Safety and Effectiveness of Somatostatin and Analogues on Chest Tube Output After Coronary Artery Bypass Grafting: A Scoping Review.

IF 2.5 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Journal of Cardiovascular Pharmacology Pub Date : 2026-08-01 Epub Date: 2026-07-20 DOI:10.1097/FJC.0000000000001810
Caitlin M Gibson, Alisa K Escaño, Katherine D Hobe, Erica R Brody, Roberto Montealgre, Josue Chery
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引用次数: 0

Abstract

Abstract: Somatostatin and analogues may reduce chest tube (CT) output in chylothorax caused by postcoronary artery bypass grafting (CABG). However, data are limited to case reports and series. This scoping review aimed to describe the efficacy and safety of somatostatin/analogue use in post-CABG chylothorax. We retrieved from PubMed, Embase, and OVID all studies and case reports describing somatostatin/analogue use in adult patients post-CABG for resolution of chylothorax. The primary outcome was time from somatostatin/analogue initiation to daily CT output <100 mL/d. CT duration, need to repeat invasive intervention, and safety events associated with somatostatin/analogues were also analyzed. Somatostatin/analogues were associated with reductions in CT output, but one-third of patients still required pleurodesis or surgical intervention. No safety events were identified. Patients with lower daily CT outputs at the time of somatostatin/analogue initiation were more likely to avoid repeat intervention than those with higher outputs. In conclusion, somatostatin/analogues seem safe and possibly effective in management of post-CABG chylothorax. Future studies should investigate which patients are most likely to benefit from this therapy.

生长抑素和类似物对冠状动脉搭桥术后胸管输出量的安全性和有效性:范围综述。
生长抑素及其类似物可减少冠状动脉旁路移植术(CABG)后乳糜胸的胸管输出量。然而,数据仅限于病例报告和系列。本综述旨在描述生长抑素/类似物在冠脉搭桥后乳糜胸治疗中的有效性和安全性。我们从PubMed、Embase和OVID中检索了所有描述成人患者冠脉搭桥后使用生长抑素/类似物治疗乳糜胸的研究和病例报告。主要终点是从开始使用生长抑素/类似物到每日CT输出的时间
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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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