{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,23]],"date-time":"2026-08-23T17:22:34Z","timestamp":1787505754747,"version":"build-2736575974"},"reference-count":20,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2014,12,27]],"date-time":"2014-12-27T00:00:00Z","timestamp":1419638400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Transplant Infectious Dis"],"published-print":{"date-parts":[[2015,2]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                        seudomonas aeruginosa\n                      <\/jats:italic>\n                      , especially multidrug\u2010resistant (\n                      <jats:styled-content style=\"fixed-case\">MDR<\/jats:styled-content>\n                      ) isolates, is an important pathogen in allogeneic hematopoietic stem cell transplant (\n                      <jats:styled-content style=\"fixed-case\">HCT<\/jats:styled-content>\n                      ) recipients. The ability to identify patients at risk for these infections and administer appropriate empiric therapy, particularly during episodes of neutropenia, may improve outcomes and also direct infection control and antimicrobial stewardship efforts. Many transplant centers obtain routine surveillance stool cultures (\n                      <jats:styled-content style=\"fixed-case\">SSC<\/jats:styled-content>\n                      s) from\n                      <jats:styled-content style=\"fixed-case\">HCT<\/jats:styled-content>\n                      recipients to test for colonization with vancomycin\u2010resistant enterococci, and extended\u2010spectrum beta lactamase\u2010producing Enterobacteriaceae. Our center initiated the performance of\n                      <jats:styled-content style=\"fixed-case\">SSC<\/jats:styled-content>\n                      s for\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                        .\u00a0aeruginosa\n                      <\/jats:italic>\n                      , because of a perceived increase in the frequency of infection with\n                      <jats:styled-content style=\"fixed-case\">MDR<\/jats:styled-content>\n                      strains. The aim of this study was to determine the utility of this practice.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      We conducted a 2\u2010year (2010\u20132011) retrospective review of the medical records of all patients who underwent allogeneic\n                      <jats:styled-content style=\"fixed-case\">HCT<\/jats:styled-content>\n                      at our cancer center to (a) determine the frequency of fecal colonization with\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                        .\u00a0aeruginosa\n                      <\/jats:italic>\n                      , including\n                      <jats:styled-content style=\"fixed-case\">MDR<\/jats:styled-content>\n                      strains; (b) to determine the overall frequency of subsequent\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                        .\u00a0aeruginosa\n                      <\/jats:italic>\n                      infection, as well as the frequency of infection with\n                      <jats:styled-content style=\"fixed-case\">MDR<\/jats:styled-content>\n                      strains; (c) to ascertain the proportion of subsequent infections likely arising from the intestinal tract; and (d) to determine risk factors for progression from colonization to infection.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Of 794 study patients, 58 (7.3%) had at least 1 positive\n                      <jats:styled-content style=\"fixed-case\">SSC<\/jats:styled-content>\n                      for\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                      <\/jats:italic>\n                      .\u00a0\n                      <jats:italic>aeruginosa;<\/jats:italic>\n                      19\/58 (32.8%) developed a subsequent pseudomonal infection (11 with matching antimicrobial resistance patterns). On the other hand, 37\/736 (5%) of the patients who were not colonized, developed a pseudomonal infection. The type of infection observed was pneumonia in 26 (46%) patients, bloodstream infection in 20 (36%), urinary tract infection in 8 (14%), and infections at other sites in 2 (4%). The incidence of\n                      <jats:styled-content style=\"fixed-case\">MDR<\/jats:styled-content>\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                        .\u00a0aeruginosa\n                      <\/jats:italic>\n                      in the entire cohort was 2.2% (18 of 794): 12 had positive\n                      <jats:styled-content style=\"fixed-case\">SSC<\/jats:styled-content>\n                      s and 7 of these patients later developed\n                      <jats:styled-content style=\"fixed-case\">MDR<\/jats:styled-content>\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                        .\u00a0aeruginosa\n                      <\/jats:italic>\n                      infections. Patients with acute myelogenous leukemia were more likely to be colonized and to develop subsequent infection. No infection\u2010related deaths were observed during the first 30\u00a0days after infection.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      The incidence of\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                        .\u00a0aeruginosa\n                      <\/jats:italic>\n                      colonization and subsequent infection was low. Patients who were not colonized had a low chance of developing\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                        .\u00a0aeruginosa\n                      <\/jats:italic>\n                      infection. Most patients who developed infection did not have fecal colonization, suggesting a different source of infection.\n                      <jats:styled-content style=\"fixed-case\">SSC<\/jats:styled-content>\n                      s for\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                        .\u00a0aeruginosa\n                      <\/jats:italic>\n                      provide incomplete information regarding the source of infection.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/tid.12323","type":"journal-article","created":{"date-parts":[[2014,12,27]],"date-time":"2014-12-27T00:45:16Z","timestamp":1419641116000},"page":"33-38","source":"Crossref","is-referenced-by-count":55,"title":["Fecal colonization and infection with\n                    <i>\n                      <scp>P<\/scp>\n                      seudomonas aeruginosa\n                    <\/i>\n                    in recipients of allogeneic hematopoietic stem cell transplantation"],"prefix":"10.1111","volume":"17","author":[{"given":"L.","family":"Nesher","sequence":"first","affiliation":[{"name":"Department of Infectious Diseases, Infection Control and Employee Health The University of Texas MD Anderson Cancer Center Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K.V.I.","family":"Rolston","sequence":"additional","affiliation":[{"name":"Department of Infectious Diseases, Infection Control and Employee Health The University of Texas MD Anderson Cancer Center Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D.P.","family":"Shah","sequence":"additional","affiliation":[{"name":"Department of Infectious Diseases, Infection Control and Employee Health The University of Texas MD Anderson Cancer Center Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J.T.","family":"Tarrand","sequence":"additional","affiliation":[{"name":"Department of Laboratory Medicine The University of Texas MD Anderson Cancer Center Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"V.","family":"Mulanovich","sequence":"additional","affiliation":[{"name":"Department of Infectious Diseases, Infection Control and Employee Health The University of Texas MD Anderson Cancer Center Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E.J.","family":"Ariza\u2010Heredia","sequence":"additional","affiliation":[{"name":"Department of Infectious Diseases, Infection Control and Employee Health The University of Texas MD Anderson Cancer Center Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R.F.","family":"Chemaly","sequence":"additional","affiliation":[{"name":"Department of Infectious Diseases, Infection 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