- Research article
- Open Access
Haemophilus influenzae type b as an important cause of culture-positive acute otitis media in young children in Thailand: a tympanocentesis-based, multi-center, cross-sectional study
BMC Pediatrics volume 14, Article number: 157 (2014)
Streptococcus pneumoniae (S. pneumoniae) and Haemophilus influenzae (H. influenzae) are considered major causes of bacterial acute otitis media (AOM) worldwide, but data from Asia on primary causes of AOM are limited. This tympanocentesis-based, multi-center, cross-sectional study assessed bacterial etiology and antimicrobial susceptibility of AOM in Thailand.
Children 3 to 59 months presenting with AOM (< 72 hours of onset) who had not received prescribed antibiotics, or subjects who received prescribed antibiotics but remained symptomatic after 48–72 hours (treatment failures), were eligible. Study visits were conducted from April 2008 to August 2009. Bacteria were identified from middle ear fluid collected by tympanocentesis or spontaneous otorrhea swab sampling (< 20% of cases). S. pneumoniae and H. influenzae serotypes were determined and antimicrobial resistance was also assessed.
Of the 123 enrolled children, 112 were included in analysis and 48% of the 118 samples were positive for S. pneumoniae (23% (27/118)), H. influenzae (18% (21/118)), Moraxella catarrhalis (6% (7/118)) or Streptococcus pyogenes (3% (4/118)). The most common pneumococcal serotypes were 19F (26%) and 14 (22%). The majority of H. influenzae isolates were encapsulated (18/21), with 13 type b (Hib) representing 62% of all H. influenzae isolate or 11% of all samples (13/118), and there were only 3 non-typeable isolates. Despite high antibiotic resistance, amoxicillin/clavulanate susceptibility was high. No pneumococcal vaccine use was reported.
S. pneumoniae and H. influenzae, both frequently antibiotic resistant, were leading causes of bacterial AOM and there was an unexpectedly high burden of Hib in this population unvaccinated by any Hib conjugate vaccine. Conjugate vaccines effective against pneumococcus and H. influenzae could potentially reduce the burden of AOM in this population.
Acute otitis media (AOM) is one of the most frequent bacterial infections in children, and one of the primary reasons for the prescription of antibiotics by pediatricians [1, 2]. Streptococcus pneumoniae (S. pneumoniae) and non-typeable Haemophilus influenzae (H. influenzae) have historically been considered the leading causes of bacterial AOM . Following introduction of the 7-valent pneumococcal conjugate vaccine (PCV7), in the United States, a relative increase in non-PCV7 serotypes and non-typeable H. influenzae (NTHi) was observed. There were few cases of AOM due to Moraxella catarrhalis (M. catarrhalis) or Streptococcus pyogenes (S. pyogenes) and no reported cases due to H. influenzae type b (Hib) . Even prior to the Hib vaccination era, encapsulated H. influenzae was rarely reported as a cause of AOM in the United States .
Most data on the topic come from North America and Europe, however, and studies of the burden, etiology and societal impact of AOM in Asia are sparse. While some studies suggest a low estimated prevalence [5, 6] and a lower physician-reported frequency of AOM visits in Asia than elsewhere , others have highlighted the importance of AOM in the region . The significant regional burden of chronic suppurative otitis media , a complication of AOM, suggests that AOM is indeed of public health concern.
Regional treatment patterns of AOM may also raise concerns given the extremely high rates of penicillin non-susceptibility of S. pneumoniae isolates and of ampicillin/amoxicillin resistance for H. influenzae non-invasive isolates documented in young children in East Asia [9–11]. A recent survey reported that most of the physicians in Asian countries use oral antibiotics as part of first line treatment of AOM , despite ‘watchful waiting’ recommendations in many countries across the world [12, 13].
There is thus a need for AOM etiology data in the region, ideally from tympanocentesis samples, as data extrapolated from pathogen distribution from nasopharyngeal samples do not necessarily represent pathogen distribution in the middle ear [14, 15]. This study aimed to add to the limited AOM data in Thailand, to characterize the bacterial etiology and serotypes of AOM cases in young children in Thailand, where both Hib and pneumococcal conjugate vaccine use are reported to be only <5% [16, 17], and to determine antibiotic susceptibility of the pathogens. These data could have important clinical implications for determining the best approach for prevention and treatment of AOM in Thailand [18, 19].
