Managing Patients With Unlabeled Passive Implants on MR Systems Operating Below 1.5 T.

The standard of care for managing a patient with an implant is to identify the item and to assess the relative safety of scanning the patient. Because the 1.5 T MR system is the most prevalent scanner in the world and 3 T is the highest field strength in widespread use, implants typically have "MR Conditional" (i.

Benefits of Using Magnetic Resonance Imaging During Breast Tissue Expansion: Literature Review and Case Series.

Breast cancer results in up to 1.6 million new candidates for yearly breast reconstruction (BR) surgery. Two-stage breast reconstruction surgery with the use of a tissue expander (TE) is a common approach to reconstructing the breast after mastectomy.

Near field communication (NFC) device: Evaluation of MRI issues.

Objective: Near field communication (NFC) is a wireless, short-range, secure communication technology that may be used for healthcare-related applications. An NFC device was recently developed that was intended for implantation in the dorsal fascia, above the interosseous compartment of the hand. This implant uses a ferrite rod to increase the distance of communication between devices.

Breast Tissue Expander With Radiofrequency Identification Port: Assessment of MRI Issues.

Breast tissue expanders with magnetic ports are MRI unsafe, preventing patients from benefiting from the diagnostic capabilities of MRI. A tissue expander was recently developed with a radiofrequency identification (RFID) port used for needle location and expansion that may be acceptable for a patient undergoing MRI. The purpose of this investigation was to evaluate MRI issues using standardized techniques and well-accepted methods for this tissue expander with RFID port.

MRI Evaluation of an Atrial-Anchored Transcatheter Mitral Valve Replacement Implant.

A medical implant that is made from metal must undergo proper MRI testing to ensure patient safety. The purpose of this investigation was to assess issues with MRI with a newly developed atrial-anchored transcatheter mitral valve replacement (TMVR) implant. The atrial-anchored TMVR implant underwent an in vitro evaluation for MRI safety issues using standardized techniques and well-accepted methods.

Evaluation of MRI Issues for a New Wirelessly Powered, Spinal Cord Stimulation Lead With Receiver.

MRI is an imaging modality frequently ordered for patients with neuromodulation systems implanted for spinal cord stimulation. The purpose of this investigation was to evaluate MRI safety issues (magnetic field interactions, MRI-related heating, functional disturbances, and artifacts) for a new wirelessly powered lead with receiver used for SCS. Lead samples underwent in vitro evaluation for MRI safety issues using standardized techniques.

MRI safety and imaging artifacts evaluated for a cannulated screw used for guided growth surgery.

Objective: Percutaneously-placed cannulated screws are the implant of choice for treatment of skeletal deformity associated with growing children that have spastic cerebral palsy (CP). These patients often require MRI examinations throughout their childhood to evaluate associated comorbidities and frequently for research protocols. There are concerns related to the use of MRI when metallic implants are present.

ACR guidance document on MR safe practices: Updates and critical information 2019.

The need for a guidance document on MR safe practices arose from a growing awareness of the MR environment's potential risks and adverse event reports involving patients, equipment, and personnel. Initially published in 2002, the American College of Radiology White Paper on MR Safety established de facto industry standards for safe and responsible practices in clinical and research MR environments. The most recent version addresses new sources of risk of adverse events, increases awareness of dynamic MR environments, and recommends that those responsible for MR medical director safety undergo annual MR safety training.

Safety Considerations of 7-T MRI in Clinical Practice.

Although 7-T MRI has recently received approval for use in clinical patient care, there are distinct safety issues associated with this relatively high magnetic field. Forces on metallic implants and radiofrequency power deposition and heating are safety considerations at 7 T. Patient bioeffects such as vertigo, dizziness, false feelings of motion, nausea, nystagmus, magnetophosphenes, and electrogustatory effects are more common and potentially more pronounced at 7 T than at lower field strengths.

Reconsidering the "MR Unsafe" breast tissue expander with magnetic infusion port: A case report and literature review.

Breast tissue expanders (TEs) with magnetic infusion ports are labeled "MR Unsafe." Therefore, patients with these implants are typically prevented from undergoing magnetic resonance imaging (MRI). We report a patient with a total submuscular breast TE who inadvertently underwent an MRI exam.

7-Tesla MRI of the brain in a research subject with bilateral, total knee replacement implants: Case report and proposed safety guidelines.

