Friday, 30 July 2021

Medical Air Sterilizer Market Size Share Trends Forecast Opportunity 2026

 

Medical Air Sterilizer Market, by Product Type (High Temperature Sterilizer, Low Temperature Sterilizer, Radiation Sterilizer, and Others), by Modality (Portable Air Sterilizers and Stand Alone Air Sterilizers), by End User (Hospitals, Research and Academic Institutes, Pharmaceutical and Biotechnology Industries, Ambulatory Surgical Centers, and Others), and by Geography (North America, Europe, Asia Pacific, Latin America, Middle East, and Africa) - Size, share, Outlook, and Opportunity Analysis 2018 – 2026

Medical air refers to a clean supply of compressed air in hospitals and healthcare facilities. Sterilized medical air plays a vital role in preventing Hospital Acquired Infections (HAIs). Moreover, lack of medical air sterilization makes patients susceptible to various diseases such as pneumonia, and flu. For instance, according to a report by Centers for Disease Control and Prevention (CDC), January 2018, around 1 in every 25 patients in a hospital on a given day acquires at least one HAI in the U.S. Therefore, high prevalence of HAI is a major factor propelling demand for medical air sterilizers. 

Medical Air Sterilizer Market – Driver

Growing awareness about HAIs is expected to boost growth of the medical air sterilizer market. For instance, according to National Centre for Disease Control 2017, in India, policies are guidelines such as guidelines for prevention and control of infections, guidelines for sterilization and disinfection, and antimicrobial use guidelines are to be implemented strictly in hospitals to minimize risk of spreading hospital acquired infections. These policies are practiced and monitored by the Hospital Infection Control Team (HICT) and Hospital Infection Control Committee (HICC) and audited periodically.

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Medical Air Sterilizer Market – Restraint

However, lack of hygienic practices and maintenance of hospitals are major factors hindering growth of the market. For instance, according to an article published in National Center for Biotechnology Information (NCBI) 2016, overcrowding in hospitals, limited hospital resources, lack of proper training and education is expected to limit growth of the medical air sterilizer market.

Medical Air Sterilizer Market – Regional Analysis

On the basis of region, the global medical air sterilizer market is segmented into North America, Latin America, Europe, Asia Pacific, Middle East, and Africa.

North America is expected to hold a dominant position in the medical air sterilizer market, owing to increasing use of air sterilizers by hospitals with latest features such as activated carbons, and U.V. lamps. For instance, Modern Alchemy Air Purifiers of U.S., are capable of treating a wide range of airborne contaminants, including allergens, chemicals, volatile organic compounds, bacterias, mycotoxins, and odors by medical-grade High Efficiency Particulate Air (HEPA) filters, activated carbons, and germicidal U.V. lamps.

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Furthermore, Middle East is expected to witness significant growth in the market, owing to increasing in improvements in healthcare sector. For instance, according to an article published in NCBI 2017, governments and private sectors are focusing in up gradation of hospitals, and clinics, due to high rates of illness and mortality rates in Gulf Cooperation Council (GCC) countries which is creating need for medical air sterilizers.

Asia Pacific is also attributed to grow in medical air sterilizer market during the forecast period, owing to increasing number of startups in medical air sterilizer system development. For instance, Biomoneta, founded in 2014, is an India-based startup focused on developing a device to extract and kill microbes in hospitals and other healthcare settings.

Key players operating in the global medical air sterilizer market include, Steris PLC, Advanced Sterilization Products Services Inc., Getinge AB, Anderson Products, TSO3 Inc., 3M Company, MMM Group, Belimed AG, Cantel Medical Corp., and SAKURA SI CO., LTD.

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Dermatology EMR Software Market Trends Forecast Opportunity Analysis-2027

 

Dermatology EMR Software Market: Regional Analysis

On the basis of region, the global Dermatology EMR Software Market is segmented into North America, Latin America, Europe, Asia Pacific, Middle East, and Africa.

North America is expected to account for largest market share in the dermatology EMR software market, owing to adoption of EMR software with advanced features in the region. For instance, in July 2018, Modernizing Medicine, Inc., a U.S.-based company, at the American Academy of Dermatology (AAD) 2018 Summer Meeting, declared introduction of EMR software with new features such as, Electronic Medical Assistant, (EMA); a mobile EHR system with touch-and-swipe technology and also features the dermatology electronic health record (EHR) system, including electronic prior authorization (ePA), Real-time Prescription Benefit, and Inventory Management.

Furthermore, in March 2018, Spectralink Corporation, a U.S.-based company, released a new line of smart phones designed specifically for use in healthcare. The Spectralink Versity phones are resistant to water and chemicals. The devices run on the latest Oreo Android operating system and has built-in software to seamlessly integrate them with in-hospital EMRs.

Electronic medical records (EMRs) is a part of Electronic Health Records (EHR). Dermatology outpatients include large number of patients with chronic diseases since they need long follow-up durations for cure. Therefore, EMRs in dermatology will be useful in recording dermatological data. EMRs in dermatology also allows streamlined, one-click retrieval of old records, previous investigation reports, medical bills, X-rays, and graphics of affected area on body on which the dermatologist can analyze skin lesions along with rashes, and ulcers.

