Current concepts regarding drug dosing for peripheral stents.


Journal

The Journal of cardiovascular surgery
ISSN: 1827-191X
Titre abrégé: J Cardiovasc Surg (Torino)
Pays: Italy
ID NLM: 0066127

Informations de publication

Date de publication:
Aug 2019
Historique:
pubmed: 8 5 2019
medline: 19 7 2019
entrez: 8 5 2019
Statut: ppublish

Résumé

Drug-eluting stent (DES) are the mainstay therapy for the treatment of coronary artery disease. Stent design and drug-elution strategies have evolved over the years leading to the last generation DES which shows optimal safety and efficacy outcome. Peripheral arteries have different mechanical and biological features and the lessons learned from the coronary field have been difficult to introduce into the development of peripheral vascular technologies. First, due to its complex biomechanical behavior the use of metallic stents is limited in some vascular segments (i.e., distal superficial fermoral artery [SFA]). Also, peripheral vascular atherosclerosis is different containing higher levels of plaque burden and calcium. Finally, peripheral arterial disease tends to be more aggressive including longer lesions and higher incidence of total chronic occlusion. In general terms, restenosis in the peripheral vascular territory is more aggressive and occurs at a later time (~12 months) requiring a different pharmacokinetic profile compared to coronary technologies. Several strategies have been evaluated in the peripheral arteries raging from the bare metal stent to the drug coated balloon and drug eluting stent with outcome varying depending on the different field of application (i.e. SFA and below-the-knee). Results coming from the clinical trial are encouraging but further studies and direct comparison among the different technologies are demanded to determine the best therapy for peripheral vascular disease.

Identifiants

pubmed: 31062571
pii: S0021-9509.19.10995-0
doi: 10.23736/S0021-9509.19.10995-0
doi:

Substances chimiques

Polymers 0
Everolimus 9HW64Q8G6G
TOR Serine-Threonine Kinases EC 2.7.11.1
Paclitaxel P88XT4IS4D
Sirolimus W36ZG6FT64

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

439-449

Auteurs

Marco Ferrone (M)

Cardiovascular Research Foundation, Skirball Center for Innovation, Orangeburg, NY, USA.
Federico II University of Naples, Naples, Italy.

Yanping Cheng (Y)

Cardiovascular Research Foundation, Skirball Center for Innovation, Orangeburg, NY, USA.

Juan F Granada (JF)

Cardiovascular Research Foundation, Skirball Center for Innovation, Orangeburg, NY, USA - jgranada@crf.org.

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Classifications MeSH