Uitgave 7/2009
Inhoudsopgave (16 Artikelen)
PatientViewpoint: a website for patient-reported outcomes assessment
Claire F. Snyder, Roxanne Jensen, S. Orion Courtin, Albert W. Wu
Predicting EQ-5D utility scores from the 25-item National Eye Institute Vision Function Questionnaire (NEI-VFQ 25) in patients with age-related macular degeneration
Nalin Payakachat, Kent H. Summers, Andreas M. Pleil, Matthew M. Murawski, Joseph Thomas III, Kristofer Jennings, James G. Anderson
The concurrent validity and responsiveness of the health utilities index (HUI 3) among patients with advanced HIV/AIDS
Bohdan Nosyk, Huiying Sun, Nick Bansback, Daphne P. Guh, Xin Li, Paul Barnett, Ahmed Bayoumi, Susan Griffin, Vilija Joyce, Mark Holodniy, Doug K. Owens, Aslam H. Anis
Quality of life from the perspective of adolescents with cerebral palsy: “I just think I’m a normal kid, I just happen to have a disability”
Keiko Shikako-Thomas, Lucy Lach, Annette Majnemer, Jodie Nimigon, Kelti Cameron, Michael Shevell
Quality of life in Serbian patients with Parkinson’s disease
Ljubomir Žiropađa, Elka Stefanova, Aleksandra Potrebić, Vladimir S. Kostić
Psychosocial adaptation status and health-related quality of life among older Chinese adults with visual disorders
Chong-Wen Wang, Cecilia L. W. Chan
Quality of life of palliative chemotherapy naive patients with advanced adenocarcinoma of the stomach or esophagogastric junction treated with irinotecan combined with 5-fluorouracil and folinic acid: results of a randomised phase III trial
Desmond Curran, Carmelo Pozzo, Jerzy Zaluski, Magdalena Dank, Carlo Barone, Vahur Valvere, Suayib Yalcin, Christian Peschel, Miklós Wenczl, Erdem Goker, Roland Bugat
Measuring pain in the context of homelessness
Rebecca Matter, Susan Kline, Karon F. Cook, Dagmar Amtmann
Development of physical and mental health summary scores from the patient-reported outcomes measurement information system (PROMIS) global items
Ron D. Hays, Jakob B. Bjorner, Dennis A. Revicki, Karen L. Spritzer, David Cella
Building PROMIS item banks: librarians as co-investigators
Mary Klem, Ester Saghafi, Rebecca Abromitis, Angela Stover, Mary Amanda Dew, Paul Pilkonis
Readability estimates for commonly used health-related quality of life surveys
Sylvia H. Paz, Honghu Liu, Marie N. Fongwa, Leo S. Morales, Ron D. Hays
Development of a battery of instruments for detailed measurement of health status in patients with COPD in routine care: the Nijmegen Clinical Screening Instrument
Jeannette Bernadette Peters, Leonie Daudey, Yvonne F. Heijdra, Johan Molema, P. N. Richard Dekhuijzen, Jan H. Vercoulen
Confirmatory and exploratory factor analysis of the caregiver quality of life index-cancer with Turkish samples
Zeynep C. Ozer, Mehmet Z. Firat, Hicran A. Bektas
Italian translation of the Manchester-Oxford Foot Questionnaire, with re-assessment of reliability and validity
Andrea Marinozzi, Nicolò Martinelli, Manlio Panascì, Francesco Cancilleri, Edoardo Franceschetti, Bruno Vincenzi, Alberto Di Martino, Vincenzo Denaro
Psychometric validation of two patient-reported outcome measures to assess symptom severity and changes in symptoms in hereditary angioedema
Margaret K. Vernon, Anne M. Rentz, Kathleen W. Wyrwich, Martha V. White, Aurelie Grienenberger
Reliability and validity of an instrument for assessing patients’ perceptions about medications for diabetes: the PAM-D
Patrick O. Monahan, Kathleen A. Lane, Risa P. Hayes, Colleen A. McHorney, David G. Marrero