Literature DB >> 32040637

An analysis of missing items in real-world electronic patient reported outcomes data: implications for clinical care.

Heather A Rosett1, Susan C Locke2, Steven P Wolf3, Kris W Herring2, Gregory P Samsa4, Jesse D Troy1,2, Thomas W LeBlanc5.   

Abstract

PURPOSE: Utilization of electronic patient-reported outcomes (ePROs) in the clinic can improve quality of life and prolong survival in cancer care. However, there remain unanswered questions regarding trends in missing data and the potential effect on real-time patient care.
METHODS: This study utilized a prospectively collected dataset of ePROs from oncology clinics that administered the Patient Care Monitor 2.0 (PCM), a validated symptoms survey assessing 78 items for men, and 86 for women. We tabulated the frequency of missing items, by item and domain (emotional, functional and physical symptom-related), and examined these by age, gender, education, race and marital status.
RESULTS: Within 20,986 encounters, there were responses to at least 1 PCM item from 6933 unique patients. The highest frequency of missing answers occurred for: "attend a paid job" (10.7%), "reduced sexual enjoyment" (3.8%), and "run" (3.7%). By domain, 12.3% of functional, 8.4% of physical symptom-related, and 1.6% of emotional constructs contained at least one missing item. For functional and physical symptom-related items, missingness was most common in patients >60 years old.
CONCLUSION: The frequency of missingness was highest for functional items, like attending a paid job, suggesting that some respondents (e.g., retirees without a paid job) skipped questions that were less applicable to them. More universal issues for cancer patients, such as emotional well-being, had much lower frequencies of missingness. This suggests differential item completion that warrants further study to understand the inherent drivers. Identifying causes of missingness could improve the clinical utility of ePROs and highlight opportunities to personalize care.

Entities:  

Keywords:  Oncology; Patient-reported outcomes; Quality of life; Supportive care

Mesh:

Year:  2020        PMID: 32040637      PMCID: PMC7415679          DOI: 10.1007/s00520-020-05338-8

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


  27 in total

1.  Overall Survival Results of a Trial Assessing Patient-Reported Outcomes for Symptom Monitoring During Routine Cancer Treatment.

Authors:  Ethan Basch; Allison M Deal; Amylou C Dueck; Howard I Scher; Mark G Kris; Clifford Hudis; Deborah Schrag
Journal:  JAMA       Date:  2017-07-11       Impact factor: 56.272

Review 2.  Electronic patient-reported outcome systems in oncology clinical practice.

Authors:  Antonia V Bennett; Roxanne E Jensen; Ethan Basch
Journal:  CA Cancer J Clin       Date:  2012-07-18       Impact factor: 508.702

3.  Assessing Psychological Toxicity and Patient-Reported Distress as the Sixth Vital Sign in Cancer Care and Clinical Trials.

Authors:  Thomas W LeBlanc; Arif H Kamal
Journal:  AMA J Ethics       Date:  2017-05-01

4.  Health status assessment for the twenty-first century: item response theory, item banking and computer adaptive testing.

Authors:  D A Revicki; D F Cella
Journal:  Qual Life Res       Date:  1997-08       Impact factor: 4.147

5.  Improving health care efficiency and quality using tablet personal computers to collect research-quality, patient-reported data.

Authors:  Amy P Abernethy; James E Herndon; Jane L Wheeler; Meenal Patwardhan; Heather Shaw; H Kim Lyerly; Kevin Weinfurt
Journal:  Health Serv Res       Date:  2008-08-28       Impact factor: 3.402

6.  Feasibility and acceptability to patients of a longitudinal system for evaluating cancer-related symptoms and quality of life: pilot study of an e/Tablet data-collection system in academic oncology.

Authors:  Amy P Abernethy; James E Herndon; Jane L Wheeler; Jeannette M Day; Linda Hood; Meenal Patwardhan; Heather Shaw; Herbert Kim Lyerly
Journal:  J Pain Symptom Manage       Date:  2009-04-25       Impact factor: 3.612

7.  Data quality and age: health and psychobehavioral correlates of item nonresponse and inconsistent responses.

Authors:  P L Colsher; R B Wallace
Journal:  J Gerontol       Date:  1989-03

8.  Symptom Monitoring With Patient-Reported Outcomes During Routine Cancer Treatment: A Randomized Controlled Trial.

Authors:  Ethan Basch; Allison M Deal; Mark G Kris; Howard I Scher; Clifford A Hudis; Paul Sabbatini; Lauren Rogak; Antonia V Bennett; Amylou C Dueck; Thomas M Atkinson; Joanne F Chou; Dorothy Dulko; Laura Sit; Allison Barz; Paul Novotny; Michael Fruscione; Jeff A Sloan; Deborah Schrag
Journal:  J Clin Oncol       Date:  2015-12-07       Impact factor: 44.544

9.  Use of tablet personal computers for sensitive patient-reported information.

Authors:  Alexandra Dupont; Jane Wheeler; James E Herndon; April Coan; S Yousuf Zafar; Linda Hood; Meenal Patwardhan; Heather S Shaw; H Kim Lyerly; Amy P Abernethy
Journal:  J Support Oncol       Date:  2009 May-Jun

Review 10.  Patient-reported outcomes in cancer care - hearing the patient voice at greater volume.

Authors:  Thomas W LeBlanc; Amy P Abernethy
Journal:  Nat Rev Clin Oncol       Date:  2017-10-04       Impact factor: 66.675

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  1 in total

1.  A narrative review of current evidence supporting the implementation of electronic patient-reported outcome measures in the management of chronic diseases.

Authors:  Olalekan Lee Aiyegbusi; Devika Nair; John Devin Peipert; Kara Schick-Makaroff; Istvan Mucsi
Journal:  Ther Adv Chronic Dis       Date:  2021-05-24       Impact factor: 5.091

  1 in total

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