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疝气修復设备的全球市场-2022-2029Global Hernia Repair Devices Market - 2022-2029 |
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对疝气修復设备开发的资金和投资不断增加,预计将推动市场增长。
一些公司已经筹集或投资于疝气修復设备的开发。例如,2020年1月,Virtual Incision Corporation宣布获得2000万美元的B+轮融资,由投资者Bluestem Capital领投,回归投资者PrairieGold Venture Partners和Genesis Innovation Group等相关投资者参投。这笔资金将用于各种应用,包括疝修补术、胆囊切除术、抗反流手术、脾切除术、肾上腺切除术、胃袖、胃旁路术、子宫切除术和肝胰胆管手术 (MIRA)。)将用于支持导致手术机器人平台商业化的监管和临床计划。因此,从上述陈述来看,预计将在预测期内推动市场。
与使用疝气修復设备相关的副作用预计会阻碍市场增长。
市场受到与使用疝气修復设备相关的副作用的阻碍。在接受疝气修復装置治疗的患者中观察到一些副作用,包括疼痛、感染、復发、粘连、肠梗阻和器官穿孔。据英国外科杂誌报导,疝气网状涂层减少了一周的粘连。 1 个月后,疝网涂层未观察到粘连预防。此外,网状物穿过身体,导致肠梗阻。根据美国食品和药物管理局 (FDA) 的说法,再生网片是患者肠道前庭形成和梗阻的主要原因。还观察到慢性感染,例如炎症、发烧和其他类似流感的症状。根据美国食品和药物管理局 (FDA) 的说法,Ethicon Physiomesh 植入物在患者之间发生了分层和迁移。这种植入物附着在患者的肠道和皮肤上。这种植入物迁移导致过度疼痛和严重损伤。
全球疝气修復设备市场受到 COVID-19 大流行的影响。随着感染 COVID-19 的患者数量增加,接受疝修补手术的患者数量正在下降。 COVID-19 可能对角膜手术的性能构成严重威胁。在全球范围内,由于接受疝气修復手术的人数减少,由于 COVID-19 流行,对疝气修復设备的需求有所下降。根据 F. Kockerling 等人 2020 年的数据,在 COVID-19 中断的 12 周高峰期间,约有 2800 万例择期手术被取消。根据疝气登记处的数据,由于 COVID-19 流行,腹股沟疝修补术已从 2020 年 2 月的 6,699 例减少到 2020 年 6 月的 3,033 例。脐疝修復从 2020 年 2 月的 1,692 例减少到 2020 年 6 月的 1,421 例。
行业分析
疝气修復设备市场根据各种行业因素(包括未满足的需求、定价分析、供应链分析和监管分析)对市场进行了深入分析。
全球疝气修復设备市场报告提供大约 45 多个市场数据表、40 多个数字和 180 页的组成。
Hernia Repair Devices Market size was valued US$ YY million in 2021 and is estimated to reach US$ YY million by 2029, growing at a CAGR of 5.65% during the forecast period (2022-2029).
Hernia is the condition in which the internal organ or fatty tissue surges out through the fascia, a weak spot present in a surrounding muscle or connective tissue. A hernia occurs most frequently within the abdominal cavity, between the chest and the hips. Inguinal hernia, femoral hernia, umbilical hernia, hiatal hernia, and others are the most prevalent hernia observed across the globe. A hernia is characterized by the signs and symptoms such as swelling in the groin or scrotum, pain at the site of the bulge, pain while lifting, increased bulge size over time, aching sensation, and bowel obstruction.
Hernia repair devices are the devices that are used for performing the surgical procedure for the correction of hernia. Hernia repair devices are used for performing laparoscopic and open repair surgery. The market is dominated by the availability of hernia mesh, including synthetic mesh & biologic mesh, and mesh fixators, including the sutures, tack applicators, and glue applicators.
Increasing funding & investment for the development of the Hernia Repair Devices is expected to drive market growth.
Several companies are raising the funding and investment for developing the Hernia Repair Devices. For instance, in January 2020, Virtual Incision Corporation raised USD 20 million in a Series B+ financing round led by the investor Bluestem Capital, with participation from returning investor PrairieGold Venture Partners and Genesis Innovation Group and other affiliated investors. This funding would be used to support the regulatory and clinical programs leading to the commercialization of the miniaturized in vivo robotic assistant (MIRA) Surgical Robotic Platform for various applications such as hernia repair, gallbladder removal, anti-reflux surgery, splenectomy, adrenalectomy, gastric sleeve, gastric bypass, hysterectomy, and hepato-pancreato-biliary procedures. Thus, from the above statements, the market is expected to drive in the forecast period.
Adverse Effects Associated with using Hernia Repair Devices are expected to hamper the market growth.
