Different antibiotic treatments for group A streptococcal pharyngitis.
Adult
Child
Humans
Infant
Azithromycin
/ adverse effects
Systematic Reviews as Topic
Anti-Bacterial Agents
/ adverse effects
Cephalosporins
/ adverse effects
Penicillins
/ adverse effects
Amoxicillin
/ adverse effects
Pharyngitis
/ drug therapy
Streptococcus pyogenes
Macrolides
/ adverse effects
Chronic Disease
Recurrence
Randomized Controlled Trials as Topic
Journal
The Cochrane database of systematic reviews
ISSN: 1469-493X
Titre abrégé: Cochrane Database Syst Rev
Pays: England
ID NLM: 100909747
Informations de publication
Date de publication:
15 11 2023
15 11 2023
Historique:
pmc-release:
15
11
2024
medline:
16
11
2023
pubmed:
15
11
2023
entrez:
15
11
2023
Statut:
epublish
Résumé
Antibiotics provide only modest benefit in treating sore throat, although their effectiveness increases in people with positive throat swabs for group A beta-haemolytic streptococci (GABHS). It is unclear which antibiotic is the best choice if antibiotics are indicated. This is an update of a review first published in 2010, and updated in 2013, 2016, and 2021. To assess the comparative efficacy of different antibiotics in: (a) alleviating symptoms (pain, fever); (b) shortening the duration of the illness; (c) preventing clinical relapse (i.e. recurrence of symptoms after initial resolution); and (d) preventing complications (suppurative complications, acute rheumatic fever, post-streptococcal glomerulonephritis). To assess the evidence on the comparative incidence of adverse effects and the risk-benefit of antibiotic treatment for streptococcal pharyngitis. We searched the Cochrane Central Register of Controlled Trials (CENTRAL 2023, Issue 2), MEDLINE Ovid, Embase Elsevier, and Web of Science (Clarivate) up to 19 March 2023. Randomised, double-blind trials comparing different antibiotics, and reporting at least one of the following: clinical cure, clinical relapse, or complications and/or adverse events. Two review authors independently screened trials for inclusion and extracted data using standard methodological procedures recommended by Cochrane. We assessed the risk of bias in the included studies according to the methods outlined in the Cochrane Handbook for Systematic Reviews of Interventions, and used the GRADE approach to assess the overall certainty of the evidence for the outcomes. We reported the intention-to-treat analysis, and also performed an analysis of evaluable participants to explore the robustness of the intention-to-treat results. We included 19 trials reported in 18 publications (5839 randomised participants): six trials compared penicillin with cephalosporins; six compared penicillin with macrolides; three compared penicillin with carbacephem; one compared penicillin with sulphonamides; one compared clindamycin with ampicillin; and one compared azithromycin with amoxicillin in children. All participants had confirmed acute GABHS tonsillopharyngitis, and ages ranged from one month to 80 years. Nine trials included only, or predominantly, children. Most trials were conducted in an outpatient setting. Reporting of randomisation, allocation concealment, and blinding was poor in all trials. We downgraded the certainty of the evidence mainly due to lack of (or poor reporting of) randomisation or blinding, or both, heterogeneity, and wide confidence intervals. Cephalosporins versus penicillin We are uncertain if there is a difference in symptom resolution (at 2 to 15 days) for cephalosporins versus penicillin (odds ratio (OR) for absence of symptom resolution 0.79, 95% confidence interval (CI) 0.55 to 1.12; 5 trials, 2018 participants; low-certainty evidence). Results of the sensitivity analysis of evaluable participants differed (OR 0.51, 95% CI 0.27 to 0.97; 5 trials, 1660 participants; very low-certainty evidence). Based on an analysis of evaluable participants, we are uncertain if clinical relapse may be lower for cephalosporins compared with penicillin (OR 0.55, 95% CI 0.30 to 0.99; number needed to treat for an additional beneficial outcome (NNTB) 50; 4 trials, 1386 participants; low-certainty evidence). Very low-certainty evidence showed no difference in reported adverse