Dartmouth-Hitchcock Medical Center, Section of Allergy and Immunology, Lebanon, and Dartmouth Geisel School of Medicine, Hanover, NH.
Division of Allergy and Immunology, Department of Pediatrics, University of British Columbia, BC Children's Hospital, Vancouver, BC, Canada.
J Allergy Clin Immunol Pract. 2021 Jul;9(7):2876-2884.e4. doi: 10.1016/j.jaip.2021.02.058. Epub 2021 Mar 18.
Across North America, 1.4% to 4.5% of children and families live with peanut allergy (PA). Preschool peanut oral immunotherapy (POIT) has been shown to be safe and effective in the real-world setting.
Evaluate the cost effectiveness of preschool POIT in North America.
Markov cohort analyses and microsimulation was used to evaluate simulated preschool children with PA over an 80-year time horizon. Models incorporated the natural history of PA, comparing children treated with preschool POIT with those not receiving immunotherapy. Costs were expressed in U.S. and Canadian dollars.
A preschool POIT strategy was associated with cost savings while improving quality-adjusted life-years (QALY), dominating a nonimmunotherapy approach. Over the model horizon, when all costs (and effectiveness) of PA were included from a societal perspective, a POIT versus a non-POIT approach cost $82,514 (18.51 QALY) versus $84,367 (17.75 QALY) in the United States, and $40,111 (18.83 QALY) versus $53,848 (18.26 QALY) in Canada. In microsimulations, systemic reactions to POIT were less frequent than anaphylaxis from accidental exposure without POIT (United States: 3.59, SD 3.49 vs 19.53, SD 11.71; Canada: 3.63, SD 3.54 vs 4.56, SD 3.30), epinephrine use was reduced with POIT (United States: 5.85, SD 5.73 vs 9.76, SD 5.85; Canada: 0.34, SD 0.36 vs 0.53, SD 0.38), and fatalities were rare but lower in the POIT strategy (United States: 0.00005, SD 0.0071 vs 0.00015, SD 0.012; Canada: 0.00005, SD 0.0071 vs 0.00009, SD 0.0095).
Preschool POIT in a real-world setting improved health and economic outcomes in the United States and Canada.
在北美,1.4%至 4.5%的儿童和家庭患有花生过敏症(PA)。在真实环境中,已证明学龄前花生口服免疫疗法(POIT)是安全有效的。
评估北美的学龄前 POIT 的成本效益。
使用马尔可夫队列分析和微模拟来评估在 80 年时间范围内患有 PA 的模拟学龄前儿童。该模型结合了 PA 的自然史,将接受学龄前 POIT 治疗的儿童与未接受免疫治疗的儿童进行比较。成本以美元和美加元表示。
与非免疫治疗方法相比,采用 POIT 策略可节省成本并提高质量调整生命年(QALY)。在模型范围内,从社会角度考虑所有 PA 的成本(和效果)时,与非 POIT 方法相比,POIT 与非 POIT 方法在美国的成本为 82514 美元(18.51 QALY)与 84367 美元(17.75 QALY),在加拿大的成本为 40111 美元(18.83 QALY)与 53848 美元(18.26 QALY)。在微模拟中,POIT 引起的全身性反应比没有 POIT 的意外暴露引起的过敏反应更为罕见(美国:3.59,SD 3.49 vs 19.53,SD 11.71;加拿大:3.63,SD 3.54 vs 4.56,SD 3.30),POIT 可减少肾上腺素的使用(美国:5.85,SD 5.73 vs 9.76,SD 5.85;加拿大:0.34,SD 0.36 vs 0.53,SD 0.38),且 POIT 策略的死亡率较低(美国:0.00005,SD 0.0071 vs 0.00015,SD 0.012;加拿大:0.00005,SD 0.0071 vs 0.00009,SD 0.0095)。
在真实环境中,学龄前 POIT 可改善美国和加拿大的健康和经济结果。