and mild pulmonary hypertension. Pediatr Pulmonol 1989, 6:53-59.
69. Elphick H.E., Mallory G. Oxygen therapy for cystic fibrosis. Cochrane Database Syst Rev 2013, (7). CD003884.
70. Cranston J.M., Crockett A.J., Moss J.R., et al. Domiciliary oxygen for chronic obstructive pulmonary disease. Cochrane Database Syst Rev 2005, (4). CD001744.
71. Balfour-Lynn I.M., Field D.J., Gringras P., et al. BTS guidelines for home oxygen in children. Thorax 2009, 64(Suppl 2):ii1-ii26.
72. Young A.C., Wilson J.W., Kotsimbos T.C., et al. Randomised placebo controlled trial of non-invasive ventilation for hypercapnia in cystic fibrosis. Thorax 2008, 63:72-77.
73. Efrati O., Modan-Moses D., Barak A., et al. Long-term non-invasive positive pressure ventilation among cystic fibrosis patients awaiting lung transplantation. Isr Med Assoc J 2004, 6:527-530.
74. Fauroux B., Burgel P.R., Boelle P.Y., et al. Practice of noninvasive ventilation for cystic fibrosis: a nationwide survey in France. Respir Care 2008, 53:1482-1489.
75. Fauroux B., Pigeot J., Polkey M.I., et al. Invivo physiologic comparison of two ventilators used for domiciliary ventilation in children with cystic fibrosis. Crit Care Med 2001, 29:2097-2105.
76. Fauroux B., Nicot F., Essouri S., et al. Setting of noninvasive pressure support in young patients with cystic fibrosis. Eur Respir J 2004, 24:624-630.
77. Piper A.J., Parker S., Torzillo P.J., et al. Nocturnal nasal IPPV stabilizes patients with cystic fibrosis and hypercapnic respiratory failure. Chest 1992, 102:846-850.
78. Granton J.T., Kesten S. The acute effects of nasal positive pressure ventilation in patients with advanced cystic fibrosis. Chest 1998, 113:1013-1018.
79. Caronia C.G., Silver P., Nimkoff L., et al. Use of bilevel positive airway pressure (BIPAP) in end-stage patients with cystic fibrosis awaiting lung transplantation. Clin Pediatr (Phila) 1998, 37:555-559.
80. Hill A.T., Edenborough F.P., Cayton R.M., et al. Long-term nasal intermittent positive pressure ventilation in patients with cystic fibrosis and hypercapnic respiratory failure (1991-1996). Respir Med 1998, 92:523-526.
81. Serra A., Polese G., Braggion C., et al. Non-invasive proportional assist and pressure support ventilation in patients with cystic fibrosis and chronic respiratory failure. Thorax 2002, 57:50-54.
82. Fauroux B., Le Roux E., Ravilly S., et al. Long-term noninvasive ventilation in patients with cystic fibrosis. Respiration 2008, 76:168-174.