Evidence map›Paper›PMID 36681747›Full record

ArticleAnnals of biomedical engineering2023

Enhanced Drug Delivery for Cardiac Microvascular Obstruction with an Occlusion-Infusion-Catheter.

Yannick Rösch, David Eggenberger, Yves Kuster, Lino Widmer, Sabrina Frey, Rob Schwartz, Cornelia Nef, Jens Ulmer, Dominik Obrist

Open access · hybridAbstract read
In one paragraph

Article in Annals of biomedical engineering, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. A Master-Follower Teleoperation System for Robotic Catheterisation: Design, Characterisation and Tracking Control.The international journal of medical robotics + computer assisted surgery : MRCAS · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Yannick RöschARTORG Center for Biomedical Engineering Research, University of Bern, Freiburgstrasse 3, 3010, Bern, Switzerland. yannick.roesch@unibe.ch.ORCID http://orcid.org/0000-0001-7284-3072
David EggenbergerInstitute for Microtechnology and Photonics, OST University of Applied Sciences, Buchs SG, Switzerland.
Yves KusterInstitute for Microtechnology and Photonics, OST University of Applied Sciences, Buchs SG, Switzerland.
Lino WidmerARTORG Center for Biomedical Engineering Research, University of Bern, Freiburgstrasse 3, 3010, Bern, Switzerland.
Sabrina FreyCorFlow Therapeutics AG, Baar, Switzerland.
Rob SchwartzCorFlow Therapeutics AG, Baar, Switzerland.
Cornelia NefInstitute for Microtechnology and Photonics, OST University of Applied Sciences, Buchs SG, Switzerland.
Jens UlmerInstitute for Microtechnology and Photonics, OST University of Applied Sciences, Buchs SG, Switzerland.
Dominik ObristARTORG Center for Biomedical Engineering Research, University of Bern, Freiburgstrasse 3, 3010, Bern, Switzerland.
University of Bern · CHUniversity of St.Gallen · CH

Funding

Innosuisse - Schweizerische Agentur für Innovationsförderung 25390.2PFLS-LSInnosuisse - Schweizerische Agentur für Innovationsförderung 31010.1IP-LS
6 · The paper itself

Abstract

Microvascular Obstruction (MVO) is a common consequence of acute myocardial infarction. MVO is underdiagnosed and treatment is often nonspecific and ineffective. A multi-scale in-vitro benchtop model was established to investigate drug perfusion in MVO affected microcirculation. The central element of the benchtop model was a fluidic microchip containing channels with diameters between [Formula: see text] and 50 μm representing [Formula: see text] of the microvascular tree fed by the left anterior descending artery (LAD). The outlets of the chip could be closed to mimic MVO. Two methods for intracoronary infusion of pharmacologic agents (simulated by dye) to regions with MVO were investigated using an occlusion-infusion catheter. The first case was a simple, bolus-like infusion into the LAD, whereas the second case consisted of infusion with concomitant proximal occlusion of the LAD phantom with a balloon. Results show that local dye concentration maxima in the chip with MVO were 2.2-3.2 times higher for the case with proximal balloon occlusion than for the conventional infusion method. The cumulated dose could be raised by a factor 4.6-5.2. These results suggest that drug infusion by catheter is more effective if the blood supply to the treated vascular bed is temporarily blocked by a balloon catheter.

Indexed as

Myocardial InfarctionPercutaneous Coronary InterventionCathetersCoronary CirculationCoronary VesselsHeartHumansMicrocirculationBalloon occlusionControlled flow infusionCoronary circulationIntracoronary drug infusionLeft-heart mock loopMicrofluidic chipMVOSTEMI

Identifiers

PMID36681747
PMCPMC10172228
OpenAlexW4317676869

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.