Bioinduction Announces the World’s First Successful Implantations of ‘PICOSTIM’, a Novel, Less Invasive, Self-Contained Cranialized ‘Brain Pacemaker’ for Parkinson’s Disease

Bioinduction Ltd., a company developing an innovative and disruptive patient-centric Deep Brain Stimulation (DBS) platform solution designed to treat cerebrovascular and neurodegenerative diseases, announces the world’s first implantations in patients with Parkinson’s disease.

DBS is the gold standard late-stage Parkinson’s treatment with worldwide regulatory approval, but adoption remains limited to ~5% due to procedure complexity and cost. The Picostim™ DBS system, developed by Bioinduction, is the world’s first miniaturized precisely targeted “brain pacemaker” that is implanted directly into the skull, making it cosmetically invisible. Being a third of the size of conventional DBS devices, it eliminates the need for extension leads, neck tissue tunneling, chest incision and a pocket for the battery.

A simpler, less invasive, single-stage intra-operative fully cranialized implantation workflow harnesses state-of-the-art, image-guided planning, navigation, and surgical-robot assistance, together demonstrating the future of brain pacemaker interventions. The result is less time in surgery for patients and elimination of the need for revision surgery for lead or extension wire fractures. Uniquely, Picostim™ also provides a wireless recording of brain signals without the cardiac artifacts associated with chest implantation, potentially helping clinicians to optimize treatment and monitor outcomes.

The device is currently undergoing a clinical trial that has been designed to evaluate the safety and efficacy of the Picostim™ system for Parkinson’s disease, with four patients implanted to date. This clinical trial[1] will recruit up to 25 patients.

Ivor Gillbe, co-founder of Bioinduction, stated: “Bioinduction’s mission is to enable a paradigm shift in the world of DBS implantations for those with chronic brain disorders. The team and partners have delivered a major milestone in the development of the next generation of elegant, evolutive cranialized brain pacemaker platform. Picostim™ harnesses state-of-the-art innovations and research enabling new possibilities to address significant unmet needs, initially focused on Parkinson’s disease. We look forward to completing the pivotal CE mark study and bringing Picostim™ to the market, as well as expanding the clinical program for significant unmet needs in cerebrovascular and cognitive disorders.”


Deep brain stimulation (DBS) is an approved, safe, and effective treatment for patients with Parkinson’s disease that cannot be adequately controlled with medication. DBS is the gold standard late-stage Parkinson’s treatment with worldwide regulatory approval, but adoption remains limited to ~5% due to procedure complexity and cost.

DBS involves surgically implanting electrodes in specific regions of the brain that are connected to an implantable device, similar to a pacemaker. Over 200,000[2] people worldwide to date have received DBS systems.

The Picostim™ DBS system is the world’s first miniaturized skull-mountable system, the IPG being one-third of the volume of conventional DBS devices. The rechargeable device is capable of meeting and exceeding conventional chest-mounted device functionality.

Skull implantation eliminates the need for tunneled extension leads. Up to a quarter of DBS patients have experienced circuit discontinuity and subsequent therapy interruption with studies showing up to 5.1%[3] of patients needing revision surgery for lead or extension wire fracture.

Employing the best available technology and practice, the implantation for a chest-mounted IPG can take five to seven hours[4] of surgical time in a multi-stage procedure. Picostim™ can be implanted in a single stage, without removing the stereotactic frame used to accurately position the electrodes, allowing for a more streamlined surgical workflow. The Picostim™ DBS system has been designed to enable a faster, single-stage implantation procedure, eliminating extension wire tunneling, reducing the risk of pain, irritation, infection, and lead breakage.

This elegant platform has been designed to evolve by integrating novel smart features, including scheduling motion responsive stimulation, and developments to further integrate real-time closed-loop features to be evaluated in future clinical studies.

Parkinson’s Disease

Parkinson’s disease is a progressive neurodegenerative disorder that can lead to tremor (trembling), stiffness, slowness of movement and poor balance, amongst other symptoms. Parkinson’s disease occurs when nerve cells, or neurons, in the substantia nigra, an area of the brain that controls movement, become impaired and/or die. There are an estimated 145,000 people in the U.K. living with Parkinson’s and 10 million people worldwide. Men are 50% more likely to be affected. The cause is poorly understood and there is no cure.

References

[2] Front. Hum. Neurosci., 2021 | https://doi.org/10.3389/fnhum.2021.644593

[3] Operative Neurosurgery, 2020 | https://doi.org/10.1093/ons/opaa215

[4] Stereotact Funct Neurosurg, 2013 | https://doi.org/10.1159/000343207

 

Hot this week

Medtronic Expands AiBLE Spine Surgery Ecosystem with New Technologies and Siemens Healthineers Partnership

New advancements in the AiBLE Spine Surgery ecosystem build upon the company's commitment to procedural innovation and execution

Axlab, Danish Medtech Pioneer, expands to US with Advanced Robotic Tissue Sectioning for Pathology Laboratories

Kris Rokke, National Sales Director for Axlab in the US. "My team and I are extremely excited and honored about this unique opportunity to also offer this advanced technology to labs across the US and thus contribute to the pathology labs of tomorrow."

Spartan Medical Broadens Single-Use Sterile Instrument Portfolio to Improve Outcomes, Increase Efficiency, and Generate Cost Savings

Spartan Medical products portfolio of single-use, sterile med tech includes micro and minor surgical convenience kits, kerrison rongeurs, spinal and general surgical retractors, dural repair kits, synthetic biologics, and a wide range of orthopedic pre-sterilized implants and devices.

Recor Medical Supports European Society of Cardiology’s Hypertension Guidelines

Record Medical notes the new guidelines, "2024 ESC Guidelines for the management of elevated blood pressure and hypertension," have been published online and recommend the consideration of renal denervation (RDN) as a safe and effective treatment option for patients who have uncontrolled resistant hypertension or those that have uncontrolled hypertension with a higher risk of cardiovascular disease, who express a preference to undergo RDN.

ConTIPI Medical Selects EVERSANA to Support U.S. Commercialization of Non-Surgical Medical Device ProVate for Women with Pelvic Organ Prolapse

EVERSANA is a leading provider of global commercial services to the life sciences industry, to support commercialization for the ProVate device in the United States to help women experiencing pelvic organ prolapse.