Wednesday, November 23, 2011

Bifacial weakness (flow chart+table)


Rhaumatoid Arthritis


- Chronic systemic inflammatory disorder involving the joints

- Peripheral symmetrical non-suppurative arthritis

- Unknown cause (autoimmune)

- Onset : 30-50 years old

- F:M = 3:1

- Mnemonic for diagnosing RA: RF RISES

Ø Rheumatoid factor

Ø Finger / hand joints involved (>6weeks)

Ø Rheumatoid nodules

Ø Involvement of 3 or more joint areas

Ø Stiffness (morning) > 1 hour > 6 weeks

Ø Erosions on X-ray

Ø Symmetrical arthritis > 6weeks

Revised Criteria for the Classification of RA

1. Guidelines for classification

a. 4 of 7 criteria are required to classify a patient as having rheumatoid arthritis (RA).

b. Patients with two or more clinical diagnoses are not excluded.

2. Criteriaav

a. Morning stiffness: Stiffness in and around the joints lasting 1 h before maximal improvement.

b. Arthritis of 3 or more joint areas: At least 3 joint areas, observed by a physician simultaneously, have soft tissue swelling or joint effusions, not just bony overgrowth. The 14 possible joint areas involved are right or left proximal interphalangeal, metacarpophalangeal, wrist, elbow, knee, ankle, and metatarsophalangeal joints.

c. Arthritis of hand joints: Arthritis of wrist, metacarpophalangeal joint, or proximal interphalangeal joint.

d. Symmetric arthritis: Simultaneous involvement of the same joint areas on both sides of the body.

e. Rheumatoid nodules: Subcutaneous nodules over bony prominences, extensor surfaces, or juxtaarticular regions observed by a physician.

f. Serum rheumatoid factor: Demonstration of abnormal amounts of serum rheumatoid factor by any method for which the result has been positive in less than 5% of normal control subjects.

g. Radiographic(X-ray) changes: Typical changes of RA on posteroanterior hand and wrist radiographs that must include erosions or unequivocal bony decalcification localized in or most marked adjacent to the involved joints.

- av Criteria a–d must be present for at least 6 weeks. Criteria b–e must be observed by a physician.

Parkinsonism


- A clinical syndrome characterized by (cardinal signs)

o Tremors (rest tremors)

o Rigidity (cogwheel)

o Bradykinesia (slowness in execution of motion / slow movement)

- Types of parkinsonism

o Primary parkinsonism = Parkinson’s disease (PD)

o Secondary parkinsonism – neuroleptics/antipsychotics (especially typical antipsychotics e.g. haloperidol), Wilson’s disease, stroke.

o Parkinsonism plus syndrome (PPS) – Progressive Supranuclear Palsy (PSP), Multiple System Atrophy (MSA).

[NB: since secondary parkinsonism is treatable thus it is important to recognized and accurately diagnose this.]

- Clinical diagnosis of PD:

o Asymmetrical signs of parkinsonism

o No clinical evidence of PPS & secondary parkinsonism

o Marked response to dopaminergic drugs

o Postural instability is the 4th cardinal sign, but it emerges late in the disease, usually after 8 years or more.











Proposed stages of Parkinson's disease (PD) based on extrapolations from pathologic, clinical and brain imaging studies. Broken black lines indicate that, by itself, Lewy (-synuclein) protofibril or fiber pathology is not sufficient to make the pathologic diagnosis of PD. Broken blue lines represent non-motor signs that usually precede clinical recognition of PD, including impaired olfaction, sleep and mood disturbances, and constipation. Broken yellow lines indicate that fluctuations may be less apparent in the late stages of PD. (Taken from Harrison's online)





- Treatment of PD:

o Early stage : dopaminergic drugs (i.e. dopamine agonist e.g. Mirapex / pramipexol & Requip / ropinirole)

o Late stage : brain surgery (Deep Brain Stimulation / DBS, pallidotomy & thalamotomy)

- Differences between PD & PPS

Parkinson’s disease (PD)

Parkinsonism plus syndrome (PPS)

1

Response to dopaminergic drugs & brain surgery are good.

Poor response

2

Better long term prognosis (less aggressive course)

Poorer long term prognosis (more aggressive course)

Unilateral Facial Weakness (flow chart)

Case based learning (COPD)


Speech disorder


Dysphasia / aphasia

Ø Impairment of the production and/or the comprehension of spoken or written words.

Ø Content of speech is abnormal. (language dysfunction)

Ø Assessment: mnemonic - CNS-RW

1. Comprehension

· 3 step instructions:

i. close your eyes/闭上您的眼睛(chinese simplified)/ अपनी आँखें बंद करो (Hindi)/ tutp mata (Malay)

ii. lift up your left hand /提起您的左手(chinese simplified)/ अपने बाएँ हाथ उठा (Hindi) / angkat tangan kiri (Malay)

iii. touch your left ear /接触您的左耳朵(chinese simplified)/ अपनी बाईं कान स्पर्श (Hindi)/ sentuh telinga kiri (Malay)

2. Naming objects

· Pen, key, book, card

3. Spontaneous speech

· Ask about his day, family, visitors, occupation

4. Repetition of sentence

· I want to go to the toilet /我想要去洗手(chinese simplified)/ मैं शौचालय जाना चाहती हूँ (Hindi)/saya nak pergi ke tandas (Malay)

5. Writing

· Write a given sentence e.g. regarding residence – I live in an apartment at Damansara Utama./ 我在公寓居住在damansara utama(chinese simplified)/ मैं एक अपार्टमेंट में damansara utama में रहते हैं (Hindi)/Saya tinggal di Damansara Utara dalam sebuah rumah bertingkat.(Malay)

· Write out a given instruction – “lift up your left hand” /提起您的左手(chinese simplified)/ अपने बाएँ हाथ उठा (Hindi) / angkat tangan kiri (Malay)











Ø Types of dysphasia :

Clinical features

Expressive (Broca’s) dysphasia

Receptive (Wernicke’s) dysphasia

Conductive dysphasia

Nominal dysphasia

Comprehension

Normal

Impaired

Normal

Normal

Naming objects

Impaired

Impaired

Impaired

Impaired

Speech

Telegraphic (staccato speech)

Paraphasia Neologism

Paraphasia Neologism

Lack nouns

Repetition

Impaired

Impaired

Impaired

Normal

Writing

Impaired

Impaired

Impaired

Pauses (lack nouns)

Spontaneous

Non-fluent (mute if severe)

Fluent

Fluent

Pauses

Site of lesion

Left inferior frontal gyrus

Left superior temporal gyrus

Left arcuate fasciculus

Left temporal lobe

Dysarthria

Ø Imperfection in articulation of speech.

Ø Content is normal.

Ø Subtypes:

o ”Hot potato” speech = Pseudobulbar dysarthria

o Nasal speech = Bulbar dysarthria

o Scanning / staccato speech(syllable by syllable) = Cerebellar dysarthria

o Monotonous, soft speech = Parkinsonian dysarthria

Dysphonia

Ø Impairment in production of voice (soft / hoarse voice)

Ø Content of speech is normal.

Ø E.g. vocal cord palsy

Speech disorder (flow chart)