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Informed Consent Breast Implant Removal2016 American Society of Plastic Surgeons. Purchasers of the Informed Consent Resource are given a limited license to modify documents contained herein and reproduce
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01
Read the informed consent document thoroughly to understand the purpose and risks of the plastic surgery procedure.
02
Ensure that you have a clear understanding of the procedure, including the expected outcomes, potential complications, and alternative options.
03
Consult with your plastic surgeon and ask any questions or concerns you may have before signing the informed consent form.
04
Provide accurate and complete personal and medical information, including any allergies, medications, or previous surgeries.
05
Follow any pre-operative instructions provided by your plastic surgeon, such as fasting requirements or medication restrictions.
06
Review and understand the confidentiality and privacy policies mentioned in the informed consent form.
07
Sign the informed consent form only after you have received satisfactory answers to your questions and feel fully informed and comfortable with proceeding.

Who needs informed consent - plastic?

01
Anyone undergoing plastic surgery, regardless of the specific procedure, needs to fill out informed consent. This includes individuals seeking cosmetic enhancements, reconstructive surgeries, or any other form of plastic surgery.
02
It is essential for both the patient's safety and legal protection to have a signed informed consent form before proceeding with any plastic surgery.
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Informed consent in plastic surgery is a legal document that ensures a patient is fully informed about the procedure, its risks, benefits, and alternatives before agreeing to undergo treatment.
Plastic surgeons and healthcare providers involved in the patient's care are required to file informed consent.
Informed consent should be filled out by providing clear information about the procedure, obtaining the patient's signature, and ensuring they understand the information provided before any procedure is performed.
The purpose of informed consent is to protect the patient's autonomy, ensuring they have the right to make informed decisions about their medical treatment.
The informed consent document must include the procedure's description, potential risks and complications, expected benefits, alternatives, and the patient's right to withdraw consent.
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