市場調查報告書
商品編碼
1446969
到 2030 年高壓顯影劑注射器的全球市場預測:按產品類型、應用、最終用戶和地區進行分析High Pressure Contrast Media Injector Market Forecasts to 2030 - Global Analysis By Product (Injector Systems and Consumables), Type (Single Head Injectors, Syringeless Injectors and Dual Head Injectors), Application, End User and By Geography |
據Stratistics MRC稱,2023年全球高壓顯影劑注射器市場規模將達到1.776億美元,預計到2030年將達到4.472億美元,預測期內年複合成長率為14.1%。
高壓顯影劑是用於放射學和成像程序的醫療設備,特別是電腦斷層掃描 (CT) 掃描和血管造影術。該裝置通常由含有顯影劑的注射器或儲液器、高壓注射器系統和電腦控制面板組成。這些注射器以受控的速率和壓力輸送顯影劑,確保在整個脈管系統中一致且均勻的分佈。其結果是提高了血管、器官和組織的可見度,從而產生更清晰、更詳細的影像。
根據世界衛生組織(WHO)的估計,癌症是世界上大多數國家的主要原因之一。
微創手術需求不斷成長
微創手術技術因其與傳統開放性手術相比的潛在優勢而越來越受歡迎。隨著微創手術在各個醫療領域變得普及普遍,在這些手術過程中對高品質影像導引的需求變得至關重要。此外,高壓顯影劑輸液設備在血管內治療、介入放射學和腹腔鏡手術等微創手術中的血管、器官和組織的即時可視化中發揮重要作用。
不利事件的風險
高壓顯影劑注射器是一種將顯影劑直接注入患者血液的醫療設備。因此,存在與顯影劑給藥相關的不利事件的風險,例如過敏反應、血管外浸潤和過敏反應。此外,顯影劑腎臟病是一種潛在的併發症,其特徵是顯影劑暴露後的急性腎損傷,尤其是有腎功能不全病史的患者。不利事件的發生可能會導致患者受傷、醫療成本增加以及醫療保健提供者和設施的責任風險。這些因素限制了市場的擴張。
成像技術的進步
隨著成像技術的發展並變得更加複雜,對造影增強成像程序以提供詳細且準確的診斷資訊的需求日益增加。高壓顯影劑注射器是造影劑增強成像程序的重要組成部分,因為它們可以以精確且受控的方式可靠地將顯影劑顯影劑輸送到患者的血流中。此外,以高壓和受控速率注射顯影劑顯影劑最佳化其在整個脈管系統中的分佈,從而可以清晰地顯示解剖結構和異常情況。因此,影像處理技術的進步已成為市場擴張的主要因素。
與替代顯像模式的衝突
超音波、磁振造影(MRI) 和光同調斷層掃瞄(OCT) 等方式可提供詳細的解剖和功能資訊,而無需注射造影顯影劑。這些替代成像方式比顯影劑增強成像方式具有優勢,包括降低副作用風險和避免電離輻射暴露。因此,醫療保健提供者可能會擴大選擇替代成像方式而不是顯影劑注射技術,從而可能減少對高壓顯影劑注射器的需求。
COVID-19 的影響
COVID-19 大流行對高壓顯影劑劑注射器市場產生了負面影響。世界各地的醫療保健系統因 COVID-19 患者的湧入而不堪重負,導致包括診斷成像在內的非緊急醫療程序被推遲或取消,並且對顯影劑的需求減少。此外,許多醫院和診斷影像中心也面臨人員短缺、供應鏈中斷和財務限制等營運挑戰。
預計消耗品領域在預測期內將是最大的
消耗品部分估計佔最大佔有率。耗材在支援顯影劑注射系統的操作和功能方面發揮關鍵作用。注射器是一種重要的消耗品,用於容納顯影劑並將其輸送到注射系統。此外,它們具有多種尺寸和配置,以適應不同的注射量和流速。因此,對耗材的需求是一致的,並且與臨床中高壓顯影劑的使用密切相關。
預計單頭注射器細分市場在預測期內年複合成長率最高
預計單頭注射器細分市場在預測期內將出現良好的成長。這些注射器旨在透過單一注射頭或注射器以受控的速率和壓力將顯影劑輸送到患者的血流中。此外,這些注射器簡單易用,適合醫療保健環境中的常規影像處理。這些注射器旨在以最小的變化提供精確數量的顯影劑,確保影像檢查中一致的影像品質和診斷準確性。
憑藉先進的醫療基礎設施、技術創新和診斷成像的高需求,北美在預測期內佔據了最大的市場佔有率。該地區包括美國、加拿大和墨西哥,擁有大量醫療支出,並專注於醫療進步和患者護理。此外,北美的技術進步和研發工作正在促進高壓顯影劑技術的持續發展。
預計歐洲在預測期內將出現盈利成長。歐洲醫療保健基礎設施的特點是擁有完善的醫院、診斷影像中心和學術機構,提供最先進的診斷影像程序。此外,該地區也是幾家主要醫療設備製造商的所在地,其中包括高壓顯影劑注射器。這些公司利用該地區強大的研發能力、監管專業知識和品質標準來開發創新注射器技術,以滿足醫療保健專業人員和患者的需求。
According to Stratistics MRC, the Global High Pressure Contrast Media Injector Market is accounted for $177.6 million in 2023 and is expected to reach $447.2 million by 2030 growing at a CAGR of 14.1% during the forecast period. A high-pressure contrast media injector is a medical device used in radiology and diagnostic imaging procedures, particularly computed tomography (CT) scans and angiography. The device typically consists of a syringe or reservoir containing the contrast media, a high-pressure injector system, and a computerized control panel. These injectors deliver contrast media at a controlled rate and pressure, ensuring consistent and uniform distribution throughout the vascular system. This results in improved visualization of blood vessels, organs, and tissues, leading to clearer and more detailed images.
