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ORIGINAL ARTICLE 
Prophylactic Antibiotics in Maxillofacial 
Fractures: A Requisite? 
S. Adalarasan, MDS, Alexander Mohan, MDS, MOMSRCPS(Glasgow), 
and Sanjay Pasupathy, MDS, DNB, MOMSRCPS(Glasgow) 
Abstract: The role of prophylactic antibiotics to prevent surgical 
wound infection (SWI) in the management of maxillofacial fractures 
is controversial. We carried out a retrospective study in 67 patients 
with 114 maxillofacial fractures, of which 9 patients each were in 
group 1 (no antibiotic) and group 3 (cefotaxime) and 49 in group 2 
(penicillin). We had an overall SWI rate of 16.66%, of which 3 of 
group 1 (33.33%), 12 of group 2 (24.48%), and 2 of group 3 (22.22%) 
constituted the SWIs. Statistical analysis showed no significant dif-ference 
between the infection rates. A strong positive correlation was 
found between infection rate and the delay in treatment, and a similar 
correlation was found in the use of catgut and SWI. Our study sug-gests 
that prophylactic antibiotic therapy may not alter the incidence 
of surgical wound infection. 
Key Words: Prophylactic antibiotics, maxillofacial fractures, 
penicillin, maxilla, mandible 
(J Craniofac Surg 2010;21: 1009Y1011) 
Management of facial fractures is an important component of 
the practice of maxillofacial surgery. With the advent of im-proved 
armamentarium, open reductionYinternal fixation has gained 
increased popularity. As with any other surgical procedure, infection 
is one of the major factors complicating the healing process. 
Antibiotics have been used not only in the management of 
postsurgical infections, but also prophylactically to prevent them. 
With the scare of antibiotic resistance, the use of antibiotics for pre-vention 
of infections needs to be reviewed. 
In this context, a retrospective study was carried out to evaluate 
the necessity of routine antibiotic administration for prevention of 
infections in the management of patients with maxillofacial fractures. 
MATERIALS AND METHODS 
Patients who visited the department of maxillofacial surgery 
in our institution for the management of maxillofacial fractures 
between April 2002 and February 2005 were included in the study. 
Patients, irrespective of sex, with maxillofacial fractures re-quiring 
surgical treatment and patients who were willing to give 
informed consent were included in the study. Patients with pre-existing 
infections at the site of fracture, medically compromised 
patients, patients allergic to penicillin and cephalosporin group of 
drugs, and patients with a history of antibiotic intake during the 
preceding 30 days were excluded. 
Patients were divided into 3 groups as follows: 
& group 1: Control group (no antibiotic group), 
& group 2: crystalline penicillin 2 million units intravenously 30 min 
before surgery, or 
& group 3: cefotaxime 2 g intravenously 30 minutes before surgery. 
A total of 67 patients who fulfilled the previously mentioned 
criteria were included in the study. Of these, 9 patients were in group 
1, 49 in group 2, and 9 in group 3. 
Surgical procedures were performed under general anesthe-sia. 
The surgical site was thoroughly prepared with povidone-iodine, 
and all universal aseptic measures were adhered to. Access to the 
surgical site was obtained intraorally, extraorally, or both, depending 
on the type and site of fracture. Open reductionYinternal fixation 
using miniplates was done in all the cases. The number of miniplates 
differed according to site of fracture and the adequacy of fixation. 
RESULTS 
The mean age in the study group was 33.4 years, ranging 
from 14 to 72 years. There were 62 males and 5 females in the study. 
A total of 38 patients had multiple fractures, whereas the remaining 
patients had fracture at a single site only, resulting in a total of 114 
fractures. The distribution of fractures and the postoperative infec-tion 
rates in the corresponding sites are shown in Figure 1. The eti-ology 
of the fractures and their distribution are shown in Figure 2. 
Of the 114 fractures, 19 developed surgical wound infection 
(SWI), resulting in an overall infection rate of 16.66%. The age-wise 
distribution of fractures and the corresponding infection rates are 
shown in Figure 3. 
