CEDIFIX (CEFIXIME 200MG TABLET)

Aztreoced

(Aztreonam 500mg/1gm/2gm Injection)

  • Aztreonam offers greater flexibility of treatment options and reduce the selective pressure from the use of Carbapenems, Piperacillin/Tazobactam, Aminoglycosides and third-generation Cephalosporins.
  • Aztreonam has clinically useful potency against aerobic Gram-negative bacteria, including those expressing Ambler class B metallo-b-lactamases (MBLs).2

INDICATIONS

  • Complicated and Uncomplicated Urinary Tract Infections (pyelonephritis and cystitis caused by E.coli, K.pneumoniae, P.mirabilis, Paeruginosa, E.cloacae, K. oxytoca, Citrobacterspp, and S. Marcescens)
  • Lower Respiratory Tract Infections (pneumonia and bronchitis caused by E.coli, K.pneumoniae, Pmirabilis, Paeruginosa, H.influenzae, Enterobacter spp, and S. Marcescens)
  • Septicemia (E.coli, K.pneumoniae, Paeruginosa, P.mirabilis, S. marcescens, and Enterobacter spp)
  • Skin and Skin-Structure Infections (those associated with postoperative wounds, ulcers, and burns, caused by E. coli, P. mirabilis, S. marcescens, Enterobacter spp, P. aeruginosa, K. pneumoniae, and Citrobacter spp)
  • Intra-abdominal Infections (peritonitis caused by E. coli, K. pneumoniae, Enterobacter spp, P. aeruginosa, Citrobacter spp and Serratia spp)
  • Gynecologic Infections (endometritis and pelvic cellulitis caused by E.coli, K. pneumoniae, Enterobacter spp and P. Mirabilis)

ADMINISTRATION AND DOSAGE

  • Route of administration and Dosage should be determined by susceptibility of the causative organisms, severity and site of infection, and the condition of the patient.
  • Administered IV (Bolus Injection & Infusion) or by IM.

Dosage Guidelines for Adults

Type of Infections Dose Frequency (hours)
Urinary Tract Infections 500 mg or 1 g 8 or 12
Moderately severe systemic infections 1 gor 2 g 8 or 12
Severe systemic or life-threatening infections 2g 6 or 8
  1. IV is recommended for patients ts requiring single doses greater than 1 or those with bacterial septicemia, localized parenchymal abscess (eg, intra-abdominal abscess) peritonitis, or other severe systemic or life-threatening infections
  2. Maximum recommended dose is 8 g per day.

Pyelonephritis Treatment Guideline

Inpatient Treatment Second-line therapy (preferred if patient is critically ill or pregnant)
Patients with Pyelonephritis who require hospitali- zation should be treated with IV antimicrobial regimens. Therapy should be given for 24-48 h or until severe symptoms improve. Duration of therapy should be 10-14 d, inclusive of initial IV therapy Monobactam (Penicillin allergy): Aztreonam 2g IV q6h

The treatment of choice should be based on local resistance data, and the drug regimen should be tailored according to susceptibility results.

Empiric Treatment of Complicated Intra-abdominal Infection

Antibiotic Adult dosage
Aztreonam 1-2 g every 6-8 h

Dosages are based on normal renal and hepatic function.

  1. J Antimicrob Chemother 2015
  2. J Antimicrob Chemother 2016: 71: 2704-2712
  3. Medscape, Updated: Dec 01, 2015
  4. Complicated Intra-abdominal Infection Guidelines: CID 2010:50 (15 January)

IDSA and ATS 2016 guidelines - Management of Adults With Hospital-acquired Pneumonia (HAP) and Ventilator-associated Pneumonia (VAP)

Empiric Treatment Option for Clinically Suspected VAP in Units Where Antipseudomonal / Gram-Negative Coverage is Appropriate

Gram-Negative Antibiotics With Antipseudomonal Activity: ẞ-Lactam-Based Agent
Monobactam - Aztreonam 2 g IV q8h

In the absence of other options, it is acceptable to use Aztreonam as an adjunctive agent with another ẞ-lactam-based agent because it has different targets within the bacterial cell wall

Recommended Initial Empiric Antibiotic Therapy for HAP (Non-VAP)

Not at High Risk of Mortality but With Factors Increasing the Likelihood of MRSA Aztreonam 2 g IV q8h
Plus: Vancomycin 15mg/kg IV q8-12h with goal to target 15-20 15-20 mg/mL mg/mL trough trough level (consider a loading dose of 25-30 mg/kg x 1 for severe illness) OR Linezolid 600 mg IV q12h
Not at High Risk of Mortality but With Factors Increasing the Likelihood of MRSA Aztreonam 2 g IV q8h
Plus: Vancomycin 15mg/kg IV q8-12h with goal to target 15-20 15-20 mg/mL mg/mL trough trough level (consider a loading dose of 25-30 mg/kg x 1 for severe illness) OR Linezolid 600 mg IV q12h
  • Risk factors for mortality include need for ventilatory support due to pneumonia and septic shock.
  • Indications for MRSA coverage include intravenous antibiotic treatment during the prior 90 days, and treatment in a unit where the prevalence of MRSA among S. aureus isolates is not known or is >20%. Prior detection of MRSA by culture or non-culture screening may also increase the risk of MRSA. The 20% threshold was chosen to balance the need for effective initial antibiotic therapy against the risks of excessive antibiotic use; hence, individual units can elect to adjust the threshold in accordance with local values and preferences. IfMRSA coverage is omitted, the antibiotic regimen should include coverage for MSSA.
  • If patient has factors increasing the likelihood of gram-negative infection, 2 antipseudomonal agents are recommended. If patient has structural lung disease increasing the risk of gram negative infection (ie, bronchiectasis or cystic fibrosis), 2 antipseudomonal agents are recommended. A high-quality Gram stain from a respiratory specimen with numerous and predominant gram-negative bacilli provides further support for the diagnosis of a gram-negative pneumonia, including fermenting and non-glucose- fermenting microorganisms.