Central Venous Access Device Registry - Improving Outcomes for Patients Diagnosed with Cancer

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Initiative Type
Data Collection
Technology
Status
Deliver
Added
Last updated

Summary

This project has not progressed in its current format and has not been implemented. 

Central Venous Access Device (CVAD) registries provide clinicians with data about device-related complications and patient outcomes. The registry collects information about the patients requiring CVADs within Cancer Care Services, type of CVADs being inserted, complications and reasons for removal.

This project was developed and driven by skills learnt during the Manage 4 Improvement program: a six-month integrated leadership and management program designed to build the confidence and capabilities of clinicians to support improvements in health service delivery.

Key dates
Apr 2016
Mar 2018
Implementation sites
Royal Brisbane and Women's Hospital

Aim

To identify variances and trends in the quality of central venous access device (CVAD) care provided.

Benefits

Provide data on CVAD failure both mechanical and infective that enables targeted quality improvement initiatives.

Background

The CVAD Registry has captured information on all adult cancer patients who received a CVAD from 1st April 2016 at the Royal Brisbane and Women’s Hospital.

Solutions Implemented

A registry was established to capture information on all CVAD received for adult cancer care services. Data includes device related-complications, patient outcomes, type of CVAD, complications and reasons for removal.

Evaluation and Results

Over 1,100 CVADs have been recorded on over 600 patients. To date less than half of the patients completed their treatment with one CVAD.

Lessons Learnt

The data has been used to identify education opportunities that are currently being provided.

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Key contact

Nicole Gavin
Nurse Researcher
Metro North Hospital and Health Services
(07) 3646 5833
nicole.gavin@health.qld.gov.au

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