You have a new patient!
A 22-year-old woman is brought to the ER because of violent, jerky movements of her limbs that started 30 minutes ago. Her husband reports that the patient has a history of epilepsy. She is unresponsive. Her examination reveals tonic-clonic episodes and blood in her mouth. How would you manage this case? What are the initial steps you would take? What actions are needed to stop the seizure?
What do you need to know?
Epidemiology and Importance
Epilepsy is one of the most common neurological diseases that can present to the emergency department [1]. It affects about 50 million people around the world, with an incidence of approximately 50.4 to 81.7 per 100,000 per year [1]. Epilepsy refers to having a lower seizure threshold than normal due to genetic, pathological, or unknown causes [2]. It is characterized by recurrent unprovoked seizures that present with motor, sensory, autonomic, or cognitive function alterations [2]. Previously diagnosed patients can present to the ED with breakthrough seizures due to factors like changes in the anti-seizure regimen or noncompliance with medication [2]. Other factors like sleep deprivation, stress, and flashing lights can also precipitate breakthrough seizures [2].
Prolonged or repetitive uncontrollable seizures are termed status epilepticus [2,3]. This emergency requires prompt treatment to prevent neuronal injury, severe disability, coma, or death [3]. The overall case fatality rates can reach up to 15% [2].
Pathophysiology
Neurons are normally stabilized by a balance between excitatory and inhibitory neurotransmitters [2]. A disruption of this balance leads to abnormal electrical discharge [2]. This discharge can propagate to nearby areas in the brain, which is evident clinically by the stepwise spread of the seizure (known as Jacksonian March) [2, 4]. Loss of consciousness in some cases is explained by the widespread involvement of large areas of the brain [2]. Many drugs used to restore this balance work by enhancing inhibitory activity through targeting GABAA subtype receptors [2]. Prolongation of the seizure leads to sequestration of GABAA receptors and upregulation of excitatory receptors; therefore, patients become unresponsive to medication [2, 5]. This explains the importance of timely treatment through early seizure control to prevent morbidity and mortality in patients with status epilepticus [2,3].
Medical History
A common scenario presenting to the ER is a patient complaining of a seizure-like episode with a sudden loss of consciousness and motor activity involvement [6]. However, various other presentations of seizures and other differential diagnoses with similar complaints should not be neglected. If the patient presents with status epilepticus, timely management, depending on the seizure type, is urgently needed (see management) [2].
Through history and examination, distinguishing a seizure from other acute medical conditions is important. An accurate diagnosis has crucial, direct consequences for activity restriction and therapy planning. Paying attention to features, especially at the onset, can help in identifying the seizure type for therapeutic implications and facilitate communication between physicians. Semiology at onset is important to classify seizures as focal, focal with impaired awareness (complex seizures), generalized, or unknown [7]. Further classification divides motor and non-motor seizures based on the descriptive assessment of the first symptom, which can vary widely according to the area of the brain affected [2].
The main aim of history-taking is to identify seizures from other similar conditions, classify them, identify triggers of new seizures, and detect a cause for a decreased seizure threshold in a patient previously diagnosed with epilepsy [8].
It is important for any patient with seizures to consider critical causes such as eclampsia, toxic ingestion, hypoglycemia, electrolyte imbalance, and increased intracranial pressure [9]. Emergent diagnoses, such as infection, acute brain injury, and serious mimics of seizure activity, must be identified and treated as soon as possible [2].
Initial history approach to a patient with suspected seizure [2] is a systematic evaluation, starting with the assessment of whether the event is likely to be a seizure, followed by differentiation of first-time versus recurrent seizures, and identifying factors that may trigger or reduce seizure thresholds [10].
Algorithmic Approach in Seizure History [2]
Determining Likelihood of a Seizure
The process begins by evaluating whether the event could be a seizure. Key indicators include:
- Aura: A subjective sensation preceding the seizure.
