Grading bloodstream infection risk using citrulline as a biomarker of intestinal mucositis in patients receiving intensive therapy

Earlier studies have suggested that severe intestinal mucositis (IM; citrulline

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2022-09, Vol.57 (9), p.1373-1381
Hauptverfasser: de Mooij, C. E. M., van der Velden, W. J. F. M., de Haan, A. F. J., Fazel, S., van Groningen, L. F. J., Blijlevens, N. M. A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1381
container_issue 9
container_start_page 1373
container_title Bone marrow transplantation (Basingstoke)
container_volume 57
creator de Mooij, C. E. M.
van der Velden, W. J. F. M.
de Haan, A. F. J.
Fazel, S.
van Groningen, L. F. J.
Blijlevens, N. M. A.
description Earlier studies have suggested that severe intestinal mucositis (IM; citrulline
doi_str_mv 10.1038/s41409-022-01719-1
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2673594523</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2709206385</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-102841baf9028ebbb46162b2ef2436e93e8c25e5b6b90f1be9f083d8d3e9bf893</originalsourceid><addsrcrecordid>eNp9kT1v1TAUhi0EoreFP8CALLGwBPydeERVKZUqscBs2clxcZvEFx-nUld-Ob7cAhIDky37eV9_PIS84uwdZ3J4j4orZjsmRMd4z23Hn5AdV73ptDT6KdkxYYZOSmNPyCniLWNcKaafkxOpjeFcmx35cVn8lNYbGuacJ6wF_ELTGmGsKa-0JLyjGx6AMdWyzXNagXqknoaUF1_uoNAcW6IC1rT6mS7bmDHVhG2R7n1NsFakBUZI94eeA7piugdav0Hx-4cX5Fn0M8LLx_GMfP148eX8U3f9-fLq_MN1N8pe144zMSgefLRtAiEEZbgRQUAUShqwEoZRaNDBBMsiD2AjG-Q0TBJsiIOVZ-TtsXdf8vetXdctCUeYZ79C3tAJ00ttlRayoW_-QW_zVtrrGtUzK5iRg26UOFJjyYgFotuX1P7kwXHmDobc0ZBrhtwvQ4630OvH6i0sMP2J_FbSAHkEsG2tN1D-nv2f2p9-6p6F</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2709206385</pqid></control><display><type>article</type><title>Grading bloodstream infection risk using citrulline as a biomarker of intestinal mucositis in patients receiving intensive therapy</title><source>SpringerLink Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>de Mooij, C. E. M. ; van der Velden, W. J. F. M. ; de Haan, A. F. J. ; Fazel, S. ; van Groningen, L. F. J. ; Blijlevens, N. M. A.</creator><creatorcontrib>de Mooij, C. E. M. ; van der Velden, W. J. F. M. ; de Haan, A. F. J. ; Fazel, S. ; van Groningen, L. F. J. ; Blijlevens, N. M. A.</creatorcontrib><description>Earlier studies have suggested that severe intestinal mucositis (IM; citrulline &lt; 10 µmol/L) is an independent risk factor for bloodstream infections (BSI) after cytotoxic therapy. Our aim was to grade IM in patients receiving commonly used chemotherapy and conditioning regimens, and characterize its relationship with BSI incidence. In a retrospective analysis of remission induction (RI) chemotherapy, or conditioning for autologous and allogeneic hematopoietic stem cell transplantation (HSCT; myeloablative conditioning [MAC] and non-myeloablative and reduced-intensity conditioning [NMA/RIC]), data were collected on central venous catheter (CVC) characteristics and BSI. The relationship between BSI occurrence and the degree of IM (determined by citrulline levels) and neutropenia was analyzed. In 626 CVC episodes, 268 (42.8%) laboratory-confirmed BSIs (LCBIs) occurred, classified as mucosal barrier injury (MBI)-LCBIs in 179 (28.6%) episodes, central line–associated BSIs in 113 (18.1%) episodes, and catheter-related BSIs in 55 (8.8%) episodes. In NMA/RIC, the mean duration of hypocitrullinemia was 0.77 days, with LCBI and MBI-LCBI occurring in 11.1% and 4.8% of episodes. In autologous HSCT, RI, and MAC allogeneic HSCT, LCBI and MBI-LCBI occurred frequently (40.0–63.8% and 22.8–53.2% of episodes, respectively) and the mean duration of hypocitrullinemia was significantly higher (9.2–13.8 days). There was a strong correlation between LCBI and the duration of hypocitrullinemia (Pearson’s correlation coefficient R = 0.96), as opposed to the relationship between LCBI and the duration of neutropenia (R = 0.42). We conclude that citrulline can be used to grade BSI risk for commonly used intensive treatment regimens.