Kubiak Catherine, Jyonouchi Soma, Kuo Caroline, Garcia-Lloret Maria, Dorsey Morna J, Sleasman John, Zbrozek Arthur S, Perez Elena E
Department of Pediatrics, Division of Allergy and Immunology, Morsani College of Medicine, University of South Florida, Tampa, Fla.
Department of Pediatrics, Division of Allergy and Immunology, Children's Hospital of Philadelphia, Philadelphia, Pa.
J Allergy Clin Immunol Pract. 2014 Nov-Dec;2(6):697-702. doi: 10.1016/j.jaip.2014.05.013. Epub 2014 Aug 28.
In the United States, newborn screening (NBS) is currently recommended for identification of 31 debilitating and potentially fatal conditions. However, individual states determine which of the recommended conditions are screened. The addition of severe combined immunodeficiency (SCID) screening to the recommended NBS panel has been fully instituted by 18 states, with another 11 states piloting programs or planning to begin screening in 2014. Untreated, SCID is uniformly fatal by 2 years of age. Hematopoietic stem cell transplantation usually is curative, but the success rate depends on the age at which the procedure is performed. Short-term implementation costs may be a barrier to adding SCID to states' NBS panels. A retrospective economic analysis was performed to determine the cost-effectiveness of NBS for early (<3.5 months) versus late (≥3.5 months) treatment of children with SCID at 3 centers over 5 years. The mean total charges at these centers for late treatment were 4 times greater than early treatment ($1.43 million vs $365,785, respectively). Mean charges for intensive care treatments were >5 times higher ($350,252 vs $66,379), and operating room-anesthesia charges were approximately 4 times higher ($57,105 vs $15,885). The cost-effectiveness of early treatment for SCID provides a strong economic rationale for the addition of SCID screening to NBS programs of other states.
在美国,目前建议进行新生儿筛查(NBS)以识别31种使人衰弱且可能致命的病症。然而,具体由各个州来决定对哪些推荐病症进行筛查。18个州已全面实施在推荐的新生儿筛查项目中增加重症联合免疫缺陷(SCID)筛查,另有11个州正在试行相关项目或计划在2014年开始筛查。若不进行治疗,SCID患儿通常在2岁前就会死亡。造血干细胞移植通常可治愈该病,但成功率取决于进行该手术时的年龄。短期实施成本可能是阻碍各州将SCID纳入新生儿筛查项目的一个因素。我们进行了一项回顾性经济分析,以确定在5年时间里3个中心对SCID患儿进行早期(<3.5个月)与晚期(≥3.5个月)治疗时新生儿筛查的成本效益。这些中心晚期治疗的平均总费用比早期治疗高出4倍(分别为143万美元和365,785美元)。重症监护治疗的平均费用高出5倍多(350,252美元对66,379美元),手术室麻醉费用高出约4倍(57,105美元对15,885美元)。对SCID进行早期治疗的成本效益为其他州将SCID筛查纳入新生儿筛查项目提供了强有力的经济依据。