Un fauteuil roulant robotique
Gyrolift: A Robotic Wheelchair With Segway Technology
(Contenu en anglais seulement)
Among Canadians who have a disability, nearly 80% require some type of assistive aid, which helps contribute to more independence and better quality of life. A variety of assistive aids are currently on the market, with requirements for mobility aids dependent upon the individual’s needs and the extent of their disability. Recent advancements have been made to incorporate robotic technology into wheelchairs to allow individuals to become more verticalized (i.e., more upright) and use their lower limbs again, potentially improving a user’s autonomy and quality of life.
This image is an illustration of a grey-and-black two-wheeled wheelchair in an upright position.
(Photo reproduced with permission from Gyrolift.)
How It Works
The Gyrolift is a robotic wheelchair that combines Segway technology and electric verticalization (i.e., when the wheelchair stands).1 Unlike other powered wheelchairs with verticalization capabilities, the Gyrolift allows users to transition continuously into a standing position, even when moving. The wheelchair system is composed of the motor, a verticalization system, and a seat, and has two large wheels (as opposed to other electric wheelchairs that usually have four wheels), which makes the wheelchair more manoeuvrable and compact.2
Who Might Benefit?
In 2017, Statistics Canada conducted a national survey that found that 13.7% of Canadians have a disability that makes daily activities difficult to perform, with mobility being one of the most common issues.3 The Gyrolift has the potential to benefit individuals with paraplegia or those with extensive immobility. As the built environment has been designed for the able-bodied person, the wheelchair’s verticalization feature may improve a user’s psychological well-being, autonomy, and overall quality of life (due to the wheelchair’s unique features and lesser need for the assistance of others).
Availability in Canada
The Gyrolift is not currently available in Canada, the US, France, or other European countries. The manufacturer noted that it expects to start marketing the device in Canada around early 2021, although the device has yet to go through Health Canada for approval (Maxime Giraux, Managing Director, Gyrolift, Paris, France: personal communication, Jan 2020).
What Does It Cost?
The manufacturer stated that the final price of the wheelchair is not yet known but it will be marketed for around €15,000 in France, depending on the chosen model (Maxime Giraux: personal communication, Jan 2020). There is no evidence to suggest that the wheelchair may require set-up costs, special training, or other financial implications to the patient or health care system.
Wheelchairs are common assistive devices for individuals with paraplegia or those with other mobility concerns. They are categorized into manual, electric, reclining, or ergonomic wheelchairs. It is unclear whether there is a standard practice for selecting the appropriate wheelchair or mobility aid for those individuals requiring an assistive device in Canada.
What Is the Evidence?
Currently, no clinical trials have taken place to examine the use of the Gyrolift. The manufacturer noted that it intends to perform future clinical trials to receive regulation and marketing approval in North America. It specified that the clinical trials will likely be conducted in early 2020 (Maxime Giraux: personal communication, Jan 2020).
A protocol study2 was published in 2014 that detailed the features and characteristics of the Gyrolift and an early experimental study2 allowing users to test out the wheelchair’s maneuverability and handling. Participants in the study reported that the Gyrolift was user friendly and easy to maneuver; however, they also reported some discomfort and sizing issues with the seat and leg rests. The seat size is important as the user’s chest needs to be in the correct position in order to control the verticalization of the wheelchair. The researchers noted that the next step will be to test out a new and enhanced version of the Gyrolift with a larger panel of test users with different morphologies.2
As with any mechanical wheelchair, a potential safety concern with the Gyrolift is the possibility of the device malfunctioning during use. This could put users in danger and compromise their safety and independence if they are injured.
Issues to Consider
While the Canadian price still unknown, the Gyrolift may be more expensive than other standing wheelchairs or electric wheelchairs and it is unclear whether potential users will have to pay out of pocket. For example, in Ontario, the current provincial health care plan does not cover standing wheelchairs and pays 75% of the cost for other mobility aids, with the remaining 25% paid out of pocket by the individual (unless they are receiving financial support from a subsidy program).4 Therefore, the Gyrolift may be available to those who can afford to pay out of pocket or who have additional insurance to cover its cost.
The Gyrolift is currently being piloted for use by individuals who are paraplegic, and the technology may be available in the future for others with limited mobility. Other stand-up robotic wheelchairs5,6 are currently on the market but do not have the same features as the Gyrolift wheelchair (such as the two-wheel Segway technology).
Results from future studies testing the maneuverability and safety of the Gyrolift, not only for individuals with paraplegia but also for those with other mobility concerns, will help to inform the best use of this technology in the future; however, there is no indication when this technology might be available for use in Canada.
- Gyrolift. Gyrolift: new mobility solution. 2019; http://www.gyrolift.fr/. Accessed 2019 Dec 12.
- Trenoras L, Gregory U, Monacelli E, Hugel V. Mechatronic design of the Gyrolift verticalization wheelchair. Paper presented at: 2014 IEEE/ASME International Conference on Advanced Intelligent Mechatronics; 2014 Jul 8-11; Besacon, France. 2014; https://ieeexplore.ieee.org/document/6878263/citations?tabFilter=papers#citations. Accessed 2019 Dec 4.
- Giesbrecht EM, Smith EM, Mortenson WB, Miller WC. Health reports: needs for mobility devices, home modifications and personal assistance among Canadians with disabilities [Catalogue no. 82-003-X]. Ottawa (ON): Statistics Canada; 2017 Aug 16: https://www150.statcan.gc.ca/n1/en/pub/82-003-x/2017008/article/54852-eng.pdf?st=d0BEWY3i. Accessed 2019 Nov 19.
- Ontario Ministry of Health and Long-Term Care. Mobility aids. 2020; https://www.ontario.ca/page/mobility-aids. Accessed 2020 Jan 9.
- UPnRIDE Robotics Ltd. Far more than a wheelchair: safety mobility outdoors and indoors while standing or sitting. 2019; https://upnride.com/. Accessed 2019 Dec 12.
