市場調查報告書
商品編碼
1453903
2030 年肺動脈瓣置換市場預測:按瓣膜類型、手術類型、應用、最終用戶和地區進行的全球分析Pulmonary Valve Replacement Market Forecasts to 2030 - Global Analysis By Valve Type, Procedure Type, Application, End User, and By Geography |
根據 Stratistics MRC 的數據,2023 年全球肺動脈瓣置換市場規模為 12 億美元,預計在預測期內年複合成長率為 7.1%,到 2030 年將達到 20 億美元。
肺動脈瓣置換術(PVR)是一種旨在替換心臟中有缺陷或損壞的肺動脈瓣的外科手術。肺動脈瓣調節從心臟右心室流向肺動脈的血流,促進肺部血液氧合。外科醫生通常使用機械或生物人工瓣膜來恢復正常的心臟功能。 PVR 可緩解呼吸急促、胸痛和疲勞等症狀,改善整體心臟健康和生活品質。術後護理包括監測併發症和心臟康復,以支持康復和長期健康。
醫療保健支出增加
隨著醫療保健支出的增加,特別是在新興經濟體和已開發國家,獲得專業心臟護理的機會也在增加。這些基礎設施的改進將使醫療保健提供者能夠為更多患者提供更廣泛的治療選擇。此外,醫療保健支出的增加通常與保險覆蓋範圍和報銷政策的改善有關,從而減少患者的財務障礙。
高成本
手術的複雜性和侵入性是導致肺動脈瓣置換術高成本的兩個主要因素。這些因素影響手術的總成本,包括術前評估、術後照護和後續觀察。此外,用於肺動脈瓣置換的材料(例如人工瓣膜和導管)可能很昂貴,這進一步增加了手術成本。
技術進步
人工瓣膜設計和材料的進步有助於提高肺動脈瓣置換術的壽命、耐用性和生物相容性。這些創新帶來更好的臨床結果並降低瓣膜關閉不全率,從而提高患者滿意度並減少再次手術的需要。此外,3D 超音波心動圖和心臟磁振造影(MRI) 等影像技術的進步正在增強術前規劃並推動該市場的成長。
缺乏意識
對肺動脈瓣疾病的症狀和後果認知不足可能會延誤診斷和干涉,導致患者預後不良。醫療保健提供者也缺乏對技術和工藝最新進展的透徹了解,這可能導致患者護理不佳和適當治療方法的利用不足。此外,患者及其家人可能對外科手術有誤解和恐懼,這可能會阻礙市場規模。
COVID-19 的影響
COVID-19 的爆發對肺動脈瓣置換市場產生了重大影響。隨著世界各地的醫療系統投入資源對抗這場流行病,包括肺動脈瓣置換術在內的選擇性手術被推遲或取消。這導致專門從事心臟介入治療的製造商和醫療機構的手術數量和收益下降。此外,患者因擔心接觸病毒而不願尋求非緊急護理,進一步減少了肺動脈瓣置換術的需求。
組織工程肺動脈瓣領域預計在預測期內成為最大
據估計,組織工程肺動脈瓣段佔最大佔有率。這些瓣膜旨在模仿天然肺動脈瓣的結構和功能,為肺動脈瓣功能障礙患者提供了一個有前景的解決方案。組織工程肺動脈瓣通常是透過將細胞接種到生物分解性的支架上來製造,從而允許生物組織生長。此外,組織工程瓣膜在長期功能和動態性能方面顯示出可喜的結果,逐漸推動了該領域的成長。
經導管肺動脈瓣置換術(TPVR)領域預計在預測期內年複合成長率最高
經導管肺動脈瓣置換術(TPVR)領域預計在預測期內年複合成長率最高,因為它是一種使用導管治療的微創肺動脈瓣置換術。這種方法對於患有先天性心臟病、肺動脈瓣狹窄和逆流的患者特別有益。此外,與傳統的外科手術相比,TPVR 手術在安全性、有效性和患者復健方面顯示出優異的結果,這正在推動這一領域的擴張。
由於先天性心臟疾病和瓣膜性心臟病的盛行率不斷增加,北美在估計期間佔據了最大的市場佔有率。該地區是Medtronic)、雅培實驗室 (Abbott Laboratories) 和波士頓科學 (Boston Scientific) 等大公司的所在地。此外,旨在改善心血管保健和促進醫學研究的政府措施也在推動市場成長方面發揮重要作用。
由於醫療技術的顯著進步和健全的醫療保健系統,預計歐洲在預測期內的年複合成長率最高。德國、法國、英國和義大利等國家對該地區的市場成長做出了重大貢獻。此外,歐洲擁有強大的法律規範,支持醫療創新、確保新型肺動脈瓣置換技術的安全性和有效性、促進競爭並促進該領域的進步。
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.