Clinical and healthcare burden of disease associated with cytomegalovirus in allogeneic hematopoietic stem cell transplantation - A retrospective single-center study

被引:3
作者
Ranti, Juha [1 ]
Perkonoja, Katariina [2 ]
Kauko, Tommi [2 ]
Korhonen, Riku [3 ]
机构
[1] Turku Univ Hosp, Dept Hematol, Hosp Dist Southwest Finland, Turku, Finland
[2] Hosp Dist Southwest Finland, Auria Clin Informat, Turku, Finland
[3] MSD Finland Oy, Keilaranta 3, Espoo 02150, Finland
关键词
allogeneic stem cell transplantation; CMV; disease burden; hospitalization; healthcare resource utilization; HLA; LEUKEMIA WORKING PARTY; QUALITY-OF-LIFE; PREEMPTIVE THERAPY; RISK-FACTORS; VIRAL LOAD; MARROW-TRANSPLANTATION; PERIPHERAL-BLOOD; CMV INFECTION; REACTIVATION; MORTALITY;
D O I
10.1111/tid.13947
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: CMV infection is a common complication in allogeneic hematopoietic stem cell transplantation (HSCT). We investigated the association of clinically significant CMV (CS-CMV) infection with clinical outcomes and healthcare resource utilization in allogeneic HSCT patients in Finland. Methods: This retrospective study included adult patients who received their first allogeneic HSCT between January 1, 2013, and December 31, 2018, at the Turku University Hospital. Data were collected from the hospital data lake. Clinical and healthcare outcomes were investigated at one year and mortality up to three years. Results: The study included 251 patients. CMV seroprevalence was 69.7%. CS-CMV infection occurred in 59.0% of the patients, and of those, 14.2% had >= 2 infections. The median time to CS-CMV infection was 34.5 days (Q(1)-Q(3) 27.0-45.0). Recipient and donor seropositivity, and lymphoproliferative diseases were associated with higher, and HLA identical sibling donors with lower CS-CMV infection risk. CS-CMV infection was not associated with mortality in three years of follow-up. One hundred thirty-three (89.8%) and 75 (72.8%) patients with and without CS-CMV infection, respectively, were readmitted to the hospital. Patients with CS-CMV infection had more hospital readmissions (incidence rate ratio [IRR] 1.38, 95% confidence interval [CI] 1.10-1.73, p = .005) and patients with one CS-CMV infection (IRR 1.48, 95% CI 1.12-1.94, p = .005) or >= 2 infections had longer length of hospital stay (IRR 2.71, 95% CI 1.76-4.35, p < .001). Conclusion: CMV seroprevalence is relatively high among Finnish allogeneic HSCT patients. CS-CMV infection was common and associated with a higher readmission rate and longer length of hospital stay.
引用
收藏
页数:11
相关论文
共 48 条
[1]   Effect of Cytomegalovirus Reactivation With or Without Acute Graft-Versus-Host Disease on the Risk of Nonrelapse Mortality [J].
Akahoshi, Yu ;
Kimura, Shun-Ichi ;
Inamoto, Yoshihiro ;
Seo, Sachiko ;
Muranushi, Hiroyuki ;
Shimizu, Hiroaki ;
Ozawa, Yukiyasu ;
Tanaka, Masatsugu ;
Uchida, Naoyuki ;
Kanda, Yoshinobu ;
Katayama, Yuta ;
Shiratori, Souichi ;
Ota, Shuichi ;
Matsuoka, Ken-ichi ;
Onizuka, Makoto ;
Fukuda, Takahiro ;
Atsuta, Yoshiko ;
Murata, Makoto ;
Terakura, Seitaro ;
Nakasone, Hideki .
CLINICAL INFECTIOUS DISEASES, 2021, 73 (03) :E620-E628
[2]   Evaluation of intervention strategy based on CMV-specific immune responses after allogeneic SCT [J].
Avetisyan, G. ;
Aschan, J. ;
Haegglund, H. ;
Ringden, O. ;
Ljungman, P. .
