Ausgabe 7/2021
Inhalt (25 Artikel)
Enhancing validity, reliability and participation in self-reported health outcome measurement for children and young people: a systematic review of recall period, response scale format, and administration modality
L. Coombes, K. Bristowe, C. Ellis-Smith, J. Aworinde, L. K. Fraser, J. Downing, M. Bluebond-Langner, L. Chambers, F. E. M. Murtagh, R. Harding
Study objectives in clinical trials in older patients with solid malignancies: do we measure what matters?
E. R. M. Scheepers, L. H. van Huis-Tanja, M. H. Emmelot-Vonk, M. E. Hamaker
Trajectories of health-related quality of life in children of parents with mental health problems: results of the BELLA study
Angela Plass-Christl, Ulrike Ravens-Sieberer, Heike Hölling, Christiane Otto
Quality of life after hospitalization predicts one-year readmission risk in a large Swiss cohort of medical in-patients
Tristan Struja, Daniel Koch, Sebastian Haubitz, Beat Mueller, Philipp Schuetz, Timo Siepmann
Moving beyond family: unequal burden across mental health patients’ social networks
Lambert Zixin Li, Jason Yucheng Bian, Senhu Wang
Social support and quality of life among rural family caregivers of persons with severe mental illness in Sichuan Province, China: mediating roles of care burden and loneliness
Baiyang Zhang, Kyaien O. Conner, Hongdao Meng, Naidan Tu, Danping Liu, Yeli Chen
Comparison of the anxiety, depression and their relationship to quality of life among adult acute leukemia patients and their family caregivers: a cross-sectional study in China
Ying Wang, Jie Yan, JingYi Chen, ChunFeng Wang, YingChun Lin, Yong Wu, Rong Hu
Depression and anxiety in cancer patients before and during the SARS-CoV-2 pandemic: association with treatment delays
Ozgen Ahmet Yildirim, Kerem Poyraz, Erkan Erdur
The association between social isolation and musculoskeletal health in older community-dwelling adults: findings from the Hertfordshire Cohort Study
Gregorio Bevilacqua, Karen A. Jameson, Jean Zhang, Ilse Bloom, Kate A. Ward, Cyrus Cooper, Elaine M. Dennison
The impact of clinical symptoms and endoscopic and histologic disease activity on health-related quality of life in patients with ulcerative colitis following treatment with multimatrix mesalazine
Aaron Yarlas, Mary Kaye Willian, Arpita Nag
Effectiveness of motivational interviewing on anxiety, depression, sleep quality and quality of life in heart failure patients: secondary analysis of the MOTIVATE-HF randomized controlled trial
Paola Rebora, Valentina Spedale, Giuseppe Occhino, Michela Luciani, Rosaria Alvaro, Ercole Vellone, Barbara Riegel, Davide Ausili
The prediction of mortality by quality of life assessed with the WHOQOL-BREF: a longitudinal analysis at the domain and item levels using a seven-year follow-up period
Robbert J. J. Gobbens, Tjeerd van der Ploeg
The association between diabetic complications and health-related quality of life in patients with type 2 diabetes: a cross-sectional study from Iran
Hassan Karami, Maryam Shirvani Shiri, Aziz Rezapour, Ranaa Sarvari Mehrabadi, Somayeh Afshari
What’s important when caring for a loved one? Population-based preference weights for the Adult Social Care Outcomes Toolkit for informal carers (ASCOT-Carer) for Austria
Birgit Trukeschitz, Assma Hajji, Laurie Batchelder, Eirini Saloniki, Ismo Linnosmaa, Juliette Malley
Willingness to pay for a quality-adjusted life year for depressive disorders compared to heart disease based on population preferences
Laura Ulbrich, Christoph Kröger
Valuation of the EQ-5D-3L in Russia
Vitaly Omelyanovskiy, Nuriya Musina, Svetlana Ratushnyak, Tatiana Bezdenezhnykh, Vlada Fediaeva, Bram Roudijk, Fredrick Dermawan Purba
Dutch utility weights for the EORTC cancer-specific utility instrument: the Dutch EORTC QLU-C10D
Femke Jansen, Irma M. Verdonck-de Leeuw, Eva Gamper, Richard Norman, Bernhard Holzner, Madeleine King, Georg Kemmler
Health state utility and quality of life measures in patients with chronic myeloid leukemia in France
Foulon S, Cony-Makhoul P, Guerci-Bresler A, Daban M, Kapso R, Tubert-Bitter P, Bonastre J
Health state utilities associated with treatment process for oral and injectable GLP-1 receptor agonists for type 2 diabetes
Louis S. Matza, Katelyn N. Cutts, Katie D. Stewart, Kirsi Norrbacka, Luis-Emilio García-Pérez, Kristina S. Boye
Comparing the measurement properties of the EQ-5D-5L and the EQ-5D-3L in hypertensive patients living in rural China
Jie Jiang, Yanming Hong, Tiantian Zhang, Zhihao Yang, Tengfei Lin, Zhuoru Liang, Peiyao Lu, Lishun Liu, Binyan Wang, Yongmei Xu, Nan Luo
Psychometric properties of the Patient-Reported Outcomes Measurement Information System (PROMIS®) pediatric item bank peer relationships in the Dutch general population
Michiel A. J. Luijten, Raphaële R. L. van Litsenburg, Caroline B. Terwee, Martha A. Grootenhuis, Lotte Haverman
Agreement between proxy- and self-report scores on PROMIS health-related quality of life domains in pediatric burn survivors: a National Institute on Disability, Independent Living, and Rehabilitation Research Burn Model System Study
Alyssa M. Bamer, Kara McMullen, Steven E. Wolf, Barclay T. Stewart, Lewis Kazis, Camerin A. Rencken, Dagmar Amtmann
How to measure fluctuating impairments in people with MS: development of an ambulatory assessment version of the EQ-5D-5L in an exploratory study
Christine Blome, Jill Carlton, Christoph Heesen, Mathieu F. Janssen, Andrew Lloyd, Marina Otten, John Brazier
The role of response domain and scale label in the quantitative interpretation of patient-reported outcome measure response options
Tessa Peasgood, Jen-Yu Chang, Robina Mir, Clara Mukuria, Philip A. Powell