Sientra breast implants represent a category of silicone-based breast implants, utilised exclusively in breast augmentation surgical procedures. However, it is important to note that patients must first provide informed consent prior to undergoing such a procedure with Sientra implants.
The initial procedure of the Sientra breast implant involves a detailed explanation of the various techniques that will be executed, the anticipated outcomes, and the plausible risks and complications. The Sientra Breast Implants Consent Form also elucidates the type of anaesthesia that will be administered during the process, in addition to the comprehensive pre-operative and post-operative guidelines that the patient must adhere to.
The Sientra Breast Implants Consent Form mandates that patients provide a comprehensive account of their medical past, encompassing all prior surgeries and health conditions that could potentially impact the safety and effectiveness of the procedure. Additionally, patients must divulge any allergies or sensitivities to medications or anaesthesia, as well as any pharmaceuticals they are presently taking.
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