Three patients of group 1 (33.33%), 14 of group 2 (24.48%), 
and 2 (22.22%) of group 3 were diagnosed with SWI. Although all 
the cases of SWI in groups 1 and 3 contained multiple fractures, only 
9 of 14 patients in group 2 had multiple fractures. Except for 2 pa-tients 
in group 2 inwhomboth the fractureswere infected, all the others 
had only a single fracture site infected. 
With the exception of one, all the other 18 infected patients 
had an average delay in treatment of 6 or more days (5Y15 days). The 
overall delay in treatment averages around 3.94 days (2Y15 days) for 
all the 67 cases. This delay in treatment could be attributed to delay 
in referral from other hospitals. Approximately 39% patients in-cluded 
in the study had a period of delay of more than 4 days. A 
positive correlation (r = 0.44) between the delay in treatment and 
infection was observed. 
Of the 67 patients, an extraoral incision was required in 16, 
intraoral incisions in 15, and a combined approach in 36 patients. Of 
the 16 patients requiring extraoral approach, 3 patients (18.75%) had 
SWI, whereas only 2 (13.33%) of the 15 patients needing intraoral 
From Sri Manakula Vinayagar Medical College and Hospital, Pondicherry, 
India. 
Received December 16, 2009. 
Accepted for publication January 24, 2010. 
Address correspondence and reprint requests to Sanjay Pasupathy, MDS, 
DNB, MOMSRCPS(Glasgow), No. 16, Cannon St, Priyadarshini Nagar, 
Gorimedu, Pondicherry, India 605006; E-mail: sanjaypasupathy@ 
yahoo.co.in 
The authors report no conflict of interest. 
Copyright * 2010 by Mutaz B. Habal, MD 
ISSN: 1049-2275 
DOI: 10.1097/SCS.0b013e3181e47d43 
The Journal of Craniofacial Surgery & Volume 21, Number 4, July 2010 1009 
Copyright ยฉ 2010 Mutaz B. Habal, MD. Unauthorized reproduction of this article is prohibited.
Adalarasan et al The Journal of Craniofacial Surgery & Volume 21, Number 4, July 2010 
incisions developed SWI. Twelve (33.33%) of 36 patients in whom 
acombined approach was required developed SWI. Of these 12, 
both incisions were infected in 2 patients (16.66%), whereas intraoral 
incisions alone were infected in 7 patients (58.33%), and extraoral 
incisions alone were infected in the remaining 3 patients (25%). 
In a majority of patients with SWI (10/19), the duration of 
surgery were more than 90 minutes, ranging from 50 to 200 minutes. 
Also, no correlation was found between number of miniplates and 
screws used and SWI. 
In 7 (41.18%) of 19 patients with SWI, catgut sutures 
were used for wound closure. There is a positive correlation (r = 1) 
between the use of catgut suture material and infection in the sur-gical 
site. 
In the management of SWI, 9 patients required deliberate 
opening of the incision by the surgeon to evacuate pus and were 
prescribed concomitant antibiotic therapy. Seven patients needed 
antibiotic therapy alone. Only one required readmission for incision 
and drainage. 
Statistical analysis was done with Pearson W2 test. The infection 
rates in all the 3 groups were found to be not statistically significant 
(the P values for groups 1, 2, and 3 were 0.71, 0.85, and 0.43, re-spectively), 
and also, intergroup evaluation did not reveal any statis-tical 
significance. 
DISCUSSION 
The use of antibiotics in the management of maxillofacial 
fractures is widespread with questionable rationale. Antibiotics have 
been used preoperatively to decrease the risk of SWI, but its role in 
preventing infection has not been evaluated properly. The main goals 
of antibiotic prophylaxis are to reduce incidence of SWI and to min-imize 
the adverse effect of antibiotics, especially the emergence of 
resistant microorganisms. 
In his landmark animal study that defined the scientific basis 
for prophylaxis, Burke1 clearly demonstrated that the use of post-operative 
antibiotics alone actually violates the basic tenets of pro-phylaxis, 
as there is no antibiotic either in the systemic circulation or 
at the site of surgery when the microorganisms invade the wound. 
This has been supported by other research articles in the litera-ture. 