- Abrupt onset: Sudden occurrence of the event.
- Non-suppressible limb shaking: Movements that are not voluntary or suppressible.
- Postictal state: A transient neurological state after the event, characterized by confusion or fatigue.
- History of epilepsy: Previous diagnosis or known history can strongly support the likelihood.
If these features are absent, the clinician is prompted to consider alternative diagnoses, such as:
- Syncope (fainting),
- Stroke,
- Complex migraine, or
- Non-epileptic spells, which may mimic seizures but lack neurological underpinnings.
Differentiating First-Time Seizures
If the event is determined to likely be a seizure, the next step is assessing whether it is the patient’s first seizure. For first-time events, the focus shifts to identifying potential triggers, including:
- Medications: Use of or withdrawal from drugs that may lower the seizure threshold.
- Exposures: Environmental or toxicological factors.
- Immunosuppression: Conditions that may predispose to infections affecting the brain.
- History of head trauma: A common precipitant for seizures.
- Pregnancy: Associated risks like eclampsia.
Characterization of the Seizure
If it is not a first-time seizure, further characterization of the event is essential. Key aspects include:
- Onset: Understanding preceding events to identify immediate triggers and auras.
- Duration: Length of the seizure episode.
- Awareness: Assessing the patient’s level of consciousness during the seizure.
- Automatisms: Involuntary, purposeless movements that occur during the seizure and can be observed by others.
- Postictal state: The presence of transient neurological deficits following the seizure (absent in some types, such as absence seizures).
The clinician also verifies whether the current event is consistent with the patient’s previous seizure patterns.
Exploring Factors Reducing the Seizure Threshold
For patients with recurrent seizures, it is crucial to evaluate factors that might decrease the seizure threshold, including:
- Non-compliance or changes to anti-seizure drug (ASD) regimens.
- Illness or trauma: Physical or psychological stressors.
- Drug or alcohol use: Acute intoxication or withdrawal.
- Catamenial exacerbations: Hormonal influences in menstruating individuals.
- Pregnancy: Increased risk of seizures due to physiological changes or complications.
- Sleep deprivation: A well-documented precipitant of seizures.
This step ensures that modifiable triggers or exacerbating factors are identified and addressed.
Physical Examination
Physical examination is crucial for identifying etiologies and directing the management plan. During an active seizure, pay close attention to posture, motor activity, eye deviation, and nystagmus, observing asymmetries and focal findings [11]. Check if the clonic activity is suppressible by applying gentle pressure. Unlike insuppressible seizures, suppression suggests a different diagnosis, such as nonepileptic spells or movement disorders. Check for mydriasis in the eyes, which is commonly found during seizures, but its persistence afterward can indicate toxic exposure [2].
Vital signs should be measured after seizure activity has ceased. They are of high importance and may direct the physician to possible causes (e.g., fever suggests meningoencephalitis, tachycardia and hypertension suggest toxic sympathomimetic exposure, while hypertension and bradycardia can indicate herniation syndromes) [2].
Moreover, a general examination should aim to search for both findings and sequelae of the seizures. Physical findings such as nuchal rigidity, stigmata of substance abuse, and lymphadenopathy may be present. Potential sequelae of seizures should also be assessed [12]. Evaluation of soft tissue and skeletal trauma is important, as injuries are common. Check for head trauma, tongue injury, shoulder dislocation, bone fractures, or aspiration [2].
Finally, a complete neurological examination should be performed. Immediately following the seizure, hyperreflexia, focal motor deficit (Todd’s paralysis), and extensor plantar response (positive Babinski) can occur and are expected to generally resolve within an hour [13]. If Todd’s paralysis does not resolve quickly, it raises the suspicion of a focal structural deficit that caused the seizure (e.g., stroke). The persistence of altered consciousness or signs of ongoing subtle seizures, such as automatisms, abnormal eye movements, and facial myoclonus, suggests the persistence of the seizure and must not be missed (nonconvulsive seizures and status epilepticus) [2].
