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Review

Cephalosporins in overcoming β-lactamase-producing bacteria and preservation of the interfering bacteria in the treatment of otitis, sinusitis and tonsillitis

Pages 939-950 | Published online: 10 Jan 2014

References

  • Brook I. The role of β-lactamase-producing bacteria in the persistence of streptococcal tonsillar infection. Rev. Inf. Dis.6, 601–607 (1984).
  • Doern GV. Resistance among problem respiratory pathogens in pediatrics. Pediatr. Infect. Dis. J.14, 420–423 (1995).
  • Richter SS, Brueggemann AB, Huynh HK et al. A 1997–1998 National Surveillance Study, Moraxella catarrhalis and Haemophilus influenzae antimicrobial resistance in 34 US institutions. Int. J. Antimicrob. Agents13, 99–107 (1999).
  • Brook I, Calhoun L, Yocum P. β-lactamase-producing isolates of Bacteroides species from children. Antimicrob. Agents Chemother.18, 264–266 (1980).
  • Brook I, Pazzaglia G, Coolbaugh JC, Walker RI. In vivo protection of group A β-hemolytic streptococci by β-lactamase producing Bacteroides species. J. Antimicrob. Chemother.12, 599–606 (1983).
  • Brook I, Pazzaglia G, Coolbaugh JC, Walker RI. In vivo protection of penicillin susceptible Bacteroides melaninogenicus from penicillin by facultative bacteria which produce β-lactamase. Can. J. Microbiol.30, 98–104 (1984).
  • Simon HM, Sakai W. Staphylococcal anatagosim to penicillin group therapy of hemolytic streptococcal pharyngeal infection, effect of oxacillin. Pediatrics31, 463–469 (1963).
  • Scheifele DW, Fussell SJ. Frequency of ampicillin resistant Haemophilus parainfluenzae in children. J. Infect. Dis.143, 495–498 (1981).
  • Brook I, Yocum P. In vitro protection of group A β-hemolytic streptococci from penicillin and cephalothin by Bacteroides fragilis.Chemotherapy29, 18–23 (1983).
  • Brook I. Presence of β-lactamase-producing bacteria and β-lactamase activity in abscesses. Am. J. Clin. Pathol.86, 97–101 (1986).
  • Brook I. Quantitative cultures and β-lactamase activity in chronic suppurative otitis media. Ann. Otol. Rhinol. Laryngol.98, 293–297 (1989).
  • Brook I, Yocum P. Bacteriology and β-lactamase activity in ear aspirates of acute otitis media that failed amoxicillin therapy. Pediatr. Infect. Dis. J.14, 805–808 (1995).
  • O’Keefe, JP, Tally FP, Barza M, Gorbach SL. Inactivation of penicillin-G during experimental infection with Bacteroides fragilis.J. Infect. Dis.137, 437–442 (1978).
  • Brook I, Yocum P, Frazier EH. Bacteriology and β-lactamase activity in acute and chronic maxillary sinusitis. Arch. Otolaryngol. Head Neck Surg.122, 418–422 (1996).
  • Brook I, Yocum P, Friedman EM. Aerobic and anaerobic flora recovered from tonsils of children with recurrent tonsillitis. Ann. Otol. Rhinol. Laryngol.90, 261–263 (1981).
  • Brook I, Yocum P. Quantitative measurement of β-lactamase levels in tonsils of children with recurrent tonsillitis. Acta Otolaryngol Scand.98, 456–459 (1984).
  • Brook I, Gober AE. Monthly changes in the rate of recovery of penicillin-resistant organisms from children. Pediatr. Infect. Dis. J.16, 255–257 (1997).
  • Brook I. β-lactamase-producing bacteria recovered after clinical failures with various penicillin therapy. Arch. Otolaryngol.110, 228–231 (1984).
  • Brook I, Gober AE. Emergence of β-lactamase-producing aerobic and anaerobic bacteria in the oropharynx of children following penicillin chemotherapy. Clin. Pediatr.23, 338–341 (1984).
  • Brook I. Emergence and persistence of β-lactamase-producing bacteria in the oropharynx following penicillin treatment. Arch. Otolaryngol. Head Neck Surg.114, 667–670 (1988).
