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Clostridioides difficile infection in solid organ and hematopoietic stem cell transplant recipients: A prospective multinational study

Background Clostridioides difficile infection (CDI) is a significant cause of morbidity and mortality in recipients of solid organ transplant (SOT) or hematopoietic stem cell transplant (HSCT). In retrospective single center analyses, severe disease and relapse are common. We undertook an internatio...

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Published in:Transplant infectious disease 2022-02, Vol.24 (1), p.e13770-n/a
Main Authors: Blumberg, Emily A., Collins, Gary, Young, Jo‐Anne H., Nguyen, M. Hong, Michonneau, David, Temesgen, Zelelem, Origȕen, Julia, Barcan, Laura, Obeid, Karam M., Belloso, Waldo H., Gras, Julien, Corbelli, Giulio Maria, Neaton, James D., Lundgren, Jens, Snydman, David R., Molina, Jean‐Michel
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cited_by cdi_FETCH-LOGICAL-c3530-99617352418fe91c76380c31114d0dcf06236cce7ed82c2dd124b059dd927303
cites cdi_FETCH-LOGICAL-c3530-99617352418fe91c76380c31114d0dcf06236cce7ed82c2dd124b059dd927303
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container_issue 1
container_start_page e13770
container_title Transplant infectious disease
container_volume 24
creator Blumberg, Emily A.
Collins, Gary
Young, Jo‐Anne H.
Nguyen, M. Hong
Michonneau, David
Temesgen, Zelelem
Origȕen, Julia
Barcan, Laura
Obeid, Karam M.
Belloso, Waldo H.
Gras, Julien
Corbelli, Giulio Maria
Neaton, James D.
Lundgren, Jens
Snydman, David R.
Molina, Jean‐Michel
description Background Clostridioides difficile infection (CDI) is a significant cause of morbidity and mortality in recipients of solid organ transplant (SOT) or hematopoietic stem cell transplant (HSCT). In retrospective single center analyses, severe disease and relapse are common. We undertook an international, prospective cohort study to estimate the response to physician determined antibiotic treatment for CDI in patients with SOT and HSCT. Methods Adults with a first episode of CDI within the first 2 years of SOT or HSCT were enrolled. Demographics, comorbidities, and medication history were collected, and over 90 days of follow‐up clinical cure, recurrences, and complications were assessed. Logistic regression was used to study associations of baseline predictors of clinical cure and recurrence. Odds ratios (ORs) and 95% confidence intervals (CIs) are cited. Results A total of 132 patients, 81 SOT and 51 HSCT (32 allogeneic), were enrolled with a median age of 56 years; 82 (62%) were males and 128 (97%) were hospitalized at enrollment. One hundred and six (80.3%) were diagnosed by DNA assay. CDI occurred at a median of 20 days post‐transplant (interquartile range, IQR: 6–133). One hundred and eight patients (81.8%) were on proton pump inhibitors; 126 patients (95.5%) received antibiotics within the 6 weeks before CDI. The most common initial CDI treatments prescribed, on or shortly before enrollment, were oral vancomycin alone (50%) and metronidazole alone (36%). Eighty‐three percent (95% CI: 76, 89) of patients had clinical cure; 18% (95% CI: 12, 27) of patients had recurrent CDI; global clinical cure occurred in 65.2%. Of the 11 patients who died, two (1.5% of total) were related to CDI. In multivariable logistic regression analyses, the type of initial treatment was associated with clinical cure (p = .009) and recurrence (p = .014). A history of cytomegalovirus (CMV) after transplant was associated with increased risk of recurrence (44% with versus 13% without CMV history; OR: 5.7, 95% CI: 1.5, 21.3; p = .01). Conclusions Among adults who develop CDI after SOT or HSCT, despite their immunosuppressed state, the percentage with clinical cure was high and the percentage with recurrence was low. Clinical cure and recurrence varied by type of initial treatment, and CMV viremia/disease was associated with an increased risk of recurrence.
