Results of an Innovative Program for Surveillance, Prophylaxis, and Treatment of Infectious Complications Following Allogeneic Stem Cell Transplantation in Hematological Malignancies (BATMO Protocol).
bacterial infections
fungal infections
multi-drug resistance
prophylaxis
viral infections
Journal
Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867
Informations de publication
Date de publication:
2022
2022
Historique:
received:
11
02
2022
accepted:
12
05
2022
entrez:
5
7
2022
pubmed:
6
7
2022
medline:
6
7
2022
Statut:
epublish
Résumé
Infectious complications are a significant cause of morbidity and mortality in patients undergoing allogeneic haematopoietic stem cell transplantation (Allo-SCT). The BATMO (Best-Antimicrobial-Therapy-TMO) is an innovative program for infection prevention and management and has been used in our centre since 2019. The specific features of the BATMO protocol regard both prophylaxis during neutropenia (abandonment of fluoroquinolone, posaconazole use in high-risk patients, aerosolized liposomal amphotericin B use until engraftment or a need for antifungal treatment, and letermovir use in CMV-positive recipients from day 0 to day +100) and therapy (empirical antibiotics based on patient clinical history and colonization, new antibiotics used in second-line according to antibiogram with the exception of carbapenemase-producing Data on the infectious complications of 116 transplant patients before BATMO protocol (Cohort A; 2016 - 2018) were compared to those of 84 transplant patients following the introduction of the BATMO protocol (Cohort B; 2019 - 2021). The clinical and transplant characteristics of the 2 Cohorts were comparable, even though patients in Cohort B were at a higher risk of developing bacterial, fungal, and CMV infections, due to a significantly higher proportion of myeloablative regimens and haploidentical donors. No change in the incidence of infections with organ localization was observed between the two Cohorts. A significant reduction in The results of this study suggest that the BATMO program is safe. In particular, the choice to avoid prophylaxis with fluoroquinolone was associated with an increase in Gram-negative BSIs by day +30, but this did not translate into higher levels of mortality. Moreover, this strategy was associated with a significant reduction of
Sections du résumé
Background
UNASSIGNED
Infectious complications are a significant cause of morbidity and mortality in patients undergoing allogeneic haematopoietic stem cell transplantation (Allo-SCT). The BATMO (Best-Antimicrobial-Therapy-TMO) is an innovative program for infection prevention and management and has been used in our centre since 2019. The specific features of the BATMO protocol regard both prophylaxis during neutropenia (abandonment of fluoroquinolone, posaconazole use in high-risk patients, aerosolized liposomal amphotericin B use until engraftment or a need for antifungal treatment, and letermovir use in CMV-positive recipients from day 0 to day +100) and therapy (empirical antibiotics based on patient clinical history and colonization, new antibiotics used in second-line according to antibiogram with the exception of carbapenemase-producing
Methods
UNASSIGNED
Data on the infectious complications of 116 transplant patients before BATMO protocol (Cohort A; 2016 - 2018) were compared to those of 84 transplant patients following the introduction of the BATMO protocol (Cohort B; 2019 - 2021). The clinical and transplant characteristics of the 2 Cohorts were comparable, even though patients in Cohort B were at a higher risk of developing bacterial, fungal, and CMV infections, due to a significantly higher proportion of myeloablative regimens and haploidentical donors.
Results
UNASSIGNED
No change in the incidence of infections with organ localization was observed between the two Cohorts. A significant reduction in
Discussion
UNASSIGNED
The results of this study suggest that the BATMO program is safe. In particular, the choice to avoid prophylaxis with fluoroquinolone was associated with an increase in Gram-negative BSIs by day +30, but this did not translate into higher levels of mortality. Moreover, this strategy was associated with a significant reduction of
Identifiants
pubmed: 35785189
doi: 10.3389/fonc.2022.874117
pmc: PMC9247274
doi:
Types de publication
Journal Article
Langues
eng
Pagination
874117Informations de copyright
Copyright © 2022 Malagola, Turra, Signorini, Corbellini, Polverelli, Masina, Del Fabro, Lorenzotti, Fumarola, Farina, Morello, Radici, Buttini, Colnaghi, Bernardi, Re, Caruso, Castelli and Russo.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Références
Clin Transplant. 2021 Feb;35(2):e14172
pubmed: 33247497
Transplant Cell Ther. 2022 Mar;28(3):168.e1-168.e8
pubmed: 34954293
Clin Infect Dis. 2008 May 1;46(9):1401-8
pubmed: 18419443
Expert Rev Hematol. 2020 Nov;13(11):1235-1251
pubmed: 32996342
Biol Blood Marrow Transplant. 2020 Jun;26(6):1179-1188
pubmed: 32004700
Bone Marrow Transplant. 2013 Mar;48(3):452-8
pubmed: 23208313
Clin Infect Dis. 2017 Nov 13;65(11):1884-1896
pubmed: 29020286
J Infect. 2019 Jun;78(6):484-490
pubmed: 30974130
Front Cell Dev Biol. 2020 Oct 27;8:534268
pubmed: 33195184
Br J Haematol. 2022 Feb;196(4):830-848
pubmed: 34599519
Transplant Cell Ther. 2022 Feb;28(2):96.e1-96.e11
pubmed: 34818581
Transplant Cell Ther. 2021 Feb;27(2):176.e1-176.e8
pubmed: 33830032
Transpl Infect Dis. 2019 Aug;21(4):e13096
pubmed: 31004545
N Engl J Med. 2017 Dec 21;377(25):2433-2444
pubmed: 29211658
Mediterr J Hematol Infect Dis. 2017 Jun 20;9(1):e2017036
pubmed: 28698779
J Antimicrob Chemother. 2016 Sep;71(9):2397-404
pubmed: 27550992
Bone Marrow Transplant. 2020 Jun;55(6):1093-1102
pubmed: 31969678
Cancer. 2020 Jan 1;126(9):1837-1855
pubmed: 32073653
J Antimicrob Chemother. 2018 Dec 1;73(12):3221-3230
pubmed: 30085172
Infection. 2017 Aug;45(4):403-411
pubmed: 28417421
J Infect. 2018 Jan;76(1):20-37
pubmed: 29079323
Hematology Am Soc Hematol Educ Program. 2019 Dec 6;2019(1):513-521
pubmed: 31808908
Transpl Infect Dis. 2015 Apr;17(2):242-9
pubmed: 25648539
Bone Marrow Transplant. 2020 Jan;55(1):126-136
pubmed: 31455899
Clin Infect Dis. 2018 Nov 13;67(suppl_2):S162-S173
pubmed: 30423054
J Infect. 2014 Jul;69(1):13-25
pubmed: 24583063
Lancet Haematol. 2020 Jan;7(1):e28-e39
pubmed: 31606445