Ventricular assist device

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Marv Slepian, M.D.; University of Arizona [2]; Juan A. Sanchez MD MPA [3], Chairman, The Stanley J. Dudrick Department of Surgery, Saint Mary's Hospital, Waterbury, CT, Syed Hassan A. Kazmi BSc, MD [4]


Overview

A Ventricular assist device, or VAD, is a mechanical device that is used in patients with advanced heart failure for Mechanical Circulatory Support (MCS). VADs are commonly employed as a strategy of bridge to heart transplant or as a destination therapy in patients ineligible for heart transplant. It has been shown that about a quarter of patients waiting for heart transplants need mechanical circulatory support with Ventricular assist devices (VADs). Some VADs are designed for short-term use, such as in patients recovering from heart attacks or heart surgery, while others are intended for long term use (months to years and in some cases for life), such as in patients suffering from congestive heart failure. Over the recent years, VADs have undergone significant improvements in size, durability, reliability and noise emission.

VADs include Left Ventricular Assist Devices (LVADs), Right Ventricular Assist Devices (RVADs) and BiVentricular Assist Devices (BiVADs) depending on the heart chamber that needs MCS.

Some VADs are percutaneous or transcutaneous, that limits patient mobility. Examples include Impella, which is an axial flow pump with non-pulsatile blood flow from left ventricle to ascending aorta and TandemHeart, which is a left atrial to iliofemoral artery bypass pump.

While some other VADs are implantable, that allow a patient to be fully mobile. Examples include HeartMate II, which is a continuous-flow system with mechanical bearings and HeartMate III which is a magnetically levitated device that is a pulsatile-flow system without mechanical bearings.

Types of Ventricular Assist Devices (VADs)

Left Ventricular Assist Device (LVAD)

  • LVADs are the most commonly transplanted VADs in heart failure patients. With robust innovation in technology, LVADs have significantly increased patient survival despite the adverse events associated with the devices. This has lead to growing proportion of patients undergoing LVAD implantations as a Destination therapy.
  • LVADs unload left ventricle and augment the cardiac outflow (nearly 10L/min) into the ascending aorta.
  • HeartMate II, HeartMate III and HeartWare HVAD are the only commercially FDA- approved LVADs for adults in North America. Worldwide efforts are being made to create the most effective and safest interface including the INCOR, Jarvik 2000, EVAHEART LVAS and more. [1]

Right Ventricular Assist Device (RVAD)

  • RVADs are implanted surgically or percutaneously. Impella RP is an example of minimally invasive percutaneous RVAD. The pump has an inflow in the inferior vena cava and outflow in the pulmonary artery.

BiVentricular Assist Device (BiVAD)

  • BiVAD is used to provide simultaneous MCS to both ventricles of heart. It is different from Total Artificial Heart (TAF) since it works in parallel to the native heart and removal of native heart is not required. Hence, BiVAD provides a potential for myocardial recovery of the retained native heart and reduces the need for a donor heart.[3]
  • BiVAD may be indicated in right ventricular dysfunction after LVAD implantation. However, early and/or long-term dual VAD therapy for biventricular support may be considered in evident right ventricular failure and conditions like acute circulatory collapse due to fulminant myocarditis, acute decompensation of dilated biventricular cardiomyopathy, massive Myocardial Infarction (involving the septum or RV), acute deterioration following toxic cardiomyopathy, infiltrative cardiomyopathy or RV cardiomyopathies with concomitant involvement of the left ventricle.[4]
  • Examples of VADs implanted as BiVAD include Abiomed BVS5000 and AB5000, Thoratec PVAD and IVAD, Berlin Heart, Levitronix, Jarvik 2000 and HeartWare HVAD.

Classification

VADs have evolved over years and are classified according to their operational characteristics. Most VADs operate on similar basic principle. A cannula is inserted into the apex of the ventricle. Blood passes through this cannula to a pump and thence through a tube into the aorta (most commonly ascending aorta) in case of an LVAD or into the pulmonary artery in case of an RVAD. The pump is powered through a lead which connects it to a controller and power supply. In some cases there is also a tube to vent the pump to the outside air. Major distinguishing features between different VADs are the pumps (which vary substantially in method of operation, size and placement), the controller and the materials used for the pump and the associated parts (tubes, cannulas, lead between the pump and the controller/power supply).

