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钙通道阻滞剂与大环内酯类抗生素合用的低血压风险。

Risk of hypotension with concomitant use of calcium-channel blockers and macrolide antibiotics.

机构信息

Lloyd L. Gregory School of Pharmacy, Palm Beach Atlantic University, 901 South Flagler Drive, West Palm Beach, FL 33416, USA.

出版信息

Am J Health Syst Pharm. 2012 Jun 15;69(12):1038-43. doi: 10.2146/ajhp110486.

Abstract

PURPOSE

The literature describing the risk of hypotension in patients receiving concomitant therapy with a calcium-channel blocker (CCB) and a macrolide antibiotic is reviewed.

SUMMARY

A literature search was conducted to identify studies and reports describing significant drug interactions between CCBs and macrolide antibiotics resulting in hypotension. One retrospective clinical trial, one pharmacokinetics study, and five case reports were found using MEDLINE. While both dihydropyridine and nondihydropyridine CCBs are cytochrome P-450 isoenzyme 3A4 (CYP3A4) substrates, verapamil was the CCB implicated in three of the five case reports. Based on currently available literature, it is unknown whether the risk of clinically significant hypotension is higher for patients receiving nondihydropyridine CCBs; however, due to the drugs' effects on the coronary arteries, there is the potential for more-serious cardiac complications with these agents. Both erythromycin and clarithromycin have been shown to prolong the Q-T interval, an effect that appears to increase when these drugs are given with CYP3A4 inhibitors. The potential for Q-T interval prolongation by both erythromycin and clarithromycin may increase the risk of clinically relevant hypotension and even shock in patients taking CCBs, in particular nondihydropyridines.

CONCLUSION

Potentially significant hypotension and shock may occur when macrolide antibiotics, particularly erythromycin and clarithromycin, are administered concomitantly with CCBs. The frequency of hypotension as a result of concomitant CCB and macrolide administration appears to be small, but the risk of adverse effects and the severity of the effects appear to be greater for those patients who are older and in those with multiple comorbidities.

摘要

目的

综述同时接受钙通道阻滞剂(CCB)和大环内酯类抗生素治疗的患者发生低血压的风险相关文献。

摘要

检索文献以确定描述 CCB 和大环内酯类抗生素之间发生显著药物相互作用导致低血压的研究和报告。使用 MEDLINE 检索到一项回顾性临床试验、一项药代动力学研究和五项病例报告。虽然二氢吡啶类和非二氢吡啶类 CCB 均为细胞色素 P-450 同工酶 3A4(CYP3A4)的底物,但在五项病例报告中有三项涉及维拉帕米。根据目前的文献,尚不清楚接受非二氢吡啶类 CCB 的患者发生临床显著低血压的风险是否更高;然而,由于这些药物对冠状动脉的影响,这些药物可能会导致更严重的心脏并发症。红霉素和克拉霉素均已被证明可延长 Q-T 间期,当这些药物与 CYP3A4 抑制剂合用时,这种作用似乎会增强。红霉素和克拉霉素均可导致 Q-T 间期延长,这可能会增加接受 CCB 治疗的患者发生临床相关低血压甚至休克的风险,尤其是非二氢吡啶类 CCB。

结论

当大环内酯类抗生素,特别是红霉素和克拉霉素与 CCB 同时给药时,可能会发生严重的低血压和休克。由于同时使用 CCB 和大环内酯类抗生素而导致低血压的频率似乎较低,但对于年龄较大和患有多种合并症的患者,不良反应的风险和严重程度似乎更高。

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