Molecular structure of amoxicillin
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Amoxicillin

Amoxicillin (INN) or amoxycillin (former BAN) is a moderate-spectrum β-lactam antibiotic used to treat bacterial infections caused by susceptible microorganisms. It is usually the drug of choice within the class because it is better absorbed, following oral administration, than other beta-lactam antibiotics. Amoxicillin is susceptible to degradation by β-lactamase-producing bacteria, and so may be given with Clavulanic acid to increase its susceptability (see below). It is currently marketed by GlaxoSmithKline under the trade name Amoxil®. more...

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Mode of action

Amoxicillin acts by inhibiting the synthesis of bacterial cell walls. It inhibits cross-linkage between the linear peptidoglycan polymer chains that make up a major component of the cell wall of Gram-positive bacteria.

Microbiology

Amoxicillin is a moderate-spectrum antibiotic active against a wide range of Gram-positive, and a limited range of Gram-negative organisms. Some examples of susceptible and resistant organisms, from the Amoxil® Approved Product Information (GSK, 2003), are listed below.

Susceptible Gram-positive organisms

Streptococcus spp., Diplococcus pneumoniae, non β-lactamase-producing Staphylococcus spp., and Streptococcus faecalis.

Susceptible Gram-negative organisms

Haemophilus influenzae, Neisseria gonorrhoeae, Neisseria meningitidis, Escherichia coli, Proteus mirabilis and Salmonella spp.

Resistant organisms

Penicillinase producing organisms, particularly penicillinase producing Staphylococcus spp. Penicillinase-producing N. gonorrhoeae and H. influenzae are also resistant

All strains of Pseudomonas spp., Klebsiella spp., Enterobacter spp., indole-positive Proteus spp., Serratia marcescens, and Citrobacter spp. are resistant.

The incidence of β-lactamase-producing resistant organisms, including E. coli, appears to be increasing.

Doubling the routinely given concentration (in pediatrics) of amoxicillin has been shown to eradicate intermediately resistant organisms (Red Book, 2003 Report of the Committee on Infectious Diseases, American Academy of Pediatrics).

Formulations

Amoxicillin in trihydrate form is avaialable as capsules or syrup for oral use, and as the sodium salt for intravenous administration.

Amoxicillin and Clavulanic acid

Amoxicillin (in either trihydrate or sodium salt forms) may be combined with Clavulanic acid (as potassium clavulanate), a β-lactamase inhibitor, to increase the spectrum of action against Gram-negative organisms, and to overcome bacterial antibiotic resistance mediated through β-lactamase production. This formulation is referred to as Co-amoxiclav (British Approved Name), but more commonly by proprietary names such as Augmentin® and Clamoxyl®.

Proprietary Preparations

The patent for amoxicillin has expired. Thus amoxicillin is marketed under many trade names including: Actimoxi®, Amoxibiotic®, Amoxicilina®, Pamoxicillin®, Lamoxy®, Ospamox®, Polymox®, Trimox®, Tolodina®, Wymox® and Zimox®.

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High-dose azithromycin or amoxicillin-clavulanate for recurrent otitis media?
From Journal of Family Practice, 3/1/04 by Adrienne Z. Ables

Arrieta A, Arguedas A, Fernandez P, et al. High-dose azithromycin versus high-dose amoxicillin-clavulanate for treatment of children with recurrent or persistent acute otitis media. Antimicrob Agents Chemother 2003; 47:3179-3186.

* BACKGROUND

High-dose amoxicillin-clavulanate is recommended for children with acute otitis media (AOM) who have not improved on previous treatment or have had recent antimicrobial exposure. (1) Azithromycin is an alternative only for patients with documented allergy to beta-lactam antibiotics.

* POPULATION STUDIED

The authors studied 304 patients aged between 6 months and 6 years with recurrent or persistent AOM. A0M was diagnosed by the presence of at least 2 of the following: decreased or absent mobility of the tympanic membrane, yellow or white discoloration, opacification, or acute perforation with purulence. In addition, 1 of the following had to be present to make the diagnosis: ear pain within 24 hours, hyperemia of the tympanic membrane, or bulging of the tympanic membrane.

Recurrent AOM was defined as at least 1 episode within 30 days of enrollment, 3 or more episodes within 6 months of enrollment, or at least 4 episodes within 12 months of enrollment. Persistent AOM was defined as the presence of signs and symptoms after at least 48 hours of antibiotic treatment. Sixty-eight percent of children had recurrent AOM and 19% had persistent AOM; the remainder had both. Forty-three percent of patients had their first episode of AOM before 6 months of age.

* STUDY DESIGN AND VALIDITY

Patients were enrolled into the trial in 13 US and 5 Latin American centers. Patients were randomly assigned to receive high-dose amoxicillin-clavulanate at 90/6.4 mg/kg/d for 10 days plus azithromycin placebo or high-dose azithromycin, 20 mg/kg/d, for 3 days plus amoxicillin-clavulanate placebo. Clinical, otoscopic, and safety assessments were made at baseline, after 2 weeks, and at the end of the study (days 28-32). Additionally, tympanocentesis was performed before the study drug was administered and pathogens from middle-ear fluid samples were isolated and identified.

Both patients/caregivers and investigators were blinded to treatment assignment. Allocation concealment was not mentioned. Analyses were performed by intention-to-treat. Of 304 patients, 4 were excluded from the safety analysis (no reason given). Of the remaining 300 patients, 4 were excluded from analysis due to incorrect diagnosis or because they did not meet inclusion criteria.

The percentage of children attending day care was similar in both treatment groups. Numbers of patients with persistent AOM, recurrent AOM, or both were not different between groups. (Level of evidence: lb)

* OUTCOMES MEASURED

The primary endpoint of the study was clinical response (cure, improvement, or worsening) at day 28 to 32. The secondary endpoint was clinical response at days 12 to 16. Adverse effects were also recorded.

* RESULTS

After 1 month, the clinical response rate (cure or improvement) of azithromycin was slightly greater than amoxicillin-clavulanate--72% vs 61%, respectively (P=.047, number needed to treat=9). At days 12 to 16, clinical success rates were similar between the 2 groups (about 85%).

With children in whom a bacterial pathogen was identified (55%), clinical success rates did not significantly differ. The incidence of diarrhea was higher in the amoxicillin-clavulanate patients (29.9% vs 19.6%; number needed to harm=10; P=.045).

* PRACTICE RECOMMENDATIONS

Use high-dose azithromycin for 3 days if antibiotics are needed, instead of a 10-day course of high-dose amoxicillin-clavulanate for the treatment of recurrent or persistent acute otitis media. For every 10 children using azithromycin instead of amoxicillin-clavulanate, there is 1 additional clinical cure at 1 month and 1 less episode of diarrhea. However, no difference in clinical success is seen at 2 weeks.

REFERENCE

(1.) Hoberman A, Marchant CD, Kaplan SL, Feldman S. Treatment of acute otitis media consensus recommendations. Clin Pediatr (Phila) 2002; 41:373-390.

DRUG BRAND NAMES Amoxicillin/clavulanate * Atacand Azithromycin * Zithromax Donepezil * Aricept Galantamine * Reminyl Ipratropium * Atrovent; Apo-Ipravent Rivasfigmine * Exelon

Adrienne Z. Ables, PharmD, and Petra K. Warren, MD, Spartanburg Family Medicine Residency Program, Spartanburg, SC. E-mail: aables@srhs.com.

COPYRIGHT 2004 Dowden Health Media, Inc.
COPYRIGHT 2004 Gale Group

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