Literature DB >> 12409335

The case identification challenge in measuring quality of cancer care.

Marjorie L Pearson1, Patricia A Ganz, Kimberly McGuigan, Jennifer R Malin, John Adams, Katherine L Kahn.   

Abstract

PURPOSE: The delivery of quality care to all patients with cancer has been named as a national priority within the American health care system. This article addresses the issues critical to case identification in cancer quality measurement and recommends possible strategies for accurately identifying a population of cancer patients.
METHODS: We present the measurement issues associated with the basic challenges of case identification strategies for quality measurement. We discuss two basic challenges: (1) accurately identifying all patients with the defining characteristics (eg, a diagnosis of breast cancer), and (2) identifying only patients with these characteristics.
RESULTS: Possible options for identifying newly diagnosed patients include using claims or other administrative data, cancer registries, cancer registry rapid case ascertainment, pathology laboratories, and physicians' offices. In the published literature, the sensitivity of claims varies from 75% to 95%, whereas central registries must have a 90% completeness rate to be certified. Most of these approaches, however, involve limitations to obtaining valid and comparable data across multiple settings.
CONCLUSION: Using an existing data collection system staffed by skilled data collectors and managers should result in substantially more accurate and timely data. Registry officials and the government agencies that provide their support should be encouraged to adopt quality-of-care analyses as an important purpose of the registry system and to enhance their capacity to rapidly ascertain cases, collect the appropriate identifying information needed for patient contact, and verify stage at diagnosis. In order to meet the growing demand for timely, accurate information about quality of care, registries are likely to require additional support so they can enhance their capacity to rapidly ascertain cases, collect the appropriate identifying information needed for patient contact, and verify stage at diagnosis.

Entities:  

Mesh:

Year:  2002        PMID: 12409335     DOI: 10.1200/JCO.2002.05.527

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  13 in total

1.  Representativeness of participants in the cancer care outcomes research and surveillance consortium relative to the surveillance, epidemiology, and end results program.

Authors:  Paul J Catalano; John Z Ayanian; Jane C Weeks; Katherine L Kahn; Mary Beth Landrum; Alan M Zaslavsky; Jeannette Lee; Jane Pendergast; David P Harrington
Journal:  Med Care       Date:  2013-02       Impact factor: 2.983

2.  Towards using administrative databases to measure population-based indicators of quality of end-of-life care: testing the methodology.

Authors:  Eva Grunfeld; Lynn Lethbridge; Ron Dewar; Beverley Lawson; Lawrence F Paszat; Grace Johnston; Frederick Burge; Paul McIntyre; Craig C Earle
Journal:  Palliat Med       Date:  2006-12       Impact factor: 4.762

3.  Association of Actual and Preferred Decision Roles With Patient-Reported Quality of Care: Shared Decision Making in Cancer Care.

Authors:  Kenneth L Kehl; Mary Beth Landrum; Neeraj K Arora; Patricia A Ganz; Michelle van Ryn; Jennifer W Mack; Nancy L Keating
Journal:  JAMA Oncol       Date:  2015-04       Impact factor: 31.777

4.  Influence of a targeted performance measure for brief intervention on gender differences in receipt of brief intervention among patients with unhealthy alcohol use in the Veterans Health Administration.

Authors:  Emily C Williams; Gwen T Lapham; Anna D Rubinsky; Laura J Chavez; Douglas Berger; Katharine A Bradley
Journal:  J Subst Abuse Treat       Date:  2017-07-19

5.  Prevalence, predictors, and patient outcomes associated with physician co-management: findings from the Los Angeles Women's Health Study.

Authors:  Danielle E Rose; Diana M Tisnado; May L Tao; Jennifer L Malin; John L Adams; Patricia A Ganz; Katherine L Kahn
Journal:  Health Serv Res       Date:  2011-12-15       Impact factor: 3.402

6.  Patients' experiences with care for lung cancer and colorectal cancer: findings from the Cancer Care Outcomes Research and Surveillance Consortium.

Authors:  John Z Ayanian; Alan M Zaslavsky; Neeraj K Arora; Katherine L Kahn; Jennifer L Malin; Patricia A Ganz; Michelle van Ryn; Mark C Hornbrook; Catarina I Kiefe; Yulei He; Julie M Urmie; Jane C Weeks; David P Harrington
Journal:  J Clin Oncol       Date:  2010-08-16       Impact factor: 44.544

7.  Cancer patients' roles in treatment decisions: do characteristics of the decision influence roles?

Authors:  Nancy L Keating; Mary Beth Landrum; Neeraj K Arora; Jennifer L Malin; Patricia A Ganz; Michelle van Ryn; Jane C Weeks
Journal:  J Clin Oncol       Date:  2010-08-16       Impact factor: 44.544

8.  Treatment decisions and employment of breast cancer patients: Results of a population-based survey.

Authors:  Reshma Jagsi; Paul H Abrahamse; Kamaria L Lee; Lauren P Wallner; Nancy K Janz; Ann S Hamilton; Kevin C Ward; Monica Morrow; Allison W Kurian; Christopher R Friese; Sarah T Hawley; Steven J Katz
Journal:  Cancer       Date:  2017-10-09       Impact factor: 6.860

9.  Validity of Race, Ethnicity, and National Origin in Population-based Cancer Registries and Rapid Case Ascertainment Enhanced With a Spanish Surname List.

Authors:  Lisa C Clarke; Rudolph P Rull; John Z Ayanian; Robert Boer; Dennis Deapen; Dee W West; Katherine L Kahn
Journal:  Med Care       Date:  2016-01       Impact factor: 2.983

10.  Variation in physician-patient discussion of breast reconstruction.

Authors:  Judy Y Chen; Jennifer Malin; Patricia A Ganz; Clifford Ko; Diana Tisnado; May Lin Tao; Martha Timmer; John L Adams; Katherine L Kahn
Journal:  J Gen Intern Med       Date:  2008-11-21       Impact factor: 5.128

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