Brazilian Journal of Otorhinolaryngology (English Edition) Brazilian Journal of Otorhinolaryngology (English Edition)
Original article
Bacteriology of peritonsillar abscess: the changing trend and predisposing factors
Bacteriologia do abscesso peritonsilar: tendência de mudança e fatores predisponentes
Yi-Wen Tsaia, Yu-Hsi Liub, Hsing-Hao Sub,c,,
a Kaohsiung Veterans General Hospital, Department of Medical Education and Research, Kaohsiung, Taiwan
b Kaohsiung Veterans General Hospital, Department of Otorhinolaryngology, Head and Neck Surgery, Kaohsiung, Taiwan
c Tajen University, Department of Pharmacy and Graduate Institute of Pharmaceutical Technology, Pingtung, Taiwan
Received 01 May 2017, Accepted 16 June 2017

Peritonsillar abscess (PTA) is the most common deep neck infection. The infectious microorganism may be different according to clinical factors.


To identify the major causative pathogen of peritonsillar abscess and investigate the relationship between the causative pathogen, host clinical factors, and hospitalization duration.


This retrospective study included 415 hospitalized patients diagnosed with peritonsillar abscess who were admitted to a tertiary medical center from June 1990 to June 2013. We collected data by chart review and analyzed variables such as demographic characteristics, underlying systemic disease, smoking, alcoholism, betel nut chewing, bacteriology, and hospitalization duration.


A total of 168 patients had positive results for pathogen isolation. Streptococcus viridans (28.57%) and Klebsiella pneumoniae (23.21%) were the most common microorganisms identified through pus culturing. The isolation rate of anaerobes increased to 49.35% in the recent 6 years (p=0.048). Common anaerobes were Prevotella and Fusobacterium spp. The identification of K. pneumoniae increased among elderly patients (age>65 years) with an odds ratio (OR) of 2.76 (p=0.03), and decreased in the hot season (mean temperature>26°C) (OR=0.49, p=0.04). No specific microorganism was associated with prolonged hospital stay.


The most common pathogen identified through pus culturing was S. viridans, followed by K. pneumoniae. The identification of anaerobes was shown to increase in recent years. The antibiotics initially selected should be effective against both aerobes and anaerobes. Bacterial identification may be associated with host clinical factors and environmental factors.


O Abscesso Peritonsilar (APT) é a infecção cervical profunda mais comum. O microrganismo infeccioso pode ser diferente de acordo com os fatores clínicos.


Identificar o principal agente causador do abscesso peritonsilar e investigar a relação entre o patógeno causador, os fatores clínicos do hospedeiro e a duração da hospitalização.


Este estudo retrospectivo incluiu 415 pacientes hospitalizados diagnosticados com abscesso peritonsilar que foram internados em um centro médico terciário de junho de 1990 a junho de 2013. Coletamos dados através da análise dos arquivos médicos dos pacientes e analisamos variáveis como características demográficas, doença sistêmica subjacente, tabagismo, alcoolismo, hábito de mascar noz de betel, bacteriologia e duração da hospitalização.


Um total de 168 pacientes apresentaram resultados positivos para isolamento de patógenos. Streptococcus viridans (28,57%) e Klebsiella pneumoniae (23,21%) foram os microrganismos mais comuns identificados pela cultura da secreção. A taxa de isolamento de anaeróbios aumentou para 49,35% nos últimos 6 anos (p=0,048). Os anaeróbios comuns foram Prevotella e Fusobacterium spp. A identificação de K. pneumoniae aumentou em pacientes idosos (idade>65 anos) com razão de chances (Odds Ratio - OR) de 2,76 (p=0,03) e diminuiu na estação do calor (temperatura média>26°C) (OR=0,49, p=0,04). Nenhum microrganismo específico foi associado à hospitalização prolongada.


O patógeno mais comumente identificado através da cultura de secreção foi S. viridans, seguido por K. pneumoniae. A identificação de anaeróbios mostrou ter aumentado nos últimos anos. Os antibióticos selecionados inicialmente devem ser efetivos contra aeróbios e anaeróbios. A identificação bacteriana pode estar associada a fatores clínicos e fatores ambientais do hospedeiro.

