S. Tatlock

发表

Content validation of a caregiver diary to monitor severity and recovery of pediatric patients with respiratory syncytial virus infection

Sarah Bentley, Robert H. Arbuckle, L. Abetz-Webb, 2022, Journal of Patient-Reported Outcomes.

Evaluation of a crosswalk between the European Quality of Life Five Dimension Five Level and the Menopause-Specific Quality of Life questionnaire

A. Bushmakin, R. Arbuckle, M. Moffatt, 2018, Climacteric : the journal of the International Menopause Society.

People living with moderate-to-severe COPD prefer improvement of daily symptoms over the improvement of exacerbations: a multicountry patient preference study

G. Criner, P. Burgel, Kirsten Phillips, 2022, ERJ Open Research.

Psychometric Evaluation of a Treatment Acceptance Measure for Use in Patients Receiving Treatment via Subcutaneous Injection.

J. Spertus, I. Khan, R. Arbuckle, 2017, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.

Development and Content Validity Testing of a Patient-Reported Treatment Acceptance Measure for Use in Patients Receiving Treatment via Subcutaneous Injection.

J. Spertus, I. Khan, R. Arbuckle, 2015, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.

Development and preliminary psychometric evaluation of an owner-completed measure of feline quality of life.

R. Arbuckle, M. Gober, N. Williamson, 2017, Veterinary journal.

Qualitative cross-cultural exploration of breast symptoms and impacts associated with hormonal treatments for menopausal symptoms to inform the development of new patient-reported measurement tools.

L. Dennerstein, T. Symonds, J. Simon, 2015, Maturitas.

What Outcomes are Important for Gout Patients? In-Depth Qualitative Research into the Gout Patient Experience to Determine Optimal Endpoints for Evaluating Therapeutic Interventions

W. Taylor, L. Harrold, T. Symonds, 2016, The Patient - Patient-Centered Outcomes Research.

Individual Differences in the Patient Experience of Relapsing Multiple Sclerosis (RMS): A Multi-Country Qualitative Exploration of Drivers of Treatment Preferences Among People Living with RMS

N. Adlard, K. Sully, S. Tatlock, 2023, The Patient - Patient-Centered Outcomes Research.

The impact of gout as described by patients, using the lens of The International Classification of Functioning, Disability and Health (ICF): a qualitative study

C. Díaz-Torné, W. Taylor, E. Pujol-Ribera, 2020, BMC Rheumatology.

PIN129 - ADAPTING INFLUENZA PATIENT-REPORTED OUTCOMES (PRO) MEASURES TO MONITOR RESPIRATORY SYNCYTIAL VIRUS (RSV) SYMPTOM SEVERITY IN ADULTS: QUALITATIVE EVIDENCE OF KEY CONCEPTS AND CONTENT VALIDITY

R. Arbuckle, K. Sully, S. Tatlock, 2018, Value in Health.

Qualitative concept elicitation and cognitive debriefing interviews of symptoms, impacts and selected customized PROMIS® Short Forms: a study in patients with axial spondyloarthritis

A. Findley, M. Bracher, Wen-Hung Chen, 2023, Journal of Patient-Reported Outcomes.

Psychometric evaluation of electronic diaries assessing side-effects of hormone therapy

A. Bushmakin, R. Arbuckle, M. Moffatt, 2018, Climacteric : the journal of the International Menopause Society.

Qualitative cross-cultural exploration of vaginal bleeding/spotting symptoms and impacts associated with hormone therapy in post-menopausal women to inform the development of new patient-reported measurement tools.

L. Dennerstein, T. Symonds, J. Simon, 2014, Maturitas.