Seizure laboratory findings: Difference between revisions

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==<s>Laboratory Findings</s>==
<s>"Obtaining postictal levels of prolactin (within 20 minutes after a convulsive event), lactate (within 1 to 2 hours), ammonia (within several hours), or creatine kinase (especially 24 to 48 hours postictally) can help differentiate convulsive seizures from psychogenic nonepileptic attacks"<ref name="WuHirsch2020">{{cite journal|last1=Wu|first1=Ken|last2=Hirsch|first2=Lawrence J.|last3=Babl|first3=Franz E.|last4=Josephson|first4=S. Andrew|title=Choosing Anticonvulsant Medications to Manage Status Epilepticus|journal=New England Journal of Medicine|volume=382|issue=26|year=2020|pages=2569–2572|issn=0028-4793|doi=10.1056/NEJMclde2004317}}</ref></s>
<s><ref name="pmid28288363">{{cite journal| author=Nass RD, Sassen R, Elger CE, Surges R| title=The role of postictal laboratory blood analyses in the diagnosis and prognosis of seizures. | journal=Seizure | year= 2017 | volume= 47 | issue=  | pages= 51-65 | pmid=28288363 | doi=10.1016/j.seizure.2017.02.013 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28288363  }} </ref></s>
<s><br /></s>
===<s>Serum Prolactin Level</s>===
<s>Two [[meta-analysis|meta-analyses]] have quantified the role of an elevated serum prolactin.
The first meta-analysis found that:<ref name="pmid14988379">{{cite journal |author=Ahmad S, Beckett MW |title=Value of serum prolactin in the management of syncope |journal=Emergency medicine journal : EMJ |volume=21 |issue=2 |pages=e3 |year=2004 |pmid=14988379 |doi=}}</ref>
"If a serum prolactin concentration is greater than  three times the baseline when taken within one hour of syncope, then in the  absence of test "modifiers":</s>
#<s>The patient is nine times more likely to have  suffered a GTCS as compared with a pseudoseizure positive LR = 8.92 (95% CI  (1.31 to 60.91)), SN = 0.62 (95% CI (0.40 to 0.83)), SP = 0.89 (95% CI (0.60 to  0.98))</s>
#<s>Five times more likely to have suffered a GTCS as compared with  non-convulsive syncope positive LR 4.60 (95% CI (1.25 to 16.90)), SN = 0.71 (95% CI (0.49 to 0.87)), SP = 0.85 (95%  CI (0.55 to 0.98)). "</s>
<s>The second meta-analysis found:<ref name="pmid16157897">{{cite journal |author=Chen DK, So YT, Fisher RS |title=Use of serum prolactin in diagnosing epileptic seizures: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology |journal=Neurology |volume=65 |issue=5 |pages=668-75 |year=2005 |pmid=16157897 |doi=10.1212/01.wnl.0000178391.96957.d0}}</ref></s>
#<s>"Elevated serum prolactin assay, when measured in the  appropriate clinical setting at 10 to 20 minutes after a suspected event, is a  useful adjunct for the differentiation of generalized tonic-clonic or complex  partial seizure from psychogenic nonepileptic seizure among adults and older  children (Level B)."</s>
#<s>"Serum prolactin assay does not distinguish  epileptic seizures from syncope (Level B).</s>
#<s>"The  use of serum PRL assay has not been established in the evaluation of status"  epilepticus, repetitive seizures, and neonatal seizures (Level U)."</s>
<s>The serum prolactin level is less [[sensitivity (tests)|sensitive]] for detecting partial seizures.<ref name="pmid15256189">{{cite journal |author=Shukla G, Bhatia M, Vivekanandhan S, ''et al'' |title=Serum prolactin levels for differentiation of nonepileptic versus true seizures: limited utility |journal=Epilepsy & behavior : E&B |volume=5 |issue=4 |pages=517-21 |year=2004 |pmid=15256189 |doi=10.1016/j.yebeh.2004.03.004}}</ref></s>


==Overview==
==Overview==

Revision as of 14:24, 30 October 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Shakiba Hassanzadeh, MD[2]

Overview

The laboratory tests for patients with seizure may include checking for: hypoglycemia, hyponatremia, uremia, and drug intoxication, and levels of ammonia, creatine kinase (CK), lactate, and prolactin. Elevated prolactin level may be helpful in differentiating generalized tonic-clonic or complex partial seizure from psychogenic nonepileptic seizures, only if the patient’s prolactin level is measured 10 to 20 minutes after a suspected seizure event. Analysis of the serum prolactin level is not effective in distinguishing a seizure from syncope. No conclusion could be established regarding serum prolactin changes following status epilepticus, repetitive seizures, and neonatal seizures.

Laboratory Findings

The chemical panel and laboratory tests for patients with seizure may include checking for:[1]

Serum Prolactin Level

  • A study found that:[2]
    • If the serum prolactin level is more than three times the baseline (taken within one hour of the event and in the absence of test modifiers):
      • The patient is nine times more likely to have had a generalized tonic-clonic seizure (GTCS) compared to a pseudoseizure, and five times more likely to have had a GTCS compared to a nonconvulsive syncope.
  • Another study found that:[3]
    • Elevated prolactin level may be helpful in differentiating GTCS or complex partial seizure from psychogenic nonepileptic seizures, only if the patient’s prolactin level is measured 10 to 20 minutes after a suspected seizure event (grade B).
    • Analysis of the serum prolactin level is not effective in distinguishing a seizure from syncope.
    • No conclusion could be established regarding serum prolactin changes following status epilepticus, repetitive seizures, and neonatal seizures (Level U).

References

  1. Gavvala JR, Schuele SU (2016). "New-Onset Seizure in Adults and Adolescents: A Review". JAMA. 316 (24): 2657–2668. doi:10.1001/jama.2016.18625. PMID 28027373.
  2. Ahmad S, Beckett MW (2004). "Value of serum prolactin in the management of syncope". Emerg Med J. 21 (2): e3. doi:10.1136/emj.2003.008870. PMC 1726305. PMID 14988379.
  3. Chen DK, So YT, Fisher RS, Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology (2005). "Use of serum prolactin in diagnosing epileptic seizures: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology". Neurology. 65 (5): 668–75. doi:10.1212/01.wnl.0000178391.96957.d0. PMID 16157897.


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