Ask the Laboratory for a Synergy Panel in Resistant Pseudomonas Infections



Ask the Laboratory for a Synergy Panel in Resistant Pseudomonas Infections


Harjot K. Singh MD

Sara E. Cosgrove MD



The use of combination therapy (double coverage) in the management of Gram-negative infections is a controversial practice. Reasons to consider combination therapy include (a) broadening empiric coverage in the event that the causative organism is resistant to one agent, (b) prevention of emergence of resistance during therapy, and (c) obtaining synergistic activity between two agents that is greater than would be expected from the sum of the activities of the individual agents.

Broadening empiric coverage should be considered in patients who are critically ill as data suggest that inappropriate empiric therapy can lead to adverse patient outcomes. Agents from two different classes of antibiotics should be used. Review of the local antibiogramis important to assess whether combination therapy is needed and what agents should be used. For example, if the usual empiric therapy regimen for a penicillin-allergic patient is a fluoroquinolone, but 40% of Pseudomonas isolates in a unit are known to be resistant to fluoroquinolones, addition of a second agent such as an aminoglycoside may effectively broaden empiric coverage if Pseudomonas is suspected. In all cases in which combination therapy is chosen for empiric coverage, therapy should be narrowed on the basis of microbiologic data.


What to Do

Prevention of emergence of resistance is often cited as a reason for combination therapy in the management of definitive infections with Gram-negative organisms; however, emergence of resistance on therapy is uncommon, occurring in 5% to 10% of Gram-negative infections. In most circumstances, long-term combination therapy is not needed and may be harmful as it increases toxicity from adverse drug reactions. It can be considered in the treatment of a deep-seated infection (such as pneumonia or severe osteomyelitis) when the organism being treated is already resistant to one or more classes of antibiotics. Discontinuing one of the agents after 5 to 7 days of therapy when the bacterial burden has decreased is an option. In all cases, attention should be given to appropriate dosing of antibiotics and to obtaining follow-up cultures if the patient is failing therapy. Of note is that when organisms that produce inducible
beta-lactamases (e.g., Enterobacter, Serratia, Citrobacter) are treated with beta-lactam agents, emergence of resistance on therapy can occur in ∼20% of cases. Monotherapy with beta-lactam agents is best avoided for treatment of serious infections in these patients if other agents are available.

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Jul 1, 2016 | Posted by in ANESTHESIA | Comments Off on Ask the Laboratory for a Synergy Panel in Resistant Pseudomonas Infections

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