Anaerobic bacteria, Bacterial infections, Klebsiella pneumoniae, Peritonsillar abscess, Viridans streptococci
Bactérias anaeróbicas, Infecções bacterianas, Klebsiella pneumoniae, Abscesso peritonsilar, Viridans streptococci
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Peritonsillar abscess (PTA), or quinsy, is the most common deep neck infection.1 The abscess may spread into the parapharyngeal space of other deep neck spaces, to the adjacent structure, and to the bloodstream. It rarely occurs but PTA is potentially life threatening. Early diagnosis of PTA is extremely crucial, and appropriate antibiotics and surgical intervention to remove the abscess are required.2 Antibiotics result in a substantial reduction in the progression of this disease. The empirical antibiotic used should be effective against the possible causative pathogen of PTA.

Our objectives were to investigate the microbiology of PTA and to identify its relationship with clinical variables including the underlying systemic disease of patients; habits such as smoking, alcoholism, and betel nut chewing; and hospitalization duration.

MethodsStudy design and sample population

This retrospective study included 415 patients with PTA who were admitted to a tertiary medical center located in Southern Taiwan from June 1990 to June 2013. Inclusion criteria were hospitalized patients who were clinically diagnosed with PTA (ICD-9 code 475) by positive pus aspiration or computed tomography (CT) imaging. We reviewed the chart of each patient to collect the following data: admission date, age, sex, height, weight, host clinical factors (diabetes mellitus [DM], hypertension, smoking habit, alcoholism, and betel nut chewing), pus culture result, antibiotic treatment, surgery, and hospitalization duration. The study was approved by the institutional review board.

We classified the bacteria into different categories according to the characteristics of Gram staining and anaerobic properties. We defined prolonged hospitalization as hospitalization duration of more than 6 days. Obesity was defined as a body mass index of more than 27, and elderly patients were defined as those aged older than 65 years. We defined the hot season as the months from May to October when the average temperature in Southern Taiwan was above 26°C according to the record of the Central Weather Bureau of R.O.C.

Statistical analysis

All data were analyzed using the SPSS statistical software (IBM Corp., Armonk, NY, USA), except for the Cochran–Armitage test, which was performed using the SAS program (SAS Institute, Cary, NC, USA). The association with each independent variable was statistically analyzed among the different groups. Categorical variables were compared using the Pearson's Chi-square test or the Fisher's exact test, as appropriate. Odds ratios (ORs) and their 95% confidence intervals (CIs) were calculated. Trends of isolated pathogens were analyzed using the Cochran–Armitage test. A p-value less than 0.05 was considered statistically significant.

Ethic statement

This study has been approved by the Institutional Review Board; the approval protocol number is VGHKS14-CT7-01.

ResultsDemographraphic characteristics

This study included 415 patients. The results of pus cultures from either surgery or needle aspiration were available for 266 patients. Adjustments for sample submitted to tonsil surgery or PTA drainage was performed, as shown in Table 1. There is no patient with history of AIDS or HIV infection in this study.

Table 1.

Demographraphic characteristics of patients with peritonsillar abscess.

Age  Overall, (n=266)  Diabetes mellitus  Smoking  Alcoholism  Betel-nut chewing 
<18 y/o  22 (8.27)  6 (27.27)  5 (22.73)  2 (9.09) 
18–64 y/o  215 (80.83)  19 (8.84)  111 (51.63)  76 (35.35)  37 (17.21) 
≥65 y/o  29 (10.90)  4 (13.79)  5 (17.24)  7 (24.14)  3 (10.34) 
Total  266 (100)  23 (8.65)  122 (45.86)  88 (33.08)  42 (15.79) 

Data are presented as n (%).

y/o indicates “year old”.


Within these patients with pus obtained, 230 (230–266, 86.47%) showed bacterial growth in their pus culture. The pus culture of the remaining 36 patients showed no bacterial growth. Of the 230 patients, 132 (132–230, 57.39%) had polymicrobial pus, including 62 cases merely reported as “normal flora” or “mixed flora” (62–230, 26.96%). Pus cultures of 168 patients (168–266, 63.15%) showed positive results for pathogen isolation. More than a single pathogen was isolated in 64 patients (64–168, 38.10%). Aerobic bacteria were isolated from 85.7% (144/168) of positive cultures, anaerobic or facultative aerobic bacteria from 44.0% (74–168), and mixed aerobic and anaerobic bacteria from 29.8% (50–168).