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Dermatology EMR Software Market: Drivers

Increasing awareness for use of EMRs in healthcare sector is expected to propel growth of the dermatology EMR software market. For instance, in November 2017, the Dubai Health Authority (DHA) completed the third and final phase of the unified electronic medical record (EMR) system Salama, in Latifa Hospital, Hatta Hospital, Thalassemia Centre, Dubai Gynecology and Fertility Centre, and all DHA Medical Fitness Centers across the United Arab Emirates (UAE). Salama stores vital patient information such as the medical history of the patient, past surgery details, lab test results, and X-ray reports, which can be easily accessed by any DHA doctor from all DHA facilities across the UAE region.

Moreover, in September 2018, MedX Health Corp., a Canadian company, launched DermSecure, its telemedicine platform, in six Ontario clinics. DermSecure telemedicine platform offers benefits to patients and primary care physicians by working with dermatologists for enhancing their skills in terms of disease diagnosis and treatment.

Furthermore, Apple Inc., in April 2018, launched Apple Health Records feature that combines data of patients’ current heath and data from their past EHR in the health app by using HL7’s Fast Healthcare Interoperability Resource (FHIR) specification. This allow users to know about their drug allergies, medications, and precautions during treatment. It also allow patients to check an EHR patient portal for information such as their laboratory test results. The users need to enter a password to view the information, as the data is encrypted.

Furthermore, advancements in the EMR software is expected to boost growth of the dermatology EMR software market. For instance, in July 2018, Yale School of Medicine in the U.S. developed voice recognition software for EMR, which will reduce time of physicians during patient consulting. Physicians can login once at the start of their shift, which will save physicians time by eliminating 20 to 140 logins per physician per day. This has improved the user experience with EMRs.

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Dermatology EMR Software Market: Restraint

Increasing cost of EHR services offered by key players is expected to hamper growth of the dermatology EMR software market. For instance, in February 2018, Practice Fusion, Inc., a company in North America, abandoned its business model that contributed to its popularity, as it was offering free EHR software to physicians when it was acquired by Allscripts in 2018. The company later started charging monthly subscription fee of US$ 100 per physician per month for EMR software. Therefore, maintaining the customer base could be a challenge for the company, as it was earlier offering the same service for free.

Moreover, mergers and acquisitions in the U.S. is also expected to drive growth of the market. For instance, in June 2017, athenahealth, a cloud-based EHR company, acquired Praxify Technologies in a US$ 63 million deal. Praxify Technologies originates with a number of applications, including a personal assistant program integrated with EHRs and artificial intelligence aimed at patient engagement. This acquisition is expected to improve athenahealth’s performance in providing their services.

Dermatology EMR Software Market: Competitive Analysis

Strategies adopted by key players such as acquisitions in Asia Pacific region is expected to boost growth of the dermatology EMR software market in this region. For instance, in August 2018, Persistent Systems, an India-based company, acquired Herald Health. Herald Health is a software platform that allows various hospital stakeholders to be automatically notified when data in the EHR and other data systems changes.

Key players operating in the dermatology EMR software market include Encite, Inc., MetaOptima Australia Pty Ltd, CureMD Healthcare, CloudPital, CollaborateMD Inc., eClinicalWorks, CompuGroup Medical, mdconnection, and Practice Fusion, Inc.

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Collagen Meniscus Implant Market To Surpass US$ 563.0 Million By 2027

 

Global Collagen Meniscus Implant Market, by Age Group (Pediatric and Adult), by End User (Hospitals, Clinics, and Ambulatory Surgical Center), and by Region (North America, Latin America, Europe, Asia Pacific, Middle East, and Africa) is estimated to be valued at US$ 389.5 million in 2019, and is expected to exhibit a CAGR of 4.7%, during the forecast period (2019-2027).

 Increasing incidences of meniscal tear, which might result into arthritis is a major factor that is expected to drive the collagen meniscus implant market growth over the forecast period. For instance, according to the Centers for Disease Control and Prevention (CDC) factsheet 2018, around 29.3% and 49.6% population aged 45 to 64 and above 65 years, respectively were diagnosed with arthritis from 2013 to 2015 in the U.S. Moreover, according to the reports published by the American Academy of Physical medicine and Rehabilitation 2017, incidence rate of knee meniscal injuries was 61 cases per 100,000 individuals in the U.S.

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Increasing number of sports injuries and rising geriatric population are major factors that are expected to drive growth of the collagen meniscus implant market over the forecast period. For instance, according to the American Journal of Sports Medicine 2014 study, the most common surgical intervention performed by orthopedic surgeons is for meniscal lesions. According to the same source, over one million surgical interventions involving meniscus are performed annually in the U.S. and around 400,000 in Europe. Moreover, adoption of inorganic strategies such as collaboration and acquisition by major players in the collagen meniscus implant market, is expected to drive growth of the market. For instance, in October 2019, Zimmer Biomet signed an exclusive license agreement with Sweden-based medical device company, Bactiguard. The licensing agreement involved usage of Bactiguard’s infection prevention technologies with Zimmer Biomet’s orthopedic implants. Moreover, in March 2017, Active Implants LLC secured funding from LS Health Science Partners, to continue clinical trials of NUsurface Meniscus Implant.