Alternative Diagnoses
Although no single clinical finding or diagnostic modality is 100% confirmatory of the diagnosis of seizures [14, 15], understanding the circumstances of the event and the factors surrounding it can help rule out or confirm diagnoses with similar presentations [2].
Findings that make the diagnosis of seizures more probable include postictal disorientation and amnesia, cyanosis during the event, lateral tongue biting, non-suppressible limb shaking, and dystonic posturing [2, 15].
If the patient experienced diaphoresis, palpitations, nausea, and vomiting before the seizure, it may suggest transient cerebral ischemia due to arrhythmias [2].
The presence of motor activity, commonly including a tonic extension of the trunk or myoclonic jerks of the extremities associated with bradycardia, raises the suspicion of convulsive syncope [16]. Once cerebral perfusion is restored, convulsions stop without any postictal period [2].
The diagnosis of migraine can sometimes be misleading due to the presence of a preceding aura that might be confused with nonconvulsive seizures (e.g., the positive visual phenomenon in occipital seizures) [17]. Unlike occipital seizures, migraines have a peak preceded by gradual evolution and followed by gradual resolution. Moreover, patients typically have a positive history of migraines with a similar presentation [2].
Nonepileptic spells or psychogenic seizures mimic status epilepticus in their presentation [18]. Due to the prolonged duration of the spells (five minutes or more, and sometimes exceeding 20 minutes), patients commonly receive high doses of benzodiazepines and need to be monitored for any respiratory compromise. Findings consistent with this diagnosis include a stop-and-go pattern of the convulsions, horizontal head shaking, forward pelvic thrusting, asynchronous bilateral convulsions with eyes closed, a short postictal period despite the long duration of spells, avoidance of noxious stimuli, and preserved recollection of events. Furthermore, laboratory testing lacks reactive leukocytosis and lactic acidosis, which are present in nearly all cases of prolonged generalized convulsive seizures or status epilepticus [2, 19].
Acing Diagnostic Testing
Due to the challenges of diagnosing a seizure, seeking diagnostic testing is of high value. Laboratory studies, radiology, and other special procedures frequently provide important elements in patient assessment [20]. Although some cases require extensive metabolic testing, it is not indicated for cases with an unremarkable history and normal examination findings. Serum glucose levels should be measured in all cases, as hypoglycemia is a common cause of provoked seizures [21]. It is also important to note that hypoglycemia could result from prolonged seizures. If correcting the glucose level does not stop a seizure, an alternate diagnosis should be evaluated. Lactic acid and creatinine kinase should also be measured in cases of prolonged seizures to assess for acute metabolic acidosis and rhabdomyolysis, respectively [22]. A low level of lactic acid during a prolonged convulsive episode makes a seizure less likely (nonepileptic convulsions) [2].
On the other hand, the presence of advanced age, comorbidities, abnormal examination findings, or an ill appearance demands comprehensive metabolic testing. Such testing includes serum glucose, creatinine kinase, lactic acid, electrolytes, complete blood count, urea nitrogen, creatinine, AST, ALT, anti-seizure drug levels, pregnancy tests, and drug-of-abuse screening. Checking for electrolyte derangements is important, as these can trigger seizures (e.g., hyponatremia, hypocalcemia, and hypomagnesemia) [23]. Patients with a low bicarbonate level should undergo blood gas analysis. An anion gap metabolic acidosis resulting from lactic acidosis is expected to decline within the first hour after the convulsive seizure stops unless another cause is present. Liver enzymes are tested to check for liver-mediated metabolic abnormalities that can impact therapeutic decisions [2].
Furthermore, patients on antiseizure medication should have their levels checked to confirm compliance. Some drugs are known to be epileptogenic, and it may be necessary to test their levels as well. Drug-of-abuse screening can also be considered in patients presenting with first-time seizures, despite the fact that such testing cannot prove causation or change outcomes [2, 24].
