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本文引用的文献

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Analysis of early clinical signs and risk factors for severe hemorrhagic cystitis after stem cell transplantation in children.儿童干细胞移植后严重出血性膀胱炎的早期临床征象及危险因素分析。
Int J Urol. 2024 Apr;31(4):335-341. doi: 10.1111/iju.15365. Epub 2024 Jan 5.
2
Endocrinopathies in beta thalassemia: a narrative review.β地中海贫血中的内分泌病:一项叙述性综述。
Hormones (Athens). 2024 Jun;23(2):205-216. doi: 10.1007/s42000-023-00515-w. Epub 2023 Dec 16.
3
Haploidentical Cord Blood Transplantation with 8 mg/kg Antithymocyte Globulin as Graft-versus-Host Disease Prophylaxis Compared to Haploidentical Transplantation with 10 mg/kg Antithymocyte Globulin in the Treatment of Acute Leukemia.采用 8mg/kg 抗胸腺细胞球蛋白预防移植物抗宿主病与采用 10mg/kg 抗胸腺细胞球蛋白预防移植物抗宿主病的半相合脐血移植治疗急性白血病的比较。
Transplant Cell Ther. 2023 Dec;29(12):771.e1-771.e10. doi: 10.1016/j.jtct.2023.09.015. Epub 2023 Sep 24.
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Impact of iron overload in hematopoietic stem cell transplantation.铁过载对造血干细胞移植的影响。
Transpl Immunol. 2023 Jun;78:101820. doi: 10.1016/j.trim.2023.101820. Epub 2023 Mar 13.
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Hematopoietic Stem Cell Transplantation in Thalassemia.地中海贫血症中的造血干细胞移植。
Hematol Oncol Clin North Am. 2023 Apr;37(2):413-432. doi: 10.1016/j.hoc.2022.12.009.
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The Clinical Phenotypes of Alpha Thalassemia.α 地中海贫血的临床表型。
Hematol Oncol Clin North Am. 2023 Apr;37(2):327-339. doi: 10.1016/j.hoc.2022.12.004.
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CMV infection is a risk factor for hemorrhagic cystitis after hematopoietic stem cell transplantation.巨细胞病毒感染是造血干细胞移植后出血性膀胱炎的一个危险因素。
Ann Hematol. 2023 May;102(5):1193-1201. doi: 10.1007/s00277-023-05121-9. Epub 2023 Feb 8.
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Incidence of late-onset hemorrhagic cystitis and its effect on PFS in acute leukemia patients after haplo-PBSCT: The 5-year single-center data.单倍体造血干细胞移植后急性白血病患者迟发性出血性膀胱炎的发生率及其对无进展生存期的影响:5年单中心数据
Front Oncol. 2022 Jul 15;12:913802. doi: 10.3389/fonc.2022.913802. eCollection 2022.
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Thalassaemia.地中海贫血症。
Lancet. 2022 Jun 18;399(10343):2310-2324. doi: 10.1016/S0140-6736(22)00536-0. Epub 2022 Jun 9.
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Current status of beta-thalassemia and its treatment strategies.β-地中海贫血的现状及其治疗策略。
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异基因造血干细胞移植后重型β地中海贫血患儿出血性膀胱炎的危险因素

Risk factors for hemorrhagic cystitis in children with severe beta-thalassemia after allogeneic hematopoietic stem cell transplantation.

作者信息

Dou Hui-Hong, Luo Jian-Ming, Zhao Yan-Jun, Wang Ji-Gan, Qin Yuan-Han

机构信息

Department of Pediatrics, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Guangxi Clinical Research Center for Pediatric Diseases, Nanning, China.

Department of Pediatrics, The First Affiliated Hospital, Guangxi Medical University, Nanning, China.

出版信息

Front Pediatr. 2025 Apr 3;13:1558099. doi: 10.3389/fped.2025.1558099. eCollection 2025.

DOI:10.3389/fped.2025.1558099
PMID:40248018
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12003309/
Abstract

PURPOSE

To investigate the risk factors for hemorrhagic cystitis (HC) in children with severe beta-thalassemia after allogeneic hematopoietic stem cell transplantation (allo-HSCT).

METHODS

The clinical data of 152 children under the age of 15 who underwent allo-HSCT between January 2011 and December 2021 were retrospectively analyzed. The incidence of HC and related variables were evaluated using univariate analysis. Variables with statistical significance ( < 0.05) were included in a multivariable logistic regression model to identify independent risk factors for HC.

RESULTS

Among the 152 children, 42 developed HC, with an incidence rate of 27.63%. The median onset time of HC was 25 days (IQR: 10-38.75 days). Univariate analysis indicated that older transplantation age, elevated pre-transplant serum ferritin levels, cytomegalovirus (CMV) infection, and prolonged neutrophil engraftment time were associated with HC occurrence ( < 0.05). Multivariable logistic regression further confirmed that older transplantation age (OR 1.236, 95% CI: 1.031-1.531,  = 0.033), elevated pre-transplant ferritin levels (OR 1.053, 95% CI: 1.028-1.086,  < 0.01), CMV infection (OR 11.522, 95% CI: 2.912-76.345,  = 0.002), and prolonged neutrophil engraftment time (OR 1.385, 95% CI: 1.109-1.793,  < 0.01) were independent risk factors for HC.

CONCLUSION

Older transplantation age (>5.95 age years old), elevated pre-transplant serum ferritin levels, CMV infection, and delayed neutrophil engraftment are independent risk factors for HC in children with severe beta-thalassemia after allo-HSCT. Early identification and intervention for these risk factors are crucial in reducing the incidence of HC.

摘要

目的

探讨重型β地中海贫血患儿异基因造血干细胞移植(allo-HSCT)后出血性膀胱炎(HC)的危险因素。

方法

回顾性分析2011年1月至2021年12月期间接受allo-HSCT的152例15岁以下儿童的临床资料。采用单因素分析评估HC的发生率及相关变量。将具有统计学意义(<0.05)的变量纳入多变量逻辑回归模型,以确定HC的独立危险因素。

结果

152例儿童中,42例发生HC,发生率为27.63%。HC的中位发病时间为25天(四分位间距:10 - 38.75天)。单因素分析表明,移植年龄较大、移植前血清铁蛋白水平升高、巨细胞病毒(CMV)感染及中性粒细胞植入时间延长与HC的发生相关(<0.05)。多变量逻辑回归进一步证实,移植年龄较大(OR 1.236,95%可信区间:1.031 - 1.531,P = 0.033)、移植前铁蛋白水平升高(OR 1.053,95%可信区间:1.028 - 1.086,P < 0.01)、CMV感染(OR 11.522,95%可信区间:2.912 - 76.345,P = 0.002)及中性粒细胞植入时间延长(OR 1.385,95%可信区间:1.109 - 1.793,P < 0.01)是HC的独立危险因素。

结论

移植年龄较大(>5.95岁)、移植前血清铁蛋白水平升高、CMV感染及中性粒细胞植入延迟是重型β地中海贫血患儿allo-HSCT后HC的独立危险因素。早期识别和干预这些危险因素对于降低HC的发生率至关重要。