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Dive into the research topics where Ashwini Shewade is active.

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Featured researches published by Ashwini Shewade.


International Review of Psychiatry | 2013

Clinical validity of cytochrome P450 metabolism and serotonin gene variants in psychiatric pharmacotherapy

C. Anthony Altar; John Hornberger; Ashwini Shewade; Victor Cruz; Jill Garrison; David A. Mrazek

Abstract Adverse events, response failures and medication non-compliance are common in patients receiving medications for the treatment of mental illnesses. A systematic literature review assessed whether pharmacokinetic (PK) or pharmacodynamic (PD) responses to 26 commonly prescribed antipsychotic and antidepressant medications, including efficacy or side effects, are associated with nucleotide polymorphisms in eight commonly studied genes in psychiatric pharmacotherapy: CYP2D6, CYP2C19, CYP2C9, CYP1A2, CYP3A4, HTR2C, HTR2A, and SLC6A4. Of the 294 publications included in this review, 168 (57%) showed significant associations between gene variants and PK or PD outcomes. Other studies that showed no association often had insufficient control for confounding variables, such as co-medication use, or analysis of medications not substrates of the target gene. The strongest gene–outcome associations were for the PK profiles of CYP2C19 and CYP2D6 (93% and 90%, respectively), for the PD associations between HTR2C and weight gain (57%), and for SLC6A4 and clinical response (54%), with stronger SLC6A4 response associations for specific drug classes (60–83%). The preponderance of evidence supports the validity of analyzing nucleotide polymorphisms in CYP and pharmacodynamic genes to predict the metabolism, safety, or therapeutic efficacy of psychotropic medications commonly used for the treatment of depression, schizophrenia, and bipolar illness.


Leukemia & Lymphoma | 2012

Cost-effectiveness of adding rituximab to fludarabine and cyclophosphamide for the treatment of previously untreated chronic lymphocytic leukemia

John Hornberger; Carolina Reyes; Ashwini Shewade; Susan Lerner; Mark Friedmann; Leona C. Han; Hialy Gutierrez; Sacha Satram-Hoang; Michael J. Keating

Abstract A recent phase III trial demonstrated improved progression-free survival (PFS) and overall survival (OS) associated with adding rituximab to fludarabine and cyclophosphamide (R-FC) compared to FC in treatment of previously untreated chronic lymphocytic leukemia (CLL). A cost-effectiveness analysis of R-FC over FC was performed from a US third-party payer perspective over a lifetime horizon in the base case. One-way, two-way and probabilistic sensitivity analyses were conducted to assess the robustness of the results. A secondary analysis was performed by also considering a societal perspective. R-FC was associated with an incremental 1.15 quality-adjusted life-years (QALYs) compared to FC and resulted in an incremental cost-effectiveness ratio of


Journal of The International Association of Physicians in Aids Care (jiapac) | 2009

Obstacles and proposed solutions to effective antiretroviral therapy in resource-limited settings.

John A. Bartlett; John Hornberger; Ashwini Shewade; Menaka Bhor; Rukmini Rajagopalan

23 530 per QALY in the base case and


Leukemia & Lymphoma | 2012

Cost-effectiveness of rituximab as maintenance therapy in patients with follicular non-Hodgkin lymphoma after responding to first-line rituximab plus chemotherapy.

John Hornberger; Rebecca Chien; Mark Friedmann; Leona C. Han; Ashwini Shewade; Sacha Satram-Hoang; Carolina Reyes

31 513 per QALY considering a societal perspective. Results were most sensitive to time horizon, discount rate and unit drug cost for rituximab. Within the limitations of modeling long-term outcomes, R-FC is cost-effective for previously untreated CLL.


Population Health Management | 2014

Health Care Coverage Decision Making in Low- and Middle-Income Countries: Experiences from 25 Coverage Schemes.