This was a tympanocentesis-based, multi-center, cross-sectional study conducted within a routine clinical setting in several regions of Thailand: 2 centers in Bangkok, one in Hatyai in southern Thailand and one in Chiang Mai in northern Thailand. Target enrollment was at least 100 patients over a year, based on the assumption that in the context of high antibiotic use, 40% of samples would be culture positive [3, 4, 20]. The study included children 3 to 59 months of age visiting Ear Nose and Throat (ENT) clinics for AOM, and from whom a middle ear fluid (MEF) sample was available either by tympanocentesis or careful sampling of spontaneous otorrhea which occurred less than 24 hours prior to the visit. Eligible patients were either subjects with a new episode of AOM (less than 72 hours since onset of symptoms) who had not yet received any antibiotics prescribed by a physician, or subjects who were diagnosed with AOM within 48–72 hours prior to study enrollment, received antibiotic therapy from a physician, but remained symptomatic at the time of study entry (treatment failures). Patients who received systemic antibiotic treatment for a disease other than AOM in the 72 hours prior to enrollment, and patients receiving antimicrobial prophylaxis for recurrent AOM, defined as at least 3 episodes in the past 6 months or 4 episodes in the past 12 months, were excluded. Children who were hospitalized during the diagnosis or treatment of AOM were also excluded. All study visits took place between 2 April 2008 and 28 August 2009.
During screening and enrollment, ENTs maintained a logbook to collect anonymized demographic information for subjects 3 to 59 months of age who were diagnosed with AOM to determine the representativeness of the AOM patients who were included in the study. ENTs obtained informed consent from parents/guardians of eligible children prior to performance of any study-specific procedures. Once enrolled, demographics, medical history, care history and general symptoms were collected and a clinical examination was performed; AOM was diagnosed after otoscopic examination of the tympanic membrane by the ENT and was classified according to the otoscopy score (8 grades) (OS-8), which measures the severity of tympanic-membrane inflammation. The OS-8 scale is only appropriate for use in children with an intact tympanic membrane, and therefore was not used for children with otorrhea. Spontaneous otorrhea or an OS-8 score of at least 2 was necessary for the child to meet AOM diagnosis criteria. The levels of the OS-8 scale from level 2 are as follows: 2 indicates hyperemia, air-fluid level, no opacification, meniscus noted; 3 indicates hyperemia, complete effusion, no opacification; 4 indicates hyperemia, opacification, air-fluid level observed, no bulging; 5 indicates hyperemia, complete effusion, opacification, and no bulging; 6 indicates hyperemia, bulging rounded doughnut appearance of tympanic membrane; 7 indicates hyperemia with bulla formation.
Middle ear fluid sample collection and sample analysis
MEF samples were collected by performing tympanocentesis. In cases of otorrhea, investigators were advised to remove and clean the ear canal material, and deep aspiration of the MEF material, via needle insertion, was attempted to avoid contamination and spurious results. Since pathogen distribution from tympanocentesis and otorrhea may differ , the study protocol limited otorrhea samples to represent no more than 20% of all subjects.
Samples were kept in Amies transport media and transferred to the central laboratory within 16 hours for plating at room temperature. Analysis of samples was performed at a central laboratory to isolate bacterial pathogens, assess serotypes and determine the antimicrobial susceptibility profile. MEF samples were inoculated in chocolate agar and blood agar with gentamycin and otorrhea samples were inoculated in chocolate agar with bacitracin and blood agar with gentamycin. S. pneumoniae serotyping was performed through polymerase chain reaction (PCR)  and H. influenzae serotyping was performed through monovalent antisera a, b, c, d, e and f at the International Emerging Infections Program of the United States Centers for Disease Control and Prevention. After initial serotyping of H. influenzae isolates the results were confirmed by a second laboratory which was blinded to the initial serotyping results. Definitions of antimicrobial susceptibility were based on the Clinical and Laboratory Standards Institute 2009 standards . Susceptibility to the following antibiotics was assessed: penicillin, amoxicillin/clavulanate, cefuroxime, cefotaxime, erythromycin, azithromycin, ampicillin, chloramphenicol, tetracycline, levofloxacin and trimethoprim/sulfamethoxazole.
Children with bilateral infections were considered a single episode but had 2 samples collected, one from each ear. Descriptive statistics were used to compare demographics, clinical characteristics, pathogen distribution and antibiotic susceptibility among enrolled children. All statistical analyses were performed using SAS, version 9.1 or later (SAS Institute Inc., Cary, NC, USA), and Microsoft Excel (2002 SP3 or later), for graphical purposes.
