Mosby's 2014 Nursing Drug Reference (407 page)

BOOK: Mosby's 2014 Nursing Drug Reference
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treprostinil (Rx)

(treh-prah′stin-ill)

Remodulin, Tyvaso

Func. class.:
Antiplatelet agent

Chem. class.:
Tricyclic benzidine prostacyclin analog

ACTION:

Direct vasodilation of pulmonary, systemic arterial vascular beds; inhibition of platelet aggregation

USES:

Pulmonary arterial hypertension (PAH) NYHA class II through IV

Unlabeled uses:
Pulmonary arterial hypertension in children/adolescents, pediatric patients transitioning from epoprostenol to treprostinil, claudication

CONTRAINDICATIONS:

Hypersensitivity to this product, other prostacyclin analogs

Precautions:
Pregnancy (B), breastfeeding, children, geriatric patients, past renal/hepatic disease, thromboembolic disease, abrupt discontinuation, IV administration

DOSAGE AND ROUTES
Calculator
Pulmonary arterial hypertension (who group 1)

• Adult:
SUBCUT INF
1.25 ng/kg/min by
CONT INF,
may reduce to 0.625 ng/kg/min if not tolerated; may increase by 1.25 ng/kg/min q wk for first 4 wk then 2.5 ng/kg/min/wk for remainder of inf;
ORAL INH
3 breaths via Tyvaso inh system qid

Hepatic dose

• Adult:
SUBCUT INF
0.625 ng/kg ideal body weight/min; increase cautiously

Available forms:
Inj 1, 2.5, 5, 10 mg/ml; neb sol 1.74 mg/2.9 ml

Administer:

• 
Sudden decreased doses, abrupt withdrawal may worsen pulmonary arterial hypertension symptoms

SUBCUT route

• 
By continuous inf

• 
No dilution required

Oral INH route

• 
Avoid skin, eyes; do not take orally; use Tyvaso Inhalation System only

• 
Patient should have backup Optineb-ir device to avoid interruptions

• 
Follow instructions for use, cleaning

• 
Do not mix with other medications in Optineb-ir device

• 
Twist off cap, squeeze total contents into medicine cup; vol is sufficient for 4 treatments

Continuous IV INF route

• 
By surgically placed CV catheter using ambulatory inf pump

• 
IV pump, product, patient education can be obtained from Priority Healthcare in United States

• 
Must be diluted with sterile water for inj or 0.9% NaCl

• 
Conc should be calculated using this formula: diluted conc = [dose (ng/kg/min) × weight (kg) × 0.00006] / inf rate (ml/hr)]

SIDE EFFECTS

CNS:
Dizziness, headache, syncope

CV:
Vasodilation, hypotension, edema, right ventricular heart failure

GI:
Nausea,
diarrhea

INTEG:
Rash
, pruritus

OTHER:
Jaw pain, cough, throat irritation

SYST:
Inf site reactions, pain; increased risk for infection

PHARMACOKINETICS

Metabolized by liver; excreted in urine, feces; terminal half-life 2-4 hr; 90% protein binding

INTERACTIONS

• 
Excessive hypotension: diuretics, antihypertensives, vasodilators, MAOIs, β-blockers, calcium channel blockers

Increase:
bleeding tendencies—anticoagulants, aspirin, NSAIDs, thrombin inhibitors, SSRIs

NURSING CONSIDERATIONS
Assess:

• 
Hypertension:
monitor B/P, baseline and periodically

• 
Hepatic studies: AST, ALT, bilirubin, creatinine with long-term therapy

 
Blood studies: CBC; CBC q2wk × 3 mo, Hct, Hgb, PT with long-term therapy, ABGs

 
Bleeding time at baseline, throughout treatment; levels may be 2-5× normal limit

Evaluate:

• 
Avoid abrupt discontinuation

• 
Therapeutic response: decreased pulmonary arterial hypertension (PAH)

Teach patient/family:

• 
That blood work will be necessary during treatment, that treatment may last for years

• 
To report side effects such as diarrhea, skin rashes

• 
That therapy will be needed for prolonged periods of time, sometimes years

• 
To prevent infection, aseptic technique must be used for preparation, administration of treprostinil

• 
That there are many product, herbal interactions

• 
About signs, symptoms of bleeding; blood in urine, stools

• 
How to use inhaled solution, how to care for equipment

Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

tretinoin (vit A acid, retinoic acid) (Rx)

(tret′i-noyn)

Avita, Renova, Retin-A, Retin-A Micro, Stieva-A

Func. class.:
Vit A acid, acne product; antineoplastic (miscellaneous)

