市場調查報告書
商品編碼
1401950
到 2030 年神經刺激的市場預測:按類型、應用和地區分類的全球分析Neurostimulation Market Forecasts to 2030 - Global Analysis By Type, Application and By Geography |
根據 Stratistics MRC 的數據,2023 年全球神經刺激市場規模為 62.212 億美元,預計到 2030 年將達到 133.29 億美元,預測期內複合年成長率為 11.5%。
使用協調的電或磁脈衝來改變神經系統的活動稱為神經刺激。它用於治療多種神經病變,包括精神疾病、運動障礙和慢性疼痛。此外,神經刺激是一種可逆且可自訂的方式來調節神經迴路並減輕相關症狀,目前正在研究新的應用,並正在最佳化現有技術。
據美國疾病管制與預防美國(CDC) 稱,北美每年估計花費 500 億美元用於治療慢性下背痛。
非侵入性替代方案的增加
由於非侵入性神經刺激方法的發展以及提供非手術方法(例如經顱磁刺激(TMS)和經皮電神經刺激(TENS))的技術進步,這些方法正在獲得認可。該方法正在減少患者的被動性和擴大市場範圍。這項轉變不僅提高了患者的舒適度和安全性,而且還提供了高效、負擔得起的微創解決方案,使我們能夠在塑造神經刺激療法和市場的方向方面發揮關鍵作用。我們正在擴大規模。
高成本
開發、製造和行銷神經刺激設備是一個昂貴的過程,需要先進的技術、廣泛的研究和監管合規性。專用零件、尖端材料和複雜的製造技術都會導致成本高昂。這些高昂的成本給患者和醫療保健提供者在負擔能力和報銷方面帶來了挑戰。因此,高昂的自付費用和缺乏保險覆蓋可能會阻礙神經刺激市場的發展。
技術進步
技術創新推動了封閉回路型或自適應神經刺激系統的發展,電極技術、程式設計能力和設備設計不斷創新,提高了神經刺激治療的準確性、有效性和安全性。此外,無線通訊技術的整合可以更好地病患監測並即時調整神經刺激參數。改善患者治療效果和解決未滿足的醫療需求正在推動整個神經刺激治療市場的發展。
副作用
神經刺激並非對所有神經系統疾病都同樣有效,侵入性手術和植入設備固有的風險(例如感染、設備故障和意外副作用)可能會限制患者的安全、性能和可靠性。此外,不利事件可能會損害產品在市場上的聲譽,引發監管問題和法律問題,並阻礙其普及。結果,神經刺激市場受到阻礙。
COVID-19 的爆發對神經刺激市場產生了負面影響,擾亂了製造、供應鏈和選擇性醫療程序。對非必要醫療保健服務的限制、患者就診的減少以及醫療資源的轉移正在推遲神經刺激設備並減少患者的就診機會。經濟不確定性也影響投資和研究經費。因此,這些因素都大大阻礙了市場的拓展。
迷走神經刺激設備部分預計在預測期內將是最大的
迷走神經刺激設備部分估計佔最大佔有率。這些植入式設備透過刺激迷走神經來運作,迷走神經向大腦發送電脈衝。技術進步、設備小型化以及對神經生理學理解的加深是有助於提高意識的一些創新。對非藥物治療選擇的需求和神經系統疾病盛行率的增加正在促進 VNS 領域在神經刺激市場的擴張。
帕金森氏症領域預計在預測期內複合年成長率最高
由於使用植入設備來緩解症狀,預計帕金森氏症領域在預測期內的複合年成長率最高。治療帕金森氏症的神經刺激稱為深部腦部刺激 (DBS),涉及在特定大腦區域植入電極以糾正異常神經活動。 DBS 可改善患者的生活品質、減少藥物依賴性並減少運動症狀。因此,DBS也為神經刺激技術的發展和進步做出了重大貢獻,支持了該領域的擴展。
由於其醫療基礎設施、報銷政策和法律規範,亞太地區在預測期內佔據了最大的市場佔有率。人口高齡化以及隨之而來的神經退化性疾病的增加導致對神經刺激療法的需求不斷成長。該地區的主要企業包括波士頓科學公司、雅培實驗室、美敦力公司和 Neuronetics, Inc.。該地區的貸款和還款政策以及新技術正在推動市場規模的成長。
預計歐洲在預測期內的複合年成長率最高。監管機構和國家衛生當局在核准和監管神經刺激設備方面發揮重要作用。治療效果和患者結果的進步包括增強的電極設計、精確定位和先進的程式功能。德國、英國和法國等歐洲國家也為引進神經病變的最尖端科技做出了重大貢獻,並正在推動該地區的成長。
According to Stratistics MRC, the Global Neurostimulation Market is accounted for $6,221.2 million in 2023 and is expected to reach $13,329.0 million by 2030 growing at a CAGR of 11.5% during the forecast period. The use of regulated electrical or magnetic impulses to alter the nervous system's activity is known as neurostimulation. It is used to treat various neurological disorders such as psychiatric disorders, movement disorders, and chronic pain. Furthermore, neurostimulation is a potentially reversible and customizable method of modulating neural circuitry and relieving symptoms associated, with ongoing research exploring new applications and optimizing existing technologies.
According to Centers for Disease Control and Prevention (CDC), an estimated USD 50 billion are spent each year for treatment of chronic lower back pain in North America.