First-generation devices

  • First generation VADs were large volume-displacement pumps with pulsatile flow generated by electronic or pneumatic compression of a blood chambers.
  • Several factors lead to discontinuation of the first generation VADs. These VADs had poor durability due to membrane rupture, bearing, and mechanical valve wear.[3]They had large control consoles that significantly reduced patient mobility and pump that was audible and caused discomfort. These VADs were also associated with higher risk of infection at external lead, significant hemolysis, thrombus formation, larger surgical incision requirement and severe postoperative bleeding. Examples include HeartMate I, Novacor and the Thoratec paracorporeal VAD.

Second-generation devices

  • The Second Generation VADs are Continuous Flow (CF) devices that use rotary centrifugal, diagonal or axial impellers. Although there is marked improvement in design and patient mobility compared to the first generation VADs, their rotary pumps are associated with increased thrombogenicity and acquired platelet dysfunction due to the lack of pulsatile flow and high shear forces near the bearings and seals. Commonly used second generation VADs include HeartMate II and Jarvik 2000. These pumps are easier to implant due to their smaller design. These are also quieter and have lower rates of infection and other complications compared to First Generation VADs. [5]
  • HeartMate II is the most commonly used LVAD. It draws blood from left ventricular apex and pumps it into ascending aorta producing a non-pulsatile flow. It is about the size of a D battery with a rotating impeller which is the shape of an Archimedes screw. Impeller is the only moving part of the pump. Due to lesser adverse events HeartMate II was approved by FDA for BTT in 2008 and later for DT in 2010 due to improved pump durability and minimal damage to blood cells. [6]
  • Jarvik 2000 Ventricular Assist System development started in 1987 with several improvements in design since then. The newer Jarvik 2000 pump is a miniaturized intraventricular pump that is placed in the cardiac apex with minimally invasive implantation procedures. It creates a blood flow towards the ascending or descending aorta through an outflow conduit and lacks a real inflow conduit. Older pumps required Cardiopulmonary Bypass (CPB) support but less invasive off-pump implantation is done with or without ExtraCorporeal Membrane Oxygenation (ECMO) instead of CPB support. [7]

Third-generation devices

  • Third Generation VADs are Continuous Flow (CF) centrifugal pumps that use contactless/bearingless impeller drive and suspension systems and hence, completely eliminate mechanical wear of the pump components. Impeller is levitated by electromagnetic and/or hydrodynamic forces while active electromagnetic forces are employed to rotate the impeller. These VADs are more durable, easier to implant and have lower risk of thrombosis and hemolysis. Examples include HeartMate III and HeartWare HVAD. [5]
  • HeartMate III is the newer LVAD technology that has shown to have fewer complications like strokes, major bleeding, GI bleeding or ventricular arrhythmias when compared to HeartMate II. Fewer pump thromboses and LVAD replacements for LVAD malfunction have also been reported with this newest LVAD. The improved function of HeartMate III is due to it's higher hemocompatibility. It has wide blood flow conduits which reduce shear of the blood.[8] It's frictionless design without mechanical bearings not only reduces wear-and-tear but also decreases the amount of heat produced during impeller rotation. [9]
  • HeartWare HVAD is placed intrapericardially in the left ventricular apex. It has a bearingless magnetically driven impeller. It is suitable for patients with smaller body surface area. Due to its small size, it has also been used as an implantable RVAD.[6]

Indications

VADs can be used for the following conditions: [8]

  • Bridge-to-Transplant (BTT): Patients who are transplant eligible and need a donor heart for survival.
  • Destination therapy (DT): Patients who need mechanical circulatory support as an alternative to heart transplant.
  • Bridge-to-Decision (BTD): Patients who are not assigned the need for heart transplant at the time of implantation.
  • Bridge-to-Candidacy (BTC): Patients who are not transplant eligible but may be reconsidered for transplant after a temporary circulatory support.
  • Bridge-to-Recovery (BTR): Patients who require temporary circulatory support after an acute insult to cardiac function, like cardiogenic shock.

