Sunday, November 6, 2016

Chloral Hydrate


Class: Anxiolytics, Sedatives, and Hypnotics; Miscellaneous
VA Class: CN309
CAS Number: 302-17-0
Brands: AquachloralSuprettes, Somnote


Genotoxic and may be carcinogenic in mice; should not be used when less potentially dangerous agents would be effective.103



Introduction

Sedative and hypnotic.100 101 103 106


Uses for Chloral Hydrate


Hypnotic


Short term treatment of insomnia for <2 weeks; effective for inducing and maintaining sleep.100 101 103


Sedation


Used for routine sedation.100 101 106


Used preoperatively to relieve anxiety and to provide sedation100 101 without depressed respiration or cough reflex.103


Also used to produce sleep prior to non-painful procedures (e.g., EEG, diagnostic imaging)104 105 to relieve anxiety and to provide sedation.100 101 103


Has been used for conscious sedation to relieve anxiety in young pediatric patients (usually <3 years of age) during procedures (e.g., diagnostic imaging).104 105 106


Used often in geriatric and pediatric patients, because many clinicians suggest that the drug is associated with paradoxical excitement less frequently than barbiturates; however, no well controlled studies confirmed this clinical impression.100 101


Postoperative Analgesia


Adjunct to opiates and analgesics for control of postoperative pain.103


Withdrawal


Reduction of anxiety associated with withdrawal of opiates or barbiturates.100 101 103


Used alone or in conjunction with paraldehyde for prevention of alcohol withdrawal symptoms and/or suppression of the syndrome once it develops.100 101


Chloral Hydrate Dosage and Administration


Administration


Administer orally100 101 or rectally.103


Withdraw chloral hydrate slowly after chronic administration to avoid possibility of precipitating withdrawal symptoms.101 c (See Withdrawal under Warnings and Precautions.)


Oral Administration


Administer capsules with a full glass of water or liquid after meals;101 dilute oral solution in 1/2 a glass of water or other liquid (e.g., fruit juice, ginger ale).100 101


Rectal Administration


Moisten finger and suppository with water before inserting suppository.103


Suppositories have been dissolved in cottonseed or olive oil and administered as a retention enema.c


Dosage


Pediatric Patients


Hypnotic

Oral

50 mg/kg or 1.5 g/m2 up to a maximum single dose of 1 g.100 101


Rectal

18 mg/kg (325 mg/18 kg) once daily before bedtime.103


Sedation

Routine Sedation

Oral

8 mg/kg or 250 mg/m2 3 times daily, up to a maximum of 500 mg 3 times daily.100 101


Some experts recommend a dosage of 25–50 mg/kg per 24 hours, (given in 3 or 4 doses; every 8 or 6 hours, respectively), up to 500 mg per dose.106


Rectal

9 mg/kg (325 mg/36 kg), do not exceed 1 dose in 24 hours.103


Some experts recommend a dosage of 25–50 mg/kg per 24 hours, (given in 3 or 4 doses; every 8 or 6 hours, respectively), up to 500 mg per dose.106


Preoperative Sedation

Oral

8 mg/kg or 250 mg/m2 3 times daily, up to a maximum of 500 mg 3 times daily.100 101


Rectal

9 mg/kg (325 mg/36 kg); do not exceed 1 dose in 24 hours.103


Procedural Sedation

Oral

20–25 mg/kg before procedure.100 101


Some experts recommend a 25- to 100-mg/kg dose before procedure; do not exceed a 1-g dose in infants or a 2-g dose in children.105 106


Rectal

Some experts recommend a 25- to 100-mg/kg dose before procedure; do not exceed a 1-g dose in infants or a 2-g dose in children.106


Conscious Sedation

Oral

Neonates: have been given 25–100 mg/kg once.104


Pediatric patients <3 years of age (excluding neonates): were given a dose of 25–100 mg/kg and a second dose of 25–50 mg/kg may be administered after 30 minutes; maximum total dosage has been 2 g or 100 mg/kg (whichever was lower).104 105


