市场调查报告书
商品编码
1577236
2030 年辅助人工心臟(VAD) 市场预测:按产品、设计、流量类型、应用、最终用户和地区进行的全球分析Ventricular Assist Devices Market Forecasts to 2030 - Global Analysis By Product, Design, Type of Flow, Application, End User and By Geography |
根据 Stratistics MRC 的数据,2024 年全球辅助人工心臟(VAD) 市场规模将达到 36 亿美元,预计到 2030 年将达到 107 亿美元,预测期内复合年增长率为 19.6%。
称为辅助人工心臟(VAD) 的机械帮浦可帮助心室将血液泵送到全身并支持心臟功能。它经常被不适合接受移植手术、患有严重心臟衰竭或正在等待心臟移植的患者使用。辅助人工心臟可插入一个或两个心室,最常见的是左心室 (LVAD)、右心室 (RVAD) 或两者 (BiVAD)。这些可以提高患者的生活水准,增加血流量,并减轻心臟负担。
根据美国心臟协会 (AHA) 的数据,预计到 2030 年,美国心臟衰竭的盛行率将显着增加,患者数量将超过 800 万人。 2020年,全球整体将有超过550万人受到心臟衰竭的影响。老年人罹患心臟衰竭的风险较高。因此,人口老化的增加也在加速这种疾病的传播。
全球心臟衰竭盛行率
在富裕国家,心臟衰竭影响 1-2% 的人口。预测表明,到 2030 年,大约 800 万美国人可能会受到这种疾病的影响。心臟衰竭患者数量的增加是增加辅助人工心臟需求的一个主要因素。此外,老年人口中常见的慢性疾病,如糖尿病和高血压,是心臟衰竭患者增加的主要原因,而可用心臟捐赠者的缺乏也增加了对辅助人工心臟的需求。
与移植相关的风险
出血风险增加是辅助人工心臟植入的手术后果之一,而抗凝血剂的使用可能会使情况变得更糟。控制器和电源等外部组件可能成为感染疾病的切入点,导致严重问题并增加移植后死亡率。血栓症是与设备相关的后果之一,需要仔细监测抗凝血治疗水平,因为它可能导致中风和帮浦衰竭。此外,心臟负荷增加引起的右心室功能障碍可能会使患者的治疗结果复杂化,需要进一步治疗。
辅助人工心臟技术持续创新
技术的进步导致了更坚固、更紧凑的设备的开发,提高了患者的舒适度和移动性。生物相容性的进步降低了血栓症和感染疾病的风险,减少了患者采用的障碍。由于小型化和侵入性较小,辅助人工心臟装置已被更多患者广泛使用,恢復时间更短,植入过程更简单。
报销政策和保险范围不足
辅助人工心臟不仅需要植入手术,还需要术后护理,这可能很昂贵。如果患者因保险范围不足而必须支付大笔自付费用,他们可能不愿意选择辅助人工心臟治疗。获得医疗服务的机会不足会导致医疗干预措施的延迟或放弃、健康状况不佳以及长期医疗费用增加,最终减少辅助人工心臟的市场需求。
COVID-19 大流行对辅助人工心臟(VAD) 市场产生了负面影响,导致择期手术显着延迟并降低了装置利用率。由于封锁和旅行限制,辅助人工心臟移植的数量减少,许多患者出于安全考虑而推迟了治疗。结果,对辅助人工心臟的需求减少,影响了製造商和医疗保健提供者的收益。然而,随着限制的放鬆,预计患者就诊和手术将有所恢復,这可能会推动随后的市场成长。
预计这两个辅助人工心臟(VAD) 细分市场将在预测期内成为最大的细分市场
由于 BiVAD 技术的需求增加和进步,例如可提高全辅助人工心臟心臟 (TAH) 植入场景中的设备性能和效用的气动驱动系统,BiVAD 细分市场预计将在预测期内实现最高增长。 BiVAD 可以实现更好的血流动力学支援、改善生活品质、提高存活率以及提高患者和医生的接受度。
预计桥接移植领域在预测期内复合年增长率最高。
由于在等待心臟移植期间保持患者稳定的关键功能,移植领域预计在预测期内将经历最高的复合年增长率。辅助人工心臟可提供 2 至 6 个月必要的机械性支持,进而改善患者的治疗效果。加深对 BTT 疗法有效性的了解将有助于其在心臟衰竭治疗中的广泛应用。
这是因为北美心臟衰竭发病率的增加和医疗设备技术的开拓共同推动了对辅助瓣膜装置 (VAD) 作为到达目的地和移植的桥接治疗的需求。此外,当可供移植的捐赠者心臟不足时,辅助人工心臟提供了重要的替代品,帮助患者永久生存或等待移植。
由于中国、印度、日本和韩国对现代医疗技术和医疗保健基础设施的投资增加,预计亚太地区在预测期内将呈现最高成长率。由于意识的提高和诊断能力的提高,对复杂心臟衰竭管理解决方案的需求不断增长。由于技术发展,包括开发较小、更有效、问题更少的设备,亚太地区辅助人工心臟(VAD) 市场正在不断扩大。
According to Stratistics MRC, the Global Ventricular Assist Devices Market is accounted for $3.6 billion in 2024 and is expected to reach $10.7 billion by 2030 growing at a CAGR of 19.6% during the forecast period. Mechanical pumps called Ventricular Assist Devices (VADs) help the ventricles pump blood to the body, hence supporting heart function. Patients who are not candidates for transplant surgery, have significant heart failure, or are awaiting a heart transplant frequently utilize them. VADs can be inserted into one or both ventricles, the most frequent being the left ventricle (LVAD), right ventricle (RVAD), or both (BiVAD). They raise the standard of living for patients, increase blood flow, and lessen cardiac strain.