The study protocol was reviewed by the ethical review committees of all participating hospitals and the Ethical Review Committee for Research in Human Subjects at the Thailand Ministry of Public Health.
Study visits took place for 123 children experiencing AOM among 263 screened children (Figure 1). One hundred and twelve children fulfilled study criteria. Nine of the 112 (8%) children were classified as treatment failures. Six of the 112 children were experiencing bilateral infections for which samples from both the left and right ears were collected. Of the 118 samples collected, 91% (107/118) were collected by tympanocentesis. The primary reason for non-enrollment was spontaneous otorrhea more than 24 hours prior to the visit (n = 52).
Demographic characteristics and clinical history
The median age of screened children was 33.5 months compared to a median age of 36 months among participating children (range 5–59 months) (Table 1). Nine percent (10/112) of participating children were between 3 and 11 months of age, 14% (16/112) were between 12 and 23 months, and the remainders were uniformly distributed between the other classes of age (24–35, 36–47 and 48–59 months). Fifty-five percent (62/112) of participating children were females. Sixty-four percent (7/11) of children with spontaneous otorrhea were less than 24 months of age, while 19% (19/101) of children in whom tympanocentesis was used were less than 24 months. None of the children had received any doses of a pneumococcal conjugate vaccine, while 4% (5/112) had received at least one dose of influenza vaccine. Antibiotic use within the past month was reported for 23% (26/112) of children. AOM was classified as recurrent for 7% (8/112) of children.
Overall, 48% (57/118) of samples yielded cultures with one of the 4 bacterial pathogens under study (S. pneumoniae, H. influenzae, M. catarrhalis or S. pyogenes) (Figure 2), 2 of which were positive for more than one bacteria. The most frequently detected bacteria was S. pneumoniae (47% (27/57)), followed by H. influenzae (37% (21/57)), M. catarrhalis (12% (7/57)) and S. pyogenes (7% (4/57)). Among the 11 samples collected from otorrhea episodes, one was positive for S. pneumoniae, 2 for H. influenzae and 3 for S. pyogenes. Two of the 9 treatment failure samples were positive for a pathogen under study, both of which were S. pneumoniae. The most common pneumococcal serotypes isolated from the 27 S. pneumoniae-isolates were 19F (7/27 (26%)), 14 (6/27 (22%)) and 3 (4/27 (15%)) (Figure 2). Out of the 21 H. influenzae isolates, 13 (62%) were serotype b (Hib), 3 (14%) were non-typeable, and the remainders were serotypes a (1 isolate (5%)), d (2 isolates (10%)) and f (1 isolate (5%)), with one (5%) missing (Figure 2). Overall, Hib was detected in 11% of all samples (13/118). The 2 co-infected samples were due to one co-infection of S. pneumoniae 23F and H. influenzae serotype a, and one co-infection of Hib and M. catarrhalis.
S. pneumoniae and Hib and non-Hib H. influenzae were the most commonly detected pathogens in all age groups (Table 1). In the youngest age range of 3–11 months, S. pneumoniae and H. influenzae were each isolated from 2/10 episodes (20%). Among children 12–35 months of age, S. pneumoniae was isolated from 7/45 (15.5%) episodes while H. influenzae was detected in 10/45 (22%). In the oldest children, 36–59 months of age, S. pneumoniae was detected from 17/57 (30%) episodes, and H. influenzae from 9/57 (16%). Potential risk and protective factors, including premature birth, HIV infection, child care attended, child breast-fed and number of household siblings less than 5, were similar when compared by pathogen (data not shown). Due to small numbers, the differences in age group and potential risk factors by pathogen were not tested for statistical significance.
The most frequently reported symptom was ear pain, reported for 95% (106/112) of episodes, followed by irritability, reported for 49% (55/112) of episodes (Table 2). Fever was reported for 12% (3/26) of children experiencing AOM due to S. pneumoniae but was not reported for any children experiencing AOM due to Hib or non-Hib H. influenzae. Trouble sleeping was reported for 2% (2/26) of children experiencing AOM due to S. pneumoniae, 31% (4/13) of those experiencing AOM due to Hib and 25% (2/8) of those experiencing AOM due to non-Hib H. influenzae (Table 2). Due to small numbers, the differences in symptoms by pathogen were not tested for statistical significance.
