School of Pharmacy, University of Waterloo, 10 Victoria St S, Kitchener, ON, N2G 2B2, Canada.
Can J Anaesth. 2013 May;60(5):492-9. doi: 10.1007/s12630-012-9879-1. Epub 2013 Jan 18.
Carcinoid crises are rare life-threatening events involving cardiac instability when carcinoid tumours release vasoactive peptides. Such events can occur in the perioperative setting. Octreotide, a somatostatin analogue, is administered as a bolus dose of 100-500 μg iv or by infusion to treat carcinoid crises. Due to the apparent low risk-to-benefit profile, a much higher dose is sometimes used in urgent situations. The purpose of this study was to assess the evidence for administering doses or hourly infusions of octreotide that exceeded 1,500 μg iv to treat carcinoid crises. We also sought to identify which patients may require large doses and to describe the adverse effects of such doses.
We systematically searched Medline, EMBASE, and Cochrane databases and hand-searched reference lists of relevant articles in 2006 and again in 2010 and 2011. All study designs were included in our search. Resolution of crisis symptoms was the primary outcome.
Eighteen articles were included. No patient died during a carcinoid crisis. A retrospective chart review of 89 patients with carcinoid heart disease reported octreotide doses of 25-54,000 μg to treat carcinoid crises, although neither crisis symptoms nor outcomes were described.
In the included case reports, carcinoid crises were managed effectively using octreotide 25-500 μg iv. Previous exposure to octreotide and carcinoid heart disease may warrant the need for higher doses. In addition to the low quality of the articles and the small sample size, inconsistent use of the term "carcinoid crisis" and paucity of reported outcomes were also limitations of this systematic review. These findings highlight the need for further investigation into dose-response relationships of octreotide for the treatment of carcinoid crisis.
类癌危象是一种罕见的危及生命的事件,当类癌肿瘤释放血管活性肽时会导致心脏不稳定。这种情况可能发生在围手术期。奥曲肽是一种生长抑素类似物,作为 100-500μg iv 推注或输注给药,用于治疗类癌危象。由于明显的低风险-效益特征,在紧急情况下有时会使用更高剂量。本研究的目的是评估给予超过 1500μg iv 的奥曲肽剂量或每小时输注剂量以治疗类癌危象的证据。我们还试图确定哪些患者可能需要大剂量,并描述这些剂量的不良反应。
我们系统地检索了 Medline、EMBASE 和 Cochrane 数据库,并于 2006 年、2010 年和 2011 年再次检索了相关文章的参考文献列表。我们的搜索包括所有研究设计。危象症状的缓解是主要结局。
纳入了 18 篇文章。没有患者在类癌危象期间死亡。对 89 例类癌性心脏病患者的回顾性图表审查报告了使用奥曲肽 25-54000μg 治疗类癌危象的剂量,尽管未描述危象症状和结局。
在纳入的病例报告中,使用奥曲肽 25-500μg iv 有效治疗了类癌危象。先前接触奥曲肽和类癌性心脏病可能需要更高的剂量。除了文章质量低和样本量小之外,术语“类癌危象”的使用不一致以及报告结果的缺乏也是本系统评价的局限性。这些发现强调了需要进一步研究奥曲肽治疗类癌危象的剂量-反应关系。