events. Macrolides versus penicillin We are uncertain if there is a difference between macrolides and penicillin for resolution of symptoms (OR 1.11, 95% CI 0.92 to 1.35; 6 trials, 1728 participants; low-certainty evidence). Sensitivity analysis of evaluable participants resulted in an OR of 0.79 (95% CI 0.57 to 1.09; 6 trials, 1159 participants). We are uncertain if clinical relapse may be different (OR 1.21, 95% CI 0.48 to 3.03; 6 trials, 802 participants; low-certainty evidence). Children treated with macrolides seemed to experience more adverse events than those treated with penicillin (OR 2.33, 95% CI 1.06 to 5.15; 1 trial, 489 participants; low-certainty evidence). However, the test for subgroup differences between children and adults was not significant. Azithromycin versus amoxicillin Based on one unpublished trial in children, we are uncertain if resolution of symptoms is better with azithromycin in a single dose versus amoxicillin for 10 days (OR 0.76, 95% CI 0.55 to 1.05; 1 trial, 673 participants; very low-certainty evidence). Sensitivity analysis for per-protocol analysis resulted in an OR of 0.29 (95% CI 0.11 to 0.73; 1 trial, 482 participants; very low-certainty evidence). We are also uncertain if there was a difference in relapse between groups (OR 0.88, 95% CI 0.43 to 1.82; 1 trial, 422 participants; very low-certainty evidence). Adverse events were more common with azithromycin compared to amoxicillin (OR 2.67, 95% CI 1.78 to 3.99; 1 trial, 673 participants; very low-certainty evidence). Carbacephem versus penicillin There is low-certainty evidence that compared with penicillin, carbacephem may provide better symptom resolution post-treatment in adults and children (OR 0.70, 95% CI 0.49 to 0.99; NNTB 14.3; 3 trials, 795 participants). Studies did not report on long-term complications, so it was unclear if any class of antibiotics was better at preventing serious but rare complications. We are uncertain if there are clinically relevant differences in symptom resolution when comparing cephalosporins and macrolides with penicillin in the treatment of GABHS tonsillopharyngitis. Low-certainty evidence in children suggests that carbacephem may be more effective than penicillin for symptom resolution. There is insufficient evidence to draw conclusions regarding the other comparisons in this review. Data on complications were too scarce to draw conclusions. Antibiotics have a limited effect in the treatment of GABHS pharyngitis and the results do not demonstrate that other antibiotics are more effective than penicillin. In the context of antimicrobial stewardship, penicillin can be used if treatment with an antibiotic is indicated. All studies were conducted in high-income countries with a low risk of streptococcal complications, so there is a need for trials in low-income countries and disadvantaged populations, where the risk of complications remains high.
Sections du résumé
BACKGROUND
Antibiotics provide only modest benefit in treating sore throat, although their effectiveness increases in people with positive throat swabs for group A beta-haemolytic streptococci (GABHS). It is unclear which antibiotic is the best choice if antibiotics are indicated. This is an update of a review first published in 2010, and updated in 2013, 2016, and 2021.
OBJECTIVES
To assess the comparative efficacy of different antibiotics in: (a) alleviating symptoms (pain, fever); (b) shortening the duration of the illness; (c) preventing clinical relapse (i.e. recurrence of symptoms after initial resolution); and (d) preventing complications (suppurative complications, acute rheumatic fever, post-streptococcal glomerulonephritis). To assess the evidence on the comparative incidence of adverse effects and the risk-benefit of antibiotic treatment for streptococcal pharyngitis.
SEARCH METHODS
We searched the Cochrane Central Register of Controlled Trials (CENTRAL 2023, Issue 2), MEDLINE Ovid, Embase Elsevier, and Web of Science (Clarivate) up to 19 March 2023.
SELECTION CRITERIA
Randomised, double-blind trials comparing different antibiotics, and reporting at least one of the following: clinical cure, clinical relapse, or complications and/or adverse events.
