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The Kybella Consent form is a crucial document that outlines the specifics of receiving Kybella® injections, an FDA-approved treatment aimed at reducing submental fullness, commonly referred to as a double chin. This consent form elaborates on the injection process, including the potential need for multiple sessions and the expected timeline for results; effects will typically manifest gradually over about a month. During the process, patients may experience swelling and other side effects, which can include bruising, numbness, and even temporary hair loss in the treated area. The form also emphasizes safety by prompting individuals to disclose any medical conditions, medications, or pregnancy status that could affect their eligibility for treatment. Additionally, it provides clear pre- and post-treatment instructions, ensuring patients understand how to care for themselves during recovery. Alternatives to Kybella® are mentioned as well, highlighting options like liposuction or neck lifts as other means to address submental fullness. By signing the form, patients not only consent to the treatment but also acknowledge the associated risks and the possibility that unforeseen circumstances may require adjustments to their treatment plan. All these elements work together to empower patients with the knowledge they need to make informed decisions regarding their aesthetic treatment.

Kybella® Injection Consent

Kybella® is an FDA approved cosmetic injection indicated for improvement in the appearance of submental fullness associated with submental fat in adults.

The results of Kybella® are not immediate. At your first treatment visit you will receive a series of injections in the submental area. At the time of injection and for several days following the injections you will have swelling in the submental area. Kybella® will cause the fat cells to diminish gradually over the course of the next month following your injection in the treated area. A series of treatments may be necessary to achieve optimal results and these will occur at no sooner than the one-month interval. Your doctor will decide the appropriate number of treatment sessions and the amount of Kybella® you will need at each session.

Side Effects:

Side effects of Kybella® may include: bruising, swelling, numbness, induration, marginal mandibular nerve injury, dysphagia (difficulty swallowing), bleeding, tenderness or discomfort, tissue necrosis, hyperpigmentation, redness, or alopecia at the site of injection.

Alopecia: Kybella® injections could cause small patches of alopecia in the treatment area. Pre- Instructions:

You should not be pregnant, nursing an infant, have a history of a bleeding disorder or infection of the area to be treated. The morning of your treatment you should take ibuprofen if you are able to tolerate this medication. Also, you should tell you physician if you take any blood thinners or aspirin or have a history of any issue with lidocaine or epinephrine.

Post Care Instructions:

Ice packs may be used to the treated area during the first 12 hours – ice for 15 minutes on every hour

Do not massage the injection site

If you are able to tolerate ibuprofen, take 200mg three times daily beginning the day of your treatment and for the following four days

Avoid heavy exercise the day of your treatment

Notify us if any significant, swelling, bleeding, pain, dusky discoloration, difficulty swallowing or smiling, or fever occurs.

Alternatives:

As explained not all submental fullness will respond to Kybella®. Other alternative treatments are liposuction to the area, a neck lift and/or platysmoplasty procedures.

The medical director will review all treatments planned for clients. The safety of all procedures are outlined in the protocols manual on site. The well-planned protocols establish safety and allow delegation to the RN to perform.

I hereby authorize ________________________________, delegated staff, and such assistants as may

be selected to perform the following procedure or treatment:

Deoxycholic acid injection injections with Kybella® for improvement in the appearance of moderate to severe convexity or fullness associated with submental (neck) fat.

I recognize that during the course of the injectable treatment, unforeseen conditions may necessitate different procedures than those above. I therefore authorize the above physician or affiliated medical personnel or designees to perform such other procedures that are in the exercise of his or her professional judgment necessary and desirable. The authority granted under this paragraph shall include all conditions that require treatment and are not known to my physician at the time the procedure is begun.

I consent to the administration of such anesthetics considered necessary or advisable. I understand that all forms of anesthetics involve risk and the possibility of complications, injury, and sometimes death.

I acknowledge that no guarantee has been given by anyone as to the results that may be obtained.

For purposes of advancing medical education, I consent to the admittance of observers to my aesthetic injectables.

I authorize the release of my Social Security number to appropriate agencies for legal reporting and medical-device registration, if applicable.

IT HAS BEEN EXPLAINED TO ME IN A WAY THAT I UNDERSTAND: A. THE ABOVE TREATMENT OR PROCEDURE TO BE UNDERTAKEN.

B. THERE MAY BE ALTERNATIVE PROCEDURES OR METHODS OF TREATMENT. C. THERE ARE RISKS TO THE PROCEDURE OR TREATMENT PROPOSED.

