This lecture is all about the recognition of an abnormal EEG, its characteristics, its appearance and all about how to differentiate the abnormal activity with normal EEG background.
This presentation looks at abnormal EEG patterns with examples for each. Benign variants, artifacts and focal ictal patterns are not part of this presentation.
This lecture is all about the recognition of an abnormal EEG, its characteristics, its appearance and all about how to differentiate the abnormal activity with normal EEG background.
This presentation looks at abnormal EEG patterns with examples for each. Benign variants, artifacts and focal ictal patterns are not part of this presentation.
This presentation looks at generalised periodic epileptiform discharges and the various disorders like Creutzfeldt Jacob disease (CJD), SSPE and metabolic encephalopathies in which it is seen. SIRPID is also discussed. Triphasic waves are described. Radermacker complexes in SSPE are described.
This presentation looks at the benign or non-epileptiform variants in EEG, their characteristics and identification. Examples of the common benign variants are provided in the presentation.
EEG variants, are always to be recognized while interpreting the EEG one must be aware of these. Major and most common EEG is variants are discussed in the stated presentation.
Syed Irshad Murtaza.
This pattern discusses the various EEG patterns seen in term as well as pre term neonates. Normal Variations as well as pathological traces are discussed
This presentation looks at generalised periodic epileptiform discharges and the various disorders like Creutzfeldt Jacob disease (CJD), SSPE and metabolic encephalopathies in which it is seen. SIRPID is also discussed. Triphasic waves are described. Radermacker complexes in SSPE are described.
This presentation looks at the benign or non-epileptiform variants in EEG, their characteristics and identification. Examples of the common benign variants are provided in the presentation.
EEG variants, are always to be recognized while interpreting the EEG one must be aware of these. Major and most common EEG is variants are discussed in the stated presentation.
Syed Irshad Murtaza.
This pattern discusses the various EEG patterns seen in term as well as pre term neonates. Normal Variations as well as pathological traces are discussed
Normal EEG patterns, frequencies, as well as patterns that may simulate diseaseRahul Kumar
This presentation discusses the vast range of traces that show the variations in normal EEG patterns, as well as discussing the frequency and amplitudes of various normal waveforms.
Most common anomaly is a cross-over of “median-to-ulnar” fibers, the Martin-Gruber anastomosis (MGA). (M U)
Occurs in 15-30% of the population
Unilateral or bilateral.
Involves only motor fibers; sensory fibers are spared.
Cross-over usually occurs in the mid-forearm, either directly from the main trunk of the median or from its branches, mostly AIN.
Crossed over fibers run with the distal ulnar nerve to innervate any of the ulnar muscles:
- hypothenar muscles (ADM),
- first dorsal interosseous muscle (FDI),
- thenar muscles (Adductor pollicis, FPB), or
- a combination.
Three Types
Type I – Cross-over fibers from Median to Ulnar supply the “hypothenar muscles (ADM).”
Differential diagnosis of this pattern:
1. Excessive stimulation of the Ulnar nerve at the ‘Wrist’ with co-stimulation of the Median nerve
2. Submaximal Stimulation of the Ulnar nerve at the ‘Elbow’,
3.Conduction block of the Ulnar nerve b/w the ‘W’ and ‘E’sites, or
4.MGA with crossing fibers innervating the ADM.
-10% drop in the ulnar CMAP ‘BE’ to ‘W’ is normal secondary to temporal dispersion.
ULNAR NERVE STIMULATION (Recorded From ADM)
Increase CMAPs at wrist.
Decrease CMAPs at elbow.
Conduction Block.
MEDIAN NERVE STIMULATION (APB)
NORMAL
MEDIAN NERVE STIMULATION (ADM)
Elbow: CMAP PRESENT AT ELBOW
Wrist: No Response
Type II (most common pattern) –
Crossover fibers Median to Ulnar supply the “thenar muscles” (adductor pollicis and the flexor pollicis brevis).
During routine median studies, when M-to-U cross-over innervates one of the ulnar innervated thenar muscles (AP/FPB).
