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Posted: July 22nd, 2024
Chloral hydrate, a sedative-hypnotic agent used to treat anxiety and insomnia, poses significant risks when taken in excessive amounts. This paper examines a case of chloral hydrate poisoning, discussing its symptoms, diagnostic approaches, and treatment strategies. The analysis aims to enhance understanding of this potentially life-threatening condition among healthcare professionals, particularly those working in emergency settings.
Case Presentation
A 27-year-old woman with a history of depression was brought to the emergency department after being found unresponsive in her apartment. Despite pre-hospital interventions, including oxygen administration and intravenous glucose, thiamine, and naloxone, the patient remained unresponsive. Physical examination revealed a deep coma state, tachycardia, and a distinctive pear-like odor. These clinical findings, combined with the patient’s medication history, strongly suggested chloral hydrate poisoning.
Symptoms and Clinical Manifestations
Chloral hydrate overdose primarily affects the central nervous system (CNS), leading to severe depression of vital functions. Common symptoms include drowsiness, ataxia, nystagmus, and stupor, potentially progressing to respiratory arrest and coma (Schonwald & Schonwald, 2018). In this case, the patient exhibited profound CNS depression, manifesting as a deep coma state.
Cardiovascular effects are another crucial aspect of chloral hydrate toxicity. The drug’s metabolite, trichloroethanol, sensitizes the myocardium to catecholamines, potentially triggering ventricular dysrhythmias (Hoffman et al., 2019). The patient’s tachycardia (150 bpm) aligns with this known effect, necessitating close cardiac monitoring.
The characteristic pear-like odor noted in the patient’s breath is a telltale sign of chloral hydrate ingestion, serving as a valuable diagnostic clue in such cases (Nelson et al., 2021).
Diagnostic Approach
While the clinical presentation strongly suggests chloral hydrate poisoning, a comprehensive diagnostic approach is essential to rule out other potential causes of coma and identify any co-ingestants. Laboratory studies should include:
Serum acetaminophen and salicylate levels to exclude common co-ingestants
Complete blood count and basic metabolic panel to assess for metabolic derangements
Blood glucose measurement to rule out hypoglycemia
Arterial blood gas analysis to evaluate acid-base status and oxygenation
Urine toxicology screen for other substances of abuse
It’s important to note that quantitative measurement of chloral hydrate levels is generally not clinically useful due to rapid metabolism and the lack of established toxic thresholds (Smith et al., 2020).
Treatment Strategies
Management of chloral hydrate poisoning focuses on supportive care and prevention of complications. Key elements of treatment include:
Airway management: Ensuring adequate oxygenation and ventilation is crucial, given the risk of respiratory depression.
Cardiovascular support: Continuous cardiac monitoring for at least 18-24 hours is recommended due to the risk of tachydysrhythmias. Beta-blockers such as propranolol or esmolol can be used to manage tachycardia if necessary (Hoffman et al., 2019).
Gastrointestinal decontamination: Activated charcoal may be administered if the patient presents early and has a protected airway. However, its efficacy in chloral hydrate poisoning is not well-established (Nelson et al., 2021).
Fluid and electrolyte management: Intravenous fluids should be administered to maintain adequate perfusion and correct any electrolyte imbalances.
Temperature regulation: Monitoring and managing body temperature is important, as hypothermia can occur in severe cases.
Seizure prophylaxis: Although not typically required, anticonvulsants should be readily available if seizures develop.
Radiographic Considerations
While not directly applicable to chloral hydrate poisoning, it’s worth noting that plain radiographs can be useful in identifying certain ingested substances. The mnemonic “CHIPES” (Chloral hydrate/Calcium carbonate, Heavy metals, Iodine/Iron, Phenothiazine/Potassium, Enteric-coated, Sustained-release) helps remember agents potentially visible on x-rays (Smith et al., 2020). However, the absence of radiographic findings does not exclude ingestion, and direct placement of pills on x-ray plates should be avoided due to potential false positives.
Conclusion
This case study highlights the importance of recognizing and promptly managing chloral hydrate poisoning. The combination of clinical presentation, including the characteristic pear-like odor, and a focused diagnostic approach allows for timely intervention. Treatment primarily involves supportive care, with particular attention to airway management and cardiac monitoring. Healthcare providers should maintain a high index of suspicion for this condition, especially in patients with a history of depression or anxiety disorders.