Thirty-eight percent (5/13) of Hib-positive AOM and 13% (1/8) of AOM due to other H. influenzae were in children 12–23 months, compared to 14% (16/112) of AOM overall. Fifteen percent (2/13) of children with Hib-positive AOM and 13% (1/8) of children with AOM due to other H. influenzae reported taking antibiotics in the past month. Two of the 3 children who experienced hearing loss had Hib-positive AOM. Irritability and ear tugging were reported for a greater proportion of children with Hib-positive AOM compared to children with AOM due to other H. influenzae (54% (7/13) and 31% (4/13) versus 0% and 13% (1/8), respectively). Seventy-seven percent (10/13) of Hib-positive and 50% (4/8) of other H-influenzae-positive children had an OS-8 scale score of greater than 5.
Among the 27 S. pneumoniae isolates, all were susceptible to amoxicillin/clavulanate and to penicillin, 11% (3/27) were non-susceptible to cefotaxime, 63% (17/27) were non-susceptible to cefuroxime, 67% (18/27) were non-susceptible to erythromycin and 78% (21/27) were non-susceptible to trimethoprim/sulfamethoxazole (Table 3). Eighty-one percent (22/27) of S. pneumoniae isolates were multidrug resistant. Among 19F isolates, the most prominent serotype, 2 out of 7 were non-susceptible to cefotaxime and 5 out of 7 were non-susceptible to cefuroxime. All H. influenzae isolates were susceptible to amoxicillin/clavulanate and to cefotaxime, 5% (1/21) was non-susceptible to cefuroxime, and 20% (4/20) were non-susceptible to ampicillin, with ampicillin data missing for one isolate (Table 3). Three of the 4 isolates not susceptible to ampicillin were Hib isolates. One (Hib) of the 21 H. influenzae isolates was beta-lactamase-negative ampicillin-resistant but susceptible to amoxicillin/clavulanate.
The AOM episodes seen in this study among children who sought care from ENTs in Thailand were generally non-recurrent episodes assessed by tympanocentesis. In this study environment, where there was minimal use of either Hib or pneumococcal vaccine, bacterial pathogens were an important cause of AOM. The leading causes of bacterial AOM were S. pneumoniae and H. influenzae, representing 47% (27/57) and 37% (21/57) of culture-positive samples, respectively. The majority of H. influenzae was serotype b (62% (13/21)). Forty-eight percent of samples were culture-positive for one of the pathogens under study, slightly lower than the 53-58% reported in other settings , but consistent with the assumption that isolation of bacteria may be lower in an environment with high antibiotic use . Other studies have found that PCR can detect bacteria in culture-negative MEF , so it is possible that these pathogens play a greater role in AOM than what was detected here.
We found slightly more S. pneumoniae than H. influenzae, consistent with what was seen elsewhere in the pre-PCV7 era . In this population, AOM episodes were generally comprised of relatively mild, sporadic cases, rather than severe or recurrent. H. influenzae was slightly more prominent than S. pneumoniae in children 12–23 months of age while the reverse was true in children 24–59 months of age. Overall, the symptom profiles and potential risk factor profiles of S. pneumoniae and H. influenzae were generally similar.
One unexpected finding in the studywas the higher than expected presence of Hib. This was a surprise in part because available data suggest a low incidence of Hib-associated invasive disease in Thailand , although there are concerns that existing data from Asia underestimate the true burden [28, 29]. Additionally, on a global level, Hib is generally perceived not to be an important AOM pathogen. Before the introduction of the Hib vaccine in the United States, for example, Hib only represented 10% of H. influenzae AOM cases , while in our study, Hib was seen in 62% of the H. influenzae isolates. Another exception to the general observation that encapsulated H. influenzae are not important causes of AOM comes from a recent, tympanocentesis-based study in Venezuela where 31% of H. influenzae AOM were encapsulated a, c, d and f strains (Venezuela has universal Hib immunization) . Interestingly, based on the OS-8 scale, the Thai Hib cases seemed to be slightly more severe than S. pneumoniae or non-Hib H. influenzae cases.
A second surprising finding was that the median age of children in the study was 36 months, which is unusual given that AOM incidence elsewhere generally peaks at 6–18 months of age. Since the age of the screened cohort was only slightly younger than the enrolled cohort it does not appear that there was significant bias in the final study sample (i.e., those who received tympanocentesis) compared to all children who came to the ENT with suspected AOM. While it is possible that the true burden of AOM in Thailand tends to be in older children, it also may be that younger children with AOM are more often treated at home or by general practitioners and do not tend to visit the ENT. We note that a number of children could not be enrolled because of otorrhea for greater than 24 hours, which may suggest more severe AOM or may suggest that access to prompt care is limited, by distance or other factors.
