The CF-ABLE Score

Chest - Tập 143 - Trang 1358-1364 - 2013
Cormac McCarthy1,2, Borislav D. Dimitrov3,4, Imran J. Meurling1,2, Cedric Gunaratnam1,2, Noel G. McElvaney1,2
1Respiratory Research Division, Royal College of Surgeons in Ireland, Dublin, Ireland
2Department of Respiratory Medicine, Beaumont Hospital, Dublin, Ireland
3Department of Medicine, and Department of General Practice, Royal College of Surgeons in Ireland, Dublin, Ireland
4Academic Unit of Primary Care and Population Sciences, University of Southampton, Southampton, England

Tài liệu tham khảo

Ramsey, 1996, Management of pulmonary disease in patients with cystic fibrosis [published correction in N Engl J Med. 1996;335(15):1167], N Engl J Med, 335, 179, 10.1056/NEJM199607183350307 Corey, 1997, Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis, J Pediatr, 131, 809, 10.1016/S0022-3476(97)70025-8 Rosenbluth, 2004, Lung function decline in cystic fibrosis patients and timing for lung transplantation referral, Chest, 126, 412, 10.1378/chest.126.2.412 Amadori, 2009, Recurrent exacerbations affect FEV(1) decline in adult patients with cystic fibrosis, Respir Med, 103, 407, 10.1016/j.rmed.2008.09.024 Sanders, 2011, Pulmonary exacerbations are associated with subsequent FEV1 decline in both adults and children with cystic fibrosis, Pediatr Pulmonol, 46, 393, 10.1002/ppul.21374 Kerem, 1992, Prediction of mortality in patients with cystic fibrosis, N Engl J Med, 326, 1187, 10.1056/NEJM199204303261804 VanDevanter, 2010, Pulmonary outcome prediction (POP) tools for cystic fibrosis patients, Pediatr Pulmonol, 45, 1156, 10.1002/ppul.21311 Liou, 2001, Predictive 5-year survivorship model of cystic fibrosis, Am J Epidemiol, 153, 345, 10.1093/aje/153.4.345 Taussig, 1973, A new prognostic score and clinical evaluation system for cystic fibrosis, J Pediatr, 82, 380, 10.1016/S0022-3476(73)80110-6 Hafen, 2006, Clinical scoring systems in cystic fibrosis, Pediatr Pulmonol, 41, 602, 10.1002/ppul.20376 Fogarty, 2012, Are measures of body habitus associated with mortality in cystic fibrosis?, Chest, 142, 712, 10.1378/chest.11-2124 Courtney, 2007, Predictors of mortality in adults with cystic fibrosis, Ped Pulmonol, 42, 525, 10.1002/ppul.20619 Milla, 1998, Risk of death in cystic fibrosis patients with severely compromised lung function, Chest, 113, 1230, 10.1378/chest.113.5.1230 Mayer-Hamblett, 2002, Developing cystic fibrosis lung transplant referral criteria using predictors of 2-year mortality, Am J Respir Crit Care Med, 166, 1550, 10.1164/rccm.200202-087OC Konstan, 2007, Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis, J Pediatr, 151, 134, 10.1016/j.jpeds.2007.03.006 Waters, 2012, Effect of pulmonary exacerbations on long-term lung function decline in cystic fibrosis, Eur Respir J, 40, 61, 10.1183/09031936.00159111 de Boer, 2011, Exacerbation frequency and clinical outcomes in adult patients with cystic fibrosis, Thorax, 66, 680, 10.1136/thx.2011.161117 Shwachman, 1958, Long-term study of one hundred five patients with cystic fibrosis; studies made over a five- to fourteen-year period, AMA J Dis Child, 96, 6, 10.1001/archpedi.1958.02060060008002 Doershuk, 1964, A 5 year clinical evaluation of a therapeutic program for patients with cystic fibrosis, J Pediatr, 65, 677, 10.1016/S0022-3476(64)80152-9 Cooperman, 1971, A simplified cystic fibrosis scoring system (a preliminary report), Can Med Assoc J, 105, 580