MAXILLOFACIAL FRACTURES AT THE TIME OF HARDWARE REMOVAL: AETIOLOGY, SURGICAL THERAPY, IDENTIFICATION OF POSTOPERATIVE INFECTIONS, AND ANTIBIOTIC PATTERN OF ISOLATES

Lutf Mohammed Al-Rahbi1,2image, Hend Naji Al-Sabri2image, Ahmed Abdulah Al-Ashwal1,2image,

Hassan Abdulwahab Al-Shamahy3,4image

1Department of Oral and Maxillo-Facial Surgery, Faculty of Dentistry, Sana’a University, Republic of Yemen.

2Yemen Medical Specialist Council, Ministry of Health and population, Yemen.

3Department of Basic Sciences, Faculty of Dentistry, Sana’a University, Republic of Yemen.

4Medical Microbiology and Clinical Immunology Department, Faculty of Medicine and Health Sciences, Sana’a University.

 

Abstract

Background and Aims: A mandibular fracture, or jaw fracture, typically occurs at two sites in about 60% of cases, potentially limiting mouth opening and causing gum bleeding and misalignment of teeth. This study aimed to identify the bacterial causes of postoperative infections, the aetiology of fractures, surgical treatment, and the antibiotic resistance profile of bacteria from patients with maxillofacial fractures at the Military Hospital in Sana'a, Yemen.

Materials and Methods: The Department of Oral and Maxillofacial Surgery at the Military Hospital in Sana'a, Yemen, treated thirty patients with maxillofacial fractures from January to December 2024. They used fracture fixation hardware and conducted follow-ups six months post-surgery. The study assessed the incidence of postoperative bacterial infections at surgical sites after hardware removal, employing standard microbiological techniques for isolate identification and the Kirby-Bauer method for antibiotic susceptibility testing, alongside collecting clinical and demographic data from participants.

Results: Most fractures were open compound fractures (56.7%), all of which were mandibular fractures. For 60% of patients, open reduction internal fixation (ORIF) was the most frequently used surgical procedure. Staphylococcus aureus accounted for 27 (90%) of all isolates from surgical sites, with Klebsiella pneumoniae coming in second at 30%. Three instances (10%) had no bacterial growth. Amoxicillin, augmentin, aztreonam, cefotaxime, cefoxitin, ceftazidime, piperacillin, ceftriaxone, and doxycycline did not work at all against isolates of S. aureus

Conclusion: According to the survey, individuals aged 20 to 24 represented 56.7% of cases, primarily due to gunshot wounds. The bacterium S. aureus, noted for its significant multidrug resistance, was the most commonly isolated pathogen. Vancomycin emerged as the most effective treatment for Staphylococcus aureus infections.

Keywords: Antibiotic pattern, bacterial causes, hardware removalmandibular fracture, maxillofacial fractures, postoperative infections. 

 

 

INTRODUCTION

 

Maxillofacial injuries account for between 7.4% and 8.7% of emergency medical care, making them one of the most frequent life-threatening crises in both industrialised and developing nations1. These injuries can outcome in serious, cosmetic, long-term functional, and psychological concerns since they impact the facial region's soft tissues as well as skeletal structures2. The maxillofacial region is the most vulnerable to fractures because of its prominent placement. The pattern and location of these fractures depend on the type of injury and the direction of trauma3. While maxillofacial skeleton fractures by themselves are rarely lethal, concurrent damage to other organs may complicate matters. Other significant diseases include neurological, orthopaedic, and ophthalmological damage frequently accompanies maxillofacial fractures4. Because these injuries are so close to important organs like the brain and cervical vertebrae, they are frequently linked to significant morbidity. 

However, they can also result in loss of function, impairment, and even death5. The epidemiology and aetiologies of facial fractures diverge with demographic in terms of severity and cause6. Falls were the most frequently reported cause of craniofacial fractures in younger individuals, while RTA and assault have been found to be the main causes in adults. Understanding maxillofacial trauma makes it easier to assess how people behave in different countries and helps create effective injury management and prevention techniques. 

