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Chloral Hydrate (Drug Study)

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0% found this document useful (0 votes)
826 views3 pages

Chloral Hydrate (Drug Study)

to download this conveniently visit: http://www.rnpedia.com/home/notes/pharmacology-drug-study-notes/chloral-hydrate
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Nursing Notes and Community

Drug Name chloral hydrate (klor' al hye' drate) Aquachloral Supprettes, PMS-Chloral Hydrate (CAN), Chloral Hydrate-Odan (CAN), Somnote Pregnancy Category C Controlled Substance C-IV Drug class Sedativehypnotic (nonbarbitura te)

Dosages Adults Single doses or daily dose should not exceed 2 g. Hypnotic: 500 mg1 g PO or rectally 1530 min before bedtime or 30 min before surgery. It is not usually considered safe practice to give oral medication to patients who are NPO for anesthesia or surgery. Sedative: 250 mg PO or rectally tid after meals. Pediatric Patients Hypnotic: 50 mg/kg/day PO up to 1 g per single dose; may be given in divided doses. Sedative: 25 mg/kg/day PO up to 500 mg per single dose; may be given in divided doses.

Therapeutic Actions Chloral hydrate is used principally as a hypnotic in the treatment of insomnia; effective only for short-term use. Its CNS depressant effect, similar to those of paraldehyde and barbiturates, may be attributed to its metabolite, trichloroethanol.

Indications Nocturnal sedation Preoperative sedation to lessen anxiety and induce sleep without depressing respiration or cough reflex Adjunct to opiates and analgesics in postoperative care and control of pain

Adverse effects Gastric irritation, abdominal distention and flatulence, vertigo, ataxia, staggering gait, rashes, malaise, lightheadedn ess, headache, ketonuria, excitement, nightmares, delirium (especially in elderly), eosinophilia, reduction in white blood cell count; dependence on prolonged use.

Contraindications Hepatic or renal impairment, cardiac disease, hypersensitivity, porphyria, esophagitis, gastritis. Pregnancy and lactation.

Nursing considerations Assessment History: Hypersensitivity to chloral derivatives, allergy to tartrazine, severe cardiac disease, gastritis, hepatic or renal impairment, acute intermittent porphyria, lactation Physical: Skin color, lesions; orientation, affect, reflexes; P, BP, perfusion; bowel sounds, normal output, liver evaluation; LFTs, renal function tests, CBC and differential, stool guaiac test Interventions Give capsules with a full glass of liquid; ensure that patient swallows capsules whole; give syrup in half glass of water, fruit juice, or ginger ale. Supervise dose and amount of drug prescribed for patients who are addiction prone or alcoholic; give least amount feasible to patients who are depressed or suicidal. Withdraw gradually over 2 wk if patient has been maintained on high doses for weeks or months; if patient has built up high tolerance, withdrawal should occur in a hospital, using supportive therapy similar to that for barbiturate

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Nursing Notes and Community

withdrawal; fatal withdrawal reactions have occurred. Reevaluate patients with prolonged insomnia; therapy for the underlying cause (eg, pain, depression) is preferable to prolonged use of sedativehypnotic drugs. Teaching points Take this drug exactly as prescribed: Swallow capsules whole with a full glass of liquid (take syrup in half glass of water, fruit juice, or ginger ale). Do not discontinue the drug abruptly. Consult your health care provider if you wish to discontinue the drug. Avoid alcohol, sleepinducing, or over-thecounter drugs; these could cause dangerous effects. You may experience these side effects: Drowsiness, dizziness, light-headedness (avoid driving or performing tasks requiring alertness); GI upset (eat frequent small meals); sleep-walking, nightmares, confusion (use caution: close doors, keep medications out of reach so inadvertent overdose does not occur while confused). Report rash, coffee ground vomitus, black or tarry stools, severe GI upset, fever, sore throat.

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Nursing Notes and Community

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