Literature DB >> 27021391

Engaging Patients as Partners in Developing Patient-Reported Outcome Measures in Cancer-A Review of the Literature.

Natasha Camuso1, Prerna Bajaj1, Deborah Dudgeon1,2, Gunita Mitera3,4.   

Abstract

PURPOSE: Tools to collect patient-reported outcome measures (PROMs) are frequently used in the healthcare setting to collect information that is most meaningful to patients. Due to discordance among how patients and healthcare providers rank symptoms that are considered most meaningful to the patient, engagement of patients in the development of PROMs is extremely important. This review aimed to identify studies that described how patients are involved in the item generation stage of cancer-specific PROM tools developed for cancer patients.
METHODS: A literature search was conducted using keywords relevant to PROMs, cancer, and patient engagement. A manual search of relevant reference lists was also conducted. Inclusion criteria stipulated that publications must describe patient engagement in the item generation stage of development of cancer-specific PROM tools. Results were excluded if they were duplicate findings or non-English.
RESULTS: The initial search yielded 230 publications. After removal of duplicates and review of publications, 6 were deemed relevant. Fourteen additional publications were retrieved through a manual search of references from relevant publications. A total of 13 unique PROM tools that included patient input in item generation were identified. The most common method of patient engagement was through qualitative interviews or focus groups.
CONCLUSIONS: Despite recommendations from international groups and the emphasized importance of incorporating patient feedback in all stages of development of PROMs, few unique tools have incorporated patient input in item generation of cancer-specific tools. Moving forward, a framework of best practices on how to best engage patients in developing PROMs is warranted to support high-quality patient-centered care.

Entities:  

Keywords:  Cancer; Patient engagement; Patient-reported outcome measurement

Mesh:

Year:  2016        PMID: 27021391     DOI: 10.1007/s00520-016-3151-0

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


  31 in total

1.  Sexual functioning along the cancer continuum: focus group results from the Patient-Reported Outcomes Measurement Information System (PROMIS®).

Authors:  Kathryn E Flynn; Diana D Jeffery; Francis J Keefe; Laura S Porter; Rebecca A Shelby; Maria R Fawzy; Tracy K Gosselin; Bryce B Reeve; Kevin P Weinfurt
Journal:  Psychooncology       Date:  2010-03-30       Impact factor: 3.894

2.  Does the medical record cover the symptoms experienced by cancer patients receiving palliative care? A comparison of the record and patient self-rating.

Authors:  A S Strömgren; M Groenvold; L Pedersen; A K Olsen; M Spile; P Sjøgren
Journal:  J Pain Symptom Manage       Date:  2001-03       Impact factor: 3.612

3.  Dermatology Life Quality Index (DLQI)--a simple practical measure for routine clinical use.

Authors:  A Y Finlay; G K Khan
Journal:  Clin Exp Dermatol       Date:  1994-05       Impact factor: 3.470

4.  The skin cancer index: clinical responsiveness and predictors of quality of life.

Authors:  John S Rhee; B Alex Matthews; Marcy Neuburg; Brent R Logan; Mary Burzynski; Ann B Nattinger
Journal:  Laryngoscope       Date:  2007-03       Impact factor: 3.325

5.  Assessing health-related quality of life for advanced basal cell carcinoma and basal cell carcinoma nevus syndrome: development of the first disease-specific patient-reported outcome questionnaires.

Authors:  Susan D Mathias; Mary-Margaret Chren; Hilary H Colwell; Yeun Mi Yim; Carolina Reyes; Diana M Chen; Scott W Fosko
Journal:  JAMA Dermatol       Date:  2014-02       Impact factor: 10.282

6.  The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology.

Authors:  N K Aaronson; S Ahmedzai; B Bergman; M Bullinger; A Cull; N J Duez; A Filiberti; H Flechtner; S B Fleishman; J C de Haes
Journal:  J Natl Cancer Inst       Date:  1993-03-03       Impact factor: 13.506

Review 7.  A systematic review of patient-reported outcome instruments of nonmelanoma skin cancer in the dermatologic population.

Authors:  Erica H Lee; Anne F Klassen; Kishwer S Nehal; Stefan J Cano; Janet Waters; Andrea L Pusic
Journal:  J Am Acad Dermatol       Date:  2012-10-24       Impact factor: 11.527

8.  Quality of life issues in nonmetastatic skin cancer.

Authors:  D Burdon-Jones; P Thomas; R Baker
Journal:  Br J Dermatol       Date:  2009-08-20       Impact factor: 9.302

Review 9.  Use of existing patient-reported outcome (PRO) instruments and their modification: the ISPOR Good Research Practices for Evaluating and Documenting Content Validity for the Use of Existing Instruments and Their Modification PRO Task Force Report.

Authors:  Margaret Rothman; Laurie Burke; Pennifer Erickson; Nancy Kline Leidy; Donald L Patrick; Charles D Petrie
Journal:  Value Health       Date:  2009-09-25       Impact factor: 5.725

10.  Content development for the Functional Assessment of Cancer Therapy-Multiple Myeloma (FACT-MM): use of qualitative and quantitative methods for scale construction.

Authors:  Lynne I Wagner; Don Robinson; Matthias Weiss; Michael Katz; Phillip Greipp; Rafael Fonseca; David Cella
Journal:  J Pain Symptom Manage       Date:  2012-05-09       Impact factor: 3.612

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  6 in total

Review 1.  Findings from the 2017 Yearbook Section on Health Information Management.

Authors:  M Bloomrosen; E S Berner
Journal:  Yearb Med Inform       Date:  2017-09-11

2.  What Do Orthopaedists Believe is Needed for Incorporating Patient-reported Outcome Measures into Clinical Care? A Qualitative Study.

Authors:  Robin R Whitebird; Leif I Solberg; Jeanette Y Ziegenfuss; Christine K Norton; Ella A Chrenka; Marc Swiontkowski; Megan Reams; Elizabeth S Grossman
Journal:  Clin Orthop Relat Res       Date:  2022-04-01       Impact factor: 4.755

3.  A randomised online experimental study to compare responses to brief and extended surveys of health-related quality of life and psychosocial outcomes among women with breast cancer.

Authors:  Kerry Ettridge; Joanna Caruso; David Roder; Ivanka Prichard; Katrine Scharling-Gamba; Kathleen Wright; Caroline Miller
Journal:  Qual Life Res       Date:  2020-09-29       Impact factor: 3.440

4.  The patient's perspective on blue light flexible cystoscopy: insight from a prospective clinical study.

Authors:  Nima Almassi; Eugene Pietzak
Journal:  Transl Androl Urol       Date:  2018-12

5.  What matters to patients and clinicians when discussing the impact of cancer medicines on health-related quality of life? Consensus-based mixed methods approach in prostate cancer.

Authors:  Emma Dunlop; Aimee Ferguson; Tanja Mueller; Kelly Baillie; Julie Clarke; Jennifer Laskey; Amanj Kurdi; Olivia Wu; Rob Jones; Hilary Glen; Marion Bennie
Journal:  Support Care Cancer       Date:  2021-12-08       Impact factor: 3.359

6.  Integrated Care Planning for Cancer Patients: A Scoping Review.

Authors:  Anum Irfan Khan; Erin Arthurs; Sharon Gradin; Marnie MacKinnon; Jonathan Sussman; Vishal Kukreti
Journal:  Int J Integr Care       Date:  2017-11-13       Impact factor: 5.120

  6 in total

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