1. Neurological history taking
Dr Mohamed Rizk Khodair
Lecturer of neurology
October 6 university
Mohamedrizk.med@edu.edu.eg
2. Aim
The neurologic history and screening examination when performed in a systematic manner provides the clinician with
the necessary data to make management decisions.
3. Agenda
• Introduction
• Personal history
• Complaints and its duration
• History of present illness
• Past history
• Family history
4. Introduction:
• The history is the most important part of the neurological assessment.
• The student should aim to be a good listener showing interest and sympathy as the patient’s story unfolds.
• It is important to get the patient’s trust and confidence.
• First introduce yourself to the patient, explain who you are and ask permission to take a history and to
carry out an examination.
• Make patient at ease : introduce yourself, exchange social pleasantries , secure privacy .
• Be friendly , attentive , courteous ( don’t haste or stereotype)
• Analyze and inquire about significant symptoms , minimize irrelevancies
• Modify your approach according to pts personality , age , education , culture and sex.
• Some clinical findings are apparent to the examiner during history taking; these include general state of
health and obvious neurological deficits and disabilities.
• If there is alteration in the level of consciousness or the patient is unable to give a history, then it may be
necessary to obtain a history and witnessed account from a relative or friend before proceeding directly to
neurological examination
• Some clinical findings are apparent to the examiner during history taking; these include general state of health
and obvious neurological deficits and disabilities.
• in some neurological disorders , it is the only key to diagnosis ( epilepsy and migraine)
6. What is the Lesion?
V Vascular
I Infectious
T Trauma
A Autoimmune
M Metabolic & Toxic
I Iatrogenic & Inflammatory
N Neoplastic
C Congenital/Familial
D Degenerative
E Epileptic
F Functional
7. Where Is the Lesion?
A. Central nervous system:
Cranial:
1. Cerebral: (Right # left, Which lobe? Cortical
#subcortical)
2. Cerebellar:
3. Brain stem:
Spinal: (Intramedullary # Extra medullary)
B. Peripheral nervous system:
Roots
Nerves
NMJ
Muscles
9. KEY POINTS IN A NEUROLOGICAL HISTORY
Personal history
Name, age, sex, occupation, handedness, marital status and no. of siblings, residence, special habits, and history of the
use of contraceptive pills, menstrual history ( age , regulatory , duration , flow , pain ).
Age: certain diseases are commonly related to age as:
-Demyelinating diseases in early and middle adulthood.
-Degenerative diseases and cerebrovascular diseases in late adulthood and elderly.
Sex: some diseases are common for each sex as:
- Myasthenia gravis and migraine are common in females.
- Myotonia atrophica and cerebrovascular stroke are common in males.
Marital status & number of siblings.
Occupation: Some diseases related to certain occupation as:
- Parkinsonism in manganese miners.
- Some occupations are avoided in epileptic patients.
10. Occupation: Some diseases related to certain occupation as:
- Parkinsonism in manganese miners.
- Some occupations are avoided in epileptic patients.
Residence: some diseases are common in certain areas as:
-Demyelinating diseases are common in Northern countries.
-Meningitis is common in tropical areas.
Special Habits:
- Smoking: smoking index= number of cigarettes/days × years of smoking
- Alcohol and Drug addiction
- Cerebrovascular diseases are common in smokers and in those who are drug adductors.
Contraceptive methods:
- Benign increased intracranial tension and venous stroke are common in females receiving oral contraceptive pills.
Handedness:
Right or left-handed to determine the dominant hemisphere.
11. Personal History & Chief Complaint
Male patient Mr. Mohamed is 26 years old worker , married , has 3 offspring
the youngest one is 3 years old ; he is smoker with no other special habit of
medical important , right-handed Caucasian gentleman presented to the OPC
complains of heavness of right side 2 months ago,
12. Complaint and its duration
Asking the patient to state what the problems are and the reason for Hospital
admission or referral.
This could begin with open questions such as “what is the main problem" or “tell me
about it from the start”.
Determine the order of the presenting complaints, These should ideally not
number more than three or four and be in order of importance. if more than one event?!
Most recent
Write in the patient's words.