  • Tuner K, Nord CE. Emergence of β-lactamase producing microorganisms in the tonsils during penicillin treatment. Eur. J. Clin. Microb.5, 399–404 (1986).
  • Brook I, Gober AE. Prophylaxis with amoxicillin or sulfisoxazole for otitis media, effect on the recovery of penicillin-resistant bacteria from children. Clin. Infect. Dis.22, 143–145 (1996).
  • Pichichero ME, Casey JR. The evidence base for cephalosporin superiority over penicillin in streptococcal pharyngitis. Diagn. Microbiol. Infect. Dis.57(3 Suppl.), S39–S45 (2007).
  • Knudsin RB, Miller JM. Significance of the Staphylococcus aureus carrier state in the treatment of disease due to group A streptococci. N. Engl. J. Med.271, 1395–1397 (1964).
  • Kovatch AL, Wald ER, Michaels RH. β-lactamase-producing Branhamella catarrhalis causing otitis media in children. J. Pediatr.102, 260–263 (1983).
  • Brook I, Yocum P. Bacteriology of chronic tonsillitis in young adults. Arch. Otolaryngol.110, 803–805 (1984).
  • Reilly S, Timmis P, Beeden AG, Willis AT. Possible role of the anaerobe in tonsillitis. J. Clin. Path.34, 542–547 (1981).
  • Chagollan JR, Macias JR, Gil JS. Flora indigena de las amigalas. Invest. Med. Int.11, 36–43 (1984).
  • Tuner K, Nord CE. β lactamase-producing microorganisms in recurrent tonsillitis. Scand. J. Infect. Dis.(Suppl.) 39, 83–85 (1983).
  • Brook I. Role of β-lactamase-producing bacteria in penicillin failure to eradicate group A streptococci. Pediatr. Infect. Dis.4, 491–495 (1985).
  • Roos K, Grahn E, Holn SE. Evaluation of β-lactamase activity and microbial interference in treatment failures of acute streptococcal tonsillitis. Scand. J. Infect. Dis.18, 313–318 (1986).
  • Brook I, Gober AE. Resistance to antimicrobials used for the therapy of otitis and sinusitis, effect of previous antimicrobial therapy and smoking. Ann. Otol. Rhinol. Laryngol.108, 645–647 (1999).
  • Heimdahl A, Von Konow L, Nord CE. Isolations of β-lactamase-producing Bacteroides strains associated with clinical failures with penicillin treatment of human orofacial infections. Arch. Oral Biol.25, 288–292 (1980).
  • Brook I, Hirokawa R. Treatment of patients with recurrent tonsillitis due to group A β-hemolytic streptococci. A prospective randomized study comparing penicillin, erythromycin and clindamycin. Clin. Pediatr.24, 331–336 (1985).
  • Casey JR, Pichichero ME. Meta-analysis of cephalosporins versus penicillin for treatment of group A strepharyngo-tonsillitisococcal tonsillopharyngitis in adults. Clin. Infect. Dis.38, 1526–1534 (2004).
  • Pichichero ME. Cephalosporins are superior to penicillin for treatment of strepharyngo-tonsillitisococcal tonsillopharyngitis, is the difference worth it? Pediatr. Infect. Dis. J.12, 268–274 (1993).
  • Brook I. Treatment of patients with acute recurrent tonsillitis due to group A β-haemolytic streptococci, a prospective randomized study comparing penicillin and amoxicillin/clavulanate potassium. J. Antimicrob. Chemother.24, 227–233 (1989).
  • Kaplan EL, Johnson DR. Eradication of group A streptococci from the upper respiratory tract by amoxicillin with clavulanate after oral penicillin V treatment failure. J. Pediatr.113, 400–403 (1988).
  • Casey JR, Pichichero ME. Meta-analysis of cephalosporin versus penicillin treatment of group A streptococcal tonsillopharyngitis in children. Pediatrics.113, 866–882 (2004).
  • Casey JR, Pichichero ME. Meta-analysis of cephalosporins versus penicillin for treatment of group A streptococcal tonsillopharyngitis in adults. Clin. Infect. Dis.38, 1526–1534 (2004).
