Bleomycin for Malignant Pericardial Effusion: A Systematic Review of Efficacy and Adverse Events.

IF 2.6 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Paulus Parholong Siahaan, Roy Bagus Kurniawan, Pandit Bagus Tri Saputra, Jannatin Nisa Arnindita, Cornelia Ghea Savitri, Luqman Hakim Andira, Estya Nadya Meitavany, Johanes Nugroho Eko Putranto, Firas Farisi Alkaff
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Abstract

Malignant pericardial effusion (MPE) is a progressive fluid accumulation in the pericardial space that can lead to pericardial tamponade. Despite the high recurrence rate associated with pericardiocentesis, it remains the mainstay therapy. Bleomycin has emerged as an intrapericardial sclerosing therapy that may reduce recurrence and improve patients' quality of life. This systematic review aimed to assess the efficacy and safety profile of Bleomycin instillation in patients with MPE. An exhaustive search was conducted in PubMed, Web of Science, Scopus, ProQuest, EBSCO, and ClinicalTrials.gov databases. Eligible studies included MPE patients as participants who were treated with intrapericardial Bleomycin, reporting the patients' outcomes and using English in the full text. Individual studies were assessed for quality using the Newcastle-Ottawa Scales for cohort studies and the Jadad Scale for trial studies. Eight studies were included in this systematic review involving 242 MPE patients treated with Bleomycin. Bleomycin demonstrated lower recurrence rates than other sclerosing agents, with only ≤5% of patients requiring repeated drainage due to recurrence. Bleomycin treatment resulted in 3.5 days less hospitalisation compared to doxycycline. Bleomycin is also safe to use, with reported less severe pain compared to other treatment agents for MPE, such as doxycycline and pericardiocentesis. Bleomycin may benefit patients by reducing recurrence rates and improving patients' quality of life. Moreover, it is safe and has low rates of adverse events following the instillation.

博来霉素治疗恶性心包积液:疗效和不良事件的系统回顾。
恶性心包积液(MPE)是一种进行性积液在心包间隙,可导致心包填塞。尽管与心包穿刺术相关的复发率很高,但它仍然是主要的治疗方法。博莱霉素已成为一种心包内硬化治疗,可减少复发并改善患者的生活质量。本系统综述旨在评估博莱霉素滴注治疗MPE患者的有效性和安全性。在PubMed、Web of Science、Scopus、ProQuest、EBSCO和ClinicalTrials.gov数据库中进行了详尽的搜索。符合条件的研究包括MPE患者作为心包内博莱霉素治疗的参与者,报告患者的结果并使用英文全文。个体研究的质量评估采用纽卡斯尔-渥太华量表(队列研究)和Jadad量表(试验研究)。本系统综述纳入了8项研究,涉及242例接受博莱霉素治疗的MPE患者。博莱霉素的复发率低于其他硬化剂,只有≤5%的患者因复发需要反复引流。与强力霉素相比,博莱霉素治疗可减少3.5天的住院时间。博莱霉素的使用也很安全,与强力霉素和心包穿刺术等其他MPE治疗药物相比,博莱霉素的疼痛程度较轻。博莱霉素可能通过降低复发率和改善患者的生活质量而使患者受益。此外,它是安全的,注射后不良事件发生率低。
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
5.10
自引率
3.30%
发文量
367
审稿时长
1 months
期刊介绍: Journal of Cardiovascular Pharmacology is a peer reviewed, multidisciplinary journal that publishes original articles and pertinent review articles on basic and clinical aspects of cardiovascular pharmacology. The Journal encourages submission in all aspects of cardiovascular pharmacology/medicine including, but not limited to: stroke, kidney disease, lipid disorders, diabetes, systemic and pulmonary hypertension, cancer angiogenesis, neural and hormonal control of the circulation, sepsis, neurodegenerative diseases with a vascular component, cardiac and vascular remodeling, heart failure, angina, anticoagulants/antiplatelet agents, drugs/agents that affect vascular smooth muscle, and arrhythmias. Appropriate subjects include new drug development and evaluation, physiological and pharmacological bases of drug action, metabolism, drug interactions and side effects, application of drugs to gain novel insights into physiology or pathological conditions, clinical results with new and established agents, and novel methods. The focus is on pharmacology in its broadest applications, incorporating not only traditional approaches, but new approaches to the development of pharmacological agents and the prevention and treatment of cardiovascular diseases. Please note that JCVP does not publish work based on biological extracts of mixed and uncertain chemical composition or unknown concentration.
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