According to the World Health Organization (WHO) estimates, cancer is the one of the leading causes of death in majority of countries globally.
Rising demand for minimally invasive surgeries
Minimally invasive surgical techniques have gained popularity due to their potential benefits compared to traditional open surgeries. As minimally invasive procedures become more widespread across various medical specialties, the need for high-quality imaging guidance during these procedures becomes paramount. Additionally, high-pressure contrast media injectors play a crucial role in providing real-time visualization of blood vessels, organs, and tissues during minimally invasive surgeries, such as endovascular procedures, interventional radiology, and laparoscopic surgeries.
Risk of adverse events
High-pressure contrast media injectors are medical devices that administer contrast agents directly into the patient's bloodstream. As such, there is a risk of adverse events associated with contrast administration, such as allergic reactions, extravasation, and anaphylaxis. Furthermore, contrast-induced nephropathy is a potential complication characterized by acute kidney injury following contrast media exposure, particularly in patients with pre-existing renal impairment. The occurrence of adverse events can result in patient harm, increased healthcare costs, and liability risks for healthcare providers and facilities. These factors limit the market's expansion.
Advancements in imaging technologies
As imaging technologies evolve and become more sophisticated, there is a growing need for contrast-enhanced imaging procedures to provide detailed and accurate diagnostic information. High-pressure contrast media injectors are essential components in contrast-enhanced imaging procedures, as they ensure the precise and controlled delivery of contrast agents into the patient's bloodstream. Moreover, by delivering contrast media at high pressures and controlled rates, these injectors optimize the distribution of contrast agents throughout the vascular system, enabling clearer visualization of anatomical structures and abnormalities. As a result, advancements in imaging technologies are a significant factor propelling market expansion.
Competition from alternative imaging modalities
Modalities such as ultrasound, magnetic resonance imaging (MRI), and optical coherence tomography (OCT) provide detailed anatomical and functional information without the need for Injectable contrast media. These alternative imaging modalities offer advantages over contrast-enhanced imaging techniques, including reduced risk of adverse reactions and avoidance of ionizing radiation exposure. As a result, healthcare providers may increasingly opt for alternative imaging modalities over contrast-enhanced techniques, leading to a decline in demand for high-pressure contrast media injectors.