  • Brook I. Microbiology and principles of antimicrobial therapy for head and neck infections. Infect. Dis. Clin. North Am.21, 355–391 (2007).
  • Edwards CA, Parrett AM. Intestinal flora during the first months of life, new perspectives. Br. J. Nutr.88(Suppl. 1), S11–S18 (2002).
  • Bibel DJ, Aly R, Bayles C, Strauss WG, Shinefield HR, Maibach HI. Competetive adherence as a mechanism of bacterial interference. Can. J. Microbiol.29, 700–703 (1983).
  • Smith H. The revival of interest in mechanisms of bacterial pathogenicity. Biol. Rev.70, 277–316 (1995).
  • Drider D, Fimland G, Hechard Y, McMullen LM, Prevost H. The continuing story of class IIa bacteriocins. Microbiol. Mol. Biol. Rev.70, 564–582 (2006).
  • Uehara Y, Agematsu K, Kikuchi K et al. Secretory IgA, salivary peroxidase, and catalase-mediated microbicidal activity during hydrogen peroxide catabolism in viridans streptococci, pathogen coaggregation. J. Infect. Dis.194, 98–107 (2006).
  • Brook I. The role of bacterial interference in otitis, sinusitis and tonsillitis. Otolaryngol. Head Neck Surg.133, 139–146 (2005).
  • Roos K, Grahm E, Lind L, Holm S. Treatment of recurrent streptococcal tonsillitis by recolonization with α-streptococci. Eur. J. Clin. Microbiol. Infect. Dis.8, 318–319 (1989).
  • Crow CC, Sandera WE Jr, Longley S. Bacterial interference. II. Role of the normal throat flora in prevention of colonization by group A Streptococcus. J. Infect. Dis.128, 527–532 (1973).
  • Sanders CC, Sanders WE Jr, Harrowe DJ. Bacterial interference, effects of oral antibiotics on the normal throat flora and its ability to interfere with group A streptococci. Infect. Immun.13, 808–812 (1976).
  • Sanders CC, Nelson GE, Sanders WE. Bacterial interference, IV, epidemiologic determinants of the antagonistic activity of the normal throat flora against group A streptococci. Infect. Immun.16, 599–603 (1977).
  • Beck A. Interference by an α-hemolytic streptococcus of β-hemolytic pathogenic streptococci. Inflammation3, 463–465 (1979).
  • Roos K, Grahn E, Holm SE. Evaluation of β-lactamase activity and microbial interference in treatment failures of acute streptococal tonsillitis. Scand. J. Infect. Dis.18, 313–319 (1986).
  • Fujimori I, Kikushima K, Hisamatsu K, Nozawa I, Goto R, Murakami Y. Interaction between oral α-streptococci and group A streptococci in patients with tonsillitis. Ann. Otol. Rhinol. Laryngol.106, 571–574 (1997).
  • Grahn E, Holm SE. Bacterial interference in the throat flora during a streptococcal tonsillitis outbreak in an apartment house area. Zentralblatt. Bakteriol. Parasitenkd. Infekt. Hyg.256, 72–79 (1983).
  • Brook I, Gober AE. Role of bacterial interference and β-lactamase-producing bacteria in the failure of penicillin to eradicate group A streptococcal pharyngotonsillitis. Arch. Otolaryngol. Head Neck Surg.121, 1405–1409 (1995).
  • Brook I, Gober AE. Bacterial interference by aerobic and anaerobic bacteria in children with recurrent group A β-hemolytic streptococcal tonsillitis. Arch. Otolaryngol. Head Neck Surg.125, 552–554 (1999).
  • Grahn E, Holm SE, Roos K. Penicillin tolerance in β-streptococci isolated from patients with tonsillitis. Scand. J. Infect. Dis.19, 421–426 (1987).
  • Brook I, Gillmore JD. Evaluation of bacterial interference and β-lactamase production in the management of experimental infection with group A β-hemolytic streptococci. Antimicrob. Agents. Chemotherapy37, 1452–1455 (1993).
  • Brook I, Foote PA. Effect of penicillin or cefprozil therapy on tonsillar flora. J. Antimicrob. Chemother.40, 725–728 (1997).
  • Brook I, Foote PA. Efficacy of penicillin versus cefdinir in eradication of group A streptococci and tonsillar flora. Antimicrob. Agents Chemother.49, 4787–4788 (2005).
