![]() |
市場調査レポート
商品コード
1593749
ステント市場の評価:製品タイプ・ステントタイプ・材料・タイプ・エンドユーザー・地域別の機会および予測 (2017-2031年)Stents Market Assessment, By Product Type, By Stent Type, By Material, By Type, By End-user, By Region, Opportunities and Forecast, 2017-2031F |
||||||
カスタマイズ可能
|
ステント市場の評価:製品タイプ・ステントタイプ・材料・タイプ・エンドユーザー・地域別の機会および予測 (2017-2031年) |
出版日: 2024年11月20日
発行: Markets & Data
ページ情報: 英文 229 Pages
納期: 3~5営業日
|
世界のステントの市場規模は、2023年の126億9,000万米ドルから、予測期間中はCAGR 6.05%で推移し、2031年には203億1,000万米ドルに成長すると予測されています。
同市場の成長を支えているのは、心血管疾患や障害の症例数の増加、新製品の導入に向けた参入事業者による取り組みの強化、高齢者人口の拡大、ステント設計の技術進歩です。
以前は避けられないと考えられていた一連の心臓手術を回避するための新しいステントの導入は、市場に有利な成長機会をもたらしています。2024年10月、FDAは先天性心疾患を持って生まれた子供たちが開心術を回避できるよう、幼児や乳児専用に設計されたステントを承認しました。通常、幼児や乳児がステントを必要とする場合、外科医は大人サイズのステントを修正したり切り詰めたりして、クルミ大の幼児の心臓の血管に押し込んでいます。この方法は、子供が成長すると血管が太くなり、開胸手術でステントを交換することになるため、理想的とは言えませんでした。RENATA MEDICALのMinimaステントは、子供の成長に合わせて大きくなるように設計されており、手術の必要がありません。FDAはまた、2つの心臓疾患 (狭窄と大動脈縮窄) の治療用としてもこれを承認しています。
ライフスタイルの変化と高齢化人口の増加に伴い、心臓疾患の発生は世界のさまざまな地域で増加しており、ステント市場の拡大にプラスの影響を与えています。
当レポートでは、世界のステントの市場を調査し、市場の定義と概要、市場規模の推移・予測、各種区分・地域/主要国別の詳細分析、産業構造、市場成長への影響因子の分析、ケーススタディ、競合情勢、主要企業のプロファイルなどをまとめています。
Global stents market is projected to witness a CAGR of 6.05% during the forecast period 2024-2031, growing from USD 12.69 billion in 2023 to USD 20.31 billion in 2031. The market's growth is supported by the rising cases of cardiovascular diseases and disorders, increasing efforts by the market players to introduce novel products, expansion of the geriatric population, and technological advancements in stent design. Small mesh-like devices are inserted in veins and arteries to keep them open and allow unrestricted fluid and blood flow. Stents are commonly used for treating conditions such as peripheral artery disease and coronary artery disease, among other blockages that can often result in life-threatening complications.
The introduction of new stents to avoid a series of heart operations that were previously considered unavoidable is providing lucrative growth opportunities for the market. In October 2024, the Food and Drug Administration (FDA) approved a stent designed specifically for young children and infants to aid kids born with congenital heart defects in avoiding a series of open-heart operations. Usually, when young children and infants require stents, surgeons modify or trim adult-size stents and squeeze them into the vessels of the infants' hearts, which are approximately the size of a walnut. This method was not ideal as when the child grows older, their blood vessels get bigger, leading to the stents getting replaced in an open-heart surgery. The Minima stent, produced by RENATA MEDICAL, is designed to grow as the child grows, eliminating the surgery requirement. The FDA has also approved it for treating two heart conditions, i.e., stenosis and coarctation.
With increasing lifestyle changes and the growth of the aging population, the occurrence of heart diseases is increasing in different regions across the globe, positively influencing the expansion of the stents market.
Expansion of Geriatric Population to Boost Market Demand
The rapid growth of the aging population is one of the major factors augmenting the requirement for stents from different regions across the globe. As per the estimates of the World Health Organization (WHO), approximately 17.9 million individuals across the globe die from cardiovascular diseases every year. Aging increases the risk of cardiovascular diseases, such as coronary artery disease, atherosclerosis, and hypertension, propelling the requirement for medical intervention and equipment for effective management of heart-related issues. Due to the minimally invasive nature of stenting procedures, they are preferred for older patients who might not be suitable for open heart surgeries due to various age-related complications. Coronary stenting is usually preferred for older people as it allows faster recovery of patients, shorter hospital stays, and minimally invasive alternatives to open heart procedures. The surgical procedures become risky with age, especially if the patients are suffering from coronary artery disease, along with other chronic conditions such as high blood pressure and diabetes. Thus, minimally invasive procedures, including stenting and coronary angioplasty, are more beneficial in elderly patients.