2Y5 Hence, use of postoperative antibiotics in the name of pro-phylaxis 
seems to have no role in the prevention of SWI. 
The criteria to identify SWI have been under a lot of scrutiny 
in recent times. Many studies3,4,6,7 have included pain and swelling 
as criteria for diagnosing SWI. But these factors are commonly seen 
as sequelae of routine inflammatory reaction after any surgical 
trauma, and they need not be pure indicators of SWI. Hence, we did 
not include these factors in our study for assessing SWI. We in-cluded 
systemic increase in temperature and purulent discharge from 
wound as the main parameters to diagnose SWI. It is well docu-mented 
in literature4,8 that systemic increase in temperature is one of 
the reliable indicators of infection, especially on the third postop-erative 
day, and the presence of purulent discharge from the wound 
within the first month postoperatively will obviously confirm the 
presence of SWI.4,8 
There are multiple risk factors involved, independent of each 
other, which are predictive for subsequent SWI. These factors in-clude 
length of preoperative stay in hospital, compromised host 
defenses, surgical wound class, and duration of surgery. Garibaldi 
et al9 collected prospective epidemiological data, and their analysis 
of those data revealed that SWI was related to the length of preop-erative 
stay in hospital. A clinical practical evidence-based guide-lines 
by the Ministry of Health, Malaysia, suggest that preoperative 
stay of more than 3 days is associated with an increased risk of SWI. 
But in our institute, we had a standard protocol of admitting the 
patients just 1 day before surgery. 
Certain medical conditions such as poorly controlled diabe-tes, 
AIDS, and so on are said to result in decreased host defenses and 
a reduced resistance to infection and a high probability of devel-oping 
SWI. But there is no conclusive evidence for compromised 
host defenses and increased SWI in literature. Hence, in our study, to 
maintain the homogeneity of sample, we excluded patients with 
these conditions. 
As the overwhelming majority of surgical management of 
maxillofacial fractures falls into class 2 (clean contaminated) variety 
and all the cases in our study too were class 2 in nature, whether the 
routine use of prophylactic antibiotics will fulfill those goals is 
controversial. Garibaldi et al9 and Culver et al10 showed that post-operative 
wound infection rate was related to the class of surgery. 
They also stated that the infection rate associated with class 1 sur-gery 
may be sufficiently low as not towarrant the use of prophylactic 
antibiotics. The infection rate associated with class 2 surgery, 
however, may be high enough to warrant the use of prophylactic 
antibiotics. The infection rate in class 2 surgeries varies between 6% 
FIGURE 1. Distribution of fractures and the SWI. 
FIGURE 2. Etiology of fractures and their distribution. 
FIGURE 3. Age-wise distribution of fractures and the 
corresponding SWI rates. 
1010 * 2010 Mutaz B. Habal, MD 
Copyright ยฉ 2010 Mutaz B. Habal, MD. Unauthorized reproduction of this article is prohibited.
The Journal of Craniofacial Surgery & Volume 21, Number 4, July 2010 Prophylactic Antibiotics in Maxillofacial Fracture 
and 20% in literature. The SWI rate in our study was 16.66%, which 
falls well within the SWI range of class 2 surgeries. 
The use of preoperative antibiotics for management of max-illofacial 
fractures is well documented in literature.4,6,11,12 All these 
studies are having wide variance of infection rates, and this may be 
attributed to various factors such as patient selection, choice of an-tibiotics, 
and so forth. But in our study, the infection rates are much 
less (16.66%) compared with those previous studies. 
Surgical wound infections in maxillofacial trauma patients 
depend on various factors such as the type of fracture, delay in 
treatment, number of fractures, and treatment modality. The most 
important among these seem to be the type of fracture, whether it is 
compound, and the period of delay in treatment. 
In the literature, many studies have shown that compound 
fractures have more chance of infection than the others.7,13,14 In our 
study in group 1, 3 of 14 compound fractures were infected, leading 
to an infection rate of 21.42%, and in group 2, 14 of 78 compound 
fractures were infected, leading to an infection rate of 17.94%. As 
the infection rate in both groups is similar in compound fractures, it 
is suggested that antibiotics are not playing much of a role in the 
prevention of SWI in this kind of fractures. 