doi_str_mv 10.1111/tid.13770
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Hong ; Michonneau, David ; Temesgen, Zelelem ; Origȕen, Julia ; Barcan, Laura ; Obeid, Karam M. ; Belloso, Waldo H. ; Gras, Julien ; Corbelli, Giulio Maria ; Neaton, James D. ; Lundgren, Jens ; Snydman, David R. ; Molina, Jean‐Michel</creator><creatorcontrib>Blumberg, Emily A. ; Collins, Gary ; Young, Jo‐Anne H. ; Nguyen, M. Hong ; Michonneau, David ; Temesgen, Zelelem ; Origȕen, Julia ; Barcan, Laura ; Obeid, Karam M. ; Belloso, Waldo H. ; Gras, Julien ; Corbelli, Giulio Maria ; Neaton, James D. ; Lundgren, Jens ; Snydman, David R. ; Molina, Jean‐Michel ; INSIGHT Clostridioides difficile Study Group ; for the INSIGHT Clostridioides difficile Study Group</creatorcontrib><description>Background Clostridioides difficile infection (CDI) is a significant cause of morbidity and mortality in recipients of solid organ transplant (SOT) or hematopoietic stem cell transplant (HSCT). In retrospective single center analyses, severe disease and relapse are common. We undertook an international, prospective cohort study to estimate the response to physician determined antibiotic treatment for CDI in patients with SOT and HSCT. Methods Adults with a first episode of CDI within the first 2 years of SOT or HSCT were enrolled. Demographics, comorbidities, and medication history were collected, and over 90 days of follow‐up clinical cure, recurrences, and complications were assessed. Logistic regression was used to study associations of baseline predictors of clinical cure and recurrence. Odds ratios (ORs) and 95% confidence intervals (CIs) are cited. Results A total of 132 patients, 81 SOT and 51 HSCT (32 allogeneic), were enrolled with a median age of 56 years; 82 (62%) were males and 128 (97%) were hospitalized at enrollment. One hundred and six (80.3%) were diagnosed by DNA assay. CDI occurred at a median of 20 days post‐transplant (interquartile range, IQR: 6–133). One hundred and eight patients (81.8%) were on proton pump inhibitors; 126 patients (95.5%) received antibiotics within the 6 weeks before CDI. The most common initial CDI treatments prescribed, on or shortly before enrollment, were oral vancomycin alone (50%) and metronidazole alone (36%). Eighty‐three percent (95% CI: 76, 89) of patients had clinical cure; 18% (95% CI: 12, 27) of patients had recurrent CDI; global clinical cure occurred in 65.2%. Of the 11 patients who died, two (1.5% of total) were related to CDI. In multivariable logistic regression analyses, the type of initial treatment was associated with clinical cure (p = .009) and recurrence (p = .014). A history of cytomegalovirus (CMV) after transplant was associated with increased risk of recurrence (44% with versus 13% without CMV history; OR: 5.7, 95% CI: 1.5, 21.3; p = .01). Conclusions Among adults who develop CDI after SOT or HSCT, despite their immunosuppressed state, the percentage with clinical cure was high and the percentage with recurrence was low. Clinical cure and recurrence varied by type of initial treatment, and CMV viremia/disease was associated with an increased risk of recurrence.</description><identifier>ISSN: 1398-2273</identifier><identifier>EISSN: 1399-3062</identifier><identifier>DOI: 10.1111/tid.13770</identifier><identifier>PMID: 34821423</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>Adults ; Anti-Bacterial Agents - therapeutic use ; Antibiotics ; Clostridioides difficile ; Clostridium difficile infection ; Clostridium Infections - drug therapy ; Clostridium Infections - epidemiology ; Confidence intervals ; Cytomegalovirus ; Demographics ; Demography ; Enrollments ; Health services ; hematopoietic stem cell transplantation ; Hematopoietic Stem Cell Transplantation - adverse effects ; Hematopoietic stem cells ; Humans ; Male ; Metronidazole ; Middle Aged ; Morbidity ; Patients ; Prospective Studies ; Proton pump inhibitors ; Recurrence ; Regression analysis ; Retrospective Studies ; solid organ transplantation ; Statistical analysis ; Stem cell transplantation ; Stem cells ; Transplant Recipients ; Vancomycin ; Viremia</subject><ispartof>Transplant infectious disease, 2022-02, Vol.24 (1), p.e13770-n/a</ispartof><rights>2021 Wiley Periodicals LLC</rights><rights>2021 Wiley Periodicals LLC.