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Standardized Informed Consent Form for Clinicians Administering Platelet-Rich Plasma
Satvik N Pai1,2, Naveen Jeyaraman3, Ravichandran Venkatasalam4
1Orthopaedic Surgery, Hospital for Orthopedics, Sports Medicine, Arthritis & Trauma (HOSMAT) Hospital, Bangalore, IND.
Cureus
|May 6, 2024
Summary
A standardized informed consent form for platelet-rich plasma (PRP) injections was developed to address legal concerns. This evidence-based document ensures patient rights and protects healthcare providers in malpractice suits.
Area of Science:
- Orthopedics
- Regenerative Medicine
- Medical Law
Background:
- Informed consent is crucial in medico-legal malpractice cases.
- Lack of a standard informed consent protocol for platelet-rich plasma (PRP) injections poses legal risks.
- Current practices may not adequately protect patients or providers.
Purpose of the Study:
- To develop a standardized, evidence-based informed consent document for PRP injections.
- To mitigate medico-legal risks associated with PRP procedures.
- To enhance patient-provider communication and transparency.
Main Methods:
- Database searches for medico-legal aspects of PRP and informed consent.
- Semi-structured interviews with healthcare providers and PRP recipients.
- Development and legal review of an informed consent document.
Main Results:
- An evidence-based informed consent document for PRP injections was created.
- The document was reviewed by a legal specialist for validity.
- The finalized form was implemented in clinical practice for over a year.
Conclusions:
- A legally valid informed consent form for PRP injections upholds patient rights.
- Standardized documentation promotes open communication and transparency.
- The form serves as a critical defense in potential legal disputes.
