TY - JOUR
T1 - In vivo model of human pathogen infection and demonstration of efficacy by an antimicrobial pouch for pacing devices
AU - Hansen, Linda K.
AU - Brown, Mary
AU - Johnson, David
AU - Palme, Donald F.
AU - Love, Charles
AU - Darouiche, Rabih
PY - 2009/7
Y1 - 2009/7
N2 - Background: Device-related infections represent a significant clinical challenge. Once established, these infections prove difficult to treat with existing antibiotic regimens, compromising the health of device recipients, and usually requiring surgical intervention to resolve. Objective: The purpose of this study was to determine the efficacy of the AIGIS RX™ antibacterial envelope (TyRx Pharma, Inc., Monmouth Junction, NJ, USA) designed to reduce device-related infections by incorporating minocycline and rifampin in a controlled release polymer. Methods: An infection was established in a rabbit model by creating bilateral subcutaneous implant pockets, into which a pacing device with or without AIGIS RX™ was placed. The incisions were closed, and a defined dose of bacteria was infused into each implant pocket. After 7 days, devices were explanted and sampled for viable bacteria by swabbing and sonication. Results: Initial studies evaluated the ability of the AIGIS RX pouch to reduce Staphylococcus epidermidis (S. epi) infection in this model using clinical and quantitative microbial endpoints. Results demonstrate S. epi infection in all control samples, while no pathogens were recovered from samples with the AIGIS RX™ pouch. Systemic antibiotic levels were undetectable. Additional studies tested the efficacy of the AIGIS RX™ pouch with additional bacterial strains, Staphylococcus capitis, Escherichia coli, and Acinetobacter Baumannii. In each case, the device and implant pocket with the AIGIS RX™ pouch was free of any signs of infection. An assessment of biofilm produced by Acinetobacter demonstrated the elimination of biofilm formation on the implanted device. Conclusion: These results demonstrate that in this animal model, the AIGIS RX™ device reduces the risk for infection of viable pathogens within implant pockets. (PACE 2009; 32:898-907)
AB - Background: Device-related infections represent a significant clinical challenge. Once established, these infections prove difficult to treat with existing antibiotic regimens, compromising the health of device recipients, and usually requiring surgical intervention to resolve. Objective: The purpose of this study was to determine the efficacy of the AIGIS RX™ antibacterial envelope (TyRx Pharma, Inc., Monmouth Junction, NJ, USA) designed to reduce device-related infections by incorporating minocycline and rifampin in a controlled release polymer. Methods: An infection was established in a rabbit model by creating bilateral subcutaneous implant pockets, into which a pacing device with or without AIGIS RX™ was placed. The incisions were closed, and a defined dose of bacteria was infused into each implant pocket. After 7 days, devices were explanted and sampled for viable bacteria by swabbing and sonication. Results: Initial studies evaluated the ability of the AIGIS RX pouch to reduce Staphylococcus epidermidis (S. epi) infection in this model using clinical and quantitative microbial endpoints. Results demonstrate S. epi infection in all control samples, while no pathogens were recovered from samples with the AIGIS RX™ pouch. Systemic antibiotic levels were undetectable. Additional studies tested the efficacy of the AIGIS RX™ pouch with additional bacterial strains, Staphylococcus capitis, Escherichia coli, and Acinetobacter Baumannii. In each case, the device and implant pocket with the AIGIS RX™ pouch was free of any signs of infection. An assessment of biofilm produced by Acinetobacter demonstrated the elimination of biofilm formation on the implanted device. Conclusion: These results demonstrate that in this animal model, the AIGIS RX™ device reduces the risk for infection of viable pathogens within implant pockets. (PACE 2009; 32:898-907)
KW - Device infection
KW - Pacemaker
UR - http://www.scopus.com/inward/record.url?scp=67650669013&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=67650669013&partnerID=8YFLogxK
U2 - 10.1111/j.1540-8159.2009.02406.x
DO - 10.1111/j.1540-8159.2009.02406.x
M3 - Article
C2 - 19572866
AN - SCOPUS:67650669013
SN - 0147-8389
VL - 32
SP - 898
EP - 907
JO - PACE - Pacing and Clinical Electrophysiology
JF - PACE - Pacing and Clinical Electrophysiology
IS - 7
ER -