</rights><rights>2022 Wiley Periodicals LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3530-99617352418fe91c76380c31114d0dcf06236cce7ed82c2dd124b059dd927303</citedby><cites>FETCH-LOGICAL-c3530-99617352418fe91c76380c31114d0dcf06236cce7ed82c2dd124b059dd927303</cites><orcidid>0000-0003-4553-3065 ; 0000-0001-8901-7850 ; 0000-0002-5193-6170 ; 0000-0002-4791-7727 ; 0000-0002-4131-647X ; 0000-0001-7247-3358 ; 0000-0001-9179-6697 ; 0000-0001-5246-7161 ; 0000-0003-4182-341X ; 0000-0002-7048-7841 ; 0000-0003-0119-3978</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34821423$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blumberg, Emily A.</creatorcontrib><creatorcontrib>Collins, Gary</creatorcontrib><creatorcontrib>Young, Jo‐Anne H.</creatorcontrib><creatorcontrib>Nguyen, M. Hong</creatorcontrib><creatorcontrib>Michonneau, David</creatorcontrib><creatorcontrib>Temesgen, Zelelem</creatorcontrib><creatorcontrib>Origȕen, Julia</creatorcontrib><creatorcontrib>Barcan, Laura</creatorcontrib><creatorcontrib>Obeid, Karam M.</creatorcontrib><creatorcontrib>Belloso, Waldo H.</creatorcontrib><creatorcontrib>Gras, Julien</creatorcontrib><creatorcontrib>Corbelli, Giulio Maria</creatorcontrib><creatorcontrib>Neaton, James D.</creatorcontrib><creatorcontrib>Lundgren, Jens</creatorcontrib><creatorcontrib>Snydman, David R.</creatorcontrib><creatorcontrib>Molina, Jean‐Michel</creatorcontrib><creatorcontrib>INSIGHT Clostridioides difficile Study Group</creatorcontrib><creatorcontrib>for the INSIGHT Clostridioides difficile Study Group</creatorcontrib><title>Clostridioides difficile infection in solid organ and hematopoietic stem cell transplant recipients: A prospective multinational study</title><title>Transplant infectious disease</title><addtitle>Transpl Infect Dis</addtitle><description>Background Clostridioides difficile infection (CDI) is a significant cause of morbidity and mortality in recipients of solid organ transplant (SOT) or hematopoietic stem cell transplant (HSCT). In retrospective single center analyses, severe disease and relapse are common. We undertook an international, prospective cohort study to estimate the response to physician determined antibiotic treatment for CDI in patients with SOT and HSCT. Methods Adults with a first episode of CDI within the first 2 years of SOT or HSCT were enrolled. Demographics, comorbidities, and medication history were collected, and over 90 days of follow‐up clinical cure, recurrences, and complications were assessed. Logistic regression was used to study associations of baseline predictors of clinical cure and recurrence. Odds ratios (ORs) and 95% confidence intervals (CIs) are cited. Results A total of 132 patients, 81 SOT and 51 HSCT (32 allogeneic), were enrolled with a median age of 56 years; 82 (62%) were males and 128 (97%) were hospitalized at enrollment. One hundred and six (80.3%) were diagnosed by DNA assay. CDI occurred at a median of 20 days post‐transplant (interquartile range, IQR: 6–133). One hundred and eight patients (81.8%) were on proton pump inhibitors; 126 patients (95.5%) received antibiotics within the 6 weeks before CDI. The most common initial CDI treatments prescribed, on or shortly before enrollment, were oral vancomycin alone (50%) and metronidazole alone (36%). Eighty‐three percent (95% CI: 76, 89) of patients had clinical cure; 18% (95% CI: 12, 27) of patients had recurrent CDI; global clinical cure occurred in 65.2%. Of the 11 patients who died, two (1.5% of total) were related to CDI. In multivariable logistic regression