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A Boy With Sudden-Onset Left Otalgia and Otorrhea

Author:
Raul G. Lopez Valle, MD, MPH

Granberry Medical Care PLLC, Humble, Texas

Citation:
Lopez Valle RG. A boy with sudden-onset left otalgia and otorrhea. Consultant. 2019;59(8):237-238, 256.


 

A 9-year-old boy was brought to a primary care office by his mother. The patient had complained of self-limited sudden left otalgia the day before his visit. The mother was unsure whether the patient had had fever or not. However, she noticed thick otorrhea from the left ear. The patient had received only acetaminophen for the pain. His medical history was positive only for hyperopia and attention-deficit/hyperactivity disorder, and he was fully up-to-date with immunizations.

The physical examination showed vital signs within the normal ranges. The patient denied pain during passive traction to the left pinna. A sample of the discharge was sent for culture and identification. Otoscopy examination showed a foul-smelling yellowish discharge in the left ear canal, without erythema of the canal walls, and a minuscule puncture on a mildly erythematous tympanic membrane. The external ear was later examined using a Wood lamp (Figure).

Wood lamp exam

 

Answer: AOM due to P aeruginosa with tympanic perforation

The attending physician, based on antibiotic susceptibility results, began treatment with ciprofloxacin, 0.3% plus fluocinolone acetonide 0.025% otic solution twice daily for 7 days and asked the parent to bring her son back for a follow-up visit in 3 days.

During the follow-up visit, the patient did not present with ear discharge, and the tympanic perforation had almost closed. Culture test results identified P aeruginosa.

DISCUSSION

AOM is one of the most frequent bacterial infections seen in children worldwide.1-4 It affects up to 4 of 5 children by the age of 3 years.2,4 Middle ear bacterial infections frequently originate from the upper respiratory tract due to asymptomatic nasopharyngeal colonization.5,6 Because of a shorter and more horizontal eustachian tube, children are more prone to develop AOM.5 Spontaneous otorrhea occurs in 3.3% to 52% of children with AOM.4

After the introduction of the pneumococcal conjugated vaccine, which has reduced the burden of pneumococcal disease,3,4 the microbiology of the condition has shifted, and the most commonly involved bacteria are Haemophilus influenzae, Streptococcus pneumoniae, Streptococcus pyogenes, Moraxella catarrhalis, and Staphylococcus aureus.1,3,4,7,8 P aeruginosa is not frequently seen as the pathologic organism of AOM in the developed world, but it is prevalent in developing countries, where can be the culprit in 14.5% to 60% of cases.5,9-14 It frequently causes otorrhea,14 and most cases (32.5%-49%) occur in those younger than 10 years.5,14

P aeruginosa is an aerobic, gram-negative, motile, non–spore-forming, oxidase-positive, and lactose non-fermenting bacterium that produces pyocyanin and pyoverdine,15 both of which are water-soluble pigments that fluoresce under a Wood ultraviolet lamp (which emits a light radiation between 320 and 400 nm, with a peak at 365 nm) that gives the typical yellow-green color.15,16 P aeruginosa fluorescence is detected if the bacterial load exceeds 105 colony forming units/cm2.15

The susceptibility of P aeruginosa to ciprofloxacin ranges from 85% to 97%,5,13,17,18 with 2% of strains being resistant.18 However, the widespread use of otic drops has promoted the emergence of P aeruginosa resistant to this antibiotic.19

The median time for otorrhea cessation using ciprofloxacin/dexamethasone is 4 days, and the improved/cured rate is 93.7% at day 3 and 96.2% at day 11.17

REFERENCES:

  1. Kung Y-H, Chiu N-C, Lee K-S, et al. Bacterial etiology of acute otitis media in the era prior to universal pneumococcal vaccination in Taiwanese children. J Microbiol Immunol Infect. 2014;47(3):239-244.
  2. Al-Mazrou KA, Shibl AM, Kandeil W, Pirçon J-Y, Marano C. A prospective, observational, epidemiological evaluation of the aetiology and antimicrobial susceptibility of acute otitis media in Saudi children younger than 5 years of age. J Epidemiol Glob Health. 2014;4(3):231-238.
  3. Abdelnour A, Arguedas A, Dagan R, Soley C, et al. Etiology and antimicrobial susceptibility of middle ear fluid pathogens in Costa Rican children with otitis media before and after the introduction of the 7-valent pneumococcal conjugate vaccine in the National Immunization Program: acute otitis media microbiology in Costa Rican children. Medicine (Baltimore). 2015; 94(2):e320.
  4. Chen Y-J, Hsieh Y-C, Huang Y-C, Chiu C-H. Clinical manifestations and microbiology of acute otitis media with spontaneous otorrhea in children. J Microbiol Immunol Infect. 2013;46(5):382-388.
  5. Elmanama AA, Abu Tayyem NE, Nassr Allah SA. The bacterial etiology of otitis media and their antibiogram among children in Gaza Strip, Palestine. Egypt J Ear Nose Throat Allied Sci. 2014;15(2):87-91.
  6. Casey JR, Kaur R, Friedel VC, Pichichero ME. Acute otitis media otopathogens during 2008 to 2010 in Rochester, New York. Pediatr Infect Dis J. 2013;32(8):805-809.
  7. Marchisio P, Bianchini S, Baggi E, et al. A retrospective evaluation of microbiology of acute otitis media complicated by spontaneous otorrhea in children living in Milan, Italy. Infection. 2013;41(3):629-635.
  8. Mayanskiy N, Alyabieva N, Ponomarenko O, et al. Bacterial etiology of acute otitis media and characterization of pneumococcal serotypes and genotypes among children in Moscow, Russia. Pediatr Infect Dis J. 2015;34(3):255-260.
  9. Seid A, Deribe F, Ali K, Kibru G. Bacterial otitis media in all age group of patients seen at Dessie referral hospital, North East Ethiopia. Egypt J Ear Nose Throat Allied Sci. 2013;14(2):73-78.
  10. DeAntonio R, Yarzabal J-P, Cruz JP, Schmidt JE, Kleijnen J. Epidemiology of otitis media in children from developing countries: a systematic review. Int J Pediatr Otorhinolaryngol. 2016;85:65-74.
  11. Ilechukwu GC, Ilechukwu CA, Ubesie AC, Okoroafor I, Ezeanolue BC, Ojinnaka NC. Bacterial agents of the discharging middle ear among children seen at the University of Nigeria Teaching Hospital, Enugu. Pan Afr Med J. 2017;26:87.
  12. Ogbogu PI, Eghafona NO, Ogbogu MI. Microbiology of otitis media among children attending a tertiary hospital in Benin City, Nigeria. J Public Health Epidemiol. 2013;5(7):280-284.
  13. Mansoor T, Musani MA, Khalid G, Kamal M. Pseudomonas aeruginosa in chronic suppurative otitis media: sensitivity spectrum against various antibiotics in Karachi. J Ayub Med Coll Abbottabad. 2009;21(2):120-123.
  14. Gul S, Eraj A, Ashraf Z. Pseudomonas aeruginosa: a common causative agent of ear infections in South Asian children. Int J Curr Microbial Appl Sci. 2014;3(6):156-160.
  15. Gupta LK, Singhi MK. Wood’s lamp. Indian J Dermatol Venereol Leprol. 2004;70(2):131-135.
  16. Cardillo H, Kohler J, Kriner E, Mehta K. Applications of Wood’s lamp technology to detect skin infections in resource-constrained settings. Presented at: IEEE Global Humanitarian Technology Conference (GHTC 2014). October 10-14, 2014; San Jose, CA. https://ieeexplore.ieee.org/document/6970337. Accessed January 28, 2019.
  17. Roland PS, Kreisler LS, Reese B, et al. Topical ciprofloxacin/dexamethasone otic suspension is superior to ofloxacin otic solution in the treatment of children with acute otitis media with otorrhea through tympanostomy tubes. Pediatrics. 2004;113(1 pt 1):e40-e46.
  18. Roland PS, Parry, DA, Stroman DW. Microbiology of acute otitis media with tympanostomy tubes. Otolaryngol Head Neck Surg. 2005;133(4):585-595.
  19. Jang CH, Park SY. Emergence of ciprofloxacin-resistant pseudomonas in pediatric otitis media. Int J Pediatr Otorhinolaryngol. 2003;67(4):313-316.