The distribution of S. pneumoniae serotypes was similar to what has been reported in the literature [10, 32] prior to PCV introduction. The generally mild profile of AOM experienced by the children in our study may explain the slightly higher than expected proportion of M. catarrhalis isolates, as this pathogen is often associated with milder disease .
Due to the risk of treatment failures, up-to-date information on antibiotic resistance has important clinical implications for determining the best approach for treatment of AOM . Our results show high levels of resistance of S. pneumoniae to some antibiotics commonly given in Thailand for respiratory infections (Azithromycin, Cefuroxime, Erythromycin, Tetracycline, Trimethoprim/Sulfamethoxazole), and a high level of multidrug resistance. This was consistent with results from another study in Asian countries , which also noted a high level of resistance to macrolides. In our study only a low rate of cefotaxime non-susceptibility was seen, likely due to the fact that cephalosporins are generally only prescribed for children presenting with severe illness (moderate to severe otalgia or fever of 39°C ) at first visit or for patients who do not respond to initial treatment. Antibiotic resistance was less common for H. influenzae, and was similar to previously published estimates, though our isolates had lower levels of resistance to chloramphenicol (10% versus 25%) and ampicillin (15% versus 48%) . It is possible that more severe AOM cases than were seen in this study would be enriched for more resistant AOM.
Currently Hib vaccine use in Thailand is extremely limited as it is not on the Expanded Program of Immunization for Thailand . Uptake of PCV7 in Thailand, which is mainly used in private settings, has also been low , and there were no reports of pneumococcal vaccine use in the children in our study. Two other pneumococcal vaccines, Prevenar/Prevnar 13™ (Wyeth, LLC) (PCV13) and Synflorix™ (GlaxoSmithKline Vaccines) (PHiD-CV), have been licensed in recent years, and differ from PCV7 in the inclusion of 6 (1, 3, 5, 6A, 7F, 19A) and 3 (1, 5, 7F) additional serotypes, respectively. PHiD-CV also utilizes as the predominant carrier protein an outer membrane protein (protein D) derived from H. influenzae, as a protein D-containing 11-valent precursor formulation of PHiD-CV was previously shown to be efficacious against both pneumococcal and H. influenzae AOM . Efficacy of PHiD-CV itself against AOM was also recently demonstrated in another double-blind randomized clinical study . Although PCV13 efficacy against AOM has not yet been assessed, such data do exist for its predecessor formulation PCV7 . Of the 22 pneumococcal isolates whose serotype could be identified, at least 16 (73%) represent a serotype contained in each of the two higher valent vaccines. Serotype 3, contained only in PCV13, was also identified in 4/22 (18%) of those pneumococcal isolates, but it remains unclear whether serotype 3 disease is vaccine-preventable . Our results thus suggest that either vaccine would likely prevent a significant proportion of AOM cases.
The study was successful in adding to the limited data on AOM in Thailand, but there are important limitations, including few cases in the youngest children, small sample size and lack of a clear population denominator. The study did cover several, but not all, regions of Thailand, and therefore is somewhat limited in geographical representativeness. As the use of a Hib vaccine is known to be very limited in Thailand, we did not collect individual Hib vaccination status, though it could have provided further insight into the previously unrecognized burden of Hib in AOM cases that was identified in this study. An additional limitation is that the over-the-counter availability of antibiotics in Thailand could mean that some children may have received antibiotics before the study visit, This could have decreased the proportion of culture positives, and meant that bacteria that were isolated from such patients may have been those with greater non-susceptibility. However, as it was impossible to know whether any antibiotics received in this manner were appropriate for AOM and/or provided in sufficient dosage, only patients receiving antibiotics prescribed by a physician 48–72 hours prior to the study visit were considered treatment failures, as per protocol.
In summary, this assessment of AOM etiology in Thai children 3 to 59 months of age visiting ENT clinics for AOM showed an unexpectedly high burden of Hib. S. pneumoniae and H. influenzae were the leading causes of AOM across all age groups, similar to what has been seen in Europe, the United States, and Latin America, and with pneumococcal serotypes similar to those found elsewhere [32, 40]. These findings contribute to the scarce tympanocentesis literature in this region, and suggest that conjugate vaccines effective against pneumococcus and H. influenzae, both encapsulated (Hib) and unencapsulated, may be important in attempts to reduce bacterial AOM in the region.
