Skip to main content
Erschienen in: Current Pulmonology Reports 3/2020

07.07.2020 | Sleeping and Breathing (A Abreu, Section Editor)

Sleep, Obstructive Sleep Apnea, and Chronic Alveolar Hypoventilation in Cystic Fibrosis: Role of Noninvasive Ventilation During Sleep

verfasst von: Pamela Barletta, Maria Tupayachi Ortiz, Alexandre R. Abreu, Matthias Salathe, Alejandro D. Chediak

Erschienen in: Current Pulmonology Reports | Ausgabe 3/2020

Einloggen, um Zugang zu erhalten

Abstract

Purpose of Review

We describe sleep disturbances in patients with cystic fibrosis emphasizing treatment of abnormal breathing during sleep with noninvasive ventilation.

Recent Findings

Advances in treatment have transformed cystic fibrosis from a pediatric disorder to an adult condition. The increase in cystic fibrosis life expectancy renders these patients at high risk for nocturnal and diurnal respiratory failure. Hypoventilation during sleep precedes diurnal hypoventilation in cystic fibrosis. In advanced cases, noninvasive ventilation improves awake ABGs, respiratory muscle strength, dyspnea, subjective sleep quality, and level of daily activities and attenuates sleep hypoventilation.

Summary

Noninvasive ventilation can ameliorate symptoms and improve gas exchange, particularly in cystic fibrosis with advanced lung dysfunction. There is insufficient literature describing the effect of noninvasive ventilation on survival in cystic fibrosis.
Literatur
1.
Zurück zum Zitat Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science. 1989;245(4922):1066–73.PubMed Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science. 1989;245(4922):1066–73.PubMed
2.
Zurück zum Zitat Elborn JS. Cystic fibrosis. Lancet. 2016;388(10059):2519–31.PubMed Elborn JS. Cystic fibrosis. Lancet. 2016;388(10059):2519–31.PubMed
3.
Zurück zum Zitat O’Sullivan BP, Freedman SD. Cystic fibrosis. Lancet. 2009;373(9678):1891–904.PubMed O’Sullivan BP, Freedman SD. Cystic fibrosis. Lancet. 2009;373(9678):1891–904.PubMed
4.
Zurück zum Zitat Cogen JD, Hall M, Loeffler DR, Gove N, Onchiri F, Sawicki GS, et al. Linkage of the CF Foundation patient registry with the pediatric health information system database. Pediatr Pulmonol. 2019;54(6):721–8.PubMed Cogen JD, Hall M, Loeffler DR, Gove N, Onchiri F, Sawicki GS, et al. Linkage of the CF Foundation patient registry with the pediatric health information system database. Pediatr Pulmonol. 2019;54(6):721–8.PubMed
5.
Zurück zum Zitat Dilokthornsakul P, Patidar M, Campbell JD. Forecasting the long-term clinical and economic outcomes of lumacaftor/ivacaftor in cystic fibrosis patients with homozygous phe508del mutation. Value Health. 2017;20(10):1329–35.PubMed Dilokthornsakul P, Patidar M, Campbell JD. Forecasting the long-term clinical and economic outcomes of lumacaftor/ivacaftor in cystic fibrosis patients with homozygous phe508del mutation. Value Health. 2017;20(10):1329–35.PubMed
6.
Zurück zum Zitat Shakkottai A, O’Brien LM, Nasr SZ, Chervin RD. Sleep disturbances and their impact in pediatric cystic fibrosis. Sleep Med Rev. 2018;42:100–10.PubMedPubMedCentral Shakkottai A, O’Brien LM, Nasr SZ, Chervin RD. Sleep disturbances and their impact in pediatric cystic fibrosis. Sleep Med Rev. 2018;42:100–10.PubMedPubMedCentral
7.
