市场调查报告书
商品编码
1453903
2030 年肺动脉瓣置换市场预测:按瓣膜类型、手术类型、应用、最终用户和地区进行的全球分析Pulmonary Valve Replacement Market Forecasts to 2030 - Global Analysis By Valve Type, Procedure Type, Application, End User, and By Geography |
根据 Stratistics MRC 的数据,2023 年全球肺动脉瓣置换市场规模为 12 亿美元,预计在预测期内复合年增长率为 7.1%,到 2030 年将达到 20 亿美元。
肺动脉瓣置换术(PVR)是一种旨在替换心臟中有缺陷或损坏的肺动脉瓣的外科手术。肺动脉瓣调节从心臟右心室流向肺动脉的血流,促进肺部血液氧合。外科医生通常使用机械或生物人工瓣膜来恢復正常的心臟功能。 PVR 可缓解呼吸急促、胸痛和疲劳等症状,改善整体心臟健康和生活品质。术后护理包括监测併发症和心臟康復,以支持康復和长期健康。
医疗保健支出增加
随着医疗保健支出的增加,特别是在新兴经济体和已开发国家,获得专业心臟护理的机会也在增加。这些基础设施的改进将使医疗保健提供者能够为更多患者提供更广泛的治疗选择。此外,医疗保健支出的增加通常与保险覆盖范围和报销政策的改善有关,从而减少患者的财务障碍。
高成本
手术的复杂性和侵入性是导致肺动脉瓣置换术高成本的两个主要因素。这些因素影响手术的总成本,包括术前评估、术后照护和后续观察。此外,用于肺动脉瓣置换的材料(例如人工瓣膜和导管)可能很昂贵,这进一步增加了手术成本。
技术进步
人工瓣膜设计和材料的进步有助于提高肺动脉瓣置换术的寿命、耐用性和生物相容性。这些创新带来更好的临床结果并降低瓣膜关闭不全率,从而提高患者满意度并减少再次手术的需要。此外,3D 超音波心动图和心臟磁振造影(MRI) 等影像技术的进步正在增强术前规划并推动该市场的成长。
缺乏意识
对肺动脉瓣疾病的症状和后果认识不足可能会延误诊断和干预,导致患者预后不良。医疗保健提供者也缺乏对技术和工艺最新进展的透彻了解,这可能导致患者护理不佳和适当治疗方法的利用不足。此外,患者及其家人可能对外科手术有误解和恐惧,这可能会阻碍市场规模。
COVID-19 的影响
COVID-19 的爆发对肺动脉瓣置换市场产生了重大影响。随着世界各地的医疗系统投入资源对抗这场流行病,包括肺动脉瓣置换术在内的选择性手术被推迟或取消。这导致专门从事心臟介入治疗的製造商和医疗机构的手术数量和收益下降。此外,患者因担心接触病毒而不愿寻求非紧急护理,进一步减少了肺动脉瓣置换术的需求。
组织工程肺动脉瓣领域预计在预测期内成为最大
据估计,组织工程肺动脉瓣段占最大份额。这些瓣膜旨在模仿天然肺动脉瓣的结构和功能,为肺动脉瓣功能障碍患者提供了一个有前景的解决方案。组织工程肺动脉瓣通常是透过将细胞接种到生物分解性的支架上来製造,从而允许生物组织生长。此外,组织工程瓣膜在长期功能和动态性能方面显示出可喜的结果,逐渐推动了该领域的成长。
经导管肺动脉瓣置换术(TPVR)领域预计在预测期内复合年增长率最高
经导管肺动脉瓣置换术(TPVR)领域预计在预测期内复合年增长率最高,因为它是一种使用导管治疗的微创肺动脉瓣置换术。这种方法对于患有先天性心臟病、肺动脉瓣狭窄和逆流的患者特别有益。此外,与传统的外科手术相比,TPVR 手术在安全性、有效性和患者復健方面显示出优异的结果,这正在推动这一领域的扩张。
由于先天性心臟疾病和瓣膜性心臟病的盛行率不断增加,北美在估计期间占据了最大的市场占有率。该地区是Medtronic)、雅培实验室 (Abbott Laboratories) 和波士顿科学 (Boston Scientific) 等大公司的所在地。此外,旨在改善心血管保健和促进医学研究的政府措施也在推动市场成长方面发挥重要作用。
由于医疗技术的显着进步和健全的医疗保健系统,预计欧洲在预测期内的复合年增长率最高。德国、法国、英国和义大利等国家对该地区的市场成长做出了重大贡献。此外,欧洲拥有强大的法律规范,支持医疗创新、确保新型肺动脉瓣置换技术的安全性和有效性、促进竞争并促进该领域的进步。
According to Stratistics MRC, the Global Pulmonary Valve Replacement Market is accounted for $1.2 billion in 2023 and is expected to reach $2.0 billion by 2030 growing at a CAGR of 7.1% during the forecast period. Pulmonary valve replacement (PVR) is a surgical procedure aimed at replacing a defective or damaged pulmonary valve in the heart. The pulmonary valve regulates blood flow from the heart's right ventricle to the pulmonary artery, facilitating oxygenation of blood in the lungs. Surgeons typically use either mechanical or biological prosthetic valves to restore proper cardiac function. PVR can alleviate symptoms like shortness of breath, chest pain, and fatigue, improving overall heart health and quality of life. Post-operative care involves monitoring for complications and cardiac rehabilitation to support recovery and long-term well-being.