Prevnar and Prevnar 13 are trademarks of Wyeth LLC.Synflorix is a trademark of the GlaxoSmithKline group of companies.
Klein JO: Otitis media. Clin Infect Dis. 1994, 19: 823-833.
McCaig LF, Hughes JM: Trends in antimicrobial drug prescribing among office-based physicians in the United States. JAMA. 1995, 273: 214-219.
Leibovitz E, Jacobs MR, Dagan R: Haemophilus influenzae: a significant pathogen in acute otitis media. Pediatr Infect Dis J. 2004, 23: 1142-1152.
Block SL, Hedrick J, Harrison CJ, Tyler R, Smith A, Findlay R, Keegan E: Community-wide vaccination with the heptavalent pneumococcal conjugate significantly alters the microbiology of acute otitis media. Pediatr Infect Dis J. 2004, 23: 829-833.
Berman S: Otitis media in developing countries. Pediatrics. 1995, 96: 126-131.
Mahadevan M, Navarro-Locsin G, Tan HK, Yamanaka N, Sonsuwan N, Wang PC, Dung NT, Restuti RD, Hashim SS, Vijayasekaran S: A review of the burden of disease due to otitis media in the Asia-Pacific. Int J Pediatr Otorhinolaryngol. 2012, 76: 623-635.
Arguedas A, Kvaerner K, Liese J, Schilder AG, Pelton SI: Otitis media across nine countries: Disease burden and management. Int J Pediatr Otorhinolaryngol. 2010, 74: 1419-1424.
World Health Organization: Chronic suppurative otitis media; burden of illness and management options. 2004, Available at http://www.who.int/pbd/deafness/activities/hearing_care/otitis_media.pdf. Accessed 01 February 2011
Levine S, Dejsirilert S, Sangsuk L, Chantra S, Feikin DR, Dowell SF, Olsen SJ: Serotypes and antimicrobial resistance of Streptococcus pneumoniae in Thailand 2002–2004. Pediatr Infect Dis J. 2006, 25: 176-178.
Srifeungfung S, Tribuddharat C, Comerungsee S, Chatsuwan T, Treerauthanaweeraphong V, Rungnobhakhun P, Nunthapisud P, Chokephaibulkit K: Serotype coverage of pneumococcal conjugate vaccine and drug susceptibility of Streptococcus pneumoniae isolated from invasive or non-invasive diseases in central Thailand, 2006–2009. Vaccine. 2010, 28: 3440-3444.
Lynch JP, Zhanel GG: Streptococcus pneumoniae: epidemiology and risk factors, evolution of antimicrobial resistance, and impact of vaccines. Curr Opin Pulm Med. 2010, 16: 217-225.
Vergison A, Dagan R, Arguedas A, Bonhoeffer J, Cohen R, Dhooge I, Hoberman A, Liese J, Marchisio P, Palmu AA, Ray GT, Sanders EA, Simoes EA, Uhari M, van Eldere J, Pelton SI: Otitis media and its consequences: beyond the earache. Lancet Infect Dis. 2010, 10: 195-203.
Cohen R, Ovetchkine P, Gehanno P: Current approaches to otitis media. Curr Opin Infect Dis. 2001, 14: 337-342.
Syrjanen RK, Herva EE, Makela PH, Puhakka HJ, Auranen KJ, Takala AK, Kilpi TM: The value of nasopharyngeal culture in predicting the etiology of acute otitis media in children less than two years of age. Pediatr Infect Dis J. 2006, 25: 1032-1036.
Eldan M, Leibovitz E, Piglansky L, Raiz S, Press J, Yagupsky P, Leiberman A, Dagan R: Predictive value of pneumococcal nasopharyngeal cultures for the assessment of nonresponsive acute otitis media in children. Pediatr Infect Dis J. 2000, 19: 298-303.
WHO vaccine-preventable diseases: monitoring system 2012 global summary. [http://apps.who.int/immunization_monitoring/globalsummary/]
Wongsawat J, Chokephaibulkit K: Implication of pneumococcal conjugate vaccines to public health: Thailand perspective. J Med Assoc Thai. 2010, 93 (Suppl 5): S53-S60.
Muangchana C, Thamapornpilas P, Karnkawinpong O: Immunization policy development in Thailand: the role of the Advisory Committee on Immunization Practice. Vaccine. 2010, 28 (Suppl 1): A104-A109.
