Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Center for Cellular and Molecular Medicine, Kyushu University Hospital, Fukuoka, Japan.
Biol Blood Marrow Transplant. 2018 Nov;24(11):2302-2309. doi: 10.1016/j.bbmt.2018.06.002. Epub 2018 Jun 15.
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.
血流感染(BSI)是异基因造血干细胞移植(allo-HSCT)受者发病率和死亡率的已知原因。在这里,我们进行了一项回顾性研究,以评估 allo-HSCT 后植入后期间(PE-BSI)BSI 的发病率、病因、危险因素和结果。316 例患者中有 43 例(13.6%)发生了 57 次 PE-BSI 发作,其中 62 种病原体被分离出来:革兰阳性菌、革兰阴性菌和真菌分别占分离物的 54.8%、35.5%和 9.7%。多变量分析显示,用于移植物抗宿主病(GVHD)预防的甲基强的松龙(甲基强的松龙)(优势比[OR],6.49;95%置信区间[CI],1.49 至 28.2;P=.013)和急性胃肠道 GVHD(GI-GVHD)(OR,8.82;95%CI,3.99 至 19.5;P <.0001)是发生 PE-BSI 的危险因素。这一发现表明,GI-GVHD 增加了细菌易位和随后败血症的风险。此外,在患有 GI-GVHD 的患者中,皮质类固醇反应不足,推测与肠道菌群失调有关,与这种并发症显著相关。与没有发生血流感染的患者相比,发生血流感染的患者预后更差(3 年总生存率,47.0%对 18.6%;P <.001)。密切监测血流感染和最大限度地减少肠道菌群失调可能是打破 GI-GVHD 和菌血症之间恶性循环的关键,尤其是在需要额外免疫抑制剂的患者中,可以改善移植结果。