According to the American Heart Association (AHA), the prevalence of heart failure is expected to increase at a significant growth rate by 2030 in the U.S., and is projected to reach over 8 million patients. In 2020, globally, more than 5.5 million individuals were affected by heart failure. Old-age people are at high risk of HF. Therefore, the increasing geriatric population has also been fueling the disease prevalence.
Global prevalence of heart failure
In wealthy nations, heart failure affects 1-2% of the population; by 2030, nearly 8 million Americans may be affected, according to forecasts. The rise in heart failure instances is a major factor driving the need for VADs. Moreover chronic illnesses that are common in aging populations, such as diabetes and hypertension, are the primary cause of the rise in heart failure patients Hence the demand for VADs is increased by the scarcity of available cardiac donors.
Risks associated with implantation
Increased bleeding risks are one of the surgical consequences associated with VAD implants, and anticoagulant medication may make matters worse. External parts such as controllers and power supplies can act as sites of entry for infections, which can cause serious problems and higher post-transplant mortality rates. Thrombosis is one device-related consequence that requires cautious anticoagulation level monitoring because it might cause strokes or pump failure. Furthermore, right ventricular dysfunction brought on by an increased stress on the heart may complicate patient outcomes and necessitate further procedures.
Continuous innovations in VAD technology
Progress in technology has resulted in more robust and compact devices, enhancing the comfort and mobility of patients. Advances in biocompatibility have lowered risks of thrombosis and infections, which has lowered obstacles to patient adoption. VAD therapy is now more widely available to a larger range of patients thanks to the less invasive nature of miniaturization, which also makes recovery times quicker and implantation processes simpler.
Inadequate reimbursement policies and insurance coverage
VADs require implantation procedures as well as post-operative care, which can be costly. Patients may be discouraged from choosing VAD therapy if they have to pay large out-of-pocket costs due to inadequate insurance coverage. Insufficient access to care can lead to postponed or abandoned medical interventions, deteriorating health outcomes and increasing long-term healthcare expenses, ultimately decreasing market demand for VADs.
The COVID-19 pandemic negatively impacted the Ventricular Assist Devices (VAD) market by causing significant delays in elective surgeries and a reduction in device utilization. Lockdowns and travel restrictions led to fewer VAD transplants, as many patients postponed seeking treatment due to safety concerns. This resulted in decreased demand for VADs, affecting revenue for manufacturers and healthcare providers. However, as restrictions eased, a rebound in patient visits and procedures is anticipated, potentially revitalizing market growth in subsequent years.
The biventricular assist devices segment is expected to be the largest during the forecast period
The biventricular assist devices segment is expected to be the largest during the forecast period owing to increased demand and advancements in BiVAD technology, such as pneumatically driven systems that improve device performance and usefulness in total artificial heart (TAH) transplant scenarios. Better hemodynamic support, improved quality of life, increased survival rates, and more patient and physician acceptance are all achieved by BiVADs.
The bridge-to-transplant segment is expected to have the highest CAGR during the forecast period
The bridge-to-transplant segment is expected to have the highest CAGR during the forecast period owing to its vital function in keeping patients stable while they await heart transplants. VADs improve patient outcomes by providing necessary mechanical support for a period of two to six months. A greater understanding of the effectiveness of BTT therapy promotes its broader use in the treatment of heart failure.
North America is expected to have the largest market share over the projection period due to the growing rate of heart failure in North America combined with technological developments in medical devices has raised demand for valve assist devices (VADs) as destination and bridge-to-transplant therapies. Moreover VADs offer a vital substitute in the event that there are insufficient donor hearts available for transplantation, assisting patients in surviving either permanently or while they wait for a transplant.
Asia Pacific is anticipated to witness the highest rate of growth during the forecast period owing to increased investment in modern medical technology and healthcare infrastructure by China, India, Japan, and South Korea is contributing to the growing use of VADs. The need for sophisticated heart failure management solutions is being driven by rising awareness and enhanced diagnostic capabilities. The Asia Pacific VAD market is expanding as a result of technological developments that include the development of smaller, more effective devices with fewer issues.
Key players in the market
Some of the key players in Ventricular Assist Devices Market include Abiomed Inc., BiVACOR Inc, Abbott Laboratories, Berlin Heart GmbH, Calon Cardio, Medtronic PLC, SynCardia Systems LLC, Terumo Corporation, Jarvik Heart Inc., ReliantHeart, Inc. and Sun Medical Technology Research Corp .
In September 2024, Abbott announced the findings of a new survey among leading infectious disease experts around the world on the state of pandemic preparedness and found that while most agree that preparation has improved since the COVID-19 pandemic.
In September 2024, Abbott announced U.S. availability of Lingo(TM), the company's first continuous glucose monitoring system available without a prescription. Lingo is based on Abbott's world-leading FreeStyle Libre(R) continuous glucose monitoring technology1, now used by more than 6 million people with diabetes globally.
In September 2024, Medtronic plc announced at the North American Spine Society (NASS) 39th Annual Meeting in Chicago the commercial launch of several software, hardware, and imaging innovations.