Literature DB >> 26887586

Electronic real-time assessment of patient-reported outcomes in routine care-first findings and experiences from the implementation in a comprehensive cancer center.

Freya Trautmann1,2, Leopold Hentschel3, Beate Hornemann4, Anke Rentsch4, Michael Baumann4, Gerhard Ehninger4, Jochen Schmitt1, Markus Schuler4,5.   

Abstract

PURPOSE: Cancer patients suffer from a variety of physical and mental complaints. Since physician assessment of symptoms seems insufficient to reveal the complete range of patients' ailments, patient-reported outcomes (PRO) have become of key importance in modern cancer treatment. The implementation and first results of a systematic electronic real-time assessment of PRO in routine care is described.
METHODS: Consecutive patients presenting for the first time to a German comprehensive cancer center were asked to fill in an adaptive self-administered electronic questionnaire consisting of standardized PRO measures. After completion, patient-reported data was linked to the patients' medical files for discussion in the first consultation with the treating physician. Interviews with staff were conducted to identify barriers in implementation.
RESULTS: Out of 160 cancer patients, 126 (79 %; mean age 63 years, 67 % males) agreed to participate. The number of recruited patients increased over time. Of participating patients, 67 % provided complete information on all PRO-related scales. On average, 31 min (range 3-140) were required to fill in the questionnaire. Of participating patients, 53.0 % comprised need for psychooncological support and 62 % revealed moderate to severe psychosocial distress. The mean score for global quality of life according to the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) was 55.2 (SD ±25.6).
CONCLUSIONS: Comprehensive oncological treatment needs to consider disease symptoms, quality of life, preferences, and comorbidities of individual patients in a structured, standardized, and transparent way. Our findings indicate that an adaptive, self-administered electronic assessment tool for cancer patients to report a broad set of PRO can be feasibly implemented and is well accepted by patients in a realistic setting.

Entities:  

Keywords:  Electronic assessment; Oncology; Patient care; Patient-reported outcomes; Quality of life; Routine care

Mesh:

Year:  2016        PMID: 26887586     DOI: 10.1007/s00520-016-3127-0

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  44 in total

1.  Evidence-based guidelines for interpreting change scores for the European Organisation for the Research and Treatment of Cancer Quality of Life Questionnaire Core 30.

Authors:  K Cocks; M T King; G Velikova; G de Castro; M Martyn St-James; P M Fayers; J M Brown
Journal:  Eur J Cancer       Date:  2012-03-12       Impact factor: 9.162

Review 2.  Implementing patient-reported outcome measures in palliative care clinical practice: a systematic review of facilitators and barriers.

Authors:  Bárbara Antunes; Richard Harding; Irene J Higginson
Journal:  Palliat Med       Date:  2013-06-25       Impact factor: 4.762

3.  The use of quality of life data in clinical practice.

Authors:  J Morris; D Perez; B McNoe
Journal:  Qual Life Res       Date:  1998-01       Impact factor: 4.147

4.  Development of computerised adaptive testing (CAT) for the EORTC QLQ-C30 dimensions - general approach and initial results for physical functioning.

Authors:  Morten Aa Petersen; Mogens Groenvold; Neil K Aaronson; Wei-Chu Chie; Thierry Conroy; Anna Costantini; Peter Fayers; Jorunn Helbostad; Bernhard Holzner; Stein Kaasa; Susanne Singer; Galina Velikova; Teresa Young
Journal:  Eur J Cancer       Date:  2010-03-16       Impact factor: 9.162

Review 5.  Impact of patient-reported outcome measures on routine practice: a structured review.

Authors:  Susan Marshall; Kirstie Haywood; Ray Fitzpatrick
Journal:  J Eval Clin Pract       Date:  2006-10       Impact factor: 2.431

6.  Patient self-reports of symptoms and clinician ratings as predictors of overall cancer survival.

Authors:  Chantal Quinten; John Maringwa; Carolyn C Gotay; Francesca Martinelli; Corneel Coens; Bryce B Reeve; Henning Flechtner; Eva Greimel; Madeleine King; David Osoba; Charles Cleeland; Jolie Ringash; Joseph Schmucker-Von Koch; Martin J B Taphoorn; Joachim Weis; Andrew Bottomley
Journal:  J Natl Cancer Inst       Date:  2011-12-07       Impact factor: 13.506

7.  Capturing patient reported outcomes and quality of life in routine clinical practice: ready for prime time?

Authors:  A Atreja; M Rizk
Journal:  Minerva Gastroenterol Dietol       Date:  2012-03

Review 8.  Prevalence of pain in patients with cancer: a systematic review of the past 40 years.

