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1.
Value Health ; 14(5 Suppl 1): S39-42, 2011.
Article in Spanish | MEDLINE | ID: mdl-21839897

ABSTRACT

UNLABELLED: Cost effectiveness of posaconazole versus fluconazole/itraconazole therapy in the prophylaxis against invasive fungal Infections among high-risk neutropenic patients in Mexico. OBJECTIVE: To estimate the cost effectiveness and long-term combined effects of Posaconazole versus fluconazole/itraconazole (standard azole) therapy in the prophylaxis against invasive fungal Infections among high-risk neutropenic patients in Mexico. METHODS: A previously validated Markov model was used to compare the projected lifetime costs and effects of two theoretical groups of patients, one receiving Posaconazole and the other receiving standard azole. The model estimates total costs, numbers of IFIs, and QALY per patient in each prophylaxis group. To extrapolate trial results to a lifetime horizon, the model was extended with one-month Markov cycles in which mortality risk is specific to the underlying disease. Data on the probabilities of IFI were obtained from Study Protocol PO1899. Drug costs were taken from average wholesale drug reports for 2009. Cost and health effects were discounted at 5% according to the Mexican guideline. The analysis was conducted from the Mexican healthcare perspective using 2008 unit cost prices. RESULTS: Our model projects an accumulated cost to the Mexican healthcare system per patient receiving the Posaconazol regimen of $US 5,634 compared to $US 7,463 for the standard azole regimen. The accumulated discounted effect is 3.13 LY or 2.25 QALYs per patient receiving Posaconazol, compared to 2.96 LY or 2.13 QALYs per patient receiving standard azole. Posaconazol remained the dominant strategy across each scenario. Probabilistic sensitivity analysis tested numerous assumptions about the model cost and efficacy parameters and found that the results were robust to most changes. CONCLUSION: Posaconazole provides modest incremental benefits compared with standard azole therapy in the prophylaxis against IFIs among high-risk neutropenic patients. Routine Posaconazole use appears a cost saving when the likelihood of IFIs or the cost of treatment medications is high.


Subject(s)
Antifungal Agents/economics , Drug Costs , Fluconazole/economics , Itraconazole/economics , Mycoses/economics , Neutropenia/economics , Outcome and Process Assessment, Health Care/economics , Triazoles/economics , Antifungal Agents/therapeutic use , Cost Savings , Cost-Benefit Analysis , Fluconazole/therapeutic use , Humans , Itraconazole/therapeutic use , Markov Chains , Mexico , Models, Economic , Mycoses/etiology , Mycoses/prevention & control , National Health Programs/economics , Neutropenia/complications , Neutropenia/drug therapy , Quality-Adjusted Life Years , Risk Assessment , Risk Factors , Time Factors , Treatment Outcome , Triazoles/therapeutic use
2.
Value Health ; 14(5 Suppl 1): S43-7, 2011.
Article in Spanish | MEDLINE | ID: mdl-21839898

ABSTRACT

OBJECTIVE: To assess the incremental cost-effectiveness of SFC compared with MON for the control of persistent asthma in children. METHODS: We conducted an economic evaluation on a 12-week prospective randomized open-label parallel-group comparison of SFC versus MON in children with symptomatic asthma receiving inhaled corticosteroids and short-acting ß2-agonists. Asthma-related medication, unscheduled physician contacts and hospitalizations were collected prospectively. The main effectiveness measure was percentage of asthma-controlled week with no short-acting ß2-agonist use during the study period. The analysis was conducted from the Mexican healthcare perspective using 2010 unit cost prices, and only direct costs were considered, all costs are reported in US dollar. . The model was made fully probabilistic to reflect the joint uncertainty in the model parameters. RESULTS: Over the whole treatment period, the median percentages of asthma-controlled weeks were 83.3% in the SFC group and 66.7% in the MON group (SFC-MON difference, 16.7%; 95% CI, 8.3-16.7; P < 0.001 in favor of SFC). The mean total cost of the SFC regimen was $ 2,323 compared with $ 3,230 for the MON regimen. The SFC was the dominant strategy (both more effective and less expensive) using the SFC was associated with an incremental cost per additional asthma-controlled of $ (5,467). Probabilistic sensitivity analysis tested numerous assumptions about the model cost and efficacy parameters and found that the results were robust to most changes. CONCLUSIONS: This analysis demonstrates that, compared with MON, SFC may be cost saving from the Mexican health care perspective for the treatment of pediatric patients with asthma. SFC provided a reduction in the number of severe exacerbations, frequent asthma symptoms and rescue medication use. Incremental cost-effectiveness analysis indicated the dominance of SFC because of both lower costs and greater efficacy.


Subject(s)
Acetates/economics , Adrenal Cortex Hormones/economics , Adrenergic beta-2 Receptor Agonists/economics , Albuterol/analogs & derivatives , Androstadienes/economics , Anti-Asthmatic Agents/economics , Asthma/economics , Drug Costs , Outcome and Process Assessment, Health Care/economics , Quinolines/economics , Acetates/therapeutic use , Adolescent , Adrenal Cortex Hormones/therapeutic use , Adrenergic beta-2 Receptor Agonists/therapeutic use , Albuterol/economics , Albuterol/therapeutic use , Androstadienes/therapeutic use , Anti-Asthmatic Agents/therapeutic use , Asthma/diagnosis , Asthma/drug therapy , Child , Cost Savings , Cost-Benefit Analysis , Cyclopropanes , Drug Combinations , Fluticasone-Salmeterol Drug Combination , Hospitalization/economics , Humans , Mexico , Models, Economic , National Health Programs/economics , Prospective Studies , Quinolines/therapeutic use , Sulfides , Time Factors , Treatment Outcome
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