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National Journal of Maxillofacial Surgery
 
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ORIGINAL ARTICLE
Year : 2014  |  Volume : 5  |  Issue : 2  |  Page : 161-165  

Evaluation of microbial flora in orofacial space infections of odontogenic origin


Department of Oral and Maxillofacial Surgery, Bharati Vidyapeeth Dental College and Hospital, Pune, Maharashtra, India

Date of Web Publication10-Apr-2015

Correspondence Address:
Amod Patankar
Shree 35/1, Padmadarshan Housing Society, Survey No.62/B, Pune-Satara Road, Parvati, Pune - 411 009, Maharashtra
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0975-5950.154820

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   Abstract 

Background: The microbiology of acute dental infections has been in the midst of many researches. Various bacteriological studies show variations in their conclusion. The purpose of our study was to evaluate the microbial flora in orofacial space infections of odontogenic origin, which is essential for appropriate antibiotic selection. Materials and Methods: Thirty-five patients with odontogenic infection causing fascial space involvement were included. Aspirated specimen was transported in nutrient broth and thyoglycollate media within an hour for further culture and sensitivity testing. Result and Conclusion: This study indicates that orofacial odontogenic infections are usually polymicrobial, consisting of a complex mixture of both anaerobes and aerobes.

Keywords: Acute dental infection, odontogenic infection, microbial flora fascial space infection, orofacial infection


How to cite this article:
Patankar A, Dugal A, Kshirsagar R, Hariram, Singh V, Mishra A. Evaluation of microbial flora in orofacial space infections of odontogenic origin. Natl J Maxillofac Surg 2014;5:161-5

How to cite this URL:
Patankar A, Dugal A, Kshirsagar R, Hariram, Singh V, Mishra A. Evaluation of microbial flora in orofacial space infections of odontogenic origin. Natl J Maxillofac Surg [serial online] 2014 [cited 2021 May 9];5:161-5. Available from: https://www.njms.in/text.asp?2014/5/2/161/154820


   Introduction Top


Infections in the orofacial region are commonly known to be of dental origin. Odontogenic infections range from simple periapical abscesses to severe infections involving superficial and deep fascial spaces in the neck often leading to septicemia.

The microbiology of acute dental infections has been in the midst of many researches. [1],[2] Various bacteriological studies show variation in their conclusions. The difference between reports undoubtedly reflects variations in the bacteriological techniques employed for their isolation and identification and may be due to gradual changes in flora due to injudicious use of antimicrobials.

The knowledge of common pathogens and resistance status can guide the clinician towards appropriate selection of empirical antibiotics. But on reviewing the available literature it has been observed that not many studies have been conducted in Indian population to list the common pathogens causing orofacial infections. Considering the above facts, this study was designed to obtain valuable information of the laboratory data regarding the microorganisms causing odontogenic infections in local population.


   Materials And Methods Top


The study was conducted as a prospective study.

Inclusion criteria

  • Patients of all age groups, with moderate to severe odontogenic fascial space infections
  • Patients not allergic to penicillin.


Exclusion criteria

  • Patients receiving antibiotic therapy more than 24 h prior to reporting to outpatient department (OPD)
  • Patients having a recent history of major illness or hospitalization for more than a week
  • Immuncompromised patients (e.g. steroids therapy and human immunodeficiency virus (HIV)).


Thirty-five patients who fulfilled the criteria were included.

The routine case history, clinical examination, and preanesthetic evaluations were carried out before these patients underwent surgical decompression/drainage either under local anesthesia or under general anesthesia.

Usual painting and draping was carried out in all the cases. The specimen (pus/exudates) was collected by aspiration with 18 gauge needle in a syringe with routine aseptic precautions before drainage. The needle was closed immediately with the plastic cap to avoid contamination.

Then part of this sample was immediately injected in two separate bottles with air tight corks, containing a nutrient broth and thyoglycollate media for aerobic and anaerobic microflora, respectively [Figure 1]. The remaining part of the sample form the syringe was used to prepare slides to examine the microorganisms under the microscope. The samples were sent to laboratory within an hour for further processing.
Figure 1: Nutrient broth and thioglycollate broth bottles

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The surgical drainage/decompression was carried out under local anesthesia or general anesthesia, and drains were placed intraorally/extraorally as required. Postoperatively all the patients were maintained on intravenous (i.v.) cephataxime (1 g tid) till culture report was obtained and after that the specific antibiotics were started if necessary.

In the laboratory following steps were done to confirm the microflora from the sample.

