ArticleBJR case reports2018
Off-label magnetic resonance imaging of an InterStim II sacral nerve stimulator device.
Article in BJR case reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
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.
Who cites it
0 citing papers in PubMed, 1 citations in OpenAlex.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The InterStim II (Medtronic, Inc., Minneapolis, MN) sacral nerve stimulator has been approved for MRI scanning of the head only. All other body areas are contraindicated by the manufacturer. This report presents the successful MRI examination of the left hand in a patient with an InterStim II device. Following an assessment of the risks and benefits of proceeding with the scan it was shown that there were minimal additional risks, which could be easily managed with appropriate patient positioning, coil selection and other established techniques. Informed consent was obtained and the scan completed without incident. Following the scan the patient reported full functioning of the device. MRI of the hand is feasible in patients with InterStim II implants using transmit/receive coils with appropriate risk controls in place. Further study of the safety of MRI of other body regions in InterStim II patients is appropriate.
Identifiers
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Registered trials
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