analyses, the type of initial treatment was associated with clinical cure (p = .009) and recurrence (p = .014). A history of cytomegalovirus (CMV) after transplant was associated with increased risk of recurrence (44% with versus 13% without CMV history; OR: 5.7, 95% CI: 1.5, 21.3; p = .01). Conclusions Among adults who develop CDI after SOT or HSCT, despite their immunosuppressed state, the percentage with clinical cure was high and the percentage with recurrence was low. Clinical cure and recurrence varied by type of initial treatment, and CMV viremia/disease was associated with an increased risk of recurrence.</description><subject>Adults</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Antibiotics</subject><subject>Clostridioides difficile</subject><subject>Clostridium difficile infection</subject><subject>Clostridium Infections - drug therapy</subject><subject>Clostridium Infections - epidemiology</subject><subject>Confidence intervals</subject><subject>Cytomegalovirus</subject><subject>Demographics</subject><subject>Demography</subject><subject>Enrollments</subject><subject>Health services</subject><subject>hematopoietic stem cell transplantation</subject><subject>Hematopoietic Stem Cell Transplantation - adverse effects</subject><subject>Hematopoietic stem cells</subject><subject>Humans</subject><subject>Male</subject><subject>Metronidazole</subject><subject>Middle Aged</subject><subject>Morbidity</subject><subject>Patients</subject><subject>Prospective Studies</subject><subject>Proton pump inhibitors</subject><subject>Recurrence</subject><subject>Regression analysis</subject><subject>Retrospective Studies</subject><subject>solid organ transplantation</subject><subject>Statistical analysis</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Transplant Recipients</subject><subject>Vancomycin</subject><subject>Viremia</subject><issn>1398-2273</issn><issn>1399-3062</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kc1u1TAQhS0EoqWw4AWQJTawSOufxInZVbcFKlVic_eRa09gKscOtgO6L8Bz4_QWFkh441l8c3TmHEJec3bO67so6M657Hv2hJxyqXUjmRJPH-ahEaKXJ-RFzveM8V63-jk5ke0geCvkKfm18zGXhA4jOsjU4TShRQ8UwwS2YAx1ojl6dDSmryZQExz9BrMpcYkIBS3NBWZqwXtakgl58SYUmsDighBK_kAv6ZJiXja9H0Dn1RcMZtM2vi6v7vCSPJuMz_Dq8T8j-4_X-93n5vbLp5vd5W1jZSdZo7XivexEy4cJNLe9kgOzsmbQOubsVM-WylrowQ3CCue4aO9Yp53TNQUmz8i7o2y1832FXMYZ82bcBIhrHoViQslOdRv69h_0Pq6pGt4oobjqqplKvT9Stt6XE0zjknA26TByNm7djLWb8aGbyr55VFzvZnB_yT9lVODiCPys-R_-rzTub66Okr8B6xGaCg</recordid><startdate>202202</startdate><enddate>202202</enddate><creator>Blumberg, Emily A.</creator><creator>Collins, Gary</creator><creator>Young, Jo‐Anne H.</creator><creator>Nguyen, M. Hong</creator><creator>Michonneau, David</creator><creator>Temesgen, Zelelem</creator><creator>Origȕen, Julia</creator><creator>Barcan, Laura</creator><creator>Obeid, Karam M.</creator><creator>Belloso, Waldo H.</creator><creator>Gras, Julien</creator><creator>Corbelli, Giulio Maria</creator><creator>Neaton, James D.</creator><creator>Lundgren, Jens</creator><creator>Snydman, David R.</creator><creator>Molina, Jean‐Michel</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4553-3065</orcidid><orcidid>https://orcid.org/0000-0001-8901-7850</orcidid><orcidid>https://orcid.org/0000-0002-5193-6170</orcidid><orcidid>https://orcid.org/0000-0002-4791-7727</orcidid><orcidid>https://orcid.org/0000-0002-4131-647X</orcidid><orcidid>https://orcid.org/0000-0001-7247-3358</orcidid><orcidid>https://orcid.org/0000-0001-9179-6697</orcidid><orcidid>https://orcid.org/0000-0001-5246-7161</orcidid><orcidid>https://orcid.org/0000-0003-4182-341X</orcidid><orcidid>https://orcid.org/0000-0002-7048-7841</orcidid><orcidid>https://orcid.org/0000-0003-0119-3978</orcidid></search><sort><creationdate>202202</creationdate><title>Clostridioides difficile infection in solid organ and hematopoietic stem cell transplant recipients: A prospective multinational study</title><author>Blumberg, Emily A. ; Collins, Gary ; Young, Jo‐Anne H. ; Nguyen, M. Hong ; Michonneau, David ; Temesgen, Zelelem ; Origȕen, Julia ; Barcan, Laura ; Obeid, Karam M. ; Belloso, Waldo H. ; Gras, Julien ; Corbelli, Giulio Maria ; Neaton, James D. ; Lundgren, Jens ; Snydman, David R. ; Molina, Jean‐Michel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3530-99617352418fe91c76380c31114d0dcf06236cce7ed82c2dd124b059dd927303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adults</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Antibiotics</topic><topic>Clostridioides difficile</topic><topic>Clostridium difficile infection</topic><topic>Clostridium Infections - drug therapy</topic><topic>Clostridium Infections - epidemiology</topic><topic>Confidence intervals</topic><topic>Cytomegalovirus</topic><topic>Demographics</topic><topic>Demography</topic><topic>Enrollments</topic><topic>Health services</topic><topic>hematopoietic stem cell transplantation</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>Hematopoietic stem cells</topic><topic>Humans</topic><topic>Male</topic><topic>Metronidazole</topic><topic>Middle Aged</topic><topic>Morbidity</topic><topic>Patients</topic><topic>Prospective Studies</topic><topic>Proton pump inhibitors</topic><topic>Recurrence</topic><topic>Regression analysis</topic><topic>Retrospective Studies</topic><topic>solid organ transplantation</topic><topic>Statistical analysis</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><topic>Transplant Recipients</topic><topic>Vancomycin</topic><topic>Viremia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blumberg, Emily A.</creatorcontrib><creatorcontrib>Collins, Gary</creatorcontrib><creatorcontrib>Young, Jo‐Anne H.</creatorcontrib><creatorcontrib>Nguyen, M. Hong</creatorcontrib><creatorcontrib>Michonneau, David</creatorcontrib><creatorcontrib>Temesgen, Zelelem</creatorcontrib><creatorcontrib>Origȕen, Julia</creatorcontrib><creatorcontrib>Barcan, Laura</creatorcontrib><creatorcontrib>Obeid, Karam M.</creatorcontrib><creatorcontrib>Belloso, Waldo H.</creatorcontrib><creatorcontrib>Gras, Julien</creatorcontrib><creatorcontrib>Corbelli, Giulio Maria</creatorcontrib><creatorcontrib>Neaton, James D.</creatorcontrib><creatorcontrib>Lundgren, Jens</creatorcontrib><creatorcontrib>Snydman, David R.</creatorcontrib><creatorcontrib>Molina, Jean‐Michel</creatorcontrib><creatorcontrib>INSIGHT Clostridioides difficile Study Group</creatorcontrib><creatorcontrib>for the INSIGHT Clostridioides difficile Study Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transplant infectious disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blumberg, Emily A.</au><au>Collins, Gary</au><au>Young, Jo‐Anne H.</au><au>Nguyen, M. Hong</au><au>Michonneau, David</au><au>Temesgen, Zelelem</au><au>Origȕen, Julia</au><au>Barcan, Laura</au><au>Obeid, Karam M.</au><au>Belloso, Waldo H.</au><au>Gras, Julien</au><au>Corbelli, Giulio Maria</au><au>Neaton, James D.</au><au>Lundgren, Jens</au><au>Snydman, David R.</au><au>Molina, Jean‐Michel</au><aucorp>INSIGHT Clostridioides difficile Study Group</aucorp><aucorp>for the INSIGHT Clostridioides difficile Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clostridioides difficile infection in solid organ and hematopoietic stem cell transplant recipients: A prospective multinational study</atitle><jtitle>Transplant infectious disease</jtitle><addtitle>Transpl Infect Dis</addtitle><date>2022-02</date><risdate>2022</risdate><volume>24</volume><issue>1</issue><spage>e13770</spage><epage>n/a</epage><pages>e13770-n/a</pages><issn>1398-2273</issn><eissn>1399-3062</eissn><abstract>Background Clostridioides difficile infection (CDI) is a significant cause of morbidity and mortality in recipients of solid organ transplant (SOT) or hematopoietic stem cell transplant (HSCT). In retrospective single center analyses, severe disease and relapse are common. We undertook an international, prospective cohort