Pre-engraftment bloodstream infection after allogeneic haematopoietic cell transplant: 18-year trends in aetiology, resistance and mortality
Bloodstream infections (BSI) are frequent complications after allogeneic hematopoietic cell transplant (HCT). This study reports data on pre-engraftment BSI in years 2016-2021 and analyses changes in incidence, aetiology, resistance and mortality compared with two previous periods (2004-2009 and 201...
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creator | Falcó-Roget, Anna Raiola, Anna Maria Balletto, Elisa Varaldo, Riccardo Gambella, Massimiliano Lanino, Emanuele Sepulcri, Chiara Ghiso, Anna Giannoni, Livia Bregante, Stefania Laudisi, Antonella Passannante, Monica Bassetti, Matteo Angelucci, Emanuele Mikulska, Malgorzata |
description | Bloodstream infections (BSI) are frequent complications after allogeneic hematopoietic cell transplant (HCT). This study reports data on pre-engraftment BSI in years 2016-2021 and analyses changes in incidence, aetiology, resistance and mortality compared with two previous periods (2004-2009 and 2010-2015). In years 2004-2021, 1364 patients received HCT. De-escalation strategy for empirical antibiotic therapy was introduced in 2011. In 381 patients from years 2016-2021, the incidence of pre-engraftment BSI was 37.8%. Independent predictors of BSI were older age, AML/MDS and active disease. In 1364 patients, the incidence of BSI increased from 22% in period 1 to 38% in period 3 (p = 0.008), particularly gram-negative BSI: from 10.1% to 19.7% (p = 0.001). Among gram-negatives, resistance to third-generation cephalosporins remained stable (40.2% in period 3), while resistance to carbapenems and fluoroquinolones decreased (respectively, 12.6% and 59.8% in period 3). Seven and 30-day mortality after the first BSI decreased, respectively, from 11% in period 1 to 1.4% in period 3 and from 20.5% to 4.9% (p |
doi_str_mv | 10.1038/s41409-024-02494-x |
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This study reports data on pre-engraftment BSI in years 2016-2021 and analyses changes in incidence, aetiology, resistance and mortality compared with two previous periods (2004-2009 and 2010-2015). In years 2004-2021, 1364 patients received HCT. De-escalation strategy for empirical antibiotic therapy was introduced in 2011. In 381 patients from years 2016-2021, the incidence of pre-engraftment BSI was 37.8%. Independent predictors of BSI were older age, AML/MDS and active disease. In 1364 patients, the incidence of BSI increased from 22% in period 1 to 38% in period 3 (p = 0.008), particularly gram-negative BSI: from 10.1% to 19.7% (p = 0.001). Among gram-negatives, resistance to third-generation cephalosporins remained stable (40.2% in period 3), while resistance to carbapenems and fluoroquinolones decreased (respectively, 12.6% and 59.8% in period 3). Seven and 30-day mortality after the first BSI decreased, respectively, from 11% in period 1 to 1.4% in period 3 and from 20.5% to 4.9% (p < 0.001 for both). Less recent transplant period was the only factor associated with higher mortality (p = 0.001). Incidence of pre-engraftment BSI is high and increased overtime, particularly for gram-negatives. Resistance rates remained stable, and mortality decreased overtime, documenting improvements in the BSI management.</description><identifier>ISSN: 1476-5365</identifier><identifier>EISSN: 1476-5365</identifier><identifier>DOI: 10.1038/s41409-024-02494-x</identifier><identifier>PMID: 39663472</identifier><language>eng</language><publisher>England</publisher><ispartof>Bone marrow transplantation (Basingstoke), 2024-12</ispartof><rights>2024. 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This study reports data on pre-engraftment BSI in years 2016-2021 and analyses changes in incidence, aetiology, resistance and mortality compared with two previous periods (2004-2009 and 2010-2015). In years 2004-2021, 1364 patients received HCT. De-escalation strategy for empirical antibiotic therapy was introduced in 2011. In 381 patients from years 2016-2021, the incidence of pre-engraftment BSI was 37.8%. Independent predictors of BSI were older age, AML/MDS and active disease. In 1364 patients, the incidence of BSI increased from 22% in period 1 to 38% in period 3 (p = 0.008), particularly gram-negative BSI: from 10.1% to 19.7% (p = 0.001). Among gram-negatives, resistance to third-generation cephalosporins remained stable (40.2% in period 3), while resistance to carbapenems and fluoroquinolones decreased (respectively, 12.6% and 59.8% in period 3). Seven and 30-day mortality after the first BSI decreased, respectively, from 11% in period 1 to 1.4% in period 3 and from 20.5% to 4.9% (p < 0.001 for both). Less recent transplant period was the only factor associated with higher mortality (p = 0.001). Incidence of pre-engraftment BSI is high and increased overtime, particularly for gram-negatives. Resistance rates remained stable, and mortality decreased overtime, documenting improvements in the BSI management.