Comparison Between 2 Types of Radiofrequency Ablation Systems in Arthroscopic Rotator Cuff Repair: A Randomized Controlled Trial.

ablation diathermy intra-articular temperature shoulder surgery

Journal

Orthopaedic journal of sports medicine
ISSN: 2325-9671
Titre abrégé: Orthop J Sports Med
Pays: United States
ID NLM: 101620522

Informations de publication

Date de publication:
Apr 2019
Historique:
entrez: 16 4 2019
pubmed: 16 4 2019
medline: 16 4 2019
Statut: epublish

Résumé

Radiofrequency ablation is commonly used in arthroscopic rotator cuff repair (RCR). New technology devices incorporating a plasma bubble may generate lower intra-articular temperatures and be more efficient. To compare a plasma ablation device with a standard ablation device in arthroscopic RCR to determine which system is superior in terms of intra-articular heat generation and diathermy efficiency. Randomized controlled trial; Level of evidence, 1. This was a single-center randomized controlled trial. The inclusion criteria were adult patients undergoing primary RCR. Patients were randomized preoperatively to the standard ablation group (n = 20) or plasma ablation group (n = 20). A thermometer was inserted into the shoulder joint during surgery, and the temperature, surgery, and diathermy times of radiofrequency ablation were measured continually. No significant differences were found between the standard ablation group and plasma ablation group for maximum temperature (38.20°C and 39.38°C, respectively; There was no difference between plasma ablation and standard ablation in terms of intra-articular temperature in the joint and diathermy efficiency. Transient high intra-articular temperatures occurred in both groups. ACTRN1261300056970 (Australian New Zealand Clinical Trials Registry).

Sections du résumé

BACKGROUND BACKGROUND
Radiofrequency ablation is commonly used in arthroscopic rotator cuff repair (RCR). New technology devices incorporating a plasma bubble may generate lower intra-articular temperatures and be more efficient.
PURPOSE OBJECTIVE
To compare a plasma ablation device with a standard ablation device in arthroscopic RCR to determine which system is superior in terms of intra-articular heat generation and diathermy efficiency.
STUDY DESIGN METHODS
Randomized controlled trial; Level of evidence, 1.
METHODS METHODS
This was a single-center randomized controlled trial. The inclusion criteria were adult patients undergoing primary RCR. Patients were randomized preoperatively to the standard ablation group (n = 20) or plasma ablation group (n = 20). A thermometer was inserted into the shoulder joint during surgery, and the temperature, surgery, and diathermy times of radiofrequency ablation were measured continually.
RESULTS RESULTS
No significant differences were found between the standard ablation group and plasma ablation group for maximum temperature (38.20°C and 39.38°C, respectively;
CONCLUSION CONCLUSIONS
There was no difference between plasma ablation and standard ablation in terms of intra-articular temperature in the joint and diathermy efficiency. Transient high intra-articular temperatures occurred in both groups.
REGISTRATION BACKGROUND
ACTRN1261300056970 (Australian New Zealand Clinical Trials Registry).

Identifiants

pubmed: 30984794
doi: 10.1177/2325967119835224
pii: 10.1177_2325967119835224
pmc: PMC6448122
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2325967119835224

Déclaration de conflit d'intérêts

The authors declared that there are no conflicts of interest in the authorship and publication of this contribution. 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.

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Auteurs

Ryan Faruque (R)

Orthopaedic Research Institute of Queensland, Pimlico, Queensland, Australia.

Brent Matthews (B)

Orthopaedic Research Institute of Queensland, Pimlico, Queensland, Australia.

Zaid Bahho (Z)

Orthopaedic Research Institute of Queensland, Pimlico, Queensland, Australia.

Kenji Doma (K)

Orthopaedic Research Institute of Queensland, Pimlico, Queensland, Australia.

Varaguna Manoharan (V)

Orthopaedic Research Institute of Queensland, Pimlico, Queensland, Australia.

Matthew Wilkinson (M)

Orthopaedic Research Institute of Queensland, Pimlico, Queensland, Australia.

Peter McEwen (P)

Orthopaedic Research Institute of Queensland, Pimlico, Queensland, Australia.

Classifications MeSH