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2
Prevention of bacterial infection in pediatric oncology: what do we know, what can we learn?儿科肿瘤的细菌感染预防:我们知道什么,我们能学到什么?
Pediatr Blood Cancer. 2012 Jul 15;59(1):16-20. doi: 10.1002/pbc.23416. Epub 2011 Nov 18.
3
Antifungal prophylaxis in pediatric hematology/oncology: new choices & new data.儿科血液学/肿瘤学中的抗真菌预防:新选择与新数据。
Pediatr Blood Cancer. 2012 Jul 15;59(1):21-6. doi: 10.1002/pbc.23415. Epub 2011 Nov 18.
4
The early addition of arsenic trioxide versus high-dose arabinoside is more effective and safe as consolidation chemotherapy for risk-tailored patients with acute promyelocytic leukemia: multicenter experience.三氧化二砷早期加入 versus 高剂量阿糖胞苷作为个体化危险分层的急性早幼粒细胞白血病巩固化疗更有效更安全:多中心经验。
Med Oncol. 2012 Sep;29(3):2088-94. doi: 10.1007/s12032-011-0099-2. Epub 2011 Oct 30.
5
Recent advances in the diagnosis and management of childhood acute promyelocytic leukemia.儿童急性早幼粒细胞白血病诊断与治疗的最新进展
Korean J Pediatr. 2011 Mar;54(3):95-105. doi: 10.3345/kjp.2011.54.3.95. Epub 2011 Mar 31.
6
Recurrent differentiation syndrome or septic shock? Unresolved dilemma in a patient with acute promyelocytic leukemia.复发性分化综合征还是感染性休克?急性早幼粒细胞白血病患者的未解决难题。
Med Oncol. 2011 Mar;28(1):279-81. doi: 10.1007/s12032-010-9462-y. Epub 2010 Mar 5.
7
Acute promyelocytic leukemia in childhood.儿童急性早幼粒细胞白血病
Curr Oncol Rep. 2009 Nov;11(6):439-45. doi: 10.1007/s11912-009-0060-0.
8
International variations in infection supportive care practices for paediatric patients with acute myeloid leukaemia.国际上小儿急性髓系白血病患儿感染支持性护理实践的差异。
Br J Haematol. 2009 Oct;147(1):125-8. doi: 10.1111/j.1365-2141.2009.07844.x. Epub 2009 Aug 5.
9
Causes and prognostic factors of remission induction failure in patients with acute promyelocytic leukemia treated with all-trans retinoic acid and idarubicin.接受全反式维甲酸和伊达比星治疗的急性早幼粒细胞白血病患者缓解诱导失败的原因及预后因素
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10
Microbiologically documented infections and infection-related mortality in children with acute myeloid leukemia.急性髓系白血病患儿的微生物学确诊感染及感染相关死亡率
Blood. 2007 Nov 15;110(10):3532-9. doi: 10.1182/blood-2007-05-091942. Epub 2007 Jul 27.

儿童急性早幼粒细胞白血病的感染:来自加拿大急性髓细胞白血病感染研究组。

Infections in pediatric acute promyelocytic leukemia: from the Canadian infections in acute myeloid leukemia research group.

出版信息

BMC Cancer. 2013 Jun 4;13:276. doi: 10.1186/1471-2407-13-276.

DOI:10.1186/1471-2407-13-276
PMID:23735034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3679857/
Abstract

BACKGROUND

It is not known whether children with acute promyelocytic leukemia (APL) have an infection risk similar to non- APL acute myeloid leukemia. The objective was to describe infectious risk in children with newly diagnosed APL and to describe factors associated with these infections.

METHODS

We conducted a retrospective, population-based cohort study that included children ≤ 18 years of age with de novo APL treated at 15 Canadian centers. Thirty-three children with APL were included; 78.8% were treated with APL -specific protocols.

RESULTS

Bacterial sterile site infection occurred in 12 (36.4%) and fungal sterile site infection occurred in 2 (6.1%) children. Of the 127 chemotherapy courses, 101 (79.5%) were classified as intensive and among these, the proportion in which a sterile site microbiologically documented infection occurred was 14/101 (13.9%). There was one infection-related death.

CONCLUSIONS

One third of children with APL experienced at least one sterile site bacterial infection throughout treatment and 14% of intensive chemotherapy courses were associated with a microbiologically documented sterile site infection. Infection rates in pediatric APL may be lower compared to non- APL acute myeloid leukemia although these children may still benefit from aggressive supportive care during intensive chemotherapy.

摘要

背景

目前尚不清楚患有急性早幼粒细胞白血病(APL)的儿童是否存在与非 APL 急性髓细胞白血病相似的感染风险。本研究旨在描述新诊断为 APL 的儿童的感染风险,并描述与这些感染相关的因素。

方法

我们进行了一项回顾性、基于人群的队列研究,纳入了在加拿大 15 个中心接受治疗的 15 岁以下初诊 APL 儿童患者。共纳入了 33 例 APL 患儿,其中 78.8%的患儿接受了 APL 特异性方案治疗。

结果

12 例(36.4%)患儿发生无菌部位细菌感染,2 例(6.1%)患儿发生无菌部位真菌感染。在 127 个化疗疗程中,101 个(79.5%)被归类为强化治疗,其中 13.9%(14/101)的无菌部位发生了微生物学证实的感染。有 1 例与感染相关的死亡。

结论

在整个治疗过程中,三分之一的 APL 患儿至少发生了一次无菌部位细菌感染,14%的强化化疗疗程与微生物学证实的无菌部位感染相关。与非 APL 急性髓细胞白血病相比,儿科 APL 的感染率可能较低,但这些患儿在强化化疗期间仍可能受益于积极的支持性护理。