DATA COLLECTION AND ANALYSIS
Two review authors independently screened trials for inclusion and extracted data using standard methodological procedures recommended by Cochrane. We assessed the risk of bias in the included studies according to the methods outlined in the Cochrane Handbook for Systematic Reviews of Interventions, and used the GRADE approach to assess the overall certainty of the evidence for the outcomes. We reported the intention-to-treat analysis, and also performed an analysis of evaluable participants to explore the robustness of the intention-to-treat results.
MAIN RESULTS
We included 19 trials reported in 18 publications (5839 randomised participants): six trials compared penicillin with cephalosporins; six compared penicillin with macrolides; three compared penicillin with carbacephem; one compared penicillin with sulphonamides; one compared clindamycin with ampicillin; and one compared azithromycin with amoxicillin in children. All participants had confirmed acute GABHS tonsillopharyngitis, and ages ranged from one month to 80 years. Nine trials included only, or predominantly, children. Most trials were conducted in an outpatient setting. Reporting of randomisation, allocation concealment, and blinding was poor in all trials. We downgraded the certainty of the evidence mainly due to lack of (or poor reporting of) randomisation or blinding, or both, heterogeneity, and wide confidence intervals. Cephalosporins versus penicillin We are uncertain if there is a difference in symptom resolution (at 2 to 15 days) for cephalosporins versus penicillin (odds ratio (OR) for absence of symptom resolution 0.79, 95% confidence interval (CI) 0.55 to 1.12; 5 trials, 2018 participants; low-certainty evidence). Results of the sensitivity analysis of evaluable participants differed (OR 0.51, 95% CI 0.27 to 0.97; 5 trials, 1660 participants; very low-certainty evidence). Based on an analysis of evaluable participants, we are uncertain if clinical relapse may be lower for cephalosporins compared with penicillin (OR 0.55, 95% CI 0.30 to 0.99; number needed to treat for an additional beneficial outcome (NNTB) 50; 4 trials, 1386 participants; low-certainty evidence). Very low-certainty evidence showed no difference in reported adverse events. Macrolides versus penicillin We are uncertain if there is a difference between macrolides and penicillin for resolution of symptoms (OR 1.11, 95% CI 0.92 to 1.35; 6 trials, 1728 participants; low-certainty evidence). Sensitivity analysis of evaluable participants resulted in an OR of 0.79 (95% CI 0.57 to 1.09; 6 trials, 1159 participants). We are uncertain if clinical relapse may be different (OR 1.21, 95% CI 0.48 to 3.03; 6 trials, 802 participants; low-certainty evidence). Children treated with macrolides seemed to experience more adverse events than those treated with penicillin (OR 2.33, 95% CI 1.06 to 5.15; 1 trial, 489 participants; low-certainty evidence). However, the test for subgroup differences between children and adults was not significant. Azithromycin versus amoxicillin Based on one unpublished trial in children, we are uncertain if resolution of symptoms is better with azithromycin in a single dose versus amoxicillin for 10 days (OR 0.76, 95% CI 0.55 to 1.05; 1 trial, 673 participants; very low-certainty evidence). Sensitivity analysis for per-protocol analysis resulted in an OR of 0.29 (95% CI 0.11 to 0.73; 1 trial, 482 participants; very low-certainty evidence). We are also uncertain if there was a difference in relapse between groups (OR 0.88, 95% CI 0.43 to 1.82; 1 trial, 422 participants; very low-certainty evidence). Adverse events were more common with azithromycin compared to amoxicillin (OR 2.67, 95% CI 1.78 to 3.99; 1 trial, 673 participants; very low-certainty evidence). Carbacephem versus penicillin There is low-certainty evidence that compared with penicillin, carbacephem may provide better symptom resolution post-treatment in adults and children (OR 0.70, 95% CI 0.49 to 0.99; NNTB 14.3; 3 trials, 795 participants). Studies did not report on long-term complications, so it was unclear if any class of antibiotics was better at preventing serious but rare complications.
