Comparison of Effects of Separate and Combined Sugammadex and Lipid Emulsion Administration on Hemodynamic Parameters and Survival in a Rat Model of Verapamil Toxicity

MakaleYayıncıda açık erişimScopus SJRQ2
  • SDG 3 · Sağlık ve Kaliteli Yaşam

Özet

Background: Toxicity of calcium channel blockers leads to high patient mortality and there is no effective antidote. The benefit of using 20% lipid emulsion and sugammadex has been reported. The present study measured the effect of sugammadex and 20% lipid emulsion on hemodynamics and survival in a rat model of verapamil toxicity. Material/Methods: In this single-blinded randomized control study, rats were separated into 4 groups of 7 rats each: Sugammadex (S), Sugammadex plus 20% lipid emulsion (SL), 20% lipid emulsion (L), and control (C). Heart rates and mean arterial pressures were monitored and noted each minute until death. Results: Average time to death was 21.0 +/- 9.57 minutes for group C, 35.57 +/- 10.61 minutes for group S, 37.14 +/- 16.6 minutes for group L and 49.86 +/- 27.56 minutes for group SL. Time to death was significantly longer in other groups than in the control group (p<0.05). Conclusions: Verapamil overdose is has a comparatively high mortality rate and there is no effective antidote. Treatment generally involves gastric decontamination and symptomatic treatment to counteract the drug's negative effects. In animal studies sugammadex and lipid emulsion had a positive effect on survival in patients with calcium channel blocker toxicity. Sugammadex and intralipid increased survival in a rat model of verapamil toxicity. The combination of both drugs may decrease cardiotoxicity. Sugammadex alone or combined with 20% lipid emulsion reduce the need for inotropic agents. The mechanism requires clarification with larger studies.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/gumushane/10540Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.12659/msm.896125Yayıncı resmi DOI adresi
Atıflar
WoS
10
OpenAlex
10
Her kaynağın kendi saydığı toplam atıf; aktarım ve zenginleştirme sırasında alındı.
Tam Kayıt
AlanDeğerDil
dc.contributor.authorTulgar, Serkan
dc.contributor.authorKose, Halil Cihan
dc.contributor.authorPiroglu, Isilay Demir
dc.contributor.authorKarakilic, Evvah
dc.contributor.authorAtes, Nagihan Gozde
dc.contributor.authorDemir, Ahmet
dc.contributor.authorGergerli, Ruken
dc.contributor.authorGuven, Selin
dc.contributor.authorPiroglu, Mustafa Devrim
dc.date.accessioned2026-10-22T09:23:04.337919761Z
dc.date.available2026-10-22T09:23:04.337919761Z
dc.date.issued2016-03
dc.description.abstractBackground: Toxicity of calcium channel blockers leads to high patient mortality and there is no effective antidote. The benefit of using 20% lipid emulsion and sugammadex has been reported. The present study measured the effect of sugammadex and 20% lipid emulsion on hemodynamics and survival in a rat model of verapamil toxicity. Material/Methods: In this single-blinded randomized control study, rats were separated into 4 groups of 7 rats each: Sugammadex (S), Sugammadex plus 20% lipid emulsion (SL), 20% lipid emulsion (L), and control (C). Heart rates and mean arterial pressures were monitored and noted each minute until death. Results: Average time to death was 21.0 +/- 9.57 minutes for group C, 35.57 +/- 10.61 minutes for group S, 37.14 +/- 16.6 minutes for group L and 49.86 +/- 27.56 minutes for group SL. Time to death was significantly longer in other groups than in the control group (p<0.05). Conclusions: Verapamil overdose is has a comparatively high mortality rate and there is no effective antidote. Treatment generally involves gastric decontamination and symptomatic treatment to counteract the drug's negative effects. In animal studies sugammadex and lipid emulsion had a positive effect on survival in patients with calcium channel blocker toxicity. Sugammadex and intralipid increased survival in a rat model of verapamil toxicity. The combination of both drugs may decrease cardiotoxicity. Sugammadex alone or combined with 20% lipid emulsion reduce the need for inotropic agents. The mechanism requires clarification with larger studies.
dc.identifier.doi10.12659/msm.896125
dc.identifier.endpage990
dc.identifier.issn1643-3750
dc.identifier.pmid27012816
dc.identifier.startpage984
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/10540
dc.identifier.volume22
dc.identifier.wosWOS:000372837700001
dc.language.isoen
dc.publisherINT SCIENTIFIC LITERATURE, INC
dc.relation.ispartofMEDICAL SCIENCE MONITOR
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectDrug Overdose
dc.subjectFat Emulsions, Intravenous
dc.subjectgamma-Cyclodextrins
dc.subjectVerapamil
dc.subject.classificationMedicine, Research & Experimental
dc.subject.classificationResearch & Experimental Medicine
dc.subject.otherCALCIUM-CHANNEL BLOCKER
dc.subject.otherEXTRACORPOREAL LIFE-SUPPORT
dc.subject.otherDRUG INTOXICATION
dc.subject.otherCARDIOGENIC-SHOCK
dc.subject.otherOVERDOSE
dc.titleComparison of Effects of Separate and Combined Sugammadex and Lipid Emulsion Administration on Hemodynamic Parameters and Survival in a Rat Model of Verapamil Toxicity
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex10
rdl.citation.wos10
rdl.oa.statushybrid
rdl.scopus.quartileQ2
rdl.sdgSDG03
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)