The antimicrobial resistance crisis: stopping mission impossible
The consequences of the AMR crisis for modern medicine
All achievements of modern medicine are only possible through the application of medical devices (MD). This is especially true for class three invasive medical devices according to the European Union’s medical device regulations (MDR). Annually, around 180,000 pacemakers, 260,000 cardiovascular stents, 200,000 hernia meshes, 365,000 hip and knee endoprostheses are implanted into patients in Germany. Furthermore, millions of central venous catheters, ports, urinary catheters, and wound dressings for example are used invasively. All of these implants are made of biomaterials with medical grade approval. Amongst them are different classes of materials, such as metal alloys, ceramics and polymers. Although these biomaterials are mainly described as ‘inert’ (they do not harm the host’s biology), or bio-active to support the host’s biology in different ways, they still remain as foreign materials. These foreign materials possess the disadvantage that bacteria and commensals of the host and pathogens interact with these biomaterials in a severely dangerous manner. Bacteria can form biofilms on the outer and inner surfaces of such biomaterials, often avoiding the host’s immune defence or applied antibiotics if the patient is suffering from an infection.
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Suppliers and Users of Technologies, Products and Services benefit from CAPI.
CAPI (Continuous AMR Partnering Initiative) unites Suppliers and Users worldwide with the aim to add to the curbing of AMR.