The market is hindered by the adverse effects associated with the use of hernia repair devices. Several adverse effects were observed among patients treated with hernia repair devices, such as pain, infection, recurrence, adhesion, bowel obstruction, organ perforation, and other adverse effects. According to the British Journal of Surgery, the hernia mesh's coating has reduced the adhesion for a week. There was no adhesion prevention through the hernia mesh coating after a month. Mesh also leads to bowel obstruction as it can migrate in the body. According to the Food and Drug Administration (FDA), the recalled mesh is the leading cause of bowel preformation and obstruction among patients. Chronic infections such as inflammation, fever, and other flu-like symptoms are observed among the patients. According to the Food and Drug Administration (FDA), the Ethicon physiomesh implant was detached and migrated among the patients. This implant was attached to the patient's intestine and the skin. Migration of the implant resulted in excess pain and severe damage.
The global hernia repair devices market has been impacted due to the COVID-19 pandemic as there is decreased number of the patients undergoing the hernia repair surgeries with the increasing number of people suffering from the COVID-19. The COVID-19 can be a serious threat for carrying out the corneal surgery. Globally, the demand of the hernia repair devices has reduced due to COVID-19 pandemic with the decrease in the number of the people undergoing the hernia repair surgery. According to the F. Kockerling et.al. 2020, approximately, 28 million elective operations were cancelled during the peak 12 weeks of disruption occurred due to COVID-19. According to the hernia registry, the number of inguinal hernia repair surgery had witnessed the decreased from the 6,699 surgeries in February 2020 to 3033 in June 2020 due to COVID-19 pandemic. The number of the umbilical hernia repair surgeries has decreased from 1, 692 in February 2020 to 1,421 in June 2020.
Industry Analysis
The hernia repair devices market provides in-depth analysis of the market based on various industry factors such as unmet needs, pricing analysis, supply chain analysis, regulatory analysis etc.
The hernia mesh segment is expected to hold the largest share in the hernia repair devices market.
The hernia mesh segment accounted for holding the largest share in the hernia repair devices market due to the rising penetration of the hernia mesh. As per Sanders DL et al., yearly, around 20 million prosthetic meshes are implanted among patients with hernias worldwide. Every year nine out of ten hernia surgeries are performed using the hernia mesh in the United States. Hernia mesh supports the damaged tissue around hernias. It can be easily placed around the hernia by attaching it with stitches, staples, or glue. Hernia mesh comprises synthetic materials that can be absorbable, non-absorbable or a combination of both materials found in knitted mesh or non-knitted sheet forms. Hernia mesh is effective in lowering the recurrence of the hernias. The market is dominated by the availability of several hernia mesh products. For instance, Atrium comprises the several hernia mesh product portfolio such as C-QUR, Vitamesh, Proloop, Prolite, and Prolite UltraQ; B. Braun comprises the several hernia mesh portfolio such as Premilene, Omyra, Optilene; LifeCell Corporation comprises the hernia mesh product portfolio such as Alloderm Select, Strattice; and Medtronic comprised of the hernia mesh product portfolio such as Parietex, Permacol, ProGrip, Symbotex, Versatex.
North American region is expected to hold the largest market share in the global hernia repair devices market.
North America dominated the global hernia repair devices market. It accounted for the largest market share in 2021, owing to the increasing adoption of hernia repair devices for performing hernia repair surgeries. According to Raquel Maia et al. 2021, published in Annals of Laparoscopic and Endoscopic Surgery, around 350,000 abdominal wall hernia repair surgeries were performed in a year. There is a high recurrence rate of hernias. The United States accounts for the highest market share due to the availability of favorable reimbursement policies for hernia repair surgeries. There is the presence of several market players developing advanced hernia repair devices. For instance, Ariste Medical gained 510(k) authorization from the US Food and Drug Administration in April 2022 to market their drug-embedded, synthetic hernia mesh in the US.
Major key players in the hernia repair devices market are Medtronic Plc, Ethicon Inc., Atrium, Lifecell Corporation, B Braun Melsungen AG, Baxter International, Inc., Cook Medical, Becton, Dickinson and Company, CooperSurgical Inc., Insightra Medical, Inc., Olympus Corporation, and Integra Lifesciences.
Medtronic plc is an American-Irish registered medical device company primarily operating in the United States. It has an operational and executive headquarters in Fridley, Minnesota, in the US. Moreover, it develops and manufactures devices and therapies to treat more than 30 chronic diseases, including heart failure, Parkinson's disease, urinary incontinence, Down syndrome, obesity, chronic pain, spinal disorders and diabetes. It is operated in 140 countries and employs over 104,950 people.
The global hernia repair devices market report would provide an access to an approx. 45+market data table, 40+figures and 180pages.