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市场调查报告书
商品编码
1558350
2030 年血管闭合装置市场预测:按产品、接取模式、应用、最终用户和地区进行的全球分析Vascular Closure Devices Market Forecasts to 2030 - Global Analysis By Product, Access Mode, Application, End User and By Geography |
根据 Stratistics MRC 的数据,2024 年全球血管闭合装置市场规模为 13 亿美元,预计在预测期内将以 8.3% 的复合年增长率成长,到 2030 年达到 21 亿美元。血管闭合装置 (VCD) 是一种用于密封或闭合血管穿孔的医疗装置,通常在血管造影术或经皮冠状动脉介入治疗等导管手术后使用。这些装置对于最大限度地减少出血、减少併发症以及透过加速穿刺部位的止血来加速恢復至关重要。 VCD 透过多种机制运行,包括机械压缩、组织黏合剂以及专用塞子或补片的部署。 VCD透过有效阻断血管入口,预防血肿、出血、感染疾病等併发症,让患者更快恢復正常活动。
据英国心臟基金会称,到 2024 年,全球将有约 6.2 亿人患有心臟或循环系统疾病。根据医疗保险和医疗补助服务中心(CMS.gov)的资料,2023年,美国将在医疗保健方面支出约4.7兆美元,占国民经济的18%。
人们越来越偏好微创治疗
人们对微创手术的日益偏好正在推动血管闭合装置 (VCD) 的进步。 VCD 对于基于导管的干预后有效闭合通路部位至关重要。随着医疗保健转向微创手术以加快患者康復时间并最大限度地减少併发症,VCD 正在不断发展以满足这些需求。现代 VCD 透过使用先进的材料和技术来确保快速、安全地闭合血管网路基地台,从而提高安全性、有效性和患者舒适度。这一趋势反映了医学领域更广泛的趋势,即采用更小切口、更少疼痛和更快恢復正常活动的手术。
临床风险和併发症
血管闭合装置 (VCD) 旨在在基于导管的手术后闭合股动脉通路部位,目的是最大限度地减少出血并加速康復。 VCD 的使用与临床风险和併发症相关,阻碍了其有效性。主要风险包括感染、血肿形成、血管损伤,可导致肢体缺血、血栓症等併发症。也可能存在与设备相关的问题,例如密封不充分或设备移位,这可能导致出血或动脉损伤。
心血管手术增加
随着血管成形术和支架置入术等手术的增加,对高效、安全和有效的 VCD 的需求正在迅速增加。现代VCD旨在快速止血,减少出血和感染等併发症,缩短復原时间。 VCD 技术的创新包括改进材料以实现更好的组织密封、提高临床医生的易用性以及适应各种血管通路部位的设计。这些进步不仅加快了患者的康復速度,还提高了手术效率,并解决了介入心臟病学增加的复杂性和频率。
智慧财产权挑战
由于智慧财产权(IP)问题,血管闭合装置(VCD)产业面临重大挑战。专利纠纷和限制性智慧财产权主张可能会阻止新参与企业开发和销售自己的设备,从而阻碍创新。现有公司通常持有涵盖基础技术的广泛专利,为新兴企业和其他竞争对手设置了障碍。这种情况可能会导致昂贵的法律诉讼并转移研发资源。严格的智慧财产权法规可能会减缓新的、可能更好的设备进入市场的速度,并限制患者照护的进步。结果,市场受到限制,创新放缓,医疗设备成本居高不下,影响了患者的取得和治疗选择。
由于选择性手术的中断和医疗保健优先事项的变化,COVID-19 大流行对血管闭合装置 (VCD) 市场产生了重大影响。由于世界各地的医院都专注于治疗新冠肺炎 (COVID-19)严重病例,许多非紧急手术,包括需要血管通路的手术,被推迟或取消。这暂时减少了对 VCD 的需求,VCD 用于在导管手术后关闭动脉通路部位。供应链中断和限制影响了这些仪器的生产和分销。这次疫情也加速了远端和微创诊断技术的采用,进一步影响了 VCD 的传统使用。
预计主动逼近器部分在预测期内将达到最大
预计主动逼近器领域在预测期内将是最大的。主动接近器显着提高了血管闭合装置的有效性和易用性,从而彻底改变了血管闭合装置。这些先进的设备利用动态机制来确保导管插入后留下的穿刺部位闭合。与依赖静压或手动操作的传统被动方法不同,主动逼近器施加受控且可调节的力来精确对准和密封血管开口。这项创新可以实现可靠的闭合,同时最大限度地减少出血和感染等併发症。
预计脑血管介入领域在预测期内复合年增长率最高
预计脑血管介入领域在预测期内复合年增长率最高。脑血管介入领域的重点是提高血管闭合的准确性、降低併发症发生率、缩短恢復时间。现代 VCD 具有创新功能,例如改进的止血剂和适应性闭合机制,以改善进入部位的密封性并最大限度地减少对周围组织的创伤。此外,结合即时影像和先进的追踪系统可以实现更精确的设备放置和监控。
由于最尖端科技的整合、医疗培训的改善、监管流程的简化等,欧洲地区在预测期内占据最大的市场占有率。先进的 VCD 对于导管插入术等手术后密封动脉穿刺至关重要,该全部区域医疗保健设施和研究的投资正在增加。增强的基础设施正在促进全部区域创新设备的开发和部署,从而提供更高的准确性、安全性和患者舒适度。配备最先进工具和设备的医院和诊所将能够更有效地利用这些先进的 VCD,从而改善手术结果并缩短恢復时间。这些因素正在推动区域成长。
由于采用血管闭合装置(VCD)并确保严格的安全性和有效性标准,预计欧洲地区在预测期内将显着成长。欧盟的法规结构,包括医疗设备法规 (MDR) 和体外诊断法规 (IVDR),要求对这些设备进行严格的临床评估、品管措施和上市后监督。这种监管监督透过要求製造商遵守高标准、推动技术进步和改善整个全部区域的患者治疗结果来促进创新。