- Matia Robotics (US) Inc. The Tek Robotic Mobilization Device (RMD). 2019; https://www.matiarobotics.com/. Accessed 2019 Dec 12.
La radiothérapie bioguidée
(Contenu en anglais seulement)
Positron Emission Tomography-Computed Tomography Biology-Guided Radiotherapy for Cancer Treatment
Biology-guided radiotherapy (BgRT) combines the functional imaging data from positron emission tomography (PET) and the anatomic data from computed tomography (CT) into a single machine that guides personalized radiotherapy.1 Currently in development, RefleXion X1 is a hybrid PET-CT linear accelerator designed to one day enable real-time tracking of tumours, which would allow for better targeting of tumour movement and the treatment of multiple tumours in one session.1,2
How It Works
It is estimated that one in two Canadians will be diagnosed with cancer during their lifetime.3 More than half of patients with cancer will have radiotherapy as part of their treatment plan, either as monotherapy or with other modalities such as surgery and/or chemotherapy.4 As radiotherapy is typically delivered in multiple treatment fractions spread over days or weeks, image-guided radiotherapy using traditional anatomical imaging technologies such as X-ray, ultrasound, or magnetic resonance (MR) can help increase patient set-up accuracy, monitor internal organ motion, and minimize toxicity to at-risk surrounding organs.5
In contrast to anatomical imaging techniques, molecular image guidance using combined PET-CT provides both anatomic and metabolic information.6 With BgRT, a patient receives an intravenous injection of a radiotracer such as fluorine-18 fluorodeoxyglucose (a glucose analogue).1 As this radiotracer is similar in structure to glucose, it accumulates in areas of elevated sugar metabolism (such as in tumours).6 As the radioisotope breaks down, resulting in positron emissions, gamma ray photons are created.2 These emissions continuously broadcast the tumour’s location in real time, and can be detected by two PET arcs on the BgRT machine.1
As the first BgRT to use the actual tumour to guide radiotherapy,7 RefleXion X1’s clinical workflow starts with a traditional planning CT scan, and clinician contouring of tumour volumes and at-risk organs.1 After an imaging-only session on the RefleXion X1 machine, where a planning PET scan is obtained, a personalized treatment plan is created.1 At each subsequent treatment session, after confirmation with a brief pre-treatment PET scan, radiotherapy can be delivered.1 Throughout the radiation delivery process, the RefleXion X1 machine continuously gathers PET emissions, which are translated into beam delivery instructions to treat various cancer types.1
Who Might Benefit?
Due to smaller treatment margins and better tissue sparing compared with CT-based image guidance, BgRT has the potential to treat oligometastatic tumours in various disease sites such as lymph nodes, lung, breast, prostate, head, and neck.2 Due to its ability to track motion,1 RefleXion X1 can also be used to treat tumours that are subject to movement.8
Availability in Canada
RefleXion X1 is not currently available for sale in any market (Marketing Department, RefleXion Medical, Hayward, CA: personal communication, Jan 14, 2020). The company’s initial focus will be commercialization in the US, and subsequently in other markets (Marketing Department, RefleXion Medical: personal communication, Jan 14, 2020). At this time, the RefleXion machine is pending its first 510(k) clearance from the US FDA (Marketing Department, RefleXion Medical: personal communication, Jan 14, 2020).
What Does It Cost?
Although pricing information for RefleXion X1 is currently unavailable, its future list price will align with other premium radiotherapy machines (excluding proton beam therapy machines) (Marketing Department, RefleXion Medical: personal communication, Nov 25, 2019).
In the delivery of radiotherapy, CT scanning is the standard imaging modality for treatment simulation, tissue contouring, treatment planning, and image guidance.9 To facilitate dose escalation to tumours and tissue sparing to healthy organs, CT imaging before each treatment fraction allows for more localized treatments and helps minimize the risk of missing the tumour.10 Due to limitations of CT imaging such as motion-related artifacts and poor soft tissue contrast,10 other technologies are being considered for image guidance.
Currently, PET-CT is used in cancer diagnosis, staging, treatment planning, and response monitoring.11 In treatment planning and response monitoring, PET-CT is considered more accurate than CT only, and can be used in the following instances:11
- tumours that are difficult to visualize with CT or MR imaging (e.g., cancer that has metastasized to sites that are distant from the original tumour)
- treatment avoidance of tissues with non-tumour cells (e.g., collapsed lung tissue in patients with lung cancer)
- evaluating tumour response to concurrent chemoradiation.
What Is the Evidence?
