Lesley-Ann Miller
West Virginia University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Lesley-Ann Miller.
Annals of Pharmacotherapy | 2007
Mariam Hassan; Suresh Madhavan; Iftekhar Kalsekar; Eugene H. Makela; Kitty Rajagopalan; Syed S. Islam; Jan Kavookjian; Lesley-Ann Miller
Background: Medication nonadherence is a significant problem among patients with bipolar disorder. Objective: To compare adherence and persistence among patients with bipolar disorder initiated on antipsychotics in a state Medicaid system over a 12 month follow-up period. Methods: Claims data for patients with bipolar disorder from a de-identified Medicaid database were examined. Patients were classified into 4 monotherapy treatment groups (risperidone, olanzapine, quetiapine, or typical antipsychotic) based on the first prescription filled between January 1, 1999, and December 31, 2001. Adherence and persistence were analyzed over a 12 month follow-up period. Adherence was measured using the Medication Possession Ratio (MPR). Persistence was defined as the total number of days from the initiation of treatment to therapy modification (ie, discontinuation, switching, or combination with another antipsychotic). Adjustment for confounding variables was undertaken using ordinary least-squares and Cox proportional hazard regression modeling. Results: The mean MPRs were 0.68 for risperidone (n = 231), 0.68 for olanzapine (n = 283), 0.71 for quetiapine (n = 106), and 0.46 for typical antipsychotics (n = 205). Patients initiated on typical antipsychotics were 23.6% less adherent than patients initiated on risperidone (p < 0.001). Mean persistence (days) was 194.8 for risperidone, 200.9 for olanzapine, 219.8 for quetiapine, and 179.2 for typical antipsychotics. Extended Cox regression modeling indicated no significant differences between antipsychotics in hazards of therapy modification within 250 days of initiation. However, patients initiated on typical antipsychotics were 5.2 times more likely to modify therapy compared with those initiated on risperidone after 250 days of antipsychotic therapy (p < 0.001). Conclusions: Adherence and persistence were similar between atypical antipsychotic groups. The typical antipsychotic group, however, demonstrated lower adherence and a greater likelihood of patients modifying therapy compared with the risperidone cohort
Current Medical Research and Opinion | 2010
Lesley-Ann Miller; Rolin Wade; Dingwei Dai; Mark J. Cziraky; Krishnan Ramaswamy; Sumeet Panjabi
Abstract Objective: To evaluate the cost effectiveness of achieving JNC 7 blood pressure goals with angiotensin II receptor blockers (ARBs). Research design and methods: Cost effectiveness of olmesartan, losartan, valsartan, and irbesartan was compared with real world patient chart and claims data from a large US health plan. Patients 18 and older with ≥2 claims for an ARB between May 1, 2002 and December 31, 2005 were identified from the claims database. Patients with a diagnosis of hypertension in the 6-month baseline period before the first (index) ARB claim and ARB-free during baseline were included. Medical charts were randomly sampled from the cohort of identified patients; effectiveness data were obtained from charts and linked to healthcare claims and costs. These data were used to populate the decision analytic model. Main outcome measures: All-cause and hypertension-attributable costs to achieve JNC 7 goals were measured. Comparisons were made within low and high-dose strata and pooled across ARB doses. Results: 121 472 patients were identified, and charts were randomly abstracted for 1600. Of these, 1293 patients were hypertensive at index. Baseline patient characteristics for the chart group were modestly different from the larger cohort. More patients treated with olmesartan (77.8%) than with losartan (66.5%), valasartan (68.8%), or irbesartan (68.8%) achieved JNC 7 BP goals. In pooled-dose comparisons, cost per patient reaching BP goal was
Journal of Clinical Epidemiology | 2009
Murali Sundaram; Michael J. Smith; Dennis A. Revicki; Betsy M. Elswick; Lesley-Ann Miller
8964 (all-cause) and
PharmacoEconomics | 2010
Murali Sundaram; Michael J. Smith; Dennis A. Revicki; Lesley-Ann Miller; Suresh Madhavan; Gerry Hobbs
2704 (hypertension-attributable) for olmesartan; compared with
Population Health Management | 2012
Pramit Nadpara; Suresh Madhavan; Rahul Khanna; Michael J. Smith; Lesley-Ann Miller
10 848 and
International journal of MS care | 2010
Vivek Pawar; Gauri Pawar; Lesley-Ann Miller; Iftekhar Kalsekar; Jan Kavookjian; Virginia Scott; Suresh Madhavan
3291 for losartan;
Journal of Managed Care Pharmacy | 2016
Lesley-Ann Miller; Stephen Stemkowski; Kim Saverno; Daniel Lane; Zhuliang Tao; Michelle D. Hackshaw; Bryan A. Loy
10 557 and
Expert Opinion on Pharmacotherapy | 2007
Lesley-Ann Miller; Anuja Roy; Reema Mody; Gerald M. Higa
3577 for valsartan; and
Annals of Pharmacotherapy | 2004
Iftekhar Kalsekar; Lesley-Ann Miller
13395 and
Journal of Managed Care Pharmacy | 2015
Anna O. D'Souza; Michael J. Smith; Lesley-Ann Miller; Joseph Doyle; Rinat Ariely
4325 for irbesartan, respectively. The trend was similar for the dose stratification analysis, except in the comparison between high-dose losartan and olmesartan, where losartan had a lower cost-effectiveness ratio. Conclusion: Overall olmesartan was the most effective and cost-saving treatment option compared to losartan, valsartan, and irbesartan for the achievement of JNC 7 BP goals in this managed-care population.