The most common pathogen identified through pus culturing was Streptococcus viridans (48–168, 28.57%), followed by Klebsiella pneumoniae (39–168, 23.21%) and the beta-hemolytic Streptococcus group (17–168, 10.12%), as shown in Table 2. We divided patients by the 4 periods of 1990–1995, 1996–2001, 2002–2007, and 2008–2013; the isolation rate of the anaerobes was 25%, 23.81%, 45.45%, and 49.35%, respectively. The isolation rate of anaerobic pathogens increased significantly between 1990 and 2013 (Cochran–Armitage test, p=0.048), as shown in Table 3 and Fig. 1. The isolation rates of gram-positive bacteria and gram-negative bacteria in these 4 periods were 100% and 25%, 57.14% and 47.62%, 62.12% and 48.48%, and 51.95% and 49.35%, respectively. Most of the anaerobic pathogens were Prevotella spp. (24–168, 14.29%) and Fusobacterium spp. (16–168, 9.52%), as shown in Table 2.

Table 2.

Bacteriology of 168 patients with peritonsillar abscess with definite isolation of pus culture.

Causative pathogen  Overall (n=168)  DM (n=17)  HTN (n=22)  Smoking (n=78)  Alcoholism (n=59)  Betel-Nut chewing (n=27)  Obesity (n=30) 
Aerobic GNB  51 (30.36)  10 (58.82)  8 (36.36)  22 (28.21)  15 (25.42)  8 (29.63)  8 (26.67) 
Klebsiella pneumoniae  39 (23.21)  7 (41.18)  7 (31.82)  19 (24.36)  13 (22.03)  7 (25.93)  7 (23.33) 
Aerobic GPB  22 (13.10)  10 (58.82)  5 (22.73)  12 (15.38)  11 (18.64)  4 (14.81)  6 (20.00) 
Aerobic GNC  4 (2.38)  1 (5.88)  1 (4.55)  1 (1.28)  1 (1.69)  1 (3.70)  2 (6.67) 
Aerobic GPC  99 (58.93)  10 (58.82)  12 (54.55)  46 (58.97)  32 (61.02)  21 (77.78)  19 (63.33) 
Staphylococcus spp.  9 (5.36)  0 (0.00)  1 (4.55)  5 (4.6)  5 (8.47)  1 (3.70)  2 (6.67) 
Beta-hemolytic streptococcus group  18 (10.71)  1 (5.88)  1 (4.55)  15 (19.23)  10 (16.95)  4 (14.81)  4 (13.33) 
Streptococcus melliri group  24 (14.29)  4 (23.53)  4 (18.18)  10 (12.82)  8 (13.56)  9 (33.33)  4 (13.33) 
Streptococcus viridans group  48 (28.57)  5 (29.41)  7 (31.82)  16 (20.51)  13 (22.03)  7 (25.93)  7 (23.33) 
Anaerobic cocci  34 (20.23)  5 (29.41)  5 (22.73)  17 (21.79)  13 (22.03)  7 (25.93)  11 (36.67) 
Peptostreptococcus spp.  9 (5.36)  1 (5.88)  1 (4.55)  7 (8.97)  6 (10.17)  3 (11.11)  4 (13.33) 
Anaerobic GPB  14 (8.33)  1 (5.88)  5 (22.73)  5 (6.41)  4 (6.78)  2 (7.41)  3 (10.00) 
Anaerobic GNB  45 (26.79)  1 (5.88)  6 (27.27)  24 (30.77)  18 (30.51)  7 (25.93)  6 (20.00) 
Fusobacterium spp.  17 (10.12)  0 (0.00)  1 (4.55)  10 (12.82)  6 (10.17)  3 (11.11)  2 (6.67) 
Prevotella spp.  24 (14.29)  1 (5.88)  4 (18.18)  11 (14.10)  10 (16.95)  4 (18.18)  4 (13.33) 

Data are presented as n (%).

Aerobic isolates included aerobic and facultative anaerobic isolates.

DM, diabetes mellitus; GNB, gram-negative bacilli; GNC, gram-negative cocci; GPB, gram-positive bacilli; GPC, gram-positive cocci; HTN, hypertension.

Table 3.

Isolation rate of different types of bacteria during each 6 year interval, 1990–2013.

Years, number of patient types (%) of bacteria  1990–1995  1996–2001  2002–2007  2008–2013  Total (1990–2013)  Test for trends (p-value) 
Gram positive (% of total patient)  4 (100)  12 (57.14)  41 (62.12)  40 (51.95)  97 (57.74)  0.120 
Gram negative (% of total patient)  1 (25)  10 (47.62)  32 (48.48)  38 (49.35)  81 (48.21)  0.569 
Anaerobes (% of total patient)  1 (25)  5 (23.81)  30 (45.45)  38 (49.35)  74 (44.05)  0.048a 
Patient  21  66  77  168   

Denotes for p-value less than 0.05.

