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Published on: September 30, 2021
A haemophilia treatment centre-administered disease management programme in patients with bleeding disorders
T Tencer1, C Roberson, N Duncan
1University of Southern California, Department of Clinical Pharmacy and Pharmaceutical Economics and Policy, Los Angeles, CA, USA.
Insights
This disease management program for bleeding disorders reduced healthcare costs and resource use, including fewer hospitalizations and ER visits. Further research is needed due to the small sample size.
Area of Science:
- Hematology
- Health Services Research
Background:
- Bleeding disorders, such as hemophilia, require comprehensive management.
- Indiana's high-risk insurance plan covers a population with significant healthcare needs.
Purpose of the Study:
- To describe a disease management program (DMP) for bleeding disorder patients.
- To assess the costs and outcomes associated with this DMP.
Main Methods:
- A pre/post-intervention study design was employed.
- Claims and medical records data were analyzed for 31 patients over two years.
- Key metrics included hospitalizations, ER visits, medical costs, and clotting factor utilization.
Main Results:
- Total healthcare costs decreased from $161,441 to $118,293 in the first year of the DMP.
- Inpatient hospital days and ER visits significantly decreased.
- Reductions were attributed to lower factor utilization and costs, but were not statistically significant due to small sample size.
Conclusions:
- The disease management program demonstrated a potential to reduce costs and resource utilization for bleeding disorder patients.
- The study was underpowered to establish statistical significance, highlighting the need for larger investigations.
Abstract:
The objective of this study is to describe a disease management programme (DMP) for the bleeding disorder population insured by Indiana's high-risk insurance plan, and to assess the associated costs and outcomes. All bleeding disorder patients, covered by the state plan as their primary health insurance, were enrolled into a DMP administered by the Indiana Hemophilia & Thrombosis Center (IHTC). A pre/post-intervention study design was used, with 1-year pre-enrollment serving as the baseline period and 1-year post-enrollment as the study period. Claims data were used to assess hospitalizations, emergency room (ER) visits, total medical and clotting factor costs and factor units dispensed. Medical records were used to assess disease severity and other comorbidities. Thirty-one continuously enrolled patients had complete data over 2 years. Approximately 84% of the population was male, 81% with haemophilia. The average costs of care in the baseline year and the first year of the programme were $161 441 and $118 293, respectively. The decrease in the total costs was primarily attributed to a decrease in outpatient factor costs, which resulted from decreased factor utilization and lower per unit factor costs. The mean number of inpatient hospital days and ER visits for the DMP population decreased from 1.3 and 1.4 to 0.4 and 0.6, baseline and first year, respectively. Owing to the small sample size and high variability of the population, the differences were not statistically significant. The DMP appears to have reduced the total costs and resource utilization, although the study was underpowered.
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