Rectal

Some experts recommend a 25- to 100-mg/kg dose before procedure; do not exceed a 1-g dose in infants or a 2-g dose in children.106


Adults


Hypnotic

Oral

0.5–1 g 15–30 minutes prior to bedtime.100 101


Some experts recommend a 0.5- to 1-g dose; do not exceed 2 g in 24 hours.106


Rectal

0.65–1.3 g 30 minutes prior to bedtime.103


Some experts recommend a 0.5- to 1-g dose; do not exceed 2 g in 24 hours.106


Sedation

Routine Sedation

Oral

250 mg 3 times daily after meals.100 101


Rectal

325–650 mg 3 times daily, up to a maximum total daily dosage of 1950 mg.103


Some experts recommend 250 mg 3 times daily.106


Preoperative Sedation

Oral

0.5–1 g 30 minutes prior surgery.c


Alcohol Withdrawal

Oral

0.5–1 g every 6 hours as needed, up to a maximum single dose or daily dosage of 2 g.100 101


Prescribing Limits


Pediatric Patients


Hypnotic

Oral

Maximum 1 g daily (as a single dose).100 101


Sedation

Oral

For routine sedation, maximum 500 mg 3 times daily.100 101 c


For procedural sedation, maximum 1-g dose in infants or a 2-g dose in children.106


For conscious sedation, maximum total dosage in children <3 years of age (excluding neonates) is 2 g or 100 mg/kg (whichever is lower).104 105


Rectal

For routine or preoperative sedation, maximum of one 9-mg/kg (325-mg/36 kg) dose daily.103


Adults


Oral

Maximum 2 g daily.100 101 c


Rectal

Maximum 1950 mg daily.103


Special Populations


No special population recommendations at this time.100 101 c 103 (See Contraindications under Cautions.)


Cautions for Chloral Hydrate


Contraindications



  • Marked hepatic impairment.100 101 c 103




  • Marked renal impairment. 100 101 c 103




  • Known hypersensitivity or idiosyncratic reaction to chloral hydrate.100 101 c 103



Warnings/Precautions


Warnings


Carcinogenicity

Although the manufacturer of Aquachloral suppositories warns about potential carcinogenicity of the drug, some experts state that the assumption that chloral hydrate is a reactive metabolite of trichloroethylene (an industrial solvent) responsible for the carcinogenicity of trichloroethylene is questionable.108 There is evidence that the carcinogenicity of trichloroethylene is due to a reactive intermediate epoxide metabolite rather than to chloral hydrate.108


Abuse Potential

Although uncommon, tolerance and psychologic dependence may occur following prolonged administration of the drug; use with caution in patients with a history of drug abuse.100 101 c 103


Symptoms of dependence are similar to those of chronic alcoholism100 101 c 103 (drowsiness, lethargy, hangover, slurring of speech, incoordination, tremulousness, and nystagmus).c


Withdrawal

Sudden withdrawal may cause delirium tremens (sometimes fatal) and hallucinations; following chronic use, withdraw slowly.100 101 c 103


Sensitivity Reactions


Hypersensitivity Reactions

Scarlatiniform or erythematous rash, urticaria, angioedema, purpura, eczema, bullous lesions, skin eruptions, and erythema multiforme reported, sometimes accompanied by fever.100 101 103


Tartrazine Sensitivity

Aquachloral 325 mg rectal suppositories contain tartrazine (FD&C yellow No. 5), which may cause allergic reactions including bronchial asthma in susceptible individuals.103 Incidence of tartrazine sensitivity is low, but it frequently occurs in patients who are sensitive to aspirin.103


General Precautions


CNS Effects

Use with caution in mentally depressed patients or those having suicidal tendencies.100 101 c 103


Rarely, somnambulistic reaction characterized by disorientation and incoherence reported.100 101 103


GI Effects

Avoid oral administration in patients with esophagitis, gastritis, or gastric or duodenal ulcers.100 101 c


Gastritis may develop following prolonged oral administration; minimize irritation by diluting oral syrup or administering other oral dosage forms with liquids.100 101 c (See Administration under Dosage and Administration.)