Zurück zum Zitat Stephenson AL, Bell SC. The Cystic Fibrosis Foundation patient registry. Design and methods of a national observational disease registry. Ann Am Thorac Soc. 2016;13(7):1014–5.PubMed Stephenson AL, Bell SC. The Cystic Fibrosis Foundation patient registry. Design and methods of a national observational disease registry. Ann Am Thorac Soc. 2016;13(7):1014–5.PubMed
8.
Zurück zum Zitat Hodson ME, Madden BP, Steven MH, Tsang VT, Yacoub MH. Non-invasive mechanical ventilation for cystic fibrosis patients--a potential bridge to transplantation. Eur Respir J. 1991;4(5):524–7.PubMed Hodson ME, Madden BP, Steven MH, Tsang VT, Yacoub MH. Non-invasive mechanical ventilation for cystic fibrosis patients--a potential bridge to transplantation. Eur Respir J. 1991;4(5):524–7.PubMed
9.
Zurück zum Zitat Regnis JA, Piper AJ, Henke KG, Parker S, Bye PT, Sullivan CE. Benefits of nocturnal nasal CPAP in patients with cystic fibrosis. Chest. 1994;106(6):1717–24.PubMed Regnis JA, Piper AJ, Henke KG, Parker S, Bye PT, Sullivan CE. Benefits of nocturnal nasal CPAP in patients with cystic fibrosis. Chest. 1994;106(6):1717–24.PubMed
10.
Zurück zum Zitat Holland AE, Denehy L, Ntoumenopoulos G, Naughton MT, Wilson JW. Non-invasive ventilation assists chest physiotherapy in adults with acute exacerbations of cystic fibrosis. Thorax. 2003;58(10):880–4.PubMedPubMedCentral Holland AE, Denehy L, Ntoumenopoulos G, Naughton MT, Wilson JW. Non-invasive ventilation assists chest physiotherapy in adults with acute exacerbations of cystic fibrosis. Thorax. 2003;58(10):880–4.PubMedPubMedCentral
11.
Zurück zum Zitat Milross MA, Piper AJ, Norman M, Becker HF, Willson GN, Grunstein RR, 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(1):129–34.PubMed Milross MA, Piper AJ, Norman M, Becker HF, Willson GN, Grunstein RR, 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(1):129–34.PubMed
12.
Zurück zum Zitat Young AC, Wilson JW, Kotsimbos TC, Naughton MT. Randomised placebo controlled trial of non-invasive ventilation for hypercapnia in cystic fibrosis. Thorax. 2008;63(1):72–7.PubMed Young AC, Wilson JW, Kotsimbos TC, Naughton MT. Randomised placebo controlled trial of non-invasive ventilation for hypercapnia in cystic fibrosis. Thorax. 2008;63(1):72–7.PubMed
13.
Zurück zum Zitat Naqvi SK, Sotelo C, Murry L, Simakajornboon N. Sleep architecture in children and adolescents with cystic fibrosis and the association with severity of lung disease. Sleep Breath. 2008;12(1):77–83.PubMed Naqvi SK, Sotelo C, Murry L, Simakajornboon N. Sleep architecture in children and adolescents with cystic fibrosis and the association with severity of lung disease. Sleep Breath. 2008;12(1):77–83.PubMed
14.
Zurück zum Zitat Katz ES. Cystic fibrosis and sleep. Clin Chest Med. 2014;35(3):495–504.PubMed Katz ES. Cystic fibrosis and sleep. Clin Chest Med. 2014;35(3):495–504.PubMed
15.
Zurück zum Zitat Shwachman H, Kulczycki LL, Mueller HL, Flake CG. Nasal polyposis in patients with cystic fibrosis. Pediatrics. 1962;30:389–401.PubMed Shwachman H, Kulczycki LL, Mueller HL, Flake CG. Nasal polyposis in patients with cystic fibrosis. Pediatrics. 1962;30:389–401.PubMed
16.
Zurück zum Zitat Bercovitch RS, Tsai SC. Respiratory medications and sleep. Current Respiratory Care Reports. 2012;1(2):123–30. Bercovitch RS, Tsai SC. Respiratory medications and sleep. Current Respiratory Care Reports. 2012;1(2):123–30.
17.
