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1.
Med Care ; 47(1): 129-33, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19106742

ABSTRACT

BACKGROUND: Black patients are more likely than white patients to prefer and receive more life-sustaining interventions in advanced stages of disease. However, little is known about potential racial differences in use of mechanical ventilation (MV), and the newer modality of noninvasive ventilation (NIV), in treatment of chronic obstructive pulmonary disease (COPD). OBJECTIVE: To determine if rates of MV and NIV use differ among black and white patients admitted to Veterans Administration (VA) hospitals for COPD exacerbation. RESEARCH DESIGN: Retrospective cohort analysis of VA database FY2003 to FY2005 including 153 hospitals nationwide. SUBJECTS: All black (n = 479) and white (n = 31,537) patients admitted with COPD exacerbation. MEASURES: Ventilation use during hospitalization as identified by ICD-9-CM codes for MV and NIV. Hierarchical logistic regression compared rates of MV or NIV use among black and white patients, adjusting for patient characteristics and accounting for hospital-level variation. RESULTS: Unadjusted rates of MV were higher in black patients than in white patients (4.1% vs. 3.0%; P < 0.001), but similar for NIV (6.0% vs. 6.1%; P = 0.65). The adjusted odds of MV for black patients relative to white patients remained higher (OR = 1.27, 95% CI: 1.01-1.54; P < 0.01) while the adjusted odds of NIV remained similar (OR = 0.94, 95% CI: 0.82-1.08; P = 0.38). CONCLUSIONS: Black patients with COPD exacerbation in VA hospitals are more likely than white patients to receive MV, and this difference is not explained by available clinical or demographic variables. By contrast, black and white patients are equally likely to receive NIV. These findings suggest that unmeasured factors, such as patient preferences or disease severity, may be affecting the use of MV in this setting and therefore warrant further investigation.


Subject(s)
Black or African American/statistics & numerical data , Continuous Positive Airway Pressure/statistics & numerical data , Healthcare Disparities , Hospitals, Veterans/standards , Life Support Care/statistics & numerical data , Pulmonary Disease, Chronic Obstructive/ethnology , Pulmonary Disease, Chronic Obstructive/therapy , Respiration, Artificial/statistics & numerical data , Respiratory Insufficiency/ethnology , Respiratory Insufficiency/therapy , White People/statistics & numerical data , Age Factors , Aged , Cohort Studies , Databases, Factual , Female , Health Services Accessibility , Humans , Male , Middle Aged , Pulmonary Disease, Chronic Obstructive/physiopathology , Quality of Health Care , Respiratory Insufficiency/etiology , Sex Factors , United States , United States Department of Veterans Affairs/standards
2.
Am J Hosp Palliat Care ; 25(6): 501-11, 2008.
Article in English | MEDLINE | ID: mdl-19106284

ABSTRACT

Goals of care are often mentioned as an important component of end-of-life discussions, but there are diverse assessments regarding the type and number of goals that should be considered. To address this lack of consensus, we searched MEDLINE (1967-2007) for relevant articles and identified the number, phrasing, and type of goals they addressed. An iterative process of categorization resulted in a list of 6 practical, comprehensive goals: (1) be cured, (2) live longer, (3) improve or maintain function/quality of life/ independence, (4) be comfortable, (5) achieve life goals, and (6) provide support for family/caregiver. These goals can be used to articulate goal-oriented frameworks to guide decision making toward the end of life and thereby harmonize patients' treatment choices with their values and medical conditions.


Subject(s)
Goals , Patient Care Planning/organization & administration , Terminal Care/organization & administration , Activities of Daily Living/psychology , Advance Care Planning , Attitude to Death , Communication , Decision Making , Family/psychology , Humans , Interpersonal Relations , Life Support Care , Longevity , Pain/etiology , Pain/prevention & control , Patient Participation , Patient-Centered Care/organization & administration , Quality of Life/psychology , Social Support , Spirituality , Terminal Care/psychology
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