Suppr超能文献

遗传性溶血性贫血脾切除术的推荐意见。

Recommendations regarding splenectomy in hereditary hemolytic anemias.

机构信息

Department of Molecular Medicine and Medical Biotechnology, University Federico II Naples, Italy

CEINGE Biotecnologie Avanzate, Naples, Italy.

出版信息

Haematologica. 2017 Aug;102(8):1304-1313. doi: 10.3324/haematol.2016.161166. Epub 2017 May 26.

Abstract

Hereditary hemolytic anemias are a group of disorders with a variety of causes, including red cell membrane defects, red blood cell enzyme disorders, congenital dyserythropoietic anemias, thalassemia syndromes and hemoglobinopathies. As damaged red blood cells passing through the red pulp of the spleen are removed by splenic macrophages, splenectomy is one possible therapeutic approach to the management of severely affected patients. However, except for hereditary spherocytosis for which the effectiveness of splenectomy has been well documented, the efficacy of splenectomy in other anemias within this group has yet to be determined and there are concerns regarding short- and long-term infectious and thrombotic complications. In light of the priorities identified by the European Hematology Association Roadmap we generated specific recommendations for each disorder, except thalassemia syndromes for which there are other, recent guidelines. Our recommendations are intended to enable clinicians to achieve better informed decisions on disease management by splenectomy, on the type of splenectomy and the possible consequences. As no randomized clinical trials, case control or cohort studies regarding splenectomy in these disorders were found in the literature, recommendations for each disease were based on expert opinion and were subsequently critically revised and modified by the Splenectomy in Rare Anemias Study Group, which includes hematologists caring for both adults and children.

摘要

遗传性溶血性贫血是一组由多种原因引起的疾病,包括红细胞膜缺陷、红细胞酶缺乏症、先天性红细胞生成异常性贫血、地中海贫血综合征和血红蛋白病。由于受损的红细胞在通过脾脏红髓时被脾脏巨噬细胞清除,因此脾切除术是治疗严重受累患者的一种可能的治疗方法。然而,除了遗传性球形红细胞增多症,脾切除术的有效性已得到充分证实,在该组中的其他贫血症中脾切除术的疗效尚未确定,并且存在短期和长期感染和血栓并发症的担忧。根据欧洲血液学协会路线图确定的优先事项,我们为每种疾病生成了具体的建议,除了地中海贫血综合征,因为针对该疾病有其他最近的指南。我们的建议旨在使临床医生能够在脾切除术、脾切除术的类型以及可能的后果方面做出更明智的疾病管理决策。由于在文献中未发现关于这些疾病的脾切除术的随机临床试验、病例对照或队列研究,因此针对每种疾病的建议均基于专家意见,并随后由脾切除术治疗罕见贫血研究小组进行了严格审查和修改,该小组包括治疗成人和儿童的血液学家。

相似文献

1
Recommendations regarding splenectomy in hereditary hemolytic anemias.
Haematologica. 2017 Aug;102(8):1304-1313. doi: 10.3324/haematol.2016.161166. Epub 2017 May 26.
2
How I approach hereditary hemolytic anemia and splenectomy.
Pediatr Blood Cancer. 2020 Nov;67(11):e28337. doi: 10.1002/pbc.28337. Epub 2020 May 11.
3
Red cell membrane disorders.
Hematology Am Soc Hematol Educ Program. 2005:13-8. doi: 10.1182/asheducation-2005.1.13.
4
Clinical and hematologic benefits of partial splenectomy for congenital hemolytic anemias in children.
Ann Surg. 2003 Feb;237(2):281-8. doi: 10.1097/01.SLA.0000048453.61168.8F.
5
Comparative effectiveness of different types of splenectomy for children with congenital hemolytic anemias.
J Pediatr. 2012 Apr;160(4):684-689.e13. doi: 10.1016/j.jpeds.2011.09.030. Epub 2011 Nov 3.
7
Confounding factors in the diagnosis and clinical course of rare congenital hemolytic anemias.
Orphanet J Rare Dis. 2021 Oct 9;16(1):415. doi: 10.1186/s13023-021-02036-4.
8
Congenital Hemolytic Anemias: Is There a Role for the Immune System?
Front Immunol. 2020 Jun 23;11:1309. doi: 10.3389/fimmu.2020.01309. eCollection 2020.
9
[Value of splenectomy in hemolytic anemias].
Chirurgia (1951). 1971 Jul;20(7):577-88.
10
Portal vein thrombosis after splenectomy for hereditary stomatocytosis in childhood.
Eur J Pediatr. 1999 Aug;158(8):628-30. doi: 10.1007/s004310051165.

引用本文的文献

1
Case Report: Post-splenectomy bulky pelvic splenosis in an adolescent with hereditary spherocytosis.
Front Pediatr. 2025 Apr 28;13:1581533. doi: 10.3389/fped.2025.1581533. eCollection 2025.
2
Underlying disease is the main risk factor in post-splenectomy complication risk: Data from a national database.
Br J Haematol. 2025 Jun;206(6):1811-1821. doi: 10.1111/bjh.20114. Epub 2025 Apr 29.
3
Feasibility of Intensive Chemotherapy in Hereditary Spherocytosis.
Hematol Rep. 2025 Feb 24;17(2):11. doi: 10.3390/hematolrep17020011.
4
An overview of hereditary spherocytosis and the curative effects of splenectomy.
Front Physiol. 2025 Feb 11;16:1497588. doi: 10.3389/fphys.2025.1497588. eCollection 2025.
6
A rare case report of hemolysis in a newborn: hereditary elliptocytosis.
Front Pediatr. 2024 Oct 22;12:1485318. doi: 10.3389/fped.2024.1485318. eCollection 2024.
7
Engineering human immune organoids for translational immunology.
Bioact Mater. 2024 Oct 18;44:164-183. doi: 10.1016/j.bioactmat.2024.10.010. eCollection 2025 Feb.
8
Clearance of pathogenic erythrocytes is maintained despite spleen dysfunction in children with sickle cell disease.
Am J Hematol. 2024 Dec;99(12):2267-2278. doi: 10.1002/ajh.27481. Epub 2024 Sep 17.
9
A Case of Adult Hereditary Spherocytosis Concomitant with Gilbert Syndrome Caused by Mutations in SPTB and UGT1A1.
J Inflamm Res. 2024 Sep 4;17:5977-5983. doi: 10.2147/JIR.S483493. eCollection 2024.

本文引用的文献

1
New insights on hereditary erythrocyte membrane defects.
Haematologica. 2016 Nov;101(11):1284-1294. doi: 10.3324/haematol.2016.142463. Epub 2016 Oct 18.
2
Advances in understanding the pathogenesis of the red cell volume disorders.
Br J Haematol. 2016 Sep;174(5):674-85. doi: 10.1111/bjh.14197. Epub 2016 Jun 29.
3
Total versus partial splenectomy in pediatric hereditary spherocytosis: A systematic review and meta-analysis.
Pediatr Blood Cancer. 2016 Oct;63(10):1713-22. doi: 10.1002/pbc.26106. Epub 2016 Jun 14.
4
Morbidity and mortality of adult patients with congenital dyserythropoietic anemia type I.
Eur J Haematol. 2017 Jan;98(1):13-18. doi: 10.1111/ejh.12778. Epub 2016 Jun 15.
5
Safe and Efficient Gene Therapy for Pyruvate Kinase Deficiency.
Mol Ther. 2016 Aug;24(7):1187-98. doi: 10.1038/mt.2016.87. Epub 2016 May 3.
6
Recent advances in the pathogenesis and treatment of paroxysmal nocturnal hemoglobinuria.
F1000Res. 2016 Feb 23;5. doi: 10.12688/f1000research.7288.1. eCollection 2016.
8
Long-term outcomes after pediatric splenectomy.
Surgery. 2016 Jun;159(6):1583-1590. doi: 10.1016/j.surg.2015.12.014. Epub 2016 Jan 30.
9
Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study.
Blood. 2016 Mar 24;127(12):1616-8. doi: 10.1182/blood-2015-11-679357. Epub 2016 Jan 15.
10
Overwhelming Postsplenectomy Infection: A Prospective Multicenter Cohort Study.
Clin Infect Dis. 2016 Apr 1;62(7):871-878. doi: 10.1093/cid/civ1195. Epub 2015 Dec 23.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验