As RefleXion X1 is awaiting clearance from the FDA,1 no published clinical trials were identified. Most identified studies pertain to treatment feasibility or dosimetry planning for PET-guided radiotherapy. In a proof-of-concept lung tumour tracking study, a phantom with spherical targets was designed to mimic respiratory motion and allow for the measurement of PET-guided target tracking accuracy.12 With the implementation of a dynamic tracking algorithm, tumour tracking error did not exceed a 2 mm threshold, and PET-guided tumour tracking was deemed to be clinically accurate.12
Simulated dose delivery studies involving digital patients with programmed 3-D motion have shown PET-guided radiotherapy to be capable of dose escalation to gross tumour volumes.13,14 With increased target accuracy, a radiation dose can be safely escalated while minimizing collateral damage to the surrounding healthy tissue, as shown by a simulation breast cancer study.14 In an ongoing clinical trial, people with early-stage lung cancer are being recruited to evaluate the planning feasibility of PET-guided radiotherapy.15 Specifically, the primary objective of the trial is to measure the variation in metabolic tumour volumes throughout a five-fraction treatment plan.15
To minimize radiation exposure to patients, health care providers, and the general public, radiation safety principles need to be followed during PET-CT scans due to the use of radioisotopes such as fluorine-18 fluorodeoxyglucose and the low radiation dose from the CT scan.16 On average, the general public naturally receives about 3 mSv of background radiation annually.17 A typical PET-CT scan gives off about 25 mSv of radiation.17 Thus, to align with the ALARA (i.e., as low as reasonably achievable) safety principle,16 RefleXion X1 BgRT could be appropriate for hypofractionated radiotherapy, where fewer treatment sessions are given.1
Immediately after the injection of a radiotracer, the patient is escorted to a secluded area to wait for 60 minutes before their PET-CT scan.16 As some radioactive material remain for a few hours after the scan, the patient should limit their contact with those who are most vulnerable to radiation (i.e., young children and pregnant people).17 Despite the use of fluorine-18 fluorodeoxyglucose, PET-CT scans are considered safe for patients with diabetes.18 Additionally, the annual occupation exposure for radiotherapy technologists setting up patients for PET-CT scans and radiation treatments would still fall under maximum allowable levels, assuming they are involved in one set-up per day.19
Issues to Consider
In addition to meeting radiation safety regulations, the implementation and use of BgRT in a cancer treatment centre would require consideration of implications to workflow,1 scheduling,19 and training.20 For cancer clinics without existing PET-CT scanners and nuclear medicine technologists, the radiation oncology team would have to coordinate closely with an external nuclear medicine team to prepare patients for their BgRT.1 In light of annual effective dose limits for nuclear energy workers, and lower limits for pregnant workers, careful consideration would have to be given in the scheduling of technologist staff.19,21 To limit the radiation exposure to staff during patient set-up, and to ensure timely and accurate image registration before radiation delivery, technologist staff would likely benefit from additional training.19,20
MR-guided linear accelerators have been developed and are in research stages at cancer centres in Edmonton and Toronto.22 With improved soft tissue contrast and the ability to image and treat in real time, MR-guided radiotherapy is likely suitable for tumour sites such as brain, liver, kidney, and lung, where lesions may not be well visualized with CT-based image-guidance techniques and/or where real-time motion tracking is critical to ensure treatment precision.9,10 Furthermore, in contrast with CT-based image guidance, MR-guided radiotherapy does not result in additional radiation exposure for those who receive the treatment.22
Due to its narrow range of dose deposition, particle therapy (such as proton therapy) can achieve superior sparing of surrounding healthy tissue when compared with photon therapy.23 To capitalize on this benefit and prevent missing the target, PET-guided particle therapy is being developed for its advantages in treatment monitoring and motion management.20
In addition to fluorine-18 fluorodeoxyglucose, the use of other radiotracers that allow for imaging tumour proliferation can be examined and used in the future for BgRT.1,20 A novel PET-CT radiotracer (68Ga-FAPI) has been recently identified to exhibit high tumour uptake and image quality, which may make it suitable for cancers such as sarcoma and esophageal cancer, where fluorine-18 fluorodeoxyglucose uptake is low.24
As a hybrid PET-CT linear accelerator designed to treat multiple lesions in one session and to better control for tumour motion, clinical trials are required to establish the efficacy of RefleXion X1.
Author: Yan Li
Image reproduced with permission from RefleXion Medical.
- Da Silva A, Mazin S. Treatment Planning and Delivery Overview of Biology-guided Radiotherapy. White paper. Hayward (CA): RefleXion: https://reflexion.com/wp-content/uploads/2019/10/BgRT_WhitePaper_Final.pdf. Accessed 2019 Nov 27
- Hwang M, Lalonde R, Heron D, Huq M. A clinical workflow for a prototype biology-guided radiation therapy (BGRT) machine. Med Phys. 2019;46 (6):e320.
- Canadian Cancer Society. Cancer statistics at a glance. Toronto: Canadian Cancer Society; 2020: https://www.cancer.ca/en/cancer-information/cancer-101/cancer-statistics-at-a-glance/?region=on. Accessed 2019 Nov 27.
- American Cancer Society. Radiation Therapy Basics. Atlanta (GA): American Cancer Society; 2018: https://www.cancer.org/treatment/treatments-and-side-effects/treatment-types/radiation/basics.html. Accessed 2019 Nov 27.
- Sun B, Chang J, Rong Y. The more IGRT systems, the merrier? J appl clin med phys. 2017;18(4):7-11.
- Farwell MD, Pryma DA, Mankoff DA. PET/CT imaging in cancer: current applications and future directions. Cancer. 2014;120(22):3433-3445.
- RefleXion Medical. RefleXion to Unveil New Approach to Cancer Treatment at ASTRO. 2018 Oct 18; https://www.globenewswire.com/news-release/2018/10/18/1623451/0/en/RefleXion-to-Unveil-New-Approach-to-Cancer-Treatment-at-ASTRO.html. Accessed Nov 27, 2019.
- Casey B. RefleXion debuts PET-guided radiation therapy. 2018; https://physicsworld.com/a/reflexion-debuts-pet-guided-radiation-therapy/. Accessed 2019 Dec 6.
- Cao Y, Tseng C-L, Balter JM, Teng F, Parmar HA, Sahgal A. MR-guided radiation therapy: transformative technology and its role in the central nervous system. Neuro-Oncology. 2017;19(suppl_2):ii16-ii29.
- Mittauer K, Paliwal B, Hill P, et al. A New Era of Image Guidance with Magnetic Resonance-guided Radiation Therapy for Abdominal and Thoracic Malignancies. Cureus. 2018;10(4):e2422.
- Jelercic S, Rajer M. The role of PET-CT in radiotherapy planning of solid tumours. Radiology and oncology. 2015;49(1):1-9.
- Yang J, Yamamoto T, Mazin SR, Graves EE, Keall PJ. The potential of positron emission tomography for intratreatment dynamic lung tumor tracking: a phantom study. Med Phys. 2014;41(2):021718.
- Fan Q, Nanduri A, Mazin S, Zhu L. Emission guided radiation therapy for lung and prostate cancers: a feasibility study on a digital patient. Med Phys. 2012;39(11):7140-7152.
- Fan Q, Nanduri A, Yang J, et al. Toward a planning scheme for emission guided radiation therapy (EGRT): FDG based tumor tracking in a metastatic breast cancer patient. Med Phys. 2013;40(8):081708.