Infections from surgical wounds can be deep (muscle and tissue), external (skin), or extend to the organ or site of the procedure. Regardless of whether the bacteria were previously on the patient's skin or oral mucous membrane or whether they were transferred to the patient from the hospital setting or from contact with infected people, surgical wound infections are commonly found and can develop within the first 30 days after surgery7-9. Recent research indicates that postoperative infections can occur years after surgery, and these infection rates go unreported for a number of reasons, such as not meeting national records requirements, missing patient follow-up, having difficulty accessing a prior surgical history, seeing a different surgeon, and more10-12. The CDC has divided SSIs into three categories: superficial infections, deep wound infections, and infections affecting organs or bodily compartments. The likelihood of an SSI is influenced by the level of contamination at the surgical site during the surgery. Wounds are categorised as clean, contaminated, unclean, or infected depending on the degree and frequency of contamination13. SSI epidemiology study presents challenges due to the heterogeneous nature of this surgical infection. The frequency varies significantly amongst surgeons, patients, institutions, and procedures14. The SSI can be changed by both foreign and internal bacteria. The majority of surgical site infections are caused by endogenous germs on the patient's skin at the time of the incision. Skin infections are more frequently caused by gram-positive bacteria like S. aureus. Microorganisms in the patient's body that are exposed during surgery are more likely to be the source of SSIs. 

Pathogens differ depending on the surgical site; gastrointestinal tract surgery, for instance, raises the risk of SSI from Gram-negative gut bacteria15. The research literature recognises several related variables given the risk factors for SSI, but the studies are not repeatable. Despite this, a number of papers have frequently identified advanced age, male sex, and considerable blood loss as risk factors for SSI16-19. Postoperative, procedure-related (peri-operative), and patient-related (preoperative) are common categories for additional risk factors for SSI19. Surgical site infection (SSI) risk factors associated with patients can generally be categorised as either changeable or non-modifiable. Poor diabetes control, immunosuppressive drug use, obesity, tobacco use, and length of preoperative hospital stay are patient-related variable risk factors. Wound type, surgical site haircut, hypoxia, length of surgery, and hypothermia are risk factors associated with the procedure. Risk factors that can be changed or not, such age and gender, have been taken into consideration20. Despite earlier research on bacterial profiles, antibiotic sensitivity, and risk factors for UTI in postoperative patients at specialist hospitals in Sana'a, Yemen21, as well as one study on general SSI, there is no information regarding SSI in craniofacial surgery in Yemen. Thus, the purpose of this investigation was to ascertain the frequency, distribution, and antibiotic susceptibility profiles of bacterial pathogens isolated from SSI linked to maxillofacial surgery postoperative wounds in a subset of hospitals in Sana'a City, Yemen.

 

 

MATERIALS AND METHODS

 

A comparative, serial clinical follow-up investigation was carried out. Patients who presented with trauma in the maxillofacial surgery department of the Military hospital between January 1, 2024, and December 31, 2024 (time for clinical works for the MD degree), were included in this study. Details were provided regarding age, sex, socioeconomic status, primary complaint, history of present illness, history of prior medical conditions, duration of injury, aetiology, and related injuries. In order to make a diagnosis, every patient in this study had a thorough clinical examination and radiological interpretation after data collection.

Data collection methods 

An experienced MD student examined patients physically to determine whether a local infection was present based on one or more of the following criteria: pain, tenderness, local swelling, redness, warmth or purulent discharge, evidence of an abscess, or fever higher than 38°C in deep incisions. 

Specimen Collection

Patients who came in for a medical evaluation had wound swabs or aspirates taken aseptically from their surgery sites. This was carried out before applying an antiseptic solution to the wound. After that, specimens were transferred to the National Centre for Public Health Laboratories' Bacteriology Department for bacteriological examination in 5 ml Stewart transport media.

Bacterial isolation and identification

Samples were tested using established bacteriological procedures for swabs and aspirates22. The conventional streak plate method was used to inoculate the samples onto blood agar, Mannitol salt agar, and MacConkey agar (Oxoid). The plates were incubated for 24 to 48 hours at 37°C in an anaerobic environment.

Bacterial growth on medium was verified by colony morphology, pigment production, blood haemolysis (beta, alpha, and gamma haemolysis), biochemical tests (lactose, mannitol, glucose, and sucrose fermentation), and motility property testing. Bacteria growing on both blood agar and mannitol salt agar are considered Gram-positive because mannitol salt agar is a selective medium for Staphylococcus. A catalase test was then performed to distinguish Streptococcus from staphylococci; if the test produced negative results, streptococcal species were ruled out. Additionally, to differentiate S. aureus from other Staphylococcus species that test negative for coagulase, a coagulase enzyme test was performed. Microorganisms grown on MacConkey agar and blood agar are assumed to be Gram-negative bacteria since they are a selective medium for such germs. The lactose fermentation characteristics of the colonies on MacConkey agar were identified. Colonies that were colourless were lactose non-fermenters, whilst colonies that were pink were lactose fermenters. Gram-negative bacteria were further investigated for motility and characterisation using a range of biochemical assays, including indole, urea, Triple Sugar Iron agar (TSI), Simmon's Citrate agar, and Lysine Decarboxylase (LDC). Oxidase was employed to assess colonies that produced colour on blood agar and non-lactose fermenter on MacConkey agar in order to verify that P. aeruginosa is an oxidase-positive bacteria. Gram-negative bacteria were also tested for motility and discrimination using a range of biochemical techniques, including triglyceride iron agar (TSI), indole, urea, Simmon's Citrate agar, and Lysine Decarboxylase (LDC).

