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Design, development and preliminary assessment in a porcine model of a novel peripheral intravenous catheter aimed at reducing early failure rates.
Doyle, Barry J; Kelsey, Lachlan J; Shelverton, Caroline; Abbate, Gabriella; Ainola, Carmen; Sato, Noriko; Livingstone, Samantha; Bouquet, Mahe; Passmore, Margaret R; Wilson, Emily S; Colombo, Sebastiano; Sato, Kei; Liu, Keibun; Heinsar, Silver; Wildi, Karin; Carr, Peter J; Suen, Jacky; Fraser, John; Li Bassi, Gianluigi; Keogh, Samantha.
Afiliación
  • Doyle BJ; Vascular Engineering Laboratory, Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands and the UWA Centre for Medical Research, The University of Western Australia, Nedlands, Western Australia, Australia.
  • Kelsey LJ; School of Engineering, The University of Western Australia, Perth, Western Australia, Australia.
  • Shelverton C; Australian Research Council Centre for Personalised Therapeutics Technologies, Australia.
  • Abbate G; British Heart Foundation Centre for Cardiovascular Science, The University of Edinburgh, UK.
  • Ainola C; Vascular Engineering Laboratory, Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands and the UWA Centre for Medical Research, The University of Western Australia, Nedlands, Western Australia, Australia.
  • Sato N; School of Engineering, The University of Western Australia, Perth, Western Australia, Australia.
  • Livingstone S; Flomatrix Pty Ltd, Brisbane, Queensland, Australia.
  • Bouquet M; Critical Care Research Group, The Prince Charles Hospital, Brisbane, Queensland, Australia.
  • Passmore MR; Critical Care Research Group, The Prince Charles Hospital, Brisbane, Queensland, Australia.
  • Wilson ES; Critical Care Research Group, The Prince Charles Hospital, Brisbane, Queensland, Australia.
  • Colombo S; Critical Care Research Group, The Prince Charles Hospital, Brisbane, Queensland, Australia.
  • Sato K; Critical Care Research Group, The Prince Charles Hospital, Brisbane, Queensland, Australia.
  • Liu K; Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia.
  • Heinsar S; Critical Care Research Group, The Prince Charles Hospital, Brisbane, Queensland, Australia.
  • Wildi K; Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia.
  • Carr PJ; Critical Care Research Group, The Prince Charles Hospital, Brisbane, Queensland, Australia.
  • Suen J; Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia.
  • Fraser J; Critical Care Research Group, The Prince Charles Hospital, Brisbane, Queensland, Australia.
  • Li Bassi G; Critical Care Research Group, The Prince Charles Hospital, Brisbane, Queensland, Australia.
  • Keogh S; Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia.
J Vasc Access ; : 11297298221127760, 2022 Oct 24.
Article en En | MEDLINE | ID: mdl-36281219
ABSTRACT

BACKGROUND:

Peripheral intravenous catheters (PIVCs) are the most commonly used invasive medical device, yet despite best efforts by end-users, PIVCs experience unacceptably high early failure rates. We aimed to design a new PIVC that reduces the early failure rate of in-dwelling PIVCs and we conducted preliminary tests to assess its efficacy and safety in a porcine model of intravenous access.

METHODS:

We used computer-aided design and simulation to create a PIVC with a ramped tip geometry, which directs the infused fluid away from the vein wall; we called the design the FloRamp™. We created FloRamp prototypes (test device) and tested them against a market-leading device (BD Insyte™; control device) in a highly-controlled setting with five insertion sites per device in four pigs. We measured resistance to infusion and visual infusion phlebitis (VIP) every 6 h and terminated the experiment at 48 h. Veins were harvested for histology and seven pathological markers were assessed.

RESULTS:

Computer simulations showed that the optimum FloRamp tip reduced maximum endothelial shear stress by 60%, from 12.7 Pa to 5.1 Pa, compared to a typical PIVC tip and improved the infusion dynamics of saline in the blood stream. In the animal study, we found that 2/5 of the control devices were occluded after 24 h, whereas all test devices remained patent and functional. The FloRamp created less resistance to infusion (0.73 ± 0.81 vs 0.47 ± 0.50, p = 0.06) and lower VIP scores (0.60 ± 0.93 vs 0.31 ± 0.70, p = 0.09) than the control device, although neither findings were significantly different. Histopathology revealed that 5/7 of the assessed markers were lower in veins with the FloRamp.

CONCLUSIONS:

Herein we report preliminary assessment of a novel PIVC design, which could be advantageous in clinical settings through decreased device occlusion and reduced early failure rates.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Vasc Access Asunto de la revista: ANGIOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Vasc Access Asunto de la revista: ANGIOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Australia