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市場調査レポート
商品コード
1576971
ペースメーカーの世界市場の評価:移植可能性別、技術別、タイプ別、適応症別、エンドユーザー別、地域別、機会、予測(2017年~2031年)Pacemakers Market Assessment, By Implantability, By Technology, By Type, By Indication, By End-user, By Region, Opportunities and Forecast, 2017-2031F |
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ペースメーカーの世界市場の評価:移植可能性別、技術別、タイプ別、適応症別、エンドユーザー別、地域別、機会、予測(2017年~2031年) |
出版日: 2024年10月25日
発行: Markets & Data
ページ情報: 英文 229 Pages
納期: 3~5営業日
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世界のペースメーカーの市場規模は、2023年の50億6,000万米ドルから2031年に69億5,000万米ドルに達すると予測され、予測期間の2024年~2031年にCAGRで4.05%の成長が見込まれます。市場は、心血管疾患(CVD)の増加、新薬の市場参入、革新的な製品に対する規制当局の承認によって牽引されています。市場の大部分は上位5社によって独占されていますが、市場の成長率はより高くなると予測されます。
ペースメーカーは、不整脈患者の心臓リズムを円滑にするために心臓に留置される医療機器です。ペースメーカーの需要は大幅に増加しており、CVDの負担が増加していることから、今後さらに拡大すると予測されています。設計の最適化を通じて患者のコンプライアンスを向上させ、このようなデバイスのサイズを小さくすることを目的とした技術の進歩は、市場の成長率をさらに高めます。しかし、複数の促進要因が存在するにもかかわらず、市場は、このようなインプラントを使用する患者が直面している電池寿命の問題や、デバイスとそれを埋め込む手術に関連する高いコストのような課題に直面しています。さらに、頻繁な規制当局の承認と戦略的な製品投入が市場の活性化を維持し、さらなる拡大に寄与しています。2023年7月、BIOTRONIK SE & Co KGは、ペースメーカーAmvia Edgeと心臓再同期療法ペースメーカー(CRT-P)のポートフォリオがUSFDAの承認を取得したことを発表しました。Amvia Edgeは、市場最小のシングルチャンバーMRコンディショナルペースメーカーで、自動化されたワークフローの効率とともに、患者中心のユニークな臨床ソリューションを導入しています。
当レポートでは、世界のペースメーカー市場について調査分析し、市場規模と予測、市場力学、主要企業の情勢などを提供しています。
Global pacemaker market is projected to witness a CAGR of 4.05% during the forecast period 2024-2031, growing from USD 5.06 billion in 2023 to USD 6.95 billion in 2031. The market for cardiac pacemakers is driven by growing cardiovascular diseases (CVD), novel drug entry into the market, and regulatory approvals for innovative products. The growth of this market is expected to be at a higher rate while the major market is served by the top 5 market players.
Pacemakers are the medical devices placed in the human heart to facilitate the cardiac rhythm in arrhythmic patients. The demand for pacemakers is rising significantly and with the growing CVD burden, it is anticipated to grow further in the future. Technological advances aim to improve patient compliance through design optimization and reducing the size of such devices further enhance the growth rate of the market. However, despite the presence of several driving forces, the market faces challenges like the high cost associated with the device and the procedure to implant it, along with the battery life issue being faced by patients with such implants. Furthermore, frequent regulatory approvals and strategic product launches keep the market active and help with further expansion. In July 2023, BIOTRONIK SE & Co KG announced the receipt of USFDA approval for its portfolio of Amvia Edge pacemakers and cardiac resynchronization therapy pacemakers (CRT-P), which highlights BIOTRONIK's latest innovation in cardiac rhythm management. Amvia Edge is the smallest single-chamber MR conditional pacemaker in the market and introduces a unique set of patient-centric clinical solutions coupled with automated workflow efficiency.
Growing Prevalence of CVD Boosts the Demand for Pacemakers
Demand for pacemakers is increasing due to the high prevalence of CVD. One very important cause for this increasing incidence is the aging population, characterized primarily by a sedentary lifestyle and poor diet. With new technology applied, the development of the pacemaker has heightened, and it is more appealing to patients as well as healthcare providers. As the awareness of CVD and its risks grows across the world, with better healthcare access, the market of pacemakers will continue to grow. It reflects the pressing need for innovative solutions in cardiovascular care with a focus on improvement in patient outcomes and quality of life. For instance, according to an article published in the European Heart Journal in November 2023, from 2010 to 2021, almost 114 thousand pacemakers were implanted. The corresponding statistics for single-chamber, double-chamber, and biventricular types make up 27.9%, 67.4%, and 4.6%, respectively. More men get a pacemaker implanted in them than women-more men get a pacemaker, as the distributions show (56.9% of men vs 43.1% were women). This trend is increasing every year. While 55.3% of the men were registered in 2010, in 2021, it will be 57.8%. The average age at the time of first pacemaker implantation is 76 years (75 years for men, 77 years for women). The average age at primary implantation increased by 1 year from 2010 to 2021 from 75.3 years to 76.3 years.