AUTHORS' CONCLUSIONS
We are uncertain if there are clinically relevant differences in symptom resolution when comparing cephalosporins and macrolides with penicillin in the treatment of GABHS tonsillopharyngitis. Low-certainty evidence in children suggests that carbacephem may be more effective than penicillin for symptom resolution. There is insufficient evidence to draw conclusions regarding the other comparisons in this review. Data on complications were too scarce to draw conclusions. Antibiotics have a limited effect in the treatment of GABHS pharyngitis and the results do not demonstrate that other antibiotics are more effective than penicillin. In the context of antimicrobial stewardship, penicillin can be used if treatment with an antibiotic is indicated. All studies were conducted in high-income countries with a low risk of streptococcal complications, so there is a need for trials in low-income countries and disadvantaged populations, where the risk of complications remains high.
Identifiants
pubmed: 37965935
doi: 10.1002/14651858.CD004406.pub6
pmc: PMC10646936
doi:
Substances chimiques
carbacephems
0
Azithromycin
83905-01-5
Anti-Bacterial Agents
0
Cephalosporins
0
Penicillins
0
Amoxicillin
804826J2HU
Macrolides
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
CD004406Commentaires et corrections
Type : UpdateOf
Informations de copyright
Copyright © 2023 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Références
Clin Pharmacol Ther. 1969 Mar-Apr;10(2):244-9
pubmed: 4887297
Eur J Pediatr. 2014 Oct;173(10):1275-83
pubmed: 25113742
Pediatr Infect Dis J. 2002 Apr;21(4):297-303
pubmed: 12075760
J Natl Cancer Inst. 1959 Apr;22(4):719-48
pubmed: 13655060
Control Clin Trials. 1986 Sep;7(3):177-88
pubmed: 3802833
J Antimicrob Chemother. 1996 Jan;37(1):133-8
pubmed: 8647754
Pediatrics. 1999 Jan;103(1):47-51
pubmed: 9917438
An Pediatr (Barc). 2011 Nov;75(5):298-306
pubmed: 21703951
Cochrane Database Syst Rev. 2010 Oct 06;(10):CD004406
pubmed: 20927734
Klin Padiatr. 1994 Jan-Feb;206(1):26-9
pubmed: 8152203
Pediatr Infect Dis J. 1998 Jan;17(1):39-43
pubmed: 9469393
Clin Pediatr (Phila). 1973 Aug;12(8):501-3
pubmed: 4579967
Pediatr Infect Dis J. 1991 Oct;10(10 Suppl):S61-3
pubmed: 1945599
J Clin Epidemiol. 2009 Aug;62(8):838-844.e3
pubmed: 19128939
J Infect Dis. 2000 Aug;182(2):509-16
pubmed: 10915082
Scand J Infect Dis. 2003;35(4):223-5
pubmed: 12839147
Am J Dis Child. 1992 Nov;146(11):1324-7
pubmed: 1415072
JAMA. 1973 Oct 29;226(5):531-5
pubmed: 4200875
J Infect Chemother. 2008 Jun;14(3):208-12
pubmed: 18574656
Allergy Asthma Proc. 2014 Nov-Dec;35(6):489-94
pubmed: 25584917
J Antimicrob Chemother. 1995 Jun;35(6):843-54
