Visiongain Publishes Transcatheter Aortic Valve Replacement Implantation (TAVRTAVI) Market Forecast 2020-2030

25 July 2020
Pharma

Visiongain has launched a new report Transcatheter Aortic Valve Replacement Implantation (TAVRTAVI) Market Forecast 2020-2030: Forecasts and Analysis by Surgery Method, by Valve Frame Material, by End-user and Geography, with Profiles of Leading Companies.

According to the report published by Visiongain, the Transcatheter Aortic Valve Replacement Implantation (TAVRTAVI) market is estimated to be valued at approximately USD xx billion in 2019 and is expected to generate around USD xx billion by 2030, at a CAGR of around xx% between 2020 and 2030. The engineering of transcatheter aortic valve implantation (TAVI) has seen fast adoption over the past 15 years and conducted in > 70 countries with > 350,000 procedures. This approach has developed in a systematic, quick and seamless way, from a complex procedure over the same era. The aim of this review article is to give an overview of the rapidly changing field of TAVI therapy and to explore past achievements, current problems and prospects. There were three sections: developments in TAVI clinical and anatomical indications, a description and progressive adoption of procedural progress and trends in complication rates over time and the discussions. One of the key trends in market growth is the increasing numbers of cardiovascular sufferers across the globe, including cardiovascular conditions like heart failure, coronary artery diseases and hypertension. The inadequate functioning of aortic valves is due to cardiovascular diseases, which then increase the demand for an effective valve replacement procedure.

Transcatheter Aortic Valve Replacement Implantation (TAVRTAVI) Market is witnessing Growth due to factors such as

Increasing Demand due to safety and effectiveness of TAVI
In an increasingly broad spectrum of patients with severe symptomatic aortic stenosis (SSS), the safety and effectiveness of TAVI was initially identified for patients with high risk of surgery [ Society of Thoracic Surgeons Predicted Mortality Risk (STP)] in the last decade. TAVI has been a beneficial alternative to surgical aortic valve replacement (SAVR) PARTNER 2A10 and SURTAVI11 subsequently examined a function for TAVI in patients at moderate surgical risk (STS 4–8Percent). Percent).

Moreover, when the aortic valve replacement surgical (STS-score) patient has remained the standard care in patients with a low surgical risk Transcatheter aortic valve (TAVI) or Transcatheter aortic valve substitution (TAVR) as it is referred to in North America, the technique in this study has been demonstrated to indicate superiority of TAVI in SAVR. STS-score is an advantageous transcatheter. The first TAVI in person was administered in 2002 on an inoperable, extreme AS and cardiogenic shock by the French cardiologist Alain Cribier.9 Originally done with septostomy through the femoral vein, the eventual invention of simpler, more straightforward femoral arterial access (as is the case in the PCI) prompted the rapid initiation of the operation. A femoral arterial (also known as transfemoral) solution is now possible for various approaches (> 90%) in the majority of the cases. For patients with complicated femoral exposure due to stenosis, calcification, tortuosity and/or small caliber channels, specific transaortic or transapical solutions may be recommended. These often involve anaesthesias of a general nature with a mini-sternotomy or a mini-thoracotomy (transapical). Both ballon expandable or self-expanding forms can be typically separated. The Edwards family of ballon expandable valves (Edwards Lifesciences) and CoreValve self expanded valve family (Medtronic) currently have significant randomized controlled test (RCT) results. These valve types are approved in Australia for implantation (Box 2), along with the Portico valve (Abbott).

Increased Funding For Research And Development Activities
New product launches and favorable refund policies are also some of the factors that are likely to contribute to the market. Cross-catheter aortic valve replacement (MIC) is anticipated to decrease overall patient resistance in tandem with technological developments. On the other hand, this is in a position to cut health costs. In addition, the growth of the market during the forecast period shall be expected to promote regional expansion, financing and adoption of advanced technologies and procedural methodologies. Transcatheter aortic vapor implantation devices (TAVI) are considered cost-effective in the treatment of high risk patients according to Annals of Cardiothoracic Surgery. TAVI systems are publicly funded in European and American nations.

The Japanese government pays treatment costs as an exception to Asian countries. Patients in the rest of Asia pay out their savings for treatment. Efforts are also made to develop and maintain the TAVR register in the area of Asia Pacific. The TAVR database has information from over 8000 TAVR procedures in Japan since 2013. The register for TAVR has been working since 2013 in Japan.

Various partnerships, mergers and acquisitions and expanded research and development investments are expected to drive the market in order to minimize risks and improve efficiency of careBoston Scientific Corporation bought, for instance, in March 2017 Symetis SA for USD 435 million to develop products such as neo / TFACURATE and valves ACURATE TA. The treatment of patients with a symptomatic aortic valve stenosis is expected to be improved globally. This acquisition helps the company to enhance its production and research and development capacities. Due to the increasing number of patients who seek effective treatment with rapid recovery, transapic implantation is most probably the highest CAGR during the forecast period. Transapical aortic valves were launched in Brazil in February 2012. This release was designed to expand the portfolio of the organization and extend its presence in the field of Latin America.