Ulnar motor studies, recording ADM are normal.
CMAP is higher when median nerve is stimulated at the ‘Elbow’ than stimulation at ‘Wrist’
This is opposite to the normal.
So Stimulate ulnar nerve at ‘W’ and ‘E’ while recording the thenar.
Normally, ulnar stimulation at the ‘W’, recording thenar, evokes a thenar CMAP, with an initial positive deflection. This CMAP reflects the normal ulnar-innervated muscles in the thenar eminence.
If no MGA is present, subsequent stimulation of the ulnar nerve at the ‘E’ site will evoke a CMAP potential with the same amplitude.
If an MGA is present, CMAP will be substantially lower when ulnar nerve is stimulated at the ‘E’ site than at the W.
Distal median motor latency is prolonged when stimulated at ’Wrist’.
All median nerve fibers stimulated at ‘W’ must travel through the carpal tunnel and therefore are delayed.
However, when the median nerve is stim. at the antecubital fossa, most fibers travel through the carpal tunnel as usual, but some median fibers bypass the carpal tunnel by traveling through the anastomosis and innerv. ulnar muscles.
Because these fibers bypass the carpal tunnel, they arrive in the hand much sooner than the median fibers that are delayed through the carpal tunnel.
When they depolarize their ulnar-innerv. muscles, a positive deflection is seen at the thenar, indicating that a
The somatosensory system is the part of the sensory system concerned with the conscious perception of touch, pressure, pain, temperature, position, movement, and vibration, which arise from the muscles, joints, skin, and fascia.
The somatosensory system is a 3-neuron system that relays sensations detected in the periphery and conveys them via pathways through the spinal cord, brainstem, and thalamic relay nuclei to the sensory cortex in the parietal lobe
Impulses are carried from receptors via sensory afferents to the dorsal root ganglia, where the cell bodies of the first-order neurons are located.
Here the fibers split into 2 functional groups: a lateral group (or anterolateral system) and a medial group (or dorsal column-medial lemniscal system).
The lateral group carries mainly unmyelinated fibers that subserve pain and temperature sensations, whereas the medial group carries mainly myelinated fibers that convey proprioceptive impulses
Their axons then travel through the spinal cord either in an ipsilateral or a contralateral fashion. Note that second-order neuron cell bodies are located in different anatomical areas depending on the sensation they carry.
Broadly, the spinal cord contains the second-order neurons for the fibers carrying pain, touch, and temperature sensations.
The lateral group of fibers enters the spinal cord, then ascend to terminate on the substantia gelatinosa and the nucleus proprius, where the second-order neurons are housed
Fibers then ascend via the brainstem to the thalamus in the spinothalamic tracts (or STT).
The medulla contains the second-order neurons for fibers carrying touch, position, and vibratory sensations. The fibers are then either conveyed to the thalamus (where the third-order neurons are located)
The medial group also sends its fibers into the posterior spinal cord; however, upon reaching it, most fibers ascend to the dorsal column nuclei in the medulla and synapse there
These tracts synapse on a second-order neuron in the nucleus gracilis and cuneatus, which are located in the medulla.
Their axons then decussate form a bundle known as the medial lemniscus.
Fibers of the posterior columns and medial lemniscus are concerned primarily with position sense and fine discriminative touch
These fibers travel to the midbrain on their way to the thalamus. Once in the thalamus, they synapse on third-order neurons in the ventral posterior lateral (VPL) nucleus.
The third-order neurons then project to the primary somatosensory cortex, which is located in the postcentral gyrus (also known as Brodmann areas 1, 2, and 3) of the parietal lobe
Primary somatosensory cortex subserves general and proprioceptive sensations and serves to integrate sensory information
Somesthetic cortex is organized in a sensory homunculus
Body areas particularly important to the sensory system (for example the face, lips, and hand) are given larger representation than other areas
Sensory receptorsperipheral nerve dorsal
AMSAN is usually severe with quadriplegia, respiratory insufficiency and delayed, incomplete recovery.