The maximum recommended delay in treatment of mandibular 
fractures and the type of treatment rendered have been the subject of 
attention of numerous studies.14,15 The literature shows that delayed 
treatment of fractures is associated with a greater rate of infection.14 
Although Champy et al16 recommended treatment within the first 
12 hours of trauma, in our setup this is not practically possible 
always because of various factors such as availability of operation 
theaters, cost factor associated with open reductions, and so on. The 
mean delay in treatment of fractures in our study is 4 days, and there is 
a positive correlation (r = +0.44) found between the delay and in-creased 
SWI. This could be attributed to the mobility of the frac-tured 
segments and concomitant development of infection. 
A strong positive correlation (r = +1) was also found between 
the use of catgut in multiple layer closures and SWI (7/17), leading 
to an infection rate of 41.18%, which is also documented in 
literature.17 
CONCLUSIONS 
Our study suggests that prophylactic antibiotic therapy may 
not alter the incidence of SWI. A multicenter, prospective, ran-domized 
controlled trial with large sample size is essential to eval-uate 
the advantage of prophylactic antibiotic therapy, if any, in the 
management of maxillofacial fractures. 
REFERENCES 
1. Burke JF. The effective period of preventive antibiotic action in 
experimental incisions and dermal lesions. Surgery 1961;50:161Y168 
2. Laskin DM. The use of prophylactic antibiotics for prevention of 
postoperative infections. Oral Maxillofac Surg Clin North Am 
2003;15:155Y160 
3. Miles BA, Porter JK, Ellis E. The efficacy of postoperative antibiotic 
regimens in the open treatment of mandibular fractures: a prospective 
randomized trial. J Oral Maxillofac Surg 2006;64:576Y582 
4. Abubaker O, Rollert MK. Post-operative antibiotic prophylaxis in 
mandibular fractures: a preliminary randomized, double blind, and 
placebo-controlled clinical study. J Oral Maxillofac Surg 2001;59: 
1415Y1419 
5. Peterson LJ. Principles of antibiotic therapy. In: Topazian RG, ed. 
Oral and Maxillofacial Infections. 3rd ed. Philadelphia, PA: WB 
Saunders Company, 1994:160Y197 
6. Heit JM, Stevens MR, Jeffords K. Comparison of ceftriaxone with 
penicillin for antibiotic prophylaxis for compound mandibular fractures. 
Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1996;83:423Y426 
7. Moreno JC, Fernandez A, Ortiz JA, et al. Complication rates associated 
with different treatments for mandibular fractures. J Oral Maxillofac 
Surg 2000;58:273Y280 
8. Larson EL, Pearson ML. Guideline for prevention of surgical site 
infection. Infect Control Hosp Epidemiol 1999;20:248Y264 
9. Garibaldi RA, et al. Risk factors for post-operative infections. Am J Med 
1991;91(suppl 3B):158Y163 
10. Culver DH, Horan TC, Gaynes RP, et al. National Nosocomial Infections 
Surveillance System: surgical wound infection rates by wound class 
operative procedure and patient risk index. Am J Med 1991;91 
(Suppl 3B):152Y157 
11. Chole RA, Yee J. Antibiotic prophylaxis for facial fractures. 
A prospective, randomized clinical trial. Arch Otolaryngol Head Neck 
Surg 1987;113:1055Y1057 
12. Zallen RD, Curry JT. A study of antibiotic usage in compound 
mandibular fractures J Oral Surg 1975;33:431Y434 
13. Edwards TJ, David DJ, Simpson DA, et al. The relationship between 
fracture severity and complication rate in miniplate osteosynthesis of 
mandibular fractures. Br J Plast Surg 1994;47:310Y311 
14. Maloney PL, Lincoln RE, Coyne CP. A protocol for management of 
compound mandibular fractures based on the time of injury to treatment. 
