Advances in the study of nebulized tranexamic acid for pulmonary hemorrhage.

IF 2.4 3区 医学 Q3 PHARMACOLOGY & PHARMACY
Ping Zhang, Jiaoni Zheng, Xuefeng Shan, Bo Zhou
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引用次数: 0

Abstract

Purpose: Pulmonary hemorrhage is a life-threatening condition characterized by blood leakage into lung tissues, leading to severe respiratory distress. Nebulized tranexamic acid (TXA) has emerged as a promising treatment option for pulmonary hemorrhage due to its localized hemostatic effects and minimal systemic side effects. This review aims to summarize the research progress on the effectiveness and safety of nebulized TXA in pulmonary hemorrhage.

Methods: A comprehensive search of the Embase, PubMed, and Scopus databases was conducted to identify relevant studies published between the date of inception of each database and November 2023. A comprehensive search was conducted in the PubMed, Embase, Scopus, and Google Scholar databases using the following keywords: "hemoptysis," "haemoptysis," "pulmonary hemorrhage," "tranexamic acid," "antifibrinolytic," "nebulize," and "inhale." Additional articles were identified by reviewing the references of the retrieved studies. Studies were selected based on their focus on the application of nebulized TXA for pulmonary hemorrhage. The authors and dates of publication, study type, patients, diseases, intervention and main outcomes of these papers are tabulated. This consisted of two randomized controlled trials (RCTs), six case series, and nine case reports.

Results: The commonly used dosage of nebulized TXA in the studies reviewed was 500 mg/5 ml, administered 3-4 times daily. Evidence suggests that nebulized TXA effectively controls bleeding in pulmonary hemorrhage with a hemostatic efficacy comparable to systemic administration, but with a lower risk of venous thrombosis. Safety data indicates that nebulized TXA is generally well-tolerated, with no significant systemic adverse reactions reported. Local reactions, such as bronchospasm, were rare and resolved with short-term bronchodilator treatment.

Conclusion: Nebulized TXA appears to be an innovative and minimally invasive therapy for pulmonary hemorrhage, providing targeted hemostatic effects with a favorable safety profile. However, the predominance of small-scale studies and case reports highlights the need for large-scale, high-quality research to establish standardized guidelines.

氨甲环酸雾化治疗肺出血的研究进展。
目的:肺出血是一种危及生命的疾病,其特征是血液渗漏到肺组织中,导致严重的呼吸窘迫。雾化氨甲环酸(TXA)由于其局部止血作用和最小的全身副作用,已成为一种有希望的治疗肺出血的选择。本文综述了气雾剂TXA治疗肺出血的有效性和安全性的研究进展。方法:对Embase、PubMed和Scopus数据库进行综合检索,确定各数据库建立日期至2023年11月之间发表的相关研究。在PubMed, Embase, Scopus和谷歌Scholar数据库中进行了全面的搜索,使用以下关键词:“咯血”,“咯血”,“肺出血”,“氨甲环酸”,“抗纤溶剂”,“雾化”和“吸入”。通过检索到的研究的参考文献来确定其他文章。选择研究的重点是雾化TXA在肺出血中的应用。列出了这些论文的作者和发表日期、研究类型、患者、疾病、干预措施和主要结局。这包括两项随机对照试验(rct), 6个病例系列和9个病例报告。结果:在回顾的研究中,TXA雾化的常用剂量为500mg / 5ml,每天给药3-4次。有证据表明,雾化TXA能有效控制肺出血出血,止血效果与全身给药相当,但静脉血栓形成的风险较低。安全性数据表明,雾化的TXA通常耐受性良好,没有明显的全身不良反应报道。局部反应,如支气管痉挛,是罕见的,并解决短期支气管扩张剂治疗。结论:雾化TXA似乎是一种创新的微创治疗肺出血,提供靶向止血效果和良好的安全性。然而,小规模研究和病例报告的优势突出了需要大规模、高质量的研究来建立标准化的指导方针。
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
CiteScore
5.40
自引率
3.40%
发文量
170
审稿时长
3-8 weeks
期刊介绍: The European Journal of Clinical Pharmacology publishes original papers on all aspects of clinical pharmacology and drug therapy in humans. Manuscripts are welcomed on the following topics: therapeutic trials, pharmacokinetics/pharmacodynamics, pharmacogenetics, drug metabolism, adverse drug reactions, drug interactions, all aspects of drug development, development relating to teaching in clinical pharmacology, pharmacoepidemiology, and matters relating to the rational prescribing and safe use of drugs. Methodological contributions relevant to these topics are also welcomed. Data from animal experiments are accepted only in the context of original data in man reported in the same paper. EJCP will only consider manuscripts describing the frequency of allelic variants in different populations if this information is linked to functional data or new interesting variants. Highly relevant differences in frequency with a major impact in drug therapy for the respective population may be submitted as a letter to the editor. Straightforward phase I pharmacokinetic or pharmacodynamic studies as parts of new drug development will only be considered for publication if the paper involves -a compound that is interesting and new in some basic or fundamental way, or -methods that are original in some basic sense, or -a highly unexpected outcome, or -conclusions that are scientifically novel in some basic or fundamental sense.
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