Survivors really want you to measure 100% recovery, not cost. WHY THE FUCK AREN'T YOU DOING THAT?
So no reporting or measurement of 100% recovery, obviously not important to the medical staff or researchers. But vastly important to stroke survivors.
“What's measured, improves.” So said management legend and author Peter F. Drucker
The latest useless stuff here:
Philips' direct-to-angio stroke pathway: new analysis demonstrates substantial cost savings in addition to improved patient outcomes
Economic analysis of cost of Vall d’Hebron University Hospital Stroke Unit shows direct-to-angio stroke pathway can save more than USD 3,000 per patient
Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced the results of a health economic analysis published
in the Journal of NeuroInterventional Surgery (JNIS) that show an
innovative approach to the stroke care pathway reduced costs by an
average of EUR 2,848 (~USD 3,120) per patient. The retrospective
analysis looked at data from the controlled single-center ANGIOCAT
clinical trial conducted at the Vall d’Hebron University Hospital Stroke
Unit (Barcelona, Spain) [1]. Earlier results from this study
demonstrated that a ‘Direct-to-Angio Suite’ (DTAS) pathway improves
clinical outcomes for patients who have suffered a stroke.
The ANGIOCAT clinical study has already shown that bringing stroke patients directly to the angio suite improves patient outcomes. The economic analysis of the data now tells us we can also significantly reduce costs.
Dr. Manuel Requena
Stroke and Interventional Neurologist, University Hospital Vall d’Hebron
“The
ANGIOCAT clinical study has already shown that bringing stroke patients
directly to the angio suite improves patient outcomes. The economic
analysis of the data now tells us we can also significantly reduce
costs,” said Dr. Manuel Requena, Stroke and Interventional Neurologist,
University Hospital Vall d’Hebron. “This indicates that the initial
up-front investment of a direct-to-angio suite workflow will result in a
fast return on investment for healthcare providers.”
Innovating the stroke pathway
After
initial triage in the emergency department, the typical treatment
pathway for stroke involves sending the patient to the radiology
department for a diagnostic CT or MRI brain scan. This adds time, often
worsened by gaps in communication, information, and access to stroke
expertise. For stroke centers, a time-saving alternative is to have a
dedicated angio-suite permanently on standby, to which stroke patients
can be transferred immediately after admission. Using cone-beam CT
imaging, such as that built into Philips Image Guided Therapy System – Azurion,
clinicians can make a diagnosis and intervene on-the-spot, saving
precious time. The health economics analysis indicates that a positive
return on investing in a dedicated angio suite can be achieved in only a
few years.
Philips cone-beam CT
Philips’
DTAS workflow is enabled by an advanced cone-beam computed tomography
(CBCT) brain scan performed directly in the angio suite to diagnose
patients. CBCT utilizes a cone-shaped beam of X-rays and a flat-panel
detector mounted on a C-arm gantry similar to that routinely used in an
angio suite, capturing multiple images from different angles to
reconstruct 3D images of the brain. Thanks to technology breakthroughs,
Philips has increased the diagnostic confidence of CBCT from 32% to 93%
in the space of a few years [3][4][5]. This technology can rule out
intracranial hemorrhages and identify large vessel occlusions (LVOs),
which account for roughly a quarter to a half of acute ischemic strokes
[2]. Patients diagnosed with an LVO can then be immediately operated on
using a minimally invasive image-guided procedure known as a mechanical
thrombectomy to open up the blocked artery causing their stroke.
Lower cost, better patient outcomes
Multiple
single-center studies have shown the positive impact of DTAS on
clinical outcomes with the result that many dedicated stroke centers
have already adopted it. A large multi-center randomized clinical trial
called WE-TRUST (Workflow Optimization to Reduce Time to Endovascular Reperfusion for Ultra-fast Stroke Treatment) [8] is currently running to confirm the patient benefit of DTAS.
Philips’ stroke portfolio includes solutions for stroke monitoring and
communication in ambulances, tele-stroke patient assessment, diagnostic
imaging and analysis, image-guided therapy, neurological monitoring and
assessment, and more. Its image-guided stroke therapy solutions are
based on the Philips Image Guided Therapy System – Azurion.
[1]
Requena M, Vanden Bavière H, Verma S, et al. Cost-utility of direct
transfer to angiography suite (DTAS) bypassing conventional imaging for
patients with acute ischemic stroke in Spain: results from the ANGIOCAT
trial.
Journal of NeuroInterventional Surgery Published Online First: 27 April 2023. doi: 10.1136/jnis-2023-020275
[2] World Stroke Organization (WSO): Global Stroke Fact Sheet 2022 (https://www.world-stroke.org/assets/downloads/WSO_Global_Stroke_Fact_Sheet.pdf)
[3] Nicholson P, Cancelliere NM, Bracken J, et al. Novel flat-panel
cone-beam CT compared to multi-detector CT for assessment of acute
ischemic stroke: A prospective study. Eur J Radiol. 2021 May;138:109645.
doi: 10.1016/j.ejrad.2021.109645. Epub 2021 Mar 10. PMID: 33725654.
[4] Cancelliere NM, Hummel E, van Nijnatten F, et al. The butterfly
effect: improving brain cone-beam CT image artifacts for stroke
assessment using a novel dual-axis trajectory. J Neurointerv Surg. 2023
Mar;15(3):283-287. doi: 10.1136/neurintsurg-2021-018553. Epub 2022 Apr
27. PMID: 35478176; PMCID: PMC9985729.
[5] Cancelliere NM, van
Nijnatten F, Hummel E, et al. Motion artifact correction for cone beam
CT stroke imaging: a prospective series. J Neurointerv Surg. 2022 Dec
23:neurintsurg-2021-018201. doi: 10.1136/jnis-2021-018201. Epub ahead of
print. PMID: 36564201.
[6] WE-TRUST. Workflow optimization to
reduce time to endovascular reperfusion for ultra-fast stroke treatment,
ClinicalTrials. gov, U.S. National Library of Medicine, identifier:
NCT04701684. n.d. Available: https://clinicaltrials.gov/ct2/show/
NCT04701684. The WE-TRUST study is sponsored by Philips.
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