Dagan R: Appropriate treatment of acute otitis media in the era of antibiotic resistance. Paediatr Drugs. 2010, 12 (Suppl 1): 3-9.
Casey JR, Pichichero ME: Changes in frequency and pathogens causing acute otitis media in 1995–2003. Pediatr Infect Dis J. 2004, 23: 824-828.
Leibovitz E, Serebro M, Givon-Lavi N, Greenberg D, Broides A, Leiberman A, Dagan R: Epidemiologic and microbiologic characteristics of culture-positive spontaneous otorrhea in children with acute otitis media. Pediatr Infect Dis J. 2009, 28: 381-384.
Pai R, Gertz RE, Beall B: Sequential multiplex PCR approach for determining capsular serotypes of Streptococcus pneumoniae isolates. J Clin Microbiol. 2006, 44: 124-131.
Clinical and Laboratory Standards Institute: Performance Standards for Antimicrobial Disk Susceptibility Tests; Approved Standard - Tenth Edition (M02-A10). 2009, http://clsi.org/,
Li WC, Chiu NC, Hsu CH, Lee KS, Hwang HK, Huang FY: Pathogens in the middle ear effusion of children with persistent otitis media: implications of drug resistance and complications. J Microbiol Immunol Infect. 2001, 34: 190-194.
Rhodes J, Hyder JA, Peruski LF, Fisher C, Jorakate P, Kaewpan A, Dejsirilert S, Thamthitiwat S, Olsen SJ, Dowell SF, Chantra S, Tanwisaid K, Maloney SA, Baggett HC: Antibiotic use in Thailand: quantifying impact on blood culture yield and estimates of pneumococcal bacteremia incidence. Am J Trop Med Hyg. 2010, 83: 301-306.
Couloigner V, Levy C, Francois M, Bidet P, Hausdorff WP, Pascal T, Boucherat M, Bingen E, Mariani P, Pierrot S, Bille E, Carbonnelle E, Varon E, Cohen R: Pathogens implicated in acute otitis media failures after 7-valent pneumococcal conjugate vaccine implementation in France: distribution, serotypes, and resistance levels. Pediatr Infect Dis J. 2012, 31: 154-158.
Rerks-Ngarm S, Treleaven SC, Chunsuttiwat S, Muangchana C, Jolley D, Brooks A, Dejsirilert S, Warintrawat S, Guiver M, Kunasol P, Maynard JE, Biggs BA, Steinhoff M: Prospective population-based incidence of Haemophilus influenzae type b meningitis in Thailand. Vaccine. 2004, 22: 975-983.
Broker M: Burden of invasive disease caused by Haemophilus influenzae type b in Asia. Jpn J Infect Dis. 2009, 62: 87-92.
Shetty S, Cohen AL, Edmond K, Ojo L, Loo J, O'Loughlin R, Hajjeh R: A systematic review and critical evaluation of invasive Haemophilus influenzae type B disease burden studies in Asia from the last decade: lessons learned for invasive bacterial disease surveillance. Pediatr Infect Dis J. 2010, 29: 653-661.
Bluestone C: Terminology and Classification. Evidence-Based Otitis Media. Edited by: Bluestone C. 1999, Saint Louis: Hamilton, 85-103.
Naranjo L, Suarez JA, DeAntonio R, Sanchez F, Calvo A, Spadola E, Rodriguez N, Andrade O, Bertuglia F, Marquez N, Castrejon MM, Ortega-Barria E, Colindres RE: Non-capsulated and capsulated Haemophilus influenzae in children with acute otitis media in Venezuela: a prospective epidemiological study. BMC Infect Dis. 2012, 12: 40-
Rodgers GL, Arguedas A, Cohen R, Dagan R: Global serotype distribution among Streptococcus pneumoniae isolates causing otitis media in children: potential implications for pneumococcal conjugate vaccines. Vaccine. 2009, 27: 3802-3810.
Broides A, Dagan R, Greenberg D, Givon-Lavi N, Leibovitz E: Acute otitis media caused by Moraxella catarrhalis: epidemiologic and clinical characteristics. Clin Infect Dis. 2009, 49: 1641-1647.
Kim SH, Song JH, Chung DR, Thamlikitkul V, Yang Y, Wang H, Lu M, So TM, Hsueh PR, Yasin RM, Carlos CC, Pham HV, Lalitha MK, Shimono N, Perera J, Shibl AM, Baek JY, Kang CI, Ko KS, Peck KR: Changing trends in antimicrobial resistance and serotypes of Streptococcus pneumoniae isolates in Asian countries: an Asian Network for Surveillance of Resistant Pathogens (ANSORP) study. Antimicrob Agents Chemother. 2012, 56: 1418-1426.