</description><identifier>ISSN: 0268-3369</identifier><identifier>EISSN: 1476-5365</identifier><identifier>DOI: 10.1038/s41409-022-01719-1</identifier><identifier>PMID: 35661156</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/67/1059/99 ; 631/67/1990 ; 692/699/1541/1990 ; Autografts ; Biomarkers ; Bone marrow ; Catheters ; Cell Biology ; Chemotherapy ; Citrulline ; Conditioning ; Correlation coefficient ; Correlation coefficients ; Cytotoxicity ; Health risks ; Hematology ; Hematopoietic stem cells ; Infections ; Internal Medicine ; Intestine ; Medical instruments ; Medicine ; Medicine &amp; Public Health ; Mucosa ; Mucositis ; Neutropenia ; Patients ; Public Health ; Remission ; Risk analysis ; Risk factors ; Stem cell transplantation ; Stem Cells ; Transplantation</subject><ispartof>Bone marrow transplantation (Basingstoke), 2022-09, Vol.57 (9), p.1373-1381</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2022</rights><rights>2022. The Author(s), under exclusive licence to Springer Nature Limited.</rights><rights>The Author(s), under exclusive licence to Springer Nature Limited 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-102841baf9028ebbb46162b2ef2436e93e8c25e5b6b90f1be9f083d8d3e9bf893</citedby><cites>FETCH-LOGICAL-c375t-102841baf9028ebbb46162b2ef2436e93e8c25e5b6b90f1be9f083d8d3e9bf893</cites><orcidid>0000-0003-3210-2215 ; 0000-0002-7002-9701</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41409-022-01719-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41409-022-01719-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35661156$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Mooij, C. E. M.</creatorcontrib><creatorcontrib>van der Velden, W. J. F. M.</creatorcontrib><creatorcontrib>de Haan, A. F. J.</creatorcontrib><creatorcontrib>Fazel, S.</creatorcontrib><creatorcontrib>van Groningen, L. F. J.</creatorcontrib><creatorcontrib>Blijlevens, N. M. A.</creatorcontrib><title>Grading bloodstream infection risk using citrulline as a biomarker of intestinal mucositis in patients receiving intensive therapy</title><title>Bone marrow transplantation (Basingstoke)</title><addtitle>Bone Marrow Transplant</addtitle><addtitle>Bone Marrow Transplant</addtitle><description>Earlier studies have suggested that severe intestinal mucositis (IM; citrulline &lt; 10 µmol/L) is an independent risk factor for bloodstream infections (BSI) after cytotoxic therapy. Our aim was to grade IM in patients receiving commonly used chemotherapy and conditioning regimens, and characterize its relationship with BSI incidence. In a retrospective analysis of remission induction (RI) chemotherapy, or conditioning for autologous and allogeneic hematopoietic stem cell transplantation (HSCT; myeloablative conditioning [MAC] and non-myeloablative and reduced-intensity conditioning [NMA/RIC]), data were collected on central venous catheter (CVC) characteristics and BSI. The relationship between BSI occurrence and the degree of IM (determined by citrulline levels) and neutropenia was analyzed. In 626 CVC episodes, 268 (42.8%) laboratory-confirmed BSIs (LCBIs) occurred, classified as mucosal barrier injury (MBI)-LCBIs in 179 (28.6%) episodes, central line–associated BSIs in 113 (18.1%) episodes, and catheter-related BSIs in 55 (8.8%) episodes. In NMA/RIC, the mean duration of hypocitrullinemia was 0.77 days, with LCBI and MBI-LCBI occurring in 11.1% and 4.8% of episodes. In autologous HSCT, RI, and MAC allogeneic HSCT, LCBI and MBI-LCBI occurred frequently (40.0–63.8% and 22.8–53.2% of episodes, respectively) and the mean duration of hypocitrullinemia was significantly higher (9.2–13.8 days). There was a strong correlation between LCBI and the duration of hypocitrullinemia (Pearson’s correlation coefficient R = 0.96), as opposed to the relationship between LCBI and the duration of neutropenia (R = 0.42). We conclude that citrulline can be used to grade BSI risk for commonly used intensive treatment regimens.