Rachael Sorg
Analysis Group
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Publication
Featured researches published by Rachael Sorg.
Journal of the American Geriatrics Society | 2013
Laurence C. Baker; Dendy Macaulay; Rachael Sorg; Melissa Diener; Scott J. Johnson; Howard G. Birnbaum
To evaluate mortality and healthcare utilization effects of an intervention that combined care management and telehealth, targeting individuals with congestive heart failure, chronic obstructive pulmonary disease, or diabetes mellitus.
Journal of Ophthalmic Inflammation and Infection | 2013
David S. Chu; Scott J. Johnson; U. Mallya; Matthew Davis; Rachael Sorg; Mei Sheng Duh
BackgroundThe purpose of this study was to describe comorbidities, healthcare costs, and resource utilization among patients with chronic non-infectious uveitis initiating corticosteroid, immunosuppressants, or biologics.In this retrospective cohort study, patients with a non-infectious uveitis diagnosis and continuous insurance coverage during a 6-month baseline were selected from a privately insured claims database with 80.7 million enrollees. Index dates were defined as the first prescription/administration of a corticosteroid, immunosuppressant, or biologic between 2003 and 2009. Comorbidities, healthcare costs, and utilization were analyzed in a per-member-per-month (PMPM) framework to account for varying between-patient treatment periods, defined as continuous medication use within the same class. Wilcoxon rank-sum and chi-square tests were used for comparisons of costs and categorical outcomes.ResultsPatients on corticosteroids (N = 4,568), immunosuppressants (N = 5,466), and biologics (N = 1,694) formed the study population. Baseline PMPM inpatient admission rates were 0.029 for patients on corticosteroids, 0.044 for patients on immunosuppressants, and 0.045 for patients on biologics (p < 0.001 immunosuppressants or biologics versus corticosteroids); during treatment, PMPM inpatient admissions increased to 0.044 and 0.048 for patients taking corticosteroids and immunosuppressants, respectively, but decreased to 0.024 for patients taking biologics (p < 0.001 versus corticosteroids and p = 0.003 versus immunosuppressants). Baseline average PMPM costs for patients taking corticosteroids, immunosuppressants, and biologics were US
Clinical Breast Cancer | 2012
Jipan Xie; Melissa Diener; Rachael Sorg; Eric Q. Wu; Madhav Namjoshi
935, US
Journal of Medical Economics | 2014
Jasmina I. Ivanova; Eleanor Hayes-Larson; Rachael Sorg; Howard G. Birnbaum; Todd Berner
1,738, and US
Journal of Comparative Effectiveness Research | 2015
James Signorovitch; Keith A. Betts; Yan Song; Rachael Sorg; Junlong Li; Ajay S Behl; Anupama Kalsekar
1,439 (p < 0.001 between groups), while on-treatment PMPM costs excluding drug costs increased to US
Clinical Therapeutics | 2015
T. Kim Le; Dendy Macaulay; Anupama Kalsekar; Yong Yuan; Rachael Sorg; Jin Wei; Eric Q. Wu
1,129 for patients taking corticosteroids but lowered to US
Gastroenterology | 2015
William J. Sandborn; Atsushi Sakuraba; A. Burak Ozbay; Rachael Sorg; William M. Reichmann; Jingdong Chao; Martha Skup
1,592 for patients taking immunosuppressants, and US
Journal of Medical Economics | 2013
Jipan Xie; Melissa Diener; Rachael Sorg; Eric Q. Wu; Madhav Namjoshi
918 for patients taking biologics (p < 0.001 versus corticosteroids or immunosuppressants).ConclusionsThere is significant economic burden associated with existing treatments of uveitis. Corticosteroids may be overused as a treatment for uveitis.
Ophthalmology | 2016
Andrew D. Dick; Namita Tundia; Rachael Sorg; Chen Zhao; Jingdong Chao; Avani Joshi; M Skup
BACKGROUND Results from a phase III clinical trial showed that denosumab significantly reduced the risk of first on-study and subsequent skeletal-related events (SREs) compared with zoledronic acid. This study aims to assess the cost-effectiveness of denosumab vs. zoledronic acid in the prevention of SREs in patients with advanced breast cancer and bone metastases. MATERIALS AND METHODS A Markov model was developed with 4-week model cycles and a 1-year time horizon. The health states were defined by SRE status (no SRE, first on-study SRE, subsequent SRE, no SRE but history of SRE) and SRE type (pathologic fracture, radiation to the bone, surgery to the bone, spinal cord compression). Costs (in 2011 US dollars) included drug, SRE treatment, and adverse event (AE) costs and were assessed from a third-party payer perspective. The primary outcome was incremental total cost per SRE avoided; the secondary outcome was incremental total cost per pathologic fracture avoided. One-way and probabilistic sensitivity analyses were used to assess the robustness of the model. RESULTS During the 1-year treatment period, denosumab incurred
Respiratory Medicine | 2013
Dendy Macaulay; Shawn X. Sun; Rachael Sorg; Sherry Y. Yan; G. De; Eric Q. Wu; Paul F. Simonelli
7522 higher costs (