Antimicrobial susceptibility testing 

The isolates' patterns of antibiotic susceptibility were investigated using the Kirby-Bauer diffusion technique on Mueller-Hilton agar (Oxoid). Four to five identically shaped bacterial colonies were suspended in five millilitres of nutritional broth. Following that, the turbidity of the solution was reduced to 0.5 McFarland, resulting in a colony count of around 107 or 108 colony-forming units per millilitre. A sterile swab was placed immediately in the centre of the Mueller-Hilton agar plate and then evenly dispersed to create confluent growth after being inserted into the solution and pushed against the tube's walls to remove any surplus. To test for streptococci susceptibility, 5% defibrinated sterile blood was aseptically added to Mueller-Hilton agar22.

After the contaminated plates had dried for three to five minutes, the appropriate anti-microbial susceptibility discs were aseptically placed and gently pushed against the medium for complete surface contact using sterile forceps. To avoid the region of inhibition overlapping, the discs were spaced around 24 mm apart and 15 mm apart from the plate's edge. The plates were incubated aerobically at 37°C for 18 to 24 hours in incubator23. The diameter of each antibiotic's zone of inhibition was measured to the nearest millimetre using a digital calliper (Market lab, UK). According to Cheesbrough22 and the Clinical Laboratory Standard Institute standards of 201523, the width of the inhibition zone of the tested bacteria surrounding the disc was measured to the closest millimetre and then categorised as sensitive and resistant. Amikacin (30 μg), clarithromycin (30 μg), amoxicillin-clavulanic acid (30 μg), ampicillin (10 μg), penicillin (30 μg), erythromycin (15 μg), ceftriaxone (30 μg), cefixime (30 μg), ceftazidime (30 μg), cefotaxime (30 μg), gentamicin (10 μg), ciprofloxacin (5 μg), norfloxacin (25 μg), and imipenem (30 μg).

Data analysis 

Epi Info version 6 (CDC, Atlanta, USA) was used to analyse the data. While the categorical variables were summarised using frequencies and proportions and displayed as tables, the continuous variable (age) was summarised using mean and standard deviation.

Ethical consideration 

The Medical Ethics and Research Committee of the Military Hospital granted ethical permission for this project (No. 12 dated December 1, 2023). Every process complied with the review committee's ethical standards. Consent was also obtained from each participant, who was told that participation was entirely optional and that they might decline at any time for any reason.

 

RESULTS 

 

The age distribution of maxillofacial fracture patients receiving device treatment at the Military Hospital is displayed in Table 1. The patient’s age ranged from 20 to 57 years, with a mean ± standard deviation of 29.9 ± 12.4 years. There was not a single instance of a female patient; all were male. The prevalence and aetiology of maxillofacial and face fractures are given in Table 2. Gunshot wounds accounted for 50% of all cases, with road accidents coming in second at 20%, bomb blasts at 16.7%, and pathological fractures at 13.3%.No cases of falls from height were recorded. There were 43.3% of closed simple fractures and 56.7% of open complicated fractures. 