BONE MARROW TRANSPLANTATION, 2007, 40 (09) :865-869
[3]   Valganciclovir is safe and effective as pre-emptive therapy for CMV infection in allogeneic hematopoietic stem cell transplantation [J].
Ayala, E ;
Greene, J ;
Sandin, R ;
Perkins, J ;
Field, T ;
Tate, C ;
Fields, KK ;
Goldstein, S .
BONE MARROW TRANSPLANTATION, 2006, 37 (09) :851-856
[4]   Health-Related Quality of Life Following Allogeneic Hematopoietic Stem Cell Transplantation [J].
Bevans, Margaret .
HEMATOLOGY-AMERICAN SOCIETY OF HEMATOLOGY EDUCATION PROGRAM, 2010, :248-254
[5]   Late cytomegalovirus disease and mortality in recipients of allogeneic hematopoietic stem cell transplants: importance of viral load and T-cell immunity [J].
Boeckh, M ;
Leisenring, W ;
Riddell, SR ;
Bowden, RA ;
Huang, ML ;
Myerson, D ;
Stevens-Ayers, T ;
Flowers, MED ;
Cunningham, T ;
Corey, L .
BLOOD, 2003, 101 (02) :407-414
[6]   Cytomegalovirus pp65 antigenemia-guided early treatment with ganciclovir versus ganciclovir at engraftment after allogeneic marrow transplantation: A randomized double-blind study [J].
Boeckh, M ;
Gooley, TA ;
Myerson, D ;
Cunningham, T ;
Schoch, G ;
Bowden, RA .
BLOOD, 1996, 88 (10) :4063-4071
[7]   Oral valganciclovir as preemptive therapy for cytomegalovirus infection post allogeneic stem cell transplantation [J].
Busca, A. ;
de Fabritiis, P. ;
Ghisetti, V. ;
Allice, T. ;
Mirabile, M. ;
Gentile, G. ;
Locatelli, F. ;
Falda, M. .
TRANSPLANT INFECTIOUS DISEASE, 2007, 9 (02) :102-107
[8]   Thiotepa, Busulfan, and Fludarabine Conditioning Regimen in T Cell-Replete HLA-Haploidentical Hematopoietic Stem Cell Transplantation [J].
Dulery, Remy ;
Bastos, Juliana ;
Paviglianiti, Annalisa ;
Malard, Florent ;
Brissot, Eolia ;
Battipaglia, Giorgia ;
Mediavilla, Clemence ;
Giannotti, Federica ;
Banet, Anne ;
Van de Wyngaert, Zoe ;
Ledraa, Tounes ;
Belhocine, Ramdane ;
Sestili, Simona ;
Adaeva, Rosa ;
Lapusan, Simona ;
Isnard, Francoise ;
Legrand, Ollivier ;
Vekhoff, Anne ;
Rubio, Marie-Therese ;
Ruggeri, Annalisa ;
Mohty, Mohamad .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2019, 25 (07) :1407-1415
[9]   Risk factors for treatment failures in patients receiving PCR-based preemptive therapy for CMV infection [J].
Einsele, H ;
Hebart, H ;
Kauffman-Schneider, C ;
Sinzger, C ;
Jahn, G ;
Bader, P ;
Klingebiel, T ;
Dietz, K ;
Löffler, J ;
Bokemeyer, C ;
Müller, CA ;
Kanz, L .
BONE MARROW TRANSPLANTATION, 2000, 25 (07) :757-763
[10]   Clinical and economic burden of pre-emptive therapy of cytomegalovirus infection in hospitalized allogeneic hematopoietic cell transplant recipients [J].
El Haddad, Lynn ;
Ghantoji, Shashank S. ;
Park, Anne K. ;
Batista, Marjorie V. ;
Schelfhout, Jonathan ;
Hachem, Jack ;
Lobo, Yadira ;
Jiang, Ying ;
Rondon, Gabriela ;
Champlin, Richard ;
Chemaly, Roy F. .
JOURNAL OF MEDICAL VIROLOGY, 2020, 92 (01) :86-95