</description><subject>631/67/1059/99</subject><subject>631/67/1990</subject><subject>692/699/1541/1990</subject><subject>Autografts</subject><subject>Biomarkers</subject><subject>Bone marrow</subject><subject>Catheters</subject><subject>Cell Biology</subject><subject>Chemotherapy</subject><subject>Citrulline</subject><subject>Conditioning</subject><subject>Correlation coefficient</subject><subject>Correlation coefficients</subject><subject>Cytotoxicity</subject><subject>Health risks</subject><subject>Hematology</subject><subject>Hematopoietic stem cells</subject><subject>Infections</subject><subject>Internal Medicine</subject><subject>Intestine</subject><subject>Medical instruments</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Mucosa</subject><subject>Mucositis</subject><subject>Neutropenia</subject><subject>Patients</subject><subject>Public Health</subject><subject>Remission</subject><subject>Risk analysis</subject><subject>Risk factors</subject><subject>Stem cell transplantation</subject><subject>Stem Cells</subject><subject>Transplantation</subject><issn>0268-3369</issn><issn>1476-5365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kT1v1TAUhi0EoreFP8CALLGwBPydeERVKZUqscBs2clxcZvEFx-nUld-Ob7cAhIDky37eV9_PIS84uwdZ3J4j4orZjsmRMd4z23Hn5AdV73ptDT6KdkxYYZOSmNPyCniLWNcKaafkxOpjeFcmx35cVn8lNYbGuacJ6wF_ELTGmGsKa-0JLyjGx6AMdWyzXNagXqknoaUF1_uoNAcW6IC1rT6mS7bmDHVhG2R7n1NsFakBUZI94eeA7piugdav0Hx-4cX5Fn0M8LLx_GMfP148eX8U3f9-fLq_MN1N8pe144zMSgefLRtAiEEZbgRQUAUShqwEoZRaNDBBMsiD2AjG-Q0TBJsiIOVZ-TtsXdf8vetXdctCUeYZ79C3tAJ00ttlRayoW_-QW_zVtrrGtUzK5iRg26UOFJjyYgFotuX1P7kwXHmDobc0ZBrhtwvQ4630OvH6i0sMP2J_FbSAHkEsG2tN1D-nv2f2p9-6p6F</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>de Mooij, C. E. M.</creator><creator>van der Velden, W. J. F. M.</creator><creator>de Haan, A. F. J.</creator><creator>Fazel, S.</creator><creator>van Groningen, L. F. J.</creator><creator>Blijlevens, N. M. A.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3210-2215</orcidid><orcidid>https://orcid.org/0000-0002-7002-9701</orcidid></search><sort><creationdate>20220901</creationdate><title>Grading bloodstream infection risk using citrulline as a biomarker of intestinal mucositis in patients receiving intensive therapy</title><author>de Mooij, C. E. M. ; van der Velden, W. J. F. M. ; de Haan, A. F. J. ; Fazel, S. ; van Groningen, L. F. J. ; Blijlevens, N. M. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-102841baf9028ebbb46162b2ef2436e93e8c25e5b6b90f1be9f083d8d3e9bf893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>631/67/1059/99</topic><topic>631/67/1990</topic><topic>692/699/1541/1990</topic><topic>Autografts</topic><topic>Biomarkers</topic><topic>Bone marrow</topic><topic>Catheters</topic><topic>Cell Biology</topic><topic>Chemotherapy</topic><topic>Citrulline</topic><topic>Conditioning</topic><topic>Correlation coefficient</topic><topic>Correlation coefficients</topic><topic>Cytotoxicity</topic><topic>Health risks</topic><topic>Hematology</topic><topic>Hematopoietic stem cells</topic><topic>Infections</topic><topic>Internal Medicine</topic><topic>Intestine</topic><topic>Medical instruments</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Mucosa</topic><topic>Mucositis</topic><topic>Neutropenia</topic><topic>Patients</topic><topic>Public Health</topic><topic>Remission</topic><topic>Risk analysis</topic><topic>Risk factors</topic><topic>Stem cell transplantation</topic><topic>Stem Cells</topic><topic>Transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Mooij, C. E. M.</creatorcontrib><creatorcontrib>van der Velden, W. J. F. M.</creatorcontrib><creatorcontrib>de Haan, A. F. J.</creatorcontrib><creatorcontrib>Fazel, S.</creatorcontrib><creatorcontrib>van Groningen, L. F. J.</creatorcontrib><creatorcontrib>Blijlevens, N. M. A.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Bone marrow transplantation (Basingstoke)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Mooij, C. E. M.</au><au>van der Velden, W. J. F. M.</au><au>de Haan, A. F. J.</au><au>Fazel, S.</au><au>van Groningen, L. F. J.</au><au>Blijlevens, N. M. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Grading bloodstream infection risk using citrulline as a biomarker of intestinal mucositis in patients receiving intensive therapy</atitle><jtitle>Bone marrow transplantation (Basingstoke)</jtitle><stitle>Bone Marrow Transplant</stitle><addtitle>Bone Marrow Transplant</addtitle><date>2022-09-01</date><risdate>2022</risdate><volume>57</volume><issue>9</issue><spage>1373</spage><epage>1381</epage><pages>1373-1381</pages><issn>0268-3369</issn><eissn>1476-5365</eissn><abstract>Earlier studies have suggested that severe intestinal mucositis (IM; citrulline &lt; 10 µmol/L) is an independent risk factor for bloodstream infections (BSI) after cytotoxic therapy. Our aim was to grade IM in patients receiving commonly used chemotherapy and conditioning regimens, and characterize its relationship with BSI incidence. In a retrospective analysis of remission induction (RI) chemotherapy, or conditioning for autologous and allogeneic hematopoietic stem cell transplantation (HSCT; myeloablative conditioning [MAC] and non-myeloablative and reduced-intensity conditioning [NMA/RIC]), data were collected on central venous catheter (CVC) characteristics and BSI. The relationship between BSI occurrence and the degree of IM (determined by citrulline levels) and neutropenia was analyzed. In 626 CVC episodes, 268 (42.8%) laboratory-confirmed BSIs (LCBIs) occurred, classified as mucosal barrier injury (MBI)-LCBIs in 179 (28.6%) episodes, central line–associated BSIs in 113 (18.1%) episodes, and catheter-related BSIs in 55 (8.8%) episodes. In NMA/RIC, the mean duration of hypocitrullinemia was 0.77 days, with LCBI and MBI-LCBI occurring in 11.1% and 4.8% of episodes. In autologous HSCT, RI, and MAC allogeneic HSCT, LCBI and MBI-LCBI occurred frequently (40.0–63.8% and 22.8–53.2% of episodes, respectively) and the mean duration of hypocitrullinemia was significantly higher (9.2–13.8 days). There was a strong correlation between LCBI and the duration of hypocitrullinemia (Pearson’s correlation coefficient R = 0.96), as opposed to the relationship between LCBI and the duration of neutropenia (R = 0.42). We conclude that citrulline can be used to grade BSI risk for commonly used intensive treatment regimens.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>35661156</pmid><doi>10.1038/s41409-022-01719-1</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-3210-2215</orcidid><orcidid>https://orcid.org/0000-0002-7002-9701</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0268-3369
ispartof Bone marrow transplantation (Basingstoke), 2022-09, Vol.57 (9), p.1373-1381
issn 0268-3369
1476-5365
language eng
recordid cdi_proquest_miscellaneous_2673594523
source SpringerLink Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects 631/67/1059/99
631/67/1990
692/699/1541/1990
Autografts
Biomarkers
Bone marrow
Catheters
Cell Biology
Chemotherapy
Citrulline
Conditioning
Correlation coefficient
Correlation coefficients
Cytotoxicity
Health risks
Hematology
Hematopoietic stem cells
Infections
Internal Medicine
Intestine
Medical instruments
Medicine
Medicine & Public Health
Mucosa
Mucositis
Neutropenia
Patients
Public Health
Remission
Risk analysis
Risk factors
Stem cell transplantation
Stem Cells
Transplantation
title Grading bloodstream infection risk using citrulline as a biomarker of intestinal mucositis in patients receiving intensive therapy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T06%3A30%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Grading%20bloodstream%20infection%20risk%20using%20citrulline%20as%20a%20biomarker%20of%20intestinal%20mucositis%20in%20patients%20receiving%20intensive%20therapy&rft.jtitle=Bone%20marrow%20transplantation%20(Basingstoke)&rft.au=de%20Mooij,%20C.%20E.%20M.&rft.date=2022-09-01&rft.volume=57&rft.issue=9&rft.spage=1373&rft.epage=1381&rft.pages=1373-1381&rft.issn=0268-3369&rft.eissn=1476-5365&rft_id=info:doi/10.1038/s41409-022-01719-1&rft_dat=%3Cproquest_cross%3E2709206385%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2709206385&rft_id=info:pmid/35661156&rfr_iscdi=true