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Pronunciation |
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(klor
HEKS i deen GLOO koe
nate) |
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U.S. Brand
Names |
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BactoShield® Topical [OTC];
Betasept®[OTC]; Dyna-Hex® Topical [OTC]; Exidine®
Scrub [OTC]; Hibiclens® Topical [OTC]; Hibistat® Topical
[OTC]; Peridex® Oral Rinse; PerioChip®;
PerioGard® |
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Generic
Available |
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No |
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Pharmacological Index |
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Antibiotic, Oral Rinse; Antibiotic, Topical |
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Use |
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Dental:
Antibacterial dental rinse; chlorhexidine is active against gram-positive and
gram-negative organisms, facultative anaerobes, aerobes, and yeast
Chip, for periodontal pocket insertion; indicated as an adjunct to scaling
and root planing procedures for reduction of pocket depth in patients with adult
periodontitis; may be used as part of a periodontal maintenance program
Medical: Skin cleanser for surgical scrub, cleanser for skin wounds,
germicidal hand rinse, and as antibacterial dental rinse. Chlorhexidine is
active against gram-positive and gram-negative organisms, facultative anaerobes,
aerobes, and yeast. |
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Pregnancy Risk
Factor |
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B |
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Contraindications |
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Known hypersensitivity to chlorhexidine gluconate |
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Warnings/Precautions |
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Staining of oral surfaces, tooth restorations, and dorsum of tongue may
occur; keep out of eyes and ears; for topical use only; there have been case
reports of anaphylaxis following chlorhexidine disinfection |
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Adverse
Reactions |
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>10%: Oral: Increase of tartar on teeth, changes in taste. Staining of
oral surfaces (mucosa, teeth, dorsum of tongue) may be visible as soon as 1 week
after therapy begins and is more pronounced when there is a heavy accumulation
of unremoved plaque and when teeth fillings have rough surfaces. Stain does not
have a clinically adverse effect but because removal may not be possible,
patient with frontal restoration should be advised of the potential permanency
of the stain.
1% to 10%: Gastrointestinal: Tongue irritation, oral irritation
<1%: Facial edema, nasal congestion, shortness of breath
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Overdosage/Toxicology |
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Symptoms of oral overdose include gastric distress, nausea, or signs of
alcohol intoxication |
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Drug
Interactions |
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No data reported |
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Stability |
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Store at room temperature |
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Mechanism of
Action |
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The bactericidal effect of chlorhexidine is a result of the binding of this
cationic molecule to negatively charged bacterial cell walls and extramicrobial
complexes. At low concentrations, this causes an alteration of bacterial cell
osmotic equilibrium and leakage of potassium and phosphorous resulting in a
bacteriostatic effect. At high concentrations of chlorhexidine, the cytoplasmic
contents of the bacterial cell precipitate and result in cell
death. |
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Pharmacodynamics/Kinetics |
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Absorption: ~30% of chlorhexidine is retained in the oral cavity following
rinsing and is slowly released into the oral fluids; chlorhexidine is poorly
absorbed from the GI tract
Serum concentrations: Detectable levels are not present in the plasma 12
hours after administration
Elimination: Primarily through the feces (approximately 90%); <1% excreted
in the urine |
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Usual Dosage |
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Adults:
Precede use of solution by flossing and brushing teeth; completely rinse
toothpaste from mouth. Swish 15 mL undiluted oral rinse around in mouth for 30
seconds, then expectorate. Caution patient not to swallow the medicine. Avoid
eating for 2-3 hours after treatment. (The cap on bottle of oral rinse is a
measure for 15 mL.)
When used as a treatment of gingivitis, the regimen begins with oral
prophylaxis. Patient treats mouth with 15 mL chlorhexidine, swishes for 30
seconds, then expectorates. This is repeated twice daily (morning and evening).
Patient should have a re-evaluation followed by a dental prophylaxis every 6
months.
Cleanser:
Surgical scrub: Scrub 3 minutes and rinse thoroughly, wash for an additional
3 minutes
Hand wash: Wash for 15 seconds and rinse
Hand rinse: Rub 15 seconds and rinse
Periodontal chip: Adults: One chip is inserted into a periodontal pocket with
a probing pocket depth greater than or equal to 5 mm. Up to 8 chips may be
inserted in a single visit. Treatment is recommended every 3 months in pockets
with a remaining depth greater than or equal to 5 mm. If dislodgment occurs 7
days or more after placement, the subject is considered to have had the full
course of treatment. If dislodgment occurs within 48 hours, a new chip should be
inserted.
Insertion of periodontal chip: Pocket should be isolated and surrounding area
dried prior to chip insertion. The chip should be grasped using forceps with the
rounded edges away from the forceps. The chip should be inserted into the
periodontal pocket to its maximum depth. It may be maneuvered into position
using the tips of the forceps or a flat instrument. The chip biodegrades
completely and does not need to be removed. Patients should avoid dental floss
at the site of PerioChip® insertion for 10 days after
placement because flossing might dislodge the chip. |
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Administration |
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Insertion of periodontal chip: Pocket should be isolated and surrounding area
dried prior to chip insertion. The chip should be grasped using forceps with the
rounded edges away from the forceps. The chip should be inserted into the
periodontal pocket to its maximum depth. It may be maneuvered into position
using the tips of the forceps or a flat instrument. The chip biodegrades
completely and does not need to be removed. |
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Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
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No information available to require special precautions |
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Dental Health:
Effects on Dental Treatment |
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Swelling of face has been reported |
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Patient
Information |
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Oral rinse: Do not swallow, do not rinse after use; may cause reduced taste
perception which is reversible; may cause discoloration of teeth
Topical administration is for external use only |
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Nursing
Implications |
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Inform patient that reduced taste perception during treatment is reversible
with discontinuation of chlorhexidine |
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Dosage Forms |
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Chip, for periodontal pocket insertion (PerioChip®):
2.5 mg
Foam, topical, with isopropyl alcohol 4%
(BactoShield®): 4% (180 mL)
Liquid, topical, with isopropyl alcohol 4%:
Dyna-Hex® Skin Cleanser: 2% (120 mL, 240 mL, 480 mL,
960 mL, 4000 mL); 4% (120 mL, 240 mL, 480 mL, 4000 mL)
BactoShield® 2: 2% (960 mL)
BactoShield®, Betasept®,
Exidine® Skin Cleanser, Hibiclens®
Skin Cleanser: 4% (15 mL, 120 mL, 240 mL, 480 mL, 960 mL, 4000 mL)
Rinse:
Oral (mint flavor) (Peridex®,
PerioGard®): 0.12% with alcohol 11.6% (480 mL)
Topical (Hibistat® Hand Rinse): 0.5% with isopropyl
alcohol 70% (120 mL, 240 mL)
Sponge/Brush (Hibiclens®): 4% with isopropyl alcohol 4%
(22 mL)
Wipes (Hibistat®): 0.5% (50s) |
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References |
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al-Tannir MA and Goodman HS,
"A Review of Chlorhexidine and Its Use in Special Populations," Spec Care
Dentist, 1994, 14(3):116-22.
Emerson D and Pierce C,
"A Case of a Single Ingestion of 4% Hibiclens®," Vet
Hum Toxicol, 1988, 30(6):583.
Ferretti GA, Brown AT, Raybould TP, et al,
"Oral Antimicrobial Agents - Chlorhexidine," NCI Monogr, 1990, 9:51-5.
Greenstein G, Berman C, and Jaffin R,
"Chlorhexidine. An Adjunct to Periodontal Therapy," J Periodontol, 1986,
57(6):370-7.
Johnson BT, "Uses of Chlorhexidine in Dentistry," Gen Dent, 1995,
43(2):126-32, 134-40.
Massano G, Ciocatto E, Rosabianca C, et al,
"Striking Aminotransferase Rise After Chlorhexidine Self-Poisoning,"
Lancet, 1982, 1(8266):289.
Quinn MW and Bini RM, "Bradycardia Associated With Chlorhexidine Spray,"
Arch Dis Child, 1989, 64(6):892-3.
Yong D, Parker FC, and Foran SM,
"Severe Allergic Reactions and Intra-Urethral Chlorhexidine Gluconate," Med J
Aust, 1995, 162(5):257-8.
Yusof ZA,
"Chlorhexidine Mouthwash: A Review of Its Pharmacological Activity, Clinical Effects, Uses and Abuses,"
Dent J Malays, 1988, 10(1):9-16.
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