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Treatment Challenges of Group A Beta-hemolytic Streptococcal Pharyngo-Tonsillitis
Introduction Despite its in vitro efficacy, penicillin often fails to eradicate Group A β-hemolytic streptococci (GABHS) from patients with acute and relapsing pharyngo-tonsillitis (PT). Objective This review of the literature details the causes of penicillin failure to eradicate GABHS PT and the...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Revinter Publicações Ltda
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5495595/ https://www.ncbi.nlm.nih.gov/pubmed/28680500 http://dx.doi.org/10.1055/s-0036-1584294 |
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author | Brook, Itzhak |
author_facet | Brook, Itzhak |
author_sort | Brook, Itzhak |
collection | PubMed |
description | Introduction Despite its in vitro efficacy, penicillin often fails to eradicate Group A β-hemolytic streptococci (GABHS) from patients with acute and relapsing pharyngo-tonsillitis (PT). Objective This review of the literature details the causes of penicillin failure to eradicate GABHS PT and the therapeutic modalities to reduce and overcome antimicrobial failure. Data Synthesis The causes of penicillin failure in eradicating GABHS PT include the presence of β lactamase producing bacteria (BLPB) that “protect” GABHS from any penicillin; the absence of bacteria that interfere with the growth of GABHS; co-aggregation between GABHS and Moraxella catarrhalis; and the poor penetration of penicillin into the tonsillar tissues and the tonsillo-pharyngeal cells, which allows intracellular GABHS and Staphylococcus aureus to survive. The inadequate intracellular penetration of penicillin can allow intracellular GABHS and S. aureus to persist. In the treatment of acute tonsillitis, the use of cephalosporin can overcome these interactions by eradicating aerobic BLPB (including M. catarrhalis), while preserving the potentially interfering organisms and eliminating GABHS. Conclusion In treatment of recurrent and chronic PT, the administration of clindamycin, or amoxicillin-clavulanic acid, can eradicate both aerobic and anaerobic BLPB, as well as GABHS. The superior intracellular penetration of cephalosporin and clindamycin also enhances their efficacy against intracellular GABHS and S. aureus. |
format | Online Article Text |
id | pubmed-5495595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Thieme Revinter Publicações Ltda |
record_format | MEDLINE/PubMed |
spelling | pubmed-54955952017-07-05 Treatment Challenges of Group A Beta-hemolytic Streptococcal Pharyngo-Tonsillitis Brook, Itzhak Int Arch Otorhinolaryngol Introduction Despite its in vitro efficacy, penicillin often fails to eradicate Group A β-hemolytic streptococci (GABHS) from patients with acute and relapsing pharyngo-tonsillitis (PT). Objective This review of the literature details the causes of penicillin failure to eradicate GABHS PT and the therapeutic modalities to reduce and overcome antimicrobial failure. Data Synthesis The causes of penicillin failure in eradicating GABHS PT include the presence of β lactamase producing bacteria (BLPB) that “protect” GABHS from any penicillin; the absence of bacteria that interfere with the growth of GABHS; co-aggregation between GABHS and Moraxella catarrhalis; and the poor penetration of penicillin into the tonsillar tissues and the tonsillo-pharyngeal cells, which allows intracellular GABHS and Staphylococcus aureus to survive. The inadequate intracellular penetration of penicillin can allow intracellular GABHS and S. aureus to persist. In the treatment of acute tonsillitis, the use of cephalosporin can overcome these interactions by eradicating aerobic BLPB (including M. catarrhalis), while preserving the potentially interfering organisms and eliminating GABHS. Conclusion In treatment of recurrent and chronic PT, the administration of clindamycin, or amoxicillin-clavulanic acid, can eradicate both aerobic and anaerobic BLPB, as well as GABHS. The superior intracellular penetration of cephalosporin and clindamycin also enhances their efficacy against intracellular GABHS and S. aureus. Thieme Revinter Publicações Ltda 2017-07 2016-06-03 /pmc/articles/PMC5495595/ /pubmed/28680500 http://dx.doi.org/10.1055/s-0036-1584294 Text en © Thieme Medical Publishers |
spellingShingle | Brook, Itzhak Treatment Challenges of Group A Beta-hemolytic Streptococcal Pharyngo-Tonsillitis |
title | Treatment Challenges of Group A Beta-hemolytic Streptococcal Pharyngo-Tonsillitis |
title_full | Treatment Challenges of Group A Beta-hemolytic Streptococcal Pharyngo-Tonsillitis |
title_fullStr | Treatment Challenges of Group A Beta-hemolytic Streptococcal Pharyngo-Tonsillitis |
title_full_unstemmed | Treatment Challenges of Group A Beta-hemolytic Streptococcal Pharyngo-Tonsillitis |
title_short | Treatment Challenges of Group A Beta-hemolytic Streptococcal Pharyngo-Tonsillitis |
title_sort | treatment challenges of group a beta-hemolytic streptococcal pharyngo-tonsillitis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5495595/ https://www.ncbi.nlm.nih.gov/pubmed/28680500 http://dx.doi.org/10.1055/s-0036-1584294 |
work_keys_str_mv | AT brookitzhak treatmentchallengesofgroupabetahemolyticstreptococcalpharyngotonsillitis |