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Acceptability of In Utero Hematopoietic Cell Transplantation for Sickle Cell Disease.

Publication ,  Journal Article
Antiel, RM; Halpern, SD; Stevens, EM; Vrecenak, JD; Patterson, CA; Tchume-Johnson, T; Smith-Whitley, K; Peranteau, WH; Flake, AW; Barakat, LP
Published in: Med Decis Making
November 2017

BACKGROUND: In utero hematopoietic cell transplantation (IUHCT) has curative potential for sickle cell disease (SCD) but carries a risk of fetal demise. METHODS: We assessed the conditions under which parents of children with SCD and young adults with SCD would consider IUHCT in a future pregnancy, given a 5% fixed risk of fetal demise. Participants were randomized to consider a hypothetical cure rate (20%, 40%, or 70%). Subsequently, cure rate was either increased or decreased depending on the previous answer to reveal the lowest acceptable rate. Participants also completed the Pediatric Research Participation Questionnaire (PRPQ) and an omission scale. RESULTS: Overall, 74 of 79 (94%) participants were willing to consider IUHCT, and 52 (66%) participants accepted IUHCT at a cure rate of 40%, the estimated rate of therapeutic mixed chimerism. Participants with higher scores on the PRPQ perceived benefits scale were more likely to participate at lower cure rates (OR 1.08, p=0.007) and participants with a greater degree of omission bias were less likely to participate at lower cure rates (OR 0.83, p=0.04). Demographics and SCD severity were not significantly associated with acceptability of IUHCT. CONCLUSION: This study suggests that the majority of parents >and young adults would consider IUHCT under expected therapeutic conditions.

Duke Scholars

Published In

Med Decis Making

DOI

EISSN

1552-681X

Publication Date

November 2017

Volume

37

Issue

8

Start / End Page

914 / 921

Location

United States

Related Subject Headings

  • Young Adult
  • Treatment Outcome
  • Surveys and Questionnaires
  • Pregnancy
  • Patient Acceptance of Health Care
  • Middle Aged
  • Male
  • Humans
  • Hematopoietic Stem Cell Transplantation
  • Health Policy & Services
 

Citation

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MLA
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Antiel, R. M., Halpern, S. D., Stevens, E. M., Vrecenak, J. D., Patterson, C. A., Tchume-Johnson, T., … Barakat, L. P. (2017). Acceptability of In Utero Hematopoietic Cell Transplantation for Sickle Cell Disease. Med Decis Making, 37(8), 914–921. https://doi.org/10.1177/0272989X17707214
Antiel, Ryan M., Scott D. Halpern, Evelyn M. Stevens, Jesse D. Vrecenak, Chavis A. Patterson, Trudy Tchume-Johnson, Kim Smith-Whitley, William H. Peranteau, Alan W. Flake, and Lamia P. Barakat. “Acceptability of In Utero Hematopoietic Cell Transplantation for Sickle Cell Disease.Med Decis Making 37, no. 8 (November 2017): 914–21. https://doi.org/10.1177/0272989X17707214.
Antiel RM, Halpern SD, Stevens EM, Vrecenak JD, Patterson CA, Tchume-Johnson T, et al. Acceptability of In Utero Hematopoietic Cell Transplantation for Sickle Cell Disease. Med Decis Making. 2017 Nov;37(8):914–21.
Antiel, Ryan M., et al. “Acceptability of In Utero Hematopoietic Cell Transplantation for Sickle Cell Disease.Med Decis Making, vol. 37, no. 8, Nov. 2017, pp. 914–21. Pubmed, doi:10.1177/0272989X17707214.
Antiel RM, Halpern SD, Stevens EM, Vrecenak JD, Patterson CA, Tchume-Johnson T, Smith-Whitley K, Peranteau WH, Flake AW, Barakat LP. Acceptability of In Utero Hematopoietic Cell Transplantation for Sickle Cell Disease. Med Decis Making. 2017 Nov;37(8):914–921.
Journal cover image

Published In

Med Decis Making

DOI

EISSN

1552-681X

Publication Date

November 2017

Volume

37

Issue

8

Start / End Page

914 / 921

Location

United States

Related Subject Headings

  • Young Adult
  • Treatment Outcome
  • Surveys and Questionnaires
  • Pregnancy
  • Patient Acceptance of Health Care
  • Middle Aged
  • Male
  • Humans
  • Hematopoietic Stem Cell Transplantation
  • Health Policy & Services