Griesshammer M, Bangerter M, Sauer T, Wennauer R, Bergmann L, Heimpel H
Department of Medicine III, University of Ulm, Germany.
J Intern Med. 1999 Mar;245(3):295-300. doi: 10.1046/j.1365-2796.1999.00452.x.
To determine the aetiology and clinical significance of an elevated platelet count (thrombocytosis) in a large cohort of patients.
A retrospective review of the medical records was performed on all patients, who had at least one platelet count > or = 500 x 10(9) L-1.
Departments of Medicine and Surgery, University of Ulm, Germany.
A total of 732 patients with thrombocytosis.
Classification of thrombocytosis and thromboembolic complications, and evaluation of laboratory parameters distinguishing between primary and secondary thrombocytosis.
Of the total of 732 patients, 89 (12.3%) had primary and 643 (87.7%) had secondary thrombocytosis. Essential thrombocythaemia was observed in 40 of 89 patients (45%) with primary thrombocytosis. The most frequent causes of secondary thrombocytosis were tissue damage (42%), infection (24%), malignancy (13%) and chronic inflammation (10%). Primary thrombocytosis was significantly associated with a higher platelet count and an increased incidence of both arterial and venous thromboembolic complications. In secondary thrombocytosis, thromboembolic events were restricted to the venous system and occurred only in the presence of other risk factors. Mean values of leucocyte count, haematocrit, erythrocyte sedimentation rate, fibrinogen, serum potassium and lactate dehydrogenase were significantly different in primary and secondary thrombocytosis.
The finding of an elevated platelet count on routine blood examination has diagnostic, prognostic and therapeutic implications. It is of clinical importance to distinguish between primary and secondary thrombocytosis, as thrombotic complications occur more frequently in primary thrombocytosis. Unless additional risk factors are present, secondary thrombocytosis is not associated with a significant risk for thromboembolic events.
确定一大群患者血小板计数升高(血小板增多症)的病因及临床意义。
对所有血小板计数至少一次≥500×10⁹/L的患者病历进行回顾性研究。
德国乌尔姆大学医学与外科系。
总共732例血小板增多症患者。
血小板增多症的分类及血栓栓塞并发症,以及区分原发性和继发性血小板增多症的实验室参数评估。
在732例患者中,89例(12.3%)为原发性血小板增多症,643例(87.7%)为继发性血小板增多症。89例原发性血小板增多症患者中有40例(45%)观察到真性红细胞增多症。继发性血小板增多症最常见的病因是组织损伤(42%)、感染(24%)、恶性肿瘤(13%)和慢性炎症(10%)。原发性血小板增多症与较高的血小板计数以及动脉和静脉血栓栓塞并发症发生率增加显著相关。在继发性血小板增多症中,血栓栓塞事件仅限于静脉系统,且仅在存在其他危险因素时发生。原发性和继发性血小板增多症患者的白细胞计数、血细胞比容、红细胞沉降率、纤维蛋白原、血清钾和乳酸脱氢酶的平均值有显著差异。
常规血液检查发现血小板计数升高具有诊断、预后和治疗意义。区分原发性和继发性血小板增多症具有临床重要性,因为原发性血小板增多症中血栓形成并发症更常见。除非存在其他危险因素,继发性血小板增多症与血栓栓塞事件的显著风险无关。