J Oral Maxillofac Surg 2001;60:133Y134 
15. Biller JA, Pletcher SD, Goldberg AN, et al. Complications and time to 
repair of mandibular fractures. Laryngoscope 2002;115:769Y772 
16. Champy, et al. Mandibular osteosynthesis by miniature screwed plates 
via buccal approach. J Oral Maxillofac Surg 1978;6:14 
17. Gabrielli F, Potenza C, Puddu P, et al. Suture materials and other factors 
associated with tissue reactivity, infection, and wound dehiscence 
among plastic surgery outpatients. Plast Reconstr Surg 2001;107:38Y45 
* 2010 Mutaz B. Habal, MD 1011 
Copyright ยฉ 2010 Mutaz B. Habal, MD. Unauthorized reproduction of this article is prohibited.

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Tashia Seeba - Antibiotics and maxillofacial fractures

  • 1. ORIGINAL ARTICLE Prophylactic Antibiotics in Maxillofacial Fractures: A Requisite? S. Adalarasan, MDS, Alexander Mohan, MDS, MOMSRCPS(Glasgow), and Sanjay Pasupathy, MDS, DNB, MOMSRCPS(Glasgow) Abstract: The role of prophylactic antibiotics to prevent surgical wound infection (SWI) in the management of maxillofacial fractures is controversial. We carried out a retrospective study in 67 patients with 114 maxillofacial fractures, of which 9 patients each were in group 1 (no antibiotic) and group 3 (cefotaxime) and 49 in group 2 (penicillin). We had an overall SWI rate of 16.66%, of which 3 of group 1 (33.33%), 12 of group 2 (24.48%), and 2 of group 3 (22.22%) constituted the SWIs. Statistical analysis showed no significant dif-ference between the infection rates. A strong positive correlation was found between infection rate and the delay in treatment, and a similar correlation was found in the use of catgut and SWI. Our study sug-gests that prophylactic antibiotic therapy may not alter the incidence of surgical wound infection. Key Words: Prophylactic antibiotics, maxillofacial fractures, penicillin, maxilla, mandible (J Craniofac Surg 2010;21: 1009Y1011) Management of facial fractures is an important component of the practice of maxillofacial surgery. With the advent of im-proved armamentarium, open reductionYinternal fixation has gained increased popularity. As with any other surgical procedure, infection is one of the major factors complicating the healing process. Antibiotics have been used not only in the management of postsurgical infections, but also prophylactically to prevent them. With the scare of antibiotic resistance, the use of antibiotics for pre-vention of infections needs to be reviewed. In this context, a retrospective study was carried out to evaluate the necessity of routine antibiotic administration for prevention of infections in the management of patients with maxillofacial fractures. MATERIALS AND METHODS Patients who visited the department of maxillofacial surgery in our institution for the management of maxillofacial fractures between April 2002 and February 2005 were included in the study. Patients, irrespective of sex, with maxillofacial fractures re-quiring surgical treatment and patients who were willing to give informed consent were included in the study. Patients with pre-existing infections at the site of fracture, medically compromised patients, patients allergic to penicillin and cephalosporin group of drugs, and patients with a history of antibiotic intake during the preceding 30 days were excluded. Patients were divided into 3 groups as follows: & group 1: Control group (no antibiotic group), & group 2: crystalline penicillin 2 million units intravenously 30 min before surgery, or & group 3: cefotaxime 2 g intravenously 30 minutes before surgery. A total of 67 patients who fulfilled the previously mentioned criteria were included in the study. Of these, 9 patients were in group 1, 49 in group 2, and 9 in group 3. Surgical procedures were performed under general anesthe-sia. The surgical site was thoroughly prepared with povidone-iodine, and all universal aseptic measures were adhered to. Access to the surgical site was obtained intraorally, extraorally, or both, depending on the type and site of fracture. Open reductionYinternal fixation using miniplates was done in all the cases. The number of miniplates differed according to site of fracture and the adequacy of fixation. RESULTS The mean age in the study group was 33.4 years, ranging from 14 to 72 years. There were 62 males and 5 females in the study. A total of 38 patients had multiple fractures, whereas the remaining patients