Informed Consent Form Template for PDO Threads

· 6 min read

Editorial illustration about an informed consent template for PDO threads

PDO (polydioxanone) threads are a procedure with particularities: the material stays inside the skin for a while, the effect has a mechanical and stimulating component, and the possible complications are not the same as with an injectable. The form must reflect that and not be a hasty adaptation of the filler consent form.

The template below is generic, with no brand, no number of threads and no technique. To understand the material, read the entry on PDO, types of PDO threads and complications with PDO threads.

When should you use this template?

Before the procedure, after the medical history and an unhurried conversation about what the thread does and does not do. Give the form to the patient for prior reading, not at the moment they lie down on the table. If the patient already has threads from an earlier time, record it.

How do you adapt it?

  • Describe the area and the type of thread by class, according to your records, without going into technique.
  • Explain that the thread is absorbable and the effect is temporary, with variation between patients. See PDO threads: how long they last and do PDO threads work?.
  • Include the specific complications: skin irregularity, palpable thread, extrusion, nodule and change in sensation. See PDO threads: risks.
  • Record the product and batch in the patient record routine. See the batch record template.
  • Align the aftercare with the post-procedure instructions template for PDO threads.
  • State what is possible in case of dissatisfaction or complication: assessment, adjustment, removal, when indicated.
  • Review with a lawyer and with your professional council's rules.

What can never be missing?

Item Reason
Nature of the procedure and the material The patient understands there is material in the body
Temporary and variable effect Avoids the expectation of a permanent effect
Common effects: pain, swelling, bruising, pulling sensation What a good share of patients notice
Complications: irregularity, asymmetry, palpable thread, infection, nodule, sensation changes Duty to inform
Possibility of removal or correction Approach in case of a problem
Conditions that call for caution The patient's duty to inform
Alternatives, including not treating Free consent
Contact, return visit and warning signs Safety after the procedure
No guarantee of results No promises
Signatures and date Validity of the record

Informed consent form template for PDO threads

Does the form protect you in case of a complication?

It helps show that the patient was informed, but it does not resolve the complication or replace care. Record the occurrence in the patient record, follow the patient closely and document the action taken, including if there was a nodule or granuloma. For the basis of consent, see informed consent, and for organizing safety in the practice, safety and complications in facial harmonization.

Frequently asked questions

What should be in the informed consent form for PDO threads?

What the threads are and how they are placed, the area, the temporary and variable effect, common effects (pain, swelling, bruising), possible complications (irregularities, palpable thread, infection, nodule, change in sensation), alternatives, the absence of any guarantee, aftercare and the professional's contact, with signatures.

What complications are possible with PDO threads?

Those described include skin irregularities or waviness, asymmetry, palpable or visible thread, extrusion, infection, nodule or granuloma and changes in sensation. Frequency varies with the technique and the patient, and complications must be known and disclosed beforehand.

Does a signed form exempt the professional if there is a complication with a PDO thread?

Not automatically. It shows that the patient was informed, but responsibility also depends on the indication, the technique, the follow-up and the care provided. Ask a lawyer to assess the scope of the document.

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