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Development and validation of a scale to predict the risk of failure on the first attempt of inserting an intravenous peripheral catheter

A-DIVA study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON27540
Enrollment
2500
Registered
2014-05-13
Start date
2014-01-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intravenous peripheral catheter insertion (inbrengen van een perifere intraveneuze canule) Prediction of difficulty of inserting a peripheral intravenous catheter (voorspellen van de moeilijkheid tijdens het inbrengen van een perifere intraveneuze canule)

Interventions

IV access was routinely obtained in the preoperative holding area by nurse anesthetists (NA), who are experienced with inserting peripheral IV catheters and familiar with the study protocol. After con

Sponsors

Catharina Hospital Eindhoven Michelangelolaan 2 5623 EJ Eindhoven
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients 18 years or older were eligible when scheduled for an elective surgical procedure and included in the study in our preoperative holding area of the operation theatre.

Exclusion criteria

Exclusion criteria: Patients were excluded when they were not adequate to answer questions or when an IV access was requested from the ward.

Design outcomes

Primary

MeasureTime frame
The primary outcome variable was defined as failed peripheral IV catheterization on the first attempt. An attempt was defined as when the needle first touches the skin until the needle was removed from the skin. A new attempt was defined as any change in vessel localization, followed by a new skin puncture. For development of the A-DIVA score, following patients’ characteristics were collected: sex, age, weight, length, body mass index, skin shade, dominant site, tympanic temperature, whether or not the patient received premedication and if it was difficult to achieve and IV access in the past. These data were collected prior to the procedure, by asking the patient or from the preoperative anesthesia screening form. Procedure-related factors were registered prior to or after insertion of an IV catheter: skin shade, size of the cannula, side of the cannulation, place of cannulation on the extremity, size of the stewed vein in millimeters, pain score after every puncture on an eleven-points NRS scale (score 0 is no pain en score 10 is the worst imaginable pain), number of attempts needed for successful IV cannulation, whether or not the vein was palpable and/or visual before puncture (answered with yes or no) and the years of experience of the NA. After the procedure, patients historical and physical status were collected by asking the patient or from the preoperative anesthesia screening forms: sex, length, weight, BMI and special attention was paid to (chronic) diseases, IV drug abuse, vessel diseases, hematological status and the use of medications.

Contacts

Public ContactF.H.J. Loon, van

Michelangelolaan 2

rick.v.loon@cze.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)