- Higgins K, Emory University. Fludeoxyglucose F-18-PET in Planning Lung Cancer Radiation Therapy. ClinicalTrials.gov. Bethesda (MD): National Library of Medicine; 2018 Apr 11; updated 2019 Apr 25: https://clinicaltrials.gov/ct2/show/NCT03493789. Accessed 2019 Dec 6.
- Anderson J, Mathews D. Site Planning and Radiation Safety in the PET Facility. Alexandria (VA): American Association of Physicists in Medicine; 2002: https://www.aapm.org/meetings/02AM/pdf/8418-39272.pdf. Accessed 2019 Dec 9.
- American Cancer Society. Understanding Radiation Risk from Imaging Tests. 2018; https://www.cancer.org/treatment/understanding-your-diagnosis/tests/understanding-radiation-risk-from-imaging-tests.html. Accessed 2019 Dec 9.
- International Atomic Energy Agency. Radiation protection of patients during PET/CT scanning. https://www.iaea.org/resources/rpop/health-professionals/nuclear-medicine/pet-ct/patients. Accessed 2019 Dec 9.
- Sam S, Shon IH, Vinod SK, Lin P, Lin M. Workflow and radiation safety implications of (18)F-FDG PET/CT scans for radiotherapy planning. J Nucl Med Technol. 2012;40(3):175-177.
- Keall P, Kron T, Zaidi H. In the future, emission-guided radiation therapy will play a critical role in clinical radiation oncology. Med Phys. 2019;46(4):1519-1522.
- Canadian Nuclear Safety Commission. Radiation doses. 2019; http://nuclearsafety.gc.ca/eng/resources/radiation/introduction-to-radiation/radiation-doses.cfm. Accessed 2019 Dec 10.
- Morrison A. MR-linac for Radiation Therapy for the Treatment of Cancer. Health technology update no.23. Ottawa: CADTH; 2019: https://cadth.ca/sites/default/files/hs-eh/EN0013-health-technology-update-march-2019.pdf. Accessed 2019 Dec 6.
- Hu M, Jiang L, Cui X, Zhang J, Yu J. Proton beam therapy for cancer in the era of precision medicine. J Hematol Oncol. 2018;11(1):136-136.
- Kratochwil C, Flechsig P, Lindner T, et al. (68)Ga-FAPI PET/CT: Tracer Uptake in 28 Different Kinds of Cancer. J Nucl Med. 2019;60(6):801-805.
La modulation de la contractilité du cœur en contexte d’insuffisance cardiaque
(Contenu en anglais seulement)
Chronic heart failure is a progressive disease characterized by a variety of ventricular or valvular dysfunctions and is often initially treated with a cocktail of medications.1 The Optimizer Smart system provides an option for the treatment of moderate-to-severe chronic heart failure patients who are symptomatic despite optimal drug therapy and who are not candidates for cardiac resynchronization therapy (CRT).2
How It Works
The Optimizer Smart system is a programmable device used for cardiac contractility modulation therapy in patients with chronic heart failure.2 The system is comprised of an implantable pulse generator, pacing leads, and a mini-charger.3 The pulse generator is subcutaneously implanted into the right pectoral region of the chest and connected to two ventricular leads.3 The device sends a high voltage electrical impulse to the right ventricular septum during the absolute refractory period, which improves cardiac muscular contraction.4 By increasing the strength of the heart’s contractions, the device may improve symptoms of chronic heart failure such as six-minute walking distance, quality of life, and the functional status of patients.2
Who Might Benefit?
Chronic heart failure is an increasingly prevalent medical condition in Canada, with 50,000 newly diagnosed Canadians each year.5 In 2016, there were an estimated 600,000 Canadians living with chronic heart failure.5
The Optimizer Smart system is indicated for up to 70% of patients classified as having New York Heart Association (NYHA) Class III heart failure.2 It is intended for those who are 18 years or older, in sinus rhythm (i.e., are not indicated for CRT, QRS duration of less than 130 milliseconds), with a left ventricular ejection fraction (LVEF) of 25% to 45%, and who remain symptomatic despite optimal drug therapy.3 It is anticipated that the majority of patients eligible for treatment with the Optimizer Smart system will also have an implantable cardioverter-defibrillator (ICD).3
Availability in Canada
The Optimizer Smart system is not currently available in Canada.6 However, the Optimizer Smart system is available in numerous other countries including the US, the UK, Australia, and Germany.3
What Does It Cost?
The Canadian cost of the Optimizer Smart system is not currently available. The total implantation cost of the Optimizer Smart system in the UK is estimated to be £18,365.7 This cost is in addition to the estimated lifetime drug therapy for heart failure (standard of care) cost of £1,362.7 Furthermore, according to a model cited by the UK’s NICE‒National Institute for Health and Care Excellence, those who use the device and drug therapy gain 5.26 quality-adjusted life-years versus 4.0 quality-adjusted life-years in those who use drug therapy alone.7
The latest update of theCanadian Cardiovascular Society guidelines for the management of heart failure1 recommends that patients with a reduced ejection fraction (i.e., LVEF ≤ 40%) and symptoms of heart failure should be initiated on triple-drug therapy with an angiotensin-converting enzyme inhibitor, beta-blocker, and mineralocorticoid receptor antagonist. A diuretic may also be used, when needed, to maintain fluid balance.1 Various drug add-on therapies are also avaiIable for those who remain symptomatic despite initial triple-drug therapy.1 However, if patients continue to have symptoms and have a LVEF < 35% despite optimal drug therapy for at least three months, ICD and CRT (i.e., a pacemaker) device therapy may be warranted.1
What Is the Evidence?
Two multi-centre, randomized controlled trials8,9 both comparing cardiac contractibility modulation via the Optimizer Smart device plus optimal medical therapy versus optimal medical therapy alone were identified. One trial9 was conducted at 50 centres in the US (n = 428) and included participants with heart failure and NYHA Class III to Class IV symptoms, normal sinus rhythm, and an ejection fraction ≤ 35%. The other trial8 was conducted in the US, Germany, and Czechia — the Czech Republic — (n = 160) and included participants with heart failure with NYHA Class III to Class IV symptoms, normal sinus rhythm, and an ejection fraction of 25% to 45%.