13. Examples
• Weakness or heaviness in limbs
• Difficulty walking
• Pins and needles or numbness in arms, legs or body
• Change in mood, memory, concentration or sleep
• Pain, headache, face or limbs·
• Loss of consciousness or dizzy spells
• Loss of vision or double vision
• loss of hearing or balance
• Difficulty speaking or swallowing
• Difficulty with passing urine, bowels and sexual function
14. HISTORY OF PRESENTING ILLNESS
A) Ask the patient to describe (of each main complaint)
Ask the patient to describe (of each main complaint)
• Onset duration between 1st symptom till complete
clinical picture (sudden, acute, rapid, subacute,
gradual):
1- Sudden over seconds or minutes (as stroke,
trauma)
2- Acute over hours (as vascular, inflammatory)
3- Subacute or rapid --- over days to weeks (as
inflammatory, demyelinating)
4- Gradual over months to years (as neoplastic,
degenerative)
• Progress (course) behavior of the disease
1. Regressive (towards improvement)(as trauma,
vascular, inflammatory, demyelinating)
2- Stationary (as inflammatory, trauma, vascular)
3- Remittent (as demyelinating, vascular)
4- Progressive (as neoplasm, degenerative)
5- intermittent ( epilepsy and migraine)
• Duration,
• Site & Side
15. B) Analysis of symptoms
1. Symptoms suggestive of motor system affection
2. Symptoms suggestive of increased intracranial tension
3. Symptoms suggestive of cranial nerve affection
4. Symptoms suggestive of sensory system affection
5. Symptoms suggestive of sphincteric disturbances
6. Symptoms of Higher brain functions disturbance.
7. Meningeal and stretch symptoms.
8. Symptoms suggesting of Epilepsy, headache, others.
9. Other systems manifestation.
16. Motor system
• OCD
• Distribution : Uni/bilateral
symmetrical/ asymmetrical
distal/proximal
flexor/extensor
simultaneous/ sequential
• Discrimination : UMN/LMN (early wasting , fasciculation, flail/stiff)
• Degree of severity (ambulation) :
I. Ambulant without support
II. Ambulant with minimum support
III. Ambulant with maximum support
IV. Wheelchair
V. Bedridden
Weakness Involuntary movements Incoordination
Weakness
analysis
Onset Course Duration Character Distribution
18. Coordination
• UL : intention tremors : increase on reaching target (key to locker , spoon to mouth ) , difficult
buttoning
• LL : clumsiness , staggering , wide base gait
• Dysarthria : staccato
Cerebellar Ataxia (Cerebellum) Sensory Ataxia (Deep Sensation)
Upper limb Lower limb Upper limb Lower limb
Upper limb is affected
lately → tremors
during eating.
المعلقة تاكل تيجي لما
بترتعش؟
Lower limb is
early affected
→ staggering
gait.
بتمشي؟ وانت بتطوح
البدلة؟ زرار تقفل بتعرف
الف سوسته تقفلي بتعرفي
ستان؟
Falling when eyes
are closed,
بتغسل وانت عينيك غمضت لو
وشك
,
بتقع؟
19. Abnormal movement :
• slow or fast
• regular or irregular
• postural / twisting / pseudopuposeful stereotype or not
• hypertonia or hypotonia
• increase or decrease by
• uni or bilateral
• association
Involuntary
movements
analysis
Onset Course Duration Character Distribution
21. The physical exam findings correlating with location of lesion
UMN dysfunction LMN dysfunction NMJ dysfunction Muscle dysfunction
• Increased muscle
tone
(spasticity/rigidity)
• Increased muscle
stretch reflex
(hyperreflexia)
• Extensor plantar
reflex (positive
Babinski’s sign)
• Decreased muscle
tone (flaccidity)
• Decreased muscle
stretch reflex
(hyporeflexia)
• Flexor plantar
reflex (absent
Babinski’s sign)
• Fluctuating
weakness
• Worsening
weakness with
repeated activity
(fatiguability)
• +/− Decreased
muscle tone
• Proximal muscles
are most
commonly
involved
• +/− Decreased
muscle tone
22. UMN VS LMN
Upper Motor Neuron Lower Motor Neuron
Mild-moderate weakness Severe weakness
Spastic tone Flaccid tone
Minimal disuse atrophy Marked muscular atrophy
Hyperreflexia Reduced or absent reflexes
Pathological Babinski sign No Babinski sign
Clonus may be present No clonus
No fasciculations Fasciculations
23. Example
The condition started 2ws ago when the patient experienced acute onset , regressive course of
weakness of RT UL and LL , such weakness was Distal >Proximal , the patient felt his limbs neither
flail or stiff , there were no fasciculation , no wasting , no manifestation as regard the other limbs, and
at the onset the patient was ambulant with maximum support and now he is ambulant without
support
26. example
The condition was also associated with diminution of sensation ( tingling and numbness ) involving
right side of the body
The patient loses his balance on closure his eyes or on entering a dark room
The patient is feeling the ground underneath as if sponge
33. Diplopia
• OCD
• Monocular or binocular
• Corrected with closure of one eye or not
• 2 images ( next to each other , above each other )
• False(outer image) or true image ( fixating eye )
• Painful or not
• Diminution of vision
• Ptosis
• Local eye manifestations
43. HISTORY SUGGESTIVE OF ENCEPHALITIS
DCL
Convulsions
Disturbed sleep rhythm
Oculogyric crisis
Behavioral or mental changes
Focal manifestations as cranial nerve palsy and long tract
lesions.
