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Seasonal variation of Pseudomonas aeruginosa in culture positive otitis externa in South East England

Published online by Cambridge University Press:  06 July 2018

A. Villedieu
Affiliation:
Department of Microbiology, Mid Essex Hospital Services NHS Trust, Chelmsford, UK
E. Papesh
Affiliation:
Department of Ear Nose and Throat, Mid Essex Hospital Service NHS Trust, Chelmsford, UK
S. E. Weinberg
Affiliation:
Department of Microbiology, Mid Essex Hospital Services NHS Trust, Chelmsford, UK
L. Teare
Affiliation:
Department of Microbiology, Mid Essex Hospital Services NHS Trust, Chelmsford, UK
J. Radhakrishnan
Affiliation:
Department of Anesthetics, Mid Essex Hospital Services NHS Trust, Chelmsford, UK
W. F. Elamin*
Affiliation:
Department of Microbiology, Mid Essex Hospital Services NHS Trust, Chelmsford, UK
*
Author for correspondence: W. F. Elamin, E-mail: [email protected]
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Abstract

Otitis externa is the inflammation of the external auditory canal. The disease is common and shows a seasonal variation with a greater incidence in warmer months. Pseudomonas aeruginosa is a common pathogen in otitis externa and in this retrospective study, we show a corresponding seasonal variation in the proportional incidence of P. aeruginosa isolates from otitis externa in South East England. In total 7770 patients were diagnosed with otitis externa over a period of 9 years from January 2008 to December 2016. P. aeruginosa was isolated from 2802 patients (proportional incidence of 36%). Incidence was higher in the months of August, September and October and in patients between 5 and 15 years of age. We postulate a combination of increased contact with water during warm weather in the holiday season and increased rainfall in the preceding season as a putative mechanism for the seasonal trends.

Type
Short Paper
Copyright
Copyright © Cambridge University Press 2018 

Otitis externa is the inflammation of the external auditory canal. It is a common problem in general practice [Reference Rowlands1]. Pseudomonas aeruginosa and Staphylococcus aureus are common pathogens in otitis externa [Reference Jayakar, Sanders and Jones2, Reference Ninkovic, Dullo and Saunders3].

Otitis externa displays a characteristic seasonal variation with a greater disease burden in warmer months [Reference Rowlands1, Reference Agius, Pickles and Burch4]. However, this seasonal variation in disease incidence has not been correlated to seasonal trends in the proportional incidence of pathogen isolates. In this retrospective, observational study, we show a seasonal variation in the proportional incidence of P. aeruginosa isolates in otitis externa and correlate the observed variation to changes in environmental conditions.

After institutional ethical approval, records of patients with the diagnosis of otitis externa on the sample request forms from January 2006 to December 2016 at Mid Essex Hospitals NHS Trust were analysed. Isolates were obtained from ear swabs cultured on agar following the standard operational procedure for ear swabs; based on the UK standards for microbiology investigations [5]. The proportional incidence of P. aeruginosa was the ratio of culture-positive patients with P. aeruginosa to the total number of patients with any other species isolate. Peak incidence date was estimated using Edward's method [Reference Edwards6]. Environmental data for the study period was obtained from the UK Meterological Office. The number of rainy days was correlated with the number of P. aeruginosa isolates. Statistical analysis was performed using IBM SPSS Statistics for Windows, Version 23.0.

In the 9-year study period, 7770 patients had a positive bacterial culture. The commonest isolate was P. aeruginosa (n = 2802, proportional incidence 36%), followed by S. aureus (n = 1850, 24%), Aspergillus and Candida sp. (n = 1410, 18%), Enterobacteriaceae (n = 1289, 17%), anaerobic bacteria (n = 1212, 16%), beta-haemolytic streptococci (n = 811, 10%) and the Haemophilus, Streptococus pneumoniae, Moraxella group (n = 610, 8%). More than one organism was isolated from 3014 patients (39%).

The average proportional incidence of P. aeruginosa was 25.9% (95% CI 25.0–26.9). However, there was a clear seasonal trend every year with a peak during the months of August–November (Fig. 1). No seasonal variation was evident for the other species isolates.