Urgent neuroimaging is indicated for most cases of a first-time seizure, whereas patients with epilepsy who have returned to baseline do not require one. Prompt neuroimaging and CT consideration in the ER is indicated for patients with coma, focal neurological deficits, immunocompromised states, advanced age, anticoagulation use, malignancy, previous intracranial hemorrhage, severe thunderclap headache, status epilepticus, neurocutaneous syndromes, or suspected trauma [25]. Computed tomography (CT) is widely available, but MRI and CT perfusion can provide additional information. If an infection is suspected, lumbar puncture is indicated [2].
Electroencephalography (EEG) is useful for diagnosing nonconvulsive seizures, epilepsy, nonepileptic spells, and status epilepticus [26]. EEG can guide therapy and monitor the treatment of refractory cases. Although it is not cost-effective, it is a high-yield modality for cases with an unclear diagnosis [2].
Lastly, ECG monitoring might benefit patients with preceding or ongoing cardiac symptoms. It can provide early clues in cases of drug toxicity and help understand the etiology of the seizure [2, 27].
Risk Stratification
The presentation and findings of a seizure case can provide clues as to whether this case has any red flags that demand urgent care. History and examination findings such as immunocompromisation, the presence of a thunderclap headache, sudden neurological deficit, status epilepticus presentation, head trauma, persistent altered consciousness, and concurrent infection can indicate a worse outcome [10]. Such patients require extensive investigations and prompt treatment to minimize morbidity and mortality due to the cause of the seizure or as a consequence of the seizures themselves [28]. Critical care for these patient groups is essential to reduce complications such as infection-related issues, irreversible intracranial structural disease, refractory status epilepticus, hemodynamic compromise, and death [2].
The risks of experiencing a secondary seizure following the current presentation may change the management plan to include secondary seizure prophylaxis. Risk stratification, weighing the chances of recurrence (higher in patients with previous brain insult, abnormal EEG, brain imaging abnormalities, and the presence of nocturnal seizures) against the risks of adverse effects from antiseizure medication, should be conducted in collaboration with a consulting neurologist [2].
Management
The initial priorities in managing unstable patients are to recognize and treat hypoxia, hypotension, and hypoglycemia, and to initiate pharmacologic treatment when needed [2, 28, 29].
Initial stabilization of patients with active seizures presenting to the ER includes the following [2, 28, 29]:
- Assess airway, breathing, and circulation: Do not use nasopharyngeal airway devices during the seizure, as they can cause injury and increase the risk of aspiration.
- Pulse oximetry.
- Electrocardiogram (ECG).
- Finger stick: If the glucose level is less than 60 mg/dL, administer IV dextrose.
- Aspiration precaution: Place the patient in the lateral decubitus position.
- Abortive treatment: Administer if the seizure lasts more than 5 minutes or in the case of hemodynamic compromise.
First-line therapy [2, 28, 29]
The first-line pharmacological therapies for managing epilepsy, include three benzodiazepine agents: diazepam, lorazepam, and midazolam. These agents are commonly used for their rapid onset and efficacy in controlling seizures, especially status epilepticus. The table includes critical details on dosing, frequency, maximum permissible dose, pregnancy category, and specific cautions.
- Diazepam
- Dose per kilogram: 0.15-0.2 mg/kg intravenously (IV).
- Frequency: Administered every 5 minutes as needed.
- Maximum Dose: Limited to 10 mg per individual dose and a cumulative total of 30 mg across all doses.
- Pregnancy Category: D (indicating a potential risk to the fetus, but benefits may outweigh risks in life-threatening situations).
- Cautions/Comments:
- Continuous monitoring of respiration is essential due to the risk of respiratory depression, a common side effect of benzodiazepines.
- Lorazepam
- Dose per kilogram: 0.1 mg/kg intravenously (IV).
- Frequency: Administered every 5 minutes as necessary.
