National Clinical Guideline Centre Pneumonia Diagnosis and management of community- and hospital-acquired pneumonia in adults

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National Clinical Guideline Centre Antibiotic classifications Pneumonia Diagnosis and management of community- and hospital-acquired pneumonia in adults Clinical guideline 191 Appendix N 3 December 2014 Final version Commissioned by the National Institute for Health and Care Excellence

Antibiotic classifications Contents Disclaimer Healthcare professionals are expected to take NICE clinical guidelines fully into account when exercising their clinical judgement. However, the guidance does not override the responsibility of healthcare professionals to make decisions appropriate to the circumstances of each patient, in consultation with the patient and/or their guardian or carer. Copyright National Clinical Guideline Centre, 2014. Confidential. Funding National Institute for Health and Care Excellence National Clinical Guideline Centre, 2014. Confidential.

Antibiotic classifications Classifications for the purposes of data pooling Contents 1 Classifications for the purposes of data pooling... 5 1.1 Rationale for using antibiotic classification... 5 1.1.1 Community-acquired pneumonia... 5 1.1.2 Hospital-acquired pneumonia... 5 National Clinical Guideline Centre, 2014. Confidential. 4

Antibiotic classifications Classifications for the purposes of data pooling 1 Classifications for the purposes of data pooling 1.1 Rationale for using antibiotic classification 1.1.1 Community-acquired pneumonia Streptococcus pneumoniae is the most frequently identified cause of community-acquired pneumonia (CAP). Staphylococcus aureus, Mycoplasma pneumoniae, Legionella pneumophila and Haemophilus influenza are also implicated as causes of CAP, depending on the population type and underlying risk factors. Moraxella catarrhalis, Chlamydophyla spp. and Coxiella burnetti are less common causes of CAP. Our search protocols placed antibiotics into narrow and broad spectrum categories based on their predicted antibacterial activity. Narrow-spectrum agents were subdivided into class 1 agents (benzylpenicillin and oral penicillin V) covering penicillin-susceptible S. pneumoniae and class 2 agents (ampicillin and amoxicillin) providing additional cover against amoxicillin-susceptible H. influenzae. Broad-spectrum agents including beta-lactam antibiotics with additional activity against beta-lactamase-producing community pathogens (H. influenzae, M. catarrhalis) and methicillinsusceptible S. aureus were split into beta-lactamase stable penicillins (isoxazolyl penicillins such as flucloxacillin, beta-lactam beta-lactamase combinations, such as co-amoxiclav) and cephalosporins. For CAP, cephalosporins were grouped together due to their similar broad-spectrum activity against susceptible community pathogens. Tetracyclines are broad-spectrum agents with activity against S. pneumoniae, S. aureus, H. influenzae and atypical pathogens such as M. pneumoniae and C. burnetti. Fluoroquinolones were subdivided into those with inadequate anti-pneumococcal activity (ciprofloxacin, ofloxacin) and the newer respiratory fluoroquinolones with broader anti-grampositive activity (levofloxacin, moxifloxacin). 1.1.2 Hospital-acquired pneumonia In addition to community pathogens, aerobic Gram-negative rods such as Klebsiella pneumoniae and Pseudomonas aeruginosa play a major role in hospital-acquired pneumonia (HAP). Beta-lactam agents with additional anti-pseudomonal activity (carbapenems, monobactams, certain third generation cephalosporins such as ceftazidime and beta lactam-beta lactamase combinations such as piperacillin-tazobactam) were specifically considered under the HAP category. Other antibiotics with predominant activity against hospital-related pathogens (glycopeptides, aminoglycosides and the oxazolidinones such as linezolid) were also considered. National Clinical Guideline Centre, 2014. Confidential. 5

Pneumonia antibiotics Table 1: BETA-LACTAMS Antibiotic classifications - separate columns denote drugs considered suitable for pooling in meta-analysis Narrow-spectrum beta-lactams Class 1 Class 2 Penicillin G (benzylpenicillin) Phenoxymethylpenicillin (penicillin V) Broad-spectrum beta-lactams Betalactamase stable penicillins All cephalosporins 1 Ampicillin Co-amoxiclav 1st Amoxicillin Piperacillintazobactam Timentin (ticarcillinclavulanic acid) All carbapenems (HAP only) 6 FLUOROQUINOLONES Non-respiratory fluoroquinolones (1st and 2nd generation) Respiratory fluoroquinolones (3rd and 4th generation) MACROLIDES TETRACYCLINES Imipenem Ciprofloxacin Levofloxacin Clarithromycin Doxycycline Cefalexin Meropenem Ofloxacin Moxifloxacin Clindamycin Tigecycline Cefradine Ertapenem Erythromycin Tetracycline Flucloxacillin Cefadroxil Azithromycin Minocycline Co-fluampicil 2nd Cefaclor Cefuroxime 3rd Cefotaxime Ceftriaxone Ceftazidime Cefixime Cefpodoxime proxetil 4th

Pneumonia antibiotics BETA-LACTAMS FLUOROQUINOLONES Narrow-spectrum beta-lactams Broad-spectrum beta-lactams Class 1 Class 2 Betalactamase stable penicillins All cephalosporins 1 All carbapenems (HAP only) Non-respiratory fluoroquinolones (1st and 2nd generation) Respiratory fluoroquinolones (3rd and 4th generation) MACROLIDES TETRACYCLINES Cefepime 5th Ceftaroline fosamil 1. All cephalosporins except for first generation agents are considered beta lactamase stable 7

Pneumonia antibiotics 8