Literature DB >> 32640313

Impact of Preemptive Therapy for Cytomegalovirus on Hospitalizations and Cost after Hematopoietic Stem Cell Transplantation.

Jiaqi Fang1, Yiqi Su1, Phaedon D Zavras1, Amit D Raval2, Yuexin Tang2, Miguel-Angel Perales3, Sergio Giralt3, Anat Stern1, Genovefa A Papanicolaou4.   

Abstract

Cytomegalovirus (CMV) viremia occurs in 40% to 80% of CMV-seropositive (R+) recipients of allogeneic hematopoietic cell transplantation (HCT). The preemptive therapy (PET) strategy has reduced the risk of CMV end-organ disease (EOD) and associated mortality but may lead to substantial healthcare resource utilization (HCRU) and costs. Real-world data on the economic impact of PET is relevant for the evaluation of alternative strategies for CMV management. We examined the impact of clinically significant CMV treated with PET on inpatient length of stay (LOS), number of readmissions, and associated costs from day 0 through day 180 post-HCT. This was a retrospective study of R+ adults who underwent peripheral blood or marrow allogeneic HCT at Memorial Sloan Kettering Cancer Center between March 2013 and December 2017. Patients were routinely screened for CMV by qPCR and received PET according to institutional standards of care. Data were extracted from electronic medical records and hospital databases. Itemized cost data per patient were obtained from the Vizient database, adjusted to 2017 dollars using inflation indices. Study outcomes included HCRU evaluated by inpatient LOS and inpatient cost in patients who received PET for clinically significant CMV (PET group) compared with those who did not receive PET (no PET group) and the frequency and cost of CMV-related readmissions compared with non CMV-related readmissions. We used generalized linear models to examine the incremental HCRU and costs associated with PET controlling for other potential factors. Of 357 patients, PET was initiated in 208 (58.3%), at a median of 35 days after HCT. By day 180, 23 patients (6.4%) had developed CMV EOD and 3 (.8%) had died of CMV. Compared with the no PET group, the PET group had a longer LOS for HCT admission (P = .0276), longer total LOS by day 180 (P = .0001), a higher number of readmissions (P = .0001), a higher mean inpatient cost for HCT admission ($189,389 versus $151,646; P = .0133), and a higher total inpatient cost ($297,563 versus $205,815; P < .0001). Among PET recipients, CMV-related readmissions were associated with higher mean cost per episode compared with non CMV-related readmissions ($165,455 versus $89,419; P = .005). CMV-related readmissions comprised 40.6% of total all-cause readmissions and incurred 55.9% of total all-cause readmission costs in PET recipients. Our data show that patients treated with currently available PET had greater inpatient HCRU and cost, by day 180 compared with patients who did not receive PET. The cost of CMV-related readmissions accounted for 56% of total readmission cost among PET recipients. Future studies are needed to examine the cost-effectiveness of alternative strategies for CMV management.
Copyright © 2020 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cytomegalovirus; Healthcare resource utilization; Hematopoietic cell transplantation; Inpatient cost; Preemptive therapy; Readmission

Mesh:

Substances:

Year:  2020        PMID: 32640313      PMCID: PMC8248281          DOI: 10.1016/j.bbmt.2020.06.025

Source DB:  PubMed          Journal:  Biol Blood Marrow Transplant        ISSN: 1083-8791            Impact factor:   5.742


  27 in total

1.  Efficacy of a viral load-based, risk-adapted, preemptive treatment strategy for prevention of cytomegalovirus disease after hematopoietic cell transplantation.

Authors:  Margaret L Green; Wendy Leisenring; Daniel Stachel; Steven A Pergam; Brenda M Sandmaier; Anna Wald; Lawrence Corey; Michael Boeckh
Journal:  Biol Blood Marrow Transplant       Date:  2012-06-07       Impact factor: 5.742

2.  Cytomegalovirus Infection in Allogeneic Hematopoietic Cell Transplantation Managed by the Preemptive Approach: Estimating the Impact on Healthcare Resource Utilization and Outcomes.

