共 393 条
- [1] Mercieca-Bebber R(2017)Preliminary evidence on the uptake, use and benefits of the CONSORT-PRO extension Qual Life Res 26 1427-1437
- [2] Rouette J(2009)Multinational trials—recommendations on the translations required, approaches to using the same language in different countries, and the approaches to support pooling the data: the ISPOR patient-reported outcomes translation and linguistic validation good research practices task force report Value Health 12 430-440
- [3] Calvert M(2006)Patient versus clinician symptom reporting using the National Cancer Institute Common Terminology Criteria for Adverse Events: results of a questionnaire-based study Lancet Oncol 7 903-909
- [4] Wild D(2013)Patient-reported outcomes (PROs) and patient-reported outcome measures (PROMs) Health Serv Insights 6 61-68
- [5] Eremenco S(2013)Reporting of patient reported outcomes in randomised trials: the CONSORT PRO extension JAMA. 309 814-822
- [6] Mear I(2012)The use of patient-reported outcomes (PRO) within comparative effectiveness research: implications for clinical practice and health care policy Med Care 50 1060-1070
- [7] Martin M(2018)Patient led PROMs must take centre stage in cancer research Res Involve Engage 4 7-988
- [8] Houchin C(2015)Assessment of patient-reported adverse events after discharge from hospital in RCTs in gastrointestinal cancer surgery: is there sufficient coverage in existing EORTC questionnaires? Trials. 16 48-977
- [9] Gawlicki M(2011)Content validity—establishing and reporting the evidence in newly developed patient-reported outcomes (PRO) instruments for medical product evaluation: ISPOR PRO good research practices task force report: part 2—assessing respondent understanding Value Health 14 978-104
- [10] Hareendran A(2014)Establishing and reporting the evidence in newly developed patient-reported outcomes (PRO) instruments for medical product evaluation: ISPOR PRO good research practices task force report: part 1 Value in Health 14 967-1178