Mid-level implemented scenario is anticipated to further increase the levels of stroke and PVL complications for new generations of TAVR systems over five to 10 years.
Although the incidence of pacemaker implantations in TAVR may continue to be increasing, the rates are slowly decreasing. Finally, while the long-term durability of the TAVR device remains inconclusive, the number of studies on durability and long-term results will increase. The results will continue to grow. Such variables would likely lead, in older patients, to a low yet strong intake of TAVR. During the mid-level adoption scenario, TAVR will be expanded to include the eligible criteria for a smaller patient pool, as the effects of the procedure on the younger patients will still be uncertain. TAVR will continue to grow in all adoption scenarios in the next ten years as there are strong evidence that transcatheter procedures significantly improve the results of patients compared to surgery. As new businesses enter the room to capitalize on market potential or acquisition targets, the competitive scene will continue to change rapidly. Although TAVR devices stay at a much better price than the SAVR products, new entrants are further promoting TAVR use, driving the price of such devices downwards.

A Number Of Key Areas Have Increased Business Expansion Capacity
When TAVR product manufacturers were able to take advantage of these prospects effectively, then the TAVR industry will expand beyond even our high estimates. Earlier procedure: mild, moderate or asymptomatic aortic stenosis While typically TAVR is documented to patients with severe, symptomatic aortic stenosis, in less severe or asymptomatic phases of the disease, a much larger possible patient pool occurs.3 Most patients with medium or mild (both asymptomatic) aortic stenosis eventually develop into a serious disease which shows early on that therapy

Studies that investigate valve operation outcomes in asymptomatic patients have produced mixed results. Some studies have revealed that valve operation has improved results, whereas others have revealed no differences or worse outcomes. Although these early studies have used SAVR, minimally invasive TAVR may well be more suitable to this patient population and two clinical trials are currently testing this theory, the TAVR assessment is tested for asymptomatic patients who have severe aortic stenosis (EARLY TAVR)

Shift in Trends

The use of TAVR devices for other heart valves
Edwards Lifesciences has recently finished studies showing that the use of its Sapien XT valve has been demonstrated by a high degree of procedural success6 other anatomical locations such as a pulmonary valve. In addition, the Edwards device has been approved by the FDA for patients with failed surgery bioprosthesis or aorta valve. When businesses will illustrate their technologies at other valve sites then the potential pool of customers, particularly those with a wider range of congenital heart disorders, will be significantly expanded again. To leverage this opportunity, businesses must provide solid evidence at every possible new location by robust clinical testing for their products.

Regional Market Analysis
The high level of implementation of advanced technologies, acquisition and acquisitions and beneficial reimbursing practices may be related to this. Patients should apply for a transcatheter aortic vent replacement operation with reimbursement by government organizations such as Centers for Medicare & Medicaid Services (CMS). Medicare was the primary payer in 2019 in almost 90% of TAVR procedures. Instead of surgical aortic valve replacement (SAVR), it enhanced the economic advantage of using TAVR.

In the forecast period, Italy is ready to report the highest growth. Increasing health care expenses as cardiovascular diseases become more prevalent and improved implant devices that place patients at a lower risk are leading to a move towards aortic valve replacement procedures. Transcatheter.

Europe's major markets are Germany and France. In 2015, 31.000 aortic valve operations in Germany had been conducted due to advances made in the aortic valve substitution process and were therefore the most prefered location for valve replacement implantations according to the National Center for Biotechnology Information (NCBI).

Top Companies
Bracco S.P.A. (Hlt, Inc.)
Jc Medical, Inc.
Meril Life Sciences Pvt. Ltd.
New Valve Technology Ag
Venus Medtech, Inc.
Transcatheter Technologies GmbH
Edwards Lifesciences Corporation
Medtronic, Inc.
Boston Scientific Corporation
Abbott Laboratories
St. Jude Medical Inc.

Notes for Editors
If you are interested in a more detailed overview of this report, please send an e-mail to sara.peerun@visiongain.com or call her on +44 (0) 20 7549 9987.

About Visiongain
Visiongain is one of the fastest growing and most innovative independent media companies in Europe. Based in London, UK, Visiongain produces a host of business-to-business reports focusing on the automotive, aviation, chemicals, cyber, defence, energy, food & drink, materials, packaging, pharmaceutical and utilities sectors.

Visiongain publishes reports produced by analysts who are qualified experts in their field. Visiongain has firmly established itself as the first port of call for the business professional who needs independent, high-quality, original material to rely and depend on.

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