pubmed: 7559195
Postgrad Med J. 1979;55 Suppl 4:50-2
pubmed: 398481
BMC Infect Dis. 2021 Sep 17;21(1):971
pubmed: 34535115
J Antimicrob Chemother. 1991 Feb;27 Suppl A:75-82
pubmed: 1827105
Scand J Infect Dis. 1994;26(1):59-66
pubmed: 8191242
Ann Fam Med. 2007 Sep-Oct;5(5):436-43
pubmed: 17893386
Pediatrics. 1999 Oct;104(4 Pt 1):911-7
pubmed: 10506234
J Fam Pract. 2006 Jul;Suppl:S9-16
pubmed: 16913668
JAMA. 2004 Apr 7;291(13):1587-95
pubmed: 15069046
Scand J Infect Dis. 2001;33(12):883-90
pubmed: 11868759
Antimicrob Agents Chemother. 1996 Apr;40(4):1005-8
pubmed: 8849215
Open Med. 2009;3(3):e123-30
pubmed: 21603045
Clin Microbiol Rev. 2004 Jul;17(3):571-80, table of contents
pubmed: 15258094
Pediatr Infect Dis J. 1992 Aug;11(8 Suppl):S20-6
pubmed: 1513608
Clin Microbiol Infect. 2015 Mar;21(3):263.e1-7
pubmed: 25658556
Scand J Infect Dis. 1997;29(2):141-5
pubmed: 9181649
CMAJ. 1998 Jan 13;158(1):75-83
pubmed: 9475915
Clin Infect Dis. 1992 Jun;14 Suppl 2:S224-30; discussion S231-2
pubmed: 1617042
Arch Pediatr Adolesc Med. 1997 Jan;151(1):45-9
pubmed: 9006528
BMJ Open. 2013 Oct 25;3(10):e003943
pubmed: 24163209
Antimicrob Agents Chemother. 1993 Feb;37(2):159-63
pubmed: 8452344
J Infect Dis. 1971 Oct;124(4):339-47
pubmed: 5143842
Ann Trop Paediatr. 2000 Sep;20(3):199-202
pubmed: 11064772
Fortschr Med Orig. 2001 Jul 19;119 Suppl 2:63-70
pubmed: 15704358
Ned Tijdschr Geneeskd. 1992 Nov 21;136(47):2314-8
pubmed: 1369534
Circulation. 2009 Mar 24;119(11):1541-51
pubmed: 19246689
J Fam Pract. 1991 Feb;32(2):138-44
pubmed: 1990041
Pediatrics. 2004 Jun;113(6):1816-9
pubmed: 15173515
Antimicrob Agents Chemother. 1993 Aug;37(8):1620-3
pubmed: 8215273
J Infect Chemother. 2013 Feb;19(1):12-9
pubmed: 22760341
Cochrane Database Syst Rev. 2016 Jul 04;7:CD010502
pubmed: 27374000
Pediatr Infect Dis J. 1991 Oct;10(10 Suppl):S68-71
pubmed: 1945601
Am J Med. 1992 Jun 22;92(6A):2S-6S
pubmed: 1621741
Pediatrics. 1953 Jan;11(1):7-13
pubmed: 13026346
Pediatrics. 2004 Apr;113(4):866-82
pubmed: 15060239
Cochrane Database Syst Rev. 2016 Sep 11;9:CD004406
pubmed: 27614728
Am J Med. 1992 Jun 22;92(6A):74S-79S
pubmed: 1621750
Med J Aust. 2016 Sep 5;205(5):201-3
pubmed: 27581260
Pediatr Infect Dis. 1986 Nov-Dec;5(6):649-54
pubmed: 3099268
Pediatr Infect Dis J. 2000 Dec;19(12 Suppl):S171-3
pubmed: 11144400
Infection. 1995;23 Suppl 2:S83-6
pubmed: 8537138
Clin Pharmacol Ther. 1970 Mar-Apr;11(2):205-13
pubmed: 4984655
Clin Pediatr (Phila). 2011 Jun;50(6):535-42
pubmed: 21317198
J Infect Dis. 1973 Nov;128:Suppl:693-5 p
pubmed: 4585968
BMJ. 1998 Sep 5;317(7159):609-10
pubmed: 9727981
J Antimicrob Chemother. 1982 Sep;10 Suppl B:125-35
