| Literature DB >> 29909153 |
Yasuo Mori1, Goichi Yoshimoto1, Ruriko Nishida1, Takeshi Sugio1, Kohta Miyawaki1, Takahiro Shima1, Yoji Nagasaki1, Noriko Miyake1, Yukiko Harada1, Yuya Kunisaki2, Kenjiro Kamezaki2, Akihiko Numata1, Koji Kato1, Motoaki Shiratsuchi3, Takahiro Maeda2, Katsuto Takenaka1, Hiromi Iwasaki1, Nobuyuki Shimono1, Koichi Akashi4, Toshihiro Miyamoto5.
Abstract
Bloodstream infection (BSI) is a well-known cause of morbidity and mortality in allogeneic hematopoietic stem cell transplant (allo-HSCT) recipients. Here, we conducted a retrospective study to assess the morbidity, etiology, risk factors, and outcomes of BSI in the postengraftment period (PE-BSI) after allo-HSCT. Forty-three of 316 patients (13.6%) developed 57 PE-BSI episodes, in which 62 pathogens were isolated: Gram-positive bacteria, gram-negative bacteria, and fungi, respectively, accounted for 54.8%, 35.5%, and 9.7% of the isolates. Multivariate analysis revealed methylprednisolone use for graft-versus-host disease (GVHD) prophylaxis (odds ratio [OR], 6.49; 95% confidence interval [CI], 1.49 to 28.2; P = .013) and acute gastrointestinal GVHD (GI-GVHD) (OR, 8.82; 95% CI, 3.99 to 19.5; P < .0001) as risk factors for developing PE-BSI. This finding suggested that GI-GVHD increases the risk of bacterial translocation and subsequent septicemia. Moreover, among patients with GI-GVHD, insufficient response to corticosteroids, presumably related to an intestinal dysbiosis, significantly correlated with this complication. Patients with PE-BSI presented worse outcome compared with those without (3-year overall survival, 47.0% versus 18.6%; P < .001). Close microbiologic monitoring for BSIs and minimizing intestinal dysbiosis may be crucial to break the vicious cycle between GI-GVHD and bacteremia and to improve transplant outcomes especially in patients who require additional immunosuppressants.Entities:
Keywords: Bacteremia; Gastrointestinal tract; Graft-versus-host disease; Hematopoietic stem cell transplantation
Mesh:
Year: 2018 PMID: 29909153 DOI: 10.1016/j.bbmt.2018.06.002
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742