Mosby's 2014 Nursing Drug Reference (317 page)

BOOK: Mosby's 2014 Nursing Drug Reference
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Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

pentoxifylline (Rx)

(pen-tox′ih-fill-in)

Trental

Func. class.:
Hemorheologic agent

Chem. class.:
Dimethylxanthine derivative

ACTION:

Decreases blood viscosity, stimulates prostacyclin formation, increases blood flow by increasing flexibility of RBCs; decreases RBC hyperaggregation; reduces platelet aggregation, decreases fibrinogen concentration

USES:

Intermittent claudication related to chronic occlusive vascular disease

Unlabeled uses:
Behçet’s syndrome, Kawasaki disease to reduce coronary artery lesions, diabetic neuropathies, sickle cell anemia

CONTRAINDICATIONS:

Hypersensitivity to this product or xanthines, retinal/cerebral hemorrhage

Precautions:
Pregnancy (C), breastfeeding, children, angina pectoris, impaired renal function, recent surgery, peptic ulceration, cardiac disease, bleeding disorders

DOSAGE AND ROUTES
Calculator

• Adult:
PO
400 mg tid with meals, may decrease to bid if side effects occur; must be taken for ≥8 wk for maximal effect

Behçet’s syndrome (unlabeled)

• Adult:
PO
300 mg bid × 2 wk then 300 mg/day

Acute claudication in sickle cell disease/diabetic neuropathy (unlabeled)

• Adult:
PO
400 mg tid

Kawasaki disease (unlabeled)

• Child:
PO
20 mg/kg/day in 3 divided doses with aspirin and IVIG

Available forms:
Cont rel tabs 400 mg; ext rel tabs 400 mg

Administer:

• 
Do not break, crush, or chew ext rel tabs

• 
With meals to prevent GI upset

SIDE EFFECTS

CNS:
Headache
, anxiety,
tremors
, confusion,
dizziness

GI:
Dyspepsia, nausea, vomiting

PHARMACOKINETICS

PO:
Peak 2-4 hr, half-life 1/2-1 hr, degradation in liver, excreted in urine

INTERACTIONS

Increase:
bleeding risk—warfarin, abciximab, eptifibatide, tirofiban, ticlopidine, clopidogrel, thrombin inhibitor

Increase:
theophylline level—theophylline

Increase:
hypotension—antihypertensives, nitrates

Increase:
pentoxifylline—cimetidine, ciprofloxacin

NURSING CONSIDERATIONS
Assess:

• 
B/P, respirations of patient also taking antihypertensives; intermittent claudication at baseline and throughout

• 
PT, Hgb, Hct in patients at risk for hemorrhage

• 
Serum creatinine/BUN

Evaluate:

• 
Therapeutic response: decreased pain, cramping, increased ambulation

Teach patient/family:

• 
That therapeutic response may take 2-4 wk, 8-12 wk to reach full benefit

• 
To observe feet for arterial insufficiency

• 
To wear cotton socks, well-fitted shoes; not to go barefoot

• 
To watch for bleeding, bruises, petechiae, epistaxis

• 
To avoid smoking to prevent blood vessel constriction

• 
That there are many drug, herb interactions

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

perindopril (Rx)

(per-in′doe-pril)

Aceon, Coversye

Func. class.:
Antihypertensive

Chem. class.:
Angiotensin-converting enzyme inhibitor

ACTION:

Selectively suppresses the renin-angiotensin-aldosterone system; inhibits ACE; prevents the conversion of angiotensin I to angiotensin II and the dilation of arterial and venous vessels

USES:

Hypertension, stable coronary artery disease

Unlabeled uses:
Heart failure

CONTRAINDICATIONS:

Hypersensitivity, history of angioedema

 

Black Box Warning:

Pregnancy (D)

Precautions:
Breastfeeding, renal disease, hyperkalemia, hepatic failure, dehydration, bilateral renal artery stenosis, cough, angioedema, severe CHF

