Predictors and impact of thirty-day readmission on patient outcomes and health care costs after reduced-toxicity conditioning allogeneic hematopoietic cell transplantation

Biol Blood Marrow Transplant. 2014 Mar;20(3):415-20. doi: 10.1016/j.bbmt.2013.12.559. Epub 2013 Dec 18.

Abstract

Thirty-day readmission (30-DR) has become an important quality-of-care measure. Allogeneic hematopoietic cell transplantation (allo-HCT) presents a medical setting with higher readmission rates. We analyzed factors affecting 30-DR and its impact on patient outcomes and on health care costs in 91 patients who underwent reduced-toxicity conditioning (RTC) allo-HCT with fludarabine and busulfan. The patient cohort was divided into 2: the readmission group (R-gp) or the no-readmission group (NR-gp). Overall, 38% (n = 35) required readmission with a median time to readmission of 14 days. In multivariate analysis, only documented infection during the index admission predicted 30-DR, P = .01. With a median follow-up of 18 months (range, 1 to 69) for surviving patients, the 2-year overall survival was 49% and 58% in the R-gp and NR-gp respectively, P = .48. The 1-year nonrelapse mortality in R-gp and NR-gp was 18% and 13% respectively, P = .43. The median post-transplantation hospital charges in the R-gp and NR-gp were $85,115 (range, $32,015 to $242,519) and $45,083 (range, $10,715 to $485,456), P = .0002. In conclusion, only documented infections during the index hospitalization influenced 30-DR after RTC allo-HCT. Although 30-DR did not adversely affect mortality or survival, it was associated with significantly increased 100-day post-transplantation hospital charges, thus supporting its role as a quality-of-care measure in allo-HCT patients.

Keywords: Allogeneic hematopoietic cell transplantation; Health care cost; Reduced-toxicity conditioning; Thirty-day readmission.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Busulfan / therapeutic use
  • Cross Infection / economics
  • Cross Infection / etiology
  • Cross Infection / immunology
  • Cross Infection / mortality
  • Female
  • Graft vs Host Disease / economics
  • Graft vs Host Disease / immunology
  • Graft vs Host Disease / mortality
  • Graft vs Host Disease / pathology
  • Health Care Costs
  • Hematologic Neoplasms / economics*
  • Hematologic Neoplasms / immunology
  • Hematologic Neoplasms / mortality
  • Hematologic Neoplasms / therapy*
  • Hematopoietic Stem Cell Transplantation / adverse effects
  • Hematopoietic Stem Cell Transplantation / economics*
  • Humans
  • Male
  • Middle Aged
  • Myeloablative Agonists / therapeutic use
  • Patient Readmission / economics*
  • Survival Analysis
  • Transplantation Conditioning / economics*
  • Transplantation Conditioning / methods
  • Transplantation, Homologous
  • Treatment Outcome
  • Vidarabine / analogs & derivatives
  • Vidarabine / therapeutic use

Substances

  • Myeloablative Agonists
  • Vidarabine
  • Busulfan
  • fludarabine