A. Steps for aerobic organisms identification: Assay time/turnaround time - 2 days

  • The pus sample was aseptically plated on blood agar plate and on MacConkey's agar plate to make a primary well. Subsequently spreading was done by a nichrome wire loop
  • Both the plates were streaked aseptically
  • Incubation was done for both the plates under aerobic conditions at 37°C for 24 h
  • The colonies on both the plates were noted. Blood agar plate was used for all organisms and MacConkey's agar plate was for gram negative organisms
  • Blood agar and MacConkey's agar plate were examined especially for the presence of following organisms: Staphylococcus aureus, Streptococcus, Klebsiella sp., and Pseudomonas aeruginosa
  • The morphology was confirmed with gram staining.
  • The identification of organism was done by biochemical tests and antimicrobial susceptibility testing was done by Kirby-Bauer method.


B. Steps for anaerobic organisms identification: Assay time/turnaround time - 5 days

  • The pus sample in thioglycollate broth was inoculated in the same and incubated at 37°C overnight
  • Subculture was done on blood agar and it was immediately put in an anaerobic biobag with indicator. The bag was sealed with parafilm. Incubation was done at 37°C for 48 h
  • The growth colonies were observed and described. Gram smear was done. Aerotolerance testing was done. If the colony grows on aerobic culture, it is unlikely to be an obligate anaerobe. (except Clostridium septicum and Actinomycetes)
  • If no growth occurs on aerobic culture, the organism is presumptively identified by means of gram reaction, colony characters, and available biochemical tests. If required antimicrobial susceptibility is done on blood agar with disc diffusion technique.



   Results Top


Of the 35 patients evaluated in this study, 18 were female and 17 were male. The highest incidence was seen in the age group of 21-30 years. The maxillary teeth were predominantly involved (66%) as a source of odontogenic infections and the highest incidence of involvement of spaces were of buccal (41%) and submandibular (31%) spaces [Figure 2] and [Figure 3].
Figure 2: Incidence of teeth involved as source of infection

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Figure 3: Incidence of fascial spaces involved

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Out of 35 patients studied, 27 patients showed mixed infection. While five and three patients showed anaerobic and aerobic infection, respectively [Figure 4].
Figure 4: Type of infection

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In our study, gram positive organisms were predominantly isolated as compared to gram negative organisms. Cocci were predominantly isolated as compared to rods. Aerobic and anaerobic organisms were nearly equal in number [Figure 5], [Figure 6] and [Figure 7].
Figure 5: Incidence of gram positive and gram negative organisms

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Figure 6: Incidence of rod and cocci organisms

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Figure 7: Incidence of aerobic and anaerobic organisms

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The incidence of isolation of anaerobic Streptococci was highest, followed by Staphylococcus aureus. The other organisms isolated were Escherichia coli, nonhemolytic Streptococci, Klebsiella pneumoniae, and Pseudomonas aeruginosa in minor percentages [Table 1] and [Figure 8].
Figure 8: Types of microorganisms isolated

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Table 1: Instances and percentages of types of organisms


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In six patients antibiotics were changed according to the culture and sensitivity reports.


   Discussion Top


For many years, the reported microbiology of odontogenic infections was inconsistent. It was difficult to compare various bacteriological investigations because of differing methods and materials used. But over a period of time, its polymicrobial nature and the changing nature of species has been noted and reported.

The pus/exudate was collected by aspiration with 18 gauge needle in a syringe with routine aseptic precautions to avoid air/surface contamination. In present study we used thioglycollate broth as it permits growth of anaerobic bacteria. The oxygen levels throughout the media are reduced via reaction with sodium thioglycollate which allows differentiation of aerobic, anaerobic, microaerophilic, and facultative anaerobic organisms based upon growth at various oxygen levels in the media.

Total number of isolates in our study was 35, with the mean number of 1 isolates per sample, which is an exception to the studies conducted in the past by many authors (Sabiston and Gold and Chow et al.,[4] ). The study revealed, less number of isolates per specimen which correlates with previous studies conducted by Hunt et al.[5]

In the study 77.14% patients were found to be having mixed microbial flora which is consistent with most of the studies. [2],[6],[7],[8]

The percentage of isolation of anaerobic bacteria (49%) was less in our study compared to studies done by Sabiston and Gold [3] and Chow et al., [4] but it is similar to the study conducted by Hunt and coworkers [5] and Aderhold and coworkers. [9] The anaerobic flora isolated was predominantly of anaerobic Streptococci (49%). Most of the earlier studies by Labriola et al.,[6] Rega et al. [7] Gill and Scully, [8] and Yuvaraj et al., [2] mentioned about mixed anaerobic flora in abscesses of orofacial region.

