Mosby's 2014 Nursing Drug Reference (280 page)

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

nafcillin (Rx)

(naf-sill′in)

Func. class.:
Antiinfective, broad-spectrum

Chem. class.:
Penicillinase-resistant penicillin

ACTION:

Bacteriocidal, interferes with cell wall replication of susceptible organisms; cell lysis mediated by cell wall autolytic enzymes

USES:

Effective for gram-positive cocci
(Staphylococcus aureus, Streptococcus viridans, Streptococcus pneumoniae)
, infections caused by penicillinase-producing
Staphylococcus

CONTRAINDICATIONS:

Hypersensitivity to penicillins or corn

Precautions:
Pregnancy (B), breastfeeding, neonates; hypersensitivity to cephalosporins or carbapenems; GI disease, asthma

DOSAGE AND ROUTES
Calculator

• Adult:
IV
500-2000 mg q4hr

• Child and infant >1 mo:
IV
50-200 mg/kg/day in divided doses q4-6hr

• Neonates >7 days (weight >2000 g):
IV
25 mg/kg q6hr

• Neonates ≤7 days (weight <2000 g):
IV
25 mg/kg q8hr

Meningitis

• Adult:
IV
100-200 mg/kg/day in divided doses q4-6hr, max 12 g/day

• Neonates >7 days (weight >2000 g):
IV
50 mg/kg q6hr

• Neonates ≤7 days (weight <2000 g):
IV
50 mg/kg q12hr

Available forms:
Powder for inj 1, 2 g, premixed or Add-Vantage vials

Administer:

• 
Product after C&S has been drawn, begin therapy while waiting for results

IM route

• 
Reconstitute vials: add 1.7 (1.8 nafcil), 3, 4, or 6.4 ml (6.6 ml NaCl) (sterile water for inj, 0.9% NaCl, bacteriostatic water for inj with benzyl alcohol or parabens) to vials with 1 g, 2 g of nafcillin, respectively (250 mg/ml)

• 
No further dilution needed; after reconstitution, inject in deep muscle mass

IV route

• 
Reconstitute vials: add 1.7 (1.8 nafcil), 3, 4, or 6.4 ml (6.6 ml NaCl) sterile water for inj, 0.9% NaCl, bacteriostatic water for inj with benzyl alcohol or parabens) to vials with 1 g, 2 g of nafcillin, respectively (250 mg/ml)

• 
Nallpen piggyback units:
reconstitute 1 or 2 g with 50-100 ml or 99 ml, respectively, of sterile water for inj, 0.45% NaCl, 0.9% NaCl

• 
Unipen piggyback units:
reconstitute according to manufacturer

Direct intermittent IV INJ route

• 
Further dilute reconstituted sol in 15-30 ml sterile water inj, 0.45% NaCl, 0.9% NaCl; inj slowly over 5-10 min into tubing of free-flowing compatible IV solution

Intermittent IV INF route

• 
Vials, further dilute reconstituted sol to 2-40 mg/ml for peripheral vein inf ≤20 mg/ml (preferred); piggyback unit, no further dilution needed; infuse ≥30-60 min, make sure entire dose is given before ≥10% of sol is inactivated

Y-site compatibilities:
Acyclovir, atropine, cyclophosphamide, diazepam, enalaprilat, esmolol, famotidine, fentaNYL, fluconazole, foscarnet, heparin, HYDROmorphone, magnesium sulfate, morphine, perphenazine, propofol, theophylline, zidovudine

SIDE EFFECTS

CNS:
Lethargy, hallucinations, anxiety, depression, twitching,
coma, seizures

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

GU:
Oliguria,
proteinuria, hematuria,
vaginitis, moniliasis,
glomerulonephritis, interstitial nephritis

HEMA:
Anemia, increased bleeding time,
bone marrow depression, neutropenia

INTEG:
Tissue necrosis, extravasation injury at inj site

SYST:
Anaphylaxis, serum sickness, Stevens-Johnson syndrome

PHARMACOKINETICS

Half-life 1 hr; metabolized by liver; excreted in bile, urine 90% protein bound

INTERACTIONS

• 
Avoid use with tetracyclines

Increase:
nafcillin concentrations—probenecid

Decrease:
effect of cycloSPORINE—warfarin

Decrease:
nafcillin effect—chloramphenicol, macrolides, sulfonamides, tetracyclines, aminoglycosides

Drug/Food

Decrease:
absorption—food, carbonated drinks, citrus fruit juices

Decrease:
Hgb/HcT, neutrophils

Drug/Lab Test

False positive:
urine glucose, urine protein

NURSING CONSIDERATIONS
Assess:

• 
I&O ratio; report hematuria, oliguria, high doses are nephrotoxic

• 
Pseudomembranous colitis:
assess for diarrhea, abdominal pain, fever, fatigue, anorexia; possible anemia, elevated WBC, low serum albumin; stop product; usually either vancomycin or IV metroNIDAZOLE given

• 
Hepatic studies: AST, ALT

• 
Blood studies: CBC with differential bleeding time

 Renal studies: urinalysis, BUN, creatinine; abnormal urinalysis may indicate nephrotoxicity

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

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

 Allergies before initiation of treatment; monitor for anaphylaxis, dyspnea, rash, laryngeal edema; stop product; keep emergency equipment nearby; skin eruptions after administration of penicillin to 1 wk after discontinuing product; cross-sensitivity with cephalosporins may occur

• 
Differential WBC 2 × per wk in patients receiving long-term therapy

• 
IV site: for redness, swelling, pain at site

Perform/provide:

• 
Extravasation management with cold packs, hyaluronidase

Evaluate:

• 
Therapeutic response: absence of fever, draining wounds

Teach patient/family:

 
To report sore throat, fever, fatigue (may indicate superinfection); CNS reactions; pseudomembraneous colitis (diarrhea, fever, abdominal pain, fatigue)

• 
To wear or carry emergency ID if allergic to penicillins

TREATMENT OF ANAPHYLAXIS:

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

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

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