pubmed: 6754685
J Infect Dev Ctries. 2011 Nov 15;5(11):804-8
pubmed: 22112735
J Antimicrob Chemother. 1993 Jun;31 Suppl E:89-94
pubmed: 8396102
BMJ. 2000 Jan 15;320(7228):150-4
pubmed: 10634735
Arch Dis Child. 2008 Jun;93(6):474-8
pubmed: 18337284
BMJ. 2004 Jun 19;328(7454):1490
pubmed: 15205295
Antimicrob Agents Chemother. 1974 Oct;6(4):501-6
pubmed: 4157353
Laryngorhinootologie. 2014 Mar;93 Suppl 1:S84-102
pubmed: 24710788
Clin Infect Dis. 1995 Nov;21(5):1294-9
pubmed: 8589159
J Pediatr. 1985 Jun;106(6):870-5
pubmed: 3923180
Eur J Clin Microbiol Infect Dis. 1991 Nov;10(11):949-53
pubmed: 1838978
J Pediatr. 1986 Sep;109(3):531-7
pubmed: 3091801
Clin Ther. 1999 Nov;21(11):1873-81
pubmed: 10890259
J Adv Pharm Technol Res. 2010 Jan;1(1):11-7
pubmed: 22247826
J Pediatr. 2008 Nov;153(5):725
pubmed: 18940364
Cochrane Database Syst Rev. 2013 Apr 30;(4):CD004406
pubmed: 23633318
Med J Aust. 2010 May 17;192(10):581-4
pubmed: 20477734
Eur J Clin Microbiol Infect Dis. 1994 Oct;13(10):846-50
pubmed: 7889958
Can Fam Physician. 2007 Nov;53(11):1961-2
pubmed: 18000276
Eur J Clin Microbiol Infect Dis. 1996 Sep;15(9):712-7
pubmed: 8922570
Antimicrob Agents Chemother. 1997 Jan;41(1):72-5
pubmed: 8980757
Ann Fam Med. 2006 Nov-Dec;4(6):494-9
pubmed: 17148626
Infection. 1992 Sep-Oct;20(5):301-8
pubmed: 1428189
Minerva Pediatr. 2012 Jun;64(3):341-6
pubmed: 22555328
Pediatr Infect Dis J. 1995 Apr;14(4):295-300
pubmed: 7603811
Clin Infect Dis. 2012 Nov 15;55(10):e86-102
pubmed: 22965026
Antimicrob Agents Chemother. 2008 Jul;52(7):2512-20
pubmed: 18332170
J Infect Dis. 1974 Jun;129(0):suppl:S178-80
pubmed: 4276096
BMC Infect Dis. 2016 Nov 25;16(1):709
pubmed: 27887585
J Antimicrob Chemother. 1990 Dec;26 Suppl E:79-85
pubmed: 2127268
Cochrane Database Syst Rev. 2021 Dec 9;12:CD000023
pubmed: 34881426
J Antimicrob Chemother. 2000 Feb;45 Suppl:23-30
pubmed: 10759359
Cochrane Database Syst Rev. 2021 Mar 17;3:CD004406
pubmed: 33728634
Health Technol Assess. 2020 Jun;24(31):1-232
pubmed: 32605705
Rev Esp Quimioter. 2008 Mar;21(1):14-21
pubmed: 18443928
Int J Antimicrob Agents. 2002 Jul;20(1):28-33
pubmed: 12127708
Antimicrob Agents Chemother. 1998 May;42(5):1073-5
pubmed: 9593129
Ghana Med J. 2014 Dec;48(4):185-8
pubmed: 25709132
Ann Intern Med. 2003 Jul 15;139(2):113-22
pubmed: 12859161
BMJ. 1993 May 1;306(6886):1170-2
pubmed: 8499823
Br J Gen Pract. 1997 May;47(418):280-4
pubmed: 9219402
J Antimicrob Chemother. 1991 Feb;27 Suppl A:67-74
pubmed: 1827104
Eur J Clin Microbiol Infect Dis. 1996 Sep;15(9):718-24
pubmed: 8922571
Clin Microbiol Infect. 2012 Apr;18 Suppl 1:1-28
pubmed: 22432746
BMJ. 2003 Sep 6;327(7414):557-60
pubmed: 12958120