The locations of our patients' maxillofacial fractures fractures were mandibular. Reconstructive plate counting accounted for 60% of the surgeries, miniplate counting for 30%, and titanium mesh for just three (10%). The clinical assessment of fracture patients is displayed in Table 3. 33.3% of cases had pain at the fracture site, 36.7% had fever, 3.3% had chills, 43.3% had night sweats, 46.7% had skin erythema, 70% had purulent discharge, 20% had discomfort at the fracture site, and 10% had movement at the fracture site.  The most prevalent surgical procedure was open reduction internal fixation (ORIF) alone in 60% of patients, followed by open reduction internal fixation with intermaxillary fixation (IMF) in 40%, and open reduction internal fixation with bone grafting in 0% of cases. The most common bacteria isolated from the surgical site was S. aureus, accounting for 27 (90%) of the total isolates, followed by K. pneumoniae at 30%, while 3 cases (10%) showed no bacterial growth.The antimicrobial susceptibility pattern of the isolated S. aureus (n=27) is displayed in Table 4.  The S. aureus isolates were totally resistant to amoxicillin, augmentin, aztreonam, cefotaxime, cefoxitin, ceftazidime, piperacillin, ceftriaxone, and doxycycline. With a 100% sensitivity rate, vancomycin was the most effective drug against S. aureus. The next greatest sensitivity rate was 88.9% for teicoplanin, followed by 55.5% for tobramycin, 66.7% for gentamicin, and 55.5% for co-trimoxazole. S. aureus's sensitivity to several antibiotics ranged from 22.2% to 59.3%. Table 5 shows the antibiotic susceptibility pattern of the nine identified K. pneumoniae.

The K. pneumoniae isolates were completely resistant to amoxicillin, augmentin, cefotaxime, cefoxitin, ceftazidime, ceftriaxone, co-trimoxazole, and gentamicin. Amikacin and ciprofloxacin sensitivity rates for K. pneumoniae are 33.3%. 

 

DISCUSSION

 

The prevalence of maxillofacial injuries has increased in both urban and rural regions, and both industrialized and developing nations have seen a shift in this trend24. While interpersonal violence has been found to be the main cause of maxillofacial injuries in wealthy countries 25, RTA has been found to be the main cause in developing countries26. It is claimed that epidemiological evaluations are more specifically required for the implementation of prevention measures and the effectiveness of therapy. This is greater than the ratio of 4.6:1 observed in Bulgaria27, in China28, in Jordan, 3:129, and 2.1:1 in an Austrian study30. Furthermore, this ratio was higher than that found in a number of Saudi studies; in Jeddah, it was 4.4:1 in one study and 4.8:131 in another32. An 8:1 ratio was noted by Shanker et al.33, and Motamedi et al.34.

Cultural factors could be the cause of this discrepancy. On the other hand, compared to the Indian report, this ratio was smaller. The ratio was estimated to be 6:1 in Jeddah35 and 10:1 in Abha City32 in the southern region of Saudi Arabia. In the current study, gunshot wounds were the most common cause, accounting for 50% of all cases. Next in line were pathological fractures (13.3%), bomb blasts (16.7%) and traffic accidents (20%). No incidents of falls from a height were reported. The current study discovered that road traffic accidents were the second major cause of maxillofacial fractures, in contrast to previous findings in other studies  by Brasileiro and Passeri36; Mijiti et al.28, Motamedi et al.34, and Saudi Arabia by Nwoku and Oluyadi37, Abdullah et al.38, Al-Masri32 where the main cause was traffic accidents. Gunshots are seen as a serious public health concern in Yemen because to the ongoing conflict and the rising number of gun owners there.

The main cause of traffic accidents in Yemen was shown to be driver mistake, mostly as a result of underage driving. Since alcohol and drugs are illegal in Yemen, they are not frequently the cause of traffic accidents. Human mistake and vehicle technical failures were the main causes of traffic accidents, which made for 20% of all road accident causes in the current study. Therefore, stringent enforcement of the legislation and national public awareness campaigns are necessary to reduce road accidents in Yemen.

The locations of maxillofacial fractures in patients who visited Military Hospital were determined in the current study; all of the fractures were mandibular. Our study's findings regarding the prevalence of mandibular fractures are comparable to those from other regions of the world27,28,36, various Middle Eastern nations34, and Saudi Arabia32,38. These results, however, are at odds with those from Australia39, Germany40, and Saudi Arabia37, where the majority of patients had orbital fractures, midfacial fractures with orbital floor injuries, and midfacial fractures were significantly more common than mandibular fractures, respectively. The difference in the affected bone may be related to the different causes reported in different studies in which gunshot was the most cause in the current study.In line with the results of Haug et al.6, the most frequently reported broken part of the maxillofacial bones in this study was the mandibular body fractures. The symphysis was the second most prevalent location for mandibular fractures after mandibular body fractures, according to another study by Mijiti et al.28. Condylar fractures and symphysis fractures were the most frequent locations of mandibular fractures, according to one study by Brasileiro and Passeri36, while symphysis–parasymphysis fractures and condylar fractures were the most frequent locations, according to a study by Motamedi et al.34. This difference in the most affected location may be caused by the mechanism and direction of the impact at the time of the accident.

