Wang Xiaoyu, Zhu Yingqiao, Liu Dan, Zhu Lijun, Tong Juan, Zheng Changcheng
Department of Hematology, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, People's Republic of China.
J Blood Med. 2024 May 7;15:217-225. doi: 10.2147/JBM.S457545. eCollection 2024.
COVID-19 infection has brought new challenges to the treatment of adult patients with immune thrombocytopenia (ITP). In adult ITP patients, there have been no relevant reports exploring the incidence, clinical characteristics, and risk factors of platelet elevation after COVID-19 infection.
A total of 66 patients with previously diagnosed ITP from December 2022 to February 2023 in a single-center were collected and analyzed for this real-world clinical retrospective observational study.
In the platelet count increased group (n = 19), 13 patients (68.4%) were using thrombopoietin receptor agonists (TPO-RA) treatment at the time of COVID-19 infection; the median platelet count was 52 (2-207) ×10/L at the last visit before infection and 108 (19-453) ×10/L at the first visit after infection. In the platelet count stable group (n = 19) and platelet count decreased group (n = 28), 9 (47.4%) and 8 (28.6%) patients were using TPO-RA at the time of infection, respectively. ITP patients treated with TPO-RA had a significantly higher risk of increased platelet count than those not treated with TPO-RA at the time of infection (platelet count increased group vs platelet count decreased group: OR: 5.745, p = 0.009; platelet count increased group vs the non-increased group: OR: 3.616, p = 0.031). In the platelet count increased group, the median platelet count at 6 months post-infection was 67 (14-235) × 10/L, which was significantly higher than the platelet level at the last visit before infection (p = 0.040).
This study showed that some adult ITP patients had an increase in platelet count after COVID-19 infection, and this phenomenon was strongly associated with the use of TPO-RA at the time of infection. Although no thrombotic events were observed in this study, it reminds clinicians that they should be alert to the possibility of thrombotic events in the long-term management of adult ITP patients during the COVID-19 pandemic.
新型冠状病毒肺炎(COVID-19)感染给成人免疫性血小板减少症(ITP)患者的治疗带来了新的挑战。在成人ITP患者中,尚无关于COVID-19感染后血小板升高的发生率、临床特征及危险因素的相关报道。
本真实世界临床回顾性观察性研究收集并分析了2022年12月至2023年2月在单中心确诊的66例ITP患者。
在血小板计数升高组(n = 19)中,13例患者(68.4%)在COVID-19感染时正在使用血小板生成素受体激动剂(TPO-RA)治疗;感染前最后一次就诊时血小板计数中位数为52(2 - 207)×10⁹/L,感染后首次就诊时为108(19 - 453)×10⁹/L。在血小板计数稳定组(n = 19)和血小板计数降低组(n = 28)中,分别有9例(47.4%)和8例(28.6%)患者在感染时使用TPO-RA。感染时接受TPO-RA治疗的ITP患者血小板计数升高的风险显著高于未接受TPO-RA治疗的患者(血小板计数升高组与血小板计数降低组:比值比(OR):5.745,p = 0.009;血小板计数升高组与未升高组:OR:3.616,p = 0.031)。在血小板计数升高组中,感染后6个月血小板计数中位数为67(14 - 235)×10⁹/L,显著高于感染前最后一次就诊时的血小板水平(p = 0.040)。
本研究表明,部分成人ITP患者在COVID-19感染后血小板计数升高,且这一现象与感染时使用TPO-RA密切相关。尽管本研究未观察到血栓事件,但提醒临床医生在COVID-19大流行期间成人ITP患者的长期管理中应警惕血栓事件的发生。