Outcomes of Irradiated Polyglactin 910 Vicryl Rapide Fast-Absorbing Suture in Oral and Scalp Wound
(Résultats de la suture des plaies de la bouche et du cuir chevelu au moyen du fil irradié de polyglactine 910 à résorption rapide Vicryl Rapide)
Dimitri Aderriotis, DDS
George K.B. Sàndor, MD, DDS, FRCD(C), FRCS(C), FACS
Historique: Dans cette étude, on a évalué les résultats de la fermeture des plaies au moyen du fil irradié de polyglactine 910 (IRPG) Vicryl Rapide (Ethicon, Somerville, N.J.).
Méthode:Soixante et onze patients, qui présentaient 80 plaies de la bouche, et 42 patients, qui présentaient 42 plaies du cuir chevelu fermées au moyen du fil IRPG, ont été évalués le jour de la chirurgie, puis à intervalles de un, sept, 14, 28 et 90 jours. On a noté l'incidence d'inflammation, de suppuration et de cicatrisation hypertrophique, ainsi que le moment de la disparition spontanée de la suture. Ce matériel de suture a été comparé aux sutures de polytétrafluoroéthylène (PTFE) utilisées chez les patients qui reçoivent des implants dentaires, aux sutures classiques à l'acide polyglycolique (PGLA) utilisées chez les patients ayant subi une ostéotomie et aux agrafes chirurgicales utilisées chez les patients qui présentent des plaies du cuir chevelu.
Résultats: Dans le groupe des plaies intrabuccales, on a observé deux cas de suppuration sans réaction inflammatoire ou cicatrisation hypertrophique au moyen des sutures de fil IRPG, contrairement à trois cas de suppuration au moyen des sutures classiques à l'acide polyglycolique (PGLA). Dans le groupe des plaies du cuir chevelu, les sutures de fil IRPG n'ont produit aucune suppuration ou cicatrisation hypertrophique, et les agrafes chirurgicales ont provoqué une réaction inflammatoire. Les sutures de fil IRPG n'ont jamais dû être enlevées, alors qu'éventuellement il a fallu enlever toutes les agrafes et les sutures PGLA et de PTFE, une par une.
Conclusion:Le fil irradié de polyglactine 910 Vicryl Rapide constitue un matériel de suture utile à la fois dans les applications intra- et extra-buccales dans les populations d'enfants et d'adultes
Mots clés MeSH: inflammation; sutures; wound healing.
© J Can Dent Assoc 1999; 65:345-7
Absorbable sutures made from animal derivatives such as gut and chromic gut generally require no suture removal. As these materials break down, however, their by-products may result in wound inflammation.1 The polyglycolic, polylactic acid polymer-derived sutures (PGLA), such as Vicryl (Ethicon, Somerville, N.J.) and Dexon (Davis & Geck, Montreal, Que.), are absorbed via enzymatic degradation by hydrolysis, resulting in less inflammation.3-5 These sutures are well suited for deeper layer, non-surface closure. When used on the surface, however, they remain for at least four to six weeks, accumulating debris at the wound site and often necessitating manual removal.
Irradiated polyglactin 910 (IRPG) Vicryl Rapide (Ethicon, Somerville, N.J.) is a braided co-polymer of glycolic and lactic acid that is surface treated with polyglactin 370 and calcium stearate6 and has received gamma radiation. This radiation alters the suture material's molecular structure and enhances its absorption rate in vivo.6 Several reports on its use in pediatric,6-8 gynecological and general surgery4 have been published.
This paper reports on the use of IRPG Vicryl Rapide in oral and maxillofacial surgery, both in intraoral and extraoral wounds, and compares this suture material with other commonly used materials and skin closure techniques.
Seventy-one patients with 80 intraoral wounds closed with IRPG sutures were evaluated. The average patient age was 28.4 years. The patients were evaluated on the day of surgery, then one, seven, 14, 28 and 90 days following surgery. The 71 patients were divided into the following three groups: group 1 consisted of 28 consecutive patients with 34 wounds from elective orthognathic procedures; group 2 consisted of 20 consecutive patients who had stage I dental implant placements; and group 3 consisted of 23 consecutive patients treated for 26 traumatic intraoral lacerations. All patients received perioperative antibiotics , either penicillin G at 2,000,000 units intravenously every six hours, or Cefazolin 1 g intravenously every eight hours for 48 hours. All patients with intraoral wounds were treated with chlorhexidine 0.12% mouth rinse every 12 hours for four weeks.
The results of group 1 were compared with the results of a group of 18 consecutive patients (average age 28.7 years) having 24 wounds from elective orthognathic procedures closed with PGLA sutures. The results of group 2 were compared with the results of a group of 22 consecutive patients (average age 24.5 years) receiving dental implants and whose incisions were closed using PTFE Gore-Tex sutures (W.L. Gore & Associates, Flagstaff, Ariz.). In all patient groups, perioperative treatment regimens and follow-up schedules were the same as described above. In a separate portion of the study, 42 patients who had a bicoronal incision for treatment of either facial trauma (22 patients) or forehead lifts (20 patients) were evaluated on the day of surgery, then one, seven, 14, 28 and 90 days following surgery. The average patient age was 38.2 years and the average incision length was 12 cm. One half of the incision was closed using metal staples and the other half using IRPG as a continuing running surface suture. The sides of staple or suture closure were varied randomly. The entire length of each incision had deep, interrupted PGLA sutures. Vacuum suction drains were placed in all cases.