Increasing healthcare expenditure
As healthcare spending rises, particularly in emerging economies and developed countries, there is a corresponding increase in access to specialized cardiac care procedures. This improved infrastructure enables healthcare providers to offer a wider range of treatment options to a greater number of patients. Moreover, increased healthcare spending often correlates with improvements in insurance coverage and reimbursement policies, reducing financial barriers for patients, which drives this market growth.
High cost
The complexity and invasiveness of the procedure are two of the primary factors contributing to the high cost of pulmonary valve replacement. These factors contribute to the overall cost of the procedure, including pre-operative assessments, post-operative care, and follow-up visits. Additionally, the materials used in pulmonary valve replacement, such as prosthetic valves or conduits, can be expensive, further driving up the cost of the procedure.
Technological advancements
Advancements in prosthetic valve design and materials contribute to improved longevity, durability, and biocompatibility of pulmonary valve replacements. These innovations result in better clinical outcomes and reduced rates of valve failure, leading to increased patient satisfaction and a decreased need for repeat interventions. Furthermore, advancements in imaging technologies, such as 3D echocardiography and cardiac magnetic resonance imaging (MRI), enhance preoperative planning, which is boosting this market growth.
Lack of awareness
Limited awareness about the symptoms and consequences of pulmonary valve conditions may lead to delays in diagnosis and intervention, resulting in poorer patient outcomes. Healthcare providers may also lack sufficient understanding of the latest advancements in techniques and technologies, leading to suboptimal patient care and the underutilization of appropriate treatments. Furthermore, patients and their families may have misconceptions or fears about surgical procedures, which can impede this market size.
Covid-19 Impact
The COVID-19 pandemic has significantly impacted the pulmonary valve replacement market. As healthcare systems worldwide diverted resources to manage the pandemic, elective procedures, including pulmonary valve replacements, experienced delays and cancellations. This led to a reduction in procedural volumes and revenue for manufacturers and healthcare facilities specializing in cardiac interventions. Moreover, patient reluctance to seek non-urgent medical care due to fear of exposure to the virus further dampened demand for pulmonary valve replacement procedures.
The tissue engineered pulmonary valves segment is expected to be the largest during the forecast period
The tissue engineered pulmonary valves segment is estimated to hold the largest share. These valves are designed to mimic the structure and function of native pulmonary valves, offering promising solutions for patients with pulmonary valve dysfunction. Tissue-engineered pulmonary valves are typically created by seeding cells onto a biodegradable scaffold, allowing for the growth of living tissue. Additionally, tissue-engineered valves have shown promising outcomes in terms of long-term functionality and hemodynamic performance, which gradually boosts this segment's growth.
The transcatheter pulmonary valve replacement (TPVR) segment is expected to have the highest CAGR during the forecast period
The transcatheter pulmonary valve replacement (TPVR) segment is anticipated to have highest CAGR during the forecast period due to its minimally invasive procedure for replacing pulmonary valves via catheterization. This approach is particularly beneficial for patients with congenital heart defects, pulmonary valve stenosis, or regurgitation. Furthermore, TPVR procedures have demonstrated excellent outcomes in terms of safety, efficacy, and patient recovery, compared to traditional surgical interventions, which are driving this segment's expansion.
North America commanded the largest market share during the extrapolated period owing to a growing prevalence of congenital heart diseases and valve disorders. This region is home to some of the major players, such as Medtronic, Abbott Laboratories, and Boston Scientific. Moreover, government initiatives aimed at improving cardiovascular healthcare and advancing medical research also play a vital role in fueling market growth.
Europe is expected to witness highest CAGR over the projection period, owing to significant advancements in medical technology, robust healthcare systems. Countries like Germany, France, the United Kingdom, and Italy are key contributors to the market's growth in the region. Additionally, Europe has a strong regulatory framework supporting medical innovation, ensuring the safety and efficacy of new pulmonary valve replacement technologies, fostering competition, and driving advancements in the field.
Key players in the market
Some of the key players in the Pulmonary Valve Replacement Market include Edwards Lifesciences, Medtronic, Terumo Corporation, CryoLife, Inc, SynCardia Systems, Inc., Abbott Laboratories, Merit Medical Systems, LivaNova PLC, Micro Interventional Devices, Inc., Boston Scientific, Braile Biomedica, JenaValve Technology, Inc., B. Braun Melsungen AG, Medistim and CardioMech AS.
In January 2024, Boston Scientific Corporation announced it has entered into a definitive agreement to acquire Axonics, Inc., a publicly traded medical technology company primarily focused on the development and commercialization of differentiated devices to treat urinary and bowel dysfunction.
In December 2023, Medtronic plc announced that it has entered into a definitive agreement to expand its partnership with Cosmo Intelligent Medical Devices, a subsidiary of Cosmo Pharmaceuticals.
In November 2023, Medtronic plc announced that the United States Food and Drug Administration (FDA) has approved the Symplicity Spyral(TM) renal denervation (RDN) system, also known as the Symplicity(TM) blood pressure procedure, for the treatment of hypertension.
In September 2023, Boston Scientific Corporation announced it has received U.S. Food and Drug Administration approval for the latest-generation WATCHMAN FLX(TM) Pro Left Atrial Appendage Closure (LAAC) Device.