Prior to undergoing a Penuma Penile Implant procedure, patients are required to provide their informed consent through the completion of a legal document. This document serves as a means to ensure that patients are fully apprised of the intended treatment, including its potential advantages, drawbacks, and anticipated results. The procedure itself aims to increase both the size and girth of the penis through the insertion of a soft, silicone-based device. Through the completion of this consent form, patients are provided with the necessary information to make an informed decision about their medical care.
The Penuma Penile Implant consent form typically covers various aspects of the treatment, including a description of the procedure, the materials used in the implant, and the surgical techniques involved. It outlines potential benefits, such as improved penile size and girth, increased self-confidence, and enhanced sexual satisfaction, as well as possible risks or side effects, like infection, bleeding, scarring, or implant displacement.
The Penuma Penile Implant consent form also provides information about post-treatment care instructions to help the patient optimise results and minimise potential side effects. Additionally, the form offers an opportunity for patients to ask questions and address any concerns they may have about the treatment.
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