References:
- 510(k) Premarket Notification: ARROWg+ard and Blue Plus™ Antimicrobial
Central Venous Catheter. March 8, 2000. Accessed April 17, 2024.
https://www.accessdata.fda.gov/cdrh_docs/pdf/K993691.pdf
- Gupta N, Weber H, Moss S, Gaire-Patel K. Are antibiotic-resistant
‘superbugs’ a real challenge to antimicrobial central venous catheter
performance? Poster presented at: Annual Meeting of the Association for
Vascular Access 2014; September 7-10, 2014; National Harbor, MD.
- O'Grady NP, Alexander M, Burns LA, et al; Healthcare Infection Control
Practices Advisory Committee (HICPAC). Guidelines for the prevention
of intravascular catheter-related infections. Clin Infect Dis.
2011;52(9):e162-e193. doi:10.1093/cid/cir257
-
Buetti N, Marschall J, Drees M, et al. Strategies to prevent central
line-associated bloodstream infections in acute-care hospitals: 2022 update.
Infect Control Hosp Epidemiol. 2022;43(5):553-569. doi:10.1017/ice.2022.87
-
Nickel B, Gorski LA, Kleidon TM, et al. Infusion therapy standards of
practice. J Infus Nurs. 2024;47(suppl1):S1-S285.
doi:10.1097/NAN.0000000000000532
-
1910.1030 - Bloodborne pathogens. US Department of Labor; Occupational
Safety and Health Administration. Accessed April 17, 2024.
https://www.osha.gov/laws-regs/regulations/standardnumber/1910/1910.1030
-
ADHX-001612: Design History File Index for VPS Rhythm™ DLX System.
-
As compared to uncoated PICCs, intravascular ovine model inoculated with
Staph aureus: AVAR-000427. No correlation between in vitro/in vivo
testing methods and clinical outcomes have currently been ascertained.
-
In vitro data on file 2010: AVER-004371, AVER-004483 and AVAR-000427. No
correlation between in vitro/in vivo testing methods and clinical
outcomes has currently been ascertained.
-
Weiss S, Qureshi M. Evaluating a novel hemodialysis central venous catheter
cap in reducing bloodstream infections: a quality improvement
initiative. Int J Nephrol Renovasc Dis. 2021;14:125-131.
doi:10.2147/IJNRD.S304605
-
Arrowg+ard Blue® Protection Clinical References MC-004390.
-
AGB AHD IFU- S-22142-105C.
-
Veenstra DL, Saint S, Sullivan SD. Cost-effectiveness of
antiseptic-impregnated central venous catheters for the prevention of
catheter-related
bloodstream infection. JAMA. 1999;282(6):554-560. doi:10.1001/jama.282.6.554
-
In vitro data on file 2010. No correlation between in vitro/in vivo testing
methods and clinical outcomes have currently been ascertained.
-
As compared to uncoated PICCs, intravascular ovine model inoculated with
Staph aureus. No correlation between in vitro/in vivo testing
methods and clinical outcomes have currently been ascertained.
-
In vitro data on file 2010: AVER-004371 and AVER-004483. No correlation
between in vitro/in vivo testing methods and clinical outcomes have
currently been ascertained.
-
Chapolini RJ. Incompatible drug infusion through the Arrow two-lumen
catheter—an in vitro analysis. White Marsh Labs, Baltimore, MD.
Unpublished, April 1987.
-
Jaimovich DG, Rose WW. In vivo evaluation of simultaneous administration of
incompatible drugs via a double-lumen peripheral catheter. Crit
Care Med. 1990;18(10):1164-1166. doi:10.1097/00003246-199010000-00022
-
Prince RA, Lucas DS, Fox JL. Effect of a dual-lumen peripheral catheter on
the delivery of known incompatible medications. Ann Pharmacother.
1998;32(9):875-877. doi:10.1345/aph.18042
-
DLX-200-OPM-US: VPS Rhythm™ DLX Operator's Manual.
-
D041679: IMH Benchtop Stylet Advancement in a Simulated Use Anatomical Model
of NaviCurve™. Product Stylet/PICC Assemblies.
-
Antimicrobial – In vitro data on file 2010; AVER-004371, AVER-004483,
AVAR-000427.
Rx only
Refer to the Instructions for Use for a complete listing of the indications,
contraindications, warnings and precautions.
Contraindications:
Arrowg+ard Blue™ and Arrowg+ard Blue Plus™ Catheters
are contraindicated for patients with known hypersensitivity to chlorhexidine and
silver sulfadiazine and/or sulfa drugs.
Clinical assessment of the patient must be completed to ensure no
contraindications exist.
The Arrowg+ard Blue Advance™ Catheters are contraindicated in the following
areas:
-Patients with known hypersensitivity to chlorhexidine
-In presence of device-related infections
-In presence of previous or current thrombosis in the intended vessel or along
the catheterized vessel pathway.
No correlation between in vitro/in vivo testing methods and clinical
outcomes have currently been ascertained.
Teleflex, the Teleflex logo, Arrow, Arrowg+ard Blue, Arrowg+ard Blue
Advance, Arrowg+ard Blue Plus, Arrow-Johans, ErgoPack, GlideThru,
QuickFlash, TipTracker, TwinCath, and VPS Rhythm are trademarks of Teleflex
Incorporated or its affiliates, in the U.S. and/or other
countries. All other trademarks are trademarks of their respective owners. MC-009786