Modern indications for short-term use of MCS include: [9]

  • Bridge-to-immediate survival
  • Brdige-to-next decision
  • Bridge-to-bridge
  • Bridge-to-surgery

Contraindications

  • Coexisting severe comorbidity like irreversible hepatic, renal, or neurological disease [8]
  • Patient non-compliance [8]
  • Severe psychosocial limitations (Unmanaged psychiatric disorders, lack of social support) [8]
  • Aortic Valve regurgitation (in case of LVAD) and Pulmonary regurgitation (in case of RVAD) [2]
  • Limited life expectancy (age >80 for DT, untreated malignancy) [8]
  • Poor nutritional status (obesity or malnutrition) [8]
  • Limitations to rehabilitation (musculoskeletal disease, severe peripheral vascular disease, active substance abuse, active infection, prolonged intubation) [8]

Complications

  • Right Ventricular(RV) failure:

Unloading of the left ventricle post-LVAD implantation may result in septal shifts, leading to increased RV preload, decreased RV contractility and function. RVAD implantation may be necessary until RV function improves, at which point RVAD can be explanted. [8]

  • Bleeding:

Bleeding is a common complication during the implantation procedure. Patients with Continuous Flow LVADs are systemically anticoagulated with Warfarin, which further increases the risk of bleeding, particularly Gastro-intestial (GI) Bleed. Patients should be evaluated and if possible, treated preoperatively for GI bleeding sources such as colonic polyps, stomach ulcers and angiodysplasias. There is also a higher risk of bleeding post-LVAD implantation from degradation of Von Willebrand Factor by VAD rotors, which is reversible once LVAD is removed.[8]

  • Thromboemolic events and Stroke:

There is an increased risk of thromboembolic events and Transient Ischemic Attacks in patients with Continous Flow LVADs despite of systemic anticoagulation. If pump thrombosis develops, there might be an emergent need for pump exchange and moving the patient up on priority list of heart transplant. [8]

  • Infection:

Infection at multiple sites of LVAD circuit is a common complication. These sites include the LVAD pocket where the LVAD is implanted, the LVAD itself or the cannulae that go from the left ventricle to the VAD and from the LVAD to the aorta. The most common infection site is the driveline which goes from the LVAD through the skin to the LVAD power source since it is a pathway from the external environment to the LVAD interior. Common causative organisms in driveline infections are the skin flora such as Staphylococcus aureus and coagulase-negative staphylococci and in infection of internal components are Serratia, Klebsiella, and Enteroccocus species, Pseudomonas aeruginosa. Candida can cause up to ten percent of infections. Treatment includes debridement of infected tissue and administration of intravenous antibiotics. Explantantion of infected LVAD is sometimes necessary. [8]

  • Ventricular arrythmias:

Ventricular arrythmias is a common complication after LVAD implantation. It is thought to be from reentrant circuits that are formed around the site of the inflow cannula in already damaged myocaFailing of power source or malfunction of different parts can also cause the device to stop workingrdium. Implantable cardioverter-defibrillator helps with these arrhythmias until the ventricles remodel as the time goes on. Anti-arrhythmic agents such as lidocaine or amiodarone are rarely necessary. [8]

  • Device Malfunction and Optimization:

Malfunction of different parts of VAD ( driveline, controller, pump) can cause the device to stop working.[10] These are complex devices that need an expert for adjustments to obtain optimal right and left ventricular hemodynamics.[8]

  • Valvular Insufficiency:

Mitral and Aortic valve insufficiency can be seen post-LVAD implantation. This can effect pump function and may worsen heart failure. [10]

History

VADs evolved over time after an external technology was used to provide cardiovascular support to a patient with Cardiopulmonary bypass (CPB) in an atrial septal defect repair surgery by John Gibbons. This lead to further interest and efforts to developing artificial heart and later implantation of VAD in the late 1960s. Thoratec pneumatic VAD was the first Food and Drug Administration (FDA) approved VAD used as a BTT. This technology further evolved into HeartMate I, a pulsatile device, but more work needed to be done to develop newer LVADs with lesser complications. The Second and Third Generation VADs were designed to have a continuous flow rather than pulsatile. [8]

Images: Ventricular Assist Devices

Fully Implantable Pumps

Most VADs currently being used are not fully implantable since they connect to an external power source, hence increasing the risk of infection. Fully implantable devices could reduce this risk of infection but more work needs to be done for further development of these VADs. The newest totally implantable LVAD (Leviticus FiVAD) uses the Jarvik VAD platform and undergoing clinical trials. [8]

List of implantable VAD devices

This is a partial list and may never be complete
Referenced additions are welcome

