Factors influencing credentialing of interventionists in the CREST-2 trial.


Journal

Journal of vascular surgery
ISSN: 1097-6809
Titre abrégé: J Vasc Surg
Pays: United States
ID NLM: 8407742

Informations de publication

Date de publication:
03 2020
Historique:
received: 11 12 2018
accepted: 01 05 2019
pubmed: 30 7 2019
medline: 30 7 2020
entrez: 30 7 2019
Statut: ppublish

Résumé

The Carotid Revascularization and Medical Management for Asymptomatic Carotid Stenosis Trial (CREST-2) is a pair of randomized trials assessing the relative efficacy of carotid revascularization in the setting of intensive medical management (IMM) in patients with asymptomatic high-grade atherosclerotic stenosis. One of the trials assesses IMM with or without carotid artery stenting (CAS). Given the low risk of stroke in nonrevascularized patients receiving IMM, it is essential that there be low periprocedural risk of stroke for CAS if it is to show incremental benefit. Thus, credentialing of interventionists to ensure excellence is vital. This analysis describes the protocol-driven approach to credentialing of CAS interventionists for CREST-2 and its outcomes. To be eligible to perform stenting in CREST-2, interventionists needed to be credentialed on the basis of a detailed Interventional Management Committee (IMC) review of data from their last 25 consecutive cases during the past 24 months along with self-reported lifetime experience case numbers. When necessary, additional prospective cases performed in a companion registry were requested after webinar training. Here we review the IMC experience from the first formal meeting on March 21, 2014 through October 14, 2017. The IMC had 102 meetings, and 8311 cases submitted by 334 interventionists were evaluated. Most were either cardiologists or vascular surgeons, although no single specialty made up the majority of applicants. The median total experience was 130 cases (interquartile range [IQR], 75-266; range, 25-2500). Only 9% (30/334) of interventionists were approved at initial review; approval increased to 46% (153/334) after submission of new cases with added training and re-review. The median self-reported lifetime case experience for those approved was 211.5 (IQR, 100-350), and the median number of cases submitted for review was 30 (IQR, 27-35). The number of CAS procedures performed per month (case rate) was the only factor associated with approval during the initial cycle of review (P < .00001). Identification of interventionists who were deemed sufficiently skilled for CREST-2 has required substantial oversight and a controlled system to judge current skill level that controls for specialty-based practice variability, procedural experience, and periprocedural outcomes. High-volume interventionists, particularly those with more recent experience, were more likely to be approved to participate in CREST-2. Primary approval was not affected by operator specialty.

Sections du résumé

BACKGROUND
The Carotid Revascularization and Medical Management for Asymptomatic Carotid Stenosis Trial (CREST-2) is a pair of randomized trials assessing the relative efficacy of carotid revascularization in the setting of intensive medical management (IMM) in patients with asymptomatic high-grade atherosclerotic stenosis. One of the trials assesses IMM with or without carotid artery stenting (CAS). Given the low risk of stroke in nonrevascularized patients receiving IMM, it is essential that there be low periprocedural risk of stroke for CAS if it is to show incremental benefit. Thus, credentialing of interventionists to ensure excellence is vital. This analysis describes the protocol-driven approach to credentialing of CAS interventionists for CREST-2 and its outcomes.
METHODS
To be eligible to perform stenting in CREST-2, interventionists needed to be credentialed on the basis of a detailed Interventional Management Committee (IMC) review of data from their last 25 consecutive cases during the past 24 months along with self-reported lifetime experience case numbers. When necessary, additional prospective cases performed in a companion registry were requested after webinar training. Here we review the IMC experience from the first formal meeting on March 21, 2014 through October 14, 2017.
RESULTS
The IMC had 102 meetings, and 8311 cases submitted by 334 interventionists were evaluated. Most were either cardiologists or vascular surgeons, although no single specialty made up the majority of applicants. The median total experience was 130 cases (interquartile range [IQR], 75-266; range, 25-2500). Only 9% (30/334) of interventionists were approved at initial review; approval increased to 46% (153/334) after submission of new cases with added training and re-review. The median self-reported lifetime case experience for those approved was 211.5 (IQR, 100-350), and the median number of cases submitted for review was 30 (IQR, 27-35). The number of CAS procedures performed per month (case rate) was the only factor associated with approval during the initial cycle of review (P < .00001).
CONCLUSIONS
Identification of interventionists who were deemed sufficiently skilled for CREST-2 has required substantial oversight and a controlled system to judge current skill level that controls for specialty-based practice variability, procedural experience, and periprocedural outcomes. High-volume interventionists, particularly those with more recent experience, were more likely to be approved to participate in CREST-2. Primary approval was not affected by operator specialty.

Identifiants

pubmed: 31353274
pii: S0741-5214(19)31449-1
doi: 10.1016/j.jvs.2019.05.035
pmc: PMC6980974
mid: NIHMS1063445
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT02089217']

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

854-861

Subventions

Organisme : NINDS NIH HHS
ID : U01 NS080165
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS080168
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS086872
Pays : United States

Informations de copyright

Copyright © 2019. Published by Elsevier Inc.

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Auteurs

Brajesh K Lal (BK)

Department of Surgery, University of Maryland, Baltimore, Md. Electronic address: blal@som.umaryland.edu.

James F Meschia (JF)

Department of Neurology, Mayo Clinic, Jacksonville, Fla.

Gary S Roubin (GS)

Department of Cardiology, Cardiovascular Associates of the Southeast/Brookwood, Baptist Medical Center, Birmingham, Ala.

Brian Jankowitz (B)

Department of Neurosurgery, UPMC Presbyterian University Hospital, Pittsburgh, Pa.

Donald Heck (D)

Department of Radiology, Novant Health Clinical Research, Winston-Salem, NC.

Tudor Jovin (T)

Department of Neurology, UPMC Presbyterian University Hospital, Pittsburgh, Pa.

Christopher J White (CJ)

Department of Cardiology, Ochsner Health System, New Orleans, La.

Kenneth Rosenfield (K)

Department of Cardiology, Massachusetts General Hospital, Boston, Mass.

Barry Katzen (B)

Department of Interventional Radiology, Miami Cardiac and Vascular Institute at Baptist Hospital of Miami, Miami, Fla.

Guilherme Dabus (G)

Department of Interventional Neuroradiology, Miami Cardiac and Vascular Institute at Baptist Hospital of Miami, Miami, Fla.

William Gray (W)

Department of Cardiology, Lankenau Medical Center, Wynnewood, Pa.

Jon Matsumura (J)

Department of Surgery, University of Wisconsin Hospital and Clinics, Madison, Wisc.

L Nelson Hopkins (LN)

Department of Neurosurgery, SUNY Buffalo, Buffalo, NY.

Sothear Luke (S)

Department of Neurology, Mayo Clinic, Jacksonville, Fla.

Jashank Sharma (J)

Department of Surgery, University of Maryland, Baltimore, Md.

Jenifer H Voeks (JH)

Department of Neurology, Medical University of South Carolina, Charleston, SC.

George Howard (G)

Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Ala.

Thomas G Brott (TG)

Department of Neurology, Mayo Clinic, Jacksonville, Fla.

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