Emphasis on Reducing Size of Pacemakers Drives the Market
One major problem with pacemakers is their design and size, along with the set of mandatory precautions they come with. To overcome such challenges, several market players and researchers have come up with novel designs and initiatives to reduce its size to enhance patient compliance. Miniaturization decreases the level of discomfort patients experience since it will reduce the invasiveness and even the time taken to recover after implantation. Devices of even smaller sizes would improve aesthetic acceptance because they can be hardly observable under the skin. Technological advancement offers a provision for extra functionalities in compact configurations like remote monitoring and efficiency in battery use. Therefore, with this aspect of consideration, demand for small pacemakers would rise. For instance, in January 2024, Medtronic plc announced the receipt of the CE (Conformite Europeenne) Mark for its Micra AV2 and Micra VR2 pacemakers. These are the next generation of Medtronic's industry-leading miniature, leadless pacemakers. The Micra AV2 and Micra VR2 are the world's smallest pacemakers. They offer longer battery life and easier programming compared to previous Micra pacemakers, while still providing the many benefits of leadless pacing, such as reduced complications compared to traditional pacemakers. With approximately 40% more battery life compared to previous generations, Medtronic estimates that the battery life of the Micra AV2 and Micra VR2 is nearly 16 and 17 years, respectively.
Dominance of Arrhythmia Indication in Pacemaker Market
The Arrhythmia indication segment is anticipated to dominate the pacemaker market owing to the high prevalence of arrhythmia worldwide coupled with the high efficacy of pacemakers to correct the heart rhythm. These conditions are increasingly common due to factors like aging populations, sedentary lifestyles, and rising rates of chronic diseases. Pacemakers play a crucial role in managing these arrhythmias by ensuring the heart maintains a regular rhythm, which is essential for effective blood circulation. For instance, an article published in The Lancet Journal in February 2024 reported that Atrial fibrillation (AF) is the most common cardiac arrhythmia, with approximately 1.5-2% prevalence among adults in Europe, with expected further increase to 9.5% in individuals above 65 years by 2060. AF is also a significant threat since it is one of the major causes of stroke, dementia, heart failure, and premature death, which is all relevant to the growing elderly population, as well as healthcare systems.
North America Dominates the Pacemaker Market
North America is anticipated to be the leading region with the highest market share in the pacemaker market. The high incidence of cardiovascular diseases in the region leads to more demand for cardiac devices. Moreover, the prevalence of heart rhythm disorders among an aging population, along with escalating rates of obesity and sedentary lifestyles, is also the major cause. With advanced health infrastructure and high expenditure on healthcare, it is easier for patients in the United States and Canada to access advanced medical technology, such as pacemakers. Proper support from regulatory mechanisms and a strong network of care providers promote access to the necessary medical assistance as soon as possible for patients. Furthermore, the increased awareness among the public about the importance of heart care and preventive measures strengthens the growth of the pacemaker market in North America. For instance, according to The University of Texas Southwestern Medical Center, approximately 3 million people in the United States live with a pacemaker, which is a battery-powered device implanted in the chest to help maintain the proper heartbeat rate. Every year, around 200,000 of these devices are implanted in the United States for patients who have bradycardia or abnormal heart rhythms.
Future Market Scenario (2024- 2031F)
Leadless pacemakers are the latest inventions that are revolutionizing the pacemaker market, creating futuristic developments through a few key innovations. The burden of traditional leads that connect the device to the heart has been abolished in leadless pacemakers, thereby giving way to some greatly valued benefits, including reduced risk of complications and improved patient comfort. It also simplifies the implantation procedure, hence having a potential and faster recovery time with lower chances of infection. In addition, leadless technology opens the possibilities for more advanced functionalities like remote monitoring as well as advanced diagnostics, through which healthcare providers can treat their patients better. For instance, in July 2024, Abbott announced that the USFDA approved its AVEIR dual chamber (DR) leadless pacemaker system, which is the world's first dual chamber leadless pacing system that can be used to treat patients with arrhythmia. The approval significantly increases access to leadless pacing for millions of people across the United States, as more than 80% of those in need of a pacemaker require pacing in both the right atrium and right ventricle of the heart.
Key Players Landscape and Outlook
The pacemaker market is quite consolidated with a very limited number of market players and a major market being sabotaged by Medtronic plc. The market players in this segment are consistently innovating technology to create more advanced pacemakers to improve patient compliance. The market has seen regulatory approvals and some deals for market growth, however, the most notable acquisition dates back to the year 2017, when Abbott Laboratories acquired St. Jude Medical to enhance its market share in the pacemaker market.
In June 2024, Boston Scientific Corporation, a leading manufacturer of pacemakers, announced a definitive agreement to acquire Silk Road Medical, Inc., a medical device company that has developed an innovative platform of products to prevent stroke in patients with carotid artery disease through a minimally invasive procedure called transcarotid artery revascularization (TCAR). The acquisition is worth approximately USD 1.16 billion.
All segments will be provided for all regions and countries covered
Companies mentioned above DO NOT hold any order as per market share and can be changed as per information available during research work.