Arthroscopic Bankart Repair With Remplissage in Anterior Shoulder Instability Results in Fewer Redislocations Than Bankart Repair Alone at Medium-term Follow-up of a Randomized Controlled Trial.

Bankart repair anterior shoulder instability arthroscopy medium-term remplissage

Journal

The American journal of sports medicine
ISSN: 1552-3365
Titre abrégé: Am J Sports Med
Pays: United States
ID NLM: 7609541

Informations de publication

Date de publication:
14 Jun 2024
Historique:
medline: 14 6 2024
pubmed: 14 6 2024
entrez: 14 6 2024
Statut: aheadofprint

Résumé

A multicenter, double-blinded randomized controlled trial comparing isolated Bankart repair (NO REMP) to Bankart repair with remplissage (REMP) reported benefits of remplissage in reducing recurrent instability at 2 years postoperative. The ongoing benefits beyond this time point are yet to be explored. To (1) compare medium-term (3 to 9 years) outcomes of these previously randomized patients undergoing isolated Bankart repair (NO REMP) or Bankart repair with remplissage (REMP) to manage recurrent anterior glenohumeral instability; (2) examine the failure rate, overall recurrent instability, and reoperation rate. Randomized controlled trial; Level of evidence, 1. Recruitment and randomization for the original randomized trial occurred between 2011 and 2017. Patients ≥14 years diagnosed with recurrent traumatic anterior shoulder instability with an engaging Hill-Sachs defect of any size were included. Those with a glenoid defect >15% were excluded. In 2020, participants were contacted by telephone and asked standardized questions regarding ensuing instances of subluxation, dislocation, or reoperation on their study shoulder. "Failure" was defined as a redislocation, and "overall recurrent instability" was described as a redislocation or ≥2 subluxations. Descriptive statistics, relative risk, and Kaplan-Meier survival curve analyses were performed. A total of 108 participants were randomized, of whom 50 in the NO REMP group and 52 in the REMP group were included in the analyses in the original study. The mean number of months from surgery to the final follow-up was 49.3 and 53.8 months for the NO REMP and REMP groups, respectively. Failure rates were 22% (11/50) in the NO REMP group versus 8% (4/52) in the REMP group. Rates of overall recurrent instability were 30% (15/50) in the NO REMP group versus 10% (5/52) in the REMP group. Survival curves were significantly different, favoring REMP in both scenarios. For the treatment of traumatic recurrent anterior shoulder instability with a Hill-Sachs lesion and subcritical glenoid bone loss (<15%), a significantly lower rate of overall postoperative recurrent instability was observed with arthroscopic Bankart repair and remplissage than with isolated Bankart repair at a medium-term follow-up (mean of 4 years). Patients who did not receive a remplissage experienced a failure (redislocated) earlier and had a higher rate of revision/reoperation than those who received a concomitant remplissage. NCT01324531 (ClinicalTrials.gov identifier).

Sections du résumé

BACKGROUND UNASSIGNED
A multicenter, double-blinded randomized controlled trial comparing isolated Bankart repair (NO REMP) to Bankart repair with remplissage (REMP) reported benefits of remplissage in reducing recurrent instability at 2 years postoperative. The ongoing benefits beyond this time point are yet to be explored.
PURPOSE UNASSIGNED
To (1) compare medium-term (3 to 9 years) outcomes of these previously randomized patients undergoing isolated Bankart repair (NO REMP) or Bankart repair with remplissage (REMP) to manage recurrent anterior glenohumeral instability; (2) examine the failure rate, overall recurrent instability, and reoperation rate.
STUDY DESIGN UNASSIGNED
Randomized controlled trial; Level of evidence, 1.
METHODS UNASSIGNED
Recruitment and randomization for the original randomized trial occurred between 2011 and 2017. Patients ≥14 years diagnosed with recurrent traumatic anterior shoulder instability with an engaging Hill-Sachs defect of any size were included. Those with a glenoid defect >15% were excluded. In 2020, participants were contacted by telephone and asked standardized questions regarding ensuing instances of subluxation, dislocation, or reoperation on their study shoulder. "Failure" was defined as a redislocation, and "overall recurrent instability" was described as a redislocation or ≥2 subluxations. Descriptive statistics, relative risk, and Kaplan-Meier survival curve analyses were performed.
RESULTS UNASSIGNED
A total of 108 participants were randomized, of whom 50 in the NO REMP group and 52 in the REMP group were included in the analyses in the original study. The mean number of months from surgery to the final follow-up was 49.3 and 53.8 months for the NO REMP and REMP groups, respectively. Failure rates were 22% (11/50) in the NO REMP group versus 8% (4/52) in the REMP group. Rates of overall recurrent instability were 30% (15/50) in the NO REMP group versus 10% (5/52) in the REMP group. Survival curves were significantly different, favoring REMP in both scenarios.
CONCLUSION UNASSIGNED
For the treatment of traumatic recurrent anterior shoulder instability with a Hill-Sachs lesion and subcritical glenoid bone loss (<15%), a significantly lower rate of overall postoperative recurrent instability was observed with arthroscopic Bankart repair and remplissage than with isolated Bankart repair at a medium-term follow-up (mean of 4 years). Patients who did not receive a remplissage experienced a failure (redislocated) earlier and had a higher rate of revision/reoperation than those who received a concomitant remplissage.
REGISTRATION UNASSIGNED
NCT01324531 (ClinicalTrials.gov identifier).