- Maximum Dose: 4 mg per dose, with a cumulative maximum of 12 mg across all doses.
- Pregnancy Category: D.
- Cautions/Comments:
- Similar to diazepam, respiratory monitoring is mandatory.
- Intramuscular (IM) administration is contraindicated for lorazepam, likely due to inconsistent absorption or slower onset compared to IV administration.
- Midazolam
- Dose per kilogram: 0.2 mg/kg, administered via multiple routes including IV, intramuscular (IM), or intranasal (IN).
- Frequency: Doses can be repeated every 5 minutes as needed.
- Maximum Dose: 10 mg per individual dose.
- Pregnancy Category: D.
- Cautions/Comments:
- Respiratory monitoring is critical due to the sedative effects of midazolam.
- The half-life of midazolam is approximately 7 hours, making it a relatively short-acting agent compared to others, which can influence its clinical use depending on seizure recurrence risk.
All three agents are effective for rapid seizure control but share common risks, including respiratory depression, necessitating vigilant monitoring, particularly in critical care or emergency settings. Their classification in pregnancy category D highlights the need for careful consideration of maternal and fetal risks versus benefits. Midazolam offers more flexibility in administration routes, making it a practical choice in situations where IV access is not readily available.
If the seizure stops, coordinate a disposition plan and consider non-convulsive status epilepticus in patients who do not return to baseline. However, if the seizure does not stop, ensure adequate dosing of first-line therapy, then proceed to second-line therapy, and finally to third-line therapy, one step at a time [2, 28, 29].
Second-line therapy [2, 28, 29]
The second-line treatment options for epilepsy, include on a variety of antiepileptic drugs. These agents are typically used when first-line benzodiazepines are insufficient to control seizures. The table details dosing, frequency, maximum permissible doses, pregnancy categories, and relevant cautions for clinical use.
- Levetiracetam
- Dose per kilogram: 40-60 mg/kg administered intravenously (IV).
- Frequency: Administered once over a 10-minute period.
- Maximum Dose: 4500 mg.
- Pregnancy Category: C (indicating that risks cannot be ruled out, but the drug may be used if benefits outweigh potential risks).
- Cautions/Comments:
- Requires renal clearance, so dose adjustments may be necessary in patients with renal impairment.
- Fosphenytoin
- Dose per kilogram: 10-20 mg PE/kg (phenytoin equivalents) given IV or intramuscularly (IM).
- Frequency: Additional 5 mg PE/kg can be administered after 10 minutes if needed.
- Maximum Dose: 150 mg PE/kg.
- Pregnancy Category: D (associated with risk but can be used in life-threatening situations).
- Cautions/Comments:
- Can cause hypotension and dysrhythmias, requiring cardiac monitoring during administration.
- Lacosamide
- Dose per kilogram: 200-400 mg IV.
- Frequency: An additional 5 mg/kg can be administered if necessary.
- Maximum Dose: 250 mg.
- Pregnancy Category: C.
- Cautions/Comments:
- Can cause arrhythmias.
- Renal clearance is required, so adjustments are needed for patients with renal insufficiency.
- Phenobarbital
- Dose per kilogram: 15-20 mg/kg IV.
- Frequency: Additional 5-10 mg/kg can be given as needed.
- Maximum Dose: Not explicitly mentioned but calculated based on repeated doses.
- Pregnancy Category: D.
- Cautions/Comments:
- Monitor respiration closely due to the sedative and respiratory depressant effects.
- A strong P450 enzyme inducer, which can affect the metabolism of other drugs.
- Phenytoin
- Dose per kilogram: 15-20 mg/kg IV.
- Frequency: Additional 5-10 mg/kg can be administered if necessary.
- Maximum Dose: 30 mg/kg.
- Pregnancy Category: D.
- Cautions/Comments:
- Risk of hypotension and dysrhythmias during administration, necessitating monitoring.