Of the 80 intraoral wounds closed with IRPG sutures, two developed suppuration of the incision line (incidence 2.5%). Both these wounds were successfully treated with a ten-day course of penicillin V at 600 mg taken orally every six hours. Both wounds were traumatic lacerations of the lower lip. There were no cases of hypertrophic scar formation and all sutures had fallen off spontaneously by day 14 (the patients were not aware of the exact disappearance date). In the PTFE patient group, there were no complications but in all cases the sutures had to be removed. All the patients whose wounds were closed with PGLA sutures for orthognathic procedures required some suture removal three to four weeks post-operatively.
There were three cases of suppuration in the PGLA group (incidence 12.5%). There were no cases of suppuration in the 34 wounds closed with IRPG (Table 1). Using the X2 test, this difference was found to be statistically significant (p < 0.05). In the bicoronal flap study, the following parameters were evaluated: inflammatory reaction, suppuration of wounds, hypertrophic scar formation and patient discomfort, which was evaluated using a visual analogue pain scale and overall patient preference. All patients expressed a preference for the IRPG material, complaining of more pain on the staple side, especially at night when lying in bed. Average pain scores were 6.7 for the staple side versus 1.8 for the IRPG side. Based on the paired t-test, the difference is statistically significant (p<0.05) (Table 2).
Table 1 Comparison of IRPG, PTFE and PGLA sutures in intraoral wounds
Table 2 Comparison of IRPG and staples in scalp wound closure
All staples had to be removed at day 14. All IRPG sutures had fallen out by day 12 in five patients, by day 13 in three patients, and were easily rubbed off on day 14 in 34 patients. All patients had been gently shampooing their hair as directed. There was one case of excessive inflammatory reaction noted on a wound closed with staples. There were no cases of suppuration, alopecia (hair loss) or hypertrophic scar formation in either patient group.
IRPG constitutes one more attempt to find an ideal suture material that is strong, handles easily, forms secure knots and causes minimal tissue reaction. Since its introduction in 1976, this suture has been used with satisfactory results in a variety of applications, including hand, plastic, gynecological, general and oral and maxillofacial surgery.
IRPG has gained particular favour among pediatric surgeons because of its fast absorption rate, which makes suture removal either unnecessary or very simple (sutures can be wiped off). Martelli and others8 showed the significant savings in time and money that can be realized by avoiding general anesthesia for very young patients needing suture removal. An added advantage of the IRPG sutures is the very mild inflammatory reaction of the surrounding tissues.6,7,9 Microscopically, the suture material is absorbed mainly through phagocytosis and disappears completely by day 35.6 The degree of inflammation is less than that observed with plain or chromic catgut sutures. IRPG is not recommended for facial skin closure; it can result in unfavourable scarring by remaining on the surface tissues longer than five days.8
The early disappearance of IRPG sutures, compared to PGLA sutures, is another advantage since many patients are irritated by the prolonged presence of intraoral sutures. The PGLA sutures can act as a potential breeding ground for bacteria, especially if sutures are braided, increasing the risk of infection. Finally, removing intraoral PGLA sutures, especially in young patients, can be a difficult and frustrating exercise. With IRPG, suture removal is unnecessary, an added advantage when one considers that many trauma patients are lost to follow-up.
After using the suture material extensively to close a variety of intraoral wounds (incisions for orthognathic surgery, implant placement and lacerations), the authors found this suture easy to handle, providing good knot security and causing minimal inflammatory reaction of the surrounding tissues. As with any new material, there is a learning curve involved with regard to its handling. IRPG is far more brittle than PGLA and will therefore snap if tugged on suddenly, frustrating the novice user. Its regular use, however, requires only a slight adjustment in suturing techniques.
In treating scalp wounds, the authors agree with Tandon and others9 that Vicryl Rapide is more visible among the hairs because of its white colour and that it has favourable handling characteristics. It is also preferred by patients because it causes negligible pain and minimal inflammatory reaction compared to staples.
From an economic point of view, Vicryl Rapide is at most 10% more expensive than similarly packaged cut or chromic sutures. PTFE sutures, on the other hand, are at least four times the cost of Vicryl Rapide.
RPG is a versatile and useful suture for oral and maxillofacial surgery. It can be used in a variety of applications, both intra- and extraorally, for pediatric as well as adult patients. The use of IRPG suture results in little wound inflammation. IRPG is absorbed over 12 to 14 days and does not require removal. It is also much more cost-effective than PTFE sutures and only slightly more expensive than catgut, chromic or PGLA sutures. Future evaluations, using clinical and economic parameters, will be necessary to compare IRPG with newer, absorbable, monofilament polymers such as the polydioxanones and caproclactones.
Dr. Aderriotis is a former senior resident in the department of oral and maxillofacial surgery, faculty of dentistry, University of Toronto. He now is engaged in a private practice in oral and maxillofacial surgery in Athens, Greece.
Dr. Sàndor is currently director of the graduate residency training program, oral and maxillofacial surgery, and an assistant professor at the faculty of dentistry, University of Toronto. He is also the coordinator of oral and maxillofacial surgery at the Hospital for Sick Children and the Bloorview MacMillan Centre in Toronto, Ont.
Reprint requests to: Dr. George K.B. Sàndor, Department of Dentistry, Hospital for Sick Children, S527-555 University Ave., Toronto, ON M5G 1X8. E-mail: email@example.com. Fax: (416) 813-6375.
While the authors received no funding from Ethicon Limited for this particular study, Dr. Sàndor has received funding from Ethicon Limited for his participation in another study involving Vicryl Rapide. The authors otherwise have no vested or commercial interest in Vicryl Rapide, Ethicon Limited, or its parent company, Johnson & Johnson Limited.
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