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慢性免疫性血小板减少性紫癜的治疗:患者视角

Treatment of chronic immune thrombocytopenic purpura: the patients' perspective.

作者信息

Matzdorff Axel, Arnold Gabriele

机构信息

Department of Haematology and Oncology, Caritasklinik St Theresia, Saarbruecken, Germany.

出版信息

Eur J Haematol. 2007 May;78(5):381-8. doi: 10.1111/j.1600-0609.2007.00829.x. Epub 2007 Feb 27.

DOI:10.1111/j.1600-0609.2007.00829.x
PMID:17331128
Abstract

BACKGROUND

The 1996 ASH guidelines recommend glucocorticoids and splenectomy as standard treatment of chronic immune thrombocytopenic purpura (ITP). We sought to find out how many German ITP-patients were treated according to these guidelines and whether high-cost treatments were offered to the patients.

METHODS

We handed out a questionnaire at two self-help group meetings in 2004 and 2005 and to all patients who contacted the ITP self-help group until the end of 2005.

RESULTS

Eighty-five questionnaires were evaluated. Age (median 34 yr) and gender distribution (38% male, 62% female) were similar to other surveys. Median duration of disease was 5.2 yr. Seventy-five percent had platelets <20,000/microL at the time of diagnosis. Twenty-four percent still had <20,000 platelets/microL at the time of this survey. Forty-two percent had oropharyngeal mucosal bleeds, 28% gastrointestinal or urological bleeds, 11% bleedings in the eye with visual impairment or intracerebral bleeds. 96% had received a trial of glucocorticoid therapy. Seventy-five percent of the patients treated with glucocorticoids perceived this treatment as particularly bothersome. Seventy-five percent of the patients with low platelet count still had their spleen. Complementary and alternative medical treatments had been used by 46% of the patients. Only 33% of the patients had ever heard of rituximab.

CONCLUSION

Despite literature suggesting that patients wish to be well informed this survey shows that chronic ITP patients know little about their disease and the various treatment modalities. This and the frequent use of complementary and alternative medicines reflects inadequate communication between doctors and ITP patients.

摘要

背景

1996年美国血液学会(ASH)指南推荐将糖皮质激素和脾切除术作为慢性免疫性血小板减少性紫癜(ITP)的标准治疗方法。我们试图了解有多少德国ITP患者按照这些指南接受治疗,以及是否向患者提供了高成本治疗。

方法

我们在2004年和2005年的两次自助小组会议上,以及在2005年底前联系ITP自助小组的所有患者中发放了问卷。

结果

共评估了85份问卷。年龄(中位数34岁)和性别分布(男性38%,女性62%)与其他调查相似。疾病的中位持续时间为5.2年。75%的患者在诊断时血小板计数<20,000/微升。在本次调查时,24%的患者血小板计数仍<20,000/微升。42%的患者有口咽黏膜出血,28%有胃肠道或泌尿系统出血,11%有导致视力障碍的眼部出血或脑出血。96%的患者接受过糖皮质激素治疗试验。75%接受糖皮质激素治疗的患者认为这种治疗特别麻烦。75%血小板计数低的患者脾脏仍在。46%的患者使用过补充和替代医学治疗。只有33%的患者听说过利妥昔单抗。

结论

尽管文献表明患者希望充分了解情况,但本次调查显示慢性ITP患者对自己的疾病和各种治疗方式了解甚少。这一点以及补充和替代药物的频繁使用反映出医生与ITP患者之间沟通不足。

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