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Key Takeaways of the Global Collagen Meniscus Implant Market:

The global collagen meniscus implant market is expected to exhibit a CAGR of 4.7% during the forecast period (2019-2027), owing to increasing initiatives by key players to develop novel collagen meniscus implant.

Increasing clinical trials by key players on collagen meniscus implants is expected to drive the global collagen meniscus implant market growth over the forecast period. For instance, in December 2015, Active Implant LLC initiated clinical trial study to gather safety and probable clinical benefit data on the NUsurface Meniscus Implant after the treatment of the patients with post-meniscectomy pain syndrome, Osteoarthritis, and Knee injuries.

Major players operating in the global collagen meniscus implant market include Zimmer Biomet Holdings, Inc., RTI Surgical Holdings, Inc., Stryker Corporation, Orthonika, Active Implants LLC, and

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Intramucosal Implants Market Size, Trends, Shares, Insights and Forecast – 2018-2026

 

Intramucosal Implants Market, by Product Type (Titanium Implants and Zirconium Implants), by End Users (Hospitals, Dental Clinics, and Others), and by Region (North America, Europe, Asia Pacific, Latin America, Middle East, and Africa) - Size, Share, Outlook, and Opportunity Analysis, 2018 – 2026

Intramucosal implants are type of dental implants made with either titanium or zirconium, attached to palatal side of partial or complete denture in mouth region. They require proper thickness of palatal to get attached hence they are inserted in maxilla region of mouth, as it is thick. Intramucosal implants are relatively easy, quick, minimally invasive, and reversible to use.

Intramucosal Implants Market Driver

Use of innovative ideas such as CAD/CAM technology in the field of dentistry is expected to boost growth of the intramucosal’ implants market. For instance, according to the Journal of Interdisciplinary Dentistry 2015, use of Computer Aided Drug Designing (CAD) and Computer Aided Manufacturing (CAM) in the dentistry offers extremely aesthetic, biocompatible intramucosal implants by using materials such as metal alloys, composites, titanium, and polyether ether ketone, and milling machines that restore implants to proper position.

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Moreover, increasing use of robotics to assist dentists with procedures such as root canal surgery and orthodontic operations are expected to increase adoption of intramuscular implants. For instance, in September 2017, a robot dentist performed first successful autonomous dental implant surgery by fitting two new teeth into a woman’s mouth in China. The robot was developed by joined collaboration of the Fourth Military Medical University’s affiliated Stomatological Hospital and the Robotic Institute at Beihang University.

Intramucosal Implants Market Restraint

The high cost of intramucosal implants is expected to restrain growth of the market. For instance, according to Dental Associates, in January 2018, the cost for a single implant is US$ 4,817 without bone grafting and US$ 5,557 with bone grafting.

Intramucosal Implants Market – Regional Analysis

On the basis of region, the global intramucosal implants market is segmented into North America, Latin America, Europe, Asia Pacific, Middle East, and Africa.

North America is expected to hold dominant position in the global intramucosal implants market, owing to marginal expansions of key players in the dental field. For instance, in July 2018, Danaher Corporation, U.S. based company, announced to expand its dental section into independent, public trading company DentalCo, to maximize dental business innovation in developing implants, services, and solutions to customers.

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Asia Pacific is projected to witness significant growth in the intramucosal implants market, owing to increasing awareness regarding use of dental implants through conferences. For instance, in February 2018, Asia Congress of Oral Implantology was held in India to engross educationalists, practitioners and researchers in eminent presentations on the technological, scientific and clinical advancements in the oral implantology sector.

Moreover, in March 2018, Dental Society of Implant Dentistry Center held first Ultra-Short conference specialized in comprehensive dental Implantology on short dental implants in India. Short dental implants allow universal brace positioning and has also been proven bacterially sealed.

Intramucosal Implants Market Competitive Analysis

Key players operating in the global intramucosal implants market include, Institut Straumann AG, Danaher Corporation, Zimmer Biomet Holdings, Inc., Camlog Biotechnologies AG, Osstem Implant Co., Ltd., Avinent Implant System, Biohorizons Iph, Inc., 3M, and Bicon, LLC.

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Levodopa Market Size, Share, Outlook, and Opportunity Analysis, 2019– 2027

 

Levodopa Market by Application (Parkinson’s disease and Dopamine Responsive Dystonia), by Drug Type (Rytary, Duopa, Sinemet, Canamet, and Others), by Distribution Channels (Hospital Pharmacies, Retail Pharmacies, and Online Pharmacies) and by Geography (North America, Europe, Asia Pacific, Latin America, Middle East, and Africa) - Size, Share, Outlook, and Opportunity Analysis 2018 – 2026.

Levodopa or L-Dopa is a chemical building-block that converts into a dopamine in body. Dopamine is the chemical messenger released in brain. It mediates pleasure, cognition, and memory functions. Nearly all patients receive the dopamine precursor levodopa, which adequately control symptoms of Parkinson's disease (PD) at early stage of the disease. Carbidopa is often included with levodopa-containing drugs in order to boost its efficacy by slowing down the metabolism of dopamine.

