“Do we perform too much antimicrobial susceptibility testing?”

As lab workers, we like to be helpful. In general, we want to provide as good a service as possible. But sometimes I think we try a little too hard…

One of our key areas of work is antimicrobial susceptibility testing. This is our bread and butter of course. This is one thing that we can do but no one else can, and we like to show off our skills! But there are many circumstances where performing antimicrobial susceptibility testing adds little value for the patient and thus unnecessarily uses up valuable laboratory resources.

Polymicrobial cultures The clinical value of antimicrobial susceptibility testing is inversely proportional to the number of different organism types present in the sample. This includes sterile site samples. Many times in my career I have been asked to do susceptibilities on samples which have grown several different organisms. I almost always push back on this. It should very much be the exception as opposed to the norm.

Eye and Ear Swabs Conjunctivitis and otitis externa are primarily managed by topical preparations, which can even be antiseptics as opposed to antibiotics. In-vitro susceptibility testing correlates poorly with response to topical antibiotics. Antimicrobial susceptibility testing on ear and eye swabs should only happen in a small minority of cases.

Enterobacteriaceae, enterococci & pseudomonas in superficial wound swabs These organisms cause infection in only a very small proportion of samples that they are actually found in. Susceptibilities should only be performed when there is compelling evidence from the clinical details that they are causing problems. 

Enterococci in urines In contrast to wounds, enterococci commonly cause urinary tract infections (they can also represent contamination). However, because amoxycillin achieves concentrations in urine which exceed the MICs of most Enterococcus faecalis and Enterococcus faecium isolates (check out this reference), susceptibility testing is essentially futile, unless the clinical details suggest the patient has a penicillin allergy. A simple comment to this effect will suffice.

Beta-haemolytic streptococci Because beta-haemolytic streptococci are inherently susceptible to beta-lactams, susceptibility testing for these antibiotics is somewhat academic in the majority of simple wound/soft tissue infections.  I would do if the clinical details suggested penicillin allergy.

Anaerobes Anaerobes rarely require formal susceptibility testing. Bacteroides fragilis has predictable response to beta-lactam/beta-lactamase inhibitor combinations. and is often part of a polymicrobial infection anyway (see polymicrobial cultures). In our lab anaerobic susceptibility testing is most often performed for C. acnes causing joint infections, where we test penicillin (almost always susceptible, maybe we don’t need to test…) and clindamycin (very occasionally resistant).

Coagulase negative staphylococci from blood cultures Again these should only be performed when it is clear that the coagulase negative staph is the suspected pathogen (prosthetic material, premature neonates, etc.) which will only be the small majority of the total number of isolates.

Pseudomonas in sputa Once a patient with COPD becomes colonised with Pseudomonas aeruginosa in their sputum, it is generally there to stay. Pseudomonas susceptibility testing should only be done when it is clear from the clinical details that it is causing a problem, i.e. the patient is failing standard management. We also need to review susceptibility testing protocols on pseudomonas isolates from patients with bronchiectasis and cystic fibrosis. There is now increasing evidence that annual susceptibility testing on Pseudomonas isolates from Cystic Fibrosis patients is more than sufficient.

Candida from vaginal swabs It’s not just bacteria! Recurrent vaginal candidiasis is a common problem, and we are often asked to perform antifungal susceptibilities on such isolates. In my opinion it is hardly ever justified. Nystatin based topical therapy often works in these patients. Candida albicans isolates are usually susceptible to generous dosing of azoles. It is only Nakaseomyces glabrata (formerly known as Candida glabrata), where I occasionally acquiesce and perform susceptibility testing…

Of course, we can perform antimicrobial susceptibility testing but not report the results, having them stored just in case. But my view is that we should minimise this approach as it is generally wasteful. We should perform antimicrobial susceptibility testing when we are confident that we are going to report the results of at least some of the antibiotics from a testing panel.

At my lab we have progressed a lot in this area over the past decade and now perform minimal amounts of antimicrobial susceptibility testing in all of the areas above. What about your own lab? Is there room for improvement, and can you think of other areas where too much antimicrobial susceptibility testing is performed, that I have not thought of?

Michael

3 thoughts on ““Do we perform too much antimicrobial susceptibility testing?”

  1. Interesting as ever. Agree. Too much work of too little value.
    Looking at some of the specific things you mention :

    Enterobacteriaceae, enterococci & pseudomonas in superficial wound swabs. We never look for them. They are not target pathogens. Just put swabs on Staph/Strep plates.

    Enterococci in urines In contrast to wounds, enterococci commonly cause urinary tract infections (they can also represent contamination). We have some new data on this that will share / try to publish. In short, they are less indicative of UTI than a mixed culture. We don’t do sens on many, and only if very convincing evidence that relevant. The default position should be that they are contaminants. So same position as for mixtures.

    Beta-haemolytic streptococci Because beta-haemolytic streptococci are inherently susceptible to beta-lactams, susceptibility testing for these antibiotics is somewhat academic in the majority of simple wound/soft tissue infections. I would do if the clinical details suggested penicillin allergy. We are now doing exactly this, after the Group A strep scare in the UK led to extraordinary expansion in work.

    Anaerobes Anaerobes rarely require formal susceptibility testing. Agree. Very rarely work these up.

    Coagulase negative staphylococci from blood cultures. We never work these up unless clearly significant. I see automation in microbiology leading people away from proper clinical assessment. Look at all the data on epidemiology that comes out of the US with CNS at the top of most lists of causative pathogens. That is not microbiology.

    1. Thanks for feedback! Enterococci in urines are tricky. At my lab we still probably overcall them as urinary pathogens but hardly any end up getting susceptibilities. We put the following comment on most “Amoxycillin is the drug of choice for treating enterococcal infections in the lower urinary tract. Alternative treatment option is nitrofurantoin. (Note: Enterococci are intrinsically resistant to all cephalosporins.”

      1. We put a similar comment on in our lab recently for E. faecalis and stopped susceptiblity testing. For E. faecium we still pefrom it for hospitalised patients, we have high rates of VRE. The paper on E. faecium amoxicillin treatment success was interesting, thanks.
        We apply many of the other rules ourselves. Interestingly we chose to temporarily restart testing S. pyogenes suceptiblities for December for surveillance info in context of near complete shortage of oral beta-lactam syrups for kids. After years of not testing non-invasive isolates and receiving few invasive isolates due to effect of NPIs/lockdowns we had little idea of our erythromycin and clindamycin local resistance rates! Clinicans were also resorting to oral clindaymycin for treatment of streptococcal sore throat and ineffective in 10% or so of our cases.

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