Fig. 1. Monthly incidence of P. aeruginosa in otitis externa infection from 2008 to 2016.

The proportional incidence of P. aeruginosa also showed age-related differences, with the greatest incidence in the 45–65 age group (25%), followed by over 65 and the 5 to 15 age groups (19% and 18% respectively). The seasonal variation in proportional incidence was clearly observed in 5–15 age group with peaks in August and September (21% and 14% respectively, compared with a yearly average of 8% (95 CI 7.1–9.6)).

The number of P. aeruginosa isolates each month correlated with the number of rainy days (r = 0.7). However, there was no correlation between the total number of patients with otitis externa and environmental factors (r = 0.2).

The relationship between diseases and seasons have been recognised since antiquity, with Hippocrates postulating changes in environmental factors such as air, water and food as explanatory causes [Reference Fisman7]. Our observational study confirms previously documented increases in otitis externa infections during summer months and the relative contributions of different agents to this incidence [Reference Rowlands1Reference Agius, Pickles and Burch4]. We have, for the first time, identified P. aeruginosa as a possible causal agent for the seasonal variation in otitis externa. This seasonal variation in the proportional incidence of P. aeruginosa occurs mainly in the 5–15 age group and correlated with the number of rainy days. These associations have only been sparsely described in the literature [Reference Rowlands1, Reference Roland and Stroman8]. Neither the seasonal variation nor the environmental association was observed with other putative pathogens.

Predisposing factors for otitis externa include the presence of moisture, long exposure to moisture with an increased risk of maceration and cerumen loss, contact with contaminated water and increased water temperatures that promote rapid growth of the organism [Reference Wang9, Reference Lieberthal10]. These factors provide a clear causal mechanism for the observed association between the proportional incidence of P. aeruginosa and the number of rainy days. The seasonal variation in the 5–15 age group can be explained by behavioural changes leading to increased exposure to water in the warm summer months.

The associations described in the study have practical relevance in choosing empirical antibiotics for otitis externa, especially in younger patients in late summer months. In the absence of a bacterial culture, empirical treatment targeting P. aeruginosa and S. aureus would cover approximately 60% of the isolates in otitis externa.

Acknowledgements

This research received no specific grant from any funding agency, commercial or not-for-profit sectors.

Conflict of interest

We have no conflicts of interest to disclose.

References

1.Rowlands, S et al. (2001) Otitis externa in UK general practice: a survey using the UK general practice research database. British Journal of General Practice 51, 533538.Google Scholar
2.Jayakar, R, Sanders, J and Jones, E (2014) A study of acute otitis externa at Wellington hospital, 2007–2011. Australasian Medical Journal 7, 392399.Google Scholar
3.Ninkovic, G, Dullo, V and Saunders, NC (2008) Microbiology of otitis externa in the secondary care in United Kingdom and antimicrobial sensitivity. Auris, Nasus, Larynx 35, 480484.Google Scholar
4.Agius, AM, Pickles, JM and Burch, KL (1992) A prospective study of otitis externa. Clinical Otolaryngology and Allied Sciences 17, 150154.Google Scholar
5.Public Health England. (2014) UK Standards for Microbiology Investigations: Investigations of ear Infections and Associated Specimens. London: Standards Unit, Microbiology Services, PHE, B1, pp. 118. Available at https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/343919/B_1i9.pdf (Accessed 1 May 2018).Google Scholar
6.Edwards, JH (1961) The recognition and estimation of cyclic trends. Annals of Human Genetics 25, 8387.Google Scholar
7.Fisman, DN (2007) Seasonality of infectious diseases. Annual Review of Public Health 28, 127143.Google Scholar
8.Roland, PS and Stroman, DW (2002) Microbiology of acute otitis externa. The Laryngoscope 112, 11661177.Google Scholar
9.Wang, MC et al. (2005) Ear problems in swimmers. Journal of the Chinese Medical Association 68, 347352.Google Scholar
10.Lieberthal, AS et al. (2013) The diagnosis and management of acute otitis media. Pediatrics 131, e964e999.Google Scholar
Figure 0

Fig. 1. Monthly incidence of P. aeruginosa in otitis externa infection from 2008 to 2016.