44. Neck pain or stiffness
Toxemic manifestations as fever, malaise
Manifestations of ICT
DCL
Focal manifestations as cranial nerve palsy and long tract lesions.
HISTORY SUGGESTIVE OF MENINGITIS
45. Special situations
Headache / pain:
• OCD , character , site , radiation
• Increase , decrease , associated
• Severity (interrupt sleep, interfere with daily activity )
• Relation ( sleep , stress , mental , physical or psychological)
Epilepsy or syncope:
• Started:
• Last attack:
• Rate (frequency) Now & on medications
• Type & Similarity of attacks:
• Sequences:
• PDF:
• Previous & Current medications & doses
47. Review of other systems
GIT: Heart burn, indigestion
Skin & orifices: rashes or tick bites, bleeding
Skeletal: arthralgias or myalgias
cardiopulmonary: chest pain, palpitations, or leg swelling
Metabolic: Fever & body weight
48. Past History
• Diseases ( chronic illness , allergies , admission to hospital )
• Operations ( type and time , anesthesia , blood transfusion )
• Drugs of neurological importance ( chronic drug intake : TB )
• Trauma of neurological importance ( site , associated symptoms )
• Fever of neurological importance .
49. Family history
• Consanguinity
• Similar condition or risk factors in the family
please establish ( pedigree chart )
• Other neuropsychiatric disorder
• Family history of medical illness : DM ,HTN ,
Cardiac .
50. Case formulation
A male patient aged 60 ys old, known to be diabetic and hypertensive and he is compliant on
treatment. One week ago, he had acute left sided hemiplegia that was associated with dysarthria, left
UMN facial N lesion. This weakness was affecting D>P, UL>LL. There was no DCL, mental changes,
fits or sensory affection.
51. Reaching provisional diagnosis
The history is the most important part of neurological evaluation that guides to establish :
• Anatomical diagnosis: focal , systemic , disseminated
• Etiological diagnosis: hereditary , symptomatic , idiopathic
52. Determine Where & What Is The Lesion:
A. Where is the lesion?
- Means the relation between different symptoms and affected structures.
- Determined by positive and negative symptoms.
Types;
1) Focal: affected structures are related anatomically.
2) Multifocal: symptoms are explained by more than one focus e.g., multiple arteriovenous malformations (AVMs),
multiple space occupying lesions.
3) Disseminated: symptoms are disseminated in place (multifocal, with selectivity) and time MS.
- For focal, multifocal or disseminated lesions determine localization e.g., right hemiparesis,
hemihypersthesia, plus cortical expressive aphasia lesion in left cortical-subcortical frontoparietal
region.
4) Systemic disease: affected structures are related physiologically or functionally:
Parkinsonism disease → (extrapyramidal system)
Myasthenia gravis (MG) → (myoneural junction).
- Determine the affected system(s) (could be single or multiple) as extrapyramidal system or peripheral
nerves.
53. B. What is the lesion?
- Means the underlying etiology and pathology.
- Types: vascular, inflammatory, degenerative, congenital, traumatic, metabolic,
neoplastic, or drug induced.
- Determined from onset, course, and duration, e.g.,
-Sudden onset, regressive or stationary course vascular (stroke), or traumatic.
-Gradual onset, progressive course degenerative, neoplastic, or metabolic.