Department of Haematology, Armed Forces Institute of Pathology (AFIP), Rawalpindi, Pakistan.
Department of Haematology, Armed Forces Institute of Transfusion (AFIT), Rawalpindi, Pakistan.
J Coll Physicians Surg Pak. 2023 Jul;33(7):760-764. doi: 10.29271/jcpsp.2023.07.760.
To analyse the predictive value of immature platelet fraction (IPF) as an independent diagnostic marker to differentiate between hyperdestructive and hypoproductive thrombocytopenia.
Cross-sectional observational study. Place and Duration of the Study: Armed Forces Institute of Pathology Rawalpindi, from February to July 2022.
A total of 164 samples were included in the study by non-probability consecutive sampling. Among these, 80 were obtained from normal individuals serving as control; 43 were obtained from patients having hyperdestructive thrombocytopenia (idiopathic thrombocytopenia, thrombotic thrombocytopenic purpura, disseminated intravascular coagulation); and 41 were obtained from those hypoproductive thrombocytopenia (acute leukaemia, aplastic anaemia, chemotherapy). Sysmex automated haematology analyzer, XN-3000 was used to determine the immature platelet fraction (IPF) of the patients. ROC curves analysis was done to ascertain area under curve.
Immature platelet fraction (IPF %) was significantly higher in consumptive / hyperdestructive thrombocytopenia group i.e. median (IQR), 21% (14.4-26.2) as compared to 6.5% (4.6-8.9) in hypoproductive thrombocytopenia, and 2.6% (1.3-4.1) in normal control group (p <0.001). Cut-off value with the highest sensitivity and specificity for IPF vs. normal population was 7.95% with sensitivity of 97.7% and specificity of 86%.
Immature platelet fraction (IPF of 7.95%) possesses high diagnostic accuracy, sensitivity and specificity for differentiation between hyperdestructive vs. hypoproductive thrombocytopenia. It can be used as a reliable marker to differentiate between the two entities.
Immature platelet fraction, Thrombocytopenia, Bone marrow failure, Peripheral destruction.
分析未成熟血小板分数(IPF)作为独立诊断标志物区分高破坏性和低生成性血小板减少症的预测价值。
横断面观察性研究。地点和研究时间:武装部队病理学研究所,拉瓦尔品第,2022 年 2 月至 7 月。
通过非概率连续抽样,共纳入 164 例研究样本。其中,80 例取自正常个体作为对照;43 例取自高破坏性血小板减少症(特发性血小板减少症、血栓性血小板减少性紫癜、弥漫性血管内凝血)患者;41 例取自低生成性血小板减少症(急性白血病、再生障碍性贫血、化疗)患者。使用 Sysmex 自动化血液分析仪 XN-3000 测定患者的未成熟血小板分数(IPF)。通过 ROC 曲线分析确定曲线下面积。
消耗性/高破坏性血小板减少症组的未成熟血小板分数(IPF%)明显更高,中位数(IQR)为 21%(14.4-26.2),而低生成性血小板减少症组为 6.5%(4.6-8.9),正常对照组为 2.6%(1.3-4.1)(p<0.001)。IPF 与正常人群相比,具有最高敏感性和特异性的最佳截断值为 7.95%,敏感性为 97.7%,特异性为 86%。
未成熟血小板分数(IPF 为 7.95%)在区分高破坏性与低生成性血小板减少症方面具有较高的诊断准确性、敏感性和特异性。它可以作为区分两者的可靠标志物。
未成熟血小板分数、血小板减少症、骨髓衰竭、外周破坏。