Do we need local guidelines for the diagnosis and management of immune thrombocytopenia in Iraq?

Q4 Medicine
Ahmed Mjali, B. Matti, N. Abbas, Hassan Abood Nassrullah, A. Naji, A. Alwan, Waseem F. Al-Tameemi, Haider Jaleel Al-Shammari, T. Saleh, Mohammed Al Qayyim, A. Mohammed
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Abstract

AIMS: Immune thrombocytopenia (ITP), also known as immune thrombocytopenic purpura, is an autoimmune disorder characterized by a low platelet count in the blood. This study aimed to assess the health infrastructure in Iraq regarding the diagnosis and management of patients with immune thrombocytopenia (ITP), with a focus on the use of guidelines in ITP management. SETTINGS AND DESIGN: This was a cross-sectional study carried out between October and November 2022 to assess ITP diagnosis, management, and the use of guidelines in 18 governorates in Iraq. MATERIALS AND METHODS: Invited to this study were 79 hematologists who were registered in the Iraqi Society of Hematology and who practiced in the 18 governorates. Out of the 79 hematologists, 65 participated in this survey. Data were collected using a questionnaire. STATISTICAL ANALYSIS USED: IBM SPSS 28 for Windows was used for the analysis and Microsoft Excel was used for creating the graphs. Descriptive statistics were presented in the form of numbers and percentages as all variables were categorical. RESULTS: The most requested routine tests were manual assessment of platelet count (83.1%), blood film (98.5%), virology screen (90.9%), connective tissue screen (85.9%), and prothrombin time and partial thromboplastin time (78.5%). More than 80% of the hematologists request bone marrow aspiration for the patients who have no response to the first-line treatment. Only the genetic test and the quantitative immunoglobulin level testing were available in the private sector both by (100%), while the other tests were available in both sectors. More than 85% treat the patients as outpatients. Active bleeding, not platelet count, was the indication for hospitalization for 60% of the hematologists. Corticosteroids were chosen as the first choice as initial treatment by (93.8%), intravenous immunoglobulin the second choice by (6.2%). In the second-line treatment, rituximab was chosen as the first choice by (75.3%), and eltrombopag as the second choice (65%). Only 83% of the hematologists referred to a guideline, and the American Society of Hematology guideline was the most referred to. CONCLUSIONS: These results showed the need to establish national guidelines for the Diagnosis and Management of Immune Thrombocytopenia in Iraq to be able to effectively treat the laboratory findings and physical symptoms of ITP in addition to address the patient's emotional and mental health needs.
我们是否需要伊拉克当地的免疫性血小板减少症诊断和管理指南?
目的:免疫性血小板减少症(ITP),也称为免疫性血小板降低性紫癜,是一种以血液中血小板计数低为特征的自身免疫性疾病。本研究旨在评估伊拉克有关免疫性血小板减少症(ITP)患者诊断和管理的卫生基础设施,重点是ITP管理指南的使用。设置和设计:这是一项在2022年10月至11月期间进行的横断面研究,旨在评估伊拉克18个省ITP的诊断、管理和指南的使用情况。材料和方法:受邀参加这项研究的是79名在伊拉克血液学学会注册并在18个省执业的血液学家。在79名血液学家中,有65人参加了这项调查。使用问卷收集数据。使用的统计分析:使用IBM SPSS 28 for Windows进行分析,使用Microsoft Excel创建图表。描述性统计以数字和百分比的形式呈现,因为所有变量都是分类的。结果:要求最多的常规检查是手动评估血小板计数(83.1%)、血膜(98.5%)、病毒学筛查(90.9%)、结缔组织筛查(85.9%)、凝血酶原时间和部分凝血活酶时间(78.5%)。超过80%的血液科医生要求对一线治疗无反应的患者进行骨髓抽吸。私营部门只有基因检测和免疫球蛋白水平定量检测(100%)可用,而其他检测在这两个部门都可用。85%以上的病人是门诊病人。60%的血液学家认为活动性出血而非血小板计数是住院的指征。(93.8%)首选皮质类固醇作为初始治疗,(6.2%)首选静脉注射免疫球蛋白。在二线治疗中,(75.3%)首选利妥昔单抗,(65%)首选艾曲波帕。只有83%的血液学家参考了指南,而美国血液学学会的指南是参考最多的。结论:这些结果表明,有必要制定伊拉克免疫性血小板减少症的诊断和管理国家指南,以便能够有效治疗ITP的实验室检查结果和身体症状,并满足患者的情绪和心理健康需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Applied Hematology
Journal of Applied Hematology Medicine-Hematology
CiteScore
0.40
自引率
0.00%
发文量
34
审稿时长
24 weeks
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