Melissa Lingohr-Smith
Bristol-Myers Squibb
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Publication
Featured researches published by Melissa Lingohr-Smith.
Current Medical Research and Opinion | 2016
Steve Deitelzweig; Amanda Bruno; Jeffrey Trocio; Natalie Tate; Kiran Gupta; Jay Lin; Melissa Lingohr-Smith
Abstract Objective: Clinical trials have demonstrated that direct oral anticoagulants (DOACs) are efficacious in reducing stroke risk among patients with nonvalvular atrial fibrillation (NVAF) with differences in the reduction of bleeding risks vs. warfarin. The objective of this study was to assess bleeding-related hospital readmissions among hospitalized NVAF patients treated with dabigatran, rivaroxaban, and apixaban in the US. Research design and methods: Patients (≥18 years) with a discharge diagnosis of NVAF who received apixaban, dabigatran, or rivaroxaban during hospitalization were identified from the Premier Hospital database (1 January 2012–31 March 2014) and the Cerner Health Facts hospital database (1 January 2012–31 August 2014). Patients identified from each database were analyzed separately and grouped into three cohorts depending on which DOAC was received. Patient characteristics, hospital resource use and costs, and frequency of readmissions within 1 month were evaluated. Results: Among study populations identified from the Premier database (N = 74,730) and the Cerner database (N = 14,201), patients who received apixaban were older, had greater comorbidity, and had higher stroke and bleeding risks. After controlling for patient characteristics, including comorbidity and stroke and bleeding risks, compared with patients who received apixaban during their index hospitalizations, the odds of bleeding-related hospital readmissions were significantly greater by 1.4-fold (p < 0.01) for patients who received rivaroxaban and 1.2-fold (p = 0.16) numerically greater for patients who received dabigatran among patients identified from the Premier Hospital database. Among patients in the Cerner Health Facts hospital database, bleeding-related hospital readmissions were significantly greater by 1.6-fold (p = 0.04) for patients who received rivaroxaban and 1.3-fold (p = 0.30) numerically greater for patients who received dabigatran compared to patients who received apixaban. Limitations: No causal relationship between treatment and outcomes can be concluded. Conclusions: NVAF patients using different DOACs had different characteristics, including stroke and bleeding risks. Use of rivaroxaban, compared to apixaban was associated with significantly greater risk of bleeding-related readmissions across two database claims analyses.
Journal of Medical Economics | 2015
Alpesh Amin; Amanda Bruno; Jeffrey Trocio; Jay Lin; Melissa Lingohr-Smith
Abstract Objective: Medical costs that may be avoided when any of the four new oral anticoagulants (NOACs), dabigatran, rivaroxaban, apixaban, and edoxaban, are used instead of warfarin for the treatment of non-valvular atrial fibrillation (NVAF) were estimated and compared. Additionally, the overall differences in medical costs were estimated for NVAF and venous thromboembolism (VTE) patient populations combined. Methods: Medical cost differences associated with NOAC use vs warfarin or placebo among NVAF and VTE patients were estimated based on clinical event rates obtained from the published trial data. The clinical event rates were calculated as the percentage of patients with each of the clinical events during the trial periods. Univariate and multivariate sensitivity analyses were conducted for the medical-cost differences determined for NVAF patients. A hypothetical health plan population of 1 million members was used to estimate and compare the combined medical-cost differences of the NVAF and VTE populations and were projected in the years 2015–2018. Results: In a year, the medical-cost differences associated with NOAC use instead of warfarin were estimated at −
Journal of Medical Economics | 2014
Alpesh Amin; Yonghua Jing; Jeffrey Trocio; Jay Lin; Melissa Lingohr-Smith; John Graham
204, −
Current Medical Research and Opinion | 2017
Steven Deitelzweig; Xuemei Luo; Kiran Gupta; Jeffrey Trocio; Jack Mardekian; Tammy Curtice; Melissa Lingohr-Smith; Brandy Menges; Jay Lin
140, −
Clinical and Applied Thrombosis-Hemostasis | 2016
Alpesh Amin; Amanda Bruno; Jeffrey Trocio; Jay Lin; Melissa Lingohr-Smith
495, and −
Journal of Hematology and Thromboembolic Diseases | 2015
Alpesh Amin; Melissa Lingohr-Smith; Amanda Bruno; Jeffrey Trocio; Jay Lin
340 per patient for dabigatran, rivaroxaban, apixaban, and edoxaban, respectively. In 2014, among the hypothetical population, the medical-cost differences were −
Journal of Medical Economics | 2017
Elias Jabbour; Jay Lin; Lisa R. Siegartel; Melissa Lingohr-Smith; Brandy Menges; Dinara Makenbaeva
3.7, −
Journal of Managed Care Pharmacy | 2017
Steven Deitelzweig; Xuemei Luo; Kiran Gupta; Jeffrey Trocio; Jack Mardekian; Tammy Curtice; Melissa Lingohr-Smith; Brandy Menges; Jay Lin
4.2, −
Current Medical Research and Opinion | 2016
Steve Deitelzweig; Michael Evans; Eric Hillson; Jeffrey Trocio; Amanda Bruno; Wilson Tan; Melissa Lingohr-Smith; Prianka Singh; Jay Lin
11.5, and −
Journal of Dermatological Treatment | 2018
Jashin J. Wu; Steven R. Feldman; Shipra Rastogi; Brandy Menges; Melissa Lingohr-Smith; Jay Lin
6.6 million for NVAF and acute VTE patients treated with dabigatran, rivaroxaban, apixaban, and edoxaban, respectively. In 2014, for the combined NVAF, acute VTE, and extended VTE patient populations, medical-cost differences were −