Adi Eldar-Lissai
Analysis Group
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Publication
Featured researches published by Adi Eldar-Lissai.
Value in Health | 2008
Adi Eldar-Lissai; Leon E. Cosler; Eva Culakova; Gary H. Lyman
OBJECTIVES Neutropenia and its complications, including febrile neutropenia (FN), are a common side effect of cancer chemotherapy. Results of clinical trials showed that prophylactic use of granulocyte colony-stimulating factors (G-CSF) is effective in preventing FN. In this study, the cost effectiveness (measured as cost per quality-adjusted time [days]) of three treatment alternatives were evaluated: no G-CSF, filgrastim administered daily for 7-12 days after chemotherapy, and a pegylated form of G-CSF pegfilgrastim, administered once per cycle. METHODS A cost-utility model based on standard clinical practice of treating FN with immediate hospitalization or with ambulatory treatment, from a societal perspective was developed. Direct medical cost estimates for hospitalization were derived from claims data reported by 115 US academic medical centers. Indirect medical costs, productivity costs, probabilities, and utilities are based on published literature. Results were subjected to sensitivity analyses and 95% confidence intervals are based on a Monte Carlo simulation. RESULTS Mean estimated costs/day of hospitalization were
PharmacoEconomics | 2007
Leon E. Cosler; Adi Eldar-Lissai; Eva Culakova; Nicole M. Kuderer; David C. Dale; Jeffrey Crawford; Gary H. Lyman
1984 (SD
Journal of Medical Economics | 2012
Caroline Korves; Adi Eldar-Lissai; Joshua McHale; Marie-Hélène Lafeuille; S.H. Ong; Mei Sheng Duh
1040, N = 24,687) for surviving patients and
Journal of Cardiac Failure | 2014
Alan H. Gradman; Francis Vekeman; Adi Eldar-Lissai; Alex Trahey; S.H. Ong; Mei Sheng Duh
3139 (SD
Journal of Interprofessional Care | 2011
Lea Hagoel; Shelley Volz; Lia M. Palileo; Adi Eldar-Lissai; Celia C. Kamath; Elizabeth D. Cox
2014, N = 1437) for dying patients. Under baseline conditions, pegfilgrastim dominated both filgrastim and no G-CSF, with expected costs and effectiveness of
Cancer treatment and research | 2010
Adi Eldar-Lissai; Gary H. Lyman
4203 and 12.361 quality adjusted life-days (QALDs) for no G-CSF,
Journal of Cardiac Failure | 2015
Alan H. Gradman; Francis Vekeman; Adi Eldar-Lissai; Alex Trahey; Mei Sheng Duh; S.H. Ong
3058 and 12.967 QALDs for pegfilgrastim, and
Value in Health | 2013
Alan H. Gradman; Francis Vekeman; Adi Eldar-Lissai; Alex Trahey; P. Lacomte; S.H. Ong; Mei Sheng Duh
5264 and 12.698 QALDs for filgrastim. CONCLUSIONS This cost-utility analysis provides strong evidence that pegfilgrastim is not only cost-effective but also cost-saving in most common clinical and economic settings. There appear to be both clinical and economic benefits from prophylactic administration of pegfilgrastim.
Value in Health | 2012
Alan H. Gradman; Francis Vekeman; Adi Eldar-Lissai; Alex Trahey; S.H. Ong; Mei Sheng Duh
BackgroundThe prophylactic use of granulocyte colony-stimulating factors (G-CSFs) reduces the severity and duration of neutropenia and reduces the incidence of febrile neutropenia after cancer chemotherapy. However, the use of G-CSFs, particularly filgrastim, to treat established neutropenia remains controversial. A recent meta-analysis of randomised controlled trials (RCTs) evaluating G-CSF treatment for established febrile neutropenia demonstrated a reduction in prolonged hospitalisations. Because more than one-third of patients in the analysis were hospitalised for at least 10 days, this finding has broad pharmacoeconomic and clinical significance. This analysis presents the potential cost implications of G-CSF treatment for established neutropenia among hospitalised patients.MethodsDirect medical costs (
Value in Health | 2012
Adi Eldar-Lissai; Caroline Korves; R. Wei; H. Sharma; Kristina Chen; S.H. Ong; Mei Sheng Duh
US, year 2003 values) related to hospitalisation for established neutropenia were modelled using a hospital perspective and according to two treatment options: (i) no use of G-CSF during the neutropenic episode (control); and (ii) addition of daily G-CSF until neutrophil recovery. Within each option, we modelled the probability of a long stay (≥10 days) and patient survival. The model used three data sets: discharge data from a consortium of academic medical institutions, drug cost data (filgrastim) from Federal payers, and estimates of G-CSF efficacy derived from a meta-analysis of RCTs of treatment in patients with established febrile neutropenia. The lowest expected total cost was predicted for both treatment options; sensitivity analyses and Monte Carlo simulations were used to evaluate the robustness of the model.ResultsThe G-CSF arm produced the lowest expected cost, and predicted net estimated savings of