Identifiants

pubmed: 38874505
doi: 10.1177/03635465241254063
doi:

Banques de données

ClinicalTrials.gov
['NCT01324531']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3635465241254063

Déclaration de conflit d'intérêts

One or more of the authors has declared the following potential conflict of interest or source of funding: The Pan Am Clinic Foundation is supported by Conmed, Arthrex, Ossur, Smith & Nephew, Stryker, and Zimmer Biomet. J.M.W. has received consulting fees from Smither & Nephew and Stryker. P.B.M. has received consulting fees from Conmed and Arthrex. AOSSM checks author disclosures against the Open Payments Database (OPD). AOSSM has not conducted an independent investigation on the OPD and disclaims any liability or responsibility relating thereto.

Auteurs

Jarret M Woodmass (JM)

Orthopaedic Surgery, Pan Am Clinic, Winnipeg, Manitoba, Canada.
Department of Surgery, Section of Orthopaedics, University of Manitoba, Winnipeg, Manitoba, Canada.

Sheila McRae (S)

Department of Surgery, Section of Orthopaedics, University of Manitoba, Winnipeg, Manitoba, Canada.
Pan Am Clinic Foundation, Winnipeg, Manitoba, Canada.

Peter Lapner (P)

The Ottawa Hospital, Ottawa, Ottawa, Canada.

Ivan Kamikovski (I)

Orthopaedic Surgery, Pan Am Clinic, Winnipeg, Manitoba, Canada.

Benjamin Jong (B)

Orthopaedic Surgery, Pan Am Clinic, Winnipeg, Manitoba, Canada.

Jason Old (J)

Orthopaedic Surgery, Pan Am Clinic, Winnipeg, Manitoba, Canada.
Department of Surgery, Section of Orthopaedics, University of Manitoba, Winnipeg, Manitoba, Canada.

Jonathan Marsh (J)

Orthopaedic Surgery, Pan Am Clinic, Winnipeg, Manitoba, Canada.
Department of Surgery, Section of Orthopaedics, University of Manitoba, Winnipeg, Manitoba, Canada.

Jamie Dubberley (J)

Orthopaedic Surgery, Pan Am Clinic, Winnipeg, Manitoba, Canada.
Department of Surgery, Section of Orthopaedics, University of Manitoba, Winnipeg, Manitoba, Canada.

Greg Stranges (G)

Orthopaedic Surgery, Pan Am Clinic, Winnipeg, Manitoba, Canada.
Department of Surgery, Section of Orthopaedics, University of Manitoba, Winnipeg, Manitoba, Canada.

Treny M Sasyniuk (TM)

Pan Am Clinic Foundation, Winnipeg, Manitoba, Canada.

Peter B MacDonald (PB)

Orthopaedic Surgery, Pan Am Clinic, Winnipeg, Manitoba, Canada.
Department of Surgery, Section of Orthopaedics, University of Manitoba, Winnipeg, Manitoba, Canada.

Classifications MeSH