had fracture at a single site only, resulting in a total of 114 fractures. The distribution of fractures and the postoperative infec-tion rates in the corresponding sites are shown in Figure 1. The eti-ology of the fractures and their distribution are shown in Figure 2. Of the 114 fractures, 19 developed surgical wound infection (SWI), resulting in an overall infection rate of 16.66%. The age-wise distribution of fractures and the corresponding infection rates are shown in Figure 3. Three patients of group 1 (33.33%), 14 of group 2 (24.48%), and 2 (22.22%) of group 3 were diagnosed with SWI. Although all the cases of SWI in groups 1 and 3 contained multiple fractures, only 9 of 14 patients in group 2 had multiple fractures. Except for 2 pa-tients in group 2 inwhomboth the fractureswere infected, all the others had only a single fracture site infected. With the exception of one, all the other 18 infected patients had an average delay in treatment of 6 or more days (5Y15 days). The overall delay in treatment averages around 3.94 days (2Y15 days) for all the 67 cases. This delay in treatment could be attributed to delay in referral from other hospitals. Approximately 39% patients in-cluded in the study had a period of delay of more than 4 days. A positive correlation (r = 0.44) between the delay in treatment and infection was observed. Of the 67 patients, an extraoral incision was required in 16, intraoral incisions in 15, and a combined approach in 36 patients. Of the 16 patients requiring extraoral approach, 3 patients (18.75%) had SWI, whereas only 2 (13.33%) of the 15 patients needing intraoral From Sri Manakula Vinayagar Medical College and Hospital, Pondicherry, India. Received December 16, 2009. Accepted for publication January 24, 2010. Address correspondence and reprint requests to Sanjay Pasupathy, MDS, DNB, MOMSRCPS(Glasgow), No. 16, Cannon St, Priyadarshini Nagar, Gorimedu, Pondicherry, India 605006; E-mail: sanjaypasupathy@ yahoo.co.in The authors report no conflict of interest. Copyright * 2010 by Mutaz B. Habal, MD ISSN: 1049-2275 DOI: 10.1097/SCS.0b013e3181e47d43 The Journal of Craniofacial Surgery & Volume 21, Number 4, July 2010 1009 Copyright ยฉ 2010 Mutaz B. Habal, MD. Unauthorized reproduction of this article is prohibited.
  • 2. Adalarasan et al The Journal of Craniofacial Surgery & Volume 21, Number 4, July 2010 incisions developed SWI. Twelve (33.33%) of 36 patients in whom acombined approach was required developed SWI. Of these 12, both incisions were infected in 2 patients (16.66%), whereas intraoral incisions alone were infected in 7 patients (58.33%), and extraoral incisions alone were infected in the remaining 3 patients (25%). In a majority of patients with SWI (10/19), the duration of surgery were more than 90 minutes, ranging from 50 to 200 minutes. Also, no correlation was found between number of miniplates and screws used and SWI. In 7 (41.18%) of 19 patients with SWI, catgut sutures were used for wound closure. There is a positive correlation (r = 1) between the use of catgut suture material and infection in the sur-gical site. In the management of SWI, 9 patients required deliberate opening of the incision by the surgeon to evacuate pus and were prescribed concomitant antibiotic therapy. Seven patients needed antibiotic therapy alone. Only one required readmission for incision and drainage. Statistical analysis was done with Pearson W2 test. The infection rates in all the 3 groups were found to be not statistically significant (the P values for groups 1, 2, and 3 were 0.71, 0.85, and 0.43, re-spectively), and also, intergroup evaluation did not reveal any statis-tical significance. DISCUSSION The use of antibiotics in the management of maxillofacial fractures is widespread with questionable rationale. Antibiotics have been used preoperatively to decrease the risk of SWI, but its role in preventing infection has not been evaluated properly. The main goals of antibiotic prophylaxis are to reduce incidence of SWI and to min-imize the adverse effect of antibiotics, especially the emergence of resistant microorganisms. In his landmark animal study that defined the scientific basis for prophylaxis, Burke1 clearly demonstrated that the use of post-operative antibiotics alone actually violates the basic tenets of pro-phylaxis, as there is no antibiotic either in the systemic circulation or at the site of surgery when the microorganisms invade