Outcomes reported by the authors8,9 include:
- change in anaerobic threshold9
- change in peak VO2
- change in Minnesota Living with Heart Failure Questionnaire (MLHFQ)
- change in six-minute hall walk
- change in NYHA classification
Furthermore, one systematic review with meta-analysis,4 which included the two randomized controlled trials previously mentioned, as well as two earlier randomized controlled trials, was identified. The systematic review4 reported all-cause mortality, total hospitalizations, worsening heart failure and heart failure-related hospitalizations, cardiac arrhythmias, ICD sensing defects and malfunction, six-minute walking distance, and MLHFQ. Overall, when the data from the four trials was combined, cardiac contractibility modulation significantly improved MLHFQ, but did not significantly improve all-cause mortality, worsening heart failure and heart failure-related hospitalizations, or six-minute walking distance.4
The identified studies reported potential safety issues related to device implantation including lead dislodgement,8,9 device pocket infections,9 and generator erosion.8 The manufacturer2 also lists the following as potential adverse effects occurring secondary to cardiac contractibility modulation signal delivery:
- abnormal cardiac function
- atrial and ventricular tachyarrhythmias
- atrial and ventricular bradyarrhythmias
- worsening heart failure
- myocardial tissue damage
- chest pain.
The Optimizer Smart system is currently being investigated for use in patients with preserved ejection fraction heart failure (i.e., LVEF ≥ 50%) with NYHA Class II or Class III symptoms.10 This pilot study is estimated to be completed by March 31, 2021.10
The incidence of cardiovascular disease is increasing with the aging Canadian population.11 Improvements to treatment methods also equates to people living longer with cardiovascular disease.5 As chronic heart failure is often the end result of cardiovascular disease, the occurrence of chronic heart failure is consequently increasing in Canada.5 This is leading to increased interest in new research in the treatment of chronic heart failure.5 Cardiac contractibility modulation is a novel method of treating patients with symptomatic heart failure.2 However, more evidence comparing the Optimizer Smart system to the standard of care is needed to ascertain the clinical benefit of cardiac contractibility modulation in improving the functional status and quality of life of patients with heart failure.
Author: Christopher Freige
- Ezekowitz JA, O'Meara E, McDonald MA, et al. 2017 comprehensive update of the Canadian Cardiovascular Society guidelines for the management of heart failure. Can J Cardiol. 2017;33(11):P1342-1433.
- Impulse Dynamics. 2020; https://impulse-dynamics.com/. Accessed 2020 Feb 7.
- PMA P180036: summary of safety and effectiveness data (SSED). Rockville (MD): U.S. Food & Drug Administration; 2019: https://www.accessdata.fda.gov/cdrh_docs/pdf18/P180036B.pdf. Accessed 2020 Feb 7.
- Mando R, Goel A, Habash F, et al. Outcomes of cardiac contractility modulation: a systematic review and meta-analysis of randomized clinical trials. Cardiovasc Ther. 2019;2019 (no pagination)(9769724).
- 2016 report on the health of Canadians: the burden of heart failure. Heart & Stroke Foundation; 2016: https://www.heartandstroke.ca/-/media/pdf-files/canada/2017-heart-month/heartandstroke-reportonhealth-2016.ashx?la=en&hash=91708486C1BC014E24AB4E719B47AEEB8C5EB93E. Accessed 2020 Feb 7.
- Government of Canada. Medical Devices Active Licence Listing (MDALL). 2019: https://health-products.canada.ca/mdall-limh/index-eng.jsp. Accessed 2020 Feb 7.
- National Institute for Health and Care Excellence. The OPTIMIZER smart system for managing heart failure. (Medtech innovation briefing MIB186) 2019: https://www.nice.org.uk/advice/mib186/resources/the-optimizer-smart-system-for-managing-heart-failure-pdf-2285963701388485. Accessed 2020 Feb 7.
- Abraham WT, Kuck KH, Goldsmith RL, et al. A randomized controlled trial to evaluate the safety and efficacy of cardiac contractility modulation. JACC Heart Fail. 2018;6(10):874-883.
- Kadish A, Nademanee K, Volosin K, et al. A randomized controlled trial evaluating the safety and efficacy of cardiac contractility modulation in advanced heart failure. Am Heart J. 2011;161(2):329-337.
- Impulse Dynamics. NCT03240237: CCM in heart failure with preserved ejection fraction (CCM-HFpEF). ClinicalTrials.gov. Bethesda (MD): U.S. National Library of Medicine; 2018: https://clinicaltrials.gov/ct2/show/NCT03240237?term=optimizer&draw=1&rank=7. Accessed 2020 Feb 7.
- Heart disease in Canada: highlights from the Canadian Chronic Disease Surveillance System. Ottawa (ON): Public Health Agency of Canada; 2017: https://www.canada.ca/en/public-health/services/publications/diseases-conditions/heart-disease-canada-fact-sheet.html. Accessed 2020 Feb 7.
Une valve auto-expansive pour traiter les malformations cardiaques congénitales
(Contenu en anglais seulement)
The Venus Pulmonary Valve (Venus P-Valve) is a self-expanding percutaneous pulmonary implantation device that offers an intervention to address right ventricle outflow tract (RVOT) complications stemming from tetralogy of fallot (ToF).1
How It Works
The purpose of the Venus P-Valve is to provide an intervention for RVOT enlargement. An RVOT enlargement is often the result of a pulmonary obstruction and can contribute to a leaky pulmonary valve that allows blood to flow back into the heart chamber.2 The Venus P-Valve is a stent consisting of a self-expanding valve and is delivered and implanted via a catheter to act as a valve replacement for the enlarged RVOT.1,3 The stent is anchored in the RVOT and is made of a fibre called nitinol.1 The design of the Venus P-Valve can accommodate RVOT diameters up to 32 mm to 33 mm, which is larger than other commercially available pulmonary valves.4 This procedure is commonly referred to as a percutaneous pulmonary valve implantation (PPVI).1,5,6
Who Might Benefit?
