Bibliography

Filters: Keyword is Quality of Life  [Clear All Filters]
2010
Gorecki CA, Brown JM, Briggs M, Nixon J. Evaluation of five search strategies in retrieving qualitative patient-reported electronic data on the impact of pressure ulcers on quality of life. J Adv Nurs. 2010;66(3):645-52. Abstract
Gorecki CA, Brown JM, Briggs M, Nixon J. Evaluation of five search strategies in retrieving qualitative patient-reported electronic data on the impact of pressure ulcers on quality of life. J Adv Nurs. 2010;66(3):645-52. Abstract
2011
Droste S, Herrmann-Frank A, Scheibler F, Krones T. Ethical issues in autologous stem cell transplantation (ASCT) in advanced breast cancer: a systematic literature review. BMC Med Ethics. 2011;12:6. Abstract
Böckerman P, Johansson E, Saarni SI. Do established health-related quality-of-life measures adequately capture the impact of chronic conditions on subjective well-being? Health Policy. 2011;100(1):91-5. Abstract
Basch E, Bennett A, Pietanza CM. Use of patient-reported outcomes to improve the predictive accuracy of clinician-reported adverse events. J Natl Cancer Inst. 2011;103(24):1808-10.
Danner M, Hummel MJ, Volz F, van Manen JG, Wiegard B, Dintsios C-, et al. Integrating patients' views into health technology assessment: Analytic hierarchy process (AHP) as a method to elicit patient preferences. Int J Technol Assess Health Care. 2011;27(4):369-75. Abstract
Hansen HP, Lee A, van Randwijk CB. Patient aspects: a review of fifty-eight Danish HTA reports. Int J Technol Assess Health Care. 2011;27(4):330-6. Abstract
2012
Oleen-Burkey M, Castelli-Haley J, Lage MJ, Johnson KP. Burden of a multiple sclerosis relapse: the patient's perspective. Patient. 2012;5(1):57-69. Abstract
Ahmed S, Berzon RA, Revicki DA, Lenderking WR, Moinpour CM, Basch E, et al. The use of patient-reported outcomes (PRO) within comparative effectiveness research: implications for clinical practice and health care policy. Med Care. 2012;50(12):1060-70. Abstract
Basch E. Beyond the FDA PRO guidance: steps toward integrating meaningful patient-reported outcomes into regulatory trials and US drug labels. Value Health. 2012;15(3):401-3.
2014
Reeve BB, Mitchell SA, Dueck AC, Basch E, Cella D, Reilly CM, et al. Recommended patient-reported core set of symptoms to measure in adult cancer treatment trials. J Natl Cancer Inst. 2014;106(7). Abstract
Engel L, Bryan S, Evers SM, Dirksen CD, Noonan VK, Whitehurst DG. Exploring psychometric properties of the SF-6D, a preference-based health-related quality of life measure, in the context of spinal cord injury. Qual Life Res. 2014;23(8):2383-93. Abstract