the wound. This has been supported by other research articles in the litera-ture. 2Y5 Hence, use of postoperative antibiotics in the name of pro-phylaxis seems to have no role in the prevention of SWI. The criteria to identify SWI have been under a lot of scrutiny in recent times. Many studies3,4,6,7 have included pain and swelling as criteria for diagnosing SWI. But these factors are commonly seen as sequelae of routine inflammatory reaction after any surgical trauma, and they need not be pure indicators of SWI. Hence, we did not include these factors in our study for assessing SWI. We in-cluded systemic increase in temperature and purulent discharge from wound as the main parameters to diagnose SWI. It is well docu-mented in literature4,8 that systemic increase in temperature is one of the reliable indicators of infection, especially on the third postop-erative day, and the presence of purulent discharge from the wound within the first month postoperatively will obviously confirm the presence of SWI.4,8 There are multiple risk factors involved, independent of each other, which are predictive for subsequent SWI. These factors in-clude length of preoperative stay in hospital, compromised host defenses, surgical wound class, and duration of surgery. Garibaldi et al9 collected prospective epidemiological data, and their analysis of those data revealed that SWI was related to the length of preop-erative stay in hospital. A clinical practical evidence-based guide-lines by the Ministry of Health, Malaysia, suggest that preoperative stay of more than 3 days is associated with an increased risk of SWI. But in our institute, we had a standard protocol of admitting the patients just 1 day before surgery. Certain medical conditions such as poorly controlled diabe-tes, AIDS, and so on are said to result in decreased host defenses and a reduced resistance to infection and a high probability of devel-oping SWI. But there is no conclusive evidence for compromised host defenses and increased SWI in literature. Hence, in our study, to maintain the homogeneity of sample, we excluded patients with these conditions. As the overwhelming majority of surgical management of maxillofacial fractures falls into class 2 (clean contaminated) variety and all the cases in our study too were class 2 in nature, whether the routine use of prophylactic antibiotics will fulfill those goals is controversial. Garibaldi et al9 and Culver et al10 showed that post-operative wound infection rate was related to the class of surgery. They also stated that the infection rate associated with class 1 sur-gery may be sufficiently low as not towarrant the use of prophylactic antibiotics. The infection rate associated with class 2 surgery, however, may be high enough to warrant the use of prophylactic antibiotics. The infection rate in class 2 surgeries varies between 6% FIGURE 1. Distribution of fractures and the SWI. FIGURE 2. Etiology of fractures and their distribution. FIGURE 3. Age-wise distribution of fractures and the corresponding SWI rates. 1010 * 2010 Mutaz B. Habal, MD Copyright ยฉ 2010 Mutaz B. Habal, MD. Unauthorized reproduction of this article is prohibited.
  • 3. The Journal of Craniofacial Surgery & Volume 21, Number 4, July 2010 Prophylactic Antibiotics in Maxillofacial Fracture and 20% in literature. The SWI rate in our study was 16.66%, which falls well within the SWI range of class 2 surgeries. The use of preoperative antibiotics for management of max-illofacial fractures is well documented in literature.4,6,11,12 All these studies are having wide variance of infection rates, and this may be attributed to various factors such as patient selection, choice of an-tibiotics, and so forth. But in our study, the infection rates are much less (16.66%) compared with those previous studies. Surgical wound infections in maxillofacial trauma patients depend on various factors such as the type of fracture, delay in treatment, number of fractures, and treatment modality. The most important among these seem to be the type of fracture, whether it is compound, and the period of delay in treatment. In the literature, many studies have shown that compound fractures have more chance of infection than the others.7,13,14 In our study in group 1, 3 of 14 compound fractures were infected, leading to an infection rate of 21.42%, and in group 2, 14 of 78 compound fractures were infected, leading to an infection rate of 