Chem. class.:
Tretinoin derivative

ACTION:

(Topical) Decreases cohesiveness of follicular epithelium, decreases microcomedone formation; (PO) induces maturation of acute promyelocytic leukemia, exact action is unknown

USES:

(Topical) Acne vulgaris (grades 1-3); (PO) acute promyelocytic leukemia, facial wrinkles, photoaging

Unlabeled uses:
Acne rosacea, actinic keratosis, ichthyosis, Kaposi’s sarcoma, keloids, keratosis follicularis, melasma

CONTRAINDICATIONS:

Hypersensitivity to retinoids or sensitivity to parabens

 

Black Box Warning:

Pregnancy (D) (PO)

Precautions:
Pregnancy (C) (topical), breastfeeding, eczema, sunburn, sun exposure

 

Black Box Warning:

Rapid-evolving leukocytosis, respiratory compromise, acute promyelocytic leukemia differentiation syndrome

DOSAGE AND ROUTES
Calculator

• Adult and child:
TOP
cleanse area, apply 0.025%-0.1% cream or 0.05% liquid gel at bedtime, cover lightly

Promyelocytic leukemia

• Adult:
PO
45 mg/m
2
/day given as 2 evenly divided doses until remission, discontinue treatment 30 days after remission or 90 days of treatment, whichever is first

Available forms:
Cream 0.01%, 0.02%, 0.025%, 0.05%, 0.1%; gel 0.01%, 0.025%, 0.04%, 0.05%, 0.1%; liquid 0.05%; caps 10 mg

Administer:
Topical route

• 
Once daily before bedtime; cover area lightly using gauze; use gloves to apply

SIDE EFFECTS
Oral

CNS:
Headache, fever, sweating
, fatigue

CV:
Cardiac dysrhythmias, pericardial effusion

GI:
Nausea, vomiting
,
hemorrhage,
abdominal pain, diarrhea, constipation, dyspepsia, distention, hepatitis

Topical

INTEG:
Rash, stinging, warmth, redness, erythema, blistering, crusting, peeling, contact dermatitis, hypo/hyperpigmentation, dry skin, pruritus, scaly skin, retinoic acid syndrome (RAS)

META:
Hypercholesterolemia, hypertriglyceridemia

RESP:
Pneumonia, upper respiratory tract disease

PHARMACOKINETICS

PO:
Terminal half-life 0.5-2 hr

TOPICAL:
Poor systemic absorption

INTERACTIONS

• 
Use with caution: medicated, abrasive soaps; cleansers that have a drying effect; products with high conc of alcohol astringents (topical)

Increase:
peeling—medication containing agents such as sulfur, benzoyl peroxide, resorcinol, salicylic acid (topical)

Increase:
plasma concentrations of tretinoin—ketoconazole (PO)

 
Increase:
ICP, risk of pseudotumor cerebri—tetracyclines; do not use together

Increase:
photosensitivity—retinoids, quinolones, phenothiazines, sulfonamides, sulfonylureas, thiazide diuretics

Increase:
thrombotic complications—aninocaproic acid, aprotinin, tranexamic acid

Drug/Lab Test

Increase:
AST, ALT

NURSING CONSIDERATIONS
Assess:
Topical route

• 
Area of body involved, what helps or aggravates condition; cysts, dryness, itching; lesions may worsen at beginning of treatment

PO route

• 
Hepatic function, coagulation, hematologic parameters; also cholesterol, triglycerides

Perform/provide:
Topical route

• 
Storage at room temp

• 
Handwashing after application

Evaluate:

• 
Therapeutic response: decrease in size, number of lesions

Teach patient/family:
Topical route

• 
To avoid application on normal skin; to avoid getting cream in eyes, nose, other mucous membranes; not to use product on areas with cuts, scrapes

• 
To use cream/gel by applying a thin layer to affected skin; to rub gently; to use liquid; to apply with fingertip or cotton swab

• 
To avoid sunlight, sunlamps; to use protective clothing, sunscreen

• 
That treatment may cause warmth, stinging; that dryness, peeling will occur

• 
That cosmetics may be used over product; not to use shaving lotions

• 
That rash may occur during first 1-3 wk of therapy

• 
That product does not cure condition, only relieves symptoms

• 
That therapeutic results may be seen in 2-3 wk but may not be optimal until after 6 wk

PO route

 

Black Box Warning:

To notify prescriber if pregnancy is planned or suspected; pregnancy (D) PO

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