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Published on: November 6, 2019
Coblation versus BiZact extra-capsular tonsillectomy in adults: a randomized control trial
Jack Tierney1, Ella Harrison1, John-Charles Hodge2
1Division of Surgery, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
This study compared Coblation and BiZact tonsillectomy devices, finding Coblation offered less pain on day 1, while BiZact showed reduced pain later. Both are safe, but Coblation may be better for same-day surgery.
Area of Science:
- Otolaryngology
- Surgical Innovation
- Pain Management
Background:
- Tonsillectomy is common but causes significant postoperative pain and bleeding.
- Coblation and BiZact devices are alternatives for tonsillectomy, with prior claims of favorable pain outcomes.
- Direct comparative studies are needed to evaluate their efficacy in reducing pain and bleeding.
Purpose of the Study:
- To directly compare the postoperative pain and bleeding outcomes of Coblation and BiZact tonsillectomy techniques.
- To evaluate secondary outcomes including surgical duration, intra-operative bleeding, and return to normal activities.
- To determine the optimal device for adult tonsillectomy regarding patient comfort and surgical safety.
Main Methods:
- A single-blinded, randomized controlled trial involving 61 patients undergoing tonsillectomy.
- Patients were randomized to either the BiZact or Coblation device group.
- Postoperative pain was assessed using a Visual Analogue Scale for 14 days, with secondary outcomes including bleeding and recovery time.
Main Results:
- Coblation demonstrated significantly lower pain on postoperative day 1 (P < 0.05).
- BiZact showed significantly reduced pain on postoperative days 7 and 11 (P < 0.05).
- BiZact was associated with longer hemostasis time (P < 0.001) and greater intraoperative blood loss (P < 0.01), with a trend towards more secondary bleeding.
Conclusions:
- Both Coblation and BiZact are safe and effective for adult tonsillectomy.
- Coblation's advantage in early postoperative pain may make it more suitable for day-case procedures.
- Further research is needed to confirm the trend in secondary bleeding rates for the BiZact device.
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