ToF accounts for 6.7% of all babies born with congenital heart disease and RVOT obstruction is a common heart abnormality associated with ToF.7,8 Patients with ToF typically undergo corrective surgery within the first six months of their lives; however, interventions in early childhood often lead to complications that require additional surgical correction later in life.7,8 Patients with right ventricle complications stemming from ToF can undergo PPVI as an alternative to repeated surgery.7,9 The commonly used PPVI devices are not suitable for large RVOT implantations, but the Venus P-Valve is designed specifically for dilated or enlarged RVOT resulting from surgical repair of ToF.2,9 Given that the Venus P-Valve is designed to accommodate larger RVOT diameters, it may provide treatment to patients who cannot receive the current commercially available PPVI devices.1,9
Availability in Canada
There is no indication that the Venus P-Valve is licensed in Canada. The Venus P-Valve has received approval from the Chinese FDA and has received Institutional Review Board approval for clinical testing;3 however, it has not been granted CE certification or US FDA approval.1,2,6 A CE feasibility and safety study is currently being conducted.2
What Does It Cost?
No information related to costs in Canada or elsewhere was identified.
The results of ToF repairment surgery are generally good, with approximately 95% of patients expected to survive to adulthood.2 In most cases, the ToF repairment surgery is associated with RVOT obstruction later in life and most centres now consider PPVI to be first-line therapy.2 The currently available PPVI devices (the Melody Valve or the Sapien Valve) are recommended for RVOT implantation, but not all patients who have undergone ToF repairment have RVOT dimensions that are compatible with the capacity of these devices.1,2
What is the Evidence?
Early procedural studies on the Venus P-Valve show safe and promising advances in PPVI. Six non-randomized studies were identified in the available literature.1,3-6,9 Five of these studies were prospective cohort studies that aimed to capture the early results regarding feasibility, effectiveness, safety, and short-term follow-up for Venus P-Valve implantations for appropriate candidates.1,3,5,6,9 One identified study used a retrospective approach to collect procedural and early-to-midterm follow-up information.4 Overall, the identified studies indicate general success related to valve implantation, encouraging health outcomes, and evidence of surgical reproducibility. The majority of studies had a follow-up of 12 months or less, and the sample sizes were from five to 55 patients.1,3-6,9 One study reported MRI follow-up data for a mean of 112 months.4 Two clinical trials were identified from the ClinicalTrials.gov database; one is in the recruitment phase10 and the status of the other is unknown.11
Of the identified studies that reported evidence related to safety for the Venus P-Valve, one study reported no severe adverse events,6` while another reported procedure complications related to sheath breakage and implantation migration and displacement.4 Additionally, one case report identified two cases of stent infolding of the Venus P-Valve after implantation.12
Issues to Consider
The Melody and Sapien devices, both currently available for smaller RVOT diameters, have reported complications related to stent fractures of the valve frame; conduit ruptures; coronary compression, which may prevent a PPVI intervention; and endocarditis or an infection associated with the PPVI procedure.7 It is possible that the Venus P-Valve could have similar complications.
The available literature identified two alternative devices similar to the Venus P-Valve. These devices include the Medtronic Harmony TPV and the Alterra Adaptive Prestent from Edwards Lifesciences.7 These devices were created to address the needs of patients with enlarged RVOTs who are not candidates for the currently recommended devices.7 The Harmony TPV device encompasses a larger valve diameter compared to the commercially available Melody Valve, similar to the Venus P-Valve.7 The Alterra Adaptive Prestent is “stent-like” and helps to reshape the RVOT13 by working similar to a docking station for the Sapien S3 valve.7
The Venus P-Valve may provide an additional valve option for patients with an enlarged RVOT who need a PPVI.9 The findings from the identified literature show reliable reproducibility and evidence of success in early cohort studies; however, more clinical trials with longer follow-up data and more reporting on patient-important outcomes are needed.2
Author: Shannon Hill
- Garay F, Pan X, Zhang YJ, Wang C, Springmuller D. Early experience with the Venus P-valve for percutaneous pulmonary valve implantation in native outflow tract. Neth Heart J. 2017;25(2):76-81.
- Qureshi SA, Jones MI. Recent advances in transcatheter management of pulmonary regurgitation after surgical repair of Tetralogy of Fallot [version 1; referees: 3 approved]. F1000Research. 1000;7.
- Cao QL, Kenny D, Zhou D, et al. Early clinical experience with a novel self-expanding percutaneous stent-valve in the native right ventricular outflow tract. Catheter Cardiovasc Interv. 2014;84(7):1131-1137.
- Morgan G, Prachasilchai P, Promphan W, et al. Medium-term results of percutaneous pulmonary valve implantation using the Venus P-valve: international experience. EuroIntervention. 2019;14(13):1363-1370.
- Zhou D, Pan W, Jilaihawi H, et al. A self-expanding percutaneous valve for patients with pulmonary regurgitation and an enlarged native right ventricular outflow tract: one-year results. EuroIntervention. 2019;14(13):1371-1377.
- Husain J, Praichasilchai P, Gilbert Y, Qureshi SA, Morgan GJ. Early European experience with the Venus P-valve: filling the gap in percutaneous pulmonary valve implantation. EuroIntervention. 2016;12(5):e643-651.
- Balzer D. Pulmonary valve replacement for Tetralogy of Fallot. Methodist Debakey Cardiovasc J. 2019;15(2):122-132.
- Driesen BW, Warmerdam EG, Sieswerda GJ, et al. Percutaneous pulmonary valve implantation: current status and future perspectives. Curr Cardiol Rev. 2019;15(4):262-273.
- Promphan W, Prachasilchai P, Siripornpitak S, Qureshi SA, Layangool T. Percutaneous pulmonary valve implantation with the Venus P-valve: clinical experience and early results. Cardiol Young. 2016;26(4):698-710.