Hialy Gutierrez; Ashwini Shewade; Minghan Dai; Pedro Mendoza-Arana; Octavio Gómez-Dantés; Nishant Jain; Irma Khonelidze; Juliet Nabyonga-Orem; Karima Saleh; Yot Teerawattananon; Sania Nishtar; John Hornberger

More than 3 million people were receiving antiretroviral therapy (ART) at the end of 2007, but this number represents only 31% of people clinically eligible for ART in resource-limited settings. The primary objective of this study is to summarize the key obstacles that impede the goal of universal access prevention, care, and treatment. We performed a systematic literature search to review studies that reported barriers to diagnosis and access to treatment of HIV/AIDS in resource-limited countries. Persons living with HIV/ AIDS commonly face economic, sociocultural, and behavioral obstacles to access treatment and care for HIV. A variety of programs to overcome these barriers have been implemented, including efforts to destigmatize HIV/AIDS, enhance treatment literacy, provide income-generation skills, decentralize HIV services, promote gender equality, and adopt a multisectoral approach to optimize limited resources. An understanding of these obstacles and suggested methods to overcome them must be addressed by global policy makers before universal ART access can be achieved.


Value in Health | 2013

Cost-Effectiveness of Gene-Expression Profiling for Tumor-Site Origin

John Hornberger; Irina Degtiar; Hialy Gutierrez; Ashwini Shewade; W. David Henner; Shawn Becker; Gauri Varadachary; Stephen S. Raab

Abstract A recent phase III trial demonstrated that maintenance rituximab® therapy after response to first-line treatment with rituximab plus chemotherapy (R-chemo) increases progression-free survival (PFS) for follicular non-Hodgkin lymphoma (f-NHL). A cost-effectiveness analysis of R-maintenance versus observation was conducted from a US payer perspective to estimate PFS and overall survival (OS) over a representative patients lifetime. Primary outcomes were cost per life-year gained (LYG) and cost per quality-adjusted life-year (QALY) gained. Compared with observation, R-maintenance increased mean PFS by 1.50 years, OS by 1.21 years and QALYs gained by 1.11 years. The incremental cost of maintenance therapy was


Advances in Therapy | 2010

Broadening the perspective when assessing evidence on boosted protease inhibitor-based regimens for initial antiretroviral therapy

John Hornberger; Kit N. Simpson; Ashwini Shewade; Birgitta Dietz; Robert W. Baran; Thomas Podsadecki

38 545. The costs per LYG and QALY gained were


Clinical Cancer Research | 2012

Abstract B9: Cost effectiveness of gene expression profiling for tumor site origin

John Hornberger; Irina Degtiar; Hialy Gutierrez; Ashwini Shewade; W. David Henner; Shawn Becker; Stephen S. Raab

31 934 and


Value in Health | 2013

Erratum: Cost-effectiveness of gene-expression profiling for tumor-site origin (Value in Health 16:1 (46-56))

John Hornberger; Irina Degtiar; Hialy Gutierrez; Ashwini Shewade; W. David Henner; Shawn Becker; Gauri R. Varadhachary; Stephen S. Raab

34 842, respectively. Within the limitations of modeling long-term outcomes, R-maintenance therapy in patients who received R-chemo for previously untreated f-NHL compared with observation alone after R-chemo for first-line treatment for f-NHL is cost-effective from the US payer perspective.


Value in Health | 2011

PHP105 HOW ARE COVERAGE DECISIONS MADE IN PUBLICLY FUNDED HEALTH CARE PROGRAMS IN LOW- AND MIDDLE-INCOME COUNTRIES?

John Hornberger; Ashwini Shewade; Hialy Gutierrez

Lessons learned by countries that have successfully implemented coverage schemes for health services may be valuable for other countries, especially low- and middle-income countries (LMICs), which likewise are seeking to provide/expand coverage. The research team surveyed experts in population health management from LMICs for information on characteristics of health care coverage schemes and factors that influenced decision-making processes. The level of coverage provided by the different schemes varied. Nearly all the health care coverage schemes involved various representatives and stakeholders in their decision-making processes. Maternal and child health, cardiovascular diseases, cancer, and HIV were among the highest priorities guiding coverage development decisions. Evidence used to inform coverage decisions included medical literature, regional and global epidemiology, and coverage policies of other coverage schemes. Funding was the most commonly reported reason for restricting coverage. This exploratory study provides an overview of health care coverage schemes from participating LMICs and contributes to the scarce evidence base on coverage decision making. Sharing knowledge and experiences among LMICs can support efforts to establish systems for accessible, affordable, and equitable health care.

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