17.94%. As the infection rate in both groups is similar in compound fractures, it is suggested that antibiotics are not playing much of a role in the prevention of SWI in this kind of fractures. The maximum recommended delay in treatment of mandibular fractures and the type of treatment rendered have been the subject of attention of numerous studies.14,15 The literature shows that delayed treatment of fractures is associated with a greater rate of infection.14 Although Champy et al16 recommended treatment within the first 12 hours of trauma, in our setup this is not practically possible always because of various factors such as availability of operation theaters, cost factor associated with open reductions, and so on. The mean delay in treatment of fractures in our study is 4 days, and there is a positive correlation (r = +0.44) found between the delay and in-creased SWI. This could be attributed to the mobility of the frac-tured segments and concomitant development of infection. A strong positive correlation (r = +1) was also found between the use of catgut in multiple layer closures and SWI (7/17), leading to an infection rate of 41.18%, which is also documented in literature.17 CONCLUSIONS Our study suggests that prophylactic antibiotic therapy may not alter the incidence of SWI. A multicenter, prospective, ran-domized controlled trial with large sample size is essential to eval-uate the advantage of prophylactic antibiotic therapy, if any, in the management of maxillofacial fractures. REFERENCES 1. Burke JF. The effective period of preventive antibiotic action in experimental incisions and dermal lesions. Surgery 1961;50:161Y168 2. Laskin DM. The use of prophylactic antibiotics for prevention of postoperative infections. Oral Maxillofac Surg Clin North Am 2003;15:155Y160 3. Miles BA, Porter JK, Ellis E. The efficacy of postoperative antibiotic regimens in the open treatment of mandibular fractures: a prospective randomized trial. J Oral Maxillofac Surg 2006;64:576Y582 4. Abubaker O, Rollert MK. Post-operative antibiotic prophylaxis in mandibular fractures: a preliminary randomized, double blind, and placebo-controlled clinical study. J Oral Maxillofac Surg 2001;59: 1415Y1419 5. Peterson LJ. Principles of antibiotic therapy. In: Topazian RG, ed. Oral and Maxillofacial Infections. 3rd ed. Philadelphia, PA: WB Saunders Company, 1994:160Y197 6. Heit JM, Stevens MR, Jeffords K. Comparison of ceftriaxone with penicillin for antibiotic prophylaxis for compound mandibular fractures. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1996;83:423Y426 7. Moreno JC, Fernandez A, Ortiz JA, et al. Complication rates associated with different treatments for mandibular fractures. J Oral Maxillofac Surg 2000;58:273Y280 8. Larson EL, Pearson ML. Guideline for prevention of surgical site infection. Infect Control Hosp Epidemiol 1999;20:248Y264 9. Garibaldi RA, et al. Risk factors for post-operative infections. Am J Med 1991;91(suppl 3B):158Y163 10. Culver DH, Horan TC, Gaynes RP, et al. National Nosocomial Infections Surveillance System: surgical wound infection rates by wound class operative procedure and patient risk index. Am J Med 1991;91 (Suppl 3B):152Y157 11. Chole RA, Yee J. Antibiotic prophylaxis for facial fractures. A prospective, randomized clinical trial. Arch Otolaryngol Head Neck Surg 1987;113:1055Y1057 12. Zallen RD, Curry JT. A study of antibiotic usage in compound mandibular fractures J Oral Surg 1975;33:431Y434 13. Edwards TJ, David DJ, Simpson DA, et al. The relationship between fracture severity and complication rate in miniplate osteosynthesis of mandibular fractures. Br J Plast Surg 1994;47:310Y311 14. Maloney PL, Lincoln RE, Coyne CP. A protocol for management of compound mandibular fractures based on the time of injury to treatment. J Oral Maxillofac Surg 2001;60:133Y134 15. Biller JA, Pletcher SD, Goldberg AN, et al. Complications and time to repair of mandibular fractures. Laryngoscope 2002;115:769Y772 16. Champy, et al. Mandibular osteosynthesis by miniature screwed plates via buccal approach. J Oral Maxillofac Surg 1978;6:14 17. Gabrielli F, Potenza C, Puddu P, et al. Suture materials and other factors associated with tissue reactivity, infection, and wound dehiscence among plastic surgery outpatients. Plast Reconstr Surg 2001;107:38Y45 * 2010 Mutaz B. Habal, MD 1011 Copyright ยฉ 2010 Mutaz B. Habal, MD. Unauthorized reproduction of this article is prohibited.