Levodopa Market Driver

Development of novel formulations and efficient drug delivery methods for levodopa are expected to drive growth of the levodopa market. For instance, a clinical study for gastric retentive Accordion Pill, an immediate drug release formulation by Intec Pharma Ltd., is ongoing in clinical phase III and is expected to complete in September 2018. Accordion Pill is a Carbidopa/Levodopa (AP-CD/LD) combinational oral drug delivery system, which is designed to improve the efficacy and safety of existing CD/LD drugs by utilizing an efficient gastric retention and specific release mechanism.

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Moreover, Impel NeuroPharma Inc. is conducting phase II clinical study for INP103, a drug-device combination product containing a drug component, L-dopa, and device component I231 Precision Olfactory Delivery (POD) device. The study is expected to complete in November 2018.

Furthermore, advancement in diagnosis of Parkinson's disease (PD) progression is expected to boost growth of levodopa market. For instance, a clinical study conducted by Washington University School of Medicine, for measuring PD progression both by using Magnetic Resonance Imaging (MRI) and by controlled dose of levodopa for discovering suitable biomarker of PD is currently in clinical phase I and is expected to complete in February 2019.

Levodopa Market Restraint

Shortage of drug supply in the market due to delay in manufacturing and supply of levodopa is expected to hamper levodopa market growth. For instance, Merck Sharp & Dohme Ireland (Human Health) Ltd. in September 2018, anticipated stock shortage of some Sinemet (Carbidopa/ Levodopa) products in the Irish market in near future due to global manufacturing delays in production and demand for resupply of these products.

Levodopa Market – Regional Analysis

On the basis of region, the global levodopa market is segmented into North America, Latin America, Europe, Asia Pacific, Middle East, and Africa.

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North America is expected to dominate the global levodopa market, owing to approval of new products by the U.S. Food and Drug Administration (FDA). For instance, in 2015, FDA approved an extended-release oral formulation of Levodopa/Carbidopa called Duopa, manufactured by AbbVie Inc., in the U.S. market. Duopa is a gel formulation of Carbidopa/Levodopa enteral suspension and is administered using a small, portable infusion pump that delivers Carbidopa and Levodopa directly into the small intestine, which continuously release over 16 hours in the body.

Europe region is expected to witness significant growth in levodopa market due to involvement of key players for marketing novel formulations in European region. For instance, Acorda Therapeutics, Inc., in March 2018, submitted a Marketing Authorization Application (MAA) to the European Medicines Agency (EMA) for INBRIJA, an investigational inhaled levodopa treatment for symptoms of OFF periods (OFF symptoms implies recurrence of symptoms such as rigidity, and tremors after long period of levodopa use) in people with PD taking a Carbidopa/Levodopa regimen.

Furthermore, in November 2015, Impax Laboratories, Inc. received European Commission (EC) marketing authorization for NUMIENT (Levodopa and Carbidopa), a modified-release oral capsule formulation for the symptomatic treatment of adult patients with Parkinson's disease in Europe region.

The key players operating in levodopa market include, Taj Pharmaceuticals Limited., Guangzhou HanFang Pharmaceutical Company Limited, Poulvet.com, Teva Pharmaceutical Industries Ltd., UBM, Zhejiang Wild Wind Pharmaceutical Co., Ltd., and SWAPNROOP.

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Thursday, 29 July 2021

Medicine Iontophoresis Market Size, Trends, Shares, Insights and Forecast – 2018-2026

 

Medicine Iontophoresis Market – Regional Analysis

On the basis of region, the global Medicine Iontophoresis Market is segmented into North America, Latin America, Europe, Asia Pacific, Middle East, and Africa.

North America is projected to hold dominant position in the global medicine iontophoresis market due to insurance and reimbursement strategies for treating hyperhidrosis patients. For instance, in the U.S., International Hyperhidrosis Society offers useful tools, information, and downloadable forms related to the insurance and reimbursement process. This comprises health plans for hyperhidrosis treatments, cost of therapy, medical insurance form for purchasing iontophoresis devices, and others. Such insurance and reimbursement services allow efficient treatment of hyperhidrosis.

Iontophoresis is a technique, which uses an electric current to deliver a medicine or other chemicals through the skin. Iontophoresis is often suggested for people with hyperhidrosis (excessive sweating) of the hands and/or feet as it aids in reducing sweating. Iontophoresis is suitable for applications such as acetic acid (calcific tendinitis), calcium chloride and magnesium sulfate (control of musculoskeletal spasms), dexamethasone (inflammation), lidocaine (inflammation of soft tissues), and zinc oxide (rheumatoid arthritis).

Medicine Iontophoresis Market Drivers

Increasing awareness for treatment of hyperhidrosis is expected to drive growth of the medicine iontophoresis market. For instance, in the U.S., the International Hyperhidrosis Society (IHhS) IHhS celebrates the month of November as Hyperhidrosis Awareness Month by making documentaries, conducting interviews of patients, and organizing various events to raise awareness of hyperhidrosis among the populace.

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Moreover, increasing research on iontophoresis in treating various diseases and symptoms is expected to boost growth of the medicine iontophoresis market. For instance, in April 2018, EyeGate Pharma Company developed a novel ocular drug delivery system called EyeGate II iontophoresis, where an electric current generated in the device delivers ionized drug into the eye and further gets absorbed into the eye by the electric current.