Staphylococcus species were isolated in 31% cases. The frequent isolation of Staphylococci in pus samples from odontogenic infections were confirmed by some previous studies (Sims [10] ). The presence of Staphylococcus aureus in the study has clinical significance, since it develops resistance to many known antibiotics.

The isolation of Pseudomonas (6%) is high, when compared to other studies (Labriola et al.,[6] and Kariyama et al.,[7] ). Pseudomonas becomes dominant and pathogenic when more susceptible bacteria of the normal flora are suppressed. [11] The injudicious use of antibiotics in dentistry may be the reason for isolation of more percentage of drug resistant pathogen [1] like Pseudomonas.

The incidence of other gram negative bacilli like Klebsiella in this study similar to earlier study reports, [1],[12] Chow and associates, [4] Sabiston and Gold, [3] and Sims [10] were able to culture gram-negative bacilli up to a proportion of 4%. According to Walton, [13] gram-negative bacilli isolated in orofacial infections are likely key players in synergism with other bacterial species.


   Conclusion Top


The microbiology of acute dental infections has been in the midst of many researches. The reported microbiology of odontogenic infections was for long time inconsistent, but a major role of anaerobes has become apparent with development of improved microbial isolation and culture techniques. The use of proper broth as carrier and culture media is necessary for identification of microorganisms. It is evident that orofacial odontogenic infections are polymicrobial, consisting both anaerobes and aerobes; as about 49% of species isolates were obligate anaerobes. Knowledge of the potential spectrum of pathogens, as well as regional resistance status is important for rational chemotherapy.

Though the sample size of this study is comparatively small, we can safely state that the microbiological flora of odontogenic abscesses consist of complex mixture of aerobic and anaerobic bacteria. This knowledge can guide us to use proper empirical antibiotics at the onset of odontogenic infection. The antibiotic sensitivity should be carried out in severe odontogenic infections for proper further management.


   Acknowledgment Top


Dr. Abhyankar, Golwilkar Metropolis Lab, Pune.

 
   References Top

1.
Haug RH. The changing microbiology of maxillofacial infections. Oral Maxillofac Surg Clin North Am 2003;15:1-15.  Back to cited text no. 1
    
2.
Yuvaraj V, Alexander M, Pasupathy S. Microflora in maxillofacial infections--a changing scenario? J Oral Maxillofac Surg 2012;70:119-25.  Back to cited text no. 2
    
3.
Sabiston CB Jr, Gold AW. Aerobic bacteria in oral infections. Oral Surg Oral Med Oral Pathol 1974;38:187-92.  Back to cited text no. 3
    
4.
Chow AW, Roser SM, Brady FA. Orofacial odontogenic infections. Ann Intern Med 1978;88:392-402.  Back to cited text no. 4
[PUBMED]    
5.
Hunt DE, King TJ, Fuller GE. Antibiotic susceptibility of bacteria isolated from oral infections. J Oral Surg 1978;36:527-9.  Back to cited text no. 5
[PUBMED]    
6.
Labriola JD, Mascaro J, Alpert B. The microbiologic flora of orofacial abscesses. J Oral Maxillofac Surg 1983;41:711-4.  Back to cited text no. 6
[PUBMED]    
7.
Rega AJ, Aziz SR, Ziccardi VB. Microbiology and antibiotic sensitivities of head and neck space infections of odontogenic origin. J Oral Maxillofac Surg 2006;64:1377-80.  Back to cited text no. 7
    
8.
Gill Y, Scully C. Orofacial odontogenic infections: Review of microbiology and current treatment. Oral Surg Oral Med Oral Pathol 1990;70:155-8.  Back to cited text no. 8
    
9.
Aderhold L, Knothe H, Frenkel G. The bacteriology of dentogenous pyrogenic infections. Oral Surg Oral Med Oral Pathol 1981;52:583-7.  Back to cited text no. 9
[PUBMED]    
10.
Sims W. The clinical bacteriology of purulent oral infections. Br J Oral Surg 1974;12:1-12.  Back to cited text no. 10
[PUBMED]    
11.
Bratton TA, Jackson DC, Nkungula-Howlett T, Williums CW, Bennett CR. Management of complex multi-space odontogenic infections. J Tenn Dent Assoc 2002;82:39-47.  Back to cited text no. 11
    
12.
Storoe W, Haug RH, Lillich TT. The changing face of odontogenic infections. J Oral Maxillofac Surg 2001;59:739-48.  Back to cited text no. 12
    
13.
Walton RE. Culturing exudates of odontogenic infection-a successful procedure? Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1999;88:525.  Back to cited text no. 13
[PUBMED]    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8]
 
 
    Tables

  [Table 1]


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