Canadian cost- utility analysis of intravenous immunoglobulin for acute childhood idiopathic thrombocytopenic purpura
| Autor: | Gord, Blackhouse, Feng, Xie, Mitchell A H, Levine, Kaitryn, Campbell, Nazila, Assasi, Kathryn, Gaebel, Daria, O'Reilly, Jean- Eric, Tarride, Ron, Goeree |
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| Rok vydání: | 2012 |
| Předmět: |
Canada
Purpura Thrombocytopenic Idiopathic Time Factors Platelet Count Cost-Benefit Analysis Body Weight Age Factors Immunoglobulins Intravenous Drug Costs Markov Chains Hospitalization Models Economic Treatment Outcome Adrenal Cortex Hormones Acute Disease Humans Immunologic Factors Quality-Adjusted Life Years Hospital Costs Child Intracranial Hemorrhages |
| Zdroj: | Journal of population therapeutics and clinical pharmacology = Journal de la therapeutique des populations et de la pharmacologie clinique. 19(2) |
| ISSN: | 2561-8741 |
| Popis: | Idiopathic thrombocytopenic purpura (ITP) is a hematological disorder and can be classified as acute or chronic. The main goal of treatment for acute childhood ITP is the prevention of potentially fatal bleeding complications, the most serious of which is intracranial hemorrhage (ICH). Treatment options for acute childhood ITP include splenectomy, corticosteroids, and blood products such as intravenous immunoglobulin.The objective was to evaluate, from a Canadian perspective, the cost-effectiveness of intravenous immunoglobulin (IVIG) compared to alternative inpatient treatments for acute childhood idiopathic thrombocytopenic purpura (ITP).A Markov model with a lifelong time horizon was used to evaluate the costs and quality-adjusted life years (QALYs) for 5 treatments for children hospitalized for ITP: 1) no treatment; 2) IVIG; 3) Anti-D; 4) prednisone; and 5) methylprednisolone. The model predicted the probability of intracranial hemorrhage for each treatment strategy based on the time children spent with platelet counts20,000µL. The time patients spent with platelet counts20,000µL with each treatment was estimated by pooling data from published randomized clinical trials. In the basecase analysis, the cohort was assumed to weigh 20kg. Cost and utility model variables were based upon various literature sources. Parameter uncertainty was assessed using probabilistic sensitivity analysis.The treatment strategies that comprised the efficiency frontier were prednisone, Anti-D and IVIG. The incremental cost per QALY was $53,333 moving from prednisone to Anti-D and $53,846 moving from Anti-D to IVIG. Results were sensitive to patient weight. If patient weight is 10kg, IVIG dominates all other strategies and if weight is increased to 30kg, the cost per QALY of IVIG is $163,708.Based on common willingness to pay thresholds, IVIG might be considered a cost effective treatment for acute childhood ITP. Cost effectiveness is highly dependent on patient weight. |
| Databáze: | OpenAIRE |
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