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Nurse-led Placement of Peripheral Venous Catheters in Overweight Patients Using Standard or Dynamic Ultrasound-guided Technique

Not Applicable
Completed
Conditions
Emergencies
Overweight and Obesity
Interventions
Device: Dynamic ultrasound-guided short-axis needle tip navigation
Other: Standard technique of placing a PVC
Registration Number
NCT04412967
Lead Sponsor
University Hospital, Linkoeping
Brief Summary

Overweight and obesity may be associated with difficult intravenous access leading to longer procedure time and more placement attempts of peripheral venous catheters (PVC). Dynamic ultrasound-guided short-axis needle tip navigation (DUST) may facilitate the procedure.

This was a prospective, randomized, non-blinded study to compare time and placement attempts for nurse-led standard (ST) and ultrasound guided PVC placement in 90 emergency patients with a BMI ≥25kg/m2.

Consenting patients were randomized at a 1:1 ratio to receive PVC by either ST or DUST.

Application time was defined as the time from applying stasis to visible blood in the PVC flash-chamber.

No difference in time was found (medians: ST 42 s; DUST 53.5 s, P = 0.535). There were on average 17 % less placement attempts in the DUST-group (median 1 attempt; Q1 = 1 Q3 = 1) compared to the ST-group (median 1 attempt; Q1 = 1 Q3 = 1.5), (p = 0.031). Patients reported no differences in perceived pain (p = 0.955) or perceived satisfaction (p = 0.342). Pain and subcutaneous infiltrations were the only side-effects reported (ST-group 6, DUST-group 5).

DUST does not decrease time to functional PVC but reduces the number of PVC placement attempts in patients with BMI ≥25 kg/m2.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
89
Inclusion Criteria
  • REETS prioritization level of "Orange", "Yellow", "Green" or "Blue"
  • 18 years old
  • BMI ≥25 Kg/m2
  • Need of PVC according to Emergency department guidelines
  • Able to give written informed consent
Exclusion Criteria
  • Unable or unwilling to provide informed consent
  • Life threatening patient status (REETS prioritization level of "Red")
  • Immunosuppression
  • Pregnant or lactating women
  • Blood infections
  • Puncture zone skin damaged (burns, eczema, infection)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
DUSTDynamic ultrasound-guided short-axis needle tip navigationDynamic ultrasound-guided short-axis needle tip navigation (DUST)
Standard Technique PVC placementStandard technique of placing a PVCStandard PVC placement technique
Primary Outcome Measures
NameTimeMethod
Number of cannulation attempts1 hour

The total number of cannulation attempts performed per patient

Time to application1 hour

Application time was defined as the time from applying stasis to visible blood in the PVC flash-chamber.

Secondary Outcome Measures
NameTimeMethod
Perceived Pain1 hour

The perceived pain of the patient as indicated by Numeric Rating scale (NRS, 0 = no pain, 10 = the worst pain possible)

Patient satisfaction1 hour

The perceived satisfaction of the patient as indicated by Numeric Rating scale (NRS, 0 = not satisfied, 10 = maximum satisfaction)

Trial Locations

Locations (1)

University Hospital Linköping

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Linköping, Östergötland, Sweden

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