Effect of Practitioner Education on Adherence to Asthma Treatment Guidelines

Author:

Coleman Craig I1,Reddy Prabashni2,Laster-Bradley N Michelle3,Dorval Sheila4,Munagala Bharathi5,White C Michael6

Affiliation:

1. Craig I Coleman PharmD, Assistant Clinical Professor, Department of Pharmacy Practice, School of Pharmacy, University of Connecticut, Storrs, CT

2. Prabashni Reddy PharmD, Lead Pharmacoeconomist, Abt Associates Clinical Trials, Cambridge, MA

3. N Michelle Laster-Bradley PhD MS BS Pharm, Health Outcomes Scientist, ACS State Healthcare, Atlanta, GA; Affiliate Assistant Professor, Pharmacy Care Systems, School of Pharmacy, Auburn University, Auburn, AL

4. Sheila Dorval BSPharm, Health Program Supervisor, Department of Social Services, Hartford, CT

5. Bharathi Munagala MS, Lead Programmer, Health Information Designs, Auburn, AL

6. C Michael White PharmD, Assistant Professor, Department of Pharmacy Practice, School of Pharmacy, University of Connecticut, Storrs; Director, Clinical Pharmacology Research, Hartford Hospital, Hartford

Abstract

OBJECTIVE: To determine whether a letter-based intervention program submitted to prescribers and pharmacists would improve drug therapy in users of high-dose β2-agonists (HDBs). STUDY DESIGN: Retrospective drug utilization review. PATIENTS AND METHODS: The intervention group consisted of 135 asthmatic patients (identified through ICD-9-CM codes) in the Connecticut Medicaid Program who submitted >1 claim per month for short-acting β2-agonists (over a 6-mo period). Patient-specific intervention packets were mailed to the patients' prescribers and pharmacists, and their use of long-term control agents and healthcare utilization was evaluated over 6 months. These variables were compared with a comparison group (n = 510) of asthmatics drawn from the same Medicaid program who were not considered to be high-dose users of short-acting β2-agonists at baseline. RESULTS: Prior to the intervention, the intervention group used fewer long-term asthma control agents as compared with the comparison group (58% vs. 96%; p < 0.001); there was no significant difference after the intervention program (65% vs. 71%; p = 0.169). The acquisition of spacers was greater in the intervention group than in the control group after the intervention (7% vs. 2%; p = 0.007). At the end of the 6-month intervention period, 46% of patients in the intervention group were no longer HDB users (p < 0.001). The higher frequency of prescriber office visits in the intervention group than the comparison group before the intervention (0.46 ± 0.82 vs. 0.25 ± 0.66; p < 0.001) was not evident after the intervention program (0.24 ± 0.63 vs. 0.18 ± 0.60; p = 0.283). CONCLUSIONS: This intervention program had modest impact on improving the use of long-term control agents and reducing prescriber office visits.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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