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Treatment of infections caused by multidrug-resistant  Pseudomonas  species is difficult because few antibiotics active against such organisms are available. Arbekacin, a relatively new aminoglycoside, is effective against  Pseudomonas  spp.  in vitro . However, no clinical report on arbekacin treatment of a human infection with a multidrug-resistant  Pseudomonas  has appeared to date. We encountered a case of pneumonia caused by a  Pseudomonas  strain producing a metallo-beta-lactamase; the patient was successfully treated with arbekacin. A 69-year-old male presented to our hospital experiencing cardiac arrest after rescue from water. Spontaneous circulation had earlier resumed after brief application of cardiopulmonary resuscitation. The patient was subjected to induced hypothermia. He experienced severe acute respiratory distress syndrome. The patient regained consciousness on day 8 post-admission. Episodes of ventilator-associated pneumonia were recorded on days 5 and 12. The causative organism was a strain of  Pseudomonas putida  that produced a metallo-beta-lactamase. Combination therapy with arbekacin and levofloxacin successfully resolved the pneumonia. The patient was transferred to another hospital on day 37 to undergo further rehabilitation. Strains of  P. putida  producing metallo-beta-lactamases have become more widespread in recent years. Colistin is traditionally the drug of last resort to treat infections with multidrug-resistant  Pseudomonas . However, colistin use is associated with a very high frequency of adverse effects, and the costs of such therapy are not covered by the Japanese health insurance system. Our results indicate that arbekacin is an efficient alternative to multidrug-resistant  Pseudomonas .

Arbekacin treatment of a patient infected with a Pseudomonas putida producing a metallo-beta-lactamase