Issue: July 2016
July 25, 2016
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Absorbable sutures associated with reduced Achilles tendon repair complications

Patients regained Achilles tendon function regardless of whether their tendon tears were treated with absorbable or nonabsorbable sutures.

Issue: July 2016
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BARCELONA — Use of absorbable sutures limited the incidence of most surgical complications in Achilles tendon repair compared with nonabsorbable sutures. However, functional outcomes were not significantly different for the two treatments, according to results presented here.

Perspective from Paul Ackermann, MD, PhD

“We can conclude the repair with absorbable sutures could be used for Achilles tendon ruptures with relatively low complication rates,” Baris Kocaoglu, MD, of Acibadem University School of Medicine, said at the European Society of Sports Traumatology, Knee Surgery and Arthroscopy Congress.

The purpose of the study was to compare the functional and clinical results of Achilles tendon repairs with an Achilles tendon suture-guiding device using nonabsorbable and absorbable sutures at a minimum follow-up.

Baris Kocaoglu, MD
Baris Kocaoglu

Comparable functional results

“We hypothesized that braided absorbable polyglactin suture, which we called Vicryl, has comparable functional results with braided nonabsorbable polyethylene terephthalate suture, which we called Ethibond,” Kocaoglu said.

Kocaoglu and colleagues randomly assigned 48 patients (mean age 38 years) with Achilles tendon ruptures to undergo treatment with either Ethibond nonabsorbable braided polyethylene terephthalate sutures (Ethicon) or Vicryl absorbable braided polyglactin suture (Ethicon). Surgeons used the Achillon Achilles tendon suture-guiding system (Integra LifeSciences).

The researchers assessed patients according to the criteria established by the clinical American Orthopaedic Foot and Ankle Society (AOFAS) rating score. They clinically evaluated all patients after surgery after 15 days, 30 days, 45 days and 90 days, and then at the end of 1 year.

Return to work

The time from injury to operation was similar in both groups at 2 days. Primary outcome measures used included the number of major surgical complications, such as infections, Achilles tendon re-ruptures and open wounds based on suture retraction.

Results showed all patients regained Achilles tendon function postoperative and returned to their previous work. The AOFAS hind foot clinical outcome scores were 98 in the nonabsorbable suture group (range 90 to 100) and 96.8 in the absorbable suture group (range 87 to 100). However, compared with the nonabsorbable group, there were fewer postoperative complications in the absorbable suture group (16% vs. 4%), Kocaoglu noted. This difference was statistically significant.

“When we look at our results, we see there is no difference between the AOFAS clinical outcome scores, but we can see some differences in terms of complications,” Kocaoglu said. “Absorbable suture group had fewer postoperative complications than nonabsorbable group.” – by Casey Tingle

Disclosure: Kocaoglu reports no relevant financial disclosures.