Literature DB >> 24126685

The quality of supportive cancer care in the veterans affairs health system and targets for improvement.

Anne M Walling1, Diana Tisnado, Steven M Asch, Jennifer M Malin, Philip Pantoja, Sydney M Dy, Susan L Ettner, Ann P Zisser, Hannah Schreibeis-Baum, Martin Lee, Karl A Lorenz.   

Abstract

IMPORTANCE: Characterizing the quality of supportive cancer care can guide quality improvement.
OBJECTIVE: To evaluate nonhospice supportive cancer care comprehensively in a national sample of veterans. DESIGN, SETTING, AND PARTICIPANTS: Using a retrospective cohort study design, we measured evidence-based cancer care processes using previously validated indicators of care quality in patients with advanced cancer, addressing pain, nonpain symptoms, and information and care planning among 719 veterans with a 2008 Veterans Affairs Central Cancer Registry diagnosis of stage IV colorectal (37.0%), pancreatic (29.8%), or lung (33.2%) cancer. MAIN OUTCOMES AND MEASURES: We abstracted medical records from diagnosis for 3 years or until death among eligible veterans (lived ≥ 30 days following diagnosis with ≥ 1 Veterans Affairs hospitalization or ≥ 2 Veterans Affairs outpatient visits). Each indicator identified a clinical scenario and an appropriate action. For each indicator for which a veteran was eligible, we determined whether appropriate care was provided. We also determined patient-level quality overall and by pain, nonpain symptoms, and information and care planning domains.
RESULTS: Most veterans were older (mean age, 66.2 years), male (97.2%), and white (74.3%). Eighty-five percent received both inpatient and outpatient care, and 92.5% died. Overall, the 719 veterans triggered a mean of 11.7 quality indicators (range, 1-22) and received a mean 49.5% of appropriate care. Notable gaps in care were that inpatient pain screening was common (96.5%) but lacking for outpatients (58.1%). With opioids, bowel prophylaxis occurred for only 52.2% of outpatients and 70.5% of inpatients. Few patients had a timely dyspnea evaluation (15.8%) or treatment (10.8%). Outpatient assessment of fatigue occurred for 31.3%. Of patients at high risk for diarrhea from chemotherapy, 24.2% were offered appropriate antidiarrheals. Only 17.7% of veterans had goals of care addressed in the month after a diagnosis of advanced cancer, and 63.7% had timely discussion of goals following intensive care unit admission. Most decedents (86.4%) were referred to palliative care or hospice before death. Single- vs multiple-fraction radiotherapy should have been considered in 28 veterans with bone metastasis, but none were offered this option. CONCLUSIONS AND RELEVANCE: These care gaps reflect important targets for improving the patient and family experience of cancer care.

Entities:  

Mesh:

Year:  2013        PMID: 24126685     DOI: 10.1001/jamainternmed.2013.10797

Source DB:  PubMed          Journal:  JAMA Intern Med        ISSN: 2168-6106            Impact factor:   21.873


  15 in total

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3.  Variations in Oncologist Recommendations for Chemotherapy for Stage IV Lung Cancer: What Is the Role of Performance Status?

Authors:  Diana Tisnado; Jennifer Malin; Katherine Kahn; Mary Beth Landrum; Robert Fletcher; Carrie Klabunde; Steven Clauser; Selwyn O Rogers; Nancy L Keating
Journal:  J Oncol Pract       Date:  2016-06-07       Impact factor: 3.840

4.  It is possible: quality measurement during serious illness.

Authors:  Melissa D Aldridge; Diane E Meier
Journal:  JAMA Intern Med       Date:  2013 Dec 9-23       Impact factor: 21.873

5.  Development and Feasibility of a Structured Goals of Care Communication Guide.

Authors:  David B Bekelman; Rachel Johnson-Koenke; Sangeeta C Ahluwalia; Anne M Walling; Jamie Peterson; Rebecca L Sudore
Journal:  J Palliat Med       Date:  2017-04-19       Impact factor: 2.947

6.  Association of Early Patient-Physician Care Planning Discussions and End-of-Life Care Intensity in Advanced Cancer.

Authors:  Sangeeta C Ahluwalia; Diana M Tisnado; Anne M Walling; Sydney M Dy; Steven M Asch; Susan L Ettner; Benjamin Kim; Philip Pantoja; Hannah C Schreibeis-Baum; Karl A Lorenz
Journal:  J Palliat Med       Date:  2015-07-17       Impact factor: 2.947

7.  Palliative Care Specialist Consultation Is Associated With Supportive Care Quality in Advanced Cancer.

Authors:  Anne M Walling; Diana Tisnado; Susan L Ettner; Steven M Asch; Sydney M Dy; Philip Pantoja; Martin Lee; Sangeeta C Ahluwalia; Hannah Schreibeis-Baum; Jennifer L Malin; Karl A Lorenz
Journal:  J Pain Symptom Manage       Date:  2016-07-09       Impact factor: 3.612

8.  Face-validation of quality indicators for the organization of palliative care in hospitals in Indonesia: a contribution to quality improvement.

Authors:  Christantie Effendy; Kris Vissers; Kathrin Woitha; Jasper van Riet Paap; Sunaryadi Tejawinata; Myrra Vernooij-Dassen; Yvonne Engels
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9.  Improving Care With a Portfolio of Physician-Led Cancer Quality Measures at an Academic Center.

Authors:  Julie Bryar Porter; Eben Lloyd Rosenthal; Marcy Winget; Andrea Segura Smith; Sridhar Belavadi Seshadri; Yohan Vetteth; Eileen F Kiamanesh; Amogh Badwe; Ranjana H Advani; Mark K Buyyounouski; Steven Coutre; Frederick Dirbas; Vasu Divi; Oliver Dorigo; Kristen N Ganjoo; Laura J Johnston; Lawrence David Recht; Joseph B Shrager; Eila C Skinner; Susan M Swetter; Brendan C Visser; Douglas W Blayney
Journal:  J Oncol Pract       Date:  2017-07-20       Impact factor: 3.840

10.  Factors Associated with Family Reports of Pain, Dyspnea, and Depression in the Last Year of Life.

Authors:  Adam E Singer; Daniella Meeker; Joan M Teno; Joanne Lynn; June R Lunney; Karl A Lorenz
Journal:  J Palliat Med       Date:  2016-07-25       Impact factor: 2.947

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