I certify that I have read all pages of this document and give my consent for my injectable procedure.

___________________

___________________

Patient Signature / Date

Witness Signature / Date

___________________

___________________

Print Patient Name

Print Witness Name

I certify that I have explained the nature, purpose, benefits, risks, complications, and alternatives to the proposed procedure to the patient. I have answered all questions fully, and I believe that the patient fully understands what I have explained.

___________________

Provider Signature / Date

File Breakdown

Fact Name Detail
FDA Approval Kybella® is an FDA approved injection specifically for treating submental fullness associated with submental fat in adults.
Injection Procedure The procedure involves a series of injections in the submental area during the first treatment visit.
Expected Results Results are not immediate; fat cells diminish over the course of the month following the injection.
Swelling After Treatment Swelling in the treated area can be expected at the time of injection and for several days afterward.
Possible Side Effects Side effects may include bruising, swelling, numbness, and others, such as tissue necrosis or difficulty swallowing.
Alopecia Risk Kybella® injections may cause small patches of alopecia in the treatment area.
Pre-Treatment Instructions Patients should not be pregnant, nursing, or have a bleeding disorder; they should also take ibuprofen if tolerated.
Post-Care Instructions Ice packs can be applied for the first 12 hours, and heavy exercise should be avoided on the day of treatment.
Alternatives Other options for submental fullness include liposuction, neck lifts, or platysmoplasty procedures.
Consent and Acknowledgments Patients give their consent for treatment and acknowledge potential risks, including the risks of anesthesia.

Getting ready for your Kybella treatment involves filling out a consent form that outlines what to expect during the procedure and the necessary precautions to take. This form is essential for ensuring your understanding and agreement to the treatment. Follow these steps carefully to complete the Kybella Consent form accurately.

  1. Start by reading the entire consent form to familiarize yourself with its content.
  2. Locate the section where you are required to fill in your name. Write your full name legibly.
  3. Find the date field next to your signature line. Write today’s date in the appropriate format.
  4. In the designated area for the witness, have a person sign their name who can confirm your consent.
  5. Next, the witness must write the date next to their signature.
  6. Look for the section where the witness must print their name. Have your witness print their full name clearly.
  7. Now, it’s your turn to print your name in the patient name section. Ensure it matches your signature.
  8. If indicated, review the section where the healthcare provider confirms that they have explained the treatment to you. This may be left blank until you confirm it with your provider.
  9. Once completed, review the form again to ensure all information is correct and legible before submission.
  10. Finally, submit the completed consent form to the appropriate healthcare staff for your records and next steps.

What is Kybella, and what does it treat?

Kybella is an FDA-approved cosmetic injection designed to enhance the appearance of submental fullness, commonly referred to as a double chin, due to submental fat in adults. By using Kybella, you can achieve a more contoured neck and jawline, as it gradually diminishes fat cells in the treated area.

What should I expect during my Kybella treatment?

During your first visit, you will receive a series of injections in the submental area. It's important to note that results are not immediate. You may experience swelling at the injection site following your treatment, which usually lasts for several days. The fat cells in the area will gradually reduce over the following month, and additional sessions may be required to reach optimal results, usually spaced at least one month apart.

What side effects should I be aware of?

The potential side effects of Kybella include:

  • Bruising
  • Swelling
  • Numbness
  • Induration (hardening of the area)
  • Marginal mandibular nerve injury
  • Dysphagia (difficulty swallowing)
  • Bleeding
  • Tenderness or discomfort
  • Tissue necrosis
  • Hyperpigmentation
  • Redness
  • Alopecia (temporary hair loss) at the injection site

Discuss any concerns with your healthcare provider to understand these risks better.

Are there any pre-treatment instructions?

Before your Kybella treatment, certain guidelines should be followed. You should:

  1. Ensure you are not pregnant or nursing
  2. Avoid any history of bleeding disorders or infections in the treatment area
  3. Take ibuprofen on the morning of your treatment, if approved by your healthcare provider
  4. Inform your physician of any blood thinners or aspirin use, as well as any previous issues with lidocaine or epinephrine

What are the post-treatment care instructions?

After your Kybella injections, follow these post-care instructions for optimal recovery:

  • Apply ice packs to the treated area for the first 12 hours (15 minutes every hour)
  • Do not massage the injection site
  • If you can tolerate ibuprofen, take 200 mg three times daily starting on the day of treatment for four days
  • Avoid heavy exercise on the day of treatment
  • Contact your provider if you experience significant swelling, bleeding, pain, dusky discoloration, difficulty swallowing or smiling, or fever

What alternatives to Kybella exist?

