Restenosis Rates After Drug-Eluting Stent Treatment for Stenotic Small-Diameter Renal Arteries.


Journal

Cardiovascular and interventional radiology
ISSN: 1432-086X
Titre abrégé: Cardiovasc Intervent Radiol
Pays: United States
ID NLM: 8003538

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 29 04 2019
accepted: 07 06 2019
pubmed: 4 7 2019
medline: 18 12 2019
entrez: 4 7 2019
Statut: ppublish

Résumé

To determine primary rates in small-diameter renal arteries, including complex bifurcation lesions, treated with drug-eluting stents (DES) in patients with atherosclerotic renal artery stenosis. This is a retrospective single-institution study. A total of 37 patients with 39 stented renal arteries were included. Patient and procedural data were obtained from the electronic medical record. Survival free from restenosis was estimated using the Kaplan-Meier method with patients stratified into two groups based on renal artery diameters (≤ 3.5 mm or > 3.5 mm). Univariate Cox proportional models were used to estimate hazard ratios associated with clinical and angiographic variables. Average renal artery diameter at time of treatment was 3.4 mm ± 0.4 mm. The median survival free from restenosis was 992 days, with 11 out of 37 (29.7%) developing an in-stent restenosis. Renal arteries < 3.5 mm in diameter had similar patency rates as renal arteries > 3.5 mm (P = 0.33). The 1-, 2-, and 5-year patency rates were 71%, 63%, and 38%, respectively. History of stroke was the only comorbidity to portend a significantly greater rate of restenosis (hazard ratio 3.77; 95%CI, 1.05-13.6; P = 0.04). Medications did not statistically alter the risk of restenosis. Revascularization of renal arteries with DES achieved similar primary patency rates irrespective of renal artery diameter. Stent configuration was not associated with time to renal replacement therapy or all-cause mortality. Level 3, Cohort Study.

Identifiants

pubmed: 31267151
doi: 10.1007/s00270-019-02264-z
pii: 10.1007/s00270-019-02264-z
pmc: PMC6679807
mid: NIHMS1533531
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1293-1301

Subventions

Organisme : NIH HHS
ID : DK107870
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK107870
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL098967
Pays : United States
Organisme : NIDDK NIH HHS
ID : R56 DK107870
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK107870
Pays : United States
Organisme : NIH HHS
ID : HL098967
Pays : United States

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Auteurs

Michael C Jundt (MC)

Department of Radiology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.
Division of Vascular and Interventional Radiology, Mayo Clinic, Rochester, USA.

Edwin A Takahashi (EA)

Department of Radiology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.
Division of Vascular and Interventional Radiology, Mayo Clinic, Rochester, USA.

William S Harmsen (WS)

Department of Clinical Statistics, Mayo Clinic, Rochester, MN, USA.

Sanjay Misra (S)

Department of Radiology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA. misra.sanjay@mayo.edu.
Division of Vascular and Interventional Radiology, Mayo Clinic, Rochester, USA. misra.sanjay@mayo.edu.

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