Cost-effectiveness of noninvasive fetal RhD blood group genotyping in nonalloimmunized and alloimmunized pregnancies

Transfusion. 2022 May;62(5):1089-1102. doi: 10.1111/trf.16826. Epub 2022 Feb 16.

Abstract

Background: We sought to determine the cost-effectiveness of noninvasive fetal RhD blood group genotyping in nonalloimmunized and alloimmunized pregnancies in Canada.

Study design and methods: We developed two probabilistic state-transition (Markov) microsimulation models to compare fetal genotyping followed by targeted management versus usual care (i.e., universal Rh immunoglobulin [RhIG] prophylaxis in nonalloimmunized RhD-negative pregnancies, or universal intensive monitoring in alloimmunized pregnancies). The reference case considered a healthcare payer perspective and a 10-year time horizon. Sensitivity analysis examined assumptions related to test cost, paternal screening, subsequent pregnancies, other alloantibodies (e.g., K, Rh c/C/E), societal perspective, and lifetime horizon.

Results: Fetal genotyping in nonalloimmunized pregnancies (at per-sample test cost of C$247/US$311) was associated with a slightly higher probability of maternal alloimmunization (22 vs. 21 per 10,000) and a reduced number of RhIG injections (1.427 vs. 1.795) than usual care. It was more expensive (C$154/US$194, 95% Credible Interval [CrI]: C$139/US$175-C$169/US$213) and had little impact on QALYs (0.0007, 95%CrI: -0.01-0.01). These results were sensitive to the test cost (threshold achieved at C$88/US$111), and inclusion of paternal screening. Fetal genotyping in alloimmunized pregnancies (at test cost of C$328/US$413) was less expensive (-C$6280/US$7903, 95% CrI: -C$6325/US$7959 to -C$6229/US$7838) and more effective (0.19 QALYs, 95% CrI 0.17-0.20) than usual care. These cost savings remained robust in sensitivity analyses.

Discussion: Noninvasive fetal RhD genotyping saves resources and represents good value for the management of alloimmunized pregnancies. If the cost of genotyping is substantially decreased, the targeted intervention can become a viable option for nonalloimmunized pregnancies.

Keywords: Rh alloimmunization; alloimmunized pregnancies; cost-effectiveness analysis; incremental cost-effectiveness ratio; non-invasive fetal RhD genotyping; nonalloimmunized pregnancies; noninvasive fetal Rh D blood group genotyping.

MeSH terms

  • Blood Group Antigens*
  • Cost-Benefit Analysis
  • Female
  • Fetal Blood
  • Genotype
  • Humans
  • Pregnancy
  • Prenatal Diagnosis / methods
  • Rh Isoimmunization* / prevention & control
  • Rh-Hr Blood-Group System / genetics
  • Rho(D) Immune Globulin / therapeutic use

Substances

  • Blood Group Antigens
  • Rh-Hr Blood-Group System
  • Rho(D) Immune Globulin