The majority of patients in the current study (60%) had open reduction internal fixation (ORIF). This is comparable to the findings of a study conducted in China by Meghettiet al.28, which found that 62.4% of afflicted patients received ORIF treatment, and a study conducted in India7, which found that 62.2% of patients received this treatment. 48% of the 1024 patients in Brazil that Brasileiro and Passeri36 retrospectively examined received conservative treatment, whereas the remaining 48% received surgical treatment, mostly by ORIF. On the other hand, in a number of other investigations by Bataine29 and Bakardjiev and Pichalova27, closed reduction was the most frequently used treatment approach.

S. aureus was found to be the most frequently isolated species (90%) in this investigation. The findings are higher than those of studies conducted in Ethiopia, where the percentages of S. aureus were 33.3%16 and 26.2%18. In Uganda, K. pneumonia was the most prevalent isolate, with a 50% rate41. This disparity in the distribution of bacterial species may be due to differences in prevalent hospital-acquired illnesses as well as policies and recommendations for infection prevention and management among countries and wound sites.

Amoxicillin, augmentin, aztreonam, cefotaxime, cefoxitin, ceftazidime, piperacillin, ceftriaxone, and doxycycline were all completely ineffective against the S. aureus isolates used in this study. Vancomycin was the most efficient antibiotic against S. aureus, with a 100% sensitivity rate. The next greatest sensitivity rates were 88.9% for teicoplanin, 55.5% for tobramycin, 66.7% for gentamicin, and 55.5% for co-trimoxazole. According to a study that was previously published in Yemen by Alhadi et al.42, Al-Makdad et al.21, and Ethiopia by Gelaw et al.43, these antibiotics were found to be reasonably efficient in treating SSIs caused by S. aureus. Conversely, the Al Shami et al. investigation found that these medications were less effective44. It is possible that the increase in antibiotic resistance brought on by the irrational use of anti-infective medications, insufficient controls to prevent the spread of infections, variations in common hospital-acquired pathogens, and the acquisition of organisms resistant to antibiotics are linked to both the duration of exposure to these microorganisms and the presence of risk factors.

Furthermore, the current study demonstrated that amoxicillin, augmentin, cefotaxime, cefoxitin, ceftazidime, ceftriaxone, co-trimoxazole, and gentamicin had no effect at all on the K. pneumoniae isolates. The sensitivity rates of K. pneumoniae to amikacin and ciprofloxacin are 33.3%. These results are almost completely different from those previously reported in Yemen21,45-49, where the sensitivity rates for the aforementioned studies were given. The current study shows that the polyclonal antibiotics amoxicillin, augmentin, cefotaxime, cefoxitin, ceftazidime, ceftriaxone, co-trimoxazole, and gentamicin are all 100% ineffective against Gram-negative bacteria, particularly K. pneumoniae. Compared to previous research conducted in Yemen, this resistance rate was higher45-49. This might be because the development and spread of resistance are mostly caused by the experimental treatment of isolates, the haphazard and frequent use of these antibiotics by inexperienced practitioners, and the absence of antibiotic usage standards21,44,50. 

Limitations of the study

The small sample size and short-term follow-up were the study's primary limitations.

 

CONCLUSION

 

According to the survey, people between the ages of 18 and 24 accounted for the majority of instances (56.7%). The most frequent cause was gunshot wounds. S. aureus, which has a very high prevalence of multidrug resistance, was the most frequently isolated bacterium. The most effective medication for treating S. aureus infections was discovered to be vancomycin.

 

ACKNOWLEDGEMENTS

 

The authors would like to acknowledge all researchers whose work contributed to the evidence summarized in this work.

 

AUTHOR’S CONTRIBUTIONS

 

Al-Sabri HN: formal analysis, conceptualization, data organization, and clinical and laboratory examinations to obtain a board’s degree in Oral and Maxillofacial Surgery. Al-Rahbi LM:  conceptualization, data organization, supervision. Al-Ashwal AA: conceptua-lization, data organization, supervision. Al-Shamahy HA: critical review. Final manuscript was checked and approved by both authors.       

 

DATA AVAILABILITY

 

The empirical data used to support the study's conclusions are available upon request from the corresponding author.

 

CONFLICT OF INTEREST 

 

Regarding this project, there are no conflicts of interest.

