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果阿三级医疗中心就诊患者真性红细胞增多症的临床谱及并发症

Clinical Spectrum and Complications of Polycythemia, in Patients presenting at Tertiary Care Centre at Goa.

作者信息

Nevrekar Ramnath, Pai Aparna, Khandeparkar Anar

机构信息

Assistant Professor.

Associate Professor, Dept. of Medicine, Goa Medical College, Goa.

出版信息

J Assoc Physicians India. 2019 Oct;67(10):20-24.

Abstract

BACKGROUND

Polycythemia is characterized by rise in hemoglobin and hematocrit, either as a result of hematopoietic clonal expansion (Vera) or secondary to hypoxic stimuli (secondary polycythemia).It is of great importance to detect early and identify the type of polycythemia and also asses the thrombotic risk so that timely and appropriate treatment can be given. The present study aims to characterize the different presentations and complications of polycythemia, evaluate genetic factors and differences between the two categories of polycythemia in ethnic Goan subjects.

AIMS AND OBJECTIVES

  1. To identify common presentations and etiologies of polycythemia 2. To evaluate and compare the differences in clinical features, hematological parameters and complications of polycythemia in primary (vera) and secondary polycythemia 3. To study the profile of JAK 2 V617F mutation in Goan patients with polycythemia Vera.

MATERIALS AND METHODS

This was a retrospective observational cohort study, conducted at the Department of Internal Medicine, Goa Medical College, a tertiary care, teaching institute in the state of Goa. We analysed clinical and laboratory data of patients of polycythemia due to all causes (polycythemia Vera and secondary causes) previously admitted or following up at the hospital from January 2014 to December 2017. In each of these 2 groups, we studied the various clinical parameters including the age at presentation,sex,residence, symptomatology and clinical findings,presence of hypertension, as well as complications arising due to polycythemia (past and at present) hematological data including Hb,HCT, total WBC count, absolute neutrophil count, RBC and platelet count, ESR, rouleaux formation, EPO levels and JAK 2 V617F mutation analysis (done by real time PCR technique) and requirement of phlebotomies in the last 4 years. Commonest clinical presentations and complications arising due to polycythemia, in each group were analysed and compared.

RESULTS

A total of 44 patients were included in the study out of which 33 were males. Polycythemia Vera was seen in 43.18% while secondary causes were seen in 56.8 % patients. Patients with Vera were found to be more symptomatic with higher levels of mean Hb, HCT, cell counts and with a higher requirement of phlebotomy and more thrombotic complications. Amongst Vera group, patients having high WBC count, increased Rouleau formation, and JAK2 positivity were found to be more prone for thrombosis. Hypertension was frequently seen to be associated with both groups. Obstructive sleep apnea followed by COPD was found to be the commonest causes of secondary polycythemia.

CONCLUSION

Our study revealed that patients with polycythemia Vera are more symptomatic and have a higher requirement of phlebotomy and a higher thrombotic tendency (arterial being more common than venous) as compared to the secondary polycythemia owing to a higher hyperviscocity in the former. Leukocytosis and JAK 2 617F positivity were found to be important predictors of thrombotic risk. Hypertension was found to be frequently associated with Vera as well as in secondary causes due to OSA.

摘要

背景

真性红细胞增多症的特征是血红蛋白和血细胞比容升高,其原因要么是造血克隆性扩增(真性红细胞增多症),要么是继发于缺氧刺激(继发性真性红细胞增多症)。早期检测并确定真性红细胞增多症的类型,同时评估血栓形成风险,以便能够给予及时、恰当的治疗,这非常重要。本研究旨在描述真性红细胞增多症的不同表现和并发症,评估种族为果阿人的受试者中两类真性红细胞增多症的遗传因素及差异。

目的

  1. 确定真性红细胞增多症的常见表现和病因。2. 评估并比较原发性(真性红细胞增多症)和继发性真性红细胞增多症在临床特征、血液学参数及并发症方面的差异。3. 研究果阿人真性红细胞增多症患者中JAK 2 V617F突变情况。

材料与方法

这是一项回顾性观察队列研究,在果阿邦一所三级医疗教学机构果阿医学院内科进行。我们分析了2014年1月至2017年12月期间在该医院既往入院或随访的所有病因所致真性红细胞增多症(真性红细胞增多症和继发性病因)患者的临床和实验室数据。在这两组中,我们研究了各种临床参数,包括就诊年龄、性别、居住地、症状和临床表现、高血压的存在情况,以及真性红细胞增多症引起的并发症(既往和目前),血液学数据包括血红蛋白、血细胞比容、白细胞总数、绝对中性粒细胞计数、红细胞和血小板计数、血沉、缗钱状形成、促红细胞生成素水平以及JAK 2 V617F突变分析(通过实时聚合酶链反应技术进行),以及过去4年放血治疗的需求。分析并比较了每组中真性红细胞增多症引起的最常见临床表现和并发症。

结果

本研究共纳入44例患者,其中33例为男性。真性红细胞增多症患者占43.18%,继发性病因患者占56.8%。真性红细胞增多症患者症状更明显,平均血红蛋白、血细胞比容、细胞计数水平更高,放血治疗需求更高,血栓形成并发症更多。在真性红细胞增多症组中,白细胞计数高、缗钱状形成增加和JAK2阳性的患者更容易发生血栓形成。高血压在两组中都经常出现。阻塞性睡眠呼吸暂停继以慢性阻塞性肺疾病被发现是继发性真性红细胞增多症的最常见病因。

结论

我们的研究表明,与继发性真性红细胞增多症相比,真性红细胞增多症患者症状更明显,放血治疗需求更高,血栓形成倾向更高(动脉血栓比静脉血栓更常见),原因是前者血液黏滞度更高。白细胞增多和JAK 2 617F阳性被发现是血栓形成风险的重要预测因素。高血压被发现经常与真性红细胞增多症以及阻塞性睡眠呼吸暂停所致继发性病因相关。

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