Cardiac Effects

Prolonged administration of therapeutic doses was not associated with adverse cardiac effects.100 101 103


Do not use high doses in patients with severe cardiac disease.100 101 103


Renal Effects

Following prolonged administration, parenchymatous renal damage reported.100 101


Porphyria

Attacks of acute intermittent porphyria reported; use caution in susceptible patients.101


Adequate Monitoring

Procedural sedation using chloral hydrate in pediatric patients should be performed only under the supervision of qualified clinicians experienced in cardiorespiratory complications.104 105 107


Specific Populations


Pregnancy

Category C.100 101 c 103


Lactation

Distributed into milk.103 Use with caution in nursing women.100 101 c 103


Pediatric Use

Used orally and rectally in pediatric patients for sedation and hypnosis.100 101 c 103 104 105 106 108


Geriatric Use

Geriatric patients may tolerate chloral hydrate even when intolerant to barbiturates.103


Common Adverse Effects


Nausea,100 101 c 103 vomiting, 100 101 c 103 diarrhea, 100 101 c 103 ataxia, 100 101 c 103 dizziness.100 101 c 103


Interactions for Chloral Hydrate


Specific Drugs
























Drug



Interaction



Comments



CNS depressants (e.g., alcohol, barbiturates, paraldehyde )



Additive CNS depression100 101 103



Vasodilation (characterized by tachycardia, palpitations, facial flushing, and dysphoria) may occur when used with alcohol100 101 103


Use with caution to avoid overdosage100 101 103



Furosemide



Possible diaphoresis, flushing, variable BP, uneasiness, in patients with acute MI and CHF receiving IV furosemide within 24 hours of chloral hydrate100 101



Consider alternative hypnotic drug (e.g., a benzodiazepine) in patients receiving IV furosemide100 101 c



Warfarin



Potential for increased warfarin metabolism and decreased warfarin efficacy (hypoprothrombinemia)100 101 c 103



Consider alternative hypnotic drug e.g., benzodiazepine).100 101 c If used concomitantly, monitor prothrombin time closely100 101 c 103



Tests for Urine Glucose



Possible false-positive results in urine glucose test using cupric sulfate as Benedict’s solution and possibly with cupric sulfate tablets (Clinitest)100 101 c



May use glucose tests based on enzymatic glucose oxidase reactions (e.g., Clinistix, Tes-Tape)100 101 c



Urine Catecholamine Test (Fluorometric)



Possible interference 100 101



Do not administer chloral hydrate for 48 hours prior to test100 101 c



Urinary 17-hydroxycorticosteroids Test



Possible interference with Reddy, Jenkins, and Thorn procedures100 101 c


Chloral Hydrate Pharmacokinetics


Absorption


Bioavailability


Rapidly absorbed following oral or rectal administration.c


Onset


Following oral administration of 0.5–1 g, sedation occurs within 30–60 minutes.c 105


Following rectal administration, sedation occurs within 60 minutes.103


Duration


Following oral administration of 0.5–1 g : 4–8 hours.c 105


Distribution


Extent


Distributed into CSF, umbilical cord blood, fetal blood, amniotic fluid, and milk.100 101 c


Elimination


Metabolism


Metabolized to trichloroethanol (active metabolite), principally in the liver and erythrocytes, by alcohol dehydrogenase and other enzymes.c Small, but variable amounts of chloral hydrate metabolized to trichloroacetic acid (inactive metabolite) in liver and kidneys.c


Elimination Route


Active and inactive metabolites are slowly and variably excreted in the kidneys.c Trichloroethanol glucuronide (urochloralic acid), an inactive metabolite, may be secreted into the bile and excreted in feces.c


Eliminated by dialysis.103


Half-life


8–11 hours.c


Stability


Storage


Oral


Capsules

25°C (may be exposed to 15–30°C).101


Solution

Tight, light resistant containers at 20–25°C; protect from freezing.100


Rectal


Suppositories

15–30°C; do not refrigerate.c 103


ActionsActions



  • Mechanism of action not fully elucidated; CNS depressant effect believed to result primarily from active metabolite trichloroethanol.c 103