DOSAGE AND ROUTES
Calculator
Hypertension

• Adult:
PO
4 mg/day, may increase or decrease to desired response, range 4-8 mg/day; may give in 2 divided doses or as single dose, max 16 mg/day

Patients on diuretics

• Adult:
PO
2-4 mg/day in 1-2 divided doses, range 4-8 mg/day

Stable CAD

• Adult:
PO
4 mg/day × 2 wk then increase as tolerated to 8 mg/day

Renal dose

• Adult:
PO
CCr 16-29 ml/min, 2 mg every other day; CCr 30-59 ml/min, 2 mg/day

Available forms:
Tabs scored 2, 4, 8 mg

Administer:

• 
As single dose or in 2 divided doses, without regard to meals

SIDE EFFECTS

CNS:
Insomnia, dizziness
, paresthesias, headache, fatigue, anxiety, depression

CV:
Hypotension
, chest pain, tachycardia, dysrhythmias, syncope

EENT:
Tinnitus;
visual changes; sore throat; double vision; dry, burning eyes

GI:
Nausea, vomiting, colitis, cramps, diarrhea, constipation, flatulence, dry mouth, loss of taste

GU:
Proteinuria, renal failure,
increased frequency of polyuria or oliguria

HEMA:
Agranulocytosis, neutropenia

INTEG:
Rash, purpura, alopecia, hyperhidrosis

META:
Hyperkalemia

RESP:
Dyspnea,
dry cough
, crackles

SYST:
Angioedema

PHARMACOKINETICS

Bioavailability 75%; peak 1 hr parent product, 3-7 hr prodrug; protein binding 68%; metabolized by liver (active metabolite perindoprilat); half-life 0.8-10 hr; excreted in urine

INTERACTIONS

Increase:
effects of neuromuscular blocking agents, antihypertensives, lithium

Increase:
antihypertensive effect—diuretics, NSAIDs

Increase:
hypersensitivity—allopurinol

Increase:
severe hypotension—diuretics, other antihypertensives

Increase:
hyperkalemia—salt substitutes, potassium-sparing diuretics, potassium supplements

Decrease:
effects of NSAIDs

Decrease:
antihypertensive effect—NSAIDs, salicylates

Drug/Herb

Increase:
antihypertensive effect—hawthorn

Decrease:
antihypertensive effect—ephedra

Drug/Lab Test

Interference:
glucose/insulin tolerance tests

NURSING CONSIDERATIONS
Assess:

• 
Hypertension:
B/P, pulse q4hr; note rate, rhythm, quality

• 
Electrolytes: K, Na, Cl during 1st 2 wk of therapy

• 
Baselines of renal, hepatic studies before therapy begins, 1 wk into therapy

• 
Skin turgor, dryness of mucous membranes for hydration status, dry mouth

• 
CHF:
edema, dyspnea, wet crackles

• 
Angioedema:
facial swelling, urticaria; product should be discontinued, may be more common in African Americans

Evaluate:

• 
Therapeutic response: decreased B/P

Teach patient/family:

• 
Not to use OTC (cough, cold, allergy) products unless directed by prescriber; to avoid salt substitutes

• 
To avoid sunlight or to wear sunscreen for photosensitivity

• 
To comply with dosage schedule, even if feeling better

• 
To notify prescriber of mouth sores, sore throat, fever, swelling of hands or feet, irregular heartbeat, chest pains, signs of angioedema

• 
That excessive perspiration, dehydration, vomiting, diarrhea may lead to fall in B/P; to consult prescriber if these occur

• 
That product may cause dizziness, fainting; that lightheadedness may occur during 1st few days of therapy

• 
That product may cause skin rash or impaired perspiration; that angioedema may occur and to discontinue product if it occurs

• 
Not to discontinue product abruptly

• 
To rise slowly to sitting or standing position to minimize orthostatic hypotension

 

Black Box Warning:

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

TREATMENT OF OVERDOSE:

Lavage, IV atropine for bradycardia, IV theophylline for bronchospasm, digoxin, O
2
, diuretic for cardiac failure

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