Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-27T21:43:51.966Z Has data issue: false hasContentIssue false

Antibiotics in treatment of peritonsillar infection: clindamycin versus penicillin

Published online by Cambridge University Press:  22 January 2021

F Hallgren*
Affiliation:
Department of Otorhinolaryngology Head and Neck Surgery, Södra Älvsborg Hospital, Borås, Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg University, Sweden
E Lindell
Affiliation:
Department of Otorhinolaryngology Head and Neck Surgery, Södra Älvsborg Hospital, Borås, Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg University, Sweden
B Nilsson-Helger
Affiliation:
Department of Otorhinolaryngology Head and Neck Surgery, Södra Älvsborg Hospital, Borås, Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg University, Sweden
A Lundqvist
Affiliation:
Department of Infectious Diseases, Södra Älvsborg Hospital, Borås, Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg University, Sweden
*
Author for correspondence: Dr Frida Hallgren, ENT Department, Södra Älvsborg Hospital, 501 82Borås, Sweden E-mail: frida.hallgren@vgregion.se

Abstract

Objective

This study aimed to compare antibiotic treatment with clindamycin versus penicillin V or G in terms of time to recovery and recurrence in patients with peritonsillar infection, including both peritonsillar cellulitis and peritonsillar abscess.

Method

This retrospective cohort study examined the records of 296 patients diagnosed with peritonsillar infection. Based on the ENT doctor's choice of antibiotics, patients were divided into clindamycin and penicillin groups.

Results

Mean number of days in follow up was 3.5 days in the clindamycin group and 3.4 days in the penicillin group. The recurrence rate within 2 months was 7 per cent in the clindamycin group and 4 per cent in the penicillin group.

Conclusion

This study found no significant differences in either recovery or recurrence between the groups. This supports the use of penicillin as a first-line treatment, considering the greater frequency of adverse effects of clindamycin shown in previous studies, as well as its profound collateral damage on the intestinal microbiota, resulting in antibiotic resistance.

