|
|
|
Pronunciation |
|
(tye
kar SIL
in) |
|
|
U.S. Brand
Names |
|
Ticar® |
|
|
Generic
Available |
|
No |
|
|
Synonyms |
|
Ticarcillin Disodium |
|
|
Pharmacological Index |
|
Antibiotic, Penicillin |
|
|
Use |
|
Treatment of susceptible infections such as septicemia, acute and chronic
respiratory tract infections, skin and soft tissue infections, and urinary tract
infections due to susceptible strains of Pseudomonas, and other
gram-negative bacteria |
|
|
Pregnancy Risk
Factor |
|
B |
|
|
Contraindications |
|
Hypersensitivity to ticarcillin or any component or
penicillins |
|
|
Warnings/Precautions |
|
Due to sodium load and adverse effects (anemia, neuropsychological changes),
use with caution and modify dosage in patients with renal impairment; serious
and occasionally severe or fatal hypersensitivity (anaphylactoid) reactions have
been reported in patients on penicillin therapy (especially with a history of
beta-lactam hypersensitivity and/or a history of sensitivity to multiple
allergens); use with caution in patients with seizures |
|
|
Adverse
Reactions |
|
Percentage unknown: Convulsions, confusion, drowsiness, fever, rash,
electrolyte imbalance, hemolytic anemia, positive Coombs' reaction,
eosinophilia, bleeding, thrombophlebitis, myoclonus, acute interstitial
nephritis, hypersensitivity reactions, anaphylaxis, Jarisch-Herxheimer
reaction |
|
|
Overdosage/Toxicology |
|
Symptoms of penicillin overdose include neuromuscular hypersensitivity
(agitation, hallucinations, asterixis, encephalopathy, confusion, and seizures)
and electrolyte imbalance with potassium or sodium salts, especially in renal
failure
Hemodialysis may be helpful to aid in the removal of the drug from the blood,
otherwise most treatment is supportive or symptom directed |
|
|
Drug
Interactions |
|
Decreased effect:
Tetracyclines may decrease penicillin effectiveness
Aminoglycosides
physical inactivation of
aminoglycosides in the presence of high concentrations of ticarcillin
Decreased effectiveness of oral contraceptives
Increased effect:
Probenecid may increase penicillin levels
Neuromuscular blockers may increase duration of blockade
Potential toxicity in patients with with mild to moderate renal dysfunction
Aminoglycosides
synergistic efficacy
Increased bleeding risk with large I.V. doses and anticoagulants
|
|
|
Stability |
|
Reconstituted solution is stable for 72 hours at room temperature and 14 days
when refrigerated; for I.V. infusion in NS or D5W solution is stable
for 72 hours at room temperature, 14 days when refrigerated or 30 days when
frozen; after freezing, thawed solution is stable for 72 hours at room
temperature or 14 days when refrigerated; incompatible with
aminoglycosides |
|
|
Mechanism of
Action |
|
Inhibits bacterial cell wall synthesis by binding to one or more of the
penicillin binding proteins (PBPs); which in turn inhibits the final
transpeptidation step of peptidoglycan synthesis in bacterial cell walls, thus
inhibiting cell wall biosynthesis. Bacteria eventually lyse due to ongoing
activity of cell wall autolytic enzymes (autolysins and murein hydrolases) while
cell wall assembly is arrested. |
|
|
Pharmacodynamics/Kinetics |
|
Absorption: I.M.: 86%
Distribution: In blister fluid, lymph tissue, and gallbladder; crosses
placenta; distributed into milk at low concentrations
Protein binding: 45% to 65%
Half-life:
Neonates: <1 week: 3.5-5.6 hours; 1-8 weeks: 1.3-2.2 hours
Children 5-13 years: 0.9 hour
Adults: 66-72 minutes, prolonged with renal impairment and/or hepatic
impairment
Peak serum levels: I.M.: Within 30-75 minutes
Elimination: Almost entirely in urine as unchanged drug and its metabolites
with small amounts excreted in feces (3.5%) |
|
|
Usual Dosage |
|
Ticarcillin is generally given I.V., I.M. injection is only for the treatment
of uncomplicated urinary tract infections and dose should not exceed 2
g/injection when administered I.M.