Authors:  Yao-Ting Huang; Yiqi Su; Seong Jin Kim; Paige Nichols; Daniel Burack; Molly Maloy; Sergio Giralt; Miguel-Angel Perales; Ann A Jakubowski; Genovefa A Papanicolaou
Journal:  Biol Blood Marrow Transplant       Date:  2018-11-24       Impact factor: 5.742

3.  Outcomes in Transplant Recipients Treated With Foscarnet for Ganciclovir-Resistant or Refractory Cytomegalovirus Infection.

Authors:  Robin K Avery; Ravit Arav-Boger; Kieren A Marr; Edward Kraus; Shmuel Shoham; Laura Lees; Brandon Trollinger; Pali Shah; Rich Ambinder; Dionysios Neofytos; Darin Ostrander; Michael Forman; Alexandra Valsamakis
Journal:  Transplantation       Date:  2016-10       Impact factor: 4.939

4.  The clinical and economic burden of cytomegalovirus management post allogeneic hematopoietic stem cell transplantation in Japan - a retrospective database study.

Authors:  Rie Ueno; Shinichi Nishimura; Go Fujimoto; Yi Piao; Katsuto Takenaka
Journal:  Curr Med Res Opin       Date:  2019-08-11       Impact factor: 2.580

5.  Impact of Preemptive Therapy for Cytomegalovirus on Toxicities after Allogeneic Hematopoietic Cell Transplantation in Clinical Practice: A Retrospective Single-Center Cohort Study.

Authors:  Phaedon Zavras; Yiqi Su; Jiaqi Fang; Anat Stern; Nitasha Gupta; Yuexin Tang; Amit Raval; Sergio Giralt; Miguel Angel Perales; Ann A Jakubowski; Genovefa A Papanicolaou
Journal:  Biol Blood Marrow Transplant       Date:  2020-04-19       Impact factor: 5.742

6.  Sequential systematic anti-mold prophylaxis with micafungin and voriconazole results in very low incidence of invasive mold infections in patients undergoing allogeneic hematopoietic stem cell transplantation.

Authors:  Claudia Rosillo; Ana Maria Avila; Yao-Ting Huang; Sean Devlin; Christina Cho; Juan Montoro; Molly A Maloy; Genovefa A Papanicolaou; Pere Barba; Miguel-Angel Perales
Journal:  Transpl Infect Dis       Date:  2018-05-07       Impact factor: 2.228

7.  Reduced Mortality of Cytomegalovirus Pneumonia After Hematopoietic Cell Transplantation Due to Antiviral Therapy and Changes in Transplantation Practices.

Authors:  Veronique Erard; Katherine A Guthrie; Sachiko Seo; Jeremy Smith; MeeiLi Huang; Jason Chien; Mary E D Flowers; Lawrence Corey; Michael Boeckh
Journal:  Clin Infect Dis       Date:  2015-03-16       Impact factor: 9.079

Review 8.  Cytomegalovirus diseases after hematopoietic stem cell transplantation: a mini-review.

Authors:  Ella J Ariza-Heredia; Lior Nesher; Roy F Chemaly
Journal:  Cancer Lett       Date:  2013-09-13       Impact factor: 8.679

9.  Definitions of Cytomegalovirus Infection and Disease in Transplant Patients for Use in Clinical Trials.

Authors:  Per Ljungman; Michael Boeckh; Hans H Hirsch; Filip Josephson; Jens Lundgren; Garrett Nichols; Andreas Pikis; Raymund R Razonable; Veronica Miller; Paul D Griffiths
Journal:  Clin Infect Dis       Date:  2016-09-28       Impact factor: 9.079

10.  Early cytomegalovirus reactivation remains associated with increased transplant-related mortality in the current era: a CIBMTR analysis.

Authors:  Pierre Teira; Minoo Battiwalla; Muthalagu Ramanathan; A John Barrett; Kwang Woo Ahn; Min Chen; Jaime S Green; Ayman Saad; Joseph H Antin; Bipin N Savani; Hillard M Lazarus; Matthew Seftel; Wael Saber; David Marks; Mahmoud Aljurf; Maxim Norkin; John R Wingard; Caroline A Lindemans; Michael Boeckh; Marcie L Riches; Jeffery J Auletta
Journal:  Blood       Date:  2016-02-16       Impact factor: 22.113

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