aminolevulinic acid
(a-meen-o-lev-yoo-lin-ic a-sid)
Levulan Kerastick

Classification
Therapeutic: none assigned
Pharmacologic: photosensitizers

Pregnancy Category C


Copyright © 2007 by F.A. Davis Company

Indications
Treatment of nonhyperkeratotic actinic keratoses of the face and scalp in conjuction with blue light illumination using the BLU-U Blue Light Photodynamic Therapy Illuminator.

Action
When applied topically, produces an accumulation of protoporphyrin IX, which when exposed to specific wavelengths of light and energy in the presence of oxygen, produces a cytotoxic photodynamic reaction. Therapeutic Effects: Resolution of nonhyperkeratotic actinic keratoses.

Pharmacokinetics
Absorption: Intended for topical application only
Distribution: Unknown
Metabolism and Excretion: Unknown
Half-life: Unknown

TIME/ACTION PROFILE (resolution of keratoses )

ROUTEONSETPEAKDURATION
Topicalunknown4–8 wk*unknown
*May take up to 12 wk


Contraindications/Precautions
Contraindicated in: Hypersensitivity. History of cutaneous photosensitization. Porphyria. Hypersensitivity to porphyrins. Pregnancy or lactation. Children.
Use Cautiously in: Other photodermatoses. Acquired or inherited coagulation defects. Concurrent wafarin therapy.

Adverse Reactions/Side Effects*
*CAPITALS indicate life threatening; underlines indicate most frequent.

Local: burning, edema, pruritus, stinging, oozing , scaling, ulceration.

Interactions
Drug–Drug: Concurrent use of other photosensitizing agents including thiazide diuretics, sulfonylureas, phenothiazines, sulfonamides, or tetracyclines may ↑ intensity of the photosensitizing reaction.

Route/Dosage

Topical (Adults): One application via the Kerastick system (contains 354 mg of aminolevulinic acid), followed 14–18 hr later by blue light illumination.

Availability
Kerastick applicator system: 354 mg aminolevulinic acid/ampule plus 1.5 ml hydroalcoholic solution vehicle.

NURSING IMPLICATIONS


Assessment
Assess skin lesions prior to and periodically during therapy.


Potential Nursing Diagnoses
Impairedskin integrity (Indications).


Implementation
Aminolevulinic acid should applied by a qualified health care professional. Medication should only be applied to actinic keratoses and not perilesional skin, eyes or mucous membranes. Application should involve scalp or face lesions, but not both simultaneously. Frequency of application and light treatment should be one site/eight wk treatment session.
Topical: Aminolevulinic acid is applied in the physician’s office and patient is told to return the following day. To prepare, hold so applicator cap is pointing up. Crush bottom ampule containing solution vehicle by applying finger pressure to lower portion of cardboard sleeve. Crush top ampule containing aminolevulinic acid powder by applying pressure to upper portion of cardboard sleeve. Continue crushing applicator downward, applying pressure to the sleeve. With applicator pointed away from face, shake gently for at least 3 min to completely dissove drug powder in solution vehicle. Remove cap and dab dry applicator tip on a gauze pad until it is uniformly wet with solution. Once application has dried, apply again in same manner. If application is not completed in 2 hr of activation, discard and use new kerastick. Upon return, actinic keratoses will be rinsed with water. Patient will be given goggles to wear as eye protection during blue light therapy. Blue light treatment is applied 14-18 hr after application of medication. Application of light lasts for approximately 17 minutes. Individual kerastick should be used for one patient only.


Patient/Family Teaching
Caution patient to avoid sunlight or bright indoor light (examination lamps, operating room lamps, tanning beds, lights at close proximity) between application and exposure to activating light. Skin will be photosensitive during this period. Exposure may result in stinging and/or burning sensation and may cause erythema and/or edema of the lesions. Protection should include a wide-brimmed hat or similar head covering of light opaque material. Sunscreens will not protect against photosensitivity reactions caused by visible light.
Instruct patient to avoid occlusive dressings; may cause excessive irritation.
Advise patient to keep treated actinic keratoses dry and out of bright light between application and exposure to activating light.
Inform patient that blue light is low intensity and will not heat skin. Inform patient that they may experience tingling, stinging, prickling or burning sensations of the treated lesions. Actinic keratoses and surrounding skin will redden and some scaling and swelling may occur. These lesion changes are temporary and should be completely resolved by 4 wks after treatment.
Instruct patient to contact health care professional if they are unable to return for blue light therapy within 14-18 hr. Caution patient to avoid exposure of photosensitized lesions to sunlight or prolonged or intense light for at least 40 hr. If stinging and/or burning is noted, exposure to light should be reduced.


Evaluation/Desired Outcomes
Resolution of nonhyperkeratotic actinic keratoses.

Copyright © 2007 by F.A. Davis Company