Postnatal age <7 days:
<2000 g: 75 mg/kg/dose every 12 hours
>2000 g: 75 mg/kg/dose every 8 hours
Postnatal age >7 days:
<1200 g: 75 mg/kg/dose every 12 hours
1200-2000 g: 75 mg/kg/dose every 8 hours
>2000 g: 75 mg/kg/dose every 6 hours
Infants and Children:
Systemic infections: I.V.: 200-300 mg/kg/day in divided doses every 4-6 hours
Urinary tract infections: I.M., I.V.: 50-100 mg/kg/day in divided doses every
6-8 hours
Maximum dose: 24 g/day
Adults: I.M., I.V.: 1-4 g every 4-6 hours, usual dose: 3 g I.V. every 4-6
hours
Dosing adjustment in renal impairment: Adults:
Clcr 30-60 mL/minute: 2 g every 4 hours or 3 g every 8 hours
Clcr 10-30 mL/minute: 2 g every 8 hours or 3 g every 12 hours
Clcr <10 mL/minute: 2 g every 12 hours
Moderately dialyzable (20% to 50%)
Continuous arteriovenous or venovenous hemodiafiltration (CAVH) effects: Dose
as for Clcr 10-50 mL/minute |
|
|
Monitoring
Parameters |
|
Serum electrolytes, bleeding time, and periodic tests of renal, hepatic, and
hematologic function; monitor for signs of anaphylaxis during first
dose |
|
|
Test
Interactions |
|
May interfere with urinary glucose tests using cupric sulfate (Benedict's
solution, Clinitest®); may inactivate aminoglycosides
in vitro; false-positive urinary or serum protein |
|
|
Mental Health: Effects
on Mental Status |
|
May cause drowsiness or confusion; penicillins reported to cause
apprehension, illusions, hallucinations, depersonalization, agitation, insomnia,
and encephalopathy |
|
|
Mental Health:
Effects on Psychiatric
Treatment |
|
None reported |
|
|
Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
|
No information available to require special precautions |
|
|
Dental Health:
Effects on Dental Treatment |
|
Prolonged use of penicillins may lead to development of oral
candidiasis |
|
|
Patient
Information |
|
This medication will be administered I.V. or I.M. Maintain adequate hydration
(2-3 L/day of fluids unless instructed to restrict fluid intake). Small frequent
meals, frequent mouth care, sucking lozenges, or chewing gum may reduce nausea
or dry mouth. Maintain good oral and vaginal hygiene to reduce incidence of
opportunistic infection. If diabetic, drug may cause false tests with
Clinitest® urine glucose monitoring; use of glucose
oxidase methods (Clinistix®) or serum glucose monitoring
is preferable. This drug may interfere with oral contraceptives; an alternate
form of birth control should be used. Report persistent diarrhea or abdominal
pain (do not use antidiarrhea medication without consulting prescriber), fever,
chills, unhealed sores, bloody urine or stool, muscle pain, mouth sores,
difficulty breathing, or skin rash. |
|
|
Nursing
Implications |
|
Draw sample for culture and sensitivity before administering first dose, if
possible |
|
|
Dosage Forms |
|
Powder for injection, as disodium: 1 g, 3 g, 6 g, 20 g, 30
g |
|
|
References |
|
Brogden RN, Heel RC, Speight TM, et al,
"Ticarcillin: A Review of Its Pharmacological Properties and Therapeutic Efficacy,"
Drugs, 1980, 20(5):325-52.
Donowitz GR and Mandell GL, "Beta-Lactam Antibiotics," N Engl J Med,
1988, 318(7):419-26 and 318(8):490-500.
Nelson JD, Kusmiesz H, Shelton S, et al,
"Clinical Pharmacology and Efficacy of Ticarcillin in Infants and Children,"
Pediatrics, 1978, 61(6):858-63.
Tan JS and File TM Jr, "Antipseudomonal Penicillins," Med Clin North
Am, 1995, 79(4):679-93.
Wright AJ, "The Penicillins," Mayo Clin Proc, 1999, 74(3):290-307.
Yoshikawa TT, "Antimicrobial Therapy for the Elderly Patient," J Am
Geriatr Soc, 1990, 38(12):1353-72.
|
|
Copyright © 1978-2000 Lexi-Comp Inc. All Rights Reserved
| |