Not everyone with submental fullness may benefit from Kybella injections. Alternative options for treatment include:

  • Liposuction
  • Neck lift procedures
  • Platysmoplasty

Your medical director will review these options to determine the best course of action tailored to your needs.

Before undergoing Kybella treatment, you will need to authorize the physician and their staff to perform the injections. You will also consent to the possibility of additional procedures based on your physician's professional judgment during the treatment, as unforeseen conditions may arise.

What should I know about anesthesia and complications?

You may be administered anesthetics deemed necessary for your procedure. Remember that all forms of anesthesia carry risks, including possible complications and rare instances of severe outcomes. It’s crucial to discuss these risks thoroughly with your medical provider to ensure you are fully informed.

Common mistakes

Filling out the Kybella Consent form requires careful attention to detail. One common mistake people make is not disclosing their full medical history. It's crucial to inform the physician of any conditions or medications that could affect the treatment. For instance, failing to mention a history of bleeding disorders or current use of blood thinners could lead to serious complications.

Another frequent oversight is not following the pre-treatment instructions. Many patients overlook the advice to take ibuprofen on the day of treatment if they can tolerate it. Skipping this step can lead to increased discomfort during and after the injections, as the medication helps reduce swelling and pain.

Additionally, patients may misunderstand the significance of side effects listed in the consent form. Some may ignore the potential for issues like difficulty swallowing or swelling, thinking these effects won't apply to them. However, being aware of and acknowledging these risks is vital for understanding what to expect during recovery.

Finally, individuals often fail to read the entire document before signing. The Kybella Consent form contains essential information about the treatment's risks and alternatives. Neglecting to fully grasp these details could lead to unrealistic expectations regarding results and recovery. Being well-informed is essential for making a confident decision involving any medical procedure.

Documents used along the form

When preparing for a Kybella treatment, various forms and documents are often required to ensure patients are informed and prepared. These documents are designed to give clear information about the procedure, outline potential risks, and set expectations for the treatment outcome. Below is a list of six commonly used documents alongside the Kybella Consent form.

  • Medical History Form: This form collects detailed information about the patient's medical background, including previous surgeries, allergies, current medications, and any pre-existing conditions. Understanding a patient's history helps healthcare providers assess the suitability of Kybella for them.
  • Post-Procedure Care Instructions: After treatment, patients receive guidelines on how to care for the injected area. This may include recommendations on using ice packs, avoiding strenuous activities, and recognizing signs of complications that may require medical attention.
  • Financial Agreement: This document outlines payment terms, methods accepted, and any applicable financing options. It ensures that patients are aware of the cost of the procedure and their financial responsibilities before undergoing treatment.
  • Pre-Treatment Instructions: Patients receive specific instructions on how to prepare for the Kybella treatment. This may include dietary recommendations, medication use, and restrictions on certain activities leading up to the appointment.
  • Risk and Benefit Disclosure: This form explains the potential risks and benefits associated with the Kybella treatment. It helps patients understand what to expect and ensures they are fully informed before consenting to the procedure.
  • Release of Information Authorization: Patients may be asked to sign this document to permit their healthcare provider to share information with relevant parties, including insurance companies, for billing and coverage verification purposes.

These documents serve to empower patients by providing essential information about their treatment. Clear communication fosters a positive treatment experience and helps establish trust between patients and healthcare providers.

Similar forms

  • Informed Consent Form for Surgical Procedures: Similar to the Kybella Consent form, this document outlines the nature of a surgical procedure, detailing risks, benefits, and possible alternatives. Both forms aim to ensure that patients understand the procedure and accept associated risks.
  • Laser Hair Removal Consent Form: This form, like the Kybella Consent, informs patients about the treatment process, expected outcomes, and potential side effects. Both documents emphasize the need for patient acknowledgment of risks and preparation prior to the procedure.
  • Botox Consent Form: This consent document shares many similarities with the Kybella Consent form, as it describes the administration process, possible side effects, and post-treatment instructions. Both ensure that patients have realistic expectations about the results.
  • Fillers Consent Form: Much like the Kybella Consent, this document covers details regarding the injection process, expected results, and risks involved. Both forms inform patients about the gradual nature of results and the need for follow-up treatments.
  • Cosmetic Surgery Consent Form: This document is comparable to the Kybella Consent form in that it provides information about the procedure, potential complications, and the importance of patient understanding. Both seek to protect patients through informed consent.
  • Chemical Peel Consent Form: This form outlines the procedure, risks, and post-care instructions similar to the Kybella Consent. Both documents assure that patients are made aware of the recovery process and any side effects associated with treatment.
  • Clinical Trial Consent Form: Though different in context, this form shares the essential goal of ensuring that participants understand the study process, risks, and benefits. The emphasis on informed consent and the potential for unexpected outcomes aligns closely with the Kybella Consent form.