Zurück zum Zitat Stokes DC, McBride JT, Wall MA, Erba G, Strieder DJ. Sleep hypoxemia in young adults with cystic fibrosis. Am J Dis Child. 1980;134(8):741–3.PubMed Stokes DC, McBride JT, Wall MA, Erba G, Strieder DJ. Sleep hypoxemia in young adults with cystic fibrosis. Am J Dis Child. 1980;134(8):741–3.PubMed
18.
Zurück zum Zitat Bradley S, Solin P, Wilson J, Johns D, Walters EH, Naughton MT. Hypoxemia and hypercapnia during exercise and sleep in patients with cystic fibrosis. Chest. 1999;116(3):647–54.PubMed Bradley S, Solin P, Wilson J, Johns D, Walters EH, Naughton MT. Hypoxemia and hypercapnia during exercise and sleep in patients with cystic fibrosis. Chest. 1999;116(3):647–54.PubMed
19.
Zurück zum Zitat Paranjape SM, McGinley BM, Braun AT, Schneider H. Polysomnographic markers in children with cystic fibrosis lung disease. Pediatrics. 2015;136(5):920–6.PubMedPubMedCentral Paranjape SM, McGinley BM, Braun AT, Schneider H. Polysomnographic markers in children with cystic fibrosis lung disease. Pediatrics. 2015;136(5):920–6.PubMedPubMedCentral
20.
Zurück zum Zitat Fauroux B, Pepin JL, Boelle PY, Cracowski C, Murris-Espin M, Nove-Josserand R, et al. Sleep quality and nocturnal hypoxaemia and hypercapnia in children and young adults with cystic fibrosis. Arch Dis Child. 2012;97(11):960–6.PubMed Fauroux B, Pepin JL, Boelle PY, Cracowski C, Murris-Espin M, Nove-Josserand R, et al. Sleep quality and nocturnal hypoxaemia and hypercapnia in children and young adults with cystic fibrosis. Arch Dis Child. 2012;97(11):960–6.PubMed
21.
Zurück zum Zitat Spier S, Rivlin J, Hughes D, Levison H. The effect of oxygen on sleep, blood gases, and ventilation in cystic fibrosis. Am Rev Respir Dis. 1984;129(5):712–8.PubMed Spier S, Rivlin J, Hughes D, Levison H. The effect of oxygen on sleep, blood gases, and ventilation in cystic fibrosis. Am Rev Respir Dis. 1984;129(5):712–8.PubMed
22.
Zurück zum Zitat Dancey DR, Tullis ED, Heslegrave R, Thornley K, Hanly PJ. Sleep quality and daytime function in adults with cystic fibrosis and severe lung disease. Eur Respir J. 2002;19(3):504–10.PubMed Dancey DR, Tullis ED, Heslegrave R, Thornley K, Hanly PJ. Sleep quality and daytime function in adults with cystic fibrosis and severe lung disease. Eur Respir J. 2002;19(3):504–10.PubMed
23.
Zurück zum Zitat Jankelowitz L, Reid KJ, Wolfe L, Cullina J, Zee PC, Jain M. Cystic fibrosis patients have poor sleep quality despite normal sleep latency and efficiency. Chest. 2005;127(5):1593–9.PubMed Jankelowitz L, Reid KJ, Wolfe L, Cullina J, Zee PC, Jain M. Cystic fibrosis patients have poor sleep quality despite normal sleep latency and efficiency. Chest. 2005;127(5):1593–9.PubMed
24.
Zurück zum Zitat Amin R, Bean J, Burklow K, Jeffries J. The relationship between sleep disturbance and pulmonary function in stable pediatric cystic fibrosis patients. Chest. 2005;128(3):1357–63.PubMed Amin R, Bean J, Burklow K, Jeffries J. The relationship between sleep disturbance and pulmonary function in stable pediatric cystic fibrosis patients. Chest. 2005;128(3):1357–63.PubMed
25.
Zurück zum Zitat Vandeleur M, Walter LM, Armstrong DS, Robinson P, Nixon GM, Horne RSC. How well do children with cystic fibrosis sleep? An actigraphic and questionnaire-based study. J Pediatr. 2017;182:170–6.PubMed Vandeleur M, Walter LM, Armstrong DS, Robinson P, Nixon GM, Horne RSC. How well do children with cystic fibrosis sleep? An actigraphic and questionnaire-based study. J Pediatr. 2017;182:170–6.PubMed