- Venus MedTech (HangZhou) Inc. NCT02846753: implantation of the Venus P-Valve™ in the pulmonic position in patients with native outflow tracts. ClinicalTrials.gov. Bethesda (MD): U.S. National Library of Medicine; 2016: https://clinicaltrials.gov/ct2/show/record/NCT02846753?term=Venus+P-Valve&draw=2&rank=2. Accessed 2020 Mar 6.
- Venus MedTech (HangZhou) Inc. NCT02071654: efficacy and safety evaluation of transcatheter pulmonary valve implantation for right ventricular outflow tract (RVOT) stenosis after congenital heart defect surgical correction complicated with severe pulmonary regurgitation. ClinicalTrials.gov. Bethesda (MD): U.S. National Library of Medicine; 2014: https://clinicaltrials.gov/ct2/show/record/NCT02071654?term=Venus+P-Valve&draw=2&rank=1. Accessed 2020 Mar 6.
- Riahi M, Ang HL, Jones M, et al. Infolding of the Venus P-Valve after transcatheter pulmonary valve implantation. Circ Cardiovasc Interv. 2018;11(4):e005923.
- Edwards Lifesciences’ Alterra adaptive prestent device used for first time to treat a malformed pulmonary valve. Cardiovascular News 2017; https://cardiovascularnews.com/edwards-lifesciences-alterra-adaptive-prestent-device-used-first-time-treat-malformed-pulmonary-valve/ Accessed 2020 Mar 19.
Le Soundbite Crossing System dans le traitement des artériopathies coronaires et périphériques
(Contenu en anglais seulement)
Chronic total occlusions (CTOs) in patients with coronary heart disease are associated with a higher risk of adverse events, a decrease in quality of life, and increased health care costs.1 Novel crossing technology by Soundbite Medical Solutions aims to break down arterial calcification using short-duration high-amplitude pressure pulses called shock waves.1
How It Works
Soundbite Medical Solutions’ Soundbite Crossing system consists of a disposable wire, guided by a supportive balloon catheter, that percutaneously penetrates the artery.1 The other component of the Soundbite system is a console that generates low-frequency, concentrated shock waves at the proximal end of the guide wire, which then mechanically propagate to the distal tip where the occlusion is located.1 Due to the shock waves, the distal tip then rapidly oscillates and crosses through arterial calcification.1 If the Soundbite system successfully creates a space within the CTO, a therapeutic system, such as a stent, can be inserted (if necessary).1
While pharmacological therapy can be sufficient for some patients with coronary heart disease, percutaneous coronary interventions (also called angioplasties) are the preferred treatment for revascularization in those with CTOs.2
Percutaneous coronary interventions consist of high-pressure balloon dilations, where an interventional cardiologist inserts a guide wire and subsequently a balloon catheter across the blockage site using fluoroscopy.3 The balloon at the tip of the catheter is then inflated and deflated continuously to push calcified plaque outward against the arterial wall, opening up the narrowed blood vessel.3 In the case of a total occlusion, new collateral blood vessels may have formed to redirect blood flow around the blockage.4 The catheter is also used to widen these collateral vessels.4
The challenges with this method of angioplasty include the risk of injuring non-calcified arterial segments when directing the guide wire, as well as the possibility of not producing enough force to fracture the calcium.5 Percutaneous coronary interventions are technically demanding, and failure to reach calcified lesions with a guide wire is the main reason for their lower success rate.1
CTOs can also be treated by a surgical procedure called coronary artery bypass grafting, which is generally reserved for patients with complex or multivessel disease.2 In this procedure, peripheral blood vessels, such as veins from the legs or arteries from the chest or arms, are used to connect to blood vessels above and below the coronary occlusion, thus redirecting blood flow.6
Who Might Benefit?
In a Canadian multi-centre registry, 18.4% of patients with coronary heart disease were found to have CTOs.7 Thus, among the 2.4 million Canadians diagnosed with heart disease,8 it is possible that 440,000 of them may require intervention to manage either coronary or peripheral CTOs. Patients who require a stent to treat their narrowed arteries could benefit from shock wave crossing to clear calcified occlusions before the insertion of a stent.9 Calcified plaques not only affect stent positioning and expansion, but also drug delivery.5
Availability in Canada
The Soundbite Crossing system is currently approved by Health Canada for the treatment of CTOs associated with peripheral artery disease, but not those associated with coronary artery disease.10 As of January 2020, Soundbite has also received 510(k) clearance by the FDA for use in the treatment of peripheral CTOs in the US.11
What Does It Cost?
The cost of the Soundbite Crossing system is currently unavailable.
What is the Evidence?
As the Soundbite system is still in development for coronary applications, there is no specific evidence regarding its clinical effectiveness in coronary CTOs. However, clinical outcomes from completed studies in peripheral CTOs may provide a basis for predicting its success.
In a prospective, single-arm feasibility study, Soundbite Medical Solutions investigated the safety and efficacy of the Soundbite system in patients with infrainguinal CTOs.1 The study used a 0.018 inch wire to deliver shock waves to peripheral CTOs, which is slightly larger than the wire being developed for coronary applications.1 The primary end point of device success, defined as, among various other outcomes, complete crossing of the target CTO lesion and freedom from major adverse events for 30 days post-procedure, was achieved in 91.9% of patients.1 The authors noted several limitations of the study, such as the small cohort of 37 patients and the lack of intravascular imaging during the procedure.1
In the Soundbite feasibility study for peripheral infrainguinal CTOs, 13.5% of patients presented angiographic evidence of arterial perforation.1 However, none of them required treatment.1
The Crosser catheter by Bard Peripheral Vascular has also emerged as a treatment option for peripheral CTOs. This option uses a higher frequency generator but similarly sized wire as the Soundbite system.12 The Crosser catheter is commercially available in the US.13
Shockwave Medical’s intravascular lithotripsy device uses low-pressure balloon dilatation with shock waves to penetrate and cross calcified plaques in both peripheral and coronary vasculature.9 By using lower pressures rather than traditional balloon-based procedures, intravascular lithotripsy is thought to minimize vascular injury.5 Currently, coronary intravascular lithotripsy catheters are commercially available in Europe but are limited to investigational use in the US.14 Shockwave Medical’s largest study to date (DISRUPT CAD III) includes 392 patients and is further examining the coronary applications of this technology. DISRUPT CAD III is expected to be completed by 2022.15
Overall, Soundbite Medical Solutions’ Soundbite Crossing system may be a promising non-surgical treatment option for patients with CTOs, but its evidence for use in coronary heart disease is lacking. As of March 2020, Soundbite Medical Solutions has received FDA approval to commence the ACTIVE study on coronary applications of the Soundbite Crossing system in the US.16 The study is expected to be conducted in 154 patients, with primary end points being device success and freedom from related major adverse events 48 hours post-procedure.17 Considering the short follow-up period, the long-term clinical effectiveness of the Soundbite Crossing system will not be an outcome of this study. As all Soundbite system investigations have been non-comparative, studies directly comparing the clinical effectiveness of shock wave technology to conventional angioplasty methods would further clarify its place in therapy.
