Eric T. Edgell
Eli Lilly and Company
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Featured researches published by Eric T. Edgell.
PharmacoEconomics | 2003
Leah Kleinman; Ana Lowin; Emuella Flood; Gian Gandhi; Eric T. Edgell; Dennis A. Revicki
AbstractBipolar disorder is a chronic affective disorder that causes significant economic burden to patients, families and society. It has a lifetime prevalence of approximately 1.3%. Bipolar disorder is characterised by recurrent mania or hypomania and depressive episodes that cause impairments in functioning and health-related quality of life. Patients require acute and maintenance therapy delivered via inpatient and outpatient treatment. Patients with bipolar disorder often have contact with the social welfare and legal systems; bipolar disorder impairs occupational functioning and may lead to premature mortality through suicide.This review examines the symptomatology of bipolar disorder and identifies those features that make it difficult and costly to treat. Methods for assessing direct and indirect costs are reviewed. We report on comprehensive cost studies as well as administrative claims data and program evaluations. The majority of data is drawn from studies conducted in the US; however, we discuss European studies when appropriate.Only two comprehensive cost-of-illness studies on bipolar disorder, one prevalence-based and one incidence-based, have been reported. There are, however, several comprehensive cost-of-illness studies measuring economic burden of affective disorders including bipolar disorder. Estimates of total costs of affective disorders in the US range from
PharmacoEconomics | 1999
S.H. Hamilton; Dennis A. Revicki; Eric T. Edgell; Laura A. Genduso; Gary D. Tollefson
US30.4–43.7 billion (1990 values). In the prevalence-based cost-of-illness study on bipolar disorder, total annual costs were estimated at
International Clinical Psychopharmacology | 2000
S.H. Hamilton; Eric T. Edgell; D. A. Revicki; Alan Breier
US45.2 billion (1991 values). In the incidence-based study, lifetime costs were estimated at
Acta Psychiatrica Scandinavica | 2005
Josep Maria Haro; Eric T. Edgell; Diego Novick; Jordi Alonso; L. Kennedy; Peter B. Jones; Mark Ratcliffe; A. Breier
US24 billion.Although there have been recent advances in pharmacotherapy and outpatient therapy, hospitalisation still accounts for a substantial portion of the direct costs. A variety of outpatient services are increasingly important for the care of patients with bipolar disorder and costs in this area continue to grow.Indirect costs due to morbidity and premature mortality comprise a large portion of the cost of illness. Lost workdays or inability to work due to the disease cause high morbidity costs. Intangible costs such as family burden and impaired health-related quality of life are common, although it has proved difficult to attach monetary values to these costs.
Value in Health | 2008
Jeonghoon Ahn; Jeffrey S. McCombs; Changun Jung; Tim Croudace; David P. McDonnell; Haya Ascher-Svanum; Eric T. Edgell; Lizheng Shi
AbstractObjective: The purpose of this study was to compare, from the payor perspective, the clinical and economic outcomes of olanzapine to those of haloperidol for the treatment of schizophrenia. Design and setting: Clinical, quality-of-life and resource utilisation data were prospectively collected for US-residing patients with schizophrenia who were participating in a multicentre, randomised, double-blind clinical trial comparing olanzapine and haloperidol. Direct medical costs were estimated by assigning standardised prices (1995 values) to the resource utilisation data. Patients and participants: 817 patients with schizophrenia who had a baseline Brief Psychiatric Rating Scale score (BPRS) ≥18 (items scored 0 to 6) and/or were no longer tolerating current antipsychotic therapy. Interventions: Olanzapine 5 to 20 mg/day (n = 551) or haloperidol 5 to 20 mg/day (n = 266) for 6 weeks. Patients showing a predefined level of clinical response entered a 46-week maintenance phase. Main outcome measures and results: After acute treatment, BPRS-based clinical improvements were seen in 38 and 27% of olanzapine and haloperidol patients, respectively (p = 0.002). Clinically important improvements on the Quality of Life Scale were achieved during acute treatment in 33% of olanzapine recipients and 25% of haloperidol recipients (p = 0.094). Olanzapine treatment in the acute phase led to significantly lower inpatient (
Acta Psychiatrica Scandinavica | 2005
Martin Lambert; Josep Maria Haro; Diego Novick; Eric T. Edgell; L. Kennedy; Mark Ratcliffe; Dieter Naber
US5125 vs
International Clinical Psychopharmacology | 2002
Lizheng Shi; M. Namjoshi; Fan Zhang; G. Gandhi; Eric T. Edgell; Mauricio Tohen; Alan Breier; Josep Maria Haro
US5795, p = 0.038) and outpatient (
PharmacoEconomics | 2000
Eric T. Edgell; Scott W. Andersen; Bryan M. Johnstone; Brian Dulisse; Dennis A. Revicki; Alan Breier
US663 vs
International Clinical Psychopharmacology | 2005
Isabelle Gasquet; Josep Maria Haro; Diego Novick; Eric T. Edgell; Liam Kennedy; Jean Pierre Lepine
US692, p = 0.001) costs, resulting in a significant overall reduction in mean total medical costs of
Acta Psychiatrica Scandinavica | 2003
Luis Prieto; Diego Novick; José Antonio Sacristán; Eric T. Edgell; Jordi Alonso
US388 (p = 0.033). This significant reduction in total costs was found despite olanzapine mean medication costs being significantly greater than haloperidol medication costs (