Evaluating the safety of daptomycin coadministered with statin medications

Tyler M. Mitzner, Michael McCormick, Krissy M. Lentz, Ryan Tomlin, Kyle J. Schmidt, Lisa E. Dumkow
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Abstract

Background

Conflicting clinical evidence and prescribing recommendations exist regarding the safety of daptomycin when coadministered with statin medications. In addition, recommendations to hold statins during daptomycin therapy do not account for atherosclerotic cardiovascular disease (ASCVD) risk. Because of this, the practice of holding or continuing statins during daptomycin therapy is variable among providers.

Objectives

This study aimed to compare the musculoskeletal and cardiovascular safety of daptomycin and statin coadministration versus monotherapy and assess the appropriateness of monitoring during daptomycin infusion therapy, including creatine kinase (CK) and musculoskeletal symptoms, and the resumption of statins held during daptomycin therapy.

Methods

This retrospective cohort study included patients who were prescribed a statin medication and daptomycin therapy. The primary outcome was to compare daptomycin discontinuation owing to suspected musculoskeletal toxicity between patients who had their statin held and received daptomycin monotherapy (monotherapy group) and those who received daptomycin coadministered with statins (coadministered group). Secondary outcomes included evaluating CK monitoring practices, ASCVD events, and the resumption of held statins at the completion of daptomycin therapy.

Results

A total of 74 patients were included (monotherapy, n = 64; coadministered, n = 10). No statistically significant differences were observed between the 2 groups regarding daptomycin discontinuation owing to suspected musculoskeletal toxicity (6.3% monotherapy vs. 10% coadministered, P = 0.527). One patient in the monotherapy group had an ASCVD event during daptomycin therapy; none occurred within the coadministered group. Within the monotherapy group, 9 patients (14.1%) did not have documentation of statin resumption and 22 (34.4%) saw a delay of 4 or more weeks in statin resumption after daptomycin completion.

Conclusion

Patients who received daptomycin coadministration with statin therapy did not experience more musculoskeletal toxicity than patients who received daptomycin monotherapy. Owing to the risk of ASCVD events and potential for errors and delays in resumption, statins should be continued during daptomycin therapy, especially in high-risk patients.
评价达托霉素与他汀类药物合用的安全性
背景:关于达托霉素与他汀类药物合用的安全性,存在相互矛盾的临床证据和处方建议。此外,在达托霉素治疗期间保留他汀类药物的建议并不能解释动脉粥样硬化性心血管疾病(ASCVD)的风险。正因为如此,在达托霉素治疗期间保持或继续使用他汀类药物的做法在提供者之间是可变的。目的:本研究旨在比较达托霉素和他汀联合使用与单药治疗的肌肉骨骼和心血管安全性,并评估在达托霉素输注治疗期间监测的适宜性,包括肌酸激酶(CK)和肌肉骨骼症状,以及在达托霉素治疗期间恢复使用他汀类药物。方法本回顾性队列研究纳入了接受他汀类药物和达托霉素治疗的患者。主要结果是比较由于怀疑肌肉骨骼毒性而停用达托霉素的患者中,保留他汀类药物并接受达托霉素单药治疗(单药治疗组)和接受达托霉素与他汀类药物联合治疗(联合治疗组)的患者。次要结局包括评估CK监测实践,ASCVD事件,以及在达托霉素治疗完成后恢复使用他汀类药物。结果共纳入74例患者(单药治疗,n = 64;共给药,n = 10)。两组因怀疑肌肉骨骼毒性而停药达托霉素的差异无统计学意义(6.3%单药vs 10%共给药,P = 0.527)。单药治疗组有1例患者在达托霉素治疗期间发生ASCVD事件;在共同管理组中没有发生。在单药治疗组中,9名患者(14.1%)没有恢复他汀类药物的记录,22名患者(34.4%)在达托霉素停用后延迟4周或更长时间恢复他汀类药物。结论达托霉素联合他汀类药物治疗的患者肌肉骨骼毒性并不比单药治疗的患者大。由于ASCVD事件的风险和潜在的错误和延迟恢复,他汀类药物应在达托霉素治疗期间继续使用,特别是在高危患者中。
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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