 

REFERENCES

 

  1. Mackenzie EJ. Epidemiology of injuries: current trends and future challenges. Epidemiol Rev 2000;22(1):112–119.https://doi.org/10.1093/oxfordjournals.epirev.a018006   
  1. Hull A, Lowe T, Devlin M, et al. Psychological consequences of maxillofacial trauma: A preliminary study. Br J Oral Maxillofac Surg 2003;41(5):317–322. https://doi.org/10.1016/s0266-4356(03)00131-1
  2. Kamath RD, Bharani S, Hammannavar R, et al. Maxillofacial trauma in central Karnataka, India: An outcome of 95 cases in a regional trauma care centre. Craniomaxillofacial Trauma Reconstruction 2012;5(4): 197–204. https://doi.org/10.1055/s-0032-1322536
  3. Van Hout WMMT, Van Cann EM, Abbink JH, et al. An epidemiological study of maxillofacial fractures requiring surgical treatment at a tertiary trauma centre between 2005 and 2010. Br J Oral Maxillofac Surg 2013;51(5):416–420. https://doi.org/10.1016/j.bjoms.2012.11.002
  4. Gali R, Devireddy SK, Kumar RVK, et al. Faciomaxillary fractures in a semi-urban South Indian teaching hospital: A retrospective analysis of 638 cases. Contemp Clin Dent 2015;6(4):539–543.https://doi.org/10.4103/0976- 237X.169847
  1. Haug RH, Prather J, Indresano AT. Fractures and concomitant lnjjury. J Oral Maxillofac Surg 1990;48(4):926–932.https://doi.org/10.1016/0278-2391(90)90004-l 
  1. Bali R, Sharma P, Garg A, et al. A comprehensive study on maxillofacial trauma conducted in Yamunanagar, India. J Injury Violence Res 2013;5(2):108–116.https://doi.org/10.5249/jivr.v5i2.331  
  1. Maliska MCDS, Lima Junior SM, Gil JN. Analysis of 185 maxillofacial fractures in the state of Santa Catarina, Brazil. Braz Oral Res 2009;23(3):268–274.https://doi.org/10.1590/s1806-83242009000300008  
  1. Alhlale MF, Humaid A, Saleh AH, Alsweedi KS, Edrees WH. Effect of most common antibiotics against bacteria isolated from surgical wounds in Aden Governorate hospitals, Yemen. Universal J Pharm Res 2020; 5(1): 21-24. https://doi.org/10.22270/ujpr.v5i1.358
  2. Agarwal A, Kelkar A, Agarwal AG, Jayaswal D, Schultz C, Jayaswal A, et al. implant retention or removal for management of surgical site infection after spinal surgery. Global Spine J 2020; 10 (5): 640–646.https://doi.org/10.1177/2192568219869330
  1. The Hardest Decision Any Spine Surgeon Has to Make | Orthopedics This Week. www.ryortho.com. Retrieved 2022-05- 24.
  2. World Health Organization (WHO). Global guidelines for the prevention of surgical site infection; 2016. https:// pubmed.ncbi.nlm.nih.gov/28139389/. Accessed May 14, 2025.
  3. Centers for Disease Control and Prevention (CDC). Procedure- associated module: Surgical Site Infection (SSI) event. Atlanta, GA: Centers for disease control and prevention; 2017
  4. Berrios-Torres SI, Umscheid CA, Bratzler DW, et al. Centers for disease control and prevention guideline for the prevention of surgical site infection. JAMA Surg 2017; 152(8):784–791. https://doi.org/10.1001/jamasurg.2017.0904
  5. Naderi HR, Ebrahim ZM. Evaluation of postoperative infections in patients undergoing abdominal surgery: A systematic review. Patient Saf Qual Improv 2015; 3(4):300– 303.
  6. Asres GS, Legese MH, Woldearegay GM. Prevalence of multidrug resistant bacteria in postoperative wound infections at Tikur Anbessa Specialized Hospital, Addis Ababa, Ethiopia. Arch Med 2017;9(4):12.
  7. Moghadamyeghaneh Z, Hwang GS, Hanna MH. Risk factors for prolonged ileus following colon surgery. Surg Endosc 2016; 30:603–609.https://doi.org/10.1007/s00464-015-4247-1  
  1. Mulu W, Kibru G, Beyene G, Damtie H. Associated risk factors for postoperative nosocomial infections among patients admitted at Felege Hiwot Referral Hospital, Bahir Dar, Northwest Ethiopia. Clin Med Res 2013; 2(6):140–147. https://doi.org/10.11648/j.cmr.20130206.15