Dos and Don'ts

When filling out the Kybella Consent form, it is essential to approach the process with care. Here are five key recommendations regarding what to do and what to avoid.

  • Do read the entire consent form thoroughly. Ensure that you understand the details of the procedure, including potential risks and side effects.
  • Do communicate openly with your physician. Discuss any medical history, especially related to allergies or previous treatments, that could impact your treatment.
  • Do ensure that you meet all pre-treatment requirements, such as not being pregnant or nursing, before proceeding with the injections.
  • Do ask questions about anything that is unclear in the consent form to ensure you have a full understanding of the matter.
  • Do follow all post-care instructions after the treatment for optimal recovery and results.
  • Don't rush through the consent form. Take your time to absorb the information to make an informed decision.
  • Don't omit any relevant medical information from your physician. Doing so could affect your treatment outcome.
  • Don't disregard the importance of discussing medications. If you are taking blood thinners or other medications, inform your healthcare provider immediately.
  • Don't ignore any severe side effects post-treatment. Seek medical attention if you experience unusual symptoms such as significant swelling or bleeding.
  • Don't overlook the significance of giving consent. Remember that this document is legally binding, so ensure you understand all provisions before signing.

Misconceptions

Understanding the Kybella Consent form is crucial for patients considering this procedure. However, there are several common misconceptions that can cause confusion. Here are some of the most prevalent misunderstandings:

  • Kybella provides immediate results. Many believe that the effects of Kybella will be noticeable right away. In reality, the results develop gradually over the course of up to a month following the treatment.
  • All submental fullness can be treated with Kybella. This is not entirely accurate. Some individuals may not respond favorably to Kybella, meaning alternative treatments might be necessary for optimal results.
  • Once you start Kybella, you will need no further treatments. Achieving the best results often requires a series of injections spaced at least one month apart, as determined by a healthcare professional.
  • There are no side effects associated with Kybella. Like any treatment, Kybella can have side effects, including bruising, swelling, and discomfort. It's essential to discuss these risks with your provider.
  • The consent form is just a formality. The consent form is a vital document that outlines the procedure, risks, and alternatives. It’s important to understand every aspect before proceeding.
  • You can engage in heavy exercise immediately after treatment. Patients are advised to avoid strenuous activity on the day of their treatment to ensure optimal recovery.
  • Every injector is equally skilled. Not all injectors have the same level of experience. It is important to choose a qualified and licensed professional for the procedure to ensure safety and effectiveness.
  • There is no need for post-treatment care. Following the recommended post-care instructions is essential. This includes managing swelling and discomfort effectively to support healing.
  • The procedure is risk-free. While Kybella is FDA approved, there are inherent risks in any medical procedure. Understanding these risks is key to making an informed decision.

Addressing these misconceptions not only enhances understanding but also empowers patients to make informed decisions regarding their health and aesthetic goals. It is always advisable to have an open conversation with a qualified healthcare provider about any concerns or questions. Your well-being is a priority, and clear communications lead to safer outcomes.

Key takeaways

1. Understand Kybella's Purpose: Kybella® is specifically designed to treat submental fullness caused by fat. The treatment is aimed at improving the appearance of the neck area for adults.

2. Recognize the Timeline: Results from Kybella® are not instant. After the first treatment, expect gradual improvement over the following month as fat cells diminish.

3. Prepare for Swelling: Swelling is a common side effect and may occur immediately after the injections and last for several days. Patience is key as your body heals.

4. Follow Pre- and Post-Care Instructions: Be sure to follow the guidance your doctor provides before and after treatment. This may include taking ibuprofen before the procedure and avoiding heavy exercise afterward.

5. Be Aware of Side Effects: Possible side effects include bruising, swelling, and even numbness. If you experience unusual symptoms, such as significant pain or difficulty swallowing, contact your medical team.

6. Acknowledge Alternative Treatments: Not all cases of submental fullness may respond to Kybella®. Discuss other options, like liposuction or a neck lift, with your provider.