EMG NCS...
Sensory and motor axonal involvement.
CMAP and SNAP amplitudes low
F and H responses were absent
Conduction block and temporal dispersion seen in demylenating neuropathy I,e AIDP
Reduce Recrument
Reduce interference pattern
After 3 weeks denervation and neurogenic changes.
Acute Motor Axonal Neuropathy (AMAN)....
Characterized by acute/subacute onset of relatively symmetric limb
weakness, diffuse
In 1916, George Guillain, Jean-Alexandre Barré, and André Strohl described acute and progressive limb weakness causing major difficulty in 2 soldiers they examined in an army hospital during the battle of the Somme (northern France, World War I).
The key features were the discovery of an unusual cerebrospinal fluid (CSF) finding of isolated albumin elevation.
Guillain–Barré syndrome, is an acute polyradiculoneuropathy,
a disorder affecting the peripheral nervous system.
Ascending paralysis, weakness beginning in the feet and hands and migrating towards the trunk, is the most typical symptom,
some subtypes cause change in sensation or pain as well as dysfunction of the autonomic nervous system.
It can cause life-threatening complications, in particular if the respiratory muscles are affected or if there is autonomic nervous system involvement.
GBS is characterized by weakness and numbness or a tingling sensation in the legs and arms and possible loss of movement and feeling in the legs, arms, upper body, and face. along with complete loss of deep tendon reflexes.
The exact cause of GBS is unknown, but it is sometimes triggered by a respiratory infection or the stomach flu.
Other causes may be campylobacter, cytomegalovirus, epstein-bar virus, HIV, vaccination, surgery, trauma, malignancy.
Acute Inflammatory Demyelinating Polyradiculo neuropathy (AIDP...
Most common variant, 85% of cases.
Primarily motor inflammatory demyelination ± secondary axonal damage.
Maximum of 4 weeks of progression.
Anti GM1 Ab
Schwan myelin cell attack
Rapid recovery
EMG NCS FINDINGS...
Sensory and motor involvement
Latency prolongation
Slow conduction velocities
Duration broad
F and H prolong
+/- axonal loss low amplitudes
Conduction block 1 or 2 unentrapment sides.
Temporal dispersion Reduce Recrument
Reduce interference pattern
After 3 weeks denervation and neurogenic changes.
Acute Motor and Sensory Axonal Neuropathy (AMSAN)...
Initially described by Feasby as axonal GBS.
Characterized by acute quadriparesis (Weakness of all four limb), areflexia, distal sensory loss, and respiratory insufficiency.
CSF with increased CSF.
EDX shows loss of motor and sensory potentials with diffuse active denervation. No evidence of primary demyelination.
EDX studies differentiate from typical GBS by showing evidence of only axonal degeneration , without demyelination.
Condition is now labeled acute motor-sensory axonal neuropathy (AMSAN)
AMSAN is usually severe with quadriplegia, respiratory insufficiency and delayed, incomplete recovery.
EMG NCS...
Sensory and motor axonal involvement.
CMAP and SNAP amplitudes low
F and H responses were absent
Conduction block and temporal dispersion seen in demylenating neuropathy I,e AIDP
Reduce Recrument
Reduce interference pattern
After 3 weeks denervation and neurogenic changes.
Acute Motor Axonal Neuropathy (AMAN)....
Characterized by acute/subacute onset of relatively symmetric limb
weakness, diffuse.
Continuous spike and wave during slow wave sleep(CSWS)Faizan Abdullah
continuous spike and wave during slow wave sleep(CSWS) was first described by patry.
The syndrome is characterized by continuous spike and wave activity during non-REM sleep and is sometimes called as “Epilepsy with electrical status Epilepticus during slow sleep” (ESES ).
Onset ranges from 1-12 years peak age around 8 years.