Device Manufacturer Type Approval Status as at December 2007
Novacor World Heart Pulsatile Approved for use in North America, European Union and Japan
Heartmate Thoratec Pulsatile Approved for use in North America
Heartmate II Thoratec Rotor driven continuous axial flow, ball and cup bearings. Approved for use in European Union. FDA approval for bridge to transplant achieved November 2007.
Incor Berlin Heart Continuous flow driven by a magnetically suspended axial flow rotor. Approved for use in European Union.
Jarvik 2000 Jarvik Heart Continuous flow, axial rotor supported by ceramic bearings Approved for use in the European Union. Clinical trials for FDA approval are planned.
MicroMed DeBakey VAD MicroMed Continuous flow driven by axial rotor supported by ceramic bearings Approved for use in the European Union. The child version is approved for use in children in USA. Undergoing clinical trials in USA for FDA approval.
VentrAssist Ventracor Continuous flow driven by a hydrodynamically suspended centrifugal rotor. Approved for use in European Union and Australia. Undergoing clinical trials for FDA approval
MTIHeartLVAD MiTiHeart Corporation Continuous flow driven by a magnetically suspended centrifugal rotor. Yet to start clinical trials.
C-Pulse Sunshine Heart Pulsatile, driven by an inflatable cuff around the aorta Yet to start clinical trials
HVAD HeartWare Similar to Ventracor - magnetic impellor similar to BLDCmotor undergoing clinical trials for CE, applied to start FDA US trials



References

  1. Han JJ, Acker MA, Atluri P (December 2018). "Left Ventricular Assist Devices". Circulation. 138 (24): 2841–2851. doi:10.1161/CIRCULATIONAHA.118.035566. PMID 30565993.
  2. 2.0 2.1 Pieri M, Pappalardo F (October 2018). "Impella RP in the Treatment of Right Ventricular Failure: What We Know and Where We Go". J. Cardiothorac. Vasc. Anesth. 32 (5): 2339–2343. doi:10.1053/j.jvca.2018.06.007. PMID 30093192.
  3. 3.0 3.1 Gregory, Shaun D.; Timms, Daniel; Gaddum, Nicholas; Mason, David G.; Fraser, John F. (2011). "Biventricular Assist Devices: A Technical Review". Annals of Biomedical Engineering. 39 (9): 2313–2328. doi:10.1007/s10439-011-0348-8. ISSN 0090-6964.
  4. Hayward, Christopher S; Shehab, Sajad (2019). "Choosing Between Left Ventricular Assist Devices and Biventricular Assist Devices". Cardiac Failure Review. 5 (1): 19. doi:10.15420/cfr.2018.23.2. ISSN 2057-7540.
  5. 5.0 5.1 Vaidya Y, Patibandla S, Dhamoon AS. PMID 29763016. Missing or empty |title= (help)
  6. 6.0 6.1 Stone ME, Pawale A, Ramakrishna H, Weiner MM (August 2018). "Implantable Left Ventricular Assist Device Therapy-Recent Advances and Outcomes". J. Cardiothorac. Vasc. Anesth. 32 (4): 2019–2028. doi:10.1053/j.jvca.2017.11.003. PMID 29338999.
  7. Zucchetta F, Tarzia V, Bottio T, Gerosa G (September 2014). "The Jarvik-2000 ventricular assist device implantation: how we do it". Ann Cardiothorac Surg. 3 (5): 525–31. doi:10.3978/j.issn.2225-319X.2014.09.09. PMC 4229469. PMID 25452914.
  8. 8.00 8.01 8.02 8.03 8.04 8.05 8.06 8.07 8.08 8.09 8.10 8.11 8.12 8.13 8.14 8.15 Eisen HJ (July 2019). "Left Ventricular Assist Devices (LVADS): History, Clinical Application and Complications". Korean Circ J. 49 (7): 568–585. doi:10.4070/kcj.2019.0161. PMC 6597447 Check |pmc= value (help). PMID 31243930.
  9. 9.0 9.1 Stone, Marc E.; Pawale, Amit; Ramakrishna, Harish; Weiner, Menachem M. (2018). "Implantable Left Ventricular Assist Device Therapy—Recent Advances and Outcomes". Journal of Cardiothoracic and Vascular Anesthesia. 32 (4): 2019–2028. doi:10.1053/j.jvca.2017.11.003. ISSN 1053-0770.
  10. 10.0 10.1 Emani S (July 2018). "Complications of Durable Left Ventricular Assist Device Therapy". Crit Care Clin. 34 (3): 465–477. doi:10.1016/j.ccc.2018.03.003. PMID 29907277.

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