Mosby's 2014 Nursing Drug Reference (321 page)

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

piperacillin/tazobactam (Rx)

(pip′er-ah-sill′in/ta-zoe-bak′tam)

Zosyn

Func. class.:
Antiinfective, broad spectrum

Chem. class.:
Extended-spectrum penicillin, β-lactamase inhibitor

ACTION:

Interferes with cell-wall replication of susceptible organisms; osmotically unstable cell wall swells and bursts from osmotic pressure; tazobactam is a β-lactamase inhibitor that protects piperacillin from enzymatic degradation

USES:

Moderate to severe infections: piperacillin-resistant, β-lactamase–producing strains causing infections in respiratory, skin, urinary tract, bone, gonorrhea, pneumonia; effective for resistant
Staphylococcus aureus
, resistant
Escherichia coli, Bacteroides fragilis, Bacteroides ovatus, Bacteroides thetaiotaomicron, Bacteroides vulgatus, Haemophilus influenzae

CONTRAINDICATIONS:

Hypersensitivity to penicillins; neonates; carbapenem allergy

Precautions:
Pregnancy (B), breastfeeding, renal insufficiency in children, hypersensitivity to cephalosporins, CHF, seizures, GI disease, electrolyte imbalances

DOSAGE AND ROUTES
Calculator
Nosocomial pneumonia

• Adult:
IV
4.5 g q6hr or 3.375 g q4hr with an aminoglycoside or antipseudomonal fluoroquinolone × 1-2 wk; continue aminoglycoside only if
Pseudomonas aeruginosa
is isolated

Other infections

• Adult:
IV INF
6-12 g/day given 2.25 g q8hr to 3.375 g q6hr over 30 min × 7-10 days

Appendicitis/peritonitis

• Child ≥40 kg (88 lb):
IV
3.375 g q6hr × 7-10 days

• Child ≥9 mo and <40 kg:
IV
100 mg/kg (piperacillin)/kg q8hr × 7-10 days

• Infant 2 mo to <9 mo:
IV
80 mg (piperacillin) q8hr × 7-10 days

Renal dose

• Adult:
IV
CCr 20-40 ml/min, give 3.375 g q6hr (nosocomial pneumonia); give 2.25 g q6hr (all other indications); CCr <20 ml/min, give 2.25 g q6hr (nosocomial pneumonia), give 2.25 g q8hr (all other indications)

Available forms:
Powder for inj 2 g piperacillin/0.25 g tazobactam, 3 g piperacillin/0.375 g tazobactam, 4 g piperacillin/0.5 g tazobactam, 36 g piperacillin/4.5 g tazobactam

Administer:

• Separate aminoglycoside from piperacillin to avoid inactivation

• 
Product after C&S is complete

Intermittent IV INF route

• 
Reconstitute each 1 g of product/5 ml 0.9% NaCl for inj or sterile water for inj, dextrose 5%; shake well; further dilute in ≥50 ml compatible IV sol, run as int inf over ≥30 min