2/3 of patients normal neurologically before onset. In time most patients have frequent seizures generalized tonic clonic , atypical absence and atonic also have a significant decline in IQ with deterioration in language, impaired memory , reduced attention span, and behavioral changes with aggression or psychosis epileptiform activity consists of generalized slow 1.5 to 2.5HZ spike wave as well as focal or multifocal spikes, which are sporadic in the waking state.
In sleep, spike-wave bursts become nearly continuous(CSWS pattern) , occupying more than 85% of the total NON-REM sleep time .
The csws pattern persists for one to several years. Similar to LKS, the EEG then tends to normalize and seizures remit spontaneously in most patients.
However recovery of neurological deficit and behavior is often incomplete and about half of the patients remain profoundly impaired.
EEG calibration are some steps which was followed by technologists in conventional EEG times. they are the steps to check the machines integrity either its properly working or not before the procedure began.it is very important to calibrate machine before the initiation of the test to interpret false results.
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
The Gram stain is a fundamental technique in microbiology used to classify bacteria based on their cell wall structure. It provides a quick and simple method to distinguish between Gram-positive and Gram-negative bacteria, which have different susceptibilities to antibiotics
Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
MIP 201T & MPH 202T
ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS : UNIT 5
APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMS By - AKANKSHA ASHTANKAR
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
1. Benign EEG Variants
Prepared by
Faizan Abdullah
NPS Trainee technologist
Aga Khan University Hospital Karachi Pakistan
21-09-2020
2. CONTENT
1.Introduction
2.Types of benign variants
3.Rhythmic EEG variants
I. Alpha variant.
II. Mu rhythm.
III. Rhythmic temporal theta burst of drowsiness (“psychomotor variant”).
IV. Subclinical rhythmic electrographic (theta) discharges in adults (SREDA).
V. Midline theta rhythm.
4.Epileptiform EEG variants
I. 14 and 6HZ positive spikes
II. Wicket spikes
III. Small spike sharps (SSS)
IV. 6HZ phantom waves
5.Lambda and lambdoids
I. Lambda waves
II. Posts pr lambdoids
III. Slow lambdoids
6.Age related variants
I. Hypnogogic and hypnopompic hypersynchrony
II. Posterior slowing of youth
III. Temporal theta in elderly
7.References
3. Introduction
Variants are the EEG patterns that look like
abnormal but considered as normal under
given circumstances.
6. Alpha Variants
• Described first by Goodwin in 1947. There are two types of alpha variants, "slow” and
“fast.”
• The slow (sub harmonic) alpha variant appears as an abrupt, usually has a bifurcated
configuration rhythm and half the frequency of the patient’s more typical waking
background rhythm, and often of greater voltage.
• The fast (harmonic) ….“double” the frequency of the patient’s more typical waking
background rhythm, appearing as beta activity.
• The fast alpha variant rhythm can be induced by hypnotic or anxiolytic medications such
as barbiturates or benzodiazepines .
• Alpha variants behave like alpha rhythm and occurs less than 1% of the normal adult
population
8. Alpha Squeak effect:
The first few seconds after closing the eyes might produce an alpha rhythm that
is slightly faster than in other resting and eyes closed state.
The frequency of the PDR should not be calculated during thisperiod.
9. Mu rhythm
• Also named as “comb” or “wicket rhythm,” or “rhythme rolandique en
arceau
• This waveform is recognized easily and has no pathological significance.
• The mu waveform occurs in the central regions in the awake patient with
the frequency of 9-11 Hz.
• Mu is usually observed bilaterally with shifting predominance; it may,
however, be asymmetrical and asynchronous. Exclusively lateralized mu
should raise a suspicion of an abnormality in the hemisphere …… mu
activity.
• Often in the alpha range frequency, it has rounded positive aspects on 1
side and sharpened negative aspects on the other.
• It is not blocked by eye opening
• It becomes obvious when the alpha disappears (i.e., alpha blocking)
• The most classical feature of mu waveform is that it blocks with motor
activity of the contralateral body.
10.
11.
12. Rhythmic Temporal Theta Bursts of
Drowsiness (“Psychomotor Variant”)
Gibbs et al. called this pattern the “psychomotor variant” because it was
thought to represent a temporal lobe or psychomotor seizure.