- A strong P450 enzyme inducer, which impacts the metabolism of other medications.
- Valproic Acid
- Dose per kilogram: 20-40 mg/kg IV.
- Frequency: Additional doses of 20 mg/kg can be administered if necessary.
- Maximum Dose: 3000 mg.
- Pregnancy Category: D.
- Cautions/Comments:
- Strong P450 enzyme inducer.
- May cause hepatotoxicity and platelet dysfunction, warranting caution in patients with liver disease or coagulopathy.
The second-line agents are reserved for scenarios where first-line therapy fails to achieve seizure control. Each agent has specific risks and monitoring requirements. For example:
- Levetiracetam and lacosamide are generally well-tolerated but require dose adjustments in renal impairment.
- Phenobarbital, phenytoin, and valproic acid necessitate respiratory and hepatic monitoring due to their systemic side effects.
- Fosphenytoin and phenytoin require cardiac monitoring due to their potential to induce arrhythmias.
The choice of agent depends on the patient’s clinical status, underlying conditions, and the safety profile of the drug.
Third-line therapy [2, 28, 29]
The third-line therapy agents for managing refractory epilepsy, particularly in patients requiring intubation, mechanical ventilation, and hemodynamic support are administered in critical care settings to control seizures when first- and second-line therapies fail. Each drug is described with its dosing regimen, frequency, maximum dose, pregnancy category, and significant precautions.
- Ketamine
- Dose per kilogram:
- Loading dose: 1.5 mg/kg intravenously (IV).
- Maintenance dose: 0.5 mg/kg every 3-5 minutes as needed.
- Maximum Dose: Not explicitly stated, but administered as required to control seizures.
- Pregnancy Category: N (Not classified).
- Cautions/Comments:
- Ketamine acts as an NMDA antagonist, a unique mechanism among anticonvulsants.
- Hypotension is a potential side effect, necessitating blood pressure monitoring.
- Midazolam
- Dose per kilogram:
- Loading dose: 0.2 mg/kg IV.
- Maintenance dose: 0.2-0.4 mg/kg every 3-5 minutes.
- Maximum Dose: 2 mg/kg for the loading dose.
- Pregnancy Category: D (Risk to the fetus exists, but use may be justified in emergencies).
- Cautions/Comments:
- Midazolam may cause hypotension and requires continuous hemodynamic monitoring.
- Pentobarbital
- Dose per kilogram:
- Loading dose: 5-15 mg/kg IV.
- Additional doses of 5-10 mg/kg may be given if required.
- Maximum Dose: 25 mg/kg for the loading dose.
- Pregnancy Category: D.
- Cautions/Comments:
- Pentobarbital has a long half-life (22 hours), which makes it effective for sustained seizure control but may prolong sedation.
- It carries significant risks, including hypotension, ileus, myocardial suppression, immunosuppression, and thrombocytopenia, requiring vigilant monitoring in an intensive care setting.
- Propofol Infusion
- Dose per kilogram:
- Loading dose: 1-2 mg/kg IV.
- Maintenance dose: 0.5-2 mg/kg every 3-5 minutes as needed.
- Maximum Dose: 10 mg/kg for the loading dose.
- Pregnancy Category: B (Lower risk, but use must be cautious).
- Cautions/Comments:
- Propofol has a short half-life (0.6 hours), allowing for rapid onset and recovery.
- Side effects include hypotension, respiratory depression, hypertriglyceridemia, pancreatitis, and the rare but potentially fatal propofol infusion syndrome. Close monitoring of triglycerides and cardiac function is necessary.
Third-line therapies are used in severe, refractory cases of epilepsy where intubation, ventilation, and hemodynamic support are required. These drugs induce deep sedation or anesthesia to suppress seizure activity effectively. Key considerations for their use include:
- Ketamine: Offers a unique mechanism (NMDA antagonism), useful in resistant cases.
