Petrou Stavros, Bischof Matthias, Bennett Charlotte, Elbourne Diana, Field David, McNally Helena
National Perinatal Epidemiology Unit, University of Oxford, Oxford, United Kingdom.
Pediatrics. 2006 May;117(5):1640-9. doi: 10.1542/peds.2005-1150.
To assess the long-term cost-effectiveness of extracorporeal membrane oxygenation (ECMO) for mature newborn infants with severe respiratory failure.
A prospective economic evaluation was conducted alongside a pragmatic randomized, controlled trial in which 185 infants were randomly allocated to ECMO (n = 93) or conventional management (n = 92) and then followed up to 7 years of age. Information about their use of health services during the follow-up period was combined with unit costs (pound sterling, 2002-2003 prices) to obtain a net cost per child. The cost-effectiveness of neonatal ECMO was expressed in terms of incremental cost per additional life year gained and incremental cost per additional disability-free life year gained. The nonparametric bootstrap method was used to present cost-effectiveness acceptability curves and net benefit statistics at alternative willingness-to-pay thresholds held by decision-makers for an additional life year and for an additional disability-free life year.
Over 7 years, neonatal ECMO was effective at reducing known death or severe disability. Mean health service costs during the first 7 years of life were 30,270 pound sterling in the ECMO group and 10,229 pound sterling in the conventional management group, generating a mean cost difference of 20,041 pound sterling that was statistically significant. The incremental cost per life year gained was estimated at 13,385 pound sterling. The incremental cost per disability-free life year gained was estimated at 23,566 pound sterling. At the notional willingness-to-pay threshold of 30,000 pound sterling for an additional life year, the probability that neonatal ECMO is cost-effective at 7 years was estimated at 0.98. This translated into a mean net benefit of 24,362 pound sterling for each adoption of neonatal ECMO rather than conventional management.
This study provides rigorous evidence of the cost-effectiveness of neonatal ECMO during childhood.
评估体外膜肺氧合(ECMO)用于患有严重呼吸衰竭的足月新生儿的长期成本效益。
在一项实用的随机对照试验的同时进行了一项前瞻性经济评估,该试验中185名婴儿被随机分配至ECMO组(n = 93)或传统治疗组(n = 92),随后随访至7岁。将他们在随访期间使用医疗服务的信息与单位成本(2002 - 2003年价格的英镑)相结合,以得出每个儿童的净成本。新生儿ECMO的成本效益通过每多获得一个生命年的增量成本以及每多获得一个无残疾生命年的增量成本来表示。使用非参数自助法呈现成本效益可接受性曲线以及在决策者为一个额外生命年和一个额外无残疾生命年设定的替代支付意愿阈值下的净效益统计数据。
在7年期间,新生儿ECMO在降低已知死亡或严重残疾方面是有效的。ECMO组在生命的前7年的平均医疗服务成本为30,270英镑,传统治疗组为10,229英镑,平均成本差异为20,041英镑,具有统计学意义。每多获得一个生命年的增量成本估计为13,385英镑。每多获得一个无残疾生命年的增量成本估计为23,566英镑。在为一个额外生命年设定的名义支付意愿阈值30,000英镑时,新生儿ECMO在7岁时具有成本效益的概率估计为0.98。这意味着每次采用新生儿ECMO而非传统治疗的平均净效益为24,362英镑。
本研究提供了新生儿ECMO在儿童期成本效益的严格证据。