Management of skin toxicity caused by epidermal growth factor receptor inhibitors: an evidence-based implementation

Xiaolu Guo1, Micah D J Peters, Zhenqi Lu

  • 11Department of Nursing, Fudan University Shanghai Cancer Center; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China 2The Joanna Briggs Institute, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.

Abstract

Insights

Implementing evidence-informed practice significantly improved management of skin toxicity from epidermal growth factor receptor inhibitors (EGFRIs). Audits showed high compliance, enhancing patient care and outcomes in chemotherapy departments.

Area of Science:

  • Oncology
  • Pharmacology
  • Evidence-Based Practice

Background:

  • Epidermal growth factor receptor inhibitors (EGFRIs) are targeted therapies for solid tumors, but commonly cause skin toxicity.
  • EGFRI-induced skin reactions can lead to treatment modification, impacting patient quality of life.
  • Effective management of EGFRI skin toxicity requires clinician and patient collaboration.

Purpose of the Study:

  • To enhance the management of skin toxicity associated with EGFRIs.
  • To implement evidence-informed practice within a chemotherapy setting.

Main Methods:

  • Developed evidence-informed recommendations and audit criteria through literature reviews.
  • Assessed current practices via audits involving nurses and patients.
  • Identified barriers and implemented strategies to improve adherence to evidence-based guidelines.

Main Results:

  • Successful implementation of multiple research-to-practice strategies.
  • Significant improvements in compliance with audit criteria observed post-intervention.
  • Achieved 100% compliance for most criteria, demonstrating effective practice change.

Conclusions:

  • Auditing and implementing evidence-informed strategies effectively improved clinical practice.
  • Sustaining these improvements is crucial for optimal patient outcomes.
  • Collaborative management strategies are key to addressing EGFRI-induced skin toxicity.

Related Concept Videos

Clinical Applications of Epidermal Stem Cells01:19

Clinical Applications of Epidermal Stem Cells

Epidermal stem cells (EpiSCs) are mainly located at the basal layer of the epidermis. These cells repair minor injuries of the skin and replace dead skin cells. However, EpiSCs’ cannot heal severe wounds such as major burns or those from diabetes or hereditary disorders. In such cases, culturing the epidermal stem cells from the patient is possible and has yielded successful treatment options, such as laboratory-grown skin grafts. These grafts are synthesized using a patient’s own...
3.3K
Mitogens and the Cell Cycle02:38

Mitogens and the Cell Cycle

Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
8.2K
Renewal of Skin Epidermal Stem Cells01:12

Renewal of Skin Epidermal Stem Cells

The skin is divided into epidermis, dermis, and hypodermis, the skin's outermost, middle, and inner layers. The human epidermal layer regularly undergoes renewal, where old, dead cells are replaced by new cells. Epidermal stem cells or EpiSCs divide and differentiate to restore the lost cells. For the renewal process, some EpiSCs continuously self-renew. In contrast, few others differentiate into transit-amplifying cells, which later form prickle or spinous cells, followed by granular...
3.1K
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase01:11

Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase

Genetic polymorphisms in drug targets have emerged as critical determinants of interindividual variability in drug response and toxicity. Pharmacogenomic investigations increasingly focus on identifying these variations to personalize and optimize therapeutic interventions. A drug target may be a receptor, enzyme, or signaling protein involved in pharmacologic responses or disease-related pathways. While early pharmacogenetic studies focused primarily on drug metabolism, current research...
24
Drug Toxicity: Allergic Reactions01:30

Drug Toxicity: Allergic Reactions

Drug-related allergies are immune-mediated responses triggered by the administration of pharmacological agents. These hypersensitivity reactions are classified based on the immune mechanisms involved. The four primary types—Type I, II, III, and IV—are mediated by different immunological pathways and exhibit distinct clinical manifestations.Type I Hypersensitivity/ IgE-Mediated Reactions: Immunoglobulin E (IgE) immediately mediates Type I hypersensitivity reactions. Upon initial...
26