</description><issn>1476-5365</issn><issn>1476-5365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpNkMtKxDAUhoMozjj6Ai4kSxdWk-bS1p0M3mBAF7MfTtOTsdImNcmAfQcf2g4quDic2_f_cA4h55xdcybKmyi5ZFXGcrmPSmafB2TOZaEzJbQ6_FfPyEmM74xxKZk6JjNRaS1kkc_J12vADN02gE09ukTrzvsmpoDQ09ZZNKn1jk5bDBS6zm_RYWvoG2APyQ--xTS1BruOpgAuDh24dEt5mY0IYZqha-LkRGEC_aQfr2jA2MYEziAF19DehwRdm8ZTcmShi3j2mxdk_XC_Xj5lq5fH5-XdKhu45ClrGigKoQwDW8uqxErXQhecQcXywmiBVomGWSuYLFXOCpMzMBZMYyteCyUW5PLHdgj-Y4cxbfo27i8Ah34XN4JLrVWuynJCL37RXd1jsxlC20MYN38PFN9plnbK</recordid><startdate>20241211</startdate><enddate>20241211</enddate><creator>Falcó-Roget, Anna</creator><creator>Raiola, Anna Maria</creator><creator>Balletto, Elisa</creator><creator>Varaldo, Riccardo</creator><creator>Gambella, Massimiliano</creator><creator>Lanino, Emanuele</creator><creator>Sepulcri, Chiara</creator><creator>Ghiso, Anna</creator><creator>Giannoni, Livia</creator><creator>Bregante, Stefania</creator><creator>Laudisi, Antonella</creator><creator>Passannante, Monica</creator><creator>Bassetti, Matteo</creator><creator>Angelucci, Emanuele</creator><creator>Mikulska, Malgorzata</creator><scope>NPM</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7896-4198</orcidid><orcidid>https://orcid.org/0000-0002-5535-4602</orcidid><orcidid>https://orcid.org/0009-0000-0676-0201</orcidid><orcidid>https://orcid.org/0000-0001-9716-5538</orcidid><orcidid>https://orcid.org/0009-0003-1774-679X</orcidid><orcidid>https://orcid.org/0000-0002-6512-6080</orcidid></search><sort><creationdate>20241211</creationdate><title>Pre-engraftment bloodstream infection after allogeneic haematopoietic cell transplant: 18-year trends in aetiology, resistance and mortality</title><author>Falcó-Roget, Anna ; Raiola, Anna Maria ; Balletto, Elisa ; Varaldo, Riccardo ; Gambella, Massimiliano ; Lanino, Emanuele ; Sepulcri, Chiara ; Ghiso, Anna ; Giannoni, Livia ; Bregante, Stefania ; Laudisi, Antonella ; Passannante, Monica ; Bassetti, Matteo ; Angelucci, Emanuele ; Mikulska, Malgorzata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p141t-dda7735c0afb498e96b36710a9027c63ef53d0ff30485207c20acfacdf91b353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Falcó-Roget, Anna</creatorcontrib><creatorcontrib>Raiola, Anna Maria</creatorcontrib><creatorcontrib>Balletto, Elisa</creatorcontrib><creatorcontrib>Varaldo, Riccardo</creatorcontrib><creatorcontrib>Gambella, Massimiliano</creatorcontrib><creatorcontrib>Lanino, Emanuele</creatorcontrib><creatorcontrib>Sepulcri, Chiara</creatorcontrib><creatorcontrib>Ghiso, Anna</creatorcontrib><creatorcontrib>Giannoni, Livia</creatorcontrib><creatorcontrib>Bregante, Stefania</creatorcontrib><creatorcontrib>Laudisi, Antonella</creatorcontrib><creatorcontrib>Passannante, Monica</creatorcontrib><creatorcontrib>Bassetti, Matteo</creatorcontrib><creatorcontrib>Angelucci, Emanuele</creatorcontrib><creatorcontrib>Mikulska, Malgorzata</creatorcontrib><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Bone marrow transplantation (Basingstoke)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Falcó-Roget, Anna</au><au>Raiola, Anna Maria</au><au>Balletto, Elisa</au><au>Varaldo, Riccardo</au><au>Gambella, Massimiliano</au><au>Lanino, Emanuele</au><au>Sepulcri, Chiara</au><au>Ghiso, Anna</au><au>Giannoni, Livia</au><au>Bregante, Stefania</au><au>Laudisi, Antonella</au><au>Passannante, Monica</au><au>Bassetti, Matteo</au><au>Angelucci, Emanuele</au><au>Mikulska, Malgorzata</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pre-engraftment bloodstream infection after allogeneic haematopoietic cell transplant: 18-year trends in aetiology, resistance and mortality</atitle><jtitle>Bone marrow transplantation (Basingstoke)</jtitle><addtitle>Bone Marrow Transplant</addtitle><date>2024-12-11</date><risdate>2024</risdate><issn>1476-5365</issn><eissn>1476-5365</eissn><abstract>Bloodstream infections (BSI) are frequent complications after allogeneic hematopoietic cell transplant (HCT). This study reports data on pre-engraftment BSI in years 2016-2021 and analyses changes in incidence, aetiology, resistance and mortality compared with two previous periods (2004-2009 and 2010-2015). In years 2004-2021, 1364 patients received HCT. De-escalation strategy for empirical antibiotic therapy was introduced in 2011. In 381 patients from years 2016-2021, the incidence of pre-engraftment BSI was 37.8%. Independent predictors of BSI were older age, AML/MDS and active disease. In 1364 patients, the incidence of BSI increased from 22% in period 1 to 38% in period 3 (p = 0.008), particularly gram-negative BSI: from 10.1% to 19.7% (p = 0.001). Among gram-negatives, resistance to third-generation cephalosporins remained stable (40.2% in period 3), while resistance to carbapenems and fluoroquinolones decreased (respectively, 12.6% and 59.8% in period 3). 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title | Pre-engraftment bloodstream infection after allogeneic haematopoietic cell transplant: 18-year trends in aetiology, resistance and mortality |
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