Kelly Julie, Sylvester Katelyn W, Rimsans Jessica, Bernier Thomas D, Ting Clara, Connors Jean M
Brigham and Women's Hospital - Department of Pharmacy Services Boston Massachusetts USA.
Brigham and Women's Hospital - Division of Hematology, Department of Medicine Boston Massachusetts USA.
Res Pract Thromb Haemost. 2021 Aug 4;5(5):e12573. doi: 10.1002/rth2.12573. eCollection 2021 Jul.
Diagnosing heparin-induced thrombocytopenia (HIT) in patients with end-stage renal disease (ESRD) can be difficult, as they are frequently exposed to heparin and have multiple etiologies for thrombocytopenia.
To correlate 4T scores, IgG heparin-platelet factor 4 (PF4-heparin) ELISA results, and serotonin release assay (SRA) results in patients with ESRD.
We performed a retrospective review of patients with ESRD (creatinine clearance < 15 mL/min or on renal replacement therapy [RRT]) who underwent PF4-heparin ELISA testing from October 2015 to September 2019. True-positive PF4s required an intermediate to high 4T score (≥4), a positive SRA, and receipt of treatment for a HIT diagnosis. False-positive PF4s were defined as a positive PF4 with a negative SRA, low 4T score (<4), or lack of treatment for HIT. Indeterminant cases were classified on the basis of clinical assessment by the treating team (eg, hematology or vascular medicine).
Of 254 patients with ESRD (92% on RRT), 29 patients (11.4%) had a positive PF4. Eleven (37.9%) had a confirmed diagnosis of HIT: 10 patients who met all of the above criteria, and one who met the 4T criteria and was treated for HIT but did not have SRA testing due to high clinical suspicion and a positive PF4 test. False-positive PF4 values occurred in 8 patients (27.5%). Of 10 (34.5%) indeterminant cases of patients with a negative SRA but intermediate to high 4T and positive PF4, only 3 patients were treated for HIT, whereas the other 7 were judged not to have HIT as assessed by the treating clinician. In patients with an intermediate to high 4T score and PF4 optical density > 0.4 but negative SRA, who were not treated for HIT, there were no adverse outcomes documented such as new or progressive thrombosis.
In our ESRD population, 4T scores and PF4 testing were not predictive of a clinical diagnosis of HIT.
诊断终末期肾病(ESRD)患者的肝素诱导的血小板减少症(HIT)可能很困难,因为他们经常接触肝素,且血小板减少有多种病因。
将4T评分、IgG肝素-血小板因子4(PF4-肝素)酶联免疫吸附测定(ELISA)结果和5-羟色胺释放试验(SRA)结果与ESRD患者进行相关性分析。
我们对2015年10月至2019年9月期间接受PF4-肝素ELISA检测的ESRD患者(肌酐清除率<15 mL/分钟或接受肾脏替代治疗[RRT])进行了回顾性研究。真正阳性的PF4需要4T评分为中到高(≥4)、SRA阳性以及因HIT诊断而接受治疗。假阳性PF4定义为SRA阴性、4T评分低(<4)或未因HIT接受治疗但PF4阳性。不确定病例根据治疗团队(如血液学或血管医学)的临床评估进行分类。
在254例ESRD患者(92%接受RRT)中,29例(11.4%)PF4呈阳性。11例(37.9%)确诊为HIT:10例符合上述所有标准,1例符合4T标准并接受了HIT治疗,但由于临床高度怀疑和PF4检测阳性而未进行SRA检测。8例(27.5%)出现假阳性PF4值。在10例(34.5%)SRA阴性但4T评分为中到高且PF4阳性的不确定病例中,只有3例接受了HIT治疗,而其他7例经治疗医生评估被判定没有HIT。在4T评分为中到高且PF4光密度>0.4但SRA阴性且未接受HIT治疗的患者中,没有记录到诸如新发或进行性血栓形成等不良结局。
在我们的ESRD患者群体中,4T评分和PF4检测不能预测HIT的临床诊断。