study to estimate the response to physician determined antibiotic treatment for CDI in patients with SOT and HSCT. Methods Adults with a first episode of CDI within the first 2 years of SOT or HSCT were enrolled. Demographics, comorbidities, and medication history were collected, and over 90 days of follow‐up clinical cure, recurrences, and complications were assessed. Logistic regression was used to study associations of baseline predictors of clinical cure and recurrence. Odds ratios (ORs) and 95% confidence intervals (CIs) are cited. Results A total of 132 patients, 81 SOT and 51 HSCT (32 allogeneic), were enrolled with a median age of 56 years; 82 (62%) were males and 128 (97%) were hospitalized at enrollment. One hundred and six (80.3%) were diagnosed by DNA assay. CDI occurred at a median of 20 days post‐transplant (interquartile range, IQR: 6–133). One hundred and eight patients (81.8%) were on proton pump inhibitors; 126 patients (95.5%) received antibiotics within the 6 weeks before CDI. The most common initial CDI treatments prescribed, on or shortly before enrollment, were oral vancomycin alone (50%) and metronidazole alone (36%). Eighty‐three percent (95% CI: 76, 89) of patients had clinical cure; 18% (95% CI: 12, 27) of patients had recurrent CDI; global clinical cure occurred in 65.2%. Of the 11 patients who died, two (1.5% of total) were related to CDI. In multivariable logistic regression analyses, the type of initial treatment was associated with clinical cure (p = .009) and recurrence (p = .014). A history of cytomegalovirus (CMV) after transplant was associated with increased risk of recurrence (44% with versus 13% without CMV history; OR: 5.7, 95% CI: 1.5, 21.3; p = .01). Conclusions Among adults who develop CDI after SOT or HSCT, despite their immunosuppressed state, the percentage with clinical cure was high and the percentage with recurrence was low. Clinical cure and recurrence varied by type of initial treatment, and CMV viremia/disease was associated with an increased risk of recurrence.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34821423</pmid><doi>10.1111/tid.13770</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-4553-3065</orcidid><orcidid>https://orcid.org/0000-0001-8901-7850</orcidid><orcidid>https://orcid.org/0000-0002-5193-6170</orcidid><orcidid>https://orcid.org/0000-0002-4791-7727</orcidid><orcidid>https://orcid.org/0000-0002-4131-647X</orcidid><orcidid>https://orcid.org/0000-0001-7247-3358</orcidid><orcidid>https://orcid.org/0000-0001-9179-6697</orcidid><orcidid>https://orcid.org/0000-0001-5246-7161</orcidid><orcidid>https://orcid.org/0000-0003-4182-341X</orcidid><orcidid>https://orcid.org/0000-0002-7048-7841</orcidid><orcidid>https://orcid.org/0000-0003-0119-3978</orcidid></addata></record>
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identifier ISSN: 1398-2273
ispartof Transplant infectious disease, 2022-02, Vol.24 (1), p.e13770-n/a
issn 1398-2273
1399-3062
language eng
recordid cdi_proquest_miscellaneous_2602635650
source Wiley
subjects Adults
Anti-Bacterial Agents - therapeutic use
Antibiotics
Clostridioides difficile
Clostridium difficile infection
Clostridium Infections - drug therapy
Clostridium Infections - epidemiology
Confidence intervals
Cytomegalovirus
Demographics
Demography
Enrollments
Health services
hematopoietic stem cell transplantation
Hematopoietic Stem Cell Transplantation - adverse effects
Hematopoietic stem cells
Humans
Male
Metronidazole
Middle Aged
Morbidity
Patients
Prospective Studies
Proton pump inhibitors
Recurrence
Regression analysis
Retrospective Studies
solid organ transplantation
Statistical analysis
Stem cell transplantation
Stem cells
Transplant Recipients
Vancomycin
Viremia
title Clostridioides difficile infection in solid organ and hematopoietic stem cell transplant recipients: A prospective multinational study
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