Publications

Barker, D.H., & Quittner, A.L. (2010). A biopsychosocial model of CF: Social and emotional functioning, adherence and quality of life. In J. Allen, H. Panitch & R. Rubenstein (Eds.) Lung Biology in Health and Disease Series: Cystic Fibrosis (pp. 468-481). New York: Informa Healthcare. [Abstract]

Cruz, I., & Quittner, A.L. (2009). Utilizing health-related quality of life measures in children with respiratory conditions. In: C. Langston, B.B. Rogers, J.E. Dimmick, & D.B. Singer (Eds). Perspectives in Pediatric Pathology, Vol 27 (pp. 266-284). Wisconsin: Society for Pediatric Pathology. [Abstract]

Olveira, G., Olveira, C., Gaspar, I., Cruz, I., Dorado, A., Pérez-Ruiz, E., Porras, N., Soriguer, F. (2010). Validation of the Spanish version of the Revised Cystic Fibrosis Quality of Life Questionnaire in adolescents and adults (CFQR 14+ Spain). Arch Bronconeumol, 46(4), 165-75 [Abstract] [Full Article]

Goss, C.H. & Quittner, A.L. (2007). Patient-reported outcomes in cystic fibrosis. Proceedings of the American Thoracic Society, 4, 378-386. [Abstract]

Havermans, T., Vreys, M., Proesmans, V., & De Boeck. (2005). Assessment of agreement between parents and children on health-related quality of life in children with cystic fibrosis. Child: Care, Health & Development, 32(1), 1-7.[Abstract]

Henry, B., Aussage, P., Grosskopf, C., & Goehrs, J-M. (2003). Development of the Cystic Fibrosis Questionnaire (CFQ) for assessing quality of life in pediatric adult patients. Quality of Life Research, 12, 63-76.[Abstract]

Klijn, P.H., van Stel, H.F., Quittner, A.L., van der Net, J., Doeleman, W., van der Schans, C.P., & van der Ent, C.K. (2004). Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults. Journal of Cystic Fibrosis, 3, 29-36. [Abstract] [Full Article]

McCoy, K.S., Quittner, A.L., Oermann, C.M., Gibson, R.L., Retsch-Bogart, G.Z., & Montgomery, A.B. (2008). Inhaled aztreonam lysine for chronic airway pseudomonas aeruginosa in Cystic Fibrosis American Journal of Respiratory Critical Care Medicine, 178, 921 - 928. [Abstract]

Modi, A. C. & Quittner, A.L. (2003). Validation of a disease-specific measure of health-related quality of life for children with cystic fibrosis. Journal of Pediatric Psychology, 28, 535-546. [Abstract]

Oerman, C.M., Retsch-Bogart, G.Z., Quittner, A.L., Gibson, R.L., McCoy, K.S., Montgomery, A.B., & Cooper, P.J. (2010). An 18-month study of the safety and efficacy of repeated courses of inhaled Aztreonam Lysine in cystic fibrosis. Pediatric Pulmonology, 45(11), 1121-34. [Abstract]

Palermo, T.M., Long, A.C., Lewandowski, A.S., Drotar, D., Quittner, A.L., & Walker, L.S. (2008). Evidenced-based assessment of health-related quality of life and functional impairment in pediatric psychology. Journal of Pediatric Psychology, 33, 983-996. [Abstract]

Quittner, A.L (1998). Measurement of quality of life in cystic fibrosis. Current Opinion in Pulmonary Medicine, 4, 326-331. [Abstract] [Full Article]

Quittner, A.L., Alpern, A., Kimberg, C.I. (In Press). Integrating patient-reported outcomes into research and clinical practice. In R.W. Wilmott, A. Bush, F. Ratjen, R. Deterding, & T. Boat (Eds.) Disorders of the Respiratory Track in Children, 8th Edition. Oxford, UK: Elsevier Inc.

Quittner, A.L., Barker, D.H., Blackwell, L.S., Romero, S.L., & Woo, M.S. (2009). The importance of measuring health-related quality of life in lung transplantation for cystic fibrosis. Proceedings of the American Thoracic Society, 6, 619-633. [Abstract]

Quittner, A.L., Buu, A., Messer, M.A., Modi A.C., & Watrous, M. (2005). Development and Validation of the Cystic Fibrosis Questionnaire (CFQ) in the United States: A health-related quality of life measure for cystic fibrosis. Chest, 128, 2347-2354. [Abstract]

Quittner, A.L., Cruz, I., Modi, A.C., & Marciel, K.K. (2009). Health-related quality of life instruments for adolescents with chronic diseases. In W. O'Donohue, & L.Tolle (Eds). Behavioral Approaches to Chronic Disease in Adolescence: A Guide to Integrative Care (pp. 311-327). New York: Springer Publishing Co. [Abstract]

Quittner, A.L., Modi, A.C., & Cruz, I. (2008). Systematic review of health-related quality of life measures for children with respiratory conditions. Pediatric Respiratory Reviews, 9, 220-232. [Abstract]

Quittner, A.L., Modi, A.C., Wainwright, C., Otto, K., Kirihara, J., Montgomery, A.B. (2009). Determination of minimal clinically important difference scores for the Cystic Fibrosis Questionnaire-Revised respiratory symptom scale in two populations of patients with Cystic Fibrosis and chronic Pseudomonas aeruginosa airway infection. Chest, 135; 1610-1618. [Abstract]

Quittner, A.L, Sweeny, S., Watrous, M., Munzenberger, P., Bearss, K., Gibson Nitza, A., Fisher, L., & Henry, B. (2000). Translation and linguistic validation of a disease-specific quality of life measure for cystic fibrosis. Journal of Pediatric Psychology, 25, 403-414. [Abstract]

Quittner, A.L., Schechter, M. Rasouliyan, L., Haselkorn, T., Pasta, D., & Wagener, J. (in press). Impact of socioeconomic status, race, and ethnicity on quality of life in patients with cystic fibrosis in the United States. Chest.

Retsch-Bogart, G.Z., Quittner, A.L., Gibson, R.L., Oermann, C.M., McCoy, K.S., Montgomery, A.B., & Cooper, P.J. (2009). Efficacy and safety of inhaled aztreonam lysine for airway pseudomonas in cystic fibrosis. Chest, 135(5), 1223-1232. [Abstract]

Rozov, T., Cunha, M.T., Nasciemento, O., Quittner, A.L., Jardim, J.R. (2006). Linguistic validation of cystic fibrosis quality of life questionnaires. Journal of Pediatrics (Rio J), 82, 151-156. [Abstract]

Sawicki, G.S., Rasouliyan, L.R., McMullen, A.H., Wagener, J.S., McColley, S.A., Pasta, D.J., & Quittner, A.L. (2011). Longitudinal assessment of health-related quality of life in an observational cohort of patients with cystic fibrosis. Pediatric Pulmonology, 46, 36-44. [Abstract]

Wainwright, C.., Quittner, A.L., Geller, D.E., Nakamura, C,. Wooldridge, J.L., Gibson, R.L., & Montgomery, A.B. (2011). Aztreonam for inhalation solution (AZLI) in patients with cystic fibrosis, mild lung impairment, and P. aeruginosa. Journal of Cystic Fibrosis, 10(4), 234-42. [Abstract]