Minimizing Medical Error-Related Adverse Events With Platelet-Rich Plasma: A Protocolized Approach to Safety

September 2024 | Volume 23 | Issue 9 | 790 | Copyright © September 2024


Published online September 1, 2024

doi:10.36849/JDD.8166

Rahul Nanda MDa, Joel L. Cohen MD FAAD FACMSb,c

aDivision of Dermatology, McGill University, Montréal, Québec, Canada
bAboutSkin Dermatology and Derm Surgery, Greenwood Village, CO
cUniversity of California Irvine Department of Dermatology, Irvine, CA

Abstract
Platelet-rich concentrates (PRCs), derived from a patient's blood, are being used in various fields of medicine, including dermatology, for an increasing number of indications. Although considered a generally safe procedure for dermatologic indications, there have been reports in the last several years linking this treatment to cases of blood-borne infections including HIV and hepatitis.1 Patient safety should always be the primary focus for physicians and other health care professionals, and systems-based protocols should exist within care settings to minimize errors. Herein, we review our protocol to decrease the risk of complications related to transmission of blood-borne infections and other medical errors related to PRCs.

J Drugs Dermatol. 2024;23(9)790-791. doi:10.36849/JDD.8166

INTRODUCTION

Platelet-rich concentrates (PRCs), including both platelet-rich plasma (PRP) and platelet-rich fibrin (PRF), have been increasing in popularity, with uses extending to various fields including orthopedics, dentistry, aesthetics, and dermatology. These concentrates are an autologous serum and contain platelets, growth factors, and fibrin. PRP specifically has evolved as a treatment modality with numerous uses in the field of dermatology, including alopecia, skin rejuvenation, scarring, pigmentary disorders, and wound healing, among others. Combined use has been reported for synergistic benefits along with various techniques, including lasers, microneedling, dermal fillers, and autologous fat grafting.2

BACKGROUND

Given the autologous nature of PRCs, the safety profile of PRCs is excellent, which likely contributes to their increasing popularity, especially in dermatology. The majority of adverse events are localized, including injection-site pain, bruising, and edema, with other complications being uncommon or rare.3 However, a review of the PubMed database (including search terms "platelet-rich concentrates," "platelet-rich plasma," "platelet-rich fibrin," "HIV," "Hepatitis B" and "Hepatitis C") revealed no reported cases of HIV, hepatitis B or hepatitis C in association with PRCs at the time of query (August 31st, 2023). Nevertheless, news outlets have reported cases of these blood-borne viruses related to the administration of PRP in the United States,1 resulting potentially from medical errors or negligence/lack of safety protocols (or both).

Patient safety and minimization of medical errors are at the center of clinical medicine. Medical errors tend to occur from the convergence of different contributory factors. Although human factors are often implicated, blaming individuals does not address nor prevent the errors from being repeated. Instead, there is a trend towards a systems-based approach, whereby care facilities recognize the potential for errors and focus on designing systems where errors are less likely to occur, along with a just culture, where workers are motivated to engage in the prevention of errors.4  

Safety Approach for PRP
Below, we describe the various steps taken at our center to minimize errors during the administration of PRCs (PRP specifically), keeping a systems-based approach to patient safety in mind. Specifically, we review the protocol we use to minimize medical error-related adverse events. Two checklists, described below (Checklist Part I and Checklist Part II), are used as part of our protocol. Evidence supports the use of checklists for improving patient safety in healthcare settings, while reducing the incidence of adverse events, leading to improved communication between staff members and importantly, minimizing human error.5

Prior to administration of PRP, the following are reviewed with the patient by the treating physician: the clinical indication, the evidence for PRP treatment as well as reasonable alternatives. Contraindications are reviewed on intake form (Checklist Part I) and all questions are reviewed once again by the physician.