26.
Zurück zum Zitat Milross MA, Piper AJ, Dobbin CJ, Bye PT, Grunstein RR. Sleep disordered breathing in cystic fibrosis. Sleep Med Rev. 2004;8(4):295–308.PubMed Milross MA, Piper AJ, Dobbin CJ, Bye PT, Grunstein RR. Sleep disordered breathing in cystic fibrosis. Sleep Med Rev. 2004;8(4):295–308.PubMed
27.
Zurück zum Zitat Douglas NJ, White DP, Pickett CK, Weil JV, Zwillich CW. Respiration during sleep in normal man. Thorax. 1982;37(11):840–4.PubMedPubMedCentral Douglas NJ, White DP, Pickett CK, Weil JV, Zwillich CW. Respiration during sleep in normal man. Thorax. 1982;37(11):840–4.PubMedPubMedCentral
28.
Zurück zum Zitat Worsnop C, Kay A, Kim Y, Trinder J, Pierce R. Effect of age on sleep onset-related changes in respiratory pump and upper airway muscle function. J Appl Physiol (1985). 2000;88(5):1831–9. Worsnop C, Kay A, Kim Y, Trinder J, Pierce R. Effect of age on sleep onset-related changes in respiratory pump and upper airway muscle function. J Appl Physiol (1985). 2000;88(5):1831–9.
29.
Zurück zum Zitat Bristow JD, Honour AJ, Pickering TG, Sleight P. Cardiovascular and respiratory changes during sleep in normal and hypertensive subjects. Cardiovasc Res. 1969;3(4):476–85.PubMed Bristow JD, Honour AJ, Pickering TG, Sleight P. Cardiovascular and respiratory changes during sleep in normal and hypertensive subjects. Cardiovasc Res. 1969;3(4):476–85.PubMed
30.
Zurück zum Zitat Gothe B, Altose MD, Goldman MD, Cherniack NS. Effect of quiet sleep on resting and CO2-stimulated breathing in humans. J Appl Physiol Respir Environ Exerc Physiol. 1981;50(4):724–30.PubMed Gothe B, Altose MD, Goldman MD, Cherniack NS. Effect of quiet sleep on resting and CO2-stimulated breathing in humans. J Appl Physiol Respir Environ Exerc Physiol. 1981;50(4):724–30.PubMed
31.
Zurück zum Zitat Tepper RS, Skatrud JB, Dempsey JA. Ventilation and oxygenation changes during sleep in cystic fibrosis. Chest. 1983;84(4):388–93.PubMed Tepper RS, Skatrud JB, Dempsey JA. Ventilation and oxygenation changes during sleep in cystic fibrosis. Chest. 1983;84(4):388–93.PubMed
32.
Zurück zum Zitat Muller NL, Francis PW, Gurwitz D, Levison H, Bryan AC. Mechanism of hemoglobin desaturation during rapid-eye-movement sleep in normal subjects and in patients with cystic fibrosis. Am Rev Respir Dis. 1980;121(3):463–9.PubMed Muller NL, Francis PW, Gurwitz D, Levison H, Bryan AC. Mechanism of hemoglobin desaturation during rapid-eye-movement sleep in normal subjects and in patients with cystic fibrosis. Am Rev Respir Dis. 1980;121(3):463–9.PubMed
33.
Zurück zum Zitat Lwin N, Giammona ST. Ventilatory responses to inspired CO 2 in patients with cystic fibrosis. Chest. 1972;61(3):206–12.PubMed Lwin N, Giammona ST. Ventilatory responses to inspired CO 2 in patients with cystic fibrosis. Chest. 1972;61(3):206–12.PubMed
34.
Zurück zum Zitat Paiva R, Krivec U, Aubertin G, Cohen E, Clement A, Fauroux B. Carbon dioxide monitoring during long-term noninvasive respiratory support in children. Intensive Care Med. 2009;35(6):1068–74.PubMed Paiva R, Krivec U, Aubertin G, Cohen E, Clement A, Fauroux B. Carbon dioxide monitoring during long-term noninvasive respiratory support in children. Intensive Care Med. 2009;35(6):1068–74.PubMed
35.
