World Journal of Emergency Medicine ›› 2024, Vol. 15 ›› Issue (2): 83-90.doi: 10.5847/wjem.j.1920-8642.2024.011
• Review Article • Next Articles
Ariella Gartenberg1(), Kayla Levine2, Alexander Petrie3
Received:
2023-07-07
Accepted:
2023-09-22
Online:
2024-03-11
Published:
2024-03-01
Contact:
Ariella Gartenberg, Email: Ariella Gartenberg, Kayla Levine, Alexander Petrie. Emergency department management of acute agitation in the reproductive age female and pregnancy[J]. World Journal of Emergency Medicine, 2024, 15(2): 83-90.
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URL: http://wjem.com.cn/EN/10.5847/wjem.j.1920-8642.2024.011
Table 1.
Five major drug classes utilized in the treatment of acute agitation, with a focus on the mechanism of action, adverse effect profiles, general recommendations for use, and use during pregnancy
Drug class | Mechanism of action | Adverse effects | General recommendations for use in agitation | Use in pregnancy |
---|---|---|---|---|
Typical psychotropics (haloperidol, droperidol) | Dopamine D2 receptor antagonism | ● QTc prolongation ● Extrapyramidal symptoms (EPS) | ● Agitation secondary to a primary psychiatric condition (WFSBP) ● Agitation secondary to alcohol intoxication (WFSBP) ● Agitation secondary to delirium (haloperidol) | ● High potency agents (haloperidol): first-line in pregnancy. No reported effects in 2nd to 3rd trimester use. Limited case reports regarding 1st trimester use ● Low potency agents (chlorpromazine, perphenazine): sedative and hypotensive effects; higher risk of congenital malformations after 1st trimester use (cleft palate, micromelia, CNS and skeletal malformations, embryonic death, decreased fetal growth, alterations in offspring behavior)[ |
Atypical psychotropics (clozapine, olanzapine, quetiapine, lurasidone, ziprasidone) | Antagonism of serotonin 5-HT2 receptors, lower affinity for D2 receptors | ● Lower EPS risk ● Higher metabolic adverse effects ● Ziprasidone: high risk of QT prolongation | ● Agitation secondary to a primary psychiatric condition (WFSBP) ● Agitation secondary to alcohol intoxication (WFSBP) ● Agitation secondary to frustration or communication difficulties including autism spectrum disorder (risperidone and aripiprazole) | ● Clozapine/risperidone: NO evidence of impaired fertility or congenital malformations in human and animal models.[ ● Other agents: increased risk of gestational metabolic complications and neonates large for gestational age[ ● Quetiapine: soft tissue anomalies and delays in skeletal ossification[ ● Olanzapine: higher rates of placental passage, early resorptions and fetal nonviability[ |
Benzodiazepines (midazolam, lorazepam) | Increase affinity of GABA to GABA-A receptors Dose dependent CNS depression | ● CNS depression ● Respiratory depression ● Sensory and motor impairments ● Anterograde amnesia | ● Agitation secondary to alcohol withdrawal ● Agitation secondary to benzodiazepine withdrawal ● Agitation from stimulant toxicity | ● Avoid if possible in pregnancy ● Animal models with mal-rotated limbs, malformed skulls, microphthalmia, gastroschisis, reduction of tibial, tarsal, metatarsal bones[ ● Absolute risk difference: 13.9 per 1,000 pregnancies for overall malformations and 11.5 per 1,000 pregnancies for heart defects in infants of mothers exposed to benzodiazepines in the 1st trimester [ ● Benzodiazepine withdrawal during post-natal period [ |
Ketamine | Noncompetitive NMDA and glutamate receptor antagonist Partial agonist on opiate receptors | ● Can worsen tachycardia and hypertension ● Dysphoric emergence phenomena[ ● Hypersalivation, vomiting, laryngospasm, increased rate of intubation, transient hypoxia[ ● Potential increase in schizophrenic symptoms[ | ● Rapid control of severe and combative agitation | ● Impaired learning abilities, spatial and conditioned memory in rat offspring [ ● Neuronal loss, pyramidal neuronal abnormalities, and reduced hippocampal cell proliferation in rat offspring [ ● Impairment of neuronal development in prefrontal cortex. Indirectly associated with abnormal offspring behaviors (depression, anxiety, memory impairment)[ ● Neurodegeneration in developing rhesus macaque brains[ |
Diphenhydramine | Competes with histamine for H1-receptor sites on effector cells in GI tract, blood vessels, and respiratory tract; anticholinergic and sedative effects | ● Anticholinergic symptoms (blurred vision; urinary retention; tachycardia; nausea, constipation) ● CNS depression or paradoxical agitation /insomnia | ● Mild to moderate agitation | ● FDA approved in pregnancy ● No major malformations reported with 1st trimester exposure ● Individual case reports of cleft palates and neonatal withdrawal [ |
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