According to Stratistics MRC, the Global Vascular Closure Devices Market is accounted for $1.3 billion in 2024 and is expected to reach $2.1 billion by 2030 growing at a CAGR of 8.3% during the forecast period. Vascular closure devices (VCDs) are medical instruments designed to seal or close punctures in blood vessels, typically following catheter-based procedures like angiography or percutaneous coronary interventions. These devices are crucial for minimizing bleeding, reducing complications, and expediting recovery by facilitating faster hemostasis at the puncture site. VCDs operate through various mechanisms, including mechanical compression, tissue adhesives, or the deployment of specialized plugs or patches. By effectively sealing the vascular entry point, VCDs help prevent complications such as hematomas, bleeding, or infections, and allow patients to resume normal activities more quickly.
According to the British Heart Foundation, in 2024, there are around 620 million people living with heart and circulatory diseases across the world. According to the data by Centers for Medicare and Medicaid Services (CMS.gov) shows that in 2023, the U.S. spent approximately USD 4.7 trillion on healthcare, constituting 18% of the national economy.
Growing preference for minimally invasive procedures
The increasing preference for minimally invasive procedures is driving advancements in Vascular Closure Devices (VCDs), which are crucial for efficiently closing access sites after catheter-based interventions. As healthcare shifts towards less invasive techniques to reduce patient recovery times and minimize complications, VCDs are evolving to meet these demands. Modern VCDs offer improved safety, efficacy, and patient comfort by using advanced materials and technologies to ensure rapid and secure closure of vascular access points. This trend reflects a broader movement in medicine towards procedures that involve smaller incisions, less pain, and quicker returns to normal activities.
Clinical risks and complications
Vascular Closure Devices (VCDs) are designed to close femoral artery access sites after catheter-based procedures, aiming to minimize bleeding and expedite recovery. Their use carries clinical risks and complications that can impede their effectiveness. Key risks include infection, hematoma formation, and vascular injury, which can lead to complications like limb ischemia or thrombosis. There is also the potential for device-related issues such as inadequate sealing or device migration, which can cause bleeding or arterial damage.
Rise in cardiovascular procedures
As the volume of procedures like angioplasty and stent placements rises, the demand for efficient, safe, and effective VCDs has surged. Modern VCDs are designed to provide faster hemostasis, reduce complications such as bleeding and infection, and shorten recovery times. Innovations in VCD technology include improved materials for better tissue sealing, enhanced ease of use for clinicians, and designs that accommodate various vascular access sites. These advancements not only facilitate quicker patient recovery but also enhance procedural efficiency, aligning with the growing complexity and frequency of cardiovascular interventions.