Furthermore, approval for new products for medicine iontophoresis therapy is expected to propel the medicine iontophoresis market growth. For instance, in May 2017, Soterix Medical Inc., the U.S.-based firm, received a 510(k) clearance from the U.S. Food and Drug Administration (U.S FDA), for its IontoDC device intended to use direct current to introduce ions of soluble salts or other drugs in the body.

Medicine Iontophoresis Market Restraints

Side effects and the limitations associated with medicine iontophoresis therapy are expected to restrain medicine iontophoresis market growth. For instance, according to British Association of Dermatologists 2016 report, people often complain symptoms of bruising or blisters incase the intensity of current is too high for iontophoresis, a sensation of mild burning in case the electrode is touched, and itchiness in the treated area after treatment. Moreover, patients with cardiac pacemakers or with metal implants are not suitable for iontophoresis treatment.

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Furthermore, product recalls due to failure in meeting regulatory standards is expected to restrain growth of the medicine iontophoresis market. For instance, in August 2016, Health Canada recalled IONTODERMA ID-1000, a product of IONTODERMA, due to failure to comply medical devices regulations and for selling medical devices without proper license.

Furthermore, increasing research and development activities to launch advanced iontophoresis devices for treating ophthalmic diseases in Asia Pacific is expected to contribute to substantial growth in the global medicine iontophoresis market. For instance, in March 2018, annual meeting of Association for Research in Vision and Ophthalmology (ARVO) 2018 was held in China where, Aciont Inc. opened up clinical data for its lead product, Dexamethasone Sodium Phosphate (DSP)-Visulex. DSP-Visulex is a non-invasive drug delivery system based on ocular iontophoresis technique. This product can be used for the treatment of non-infectious anterior uveitis.

Medicine Iontophoresis Market Competitor Analysis

Key players operating in the global medicine iontophoresis market include, ORGANIX GmbH & Co. KG, Hidrex USA, Drionic, IOMED, R.A. Fischer, Iskra Medical d.o.o., Chattanooga, Encore Medical, L.P., iTech Medical, Inc., Kimetec GmbH, and AAM.

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Calciphylaxis Treatment Market To Surpass US$ 2,400 Million By 2026

 

The Global Calciphylaxis Treatment Market, by Treatment (Drug Therapy, and Hyperbaric Oxygen Therapy), by End User (Hospital and Clinics, Homecare, and Ambulatory Centers), and by Region (North America, Latin America, Europe, Asia Pacific, Middle East, and Africa) was valued at US$ 1,097.7 million in 2017 and is projected to exhibit a CAGR of 9.6% over the forecast period (2018 - 2026).

Calciphylaxis is a rare condition characterized by calcification or the aggregation of calcium in a patient’s blood vessels and the development of thrombosis. This can lead to the death of cells in a patient’s skin and fatty tissues, thereby causing death. Diagnosis of calciphylaxis is symptoms-based and various tests such as skin biopsy, blood tests, and imaging studies confirm the condition. There is no specific treatment available for calciphylaxis. Healthcare professionals often focus on balancing the minerals in the body such as calcium and phosphate that may aid in treatment of the disease. This can be achieved by changing dialysis regimes, medications, or considering surgery for parathyroid glands. Major surgical treatments such as parathyroidectomy are mostly recommended for patients with known primary hyperparathyroidism. However, surgical debridement to remove necrotic tissue and healing of healthy tissue is more widely used, however, its efficacy is debated.

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Doctors also focus on pain control, good nutrition, and excellent ulcer care in case the skin has broken down. Wound management therapies for calciphylaxis include, nonsurgical wound cleansing and Hyperbaric Oxygen Therapy (HBOT). HBOT can be considered as a second line of treatment incase wounds do not improve. Researchers and key players in the market are focused on finding efficient treatment for calciphylaxis. According to the Journal of the American Society of Nephrology 2017 study, Vitamin K deficiency can have a role in development of calciphylaxis. Moreover, according a study published in 2017 by BioMed Central Nephology Journal, four week supplementation of Vitamin K2 can significantly improve vascular calcification.

Browse 24 Market Data Tables and 21 Figures spread through 165 Pages and in-depth TOC on "Calciphylaxis Treatment Market, by Treatment (Drug Therapy, and Hyperbaric Oxygen Therapy), by End User (Hospital and Clinics, Homecare, and Ambulatory Centers), and by Region (North America, Latin America, Europe, Asia Pacific, Middle East, and Africa) - Global Forecast to 2026"

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Key Takeaways of the Global Calciphylaxis Treatment Market:

The global calciphylaxis treatment market is expected to witness a CAGR of 9.6% during the forecast period, owing to increasing cases of calciphylaxis associated with dialysis. According to the Nephrology Dialysis Transplantation Journal 2017 study, the German Calciphylaxis Registry recorded calciphylaxis reporting rate of approximately 30 new cases per year among the dialysis patients between 2006 to 2015

Among region, North America calciphylaxis treatment market is expected to generate maximum revenue during the forecast period, owing to increasing demand for kidney transplantation procedures and rising number of dialysis patients. According to the National Kidney Foundation, in 2016, around 3,000 patients every month underwent kidney transplant in the U.S.