Increasing Investments to Support Market Expansion
The continuous innovations and technological advancements in stent design and manufacturing are providing lucrative growth opportunities to the global stents market. Various medical device companies are actively working on raising investments to propel the development of novel treatment solutions for different cardiac conditions. In February 2024, CeroFlo, an Irish medical device company, announced that they had raised approximately USD 6.9 million (EUR 6.4 million) in investment round funding to advance the development of their novel stent, SubMax device, intended to revolutionize intracranial atherosclerotic disease treatments. The company announced that the funds will aid them in supporting first-in-human clinical trials across thirty patients. Such investments are expected to propel the development and availability of novel technologies, providing lucrative growth opportunities to the market.
Additionally, increasing investments are aiding the leading medical device companies in producing stents that are compatible with the complex anatomical structure of the heart, allowing healthcare professionals to provide customized treatments for patients with varying requirements.
Coronary Stenting to Account for a Significant Market Share
The rising investments by medical device companies in research and development activities for coronary stents are supporting the segment's expansion. The increasing efforts by the leading market players to ensure the availability of coronary stent systems in different regions across the globe are boosting the segment's growth. Additionally, the growing research activities for managing coronary artery perforations further aid the segment's growth. Research institutions across the globe are working on developing a bioresorbable polymer membrane to seal coronary artery perforations effectively. Such coatings could effectively correct symptomatic aneurysms and mitigate neointimal hyperplasia in the vascular lumen.
Coronary stents, including drug-eluting stunts, are increasingly being deployed to treat narrowed or blocked arteries caused by plaque buildup. Additionally, the minimally invasive nature of coronary stenting is bolstering its adoption and providing lucrative growth opportunities to the market. The shorter recovery time, lower risk of complications, and reduced hospital stays associated with the stenting procedure drive the market's demand.
North America to Hold Major Market Share
The increasing awareness among the general population about cardiovascular health, the presence of well-established healthcare infrastructure, and the expansion of the geriatric population are some of the major factors bolstering the growth of the North America stents market. The rising cases of cardiovascular diseases are propelling the market's expansion. According to the estimates by the US Centers for Disease Control and Prevention, 702,880 individuals died from heart disease in 2022. Additionally, the increasing efforts by key market players and research organizations boost the development of innovative devices for different cardiac conditions, providing lucrative growth opportunities to the market.
Meanwhile, the Asia-Pacific market is expected to witness significant growth over the forecast period as an increasing number of patients undergo stenting procedures in countries such as Japan, India, and China due to the expansion of insurance coverage and accessibility to affordable healthcare solutions. Furthermore, the rising awareness about heart health and the importance of regular health checkups and early treatments is propelling the demand for stenting procedures in the region. To meet the rising requirements, local manufacturers are stepping up and producing cost-effective options to increase the accessibility of the procedure for a wider population base.
Future Market Scenario (2024-2031F)
The market is expected to witness significant growth in the forecast years due to the increasing prevalence of cardiovascular diseases, rising partnerships between leading healthcare companies, and growing emphasis on innovation and novel product development. The growing awareness about cardiovascular health and the rapid expansion of the geriatric population is expected to provide lucrative growth opportunities for the market. As per the estimates of the WHO, one in six people across the globe will be 60 years or older by 2030.
Additionally, the market is expected to witness significant growth as different emerging economies, such as South America and Asia-Pacific, invest in improving their healthcare infrastructure. The key market players are expected to increasingly invest in producing more effective and safer stents, improving their designs to cater to the specific requirements of the patient population. The rising emphasis on minimally invasive treatments, in combination with rapid innovations in stent technology, is expected to positively influence the market's expansion.
Key Players Landscape and Outlook
The key players in the market are investing in introducing newer products to expand their market share. In May 2024, Abbott introduced the new generation of XIENCE Sierra Everolimus drug-eluting coronary stent system in India. XIENCE stents are effective in cases of narrow and difficult-to-treat lesions and chronic cases. The improved deliverability and innovative design allow physicians to unblock difficult-to-treat lesions with precision and flexibility. The product contains a highly specialized coating that decreases the probability of arteries re-blocking.
Additionally, the market players are receiving approval from different regulatory bodies, allowing them to distribute their products across the globe and aiding them in expanding their market share. In April 2022, Biosensors International Group, Ltd. announced that they received approval for BioFreedom from the United States FDA and the Japanese Pharmaceuticals and Medical Devices Agency (PMDA). The BioFreedom stent systems optimize the percutaneous coronary intervention (PCI) procedure for patients with high bleeding risk by simplifying stent choice prior to the procedure. Such approvals are aiding the market players in expanding their global footprint and positively influencing the expansion of the global stents market.
All segments will be provided for all regions and countries covered
Companies mentioned above DO NOT hold any order as per market share and can be changed as per information available during research work.