Intellectual property challenges
The vascular closure device (VCD) industry faces significant challenges due to intellectual property (IP) issues. Patent disputes and restrictive IP claims can stifle innovation by preventing new entrants from developing or marketing their own devices. Established companies often hold broad patents that cover fundamental technologies, creating barriers for startups and other competitors. This situation can lead to expensive legal battles, which divert resources away from research and development. Stringent IP regulations can delay the introduction of new, potentially better devices to the market, limiting advancements in patient care. The result is a constrained market where innovation is slowed, and the cost of devices may remain high, impacting accessibility and treatment options for patients.
The COVID-19 pandemic significantly impacted the vascular closure devices (VCDs) market due to disruptions in elective procedures and a shift in healthcare priorities. As hospitals worldwide focused on managing severe COVID-19 cases, many non-urgent procedures, including those requiring vascular access, were postponed or canceled. This led to a temporary decline in demand for VCDs, which are used to close the arterial access site after catheter-based procedures. Supply chain disruptions and restrictions affected the production and distribution of these devices. The pandemic also accelerated the adoption of remote and less invasive diagnostic techniques, further impacting the traditional usage of VCDs.
The Active Approximators segment is expected to be the largest during the forecast period
Active Approximators segment is expected to be the largest during the forecast period. Active approximators are revolutionizing vascular closure devices by significantly improving their efficacy and ease of use. These advanced devices utilize dynamic mechanisms to securely close the puncture site left after catheterization procedures. Unlike traditional passive methods that rely on static pressure or manual manipulation, active approximators apply controlled, adjustable forces to precisely align and seal the vascular opening. This innovation enhances the device's ability to achieve a reliable closure with minimal complications, such as bleeding or infection.
The Cerebrovascular Interventions segment is expected to have the highest CAGR during the forecast period
Cerebrovascular Interventions segment is expected to have the highest CAGR during the forecast period. Cerebrovascular Interventions segment focus on increasing the precision of vascular closure, reducing complication rates, and shortening recovery times. Modern VCDs are designed with innovative features such as improved hemostatic agents and more adaptable closure mechanisms, which ensure better sealing of the access site and minimal trauma to surrounding tissues. Additionally, the incorporation of real-time imaging and advanced tracking systems allows for more accurate device placement and monitoring.
Europe region commanded the largest market share over the extrapolated period driven by the integration of cutting-edge technologies, improved medical training, and streamlined regulatory processes. Advanced VCDs, which are crucial for sealing arterial punctures after procedures like catheterizations, are benefiting from increased investment in healthcare facilities and research across the region. Enhanced infrastructure facilitates the development and deployment of innovative devices that offer greater precision, safety, and patient comfort throughout the region. Hospitals and clinics equipped with state-of-the-art tools and facilities can more effectively utilize these advanced VCDs, leading to improved procedural outcomes and reduced recovery times. These elements are boosting the regional growth.
Europe region is projected to witness substantial growth during the forecast period due to the adoption of Vascular Closure Devices (VCDs) by ensuring stringent safety and efficacy standards. The European Union's regulatory framework, including the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR), mandates rigorous clinical evaluations, quality control measures, and post-market surveillance for these devices. This regulatory oversight fosters innovation by encouraging manufacturers to adhere to high standards, thus driving advancements in technology and improving patient outcomes across the region.
Key players in the market
Some of the key players in Vascular Closure Devices market include Abbott Laboratories, Boston Scientific Corporation, Cardinal Health, Inc, Endologix, Inc, GE Healthcare, HeartWare International, Inc, Medtronic PLC, Nipro Corporation, Stryker Corporation and Terumo Corporation.
In June 2024, Haemonetics Corporation has announced the launch of its new VASCADE MVP XL mid-bore venous closure device. The VASCADE MVP XL system adds to Haemonetics VASCADE line of vascular closure devices by using novel collapsible disc technology with a patented resorbable collagen patch that promotes fast hemostasis.
In November 2023, Johnson & Johnson Service Inc., a biotechnology company, announced the completion of the acquisition of Laminar, Inc., a privately held medical device company focused on eliminating the left atrial appendage (LAA) in patients with non-valvular atrial fibrillation (AFib).
In February 2023, the LockeT product was introduced to the market by Catheter Precision, Inc., a wholly-owned subsidiary of Ra Medical Systems, Inc. The first shipments of the product to its distributors will start right away. When a catheter is inserted through the skin into a blood artery and subsequently removed after an operation, LockeT can be utilized in combination with the closure of the percutaneous wound site.