Srifuengfung S, Chayakulkeeree M, Chokephaibulkit K, Tribuddharat C: Five-year study of antimicrobial susceptibility and beta-lactamase production in Haemophilus influenzae. Southeast Asian J Trop Med Public Health. 2007, 38: 732-736.
Prymula R, Peeters P, Chrobok V, Kriz P, Novakova E, Kaliskova E, Kohl I, Lommel P, Poolman J, Prieels JP, Schuerman L: Pneumococcal capsular polysaccharides conjugated to protein D for prevention of acute otitis media caused by both Streptococcus pneumoniae and non-typable Haemophilus influenzae: a randomised double-blind efficacy study. Lancet. 2006, 367: 740-748.
Tregnaghi MW, Sáez-Llorens X, López P, Abate H, Smith E, Pósleman A, Calvo A, Wong D, Cortes-Barbosa C, Ceballos A, Tregnaghi M, Sierra A, Rodriguez M, Troitiño M, Carabajal C, Falaschi A, Leandro A, Castrejón MM, Lepetic A, Lommel P, Hausdorff WP, Borys D, Ruiz Guiñazú J, Ortega-Barría E, Yarzábal JP, Schuerman L, on behalf of the COMPAS Group: Efficacy of PHiD-CV in Young Latin American Children: A Double-Blind, Randomized Controlled Trial. PLoS Med. 2014, 11 (6): e1001657-
Eskola J, Kilpi T, Palmu A, Jokinen J, Haapakoski J, Herva E, Takala A, Kayhty H, Karma P, Kohberger R, Siber G, Makela PH: Efficacy of a pneumococcal conjugate vaccine against acute otitis media. N Engl J Med. 2001, 344: 403-409.
Mrkvan T, Clarke C, Hausdorff WP: Should the next generation of pneumococcal conjugate vaccines (PCVs) contain serotype 3? Lessons learned and rediscovered. 2013, Denver, USA: Third Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC), Abstract B-498
Hausdorff WP, Yothers G, Dagan R, Kilpi T, Pelton SI, Cohen R, Jacobs MR, Kaplan SL, Levy C, Lopez EL, Mason EO, Syriopoulou V, Wynne B, Bryant J: Multinational study of pneumococcal serotypes causing acute otitis media in children. Pediatr Infect Dis J. 2002, 21: 1008-1016.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2431/14/157/prepub
The authors thank Drs Barbara Pelgrims, Véronique Mouton and Marie-Line Seret (XPE Pharma & Science c/o GlaxoSmithKline Vaccines) for editorial assistance and manuscript coordination and Dr Anna Dow (Freelance) for scientific writing support on behalf of the GlaxoSmithKline Group of companies.
GlaxoSmithKline Biologicals SA funded all costs associated with the study and with the development and publishing of the present manuscript. GM and SN declare no conflicts of interest. PI received an institutional grant and a travel grant from the GlaxoSmithKline group of companies. NS has received a grant, travel grant funding and payment for lectures from the GlaxoSmithKline group of companies. JYP and WPH are employees of the GlaxoSmithKline group of companies. WPH own stock in GlaxoSmithKline Biologicals and is co-holder of the patent for Prevnar 13™. YFL and MVD were previously employed by the GlaxoSmithKline group of companies and had stock options.
PI, YL and WPH participated in the conception and design of the study and together with NS, MKV, SN and GM contributed to the development of the protocol. PI, NS, SN and GM contributed to the acquisition of data. JYP (study and project statistician), PI, GM, NS, SN, YL and MKV contributed to data processing, to the statistical analysis and to the study report. MKV contributed to the interpretation of the statistical analysis and together with NS, WPH and YL to the development of the manuscript. All authors had full access to the data, read and reviewed drafts of the manuscripts and approved its final content.
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Intakorn, P., Sonsuwan, N., Noknu, S. et al. Haemophilus influenzae type b as an important cause of culture-positive acute otitis media in young children in Thailand: a tympanocentesis-based, multi-center, cross-sectional study. BMC Pediatr 14, 157 (2014). https://doi.org/10.1186/1471-2431-14-157
- Acute otitis media
- Streptococcus pneumoniae
- Haemophilus influenzae and antibiotic resistance