  2. Zahran WA, Zein-Eldeen AA, Hamam SS, et al. Surgical site infections: Problem of multidrug-resistant bacteria. Menoufia Med J 2017; 30(4):1005–1013.https://doi.org/0.4103/mmj.mmj_119_17  
  1. Anderson DJ, Moehring RW, Sloane R, et al. Bloodstream infections in community hospitals in the 21st century: A Multicenter Cohort Study. PLoS One 2014; 9:e91713. https://doi.org/10.1371/journal.pone.0091713
  2. Al Makdad ASM, Al-Haifi AY, Salah MK, Al-Shamahy HA, Al-Falahi TH. Urinary tract infections in post operative patients: Prevalence rate, bacterial profile, antibiotic sensitivity and specific risk factors. Universal J Pharm Res 2020; 5(3):21-26.https://doi.org/10.22270/ujpr.v5i3.329
  1. Cheesbrough M. District Laboratory Practice in Tropical Countries. 2nd New York 106. Cambridge, UK: Cambridge University Press; 2006.
  2. Clinical and Laboratory Standard Institute. Performance Standards for Antimicrobial Disk Susceptibility Tests. 25th ed. CLSI document M100-S25. Wayne, United State; 2015.
  3. Al-Khateeb T, Abdullah FM. Craniomaxillofacial injuries in the United Arab Emirates: a retrospective study. J Oral Maxillofac Surg 2007;65(6):1094–1101.https://doi.org/10.1016/j.joms.2006.09.013  
  1. Telfer MR, Jones GM, Shepherd JP. Trends in the etiology of maxillofacial fractures in the United Kingdom (1977-1987). Br J Oral Maxillofac Surg 1991;29(4):250–255. https://doi.org/10.1016/0266-4356(91)90192-8   
  2. Cheema SA, Amin F. Incidence and causes of maxillofacial skeletal injuries at the Mayo Hospital in Lahore, Pakistan. Br J Oral Maxillofac Surg 2006;44(3):232–234. https://doi.org/10.1016/j.bjoms.2005.05.017
  3. Bakardjiev A, Pechalova P. Maxillofacial fractures in Southern Bulgaria - A retrospective study of 1706 cases. J Cranio-Maxillofac Surg 2007;35(3):147–150.https://doi.org/10.1016/j.jcms.2007.01.005  
  1. Mijiti A, Ling W, Tuerdi M, et al. Epidemiological analysis of maxillofacial fractures treated at a University hospital, Xinjiang, China: A 5-year retrospective study. J Cranio-Maxillofac Surg 2014;42(3): 227–233.https://doi.org/10.1016/j.jcms.2013.05.005  
  1. Bataineh AB. Etiology and incidence of maxillofacial fractures in the north of Jordan. Oral Surg Oral Med Oral Pathol, Oral Radiol Endodontol 1998;86(1):31–35.https://doi.org/10.1016/s1079-2104(98)90146-9   
  1. Gassner R, Tuli T, Hächl O, et al. Cranio-maxillofacial trauma: a 10-year review of 9543 cases with 21 067 injuries. J Cranio Maxillofac Surg 2003;31(1):51–61. https://doi.org/10.1016/s1010-5182(02)00168-3
  2. Rabi AG, Khateery SM. Maxillofacial trauma in Al-Madinah region of Saudi Arabia: A 5-year retrospective study. Asian J Oral Maxillofac Surg 2002;14(1):10–14.
  3. Al-Masri M. Severity and causality of maxillofacial trauma in the Southern region of Saudi Arabia. Saudi Dent J 2013;25(3):107–110.https://doi.org/10.1016/j.sdentj.2013.04.001  
  1. Shankar VN, Hegde N, Prasad R. The pattern of the maxillofacial fractures: A multicenter retrospective study. J Craniomaxillofac Surg 2014;40(4):675–679.
  2. Motamedi MHK, Dadgar E, Ebrahimi A, et al. Pattern of maxillofacial fractures: A 5-year analysis of 8,818 patients. J Trauma Acute Care Surg 2014;77(4):630–634. https://doi.org/10.1097/TA.0000000000000369
  3. Jan AM, Alsehaimy M, Al-Sebaei M, et al. A retrospective study of the epidemiology of maxillofacial trauma in Jeddah, Saudi Arabia. J Am Sci 2015;11(1):57–61.