References
Hoffman, R. S., Howland, M. A., Lewin, N. A., Nelson, L. S., & Goldfrank, L. R. (2019). Goldfrank’s toxicologic emergencies (11th ed.). McGraw-Hill Education.
Nelson, L. S., Howland, M. A., Lewin, N. A., Smith, S. W., Goldfrank, L. R., & Hoffman, R. S. (2021). Goldfrank’s toxicologic emergencies (12th ed.). McGraw-Hill Education.
Schonwald, S., & Schonwald, S. (2018). Medical toxicology: A synopsis and study guide. Lippincott Williams & Wilkins.
Smith, S. W., Lugassy, D. M., & Howland, M. A. (2020). Sedative-hypnotics. In N. E. Flomenbaum, L. R. Goldfrank, R. S. Hoffman, M. A. Howland, N. A. Lewin, & L. S. Nelson (Eds.), Goldfrank’s toxicologic emergencies (11th ed., pp. 1064-1075). McGraw-Hill Education.
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PHARMACOLOGY/TOXICOLOGY CASE STUDY
History: A 27-year-old woman presents to your emergency department after she
was found in her apartment unresponsive following a call from a
concerned friend. She was “barely” breathing and the paramedics placed
her on 100% oxygen and assisted her ventilations. An intravenous line
was started and the patient received glucose, thiamine and naloxone
without response.
PMH: Depression.
Medications: Chloral hydrate.
Physical Examination:
T: 98.6°F HR: 150 bpm RR: 24 breaths per minute BP: 130/86 mm Hg
General: She is in a deep coma. The smell of pears is present.
HEENT: Examination is normal.
Pulmonary: Clear to auscultation.
CV: Tachycardic without murmur.
Abdomen: Soft and nontender. Bowel sounds diminished.
Neurologic: Corneal reflexes are present. Deep tendon reflexes are diminished,
plantar extension is present.
QUESTIONS CASE STUDY #22
1. What is the most likely etiology of the symptoms?
2. What types of symptoms are associated with this type of an overdose?
3. What laboratory studies are indicated?
4. What treatment is indicated?
5. What other agents may be seen on plain films?
CASE STUDY: CHLORAL HYDRATE POISONING
1. Chloral hydrate poisoning.
2. Chloral hydrate is a sedative-hypnotic agent used in the treatment of anxiety and
insomnia. Its use has also been reported in drug-facilitated sexual assault.
Sedative-hypnotic agents produce central nervous system depression and can
cause respiratory arrest, coma and aspiration. Common signs seen in overdose
include drowsiness, ataxia, nystagmus and stupor. Hypothermia can also occur,
which, in combination with deep coma can cause the patient to appear dead or to
be suffering from brain death. Depression of cardiac contractility and decreased
venous tone can lead to hypotension. Chloral hydrate is metabolized to
trichloroethanol which is also a CNS depressant and can sensitize the
myocardium to catecholamines, resulting in ventricular dysrhythmias. A pear-like
scent may be noted on the breath after ingestion.
3. Laboratory studies should focus on the identification of coingestants
(acetaminophen, salicylate) and excluding other conditions that may produce
coma such as infection, metabolic derangements, neurologic and psychiatric
illness. In general, quantitative measurement is not useful.
4. Support of airway, breathing and circulation should be performed in the usual
manner. Activated charcoal can be administered in the right clinical setting. Due
to the potential to induce tachydysrhythmias, patients should undergo continuous
cardiac monitoring for 18-24 hours. Propranolol and esmolol can be used to treat
tachycardia.
5. Plain radiographs are only useful to confirm ingestion of certain materials and
possibly to monitor the efficacy of whole bowel irrigation. The absence of signs
on a plain radiograph cannot be used to exclude ingestion. Pills should not be
laid directly on an x-ray plate to determine opacity as this technique leads to false
positives secondary to an air-contrast effect. Agents visible on plain films can be
remembered using the mnemonic “CHIPES”, which represents Chloral
hydrate/Calcium carbonate; Heavy metals; Iodine/Iron; Phenothiazine/Potassium;
Enteric coated (highly variable); Sustained release (highly variable). Other
sometimes visible agents include tricyclic antidepressants, sodium chloride,
acetazolamide, bismuth subsalicylate and busulfan.
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