  • Brook I, Shah K, Jackson W. Microbiology of healthy and diseased adenoids. Laryngoscope110, 994–999 (2000).
  • Faden H, Zaz MJ, Bernstein JM, Brodsky L, Stamievich J, Ogru PL. Nasopharyngeal flora in the first three years of life in normal and otitis-prone children. Ann. Otolo. Rhinolo. Laryngolo.100, 612–615 (1991).
  • Bernstein JM, Sagahtaheri-Altaie S, Dryjd DM, Wactawski-Wende J. Bacterial interference in nasopharyngeal bacterial flora of otitis-prone and non-otitis-prone children. Acta Otorhinolaryngol. Belg.48, 1–9 (1994).
  • Tano K, Hakansson EG, Holm SE, Hellstrom S. Bacterial interference between pathogens in otitis media and α-haemolytic streptococci analysed in an in vitro model. Acta Otolaryngol.122, 78–85 (2002).
  • Brook I, Yocum P. Bacterial interference in the adenoids of otitis media prone children. Pediatr. Infect. Dis. J.18, 835–837 (1999).
  • Brook I, Gober A. Bacterial interference in the nasopharynx of otitis media prone and not otitis media prone children. Arch. Otolaryngol. Head Neck Surg.126, 1011–1013 (2000).
  • Brook I, Gober AE. Long-term effects on the nasopharyngeal flora of children following antimicrobial therapy of acute otitis media with cefdinir or amoxycillin–clavulanate. J. Med. Microbiol.54, 553–556 (2005).
  • Tano K, Grahn Hakansson E, Holm SE, Hellstrom S. A nasal spray with α-haemolytic streptococci as long term prophylaxis against recurrent otitis media. Int. J. Pediatr. Otorhinolaryngol.11(62), 17–23 (2002).
  • Brook I, Foote PA. Effect of antimicrobial therapy with amoxicillin and cefprozil on bacterial interference and β-lactamase production in the adenoids. Ann. Otol. Rhinol. Laryngol.113, 902–905 (2004).
  • Brook I, Gober AE. Bacterial interference in the nasopharynx following antimicrobial therapy of acute otitis media. J. Antimicrob. Chemother.41, 489–492 (1998).
  • Brook I. The role of anaerobic bacteria in sinusitis. Anaerobe12, 5–12 (2006).
  • Jousimies-Somer HR, Savolainen S, Ylikoski JS. Comparison of the nasal bacterial floras in two groups of healthy subjects and in patients with acute maxillary sinusitis. Clin. Micrbiol.27, 2736–2743 (1989).
  • Gwaltney JM Jr, Sydnor A Jr, Sande MA. Etiology and antimicrobial treatment of acute sinusitis. Ann. Otol. Rhinol. Laryngol. Suppl.90(3 Pt 3), 68–71 (1981).
  • Nylen O, Jeppsson PH, Branefors-Helander P. Acute sinusitis. A clinical bacteriological and serological study with special reference to Haemophilus influenzae.Scand J. Infect. Dis.4, 43–48 (1972).
  • Brook I, Gober A. Bacterial interference in the nasopharynx and nasal cavity of sinusitis prone and not sinusitis prone children. Acta Otolaryngol.119, 832–836 (1999).
  • Stenfors L E, Raisanen S. The flora of the nasopharynx, with special reference to middle ear pathogens. Acta Otolaryngol. (Stockholm)108, 122–125 (1989).
  • Martin JM, Green M, Barbadora KA, Wald ER. Erythromycin-resistant group A strepharyngo–tonsillitisococci in schoolchildren in Pittsburgh. N. Engl. J. Med.346, 1200–1206 (2002).
  • Tanz R, Shulman T, Sroka A, Marubio S, Brook I, Yogev R. Lack of influence of β-lactamase-production flora on recovery of group A strepharyngo–tonsillitisococci after treatment of acute pharyngitis. J. Pediatrics117, 859–863 (1990).
  • Tanz RR, Shulman ST. Strepharyngo– tonsillitisococcal pharyngitis, the carrier state, definition, and management. Pediatr. Ann.27, 281–285 (1998).

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