- Midazolam and pentobarbital: Provide effective sedation but require careful respiratory and cardiovascular monitoring due to risks of hypotension and prolonged sedation.
- Propofol: Its short duration of action allows for precise titration, but metabolic side effects and infusion syndrome necessitate caution.
The choice of agent depends on the clinical scenario, patient stability, and institutional protocols. These medications are used alongside comprehensive critical care support to manage complications and optimize outcomes.
Special Patient Groups
Certain notes are important to remember regarding special patient groups. In cases of seizures during pregnancy, considering the diagnosis of eclampsia is a high priority. Magnesium is the drug of choice for acute eclamptic seizures [30]. If a pregnant patient was previously diagnosed with epilepsy, a lower seizure threshold may result due to noncompliance, adjusted regimens, sleep deprivation, nausea and vomiting, or increased drug clearance. When managing status epilepticus, the risks to the fetus from the seizure are higher than the risks from the medication; therefore, manage the patient as you would a nonpregnant individual [31]. In the case of a new, non-eclamptic seizure, a workup is indicated as previously mentioned [2].
When To Admit This Patient
The decision to admit or discharge should be individualized based on the underlying illness, recurrence risk, and need for maintenance pharmacotherapy [32]. Admission for observation alongside neurological consultation should be considered for patients with an uncertain diagnosis, a history of neurological disease or other comorbidities, or in situations where follow-up is unlikely. In contrast, patients can be discharged home with early referral to a neurologist if they have normal examination findings, no significant comorbidities, no known structural brain disease, did not require more than a single dose of benzodiazepines, and are expected to comply with follow-up instructions [2].
Discharge instructions should include guidance on car driving, potentially dangerous activities (e.g., swimming, cycling, climbing ladders), and information regarding any needed follow-up [2, 33].
Revisiting Your Patient
A 22-year-old woman with a previous history of epilepsy was brought to the ER due to generalized tonic-clonic insuppressible movements of her limbs that started 15 minutes ago.
You immediately assessed the airway, breathing, and circulation and placed the patient in the lateral decubitus position to prevent aspiration, as she had a tongue injury. Blood sugar was measured using a finger stick, ruling out hypoglycemia. Lorazepam was then administered as abortive treatment.
You began taking a history from her husband. They were having lunch together when his wife suddenly started seizing, and he was unable to stop it. She had not regained consciousness since then. He mentioned that she had been inconsistent with her antiepileptic medication because she wanted to get pregnant and had read online about potential harms of the medications on a growing baby.
Her lactic acid level was high, her pregnancy test was negative, and the rest of her laboratory findings were within normal limits.
The patient was diagnosed with status epilepticus, a medical emergency requiring urgent management. The ABC approach was performed to ensure the patient’s safety, followed by the administration of benzodiazepines. If first-line therapy fails, second- and third-line therapies should be administered sequentially. Inconsistency with antiepileptic medication highlights the need for patient education and further discussion regarding her concerns and available treatment options.
Authors
Rand Redwan Al Sari
Dr Rand Al Sari is a dedicated General Physician practicing in Saudi Arabia. With a strong commitment to patient care, she is also actively engaged in medical research, staying at the forefront of healthcare advancements and integrating this knowledge into her clinical practice. Passionate about medical writing and journaling, Dr Al Sari reflects on her experiences to contribute meaningfully to the medical community, with a focus on evidence-based healthcare and improving patient outcomes.
Imad Khojah
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Reviewed and Edited By
Arif Alper Cevik, MD, FEMAT, FIFEM
Prof Cevik is an Emergency Medicine academician at United Arab Emirates University, interested in international emergency medicine, emergency medicine education, medical education, point of care ultrasound and trauma. He is the founder and director of the International Emergency Medicine Education Project – iem-student.org, chair of the International Federation for Emergency Medicine (IFEM) core curriculum and education committee and board member of the Asian Society for Emergency Medicine and Emirati Board of Emergency Medicine.
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