The Journal of Pediatrics
Volume 151, Issue 2 , Pages 115-120.e3, August 2007

Cost-Effectiveness of Neonatal Screening for Medium Chain acyl-CoA Dehydrogenase Deficiency: The Homogeneous Population of the Netherlands

  • Christian S. van der Hilst, MSc

      Affiliations

    • Office for Medical Technology Assessment, University of Groningen, University Medical Center Groningen, The Netherlands
    • Corresponding Author InformationReprint requests: Christian S. van der Hilst, MSc, Office for Medical Technology Assessment, University Medical Center Groningen, PO Box 30 001, 9700 RB Groningen, The Netherlands.
  • ,
  • Terry G.J. Derks, MD, PhD

      Affiliations

    • Division of Metabolic Diseases, Beatrix Children’s Hospital, University of Groningen, University Medical Center Groningen, The Netherlands
  • ,
  • Dirk-Jan Reijngoud, PhD

      Affiliations

    • Laboratory of Metabolic Diseases, Beatrix Children’s Hospital, University of Groningen, University Medical Center Groningen, The Netherlands.
  • ,
  • G. Peter A. Smit, MD, PhD

      Affiliations

    • Division of Metabolic Diseases, Beatrix Children’s Hospital, University of Groningen, University Medical Center Groningen, The Netherlands
  • ,
  • Elisabeth M. TenVergert, PhD

      Affiliations

    • Office for Medical Technology Assessment, University of Groningen, University Medical Center Groningen, The Netherlands

Received 19 July 2006; received in revised form 1 February 2007; accepted 6 March 2007.

Objective

To assess the cost-effectiveness of neonatal screening on medium chain acyl-CoA dehydrogenase (MCAD) deficiency in a homogeneous population.

Study design

For the scenario without neonatal screening, medical chart review and interviews were performed with physicians and families of 116 Dutch patients born between 1985 and July 2003 with clinically ascertained MCAD deficiency. For the scenario with neonatal screening, 66,205 unaffected and 11 affected newborns identified by prospective neonatal screening for MCAD deficiency in the northern part of the Netherlands were evaluated. The incremental cost-effectiveness ratio (ICER) used life years (LYs) as the outcome measure by combining both scenarios in a decision model with second-order Monte Carlo simulation.

Results

For the scenarios with and without neonatal screening for MCAD deficiency, costs were $6.10 and $4.22 per newborn, respectively. The main cost categories were institutionalization (64%), admissions (17%), special education (8%), laboratory testing (4%), and (para)medical contact (4%). The resulting ICER was $1653 per LY gained. Sensitivity analysis generated an ICER between $14,839 and $4345 per LY gained.

Conclusions

Screening for MCAD deficiency in a well-defined population generates an ICER well within accepted boundaries for cost-effective interventions, even after sensitivity analysis.

Abbreviations: CI, Confidence interval, CRFs, Case record forms, DPSU, Dutch Pediatric Surveillance Unit, ICER, Incremental cost-effectiveness ratio, LY, Life year, MCAD, Medium chain acyl-CoA dehydrogenase, MS/MS, Tandem mass spectrometry

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 Supported by ZonMw.

PII: S0022-3476(07)00249-1

doi:10.1016/j.jpeds.2007.03.013

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The Journal of Pediatrics
Volume 151, Issue 2 , Pages 115-120.e3, August 2007