Figure 1.

Isolation rate of different types of bacteria during each 6 year interval.

Host clinical factors were associated with several isolated pathogens. Betel nut chewing was associated with the isolation of gram-positive cocci (GPC) (OR=2.67, p=0.04). The association of bacterial isolation with smoking habit and alcoholism was not statistically significant. Elderly patients (age>65 years) had higher K. pneumoniae isolation (OR=2.76, p=0.03). Obesity (BMI>27) was associated with a higher isolation of Peptostreptococcus (OR=4.19, p=0.04), as shown in Table 4.

Table 4.

Association between the predisposing factors and the pathogen.a

Predisposing factors  Causative pathogen  OR  95% CI  p-value 
Elderb  KP  2.76  1.10–6.93  0.03e 
Obesityc  Peptostreptococcus  4.19  0.98–17.88  0.04e 
Hot seasondGPB  3.22  1.13–9.19  0.02e 
KP  0.49  0.23–1.01  0.04e 
Betel-Nut chewing  GPC  2.67  1.02–7.02  0.04e 

No statistically difference was observed among bacterial isolates and smoking, alcoholism, and DM.


Elderly indicates patient's age was more than 65 years old.


Obesity indicates patient's body mass index was more than 27.


Hot season indicates the admission date was between May and October, during which time the average temperature in southern Taiwan was more than 27°C.


Denotes for p-value less than 0.05.

CI, confidence interval; DM, diabetes mellitus; GPB, gram-positive bacilli; GPC, gram-positive cocci; HTN, hypertension; KP, Klebsiella pneumoniae; OR, odds ratio.

In addition, in the hot season, we found that the risk of isolating gram-positive bacilli (GPB) increased (OR=3.22, p=0.02), but that of K. pneumoniae isolation decreased (OR=0.49, p=0.04), as shown in Table 4. There was no specific microorganism associated with prolonged hospital stay.

Searching from the PubMed database, there were 30 studies involved in bacteriology of PTA during 1980–2016. The timeframes, the geographical locations and the predominant bacterial species identified in these studies were listed in Table 5.

Table 5.

Studies involved in bacteriology of PTA during 1980–2016.

