Core Conditions Flashcards

1
Q

Respiratory Malignancy

A

Definition:

Bronchial carcinoma, malignant tumour of the bronchial tree.

Most common malignancy and third most common cause of death in UK

Types:

Small Cell 20-30%

Non-small cell

Squamous 40%

Large Cell 25%

Adenocarcinoma 10%

Bronchoalveolar 1-2%

Aetiology:

Smoking (including passive) - squamous

Urban>rural

Occupational - adeno (asbestos, coal, chromium, aresenic, petroleum products and oils, radiation

Clinical Features:

Cough 41%

Chest Pain 22%

Cough & Pain 15%

Haemoptysis 7%

Chest Infection

Others (SoB, malaise)

Investigations:

CXR

Bloods - hyponatraemia, polycythaemia, anaemia

CT & PET for staging

Bronchoscopy biopsy

Management:

MDT

Surgery - 5-10% of cases suitable. Non-small cell only

Radiotherapy - squamous, symptom control, SVC obstr.

Chemotherapy - combination therapy

Prognosis:

55-67% 5-year survival with local disease

23-40% 5-year survival with locally advanced

1-3% 5-year survival with advanced disease

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1
Q

Hyperthyroidism

A

Definition:

Characterised by increased plasma concentration of free T4

Aetiology:

Grave’s Disease
Toxic multinodular goitre
Single toxic nodule
Gestational

Clinical Features:

Heat intolerance
Weight loss
Increased appetite
Diarrhoea
Irritability
Sleepleessness, tiredness
Exertional SoB
Goitre
Tachy / AF
Tremor
Hyperkinesia
Proximal muscle wasting
Cardiac failure
Pretibial myxedema

Eye Signs (Grave’s):

Exopthalmos
Lid lag
Lid retraction
Opthalmoplegia

Investigations:

T4 up

TSH down

Management:

Carbimazole
Propylthiouracil
Radioiodine

Surgical for:

Malignancy
Pressure symptoms
Failure of medical treatment

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2
Q

COPD

A

Definition:

Non-reversible progressive airflow limitation

Aetiology:

Smoking 90% of cases

Rarely alpha1-antitrypsin deficiency

Clinical Features:

Cough & sputum

Wheeze

SoB

Exacerbating factors - URTI, cold weather, pollution

Tachypnoea

Signs respiratory compromise or RHF

Investigations:

Spirometry

CXR - hyperinflation, flat diaphragm

ABG

ECG - P pulmonale, RBBB, RV hypertrophy

FBC -

Management:

Stop Smoking

Flu & pneumococcal vaccines

ß2 agonists

Antimuscarinics

Corticosteroids

Abx if required

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2
Q

Mitral Stenosis

A

Aetiology:

Rheumatic Fever

Clinical Features:

Secondary to Pulmonary HPT

Progressive SoB
PND
Orthopnoea
Haemoptosis
Recurrent Bronchitis

Others

Malar Flush
⇓Pulse Volume
AF

Heart Sounds

Tapping Apex Beat
Loud 1st Heart Sound
Opening Snap
Rumbling Mid-diastolic Murmur @ Apex
Signs of RVF

Investigations:

CXR – large L atrium, convex L heart border
ECG – bifid ‘P’ wave, AF, R ventricular hypertrophy, R axis deviation
Echocardiogram –

Management:

Medical:

Diruretics
Rate control for AF (β-blockers, Ca2+-blockers, Digoxin)
Anticoagulation
Endocarditis Prophylaxis

Surgical:

Balloon Valvotomy
Closed Valvotomy
Open Valvotomy
Replacement

Complications

AF
Emboli
Pulmonary HPT
Pulmonary Infarction
Chest Infections
Tricuspid Regurgitation
RVF

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3
Q

Dementia

A

Definition:

Progressive decline of cognitive function in the absence of clouded consciousness

Alzheimer’s - Neuronal loss, neurofibrillary tangles, senile plaques, amyloid deposition

Lewy Bodies shown on CT

Aetiology:

Alzheimer’s (65%) - may be familial

Lewy Body (25%)

CVD

Clinical Features:

Alzheimer’s - Inability to learn new or recall old information, decline in language (names), apraxia, impaired organizing / sequencing, behavioural change, paranoia & loss of insight

Lew Body - Fluctuating cognition with pronounced variation in attention / alertness, memory loss uncommon early on, sleep disorders, visual hallucinations, delusions & transient LOC

Vascular - Hx of stroke

Investigations:

Rule out delerium:

FBC, U&Es, ABG, BM, cultures, LFTs, TFTs, ECG, CXR

?CT / MRI, LP

MMSE

Management:

Alzheimer’s - cholinesterase inhibitors (eg rivastigmine, galantamine), NMDA (eg Memantine)

Lewy Body - avoid neuroleptics (antipsychotics)

Vascular - Stroke prevention

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4
Q

Anorexia

A

Definition:

Reduced nutritional intake and an irrational fear of gaining weight due to distorted fears of body image

Aetiology:

Genetic

Childhood sexual abuse

Dietary problems in early life

Social - higher class, ballet dancers, medical students

Clinical Features:

BMI

Intense wish to be thin & morbid fear of fattness

Amenorrhoea

F>>M with adolescent onset

Previously fat or chubby

Avoids carbs

Vomiting / excess exercise / purging

Loss of libido

Investigations:

Clinical diagnosis

Management:

CBT - goal setting with rewards

Psychotherapy

Family therapy

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5
Q

Pulmonary Embolism

A

Definition:

Embolus causing partial or total occulsion of the pulmonary artery or its tributaries.

Aetiology:

Usually arise from a venous thrombus in the pelvis or leg which gives of a clot whch travel through the right heart.

Risk Factors:

Recent surgery or prolonged bedrest

Recent stroke / MI

Disseminated malignancy

Thrombophillia / antiphospholipid syndrome

Pregnancy / post-partum / ?OCP/HRT

Clinical Features:

SoB, pleuritic chest pain, haemoptysis, dizziness, syncope COULD BE NO SYMPTOMS

Tachy, hypotension, cyanosis, tachypnoea, raised JVP, pleural rub, pleural effusion

Investigations:

FBC - infection (WCC), Anaemia (Hb), Platelets

U&Es – Electrolyte disturbances, renal function
Clotting Screen – baseline

*D-Dimer – only if no other explaination for clinical features

ABG – May show ¬⇓Pa02 and ⇓PaC02 (hyperventilation)

CXR – May be normal, or show oligaemia, dilated pulmonary artery, effusion, wedge-shaped opacities.

ECG – May be normal, or show tachy, RBBB, R vent. Strain (inverted T in V1 – V4). *(S1, Q3, T3 pattern is rare)*

Management:

WELLS SCORE FOR PE (gives probability)

Sit up and 15L O2

Analgesia

Fluids if low BP

Senior Help

CTPA +/- echo urgently

Consider thrombolysis

Enoxaparin 1.5mg/kg/24hr

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6
Q

Epilepsy

A

Definition:

A continuing tendency to suffer epileptic seizures, a seizure being an abnormal event resulting from paroxysmal discharge or cerebral neurons.

2% of the population has two or more seizures

Aetiology:

Genetic, Developmental, Trauma, Surgery, Pyrexia, Intracranial Mass, Infarction, Alcohol / Drug Withdrawal, Encephalitis, Metabolic Abnormalities (hyponatraemia/hypoglycaemia)

Clinical Features:

Classification

Generalised:

Absence (Petit Mal)
Myoclonic
Tonic-Clonic (Grand Mal)
Tonic
Akinetic

Partial:

Simple (Jacksonian - motor. No impairment of consciousness)
Complex (impairment of consciousness)

Investigations:

EEG – normal between seizures
CT/MRI Head
Serum Biochemistry
CXR - checking aspiration pneumonia

Management:

During Seizure:

ABCDEFG Approach
Maintain Airway & Physical Safety
Rectal or IV Diazepam 5-10mg if seizure doesn’t cease spontaneously