Zurück zum Zitat Francis PW, Muller NL, Gurwitz D, Milligan DW, Levison H, Bryan AC. Hemoglobin desaturation: its occurrence during sleep in patients with cystic fibrosis. Am J Dis Child. 1980;134(8):734–40.PubMed Francis PW, Muller NL, Gurwitz D, Milligan DW, Levison H, Bryan AC. Hemoglobin desaturation: its occurrence during sleep in patients with cystic fibrosis. Am J Dis Child. 1980;134(8):734–40.PubMed
36.
Zurück zum Zitat Coffey MJ, FitzGerald MX, McNicholas WT. Comparison of oxygen desaturation during sleep and exercise in patients with cystic fibrosis. Chest. 1991;100(3):659–62.PubMed Coffey MJ, FitzGerald MX, McNicholas WT. Comparison of oxygen desaturation during sleep and exercise in patients with cystic fibrosis. Chest. 1991;100(3):659–62.PubMed
37.
Zurück zum Zitat McEvoy RD, Pierce RJ, Hillman D, Esterman A, Ellis EE, Catcheside PG, et al. Nocturnal non-invasive nasal ventilation in stable hypercapnic COPD: a randomised controlled trial. Thorax. 2009;64(7):561–6.PubMed McEvoy RD, Pierce RJ, Hillman D, Esterman A, Ellis EE, Catcheside PG, et al. Nocturnal non-invasive nasal ventilation in stable hypercapnic COPD: a randomised controlled trial. Thorax. 2009;64(7):561–6.PubMed
38.
Zurück zum Zitat Spicuzza L, Sciuto C, Leonardi S, La Rosa M. Early occurrence of obstructive sleep apnea in infants and children with cystic fibrosis. Arch Pediatr Adolesc Med. 2012;166(12):1165–9.PubMed Spicuzza L, Sciuto C, Leonardi S, La Rosa M. Early occurrence of obstructive sleep apnea in infants and children with cystic fibrosis. Arch Pediatr Adolesc Med. 2012;166(12):1165–9.PubMed
39.
Zurück zum Zitat Chervin RD, Hedger K, Dillon JE, Pituch KJ. Pediatric Sleep Questionnaire (PSQ): validity and reliability of scales for sleep-disordered breathing, snoring, sleepiness, and behavioral problems. Sleep Med. 2000;1(1):21–32.PubMed Chervin RD, Hedger K, Dillon JE, Pituch KJ. Pediatric Sleep Questionnaire (PSQ): validity and reliability of scales for sleep-disordered breathing, snoring, sleepiness, and behavioral problems. Sleep Med. 2000;1(1):21–32.PubMed
40.
Zurück zum Zitat Nagappa M, Liao P, Wong J, Auckley D, Ramachandran SK, Memtsoudis S, et al. Validation of the STOP-Bang Questionnaire as a screening tool for obstructive sleep apnea among different populations: a systematic review and meta-analysis. PLoS One. 2015;10(12):e0143697.PubMedPubMedCentral Nagappa M, Liao P, Wong J, Auckley D, Ramachandran SK, Memtsoudis S, et al. Validation of the STOP-Bang Questionnaire as a screening tool for obstructive sleep apnea among different populations: a systematic review and meta-analysis. PLoS One. 2015;10(12):e0143697.PubMedPubMedCentral
41.
Zurück zum Zitat Medarov BI, Victorson DE, Judson MA. Patient-reported outcome measures for sleep disorders and related problems: clinical and research applications. Chest. 2013;143(6):1809–18.PubMed Medarov BI, Victorson DE, Judson MA. Patient-reported outcome measures for sleep disorders and related problems: clinical and research applications. Chest. 2013;143(6):1809–18.PubMed
42.
Zurück zum Zitat Clinical indications for noninvasive positive pressure ventilation in chronic respiratory failure due to restrictive lung disease, COPD, and nocturnal hypoventilation--a consensus conference report. Chest. 1999;116(2):521–34. Clinical indications for noninvasive positive pressure ventilation in chronic respiratory failure due to restrictive lung disease, COPD, and nocturnal hypoventilation--a consensus conference report. Chest. 1999;116(2):521–34.
43.