Investigator  Country  Year  Positive culture  Predominant aerobes  Predominant anaerobes 
Brook et al. (1981)19U.S.  –  16  Gamma-hemolytic streptococci  Bacteroides sp. 
      Alpha-hemolytic streptococci  Anaerobic GPC 
Jokipii et al. (1988)8Finland  –  42  Group A streptococcus  Peptostreptococcus sp. 
      Streptococcus viridans group  Bacteroides sp. 
Brook et al. (1991)37U.S.  1978–1985  34  Staphylococcus aureus  Bacteroides sp. 
      Streptococcus pyogenes  Peptostreptococcus sp. 
Snow et al. (1991)38UK  –  55  Beta hemolytic streptococci  – 
      Staphylococcus aureus   
Jousimies-Somer et al. (1993)20Finland  –  122  Streptococcus pyogenes  Fusobacterium necrophorum 
      Streptococcus milleri group  Prevotella melaninogenica 
Mitchelmore et al. (1995)9UK  1982–1992  45  Group A streptococcus  Peptostreptococcus sp. 
Muir et al. (1995)39  New Zealand  1990–1992  39  Group A streptococcus  – 
Prior et al. (1995)40
Cherukuri (2002)
UK  –  45  –  – 
USA  1990–1999  82  Streptococcus sp.  – 
      Haemophilus sp.   
Matsuda et al. (2002)10Japan  1988–1999  386  Alpha-hemolytic streptococci  Anaerobic gram-negative rods 
      Neisseria sp.  Porphyromnas sp. 
Hanna et al. (2006)41  Northern Ireland  2001–2002  37  Group A streptococci  Bacteroides sp. 
Sakae et al. (2006)42Brazil  2001  26  Streptococcus viridans  Peptostreptococcus sp. 
      Streptococcus pyogenes  Prevotella sp. 
Zagolski et al. (2007)  Poland  –  12  Streptococcus sp.  Bacteroides sp. 
Megalamani et al. (2008)India  2003–2006  39  Beta hemolytic streptococcus  – 
Sunnergren et al. (2008)7  Sweden  2000–2006  67  Group A streptococcus  Bacteroides sp. 
Klug et al. (2009)11Denmark  2001–2006  405  Group A streptococcus  Fusobacterium sp. 
      Groups C or G streptococci   
Gavriel et al. (2009)6Israel  1996–2002  137  Streptococcus pyogenes  Prevotella sp. 
      Streptococcus intermedius  Peptostreptococcus sp. 
Segal et al. (2009)4Israel  2004–2007  64  Group A streptococcus  – 
      Group C streptococcus   
Repanos et al. (2009)32  UK  1998–2005  107  Streptococcal sp.  – 
Rusan et al. (2009)  Denmark  2001–2006  623  Group A streptococcus  Fusobacterium sp. 
Acharya et al. (2010)5Nepal  2007–2008  18  Streptococcus pyogenes  – 
      Staphylococcus aureus   
Marom et al. (2010)17Canada  1998–2007  180  Streptococcus viridans  – 
      Group A streptococcus   
Hidaka et al. (2011)43Japan  2002–2007  65  Streptococcus milleri group  Prevotella sp. 
      Other Streptococcus sp.  Peptostreptococcus sp. 
Klug et al. (2011)12Denmark  2005–2009  36  Streptococcus viridans  Prevotella sp. 
      Neisseria sp.  Fusobacterium sp. 
Love et al. (2011)13  New Zealand  2006–2008  147  Group A streptococcus Other beta-hemolytic streptococci  Fusobacterium sp. 
Albertz et al. (2012)16Chile  2000–2012  112  Streptococcus pyogenes  Bacteroides sp. 
      Other streptococci  Peptostreptococcus sp. 
        Fusobacterium sp. 
Takenaka et al. (2012)3Japan  2005–2009  50  Streptococcus pyogenes  Anaerobic 
        Fusobacterium sp. 
Sowerby et al. (2013)14Canada  2009–2010  42  Group A streptococcus  – 
      Streptococcus anginosus   
Gavriel et al. (2015)Israel  1996–2003  132  Streptococcus pyogenes  Prevotella sp. 
        Peptostreptococcus sp. 
Mazur et al. (2015)18Poland  2003–2013  45  Streptococcus viridans group  Fusobacterium sp. 
      Streptococcus pyogenes  Prevotella sp. 
Plum et al. (2015)44USA  2002–2012  69  Streptococcus milleri in adults  – 
      β-hemolytic streptococcus in children   
Lepelletier et al. (2016)36  French  2009–2012  412  Group A streptococci  Fusobacterium spp. 
Tachibana et al. (2016)45  Japan  2008–213  100  Streptococcus viridans  Fusobacterium sp. 
Vaikjarv et al. (2016)46  Estonia  2011–2012  22  Streptococcus sp.  Streptococcus spp. 
Present study (2017)Taiwan  1990–2013  168  Streptococcus Viridans  Prevotella sp. 
      Klebsiella Pneumoniae  Fusobacterium sp. 

–, indicates “not disclosed”.

Several broad-spectrum antibiotics such as penicillin or cefazolin combined with gentamycin (GM) and metronidazole, clindamycin plus GM, or augmentin along were used in our series. All these antibiotics were effective without any significant difference.


In our study, the most common pathogen identified through pus culturing in patients with PTA was S. viridans, followed by K. pneumoniae; commonly isolated anaerobes in our study were Prevotella and Fusobacterium spp. We reviewed the bacteriology data from previous studies, as shown in Table 5. Most of the studies3–16 have reported group A Streptococcus as the most common aerobic pathogen in PTA; some studies12,17,18 have reported that common aerobic pathogens were S. viridans, followed by group A β-hemolytic streptococci. The prevalence of K. pneumoniae has been rarely reported in previous studies. In previous studies, Fusobacterium nucleatum,3,8,11,12,15,19,20Prevotella,3,12,19–21Bacteroides,7,8,19Peptostreptococcus,8,9,20 and anaerobic streptococcus12 were the most common anaerobic pathogens. The divergence of bacterial culture may be owing to different geographical location. With difference between diets and lifestyle, the bacterial flora within each people may be also different.

