159252 Cardiometabolic risk factors and healthcare cost for a sample of health plan members

Wednesday, November 7, 2007: 2:45 PM

Sarah J. Beaton, PhD , Lovelace Clinic Foundation, Albuquerque, NM
Scott B. Robinson, MA, MPH , Lovelace Clinic Foundation, Albuquerque, NM
Ann Von Worley, RN, BSHS , Lovelace Clinic Foundation, Albuquerque, NM
Herbert T. Davis, PhD , Lovelace Clinic Foundation, Albuquerque, NM
Audra Boscoe, PhD , United BioSource Corporation, Bethesda, MD
Rami Ben-Joseph, PhD , sanofi-aventis, Bridgewater, NJ
Lynn J. Okamoto, PharmD , United BioSource Corporation, Bethesda, MD
Cardiometabolic Risk Factors (CMRFs) are a set of risk factors which, when occurring together, increase a patient's chance for developing diabetes, heart disease, or stroke. Study objectives were to understand and quantify the prevalence and healthcare cost of CMRFs for female Hispanic and non-Hispanic health plan members in a Health Maintenance Organization located in southwestern US. This study used a retrospective database design to determine the prevalence of 6 different groupings of CMRFs among 2578 females (27.6% Hispanic) who had a bone mineral density test during 2003-2004. This population was selected since these patients had, in addition to their DEXA results, an electronic measure of height and weight, allowing us to calculate BMI. The presence of one or more of the following risk factors was used to define CMRF groupings: obesity (measured using BMI), triglycerides, HDL, blood pressure, and fasting glucose. Study analyses identified differences between cohorts of individuals with CMRFs and controls with respect to prevalence and healthcare costs. Generalized linear models were utilized to analyze adjusted costs associated with CMRFs. Results showed that Hispanics had significantly higher prevalence rates compared to non-Hispanics across all CMRF groupings (65.8% vs. 52.3%, respectively, met inclusion criteria for at least one of the 6 CMRF groupings). After adjusting for age and ethnicity, patients with CMRFs had significantly higher total costs (including inpatient, outpatient, emergency, and pharmacy utilization) than controls (p-values < .0001 across all risk groupings). Adjusted mean total costs for patients with CMRFs ranged from $3,923 to $6,056 vs. $3,203 to $3,488 for controls. Further cost analyses showed non-Hispanics had higher costs than Hispanics for all 6 risk groupings (F-values ranged from 5.11 to 6.70, p < .02 in all cases). The adjusted mean total costs for Hispanics ranged from $3130 to $4011 vs. $3648 to $4660 for non-Hispanics, with higher costs for both ethnicities where one of the risk factors was diabetes. Our higher CMRF prevalence rates among female Hispanics compared to non-Hispanics are consistent with earlier studies. The higher cost for those with CMRFs suggests the need for HMOs to address identification and monitoring of patients with CMRFs. Higher costs for non-Hispanics in the face of higher Hispanic CMRF prevalence may indicate under-utilization of healthcare resources for Hispanics. Future research should explore cultural diversity as it relates to CMRFs, including differences between Hispanics and non-Hispanics in access to care and disease management programs.

Learning Objectives:
1. Recognize cardiometabolic risk factors. 2. Identify prevalence and cost of cardiometabolic risk for a sample of health plan members. 3. Discuss differences between Hipanic and non-Hispanic patients with respect to cardiometabolic risk factors.

Keywords: Health Risks, Cost Issues

Presenting author's disclosure statement:

Any relevant financial relationships? Yes

Name of Organization Clinical/Research Area Type of relationship
United BioSource Corp Health Outcomes Independent Contractor (contracted research and clinical trials) and Lovelace Clinic Foundation subcontracted with United BioSource on a retrospective data project which was funded by sanofi-aventis

Any company-sponsored training? No
Any institutionally-contracted trials related to this submission? Yes
Have you received salary support, retainer, or other monies to support your position as part of the research/clinical trials? Yes
Have you served as the Principal Investigator) for the research/clinical trials? Yes
Have the results of your research/clinical trials been published? No

I agree to comply with the American Public Health Association Conflict of Interest and Commercial Support Guidelines, and to disclose to the participants any off-label or experimental uses of a commercial product or service discussed in my presentation.