Covid-19 Impact
The COVID-19 pandemic had negatively impacted the high-pressure contrast media injector market. With healthcare systems worldwide overwhelmed by the influx of COVID-19 patients, non-urgent medical procedures, including diagnostic imaging, have been postponed or cancelled, leading to a decline in demand for contrast media injectors. Moreover, many hospitals and imaging centers faced operational challenges, such as staffing shortages, supply chain disruptions, and financial constraints.
The consumables segment is expected to be the largest during the forecast period
The consumables segment is estimated to hold the largest share. Consumables play a crucial role in supporting the operation and functionality of contrast media injection systems. Syringes are essential consumables that hold and deliver the contrast media to the injector system. Moreover, they come in various sizes and configurations to accommodate different injection volumes and flow rates. As a result, demand for consumables remains consistent and is closely related to the use of high-pressure contrast media injectors in clinical practice.
The single head injectors segment is expected to have the highest CAGR during the forecast period
The single head injectors segment is anticipated to have lucrative growth during the forecast period. These injectors are designed to deliver contrast media into the patient's bloodstream at a controlled rate and pressure through a single injection head or syringe. Furthermore, these injectors offer simplicity and ease of use, making them suitable for routine imaging procedures in healthcare settings. They are engineered to deliver precise volumes of contrast media with minimal variability, ensuring consistent image quality and diagnostic accuracy across imaging studies.
North America commanded the largest market share during the extrapolated period due to its advanced healthcare infrastructure, technological innovation, and high demand for diagnostic imaging procedures. The region encompasses the United States, Canada, and Mexico, where healthcare expenditure is substantial and there is a strong emphasis on medical advancements and patient care. Moreover, technological advancements and research and development initiatives in North America contribute to the continuous evolution of high-pressure contrast media injector technologies.
Europe is expected to witness profitable growth over the projection period. Europe's healthcare infrastructure is characterized by well-established hospitals, imaging centers, and academic institutions, providing access to state-of-the-art diagnostic imaging procedures. Furthermore, the region is home to several leading manufacturers of medical devices, including high-pressure contrast media injectors. These companies leverage the region's strong research and development capabilities, regulatory expertise, and quality standards to develop innovative injector technologies that meet the needs of healthcare providers and patients.
Key players in the market
Some of the key players in the High Pressure Contrast Media Injector Market include Guerbet Group, Bayers Healthcare LLC, Bracco Group, Ulrich GmbH & Co. KG, Medtron AG, GE Healthcare, NemotoKyorindo Co. Ltd, Apollo RT Co. Ltd, Vivid Imaging and Sino Medical Device Technology Co.
In September 2023, GE HealthCare and Mayo Clinic announced a strategic healthcare collaboration for research and product development programs aimed to transform the experience of patients and clinicians in the practice of radiology and the delivery of novel therapies.
In December 2022, Bayer announced the U.S. launch of the Bayer Science Collaboration Explorer (BSCE) as part of its ongoing efforts to enhance public trust in scientific innovations, processes, and R&D activities.
In November 2022, GE Healthcare announced agreement with ulrich medical aimed at enhancing its market position in the growing U.S. market. As per the agreement, these two companies will co-ordinate to develop and offer multi-dose contrast media injector in the country.
In March 2022, Bracco Imaging and Philochem, a subsidiary of the Philogen Group collaborated on the development of a molecule for diagnostic applications
In December 2021, Bracco Imaging announced a global strategic collaboration agreement with Guerbet for Gadopiclenol, a high-relaxivity, macrocyclic contrast agent. Bracco Imaging and Guerbet will manufacture, as well as support research and development for future indications of Gadopiclenol, which the parties will commercialize independently under different brands.