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Delayed Vesicular Urticarial Dermatosis Due to Apixaban
Wendy T Garzon-Siatoya1, Dan Morgenstern-Kaplan1, Karol Avila-Castano1
1Division of Pulmonary, Allergy, and Sleep Medicine, Department of Medicine, Mayo Clinic, Jacksonville, USA.
A woman experienced a non-severe cutaneous adverse drug reaction (cADR) to apixaban, a Factor Xa inhibitor. Diagnosis involved patch testing, highlighting its utility in evaluating such reactions.
Area of Science:
- Pharmacology
- Dermatology
- Immunology
Background:
- Novel oral anticoagulants (NOACs), particularly Factor Xa inhibitors like apixaban, are widely prescribed for thrombosis and atrial fibrillation.
- Cutaneous adverse drug reactions (cADR) are T-cell mediated delayed hypersensitivity responses.
- Evaluating cADR to NOACs presents diagnostic challenges due to a lack of standardized protocols.
Observation:
- A 78-year-old female developed a vesicular-urticated erythematous rash approximately nine days after initiating apixaban for stroke prophylaxis.
- The rash initially appeared on her upper extremity and spread to her face.
- Symptoms improved with hydroxyzine and prednisone, and the patient was switched to warfarin.
Findings:
- Patch testing with apixaban, rivaroxaban, and edoxaban yielded negative results.
- The Naranjo scale indicated a probable drug reaction (score 5-6).
- This case represents the first reported instance of a non-severe cADR to apixaban.
Implications:
- Patch testing, alongside careful clinical evaluation and consideration of alternative anticoagulants, is valuable for diagnosing cADR to Factor Xa inhibitors.
- Further research is needed to establish standardized diagnostic approaches for NOAC-induced cutaneous reactions.
- Prompt recognition and management of cADR are crucial for patient safety and adherence to anticoagulation therapy.
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