Central venous Access device SeCurement And Dressing Effectiveness for peripherally inserted central catheters in adult acute hospital patients (CASCADE): a pilot randomised controlled trial
Autor: | Emily Larsen, Peter Hancock, Raymond Javan Chan, David Wyld, Nicole Gavin, Abu Choudhury, Emily Russell, Sarah Northfield, Amanda J. Ullman, Nicole Marsh, Julie Flynn, Claire M. Rickard, Anthony M. Allworth, Gabor Mihala |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
Catheter Obstruction
Male Time Factors Complications medicine.medical_treatment Polyurethanes Medicine (miscellaneous) Peripherally inserted central catheter (PICC) Pilot Projects law.invention Central venous 0302 clinical medicine Catheters Indwelling Randomized controlled trial law Acute care Medicine Central Venous Catheters Pharmacology (medical) 030212 general & internal medicine Treatment Failure lcsh:R5-920 Chlorhexidine Equipment Design Middle Aged Catheter Patient Satisfaction 030220 oncology & carcinogenesis Female Vascular access devices Queensland lcsh:Medicine (General) Adult medicine.medical_specialty Catheterization Central Venous Attitude of Health Personnel Randomised controlled trials Peripherally inserted central catheter Catheterization 03 medical and health sciences Patient satisfaction Catheterization Peripheral Humans Device Removal Aged Inpatients Dressing and securement methods business.industry Research Bandages Surgery Clinical trial Intravenous therapy Catheter-Related Infections Anti-Infective Agents Local Feasibility Studies Tissue Adhesives business Complication |
Zdroj: | Trials, Vol 18, Iss 1, Pp 1-13 (2017) Trials |
ISSN: | 1745-6215 |
Popis: | Background Peripherally inserted central catheters (PICCs) are commonly used for delivering intravenous therapy. PICC failure is unacceptably high (up to 40%) due to mechanical, infectious and thrombotic complications. Poor securement potentiates all complication types. This randomised controlled trial (RCT) aimed to examine the feasibility of a large RCT of four dressing and securement methods to prevent PICC failure. Methods This single-centre pilot RCT included 124 admitted medical/surgical/cancer patients aged ≥ 16 years with a PICC. Interventions were: (i) standard polyurethane dressing and sutureless securement device (SPU + SSD, control); (ii) polyurethane with absorbent lattice pad dressing (PAL + Tape); (iii) combination securement-dressing (CSD); and (iv) tissue adhesive (TA + SPU). All groups except TA + SPU had a chlorhexidine-gluconate (CHG) impregnated disc. Feasibility outcomes were recruitment and safety/acceptability of the interventions. The primary outcome was PICC failure, a composite of PICC removal for local infection, catheter-associated bloodstream infection, dislodgement, occlusion, and/or catheter fracture. Secondary outcomes included individual complications, dressing failure and dwell time, PICC dwell time, skin complications/phlebitis indicators, product costs, and patient and staff satisfaction. Qualitative feedback was also collected. Results PICC failure incidence was: PAL + CHG + Tape (1/5; 20%; 17.4/1000 days), SPU + SSD + CHG (control) (4/39; 10%; 9.0/1000 days), TA + SPU (3/35; 9%; 9.6/1000 days), and CSD + CHG (3/42; 7%; 9.4/1000 days). Recruitment to PAL + CHG + Tape was ceased after five participants due to concerns of PICC dislodgement when removing the dressing. CSD + CHG, TA + SPU (TA applied only at PICC insertion time), and control treatments were acceptable to patients and health professionals. Conclusion A large RCT of CSD + CHG and TA + SPU (but not PAL + CHG + Tape) versus standard care is feasible. Trial registration Australian and New Zealand Clinical Trials Registry, ACTRN12616000027415 . Registered on 15 January 2016. |
Databáze: | OpenAIRE |
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