But discarded because this pattern is observed in asymptomatic healthy
individuals and exhibits poor correlation with patients with true temporal
lobe or psychomotor seizures.
Also called “rhythmic mid-temporal discharges” describing its …. mid-
temporal head regions, but can spread parasagittally.
This pattern may be present in waking or early drowsiness and usually in
tracings of adults and adolescents. It wanes with deepening sleep. As its
name implies, this particular pattern
5- to 7-Hz rhythms in bursts or trains lasting often longer than 10 s and
sometimes beyond a minute. often sharply contoured, monomorphic; it
does not evolve significantly in frequency or amplitude, as occurs in most
ictal patterns.
Rhythmic mid-temporal discharges can occur bilaterally or independently
with shifting hemispheric predominance.
13.
14.
15.
16. SREDA
• This variant pattern involves sharply contoured 5- to 7-Hz
activities with a wide distribution, mainly over temporo-parietal
derivations.
• It is usually bilateral, but can be asymmetrically disposed.
• can appear as repetitive monophasic sharp waves or as a single
discharge of sharp waves that gradually accelerate to form a
sustained, rhythmic train of theta activity. This may last from 20
s to several minutes, usually 40 to 80 s.
• Because of its duration and evolution, SREDA can easily be
misinterpreted as an ictal pattern
• SREDA is more typically seen in older adults (older than 50
years), and more common at rest, drowsiness, or during
hyperventilation.
17.
18. Midline theta rhythm
• The midline theta rhythm is most prominent at Cz
but may spread to nearby contacts.
• This 5- to 7-Hz frequency exhibits either a smooth,
arc-shaped (mu-like) or spiky appearance.
• Duration.. Variable, tends to wax and wane, more
common in wakeful and drowsy states
• Reacts variably to limb movements, alerting, and/or
eye opening.
• Now regarded to be a nonspecific variant, although
initially it was considered a marker of an underlying
epileptic tendency.
20. 2. EPILEPTIFORM VARIANT PATTERNS
There are 4 major types of Epileptiform
variant patterns:
• 14- and 6-Hz positive bursts.
• Small sharp spikes (benign Epileptiform
transients of sleep [BETS]).
• 6-Hz spike and wave (phantom spike and
wave).
• Wicket spikes.
21. FOURTEEN AND SIX HZ ACTIVITY
• comb-shaped positive spikes maximum at the
posterior temporal/occipital electrodes with a
frequency of 13 to 17 Hz and/or 5 to 7 Hz,
mostly consisting of 14 Hz and/or 6 Hz. .
• Seen during drowsy or light sleep.
• Well seen on contralateral ear referential
montage .
• It occur independently over both sides.
• Best seen in the age group of 13-14yrs.
22. 14 & 6 Hz SPIKES in
longitudinal bipolar montage
27. • Resemble mu or wicket rhythm seen in the central
region but they occur in the temporal electrodes.
• Appear as brief (<1 s) bursts at 6 to 11 Hz in a
crescendodecrescendo form of sharply contoured
alpha or sharp activity.
• They are predominantly seen in adults older than 50
years.
WICKET SPIKES:
28. Cont’d
• When wicket spikes occur in isolation, they may be mistaken
for an epileptiform discharge. Several features help
differentiate isolated wicket spikes from pathological spikes.
A similar morphology of the isolated wicket spike to those in a
later train or cluster argues for the variant pattern and against
an epileptiform discharge. The absence of a following slow-
wave argues for the variant and against an epileptiform
discharge. An unchanged background also argues more for the
variant and against an epileptiform event.
34. Small Sharp Spikes/BETS
• As these names imply, small sharp spikes or benign epileptiform transients of
sleep (BETS) are low in amplitude (~50 µV) and brief (~50 ms).
• Their morphology can be monophasic or diphasic. When diphasic, the ascending
limb is quite abrupt and the descending limb slightly less so They may exhibit a
subtle following slow wave.