Type
Main Articles
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

Dr F Hallgren takes responsibility for the integrity of the content of the paper

References

Paras, ML. Acute pharyngitis, tonsillitis, and peritonsillar abscess. In: Durand, ML, Deschler, DG, eds. Infections of the Ear Nose, Throat, and Sinuses. New York: Springer, 2018Google Scholar
Risberg, S, Engfeldt, P, Hugosson, S. Incidence of peritonsillar abscess and relationship to age and gender: retrospective study. Scand J Infect Dis 2008;40:792–6CrossRefGoogle ScholarPubMed
Powell, J, Wilson, JA. An evidence-based review of peritonsillar abscess. Clin Otolaryngol 2012;37:136–45CrossRefGoogle ScholarPubMed
Wiksten, J, Blomgren, K, Eriksson, T, Guldfred, L, Bratt, M, Pitkaranta, A. Variations in treatment of peritonsillar abscess in four Nordic countries. Acta Otolaryngol 2014;134:813–7CrossRefGoogle ScholarPubMed
Chang, BA, Thamboo, A, Burton, MJ, Diamond, C, Nunez, DA. Needle aspiration versus incision and drainage for the treatment of peritonsillar abscess. Cochrane Database Syst Rev 2016;(12):CD006287CrossRefGoogle ScholarPubMed
Mehanna, HM, Al-Bahnasawi, L, White, A. National audit of the management of peritonsillar abscess. Postgrad Med J 2002;78:545–8CrossRefGoogle Scholar
Simon, LM, Matijasec, JW, Perry, AP, Kakade, A, Walvekar, RR, Kluka, EA. Pediatric peritonsillar abscess: Quinsy ie versus interval tonsillectomy. Int J Pediatr Otorhinolaryngol 2013;77:1355–8CrossRefGoogle ScholarPubMed
Brook, I. Aerobic and anaerobic bacteriology of peritonsillar abscess in children. Acta Paediatr Scand 1981;70:831–5CrossRefGoogle ScholarPubMed
Klug, TE, Henriksen, JJ, Fuursted, K, Ovesen, T. Significant pathogens in peritonsillar abscesses. Eur J Clin Microbiol Infect Dis 2011;30:619–27CrossRefGoogle ScholarPubMed
Acharya, A, Gurung, R, Khanal, B, Ghimire, A. Bacteriology and antibiotic susceptibility pattern of peritonsillar abscess. J Nepal Med Assoc 2010;49:139–42CrossRefGoogle ScholarPubMed
Powell, EL, Powell, J, Samuel, JR, Wilson, JA. A review of the pathogenesis of adult peritonsillar abscess: time for a re-evaluation. J Antimicrob Chemother 2013;68:1941–50CrossRefGoogle ScholarPubMed
Klug, TE. Peritonsillar abscess: clinical aspects of microbiology, risk factors, and the association with parapharyngeal abscess. Dan Med J 2017;64:B5333Google ScholarPubMed
Repanos, C, Mukherjee, P, Alwahab, Y. Role of microbiological studies in management of peritonsillar abscess. J laryngol Otol 2009;123:877–9CrossRefGoogle ScholarPubMed
Fairbanks, DNF. Pocket guide to antimicrobial therapy in otolaryngology-head and neck surgery, 13th edn. In: https://www.entnet.org/content/pocket-guide-antimicrobial-therapy-otolaryngology [30 July 2020]Google Scholar
Tuner, K, Nord, CE. Impact on peritonsillar infections and microflora of phenoxymethylpenicillin alone versus phenoxymethylpenicillin in combination with metronidazole. Infection 1986;14:129–33CrossRefGoogle ScholarPubMed
Wiksten, JE, Pitkaranta, A, Blomgren, K. Metronidazole in conjunction with penicillin neither prevents recurrence nor enhances recovery from peritonsillar abscess when compared with penicillin alone: a prospective, double-blind, randomized, placebo-controlled trial. J Antimicrob Chemother 2016;71:1681–7CrossRefGoogle ScholarPubMed
Kieff, DA, Bhattacharyya, N, Siegel, NS, Salman, SD. Selection of antibiotics after incision and drainage of peritonsillar abscesses. Otolaryngol Head Neck Surg 1999;120:5761CrossRefGoogle ScholarPubMed
DeMuri, GP, Sterkel, AK, Kubica, PA, Duster, MN, Reed, KD, Wald, ER. Macrolide and clindamycin resistance in group a streptococci isolated from children with pharyngitis. Pediatr Inf Dis J 2017;36:342–4CrossRefGoogle Scholar
Plainvert, C, Martin, C, Loubinoux, J, Touak, G, Dmytruk, N, Collobert, G et al. Highly virulent M1 Streptococcus pyogenes isolates resistant to clindamycin. Med Mal Infect 2015;45:470–4CrossRefGoogle ScholarPubMed
Pesola, AK, Sihvonen, R, Lindholm, L, Patari-Sampo, A. Clindamycin resistant emm33 Streptococcus pyogenes emerged among invasive infections in Helsinki metropolitan area, Finland, 2012 to 2013. Euro Surveill 2015;20:21117CrossRefGoogle Scholar
Sowerby, LJ, Hussain, Z, Husein, M. The epidemiology, antibiotic resistance and post-discharge course of peritonsillar abscesses in London, Ontario. J Otolaryngol 2013;42:5Google ScholarPubMed
Macris, MH, Hartman, N, Murray, B, Klein, RF, Roberts, RB, Kaplan, EL et al. Studies of the continuing susceptibility of group A streptococcal strains to penicillin during eight decades. Pediatr Inf Dis J 1998;17:377–81CrossRefGoogle Scholar
Hanage, WP, Shelburne, SA. Streptococcus pyogenes with reduced susceptibility to beta-lactams: how big an alarm bell? Clin Infect Dis 2020;71:205–6CrossRefGoogle ScholarPubMed
Abraham, T, Sistla, S. Trends in antimicrobial resistance patterns of Group A streptococci, molecular basis and implications. Indian J Med Microbiol 2018;36:186–91CrossRefGoogle Scholar
Rashid, MU, Zaura, E, Buijs, MJ, Keijser, BJ, Crielaard, W, Nord, CE, et al. Determining the long-term effect of antibiotic administration on the human normal intestinal microbiota using culture and pyrosequencing methods. Clin Infect Dis 2015;60(suppl 2):S7784CrossRefGoogle ScholarPubMed
Zimmermann, P, Curtis, N. The effect of antibiotics on the composition of the intestinal microbiota – a systematic review. J Infect 2019;79:471–89CrossRefGoogle ScholarPubMed
Brindle, R, Williams, OM, Davies, P, Harris, T, Jarman, H, Hay, AD et al. Adjunctive clindamycin for cellulitis: a clinical trial comparing flucloxacillin with or without clindamycin for the treatment of limb cellulitis. BMJ open 2017;7:e013260CrossRefGoogle ScholarPubMed
Slimings, C, Riley, TV. Antibiotics and hospital-acquired Clostridium difficile infection: update of systematic review and meta-analysis. J Antimicrob Chemother 2014;69:881–91CrossRefGoogle ScholarPubMed
Smits, WK, Lyras, D, Lacy, DB, Wilcox, MH, Kuijper, EJ. Clostridium difficile infection. Nat Rev Dis Primers 2016;2:16020CrossRefGoogle ScholarPubMed
Thornhill, MH, Dayer, MJ, Prendergast, B, Baddour, LM, Jones, S, Lockhart, PB. Incidence and nature of adverse reactions to antibiotics used as endocarditis prophylaxis. J Antimicrob Chemother 2015;70:2382–8CrossRefGoogle ScholarPubMed
Brown, KA, Khanafer, N, Daneman, N, Fisman, DN. Meta-analysis of antibiotics and the risk of community-associated Clostridium difficile infection. Antimicrob Agents Chemother 2013;57:2326–32CrossRefGoogle ScholarPubMed
Thornhill, MH, Dayer, MJ, Durkin, MJ, Lockhart, PB, Baddour, LM. Risk of adverse reactions to oral antibiotics prescribed by dentists. J Dent Res 2019;98:1081–7CrossRefGoogle ScholarPubMed
STRAMA. The Swedish strategic programme against antibiotic resistance: antibiotic treatment recommendations. In: http://strama.se/behandlingsrekommendationer/2019 [30 July 2020]Google Scholar
Munck, H, Jorgensen, AW, Klug, TE. Antibiotics for recurrent acute pharyngo-tonsillitis: systematic review. Eur J Clin Microbiol Infect Dis 2018;37:1221–30CrossRefGoogle ScholarPubMed