K. pneumoniae and Streptococcus spp. are common oral flora normally found in the mouth and are odontogenic pathogens of deep neck infection.22–24 The S. viridans group is the etiological agent of dental caries, pericoronitis, or, if introduced into the bloodstream, endocarditis. In Taiwan, K. pneumoniae has been linked to lung infection in aspiration patients or a liver abscess25 in immunocompromised patients or those with diabetes.26

Patients with old age27 or diabetes mellitus28 are considered to be immunocompromised and have more chance to get infection. DM and elder are also linked with more complications and higher mortality rate in deep neck infection.29,30 Thus PTA patients with above characteristics often have longer hospital stay.30 We reported the microbiology of PTA in such immunocompromised patients. Patients with DM had no increased risk of isolating K. pneumoniae as the causative pathogen of PTA. By contrast, elderly patients with PTA in the current series had a higher risk of K. pneumoniae isolation.

A trend toward a higher isolation rate for anaerobes was observed during 2002–2013 (p=0.048). Gavriel6 reported a significant increase in anaerobic growth during 1996–1999 and then a slow nonsignificant decline until 2002. Takenaka3 reported no change in the percentage of cases with anaerobic growth between 2 periods (2005–2007 and 2008–2009). Such a phenomenon might result from a real change in pathogens; the alteration of antibiotics used, or improved culture methods for anaerobic pathogens. In our series, no major alteration of antibiotics used or improvement of the culture methods was observed. Physicians should prescribe empirical antibiotics to cover anaerobes.

PTA is often a polymicrobial infection. Polymicrobial growth was observed in the pus cultures of 57.39% of patients. The rationale of using empirical antibiotics was to cover GPCs, GNBs, and respiratory anaerobes. If necessary, suitable antibiotics should be chosen on the basis of culture results. However, the management of most uncomplicated patients may not be affected by the culture result.31 Repanos et al.32 suggested that using broad-spectrum antibiotics such as cephalosporin or penicillin combined with metronidazole was effective. In our study, no significant difference was found among several combinations of broad-spectrum antibiotics.

Smoking habit has been commonly observed in patients with PTA in several studies17,18,33,34; these studies have reported smoking as a risk factor for PTA. Marom et al.17 reported a significantly higher incidence for S. viridans, other gram-positive cocci isolates, and anaerobes. In our study, no statistical significance was observed in the causative pathogen between smokers and nonsmokers with PTA, similar to the findings of the study by Klug.34

Betel nut chewing is a popular habit in Southeast Asia. To the best of our knowledge, no study has found an association between the bacteriology of PTA and betel nut chewing. In our series, this habit was associated with a higher risk of GPC as a pathogen. In the study by Ling et al.,35 it was associated with a likelihood of subgingival infection by Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis.

In our study, elderly patients (older than 65 year-old) had a high risk of K. pneumoniae isolation. The study by Marom17 reported a significantly higher isolation rate for infection by GPC (mixed Streptococcus species) and gram-negative rods in older patients (40 year-old or older) than in younger patients.

The hot season increased the risk of GPB infection and reduced the risk of K. pneumoniae infection in patients with PTA in our current study. Our institute is located in a tropical region that has approximately six months (May to October) of hot weather, with a mean temperature of 27°C. By contrast, Klug et al.15 from another institute located in a temperate zone reported a higher incidence of F. nucleatum infection during summer than during winter. It also reported Group A streptococcus was significantly more frequently identified from in the winter and spring. The study in French36 reported PTA caused by S. pyogenes or anaerobes were more prevalent in the winter and spring than summer. Such fluctuation in the microbiology of PTA might be weather related.

In our series, no specific microorganism was associated with the poor prognosis of PTA. This finding is considerably similar to the reports by Marom17 and Mazur.18

Our study has several limitations. Because we retrospectively collected data by chart review, data from the medical record might be lost during the early years. As we used several small populations of isolated pathogens, a larger sample size is necessary to determine the relationship between the isolated pathogen and the predisposing factors.


The most common causative pathogen of PTA was S. viridans, followed by K. pneumoniae. The isolation of anaerobes significantly increased in recent years. The common ones were Prevotella and Fusobacterium spp. Empirical antibiotics targeting both aerobes and anaerobes should be appropriate as treatment. Bacterial isolation may be associated with host clinical factors, environmental factors, and hospitalization duration.

Conflicts of interest

The authors declare no conflicts of interest.


The authors thank Professor Hsueh-Wen Chang (Department of Biological Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan) for his help in the statistical analysis.

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Please cite this article as: Tsai Y-W, Liu Y-H, Su H-H. Bacteriology of peritonsillar abscess: the changing trend and predisposing factors. Braz J Otorhinolaryngol. 2017.

Peer Review under the responsibility of Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial.

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