Anaerobic bacteria in cystic fibrosis: pathogens or harmless commensals?

نویسنده

  • Andrew M Jones
چکیده

2004;27:453e8. 9. Hillman DR, Murphy AS, Pezzullo L. The Economic Cost of Sleep Disorders. Sleep 2006;29:299e305. 10. Mar J, Rueda JR, Durán-Cantolla J, et al. The costeffectiveness of nCPAP treatment in patients with moderate-to-severe obstructive sleep apnoea. Eur Respir J 2003;21:515e22. 11. Tan MC, Ayas NT, Mulgrew A, et al. Costeffectiveness of continuous positive airway pressure therapy in patients with obstructive sleep apneahypopnea in British Columbia. Can Respir J 2008;15:159e65. 12. Guest JF, Helter MT, Morga A, et al. Costeffectiveness of using continuous positive airway pressure in the treatment of severe obstructive sleep apnoea/hypopnoea syndrome in the UK. Thorax 2008;63:860e5. 13. Kapur VK, Alfonso-Cristancho R. Just a good deal or truly a steal? Medical cost savings and the impact on the cost-effectiveness of treating sleep apnea. Sleep 2009;32:135e6. 14. Groot W, van den Brink HM. The value of health. BMC Health Serv Res 2008;8:136. 15. McDaid C, Griffin S, Weatherly H, et al. Continuous positive airway pressure devices for the treatment of obstructive sleep apnoea-hypopnoea syndrome: a systematic review and economic analysis. Health Technol Assess 2009;13:iiieiv, xi-xiv, 1e119, 143e274. 16. Ayas NT, Fox J, Epstein L, et al. Initial use of portable monitoring versus polysomnography to confirm obstructive sleep apnea in symptomatic patients: an economic decision model. Sleep Med 2010;11:320e4. 17. Hedner J, Grote L, Lavie P, et al. The European Sleep Apnea Database (ESADA)ddesign and first interim cross-sectional description of results from 22 European sleep laboratories. Am J Respir Crit Care Med 2010;181:A6857.

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عنوان ژورنال:
  • Thorax

دوره 66 7  شماره 

صفحات  -

تاریخ انتشار 2011