Major players operating in the global calciphylaxis treatment market include, 3M, Amgen Inc., BSN Medical, ConvaTec Inc., Medtronic Plc., Smith & Nephew Plc., and Laboratoris Sanifit S.L.

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Pertuzumab Market Size, Share, Outlook, and Opportunity Analysis, 2019– 2027

 

Furthermore, increasing number of drug approvals are expected to propel growth of the global Pertuzumab Market. For instance, in December 2017, the U.S. Food and Drug Administration (U.S FDA) granted approval to PERJETA, a pertuzumab produced by Genentech, Inc. for its use in combination with trastuzumab and chemotherapy as adjuvant treatment of patients with HER2-positive early breast cancer at high risk of recurrence.

Pertuzumab is a recombinant monoclonal antibody that acts as an antineoplastic agent, which targets the human epidermal growth factor receptor 2 protein known as HER2. The drug blocks signaling pathways that leads to cell growth arrest and apoptosis (cell destruction), thereby inhibiting the proliferation of human tumor cells. Pertuzumab was found to aid in the treatment of HER2 associated breast cancer and was developed by Genentech, Inc., a subsidiary of F. Hoffmann-La Roche AG. It was first approved by U.S. Food and Drug Administration in 2012.

Pertuzumab Market– Drivers

There are increasing number of clinical trials for use of pertuzumab in combination with other drugs for the treatment of breast cancer . For instance, Helsinki University Central Hospital is undergoing phase III clinical study for adjuvant trastuzumab, pertuzumab, and docetaxel in the treatment of early HER2 positive breast cancer. The study was started in December 2015 and is estimated to complete by June 2023.

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Moreover, development of novel anticancer drug delivery technologies is expected to boost growth of the market. For instance, in July 2018, Gentech, Inc., in partnership with Halozyme Therapeutics, Inc., used proprietary ENHANZE drug-delivery technology of Halozyme Therapeutics, Inc., for subcutaneous administration of fixed-dose combination of pertuzumab (PERJETA) and trastuzumab (Herceptin). This study is under clinical phase III trial. ENHANZE technology aids in reducing the need for multiple injections and reduces time required for drug administration.

Pertuzumab Market– Restraint                                                

Increasing cost of anticancer drugs is expected to be a major factor hampering growth of the market. For instance, in June 2017, The Scottish Medicines Consortium (SMC) denied access to pertuzumab in England, which was available via the Cancer Drugs Fund (CDF) in Europe. The drug was rejected by SMC as the treatment of HER2 positive breast cancer was not cost effective when pertuzumab was used in combination with trastuzumab and docetaxel.

Moreover, according to a study published in the journal Oncology, September 2015, although the use of pertuzumab with docetaxel and trastuzumab as first-line therapy for HER2 positive breast cancer has been shown to yield a substantial survival benefit, the therapy is not cost effective in the U.S. Also, according to the same source, the cost of treating HER2 positive breast cancer with pertuzumab and other drugs is US$ 509,845 and that with only docetaxel and trastuzumab is US$ 135,092.

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Pertuzumab Market– Regional Analysis

On the basis of region, the global pertuzumab market is segmented into North America, Latin America, Europe, Asia Pacific, Middle East, and Africa.

North America is expected to hold dominant position in the global pertuzumab market due to increasing prevalence of breast cancer among women in the U.S. For instance, according to American Cancer Society 2017, around 52,710 new cases of invasive breast cancer were diagnosed in 2017 among women in the U.S. and around 40,610 women were expected to die due to breast cancer in the U.S. in same year.

Furthermore, Asia Pacific is expected to witness significant growth in the global pertuzumab market, owing to increasing awareness of breast cancer and its management. For instance, in November 2016, India launched National Cancer Screening Program to increase awareness and early detection of breast cancer. This framework aims to offer mechanism for effective screening and management of common cancers.

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Prophylactic Human Vaccine Market Size Share Trends Forecast 2026

 

Prophylactic Human Vaccine Market – Regional Analysis

On the basis of region, the global Prophylactic Human Vaccine Market is segmented into North America, Latin America, Europe, Asia Pacific, Middle East, and Africa.

Geographically, North America is probable to lead in the global prophylactic human vaccine market, owing to receiving large number of research grants by government. For instance, in September 2018, GeoVax Labs, Inc., U.S.-based company recieved grant of US$ 2,442,307 by the U.S. Army Medical Research Acquisition Activity. The grant was awarded as a cooperative agreement for novel Lassa Fever (LF) vaccine (GEO-LM01) development program. GEO-LM01 uses Modified Vaccinia Ankara (MVA) and Virus-Like Particle (VLP) vaccine platform that has been demonstrated to be safe and induce antibody responses in patients. Moreover, MVA-VLP platform has shown effective results in other cases such as GeoVax’s prophylactic HIV vaccine, GeoVax’s Ebola (EBOV) vaccine, and GeoVax’s Zika vaccine in its respective preclinical studies.

Prophylactic human vaccines stimulate the immune response and are intended for ameliorating the effects of future infection caused by pathogens in human beings. Novel vaccine development technologies such as viral-like particles are used in developing Hepatitis B Virus (HBV) vaccines, and Human Papilloma Virus (HPV) vaccines. For instance, in March 2014, CureVac AG received EUR 2 million Vaccine Prize from European Commission for its novel RNActive vaccine technology. This RNActive vaccine technology enables production of safe, efficacious, and cost-effective vaccines that are protected against elevated temperature as well as inadvertent freezing.

