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Rahnella aquatilis is a member of the family Enterobacteriaceae, and its natural habitat is water. The organism is rarely isolated in clinical specimens. The infections ascribed to this organism are bacteremia (6, 10), sepsis (4), respiratory infection (5), urinary tract infection (1), and wound infection (7) in immunocompromised patients and infective endocarditis (8) in patients with congenital heart disease.

In this paper we report what we believe to be the first case of sepsis due to an infusion of fluid contaminated with R. aquatilis in an immunocompetent adult.

Case report. The 26-year-old male patient was in good health with no previous history of chronic debilitating diseases, such as diabetes mellitus, hypertension, hepatitis, or renal failure. Three weeks before his visit to the emergency room, he purchased a bottle of 1,000-ml 5% dextrose water mixed with 15 mg of vitamin B complex and 100 mg of vitamin C in a private drugstore; 250 ml of the fluid was infused by an unlicensed person. It is prohibited to sell intravenous infusion fluid in a drugstore without a doctor's prescription in Korea, but it is not uncommon for someone to buy the fluid with no prescription, even when he or she feels only fatigue or mild discomfort. The male patient stopped the infusion and removed the intravenous line, and the remaining fluid was kept in his room at room temperature for 3 weeks. On 19 March 1999, his day of admission, he infused 250 ml of the remaining fluid and removed the intravenous line by himself. Five hours after that, he had a headache, blurred vision, and substernal pain radiating to his left shoulder and neck. He was immediately taken to the emergency room of Pusan National University Hospital. An examination of his initial vital signs showed low blood pressure (60/40 mm Hg), high fever (38.2°C), a respiratory rate of 24/min, and a pulse rate of 88/min, indicating septic shock. The leukocyte count was 11.7 × 10⁹/liter with a shift to the left, and the D-dimer was 1.6 mg/liter. Three sets of blood for culture were drawn with a 30-min interval between each, and intravenous ceftriaxone and imipenem were started. Blood cultures were performed with the VITAL automatic system (Biomerieux Marcy l'Etoile, France). All four aerobic and anaerobic bottles of the first two sets showed positive signals, and gram-negative bacilli were discovered by Gram stain. The bacteria were all identified as R. aquatilis. The infusion fluid was cultured in a blood agar plate and a MacConkey agar plate, because it was suspected as a possible contaminant, and the same bacillus was grown. All bacteria isolated from blood and infusion fluid were identified as R. aquatilis initially by the API 20E commercial system version 4.0 (Biomerieux) with code no. 1205573 (80.5%). Because R. aquatilis is a very uncommon pathogen, we tried to identify the isolate by using two more commercial kits. The additional kits showed good identification: code no. 6764675051 (99%) of BBL Crystal ID System E/NF version 4.0 (Becton Dickinson Microbiology System, Sparks, Nev.) and bionumber 6664770430 (98%) of Vitek GNI version VTK-R06.01 (Biomerieux Vitek, Hazelwood, Mo.). The species identification was confirmed by temperature-dependent motility and growth characteristics and lack of yellow pigment production (Table 1). On the third day of admission, the antimicrobial susceptibility test by the National Committee for Clinical Laboratory Standards-recommended disk diffusion method (9) resulted in susceptibility to ciprofloxacin, cefotaxime, cefoxitin, gentamicin, imipenem, cefamandole, and trimethoprim-sulfamethoxazole and resistance to ampicillin and cephalothin. The treatment with intravenous ceftriaxone and imipenem was continued for the first 3 days, because the isolate was susceptible to ceftriaxone and imipenem and because cefotaxime and ceftriaxone are a relative group of agents that has an almost identical spectrum of activity and interpretative results and for which cross-resistance and susceptibility are nearly complete (9). Supportive electrolyte and fluid therapy was undergone for 3 additional days. On the sixth day of admission, the man's vital signs had normalized: blood pressure, 110/80 mm Hg; body temperature, 36.3°C; respiratory rate, 22/min; and pulse rate, 76/min. The leukocyte count and D-dimer had also normalized. He was discharged on the 13th day of admission with good health. At the time of discharge, the human immunodeficiency virus antibody was negative and the lymphocyte count was 2.66 × 10⁹/liter, with a normal CD4/CD8 ratio. The blood culture was not done.