Prophylactic:

First-Line:

Generalised Tonic-Clonic – Phenytoin, Carbamazepine, Sodium Valproate
Generalized Absence – Sodium Valproate, Ethosuximide
Partial Seizures – Carbamazepine, Phenytoin, Sodium Valproate

Common SE:

Phenytoin – Rash, blood dyscasias, lymphadenopathy
Carbamazepine – Rash, leucopenia
Sodium Valproate – Anorexia, hair loss, liver damage
Ethosuximide – Rash, blood dyscrasias, night terrors

Other Drugs:

Felbamate
Gabaentin
Lamotragine
Levetiracetam
Oxcarbazapine
Tiagabine
Topiramate
Vigabatrin

Driving

It is illegal to drive for 12 months post any form of seizure or unexplained LoC. It is the responsibility of the doctor to inform the patient, but patient’s responsibility to inform DVLA.

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7
Q

Pleural Effusion

A

Definition:

Excessive liquid in the pleural space

Aetiology:

Transudates (

Exudates (>35g/l protein) - malignancy, infection, vasculitidies, rheumatoid.

If purulent and pH

Clinical Features:

SoB

Pleuritic Chest Pain

Investigations:

CXR - loss of costophrenic angle with a meniscus

Management:

o2

Investigate cause

? aspiration

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7
Q

Hyponatraemia

A

Definition:

Normal range 135-145 mmols/L

May be associated with normal extracellular volume and body Na+ content, salt deficiency or water excess.

Aetiology:

Abnormal ADH release - SIADH, Addison’s, Hypothyroid

Psychiatric Illness - psychogenic polydipsia, TCAs

Drugs - Oxytocin

GI Loss - D&V, haemorrhage

Renal Loss - hyperglycaemia, diuretics

Clinical Features:

Normovolaemia & signs of underlying disease

Hypovolaemia in GI / Renal losses

Investigations:

Determine cause if unknown

Management:

Replace lost fluids & electrolytes

Treat underlying cause

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8
Q

Ectopic Pregnancy

A

Definition:

The fertilised ovum implants outside the uterine cavity

Aetiology:

2° to salpingitis, tubal surgery, prev ectopic, endometriosis, older IUCD, PoP

Clinical Features:

Abdo pain

PV bleeding (prune juice)

~8 weeks amenorrhoea

Rupture - severe pain, shock, peritonism

Investigations:

Pregnancy test - +ve, ßHCG lower than normal

USS - TV probably better than abdo

Management:

Resus

x-match 6 units

Rhesus status - anti-D

Refer Gynae

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9
Q

Asthma

A

Definition:

Chronic inflammatory disease of the airways

Reversible airflow limitation

Hyperesponsiveness to stimuli

Inflammation of the bronchi

Aetiology and Precipitatin Factors:

Atopy & allergy

Increased airway responsiveness

Cold air, exercise, pollution

Occupational (paint sprayers)

Drugs eg NSAIDs, Beta-blockers

Clinical Features:

Cough

Wheeze

SoB

Chest tightness

Investigations:

CXR

Spirometry

Peak flow charts

Skin testing for allergies

Management:

BTS guidelines

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9
Q

GORD

A

Definition:

Decreased lower oesophageal sphincter; sustained or transient.

Aetiology:

Usually no obvious cause; secondary causes include smoking, pregnancy, scleroderma, drugs, trauma, alcohol, obesity

Helicobacter Pylori is not associated with GORD

Clinical Features:

Heartburn, regurgitation

Investigations:

OGD, 24hr pH monitoring in difficult cases

Management:

Conservative:

weight loss, avoidance of smoking and alcohol

Medical:

simple antacids, H2 blockers (Ranitadine), PPIs

Surgery:

Nissen fundoplication (fundus wrapped around distal oesophagus)

Complications

Reflux oesophagitis, peptic stricture, Barrett’s oesophagus

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10
Q

Guillian-Barre

A

Definition:

Acute inflammatory post