Y-site compatibilities:
Alfentanil, allopurinol, amifostine, amikacin, aminocaproic acid, aminophylline, amphotericin B lipid complex, amphotericin B liposome, anidulafungin, atenolol, aztreonam, bivalirudin, bleomycin, bumetanide, buprenorphine, busulfan, butorphanol, calcium acetate/chloride/gluconate, CARBOplatin, carmustine, cefepime, chloramphenicol, cimetidine, clindamycin, cyclophosphamide, cycloSPORINE, cytarabine, DACTINomycin, DAPTOmycin, dexamethasone, dexrazoxane, diazepam, digoxin, diphenhydrAMINE, DOCEtaxel, DOPamine, doxacurium, enalaprilat, ePHEDrine, EPINEPHrine, eptifibatide, erythromycin, esmolol, etoposide, fenoldopam, fentaNYL, floxuridine, fluconazole, fludarabine, fluorouracil, foscarnet, fosphenytoin, furosemide, gallium, granisetron, heparin, hydrocortisone, HYDROmorphone, ifosfamide, isoproterenol, ketorolac, lansoprazole, leucovorin, lidocaine, linezolid, LORazepam, magnesium sulfate, mannitol, mechlorethamine, melphalan, meperidine, mesna, metaraminol, methotrexate, methylPREDNISolone, metoclopramide, metoprolol, metroNIDAZOLE, milrinone, morphine, naloxone, nitroglycerin, nitroprusside, norepinephrine, octreotide, ondansetron, oxytocin, PACLitaxel, palonosetron, pamidronate, pancuronium, pantoprazole, PEMEtrexed, PENTobarbital, PHENobarbital, phenylephrine, plicamycin, potassium chloride/phosphates, procainamide, ranitidine, remifentanil, riTUXimab, sargramostim, sodium acetate/bicarbonate/phosphates, succinylcholine, SUFentanil, sulfamethoxazole-trimethoprim, tacrolimus, teniposide, theophylline, thiotepa, tigecycline, tirofiban, trimethobenzamide, vasopressin, vinBLAStine, vinCRIStine, voriconazole, zidovudine, zoledronic acid

SIDE EFFECTS

CNS:
Lethargy, hallucinations, anxiety, depression, twitching, insomnia, headache, fever, dizziness,
seizures,
vertigo

CV:
Cardiac toxicity

GI:
Nausea, vomiting, diarrhea;
increased AST, ALT; abdominal pain, glossitis,
pseudomembranous colitis,
constipation

GU:
Oliguria, proteinuria, hematuria,
vaginitis, moniliasis
,
glomerulonephritis, renal failure

HEMA:
Anemia, increased bleeding time,
bone marrow depression, agranulocytosis, hemolytic anemia

INTEG:
Rash, pruritus,
exfoliative dermatitis

META:
Hypokalemia, hypernatremia

SYST:
Serum sickness, anaphylaxis, Stevens-Johnson syndrome

PHARMACOKINETICS

Half-life 0.7-1.2 hr; excreted in urine, bile, breast milk; crosses placenta; 33% bound to plasma proteins

IV:
Peak completion of IV

INTERACTIONS

Increase:
effect of neuromuscular blockers, oral anticoagulants, methotrexate

Increase:
piperacillin concentrations—aspirin, probenecid

Decrease:
antimicrobial effect of piperacillin—tetracyclines, aminoglycosides IV

Drug/Lab Test

Increase:
platelet count, eosinophilia, neutropenia, leukopenia, serum creati
nine, PTT, AST, ALT, alk phos, bilirubin, BUN, electrolytes

Decrease:
Hct, Hgb, electrolytes

False positive:
urine glucose, urine protein, Coombs’ test

NURSING CONSIDERATIONS
Assess:

• 
Infection:
temp, stools, urine, sputum, wounds

• 
I&O ratio; report hematuria, oliguria because penicillin in high doses is nephrotoxic; maintain hydration unless contraindicated

• 
Hepatic studies: AST, ALT before treatment and periodically thereafter

• 
Blood studies: WBC, RBC, Hct, Hgb, bleeding time before treatment and periodically thereafter; serum potassium

• 
Renal studies: urinalysis, protein, blood, BUN, creatinine before treatment and periodically thereafter

• 
C&S before product therapy; product may be given as soon as culture is taken

• Pseudomembranous colitis:
diarrhea, bloody stools, fever, abdominal cramps; may occur ≤2 mo after treatment; bowel pattern before and during treatment

• 
Skin eruptions after administration of penicillin to 1 wk after discontinuing product

• 
Respiratory status: rate, character, wheezing, tightness in chest

• Anaphylaxis:
wheezing, laryngeal edema, rash, itching; discontinue product, have emergency equipment nearby

Perform/provide:

• 
Adequate intake of fluids (2 L) during diarrhea episodes

• 
Discard after 24 hr if stored at room temp or after 48 hr if refrigerated; use single-dose vials immediately after reconstitution; stable in ambulatory IV pump for 12 hr

Evaluate:

• 
Therapeutic response: absence of fever, purulent drainage, redness, inflammation; culture shows decreased organisms

Teach patient/family:

• 
That culture may be taken after completed course of medication

• To report sore throat, fever, fatigue (superinfection); CNS effects (anxiety, depression, hallucinations, seizures);
pseudomembranous colitis:
fever, diarrhea with blood, pus, mucous

• 
To wear or carry emergency ID if allergic to penicillins

• 
To notify nurse of diarrhea

TREATMENT OF OVERDOSE:

Withdraw product, maintain airway, administer EPINEPHrine, aminophylline, O
2
, IV corticosteroids for anaphylaxis

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

pirbuterol (Rx)

(peer-byoo′ter-ole)

Maxair

Func. class.:
Bronchodilator

Chem. class.:
β-Adrenergic agonist

ACTION:

Causes bronchodilation with little effect on heart rate by action on β-receptors, causing increased cAMP and relaxation of smooth muscle

USES:

Reversible bronchospasm (prevention, treatment) including asthma; may be given with theophylline or steroids

CONTRAINDICATIONS:

Hypersensitivity to sympathomimetics, tachycardia

Precautions:
Pregnancy (C), breast-feeding, cardiac disorders, hyperthyroidism, hypertension, diabetes mellitus, prostatic hypertrophy

DOSAGE AND ROUTES
Calculator

• Adult and child
>
12 yr:
INH 1-2 puffs (0.4 mg) q4-6hr; max 12 INH/day

Available forms:
Aerosol delivery 0.2 mg pirbuterol/actuation

Administer:

• 
After shaking; exhale; place mouthpiece in mouth; inhale slowly; hold breath; remove; exhale slowly

• 
Gum, sips of water for dry mouth

SIDE EFFECTS

CNS:
Tremors, anxiety, insomnia, headache, dizziness, stimulation, restlessness, hallucinations, drowsiness, irritability

CV:
Palpitations, tachycardia, hypertension, angina, hypotension, dysrhythmias

EENT:
Dry nose and mouth, irritation of nose, throat

GI:
Gastritis, nausea, vomiting, anorexia

MS:
Muscle cramps

RESP:
Paradoxical bronchospasm,
dyspnea, coughing

PHARMACOKINETICS

INH:
Onset 3 min, peak ½-1 hr, duration 5 hr, terminal half-life 2 hr

INTERACTIONS

 
Hypertensive crisis: MAOIs

Increase:
action of other aerosol bronchodilators

Increase:
pirbuterol action—tricyclics, antihistamines, levothyroxine

Decrease:
pirbuterol action—β-blockers

Drug/Herb

Increase:
action of both—cola nut, guarana, yerba maté

Increase:
effect—green tea (large amounts), guarana

NURSING CONSIDERATIONS
Assess:

• 
Respiratory function: vital capacity, forced expiratory volume, ABGs, B/P, lung sounds, pulse, characteristics of sputum

 
Paradoxical bronchospasm, that can occur rapidly, hold product, notify prescribeer

Perform/provide:

• 
Storage in light-resistant container; do not expose to temperatures over 86° F (30° C)

• 
Fluid intake >2 L/day to liquefy thick secretions

Evaluate:

• 
Therapeutic response: absence of dyspnea, wheezing over 1 hr

Teach patient/family:

• 
Not to use OTC medications; extra stimulation may occur

• 
Use of inhaler; review package insert with patient

• 
To avoid getting aerosol in eyes

• 
Actuator is for Maxair autoinhaler; do not use with other inhaler canister

• 
About all aspects of product; avoid smoking, smoke-filled rooms, persons with respiratory infections

• 
To keep fluid intake >2 L/day to liquefy thick secretions

TREATMENT OF OVERDOSE:

Administer a β-adrenergic blocker

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