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Prophylactic Human Vaccine Market – Drivers

Increasing number of pipeline studies and rising involvement of key players for vaccine development is expected to propel growth of the prophylactic human vaccine market during the forecast period. For instance, in October 2018, CureVac AG, announced to initiate dose escalation phase I clinical trial for CV7202 mRNA-based rabies vaccine. CV7202 is a prophylactic vaccine encoding RABV-G, the rabies virus glycoprotein. This will enable vaccinated individual's own cells to produce RABV-G protein, by which immune response gets triggered. This study is estimated to complete in January 2021.

Moreover, in October 2018, Valneva SE announced progress in its Phase 1 program targeting a single-shot vaccine against Chikungunya. It is designed for prophylactic, active, single-dose immunization against Chikungunya in humans. The vaccine aims for long-lasting protection and an anticipated safety profile similar to other approved vaccines for active immunization in adults and children.

Furthermore, rising initiatives by various scientists to develop innovative solutions to fight against infectious diseases is expected to drive growth of the market. For instance, VBI Vaccines Inc., in September 2018, announced formation of three Scientific and Clinical Advisory Boards (SABs) comprising leading experts in infectious disease and immuno-oncology research and vaccine development targeting hepatitis B, Cytomegalovirus (CMV), and Glioblastoma (GBM). This collaboration is expected to propel growth of the market, owing to enhanced vaccine development.

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Prophylactic Human Vaccine Market – Restraint

Significant barriers in the vaccine development such as virus diversity and limited number of animal models are estimated to hamper growth of the prophylactic human vaccine market. For instance, according to Gastroenterology, in October 2018, vaccine development requires huge investment from various resources and is very challenging. Designing vaccine trials in human is difficult since following immunization the chances for develop an acute infection is very high. Therefore, anti-viral treatment has to be offered immediately, which makes it a challenging task to manage disease.

Europe region is also expected to perceive extensive growth in prophylactic human vaccine market, due to rising initiatives by government for developing efficient and safe vaccines. For instance, in October 2017, the European Commission funded TRANSVAC, a new infrastructure project. This project aims to rapidly develop effective vaccines in order to address European health challenges and in turn increase the sustainability of EC vaccine projects in Europe. TRANSVAC offers high-quality technical services to support development of prophylactic and therapeutic vaccines for both human and animal use.

The key players operating in prophylactic human vaccine market include, GlaxoSmithKline Plc., Merck & Co., Inc., Pfizer Inc., Janssen Pharmaceuticals, Inc., Altimmune, Inc., Bharat Biotech International Limited, Serum Institute of India Pvt. Ltd., Sanofi Pasteur SA, Shanghai BravoBio Co., Ltd., SK Chemicals Co., Ltd., Takeda Pharmaceutical Company Limited, BiondVax Pharmaceuticals Ltd., and SK Chemicals Co., Ltd.

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Sulfachloropyridazine Sodium Market Forecast Opportunity Analysis - 2027

 

Sulfachloropyridazine Sodium Market by Patient Type (Cows, Pigs, Chickens, Cattles, and Pediatrics), and by Region (North America, Europe, Asia Pacific, Latin America, Middle East, and Africa) - Size, Share, Outlook, and Opportunity Analysis 2018 – 2026

Sulfachloropyridazine sodium is a sulfonamide antibiotic used to study kinetics and reaction pathways. Also, it is used to treat acute Urinary Tract Infections (UTIs) in pediatric patients. Sulfachloropyridazine sodium blocks the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase and bacterial Para-Amino Benzoic Acid (PABA), which is required for bacterial growth. The compound Sulfachloropyridazine sodium powder has a curative effect for various animals with pasteurellosis and is popular for use in animal husbandry.

Sulfachloropyridazine Sodium Market Drivers

Rising use of antibiotics in animals to treat certain infections is expected to drive growth of the sulfachloropyridazine sodium market. For instance, according to an article published in journal Science, 2017, almost 80% of all antibiotics in the U.S. are administered to cows, pigs, and chickens to keep them healthy and accelerate their growth and development.

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Moreover, according to the Louisiana Department of Health, U.S., due  to  low  cost  and  relatively better  efficacy against many common bacterial infections, sulfonamides  are  some  of  the  most common antibacterial agents utilized in veterinary medicine, which is in turn is boosting growth of the sulfachloropyridazine sodium market.

Sulfachloropyridazine Sodium Market Restraint

Over the years, bacterial pathogens have acquired resistance to sulfonamide class of antibiotics, due to mutations in pre-existing DNA or by acquisition of Antibiotic Resistance Genes (ARGs), which is expected to hinder growth of the sulfachloropyridazine sodium market. For instance, according to an article published in journal Microbiome, 2017, use of sulfonamide class of antibiotics is restricted to topical use only extensively for animals.  For instance, in the U.S., around 380,186 kg of sulfonamides was distributed legally during 2015, to increase the resistance power of food-producing animals. Hence, further spread of sulfonamide resistance would have hamper the market particularly in the animal sector.

