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伦巴第血栓性微血管病诊断与治疗网络。

Lombardy diagnostic and therapeutic network of thrombotic microangiopathy.

机构信息

Department of Pathophysiology and Transplantation, Università Degli Studi Di Milano, and Fondazione Luigi Villa, Via Pace 9, 20122, Milan, Italy.

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Milan, Italy.

出版信息

Orphanet J Rare Dis. 2022 Jun 23;17(1):246. doi: 10.1186/s13023-022-02400-y.

Abstract

BACKGROUND

Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening thrombotic microangiopathy (TMA) requiring urgent treatment. Standardization of its diagnosis and optimal management is challenging. This study aimed to evaluate the role of centralized, rapid testing of ADAMTS13 in patients experiencing acute TMAs requiring plasma-exchange (PEX) and to estimate the incidence of TTP in a large Italian Region.

METHODS

We perfomed a cohort study in the frame of the project "Set-up of a Lombardy network for the study and treatment of patients undergoing apheresis", including 11 transfusion centers in the Region. Consecutive patients referred from 2014 to 2016 with acute TMAs requiring PEX were enrolled. Centralized ADAMTS13 activity testing was performed at the Milan Hemophilia and Thrombosis Center within 24 h.

RESULTS

Forty-three TMA patients (44 events) were enrolled, of whom 35 (81%) had severe ADAMTS13 deficiency. Patients with severe ADAMTS13 deficiency were younger, mainly women, with a higher prevalence of autoimmune disorders and a lower prevalence of cancer. Clinical and laboratory characteristics of patients with and without severe ADAMTS13 deficiency largely overlapped, with a lower platelet count being the only baseline marker that significantly differed between the two patient groups (ADAMTS13 activity < 10% vs ≥ 10%: median difference of -27 × 10/l, 95% CI - 37 to - 3). PEX treatment was initiated in all patients, but soon discontinued in cases without severe ADAMTS13 deficiency. In this group, the mortality rate was higher and no episode exacerbations or relapses within 6 months occured. The estimated average annual incidence of acute acquired TTP events was 1.17 [0.78-1.55] per million people.

CONCLUSIONS

Severe ADAMTS13 deficiency distinguished two groups of patients with largely overlapping clinical features but different treatment and disease course. This study provides a feasible model implemented in a large Italian region for the practical clinical approach to TMAs and underlines the importance of urgent ADAMTS13 activity testing for an accurate differential diagnosis and therapeutic approach.

摘要

背景

血栓性血小板减少性紫癜(TTP)是一种罕见的、危及生命的血栓性微血管病(TMA),需要紧急治疗。其诊断和最佳治疗方法的标准化具有挑战性。本研究旨在评估在接受血浆置换(PEX)治疗的急性 TMA 患者中,集中快速检测 ADAMTS13 的作用,并估计意大利一个大区的 TTP 发病率。

方法

我们在“伦巴第地区开展治疗和研究患者接受血浆置换的网络项目”的框架内进行了一项队列研究,包括该地区的 11 个输血中心。纳入了 2014 年至 2016 年间因急性 TMA 需要 PEX 治疗的连续患者。在米兰血友病和血栓形成中心在 24 小时内进行集中的 ADAMTS13 活性检测。

结果

共纳入 43 例 TMA 患者(44 例),其中 35 例(81%)存在严重 ADAMTS13 缺乏。严重 ADAMTS13 缺乏的患者年龄较小,主要为女性,自身免疫性疾病患病率较高,癌症患病率较低。有和没有严重 ADAMTS13 缺乏的患者的临床和实验室特征基本重叠,血小板计数较低是两组患者之间唯一显著不同的基线标志物(ADAMTS13 活性 < 10%与 ≥ 10%:中位数差异 -27×10/L,95%CI-37 至 -3)。所有患者均开始接受 PEX 治疗,但在无严重 ADAMTS13 缺乏的患者中很快停止。在该组中,死亡率较高,且 6 个月内无发作加重或复发。急性获得性 TTP 事件的估计平均年发病率为每百万人 1.17[0.78-1.55]。

结论

严重 ADAMTS13 缺乏将两组具有基本重叠的临床特征但不同治疗和病程的患者区分开来。本研究为意大利一个大区提供了一种可行的模型,用于 TMAs 的实际临床方法,并强调了紧急 ADAMTS13 活性检测对准确鉴别诊断和治疗方法的重要性。

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本文引用的文献

1
Plasma exchange and thrombotic microangiopathies: From pathophysiology to clinical practice.
Transfus Apher Sci. 2020 Dec;59(6):102990. doi: 10.1016/j.transci.2020.102990. Epub 2020 Nov 19.
2
ISTH guidelines for the diagnosis of thrombotic thrombocytopenic purpura.
J Thromb Haemost. 2020 Oct;18(10):2486-2495. doi: 10.1111/jth.15006. Epub 2020 Sep 11.
4
International Council for Standardization in Haematology (ICSH) recommendations for laboratory measurement of ADAMTS13.
Int J Lab Hematol. 2020 Dec;42(6):685-696. doi: 10.1111/ijlh.13295. Epub 2020 Jul 16.
5
6
Incidence of acquired thrombotic thrombocytopenic purpura in Germany: a hospital level study.
Orphanet J Rare Dis. 2019 Nov 15;14(1):260. doi: 10.1186/s13023-019-1240-0.
7
Clinical factors and biomarkers predict outcome in patients with immune-mediated thrombotic thrombocytopenic purpura.
Haematologica. 2019 Jan;104(1):166-175. doi: 10.3324/haematol.2018.198275. Epub 2018 Aug 31.
8
Thrombotic thrombocytopenic purpura: diagnostic criteria, clinical features, and long-term outcomes from 1995 through 2015.
Blood Adv. 2017 Apr 6;1(10):590-600. doi: 10.1182/bloodadvances.2017005124. eCollection 2017 Apr 11.
9
Derivation and external validation of the PLASMIC score for rapid assessment of adults with thrombotic microangiopathies: a cohort study.
Lancet Haematol. 2017 Apr;4(4):e157-e164. doi: 10.1016/S2352-3026(17)30026-1. Epub 2017 Mar 2.

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