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接受异基因骨髓移植的儿童可能会在后期(100天后)发生血流感染,和/或在无中性粒细胞减少的情况下发生血流感染。

Bloodstream infections can develop late (after day 100) and/or in the absence of neutropenia in children receiving allogeneic bone marrow transplantation.

作者信息

Romano V, Castagnola E, Dallorso S, Lanino E, Calvi A, Silvestro S, Morreale G, Giacchino R, Dini G

机构信息

Department of Hematology-Oncology, G Gaslini Children's Hospital, Genoa, Italy.

出版信息

Bone Marrow Transplant. 1999 Feb;23(3):271-5. doi: 10.1038/sj.bmt.1701562.

Abstract

We retrospectively evaluated the incidence and time from transplantation of bloodstream infections occurring in children receiving bone marrow transplant (BMT) at G Gaslini Children's Hospital between September 1984 and December 1997. During this period the incidence was 35% after allogeneic and 26% after autologous BMT (P=0.08). Among these episodes, 38% after allogeneic BMT and 90% after autologous BMT were detected in the presence of neutropenia within the first 30 days from reinfusion (P < 0.001). Incidence of catheter-related bloodstream infections was 40% after allogeneic and 8% after autologous BMT (P < 0.001). Bloodstream infections in the absence of neutropenia were 55% after allogeneic BMT vs 10% after autologous BMT (P < 0.001) and occurred later after reinfusion (mean 199 vs 41 days, P <0.001). Among the episodes occurring after allogeneic BMT and in the absence of neutropenia, 61% were related to the presence of a central venous catheter, 15% were related to the presence of GVHD, but 23% were not associated with any of major risk factors for infection. Finally, 38% of episodes following allogeneic BMT were detected after day 100 vs 1% after autologous BMT. We concluded that patients receiving allogeneic BMT experience a high incidence of bloodstream infections in the absence of neutropenia and that a significant proportion of these episodes is not clearly associated with well known risk factors such as GVHD or central venous catheters. Moreover, many episodes develop a long time after the transplantation procedure. Therefore, any febrile episode following allogeneic BMT even late and/or in the absence of neutropenia should be intensively managed.

摘要

我们回顾性评估了1984年9月至1997年12月在G加斯利尼儿童医院接受骨髓移植(BMT)的儿童发生血流感染的发生率及自移植后的时间。在此期间,异基因BMT后发生率为35%,自体BMT后为26%(P = 0.08)。在这些感染事件中,异基因BMT后38%以及自体BMT后90%是在再输注后的前30天内中性粒细胞减少的情况下检测到的(P < 0.001)。异基因BMT后导管相关血流感染的发生率为40%,自体BMT后为8%(P < 0.001)。无中性粒细胞减少情况下的血流感染,异基因BMT后为55%,自体BMT后为10%(P < 0.001),且在再输注后发生时间较晚(平均199天对41天,P < 0.001)。在异基因BMT后且无中性粒细胞减少的感染事件中,61%与中心静脉导管的存在有关,15%与移植物抗宿主病(GVHD)的存在有关,但23%与任何主要感染危险因素均无关。最后,异基因BMT后的感染事件中有38%是在第100天后检测到的,而自体BMT后为1%。我们得出结论,接受异基因BMT的患者在无中性粒细胞减少的情况下血流感染发生率较高,且这些感染事件中有很大一部分与移植物抗宿主病或中心静脉导管等知名危险因素无明显关联。此外,许多感染事件在移植手术后很长时间才发生。因此,异基因BMT后的任何发热事件,即使发生较晚和/或无中性粒细胞减少,都应进行强化处理。

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