Sulfachloropyridazine Sodium Market – Regional Analysis

On the basis of region, the global sulfachloropyridazine sodium market is segmented into North America, Latin America, Europe, Asia Pacific, Middle East, and Africa.

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North America region is expected to gain maximum share in the sulfachloropyridazine sodium market, owing to high prevalence of Urinary Tract Infections (UTIs) in the U.S. For instance, according to American Urological Association 2016, more than 1 million catheter-associated UTIs are reported annually in the U.S. and up to 40% of hospital gram negative bacteremias originate as UTIs annually, which are treated by antibiotics.

Asia Pacific region is expected to witness significant growth in the sulfachloropyridazine market due to involvement of key players in manufacturing antibiotics solely for veterinary purposes. One of the company named Weifang Premier Animal Pharmaceutical Industries Co., Ltd, a China-based company also involved in animal husbandry. They contributes to animal health by manufacturing sulfachloropyridazine sodium soluble powder as one of the key product in China.

Key players involved in Sulfachloropyridazine market include Sigma-Aldrich, Inc., Zhengzhou Fuyuan Chemical Industry Co., Ltd, Santa Cruz Biotechnology, Inc., UBM, Hefei TNJ Chemical Industry Co., Ltd., AK Scientific Inc., SuZhou Wugan Pharmaceutical Co., Quimica Alkano, Shanghai Danfan Network Science&Technology Co., Ltd., and Ofichem Group.

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Wednesday, 28 July 2021

Surgery Shadow less Light Market Size Share Trends Forecast 2026

 

Surgery Shadow less Light Market by Product Type (Mobile Shadow less Lamp, Light Emitting Diode (LED) Shadow less lamp, Holes Shadow less Lamp, and Integral Reflex Shadow less Lamp), by Modality (Portable Shadow less Lamps, and Standalone Shadow less Lamps), by End Users (Hospitals, Specialty Clinics, and Ambulatory Surgical Centers), and by Geography - Size, Share, Outlook, and Opportunity Analysis 2018 – 2026

Proper surgical lighting is crucial during surgery for patient safety and comfort. It should be designed so as to enable the medical team to focus exclusively on the surgical operation. Successful surgery requires a special balance of luminance of light, shadow management, volume, and temperature which maximizes visibility at the surgical site while minimizing eye fatigue.

Surgery Shadow less Light Market – Driver

Development in the use of surgery lamps technology is expected to drive growth of the surgery shadow less light market. For instance, development of Light Emitting Diode (LED) Shadowless lamps by Sansi Technology Inc., in June 2018, has opened up a new era in medical lighting and provides advantages over traditional lamps such as high shadow less degree, less energy consumption, and environment friendly nature.

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Furthermore, mobile operational shadowless lamps with internal camera arrangement launched by MTMED GROUP in August 2018, also allows same advantages such as environment friendly and long life. 

Surgery Shadow less Light Market – Restraint

Product recalls by U.S. Food and Drug Administration (USFDA) due to faulty surgery shadow less lamps and further chances of injuries is expected to affect the growth of surgery shadow less light market. For instance, in June 2018, FDA recalled VOLISTA StandOP Surgical Light manufactured by Maquet SAS firm. The lamps were recalled due to potential light head detachment issue. Improper assembly of the bracket that connects the light head to the axle fork could result in the light head bracket breaking, causing the light head to detach from the arm. Use of such affected device may result in serious injury to patient and/or medical staff if the light head detaches and drops.

Surgery Shadow less Light Market – Regional Analysis

On the basis of region, the global surgery shadow less light market is segmented into North America, Latin America, Europe, Asia Pacific, Middle East, and Africa.

Geographically, North America is likely to lead in the global surgery shadow less light market owing to rising preference to use of LED surgical shadow less lights due to its advantages such as low heating, No mercury pollution and no infrared radiation or ultraviolet radiation, actively preventing water loss of the surface of a wound and infection and low energy consumption. For instance, MAQUET Holding B.V. & Co. KG. KG. Headquartered in U.S., provides POWERLED light that is intuitively easy to use and generates reduced shadows and low heat emission. The irradiance is less than 500 W/m2, which helps to eliminate heat and the associated potential for drying of tissue; even in the most sensitive patients.

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Europe region is also expected to observe substantial growth in surgery shadow less light market due to development of new technologies in surgery shadow less light market by various players. For instance, Ergonoptix.com., Netherlands based company in 2018 has emerged with number of new innovations in the field of surgery optics and headlights, including the revolutionary D-Light DUO, a dual headlight which provides 70% shadow reduction. D-Light Duo LED headlamps utilize an advanced cooling system ensuring the lamp does not get too hot to touch.

Surgery Shadow less Light Market – Competitive Analysis

The key players operating in this market include, Heal Force., Getinge Group, Shangdong Mingtai Medical Devices Co., Ltd., Welch Allyn, Skytron, Derungs Licht AG, Integra Life Sciences, Sansi Technology Inc., Lumitex, Inc., Yamada Shadowless Lamp Co., Ltd., HongKong Chenyang Trading Ltd., Integra Life Sciences, United Surgical Industries, Meditech (India)., and Hospedia Medicare Pvt. Ltd.

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