• BETS are isolated and sporadic.
• They appear during drowsiness and light sleep in adults.
• They are usually unilateral but can appear independently (and rarely
synchronously) from bilateral regions.
35. Cont’d
.Other distinguishing features BETS and epileptiform activity are that BETS
do not run in trains, distort the background, or coexist with rhythmic slowing,
and BETS diminish with deepening sleep, whereas epileptiform discharges
worsen with deeper sleep stages.
36.
37. • 6Hz spike and wave (Phantom spike and wave):
• These occur as bursts of miniature spike and wave complexes or runs of
such complexes at 6 Hz rather than the usual 2-4 Hz.
• Their significance is debated, but generally those occurring in the
posterior head regions are regarded as benign.
• Seen at all ages (but especially in adults) they often are confused with 14-
and 6-Hz waves and may merge into them.
38. Phantom spike has further two variants as,
WHAM
wake high amplitudes anterior dominant in males.
FOLD
female occipital low amplitude in drowsiness.
Differentiate wicket spikes from epileptiform spikes:
1. The absence of slow waves following and a preserved background favor
wicket spikes.
2. An equal rise and decay of the sharp waveform also favors a wicket
spike.
44. LAMBDA WAVE
• A Normal EEG pattern.
• They resemblance to the Greek lowercase letter lambda ( ) so called lambda
waves.
• Positive waves
• Seen over the occipital region when patient is looking at a picture of pattern.
• It blocks on eye closing or looking at white card.
• They have a duration of 160 to 250 ms, an amplitude of 20 to 50 µV, and
usually appear over bi-occipital leads, although occasionally may be unilateral
48. Positive occipital sharp transients of sleep or
Lambdoid
• Normal EEG pattern
• Morphologically they are surface positive potentials
• They are seen maximum at 01-02 leads.
• They are seen during drowsiness.
• POSTS are usually synchronous but can be asymmetric in
size. There are most commonly seen between 15 and 35 yr
of age, and usually in light sleep.
51. Slow lambdoids
• Slow lambdoids of youth, also known as cone-shaped
waves or O-waves, are high voltage, diphasic slow
transients seen over the occipital contacts and frequently
with the occipital delta activity in deeper sleep states
• As the name implies, they are cone-shaped. They can be
seen up to 5 yr of age.
• OTHER NAMES ARE
1.RHO WAVES,
2. CONE SHAPED WAVES
3.O WAVES
4.SLOW LAMBDOIDS OF YOUTH
52.
53. Age related variants
Posterior slow waves of youth, also called youth waves, posterior fused
transients, and sail waves, are triangular, 2- to 4-Hz waveforms that coexist with other
waking background rhythms.
Less prevalent toward the age of 20 years but could be seen as late as 25 years of age.
Distinguish between normal and abnormal posterior delta :
(a) disproportionately high amplitude as compared to the alpha rhythm (>1.5 times the
voltage of the alpha rhythm or >200 μV),
(b) serial rhythmic waveform which constitutes OIRDA (Occipital Intermittent
Rhythmic Delta Activity
(c) widespread distribution involving the central or midtemporal electrodes,
(d) predominantly unilateral.
(e) persistent after eye opening.
55. Temporal theta in the elderly
It is a commonly encountered age-dependent pattern. This is a 4- to 5-Hz activity
involving temporal channels and is thought by some to represent a subharmonic
of the 8- to 10-Hz background rhythm common in the asymptomatic elderly
individuals. However, this rhythm is distinct from the alpha rhythm in that it
persists with eye opening and even into drowsiness and light sleep.
Hyperventilation augments this pattern’s voltage and persistence.
Some have observed them to be more prevalent over the left hemisphere. Their
significance remains controversial.
56. HYNOGOGIC and HPYNOPOMPIC
• Synchronous high voltage theta, delta at
beginning of sleep
• < 2 yrs of age
• May be notched and/or have a spiky
component only occurs at transition phase.
• Reverse phenomena could also in opposite
phase which is hypnopompic response.