  4. Brasileiro BF, Passeri LA. Epidemiological analysis of maxillofacial fractures in Brazil: A 5-year prospective study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2006;102(1):28–34.https://doi.org/10.1016/j.tripleo.2005.07.023   
  1. Nwoku AL, Oluyadi BA. Retrospective analysis of 1206 maxillofacial fractures in an Urban Saudi Hospital: 8 year review. Pakistan Oral Dent J 2004;24(1):13–16.
  1. Abdullah WA, Al-Mutairi K, Al-Ali Y, et al. Patterns and etiology of maxillofacial fractures in Riyadh City, Saudi Arabia. Saudi Dent J 2013;25(1):33–38.https://doi.org/1016/j.sdentj.2012.10.004  
  1. Cabalag MS, Wasiak J, Andre NE, et al. Epidemiology and management of maxillofacial fractures in an Australian trauma center. J Plastic, Reconstruc Aesthet Surg 2014;67(2):183–189.https://doi.org/10.1016/j.bjps.2013.10.022   
  1. Schneider D, Kammerer PW, Schon G, et al. Etiology and injury patterns of maxillofacial fractures from the years 2010 to 2013 in Mecklenburg-Western Pomerania, Germany: A retrospective study of 409 patients. J Cranio-Maxillofac Surg 2015;43(10):1948–1951.
  2. Lubega A, Joel B, Justina Lucy N. Incidence and etiology of surgical site infections among emergency postoperative patients in mbarara regional referral hospital, South Western Uganda. Surg Res Pract 2017; 2017:1–6.https://doi.org/10.1155/2017/6365172
  1. Alhadi YAA, Al-Kibsi TAM, Al-Shamahy HA, Aldeen YAAS. Surgical site Infections: Prevalence, associated factors and antimicrobial susceptibility patterns of the bacterial isolates among postoperative patients in Sana’a, Yemen. Universal J Pharm Res 2022; 7(3):32-39.https://doi.org/10.22270/ujpr.v7i3.777
  1. Gelaw A, Gebre-Selassie S, Tiruneh M, Mathios E, Yifru S. Isolation of bacterial pathogens from patients with postoperative surgical site infections and possible sources of infections at the University of Gondar Hospital, Northwest Ethiopia. J Environ Occup Health 2014; 3(2):103-108.
  2. Al-Shami HZ, Al-Haimi MA, Al-Shamahy HA, et al. Patterns of antimicrobial resistance among major bacterial pathogens isolated from clinical samples in two tertiary’s hospitals, in Sana'a, Yemen. Universal J Pharm Res 2021; 6(5):60-67. https://doi.org/10.22270/ujpr.v6i5.674
  3. Abbas AM, Al-Kibsi TAM, Al-Shamahy HA, et al. Characterization and antibiotic sensitivity of bacteria in orofacial abscesses of odontogenic origin. Universal J Pharm Res 2020; 5(6):36-42.https://doi.org/10.22270/ujpr.v5i6.510  
  1. Al-Akwa AA, Zabara A, Al-Shamahy HA. Prevalence of Staphylococcus aureus in dental infections and the occurrence of MRSA in isolates. Universal J Pharm Res 2020; 5( 2):1-6. https://doi.org/10.22270/ujpr.v5i2.384
  2. Shogaa Al-Deen SH, Al-Ankoshy AAM, Al-Najhi MMA, Al-Shamahy HA, et al. Porphyromonasgingivalis: Biofilm formation, antimicrobial susceptibility of isolates from cases of Localized Aggressive Periodontitis (LAP). Universal J Pharm Res 2021; 6 (4): 1-6.https://doi.org/10.22270/ujpr.v6i4.633  
  1. Al-Eryani SA, Alshamahi EYA, Al-Shamahy HA, Alfalahi GHA, Al-Rafiq AA. Bacterial conjunctivitis of adults: causes and ophthalmic antibiotic resistance patterns for the common bacterial isolates. Universal J Pharm Res 2021; 6: (1). https://doi.org/10.22270/ujpr.v6i1.535
  2. AL-Haddad KA, Ali Al-Najhi MM, Al-Akwa AAY, et al. Antimicrobial susceptibility of Aggregati-bacter-actinomycetemcomitans isolated from Localized Aggressive Periodontitis (LAP) cases. J Dent Ora Heal Ad Re 2007; 103.https://doi.org/10.1111/j.1600-0463.2007.apm_630.x
  1. Ishak AA, Alhadi AM, Al-Moyed KAA, Al-Shamahy HA. Childhood urinary tract infection: Clinical signs, bacterial causes and antibiotic susceptibility. Universal J Pharm Res 2021; 6(4). https://doi.org/10.22270/ujpr.v6i4.643