Treatment of Critical Bleeds in Patients With Immune Thrombocytopenia: A Systematic Review.

IF 2.3 3区 医学 Q2 HEMATOLOGY European Journal of Haematology Pub Date : 2024-11-18 DOI:10.1111/ejh.14351
Saifur R Chowdhury, Emily Sirotich, Gordon Guyatt, Daya Gill, Dimpy Modi, Laura M Venier, Syed Mahamad, Mahmudur Rahman Chowdhury, Kerolos Eisa, Carolyn E Beck, Vicky R Breakey, Kerstin de Wit, Stephen Porter, Kathryn E Webert, Adam Cuker, Clare O'Connor, Jennifer MacWhirter -DiRaimo, Justin W Yan, Charles Manski, John G Kelton, Matthew Kang, Gail Strachan, Ziauddin Hassan, Barbara Pruitt, Menaka Pai, Rachael F Grace, Dale Paynter, Jay Charness, Nichola Cooper, Steven Fein, Arnav Agarwal, Hasmik Nazaryan, Ishaq Siddiqui, Russell Leong, Sushmitha Pallapothu, Aaron Wen, Emily Xu, Bonnie Liu, Amirmohammad Shafiee, Preksha Rathod, Henry Kwon, Jared Dookie, Dena Zeraatkar, Lehana Thabane, Rachel Couban, Donald M Arnold
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Abstract

Objectives: Evidence-based protocols for managing bleeding emergencies in patients with immune thrombocytopenia (ITP) are lacking. We conducted a systematic review of treatments for critical bleeding in patients with ITP.

Methods: We included all study designs and extracted data in aggregate or individually for patients who received one or more interventions and for whom any of the following outcomes were reported: platelet count response, bleeding, disability, or death.

Results: We identified 49 eligible studies reporting 112 critical bleed patients with ITP, including 66 children (median age, 10 years), 36 adults (median age, 41.5 years), and 10 patients with unreported age. Patients received corticosteroids (n = 67), IVIG (n = 49), platelet transfusions (n = 41), TPO-RAs (n = 17), and splenectomy (n = 28) either alone or in combination. Studies reported 29 different treatment combinations, the 5 most common were corticosteroids, platelet transfusion and splenectomy (n = 13), corticosteroids and IVIG (n = 13), or splenectomy alone (n = 13); IVIG alone (n = 11); and corticosteroids, IVIG and TPO-RA (n = 8). Mortality among patients with critical bleeds in ITP was 30.6% for adults and 19.7% for children.

Conclusions: The effects of individual treatments on patient outcomes were uncertain due to very low-quality evidence. There is a need for a standardized approach to the treatment of ITP critical bleeds.

Systematic review registration: CRD42020161206.

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免疫性血小板减少症患者严重出血的治疗:系统回顾。
目的:免疫性血小板减少症(ITP)患者出血紧急情况的处理缺乏循证方案。我们对治疗 ITP 患者严重出血的方法进行了系统回顾:我们纳入了所有研究设计,并提取了接受一种或多种干预措施的患者的总数据或单个数据,这些患者报告了以下任何一种结果:血小板计数反应、出血、残疾或死亡:我们确定了 49 项符合条件的研究,报告了 112 名严重出血的 ITP 患者,包括 66 名儿童(中位年龄为 10 岁)、36 名成人(中位年龄为 41.5 岁)和 10 名未报告年龄的患者。患者单独或联合接受了皮质类固醇(67 例)、IVIG(49 例)、血小板输注(41 例)、TPO-RAs(17 例)和脾切除术(28 例)。研究报告了 29 种不同的治疗组合,最常见的 5 种组合是皮质类固醇、血小板输注和脾切除术(13 例)、皮质类固醇和 IVIG(13 例)或单独脾切除术(13 例);单独 IVIG(11 例);以及皮质类固醇、IVIG 和 TPO-RA(8 例)。ITP危重出血患者的死亡率成人为30.6%,儿童为19.7%:结论:由于证据质量很低,因此无法确定各种治疗方法对患者预后的影响。系统综述注册:CRD42020161206。
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来源期刊
CiteScore
5.50
自引率
0.00%
发文量
168
审稿时长
4-8 weeks
期刊介绍: European Journal of Haematology is an international journal for communication of basic and clinical research in haematology. The journal welcomes manuscripts on molecular, cellular and clinical research on diseases of the blood, vascular and lymphatic tissue, and on basic molecular and cellular research related to normal development and function of the blood, vascular and lymphatic tissue. The journal also welcomes reviews on clinical haematology and basic research, case reports, and clinical pictures.
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