Zurück zum Zitat Mehta S, Hill NS. Noninvasive ventilation. Am J Respir Crit Care Med. 2001;163(2):540–77.PubMed Mehta S, Hill NS. Noninvasive ventilation. Am J Respir Crit Care Med. 2001;163(2):540–77.PubMed
44.
Zurück zum Zitat Simonds AK. Home ventilation. Eur Respir J Suppl. 2003;47:38 s–46 s. Simonds AK. Home ventilation. Eur Respir J Suppl. 2003;47:38 s–46 s.
45.
Zurück zum Zitat Brochard L, Mancebo J, Wysocki M, Lofaso F, Conti G, Rauss A, et al. Noninvasive ventilation for acute exacerbations of chronic obstructive pulmonary disease. N Engl J Med. 1995;333(13):817–22.PubMed Brochard L, Mancebo J, Wysocki M, Lofaso F, Conti G, Rauss A, et al. Noninvasive ventilation for acute exacerbations of chronic obstructive pulmonary disease. N Engl J Med. 1995;333(13):817–22.PubMed
46.
Zurück zum Zitat Kohnlein T, Windisch W, Kohler D, Drabik A, Geiseler J, Hartl S, et al. Non-invasive positive pressure ventilation for the treatment of severe stable chronic obstructive pulmonary disease: a prospective, multicentre, randomised, controlled clinical trial. Lancet Respir Med. 2014;2(9):698–705.PubMed Kohnlein T, Windisch W, Kohler D, Drabik A, Geiseler J, Hartl S, et al. Non-invasive positive pressure ventilation for the treatment of severe stable chronic obstructive pulmonary disease: a prospective, multicentre, randomised, controlled clinical trial. Lancet Respir Med. 2014;2(9):698–705.PubMed
47.
Zurück zum Zitat • Murphy PB, Rehal S, Arbane G, Bourke S, PMA C, Crook AM, et al. Effect of home noninvasive ventilation with oxygen therapy vs oxygen therapy alone on hospital readmission or death after an acute COPD exacerbation: a randomized clinical trial. JAMA. 2017;317(21):2177–86 Suggests that the use of NIV in patients with COPD with diurnal hypoventilation can also be used in patients with CF and diurnal hypoventilation and have the same therapeutic benefits.PubMedPubMedCentral • Murphy PB, Rehal S, Arbane G, Bourke S, PMA C, Crook AM, et al. Effect of home noninvasive ventilation with oxygen therapy vs oxygen therapy alone on hospital readmission or death after an acute COPD exacerbation: a randomized clinical trial. JAMA. 2017;317(21):2177–86 Suggests that the use of NIV in patients with COPD with diurnal hypoventilation can also be used in patients with CF and diurnal hypoventilation and have the same therapeutic benefits.PubMedPubMedCentral
48.
Zurück zum Zitat Bright-Thomas RJ, Johnson SC. What is the role of noninvasive ventilation in cystic fibrosis? Curr Opin Pulm Med. 2014;20(6):618–22.PubMed Bright-Thomas RJ, Johnson SC. What is the role of noninvasive ventilation in cystic fibrosis? Curr Opin Pulm Med. 2014;20(6):618–22.PubMed
49.
Zurück zum Zitat Gozal D. Nocturnal ventilatory support in patients with cystic fibrosis: comparison with supplemental oxygen. Eur Respir J. 1997;10(9):1999–2003.PubMed Gozal D. Nocturnal ventilatory support in patients with cystic fibrosis: comparison with supplemental oxygen. Eur Respir J. 1997;10(9):1999–2003.PubMed
50.
Zurück zum Zitat Andrade RG, Madeiro F, Piccin VS, Moriya HT, Schorr F, Sardinha PS, et al. Impact of acute changes in CPAP flow route in sleep apnea treatment. Chest. 2016;150(6):1194–201.PubMed Andrade RG, Madeiro F, Piccin VS, Moriya HT, Schorr F, Sardinha PS, et al. Impact of acute changes in CPAP flow route in sleep apnea treatment. Chest. 2016;150(6):1194–201.PubMed
51.
