Bibliography | HTAi vortal

Patient and Citizen Involvement Group

DCIG Resources

List
Filter

Bibliography

Export 5 results:

Filters: Keyword is Health Status [Clear All Filters]

U

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

S

Sullivan SM, Tsiplova K, Ungar WJ. A scoping review of pediatric economic evaluation 1980-2014: do trends over time reflect changing priorities in evaluation methods and childhood disease? Expert Rev Pharmacoecon Outcomes Res. 2016;16(5):599-607. Abstract

R

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

H

Fleurette F, Banta D. Health technology assessment in France. Int J Technol Assess Health Care. 2000;16(2):400-11. Abstract

D

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