Author: Diksha Kumar
- Brodmann M, Therasse E, Benko A, Riel LP, Dion S, Genereux P, et al. Recanalization of CTOs with SoundBiteTM Active Wire. J Cardiovasc Surg. 2018;59(4):529-537.
- Khatri J, Abdallah M, Ellis S. Management of coronary chronic total occlusion. Cleve Clin J Med. 2017;84(12 suppl 3):27-38.
- Heart and Vascular Institute, University of Pittsburgh Medical Center. Chronic coronary total occlusion - Treatment. Pittsburgh (PA): University of Pittsburgh Schools of Health Sciences: https://www.upmc.com/services/heart-vascular/conditions-treatments/chronic-coronary-total-occlusion#treatment. Accessed 2020 Feb 14.
- Heart Center. Chronic Total Occlusion Percutaneous Coronary Intervention. Boston (MA): Massachusetts General Hospital; 2020: https://www.massgeneral.org/heart-center/treatments-and-services/chronic-total-occlusion-percutaneous-coronary-intervention-cto-pci. Accessed 2020 Feb 21.
- Brinton TJ, Ali ZA, Hill JM, Meredith IT, Maehara A, Illindala U, et al. Feasibility of Shockwave Coronary Intravascular Lithotripsy for the Treatment of Calcified Coronary Stenoses. Circulation. 2019;139(6):834-836.
- National Heart, Lung, and Blood Institute. Coronary artery bypass grafting. Bethesda (MD): U.S. Department of Health and Human Services; 2020: https://www.nhlbi.nih.gov/health-topics/coronary-artery-bypass-grafting. Accessed 2020 Mar 3.
- Fefer P, Knudtson ML, Cheema AN, Galbraith PD, Osherov AB, Yalonetsky S, et al. Current Perspectives on Coronary Chronic Total Occlusions: The Canadian Multicenter Chronic Total Occlusions Registry. J Am Coll Cardiol. 2012;59(11):991-997.
- Heart disease in Canada. Ottawa (ON): Government of Canada; 2017: https://www.canada.ca/en/public-health/services/publications/diseases-conditions/heart-disease-canada.html. Accessed 2020 Mar 17.
- Aksoy A, Salazar C, Zimmer S, Escaned J, Nickenig G, Sinning JM, et al. TCT-653 Intravascular Lithotripsy for Lesion Preparation in Calcified Coronary Lesions: First Data of Prospective, Observational Multicenter Registry. J Am Coll Cardiol. 2019;74 (13 Supplement):B641.
- SoundBite announces Health Canada approval of the SoundBite™ Crossing System – Peripheral. Montreal (QC): SoundBite Medical Solutions; 2020: https://soundbitemedical.com/soundbite-announces-health-canada-approval-of-the-soundbite-crossing-system-peripheral/. Accessed 2020 Feb 14.
- SoundBite receives FDA 510(k) Clearance of the SoundBite™ Crossing System – Peripheral. Montreal (QC): SoundBite Medical Solutions; 2020: https://soundbitemedical.com/soundbite-receives-fda-510k-clearance-of-the-soundbite-crossing-system-peripheral/. Accessed 2020 Feb 14.
- Laird J, Joye J, Sachdev N, Huang P, Caputo R, Mohiuddin I, et al. Recanalization of infrainguinal chronic total occlusions with the crosser system: results of the PATRIOT trial. J Invasive Cardiol. 2014;26(10):497-504.
- Crosser™ CTO recanalization catheters. Tempe (AZ): Bard Peripheral Vascular, Inc.; 2018: https://www.crbard.com/Peripheral-Vascular/en-US/Products/Crosser-CTO-recanalization-catheters. Accessed 2020 Mar 13.
- Shockwave receives FDA Breakthrough Device designation for the Coronary IVL System. Santa Clara (CA): Shockwave Medical, Inc. ; 2019: https://shockwavemedical.com/about/press-releases/shockwave-receives-fda-breakthrough-device-designation-for-the-coronary-ivl-system/. Accessed 2020 Mar 20.
- Shockwave Medical Inc. NCT03595176: Disrupt CAD III with the Shockwave Coronary IVL System. Clinicaltrials.gov. Bethesda (MD): U.S. National Library of Medicine; 2019: https://clinicaltrials.gov/ct2/show/NCT03595176. Accessed 2020 Feb 14.
- SoundBite receives FDA IDE Approval for the ACTIVE Clinical Study with the SoundBite™ Crossing System – Coronary. Montreal (QC): Soundbite Medical Solutions, Inc. ; 2020: https://soundbitemedical.com/soundbite-receives-fda-ide-approval-for-the-active-clinical-study-with-the-soundbite-crossing-system-coronary/. Accessed 2020 Mar 13.
- Soundbite Medical Solutions. NCT03521804: Safety and efficacy study of the SoundBite™ Crossing System With ACTIVE Wire in Coronary CTOs. (ACTIVE). Clinicaltrials.gov. Bethesda (MD): U.S. National Library of Medicine; 2020: https://clinicaltrials.gov/ct2/show/NCT03521804. Accessed 2020 Mar 13.