Recently, the first 7-T MR system was approved for clinical use in the United States. Unfortunately, relatively few metallic implants have undergone testing to determine if they are acceptable or pose hazards to research subjects and patients at this ultra-high-field strength. Therefore, in lieu of not performing a research or clinical MRI exam at 7-T, the supervising physician may make a decision to scan the individual with an untested metallic implant based on an analysis of the risks vs.

Assessment of metallic patient support devices and other items at 7-Tesla: Findings applied to 46 additional devices.

Objective: Recently, the first 7-Tesla MR system was approved for clinical use in Europe and the United States. Unfortunately, few metallic objects have undergone testing in association with this high-field-strength scanner, including essential equipment such as patient support devices and other items. Therefore, the objective of this investigation was to assess metallic patient support devices and other items for translational attraction at 7-Tesla.

Assessment of MRI safety issues for stainless steel sutures used for microtia reconstruction.

Introduction: Potential magnetic resonance imaging issues for stainless steel sutures used for microtia reconstruction could be clinically significant for safety and diagnostic yield considerations. Therefore, the purpose of this investigation was to assess magnetic resonance issues (magnetic field interactions, heating, and artifacts) for different types of stainless steel sutures used for microtia reconstruction.

Methods: Small gauge, commonly used stainless steel sutures from four different manufacturers (5/0 Steelex, Aesculap/B, Braun Medical, Inc.

Assessment of MRI issues at 1.5 T for the Temperature Logger Implant.

Purpose: The Temperature Logger Implant is a newly developed device that is capable of providing data for animal studies on thermoregulatory function, hibernation, hypothermia, and general health. During research, it may be necessary to conduct a magnetic resonance imaging (MRI) examination on an animal with this device implanted to assess anatomical changes or other conditions. Notably, this new device was specially designed to be unaffected by the electromagnetic fields used for MRI.

In Vitro Magnetic Resonance Imaging Evaluation of Fragmented, Open-Coil, Percutaneous Peripheral Nerve Stimulation Leads.

Objective: Percutaneous peripheral nerve stimulation (PNS) is an FDA-cleared pain treatment. Occasionally, fragments of the lead (MicroLead, SPR Therapeutics, LLC, Cleveland, OH, USA) may be retained following lead removal. Since the lead is metallic, there are associated magnetic resonance imaging (MRI) risks.

Evaluation of Magnetic Resonance Imaging Safety and Imaging Issues Associated with the Occlusion Balloon Used during Fetoscopic Endoluminal Tracheal Occlusion.

Introduction: Congenital diaphragmatic hernias can be successfully treated by fetoscopic tracheal occlusion (FETO), a minimally invasive procedure that may improve postnatal survival. The endoluminal balloon utilized for FETO contains a metallic component that may pose possible risks for the fetus and mother related to the use of magnetic resonance imaging (MRI). The objective of this study is to evaluate MRI-related imaging and safety issues (magnetic field interactions, heating, and artifacts) for the occlusion balloon used in FETO.

Assessment of MRI issues for a new cerebral spinal fluid shunt, gravitational valve (GV).

Purpose: A gravitational valve (GV) may be used to treat hydrocephalus, offering possible advantages that include avoidance of over drainage and long-term complications. Because a GV is made from metal, there are potential safety and other problems related to the use of MRI. The objective of this investigation was to evaluate MRI-related issues (i.

Gadolinium deposition in the brain: summary of evidence and recommendations.

Emerging evidence has linked MRI signal changes in deep nuclei of the brain with repeated administration of gadolinium-based contrast agents. Gadolinium deposits have been confirmed in brain tissue, most notably in the dentate nuclei and globus pallidus. Although some linear contrast agents appear to cause greater MRI signal changes than some macrocyclic agents, deposition of gadolinium has also been observed with macrocyclic agents.

Assessment of MRI Issues at 3 Tesla for a New Metallic Tissue Marker.

Purpose. To assess the MRI issues at 3 Tesla for a metallic tissue marker used to localize removal areas of tissue abnormalities. Materials and Methods.

Evaluation of MRI issues at 3-Tesla for a transcatheter aortic valve replacement (TAVR) bioprosthesis.

Objective: Replacement of the aortic heart valve typically requires open-heart surgery. A new transcatheter aortic valve replacement (TAVR) bioprosthesis made from metallic material was recently developed that is an advantageous alternative insofar as it is implanted using a minimally invasive procedure. Because of the presence of metal, there are safety issues related to MRI.