Zurück zum Zitat Andrade RGS, Viana FM, Nascimento JA, Drager LF, Moffa A, Brunoni AR, et al. Nasal vs oronasal CPAP for OSA treatment: a meta-analysis. Chest. 2018;153(3):665–74.PubMed Andrade RGS, Viana FM, Nascimento JA, Drager LF, Moffa A, Brunoni AR, et al. Nasal vs oronasal CPAP for OSA treatment: a meta-analysis. Chest. 2018;153(3):665–74.PubMed
52.
Zurück zum Zitat Nava S, Navalesi P, Gregoretti C. Interfaces and humidification for noninvasive mechanical ventilation. Respir Care. 2009;54(1):71–84.PubMed Nava S, Navalesi P, Gregoretti C. Interfaces and humidification for noninvasive mechanical ventilation. Respir Care. 2009;54(1):71–84.PubMed
53.
Zurück zum Zitat Navalesi P, Fanfulla F, Frigerio P, Gregoretti C, Nava S. Physiologic evaluation of noninvasive mechanical ventilation delivered with three types of masks in patients with chronic hypercapnic respiratory failure. Crit Care Med. 2000;28(6):1785–90.PubMed Navalesi P, Fanfulla F, Frigerio P, Gregoretti C, Nava S. Physiologic evaluation of noninvasive mechanical ventilation delivered with three types of masks in patients with chronic hypercapnic respiratory failure. Crit Care Med. 2000;28(6):1785–90.PubMed
54.
Zurück zum Zitat Hart N, Polkey MI, Clement A, Boule M, Moxham J, Lofaso F, et al. Changes in pulmonary mechanics with increasing disease severity in children and young adults with cystic fibrosis. Am J Respir Crit Care Med. 2002;166(1):61–6.PubMed Hart N, Polkey MI, Clement A, Boule M, Moxham J, Lofaso F, et al. Changes in pulmonary mechanics with increasing disease severity in children and young adults with cystic fibrosis. Am J Respir Crit Care Med. 2002;166(1):61–6.PubMed
55.
Zurück zum Zitat •• Moran F, Bradley JM, Piper AJ. Non-invasive ventilation for cystic fibrosis. Cochrane Database Syst Rev. 2017;2:CD002769 The Cochrane analysis provides a thorough description of how nocturnal NIV used together with overnight oxygen improves gas exchange during sleep to a greater extent than oxygen therapy alone in patients with CF.PubMed •• Moran F, Bradley JM, Piper AJ. Non-invasive ventilation for cystic fibrosis. Cochrane Database Syst Rev. 2017;2:CD002769 The Cochrane analysis provides a thorough description of how nocturnal NIV used together with overnight oxygen improves gas exchange during sleep to a greater extent than oxygen therapy alone in patients with CF.PubMed
Metadaten
Titel
Sleep, Obstructive Sleep Apnea, and Chronic Alveolar Hypoventilation in Cystic Fibrosis: Role of Noninvasive Ventilation During Sleep
verfasst von
Pamela Barletta
Maria Tupayachi Ortiz
Alexandre R. Abreu
Matthias Salathe
Alejandro D. Chediak
Publikationsdatum
07.07.2020
Verlag
Springer US
Erschienen in
Current Pulmonology Reports / Ausgabe 3/2020
Elektronische ISSN: 2199-2428
DOI
https://doi.org/10.1007/s13665-020-00252-0

Weitere Artikel der Ausgabe 3/2020

Current Pulmonology Reports 3/2020 Zur Ausgabe

Pulmonary Radiology (M Stephens and S Kapur, Section Editors)

Current Applications for Nuclear Medicine Imaging in Pulmonary Disease

Sleeping and Breathing (A Abreu, Section Editor)

Management of Insomnia in Chronic Lung Diseases

Sleeping and Breathing (A Abreu, Section Editor)

Cannabinoids and Sleep: Helpful or Harmful?

Environmental and Occupational Health (S Cherian, Section Editor)

Imaging in Occupational and Environmental Lung Disease

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.