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1.
J Pharm Pract ; 30(6): 672-675, 2017 Dec.
Article in English | MEDLINE | ID: mdl-27876693

ABSTRACT

Sodium-glucose cotransporter 2 (SGLT2) inhibitors have been associated with serious urinary tract infections (UTIs) including pyelonephritis and urosepsis. The Food and Drug Administration (FDA) issued a label change to include this warning in December 2015 due to a small number of cases (n = 19) reported to the FDA Adverse Event Reporting System. Details of these cases are limited and none involved empagliflozin. To date, there has been no published literature comprehensively describing serious UTIs attributed to empagliflozin. We describe a case of septic shock due to Serratia marcescens pyelonephritis and bacteremia that required intensive care unit admission in a well-controlled, type 2 diabetic patient who had begun taking empagliflozin 2 months prior. The patient was treated successfully with intravenous antibiotics followed by oral ciprofloxacin. After discontinuation of empagliflozin and completion of antibiotic therapy, no subsequent UTIs were documented in the following 4 months.


Subject(s)
Bacteremia/chemically induced , Benzhydryl Compounds/adverse effects , Glucosides/adverse effects , Pyelonephritis/chemically induced , Serratia Infections/chemically induced , Serratia marcescens/isolation & purification , Shock, Septic/chemically induced , Aged , Bacteremia/complications , Bacteremia/diagnosis , Diabetes Mellitus, Type 2/drug therapy , Humans , Hypoglycemic Agents/adverse effects , Male , Pyelonephritis/complications , Pyelonephritis/diagnosis , Serratia Infections/complications , Serratia Infections/diagnosis , Serratia marcescens/drug effects , Shock, Septic/complications , Shock, Septic/diagnosis
2.
Clin J Pain ; 24(5): 374-80, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18496300

ABSTRACT

OBJECTIVES: To determine the cause of an outbreak of Serratia marcescens infections in patients after interventional pain management procedures at an outpatient pain clinic. METHODS: We conducted a case-control study and collected clinical and environmental samples. RESULTS: We identified 5 culture-confirmed case-patients and 2 presumptive case-patients who had no bacteria recovered from cultures. The 7 case-patients were compared with 28 controls who underwent procedures at the same clinic but did not develop symptoms of infection. All confirmed case-patients had S. marcescens bloodstream infections; 2 had concurrent S. marcescens central nervous system infections. Case-patients were more likely than controls to have procedures that used contrast solution or entered the epidural or intervertebral disc space (P< or =0.01 for each). All S. marcescens clinical isolates were indistinguishable by pulsed-field gel electrophoresis. We did not isolate S. marcescens from medications or environmental samples; however, S. marcescens was shown to survive and grow in contrast solution that was experimentally contaminated for up to 30 days. Single-dose vials of medication, including contrast solution, were used for multiple procedures; multiple medications were accessed with a common needle and syringe. DISCUSSION: The findings of this investigation suggest contamination of a common medication, likely contrast solution, as the source of the outbreak. Practices, such as reusing single-dose medication vials and using a common needle and syringe to access multiple medications, could have led to contamination and propagation of S. marcescens and should be avoided in interventional pain management procedures.


Subject(s)
Central Nervous System Bacterial Infections/chemically induced , Central Nervous System Bacterial Infections/diagnosis , Contrast Media/adverse effects , Disease Outbreaks/prevention & control , Serratia Infections/chemically induced , Serratia Infections/diagnosis , Serratia marcescens/isolation & purification , Adult , Aged , Aged, 80 and over , Case-Control Studies , Female , Humans , Male , Middle Aged , Pain/diagnosis , Pain/drug therapy
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