Increase in non-invasive alternatives
The development of non-invasive neurostimulation methods and their increasing acceptance as a result of technological advancements like transcranial magnetic stimulation (TMS) and transcutaneous electrical nerve stimulation (TENS) which offer non-surgical approaches, reducing patient reluctance and expanding the market reach. This shift not only improve patient comfort and safety but also provide efficient, affordable, and minimally invasive solutions which place them in a position to play a significant role in influencing the direction of neurostimulation therapy, which are driving the market size.
High cost
Neurostimulation device development, manufacture, and distribution are expensive processes that require sophisticated technology, a great deal of research, and adherence to regulations. Specialized parts, cutting-edge materials, and complex manufacturing techniques all contribute to the higher expenses. In terms of affordability and reimbursement, these exorbitant cost present difficulties for patients and healthcare providers. Therefore, high out-of-pocket costs and a lack of insurance coverage may impede neurostimulation market.
Technological advancements
Technological innovations have facilitated the development of closed-loop or adaptive neurostimulation systems with constant innovations including electrode technologies, programming capabilities, and device design which improves the accuracy, effectiveness, and safety of neurostimulation treatments. In addition, integration of wireless communication technologies enables better patient monitoring and real-time adjustments to neurostimulation parameters. By improving patient outcomes and addressing unmet medical needs overall propels the neurostimulation market.
Side effects
Neurostimulation may not be equally effective for all neurological conditions which effects patient safety and confidence by the inherent risks associated with invasive procedures and implantable devices, which include infection, malfunctioning of the device, and unintended side effects. Moreover, adverse events can damage a product's reputation in the market and prevent its widespread adoption by giving rise to regulatory worries and legal issues. Thus, consequently hinder the neurostimulation market.
The COVID-19 pandemic has negatively impacted the neurostimulation market, causing disruptions in manufacturing, supply chains, and elective medical procedures. Restrictions on non-essential healthcare services, reduced patient visits, and diverted healthcare resources have led to delays in neurostimulation device implantations and decreased patient access. Economic uncertainties have also affected investment and research funding. Therefore, these factors significantly impede market expansion.
The vagus nerve stimulators segment is expected to be the largest during the forecast period
The vagus nerve stimulators segment is estimated to hold the largest share. These implantable devices stimulate the vagus nerve, which operates by sending electrical impulses to the brain. Technological advancements, miniaturization of devices, and improved understanding of neurophysiology are some of the innovations contributing awareness. The demand for non-pharmacological treatment options and the increasing prevalence of neurological disorders contribute to the expansion of the VNS segment in the Neurostimulation market.
The parkinson's disease segment is expected to have the highest CAGR during the forecast period
The parkinson's disease segment is anticipated to have the highest CAGR during the forecast period due to reducing symptoms by using implantable devices. Neurostimulation for Parkinson's disease is called deep brain stimulation (DBS), which involves implanting electrodes in particular brain areas to modify aberrant neural activity. The patients' quality of life is improved, medication dependence is decreased, and motor symptoms are reduced with DBS. Hence, it also makes a substantial contribution to the development and advancement of neurostimulation technologies which are propelling this segment expansion.
Asia Pacific commanded the largest market share during the extrapolated period owing to evaluations of the healthcare infrastructure, reimbursement policies, and regulatory frameworks. The aging population and the subsequent increase in neurodegenerative diseases contribute to the expanding demand for neurostimulation therapies. The region is home to major key players such as Boston Scientific Corporation, Abbott Laboratories, Medtronic plc and Neuronetics, Inc. The region's financing and reimbursement policies and new technologies is driving the market size.
Europe is expected to witness highest CAGR over the projection period. Regulatory bodies and national health authorities play a crucial role in approving and regulating neurostimulation devices. Advancements in treatment efficacy and patient outcomes include enhanced electrode designs, precise targeting, and advanced programming capabilities. Countries within Europe, including Germany, the United Kingdom, France, and others, also contribute significantly to the adoption of cutting-edge technologies for neurological disorders which thereby driving region growth.
Some of the key players in the Neurostimulation Market include Medtronic, LivaNa PLC, Abbott, Neuronetics, Boston Scientific Corporation, Nevro Corp, Laborie, Johnson & Johnson Services, NeuroPace, Inc., Synapse Biomedical Inc, NeuroSigma, Inc, Modulus, Inc and Biegler GmbH.
In October 2023, Boston Scientific Corporation announced that the U.S. Food and Drug Administration (FDA) has approved an expanded indication of the WaveWriter Alpha™ Spinal Cord Stimulator (SCS) Systems for the treatment of painful diabetic peripheral neuropathy (DPN), a complication of diabetes that can affect the lower extremities of the body.
In September 2023, Abbott announced it has completed the acquisition of Bigfoot Biomedical, a leader in developing smart insulin management systems for people with diabetes.
In August 2023, Medtronic announced the outcome of the U.S. Food & Drug Administration (FDA) Circulatory System Devices Panel (CSDP) meeting to review data presented in support of the Medtronic Symplicity Spyral™ Renal Denervation (RDN) System.
In June 2023, the American Diabetes Association® (ADA) and Abbott announced a collaboration aimed at better understanding how diabetes technology like continuous glucose monitoring (CGM) systems can help people living with diabetes make informed decisions about their food and activity.