  • CNS depressant effects similar to paraldehyde and barbiturates.c




  • Hypnotic doses produce mild cerebral depression and quiet, deep sleep.c




  • Higher doses may lead to general anesthesia and concurrent depression of respiratory and vasomotor centers; death may result from respiratory failure.c




  • Sedative or hypnotic doses have little anticonvulsant activity.c




  • Has little analgesic activity and may produce excitement or delirium in the presence of pain.c



Advice to Patients



  • Administer capsules with a full glass of water or liquid101 and oral solution with half glass of liquid (i.e., water, fruit juice, or ginger ale).100 (See Administration under Dosage and Administration)




  • Advise patients not to take CNS depressant drugs or alcohol concomitantly with chloral hydrate.100 101 103




  • Risk of dizziness or fatigue; potential for drug to impair mental alertness or physical coordination; use caution when driving or operating machinery until effects on the individual are known.100 101 c 103




  • Importance of informing clinicians of hypersensitivity to aspirin.103 (See Tartrazine Sensitivity under Warnings and Precautions.)




  • Importance of informing clinicians of existing or contemplated therapy, including prescription and OTC drugs and dietary or herbal supplements, as well as concomitant illnesses.100 101 c 103




  • Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed; breast-feeding may result in sedation of the infant.c 103




  • Importance of informing patients of other important precautionary information. (See Cautions.)



Preparations


Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.


Chloral hydrate is subject to control under the Federal Controlled Substances Act of 1970 as a schedule IV (C-IV) drug.c


* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name

































Chloral Hydrate

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Oral



Capsules, liquid-filled



500 mg*



Somnote (C-IV)



Breckenridge



Solution



500 mg/5 mL*



Chloral Hydrate Syrup (C-IV)



Pharmaceutical Associates



Rectal



Suppositories



325 mg



Aquachloral Supprettes (with tartrazine, C-IV)



Amerifit Pharma



500 mg



Chloral Hydrate Suppositories (C-IV)



G&W



650 mg



Aquachloral Supprettes (with tartrazine, C-IV)



Amerifit Pharma


Comparative Pricing


This pricing information is subject to change at the sole discretion of DS Pharmacy. This pricing information was updated 03/2011. Actual costs to patients will vary depending on the use of specific retail or mail-order locations and health insurance copays.


Somnote 500MG Capsules (BRECKENRIDGE): 50/$86.39 or 150/$232.19



Disclaimer

This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.


The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.

AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions April 2009. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.


† Use is not currently included in the labeling approved by the US Food and Drug Administration.




References



100. Pharmaceutical Associates. Chloral hydrate syrup prescribing information. Greenville, SC; 2002 Oct.



101. Breckenridge Pharmaceutical. Somnote capsules prescribing information. Boca Raton, FL; 2004 Dec.



103. Amerifit Pharma. AquachloralSupprettes prescribing information. Woburn, MA; 2006 May.



104. Krauss B, Green SM. Sedation and analgesia for procedures in children. N Engl J Med. 2000; 342:938-45. [PubMed 10738053]



105. Sectish TC. Use of sedation and local anesthesia to prepare children for procedures. Am Fam Physician. 1997; 55:909-16. [PubMed 9048510]



106. Siberry GK, Iannone R, eds. The Harriet Lane handbook: a manual for pediatric house officers. 15th ed. Philadelphia, PA: Mosby: 2000:667.



107. American Academy of Pediatrics, American Academy of Pediatric Dentistry, Coté CJ, Wilson S, and the Work Group on Sedation. Guidelines for monitoring and management of pediatric patients during and after sedation for diagnostic and therapeutic procedures; an update. Pediatrics. 2006; 118::836-8.



108. American Academy of Pediatrics Committee on Drugs and Committee on Environmental Health. Use of chloral hydrate for sedation in children. Pediatrics. 1993; 92:471-3. [PubMed 8361811]



c. AHFS drug information 2007. McEvoy GK, ed. Chloral hydrate. Bethesda, MD: American Society of Health-System Pharmacists; 2007;2547-8.



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