Authors:  M H J van den Beuken-van Everdingen; J M de Rijke; A G Kessels; H C Schouten; M van Kleef; J Patijn
Journal:  Ann Oncol       Date:  2007-03-12       Impact factor: 32.976

9.  Screening for distress in lung and breast cancer outpatients: a randomized controlled trial.

Authors:  Linda E Carlson; Shannon L Groff; Olga Maciejewski; Barry D Bultz
Journal:  J Clin Oncol       Date:  2010-10-12       Impact factor: 44.544

10.  High levels of untreated distress and fatigue in cancer patients.

Authors:  L E Carlson; M Angen; J Cullum; E Goodey; J Koopmans; L Lamont; J H MacRae; M Martin; G Pelletier; J Robinson; J S A Simpson; M Speca; L Tillotson; B D Bultz
Journal:  Br J Cancer       Date:  2004-06-14       Impact factor: 7.640

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  14 in total

1.  CORR Insights®: What is the Incidence of Suicide in Patients with Bone and Soft Tissue Cancer?

Authors:  Kenneth R Gundle
Journal:  Clin Orthop Relat Res       Date:  2017-01-03       Impact factor: 4.176

2.  Feasibility of health-related quality of life (HRQoL) assessment for cancer patients using electronic patient-reported outcome (ePRO) in daily clinical practice.

Authors:  Guillaume Mouillet; Antoine Falcoz; Joëlle Fritzsch; Hamadi Almotlak; Pascale Jacoulet; Xavier Pivot; Cristian Villanueva; Laura Mansi; Stefano Kim; Elsa Curtit; Nathalie Meneveau; Olivier Adotevi; Marine Jary; Guillaume Eberst; Angelique Vienot; Fabien Calcagno; Astrid Pozet; Oumelkheir Djoumakh; Christophe Borg; Virginie Westeel; Amélie Anota; Sophie Paget-Bailly
Journal:  Qual Life Res       Date:  2021-01-02       Impact factor: 4.147

Review 3.  Quality of Life Measurements: Any Value for Clinical Practice?

Authors:  Matthias Büttner; Veit Zebralla; Andreas Dietz; Susanne Singer
Journal:  Curr Treat Options Oncol       Date:  2017-05

4.  Cancer patients' control preferences in decision making and associations with patient-reported outcomes: a prospective study in an outpatient cancer center.

Authors:  Markus Schuler; Jan Schildmann; Freya Trautmann; Leopold Hentschel; Beate Hornemann; Anke Rentsch; Gerhard Ehninger; Jochen Schmitt
Journal:  Support Care Cancer       Date:  2017-03-29       Impact factor: 3.603

5.  Ethnography and user-centered design to inform context-driven implementation.

Authors:  Emily R Haines; M Alexis Kirk; Lauren Lux; Andrew B Smitherman; Byron J Powell; Alex Dopp; Angela M Stover; Sarah A Birken
Journal:  Transl Behav Med       Date:  2022-01-18       Impact factor: 3.626

6.  Reliability of an e-PRO Tool of EORTC QLQ-C30 for Measurement of Health-Related Quality of Life in Patients With Breast Cancer: Prospective Randomized Trial.

Authors:  Joachim Graf; Sara Y Brucker; Markus Wallwiener; Lina Matthies; Elisabeth Simoes; Lucia Keilmann; Andreas D Hartkopf; Alexander N Sokolov; Christina B Walter; Nina Sickenberger; Stephanie Wallwiener; Manuel Feisst; Paul Gass; Peter A Fasching; Michael P Lux; Diethelm Wallwiener; Florin-Andrei Taran; Joachim Rom; Andreas Schneeweiss
Journal:  J Med Internet Res       Date:  2017-09-14       Impact factor: 5.428

7.  Electronic Patient-Reported Outcome-Based Interventions for Palliative Cancer Care: A Systematic and Mapping Review.

Authors:  Christina Karamanidou; Pantelis Natsiavas; Lefteris Koumakis; Kostas Marias; Fatima Schera; Michael Schäfer; Sheila Payne; Christos Maramis
Journal:  JCO Clin Cancer Inform       Date:  2020-07

8.  Acceptability of patient reported outcome measures (PROMs) in a cystic fibrosis data registry.

Authors:  Irushi Ratnayake; Susannah Ahern; Rasa Ruseckaite
Journal:  BMJ Open Respir Res       Date:  2021-07

9.  An Electronic Patient-Reported Outcome Tool for the FACT-B (Functional Assessment of Cancer Therapy-Breast) Questionnaire for Measuring the Health-Related Quality of Life in Patients With Breast Cancer: Reliability Study.

Authors:  Lina Maria Matthies; Florin-Andrei Taran; Joachim Graf; Markus Wallwiener; Lucia Keilmann; Andreas Schneeweiss; Elisabeth Simoes; Andreas D Hartkopf; Alexander N Sokolov; Christina B Walter; Nina Sickenberger; Stephanie Wallwiener; Manuel Feisst; Paul Gass; Michael P Lux; Florian Schuetz; Peter A Fasching; Christof Sohn; Sara Y Brucker
Journal:  J Med Internet Res       Date:  2019-01-22       Impact factor: 5.428

10.  The acceptance and applicability of a patient-reported experience measurement tool in oncological care: a descriptive feasibility study in northern Germany.

Authors:  Christiane Rudolph; Gitte Stentebjerg Petersen; Ron Pritzkuleit; Hans Storm; Alexander Katalinic
Journal:  BMC Health Serv Res       Date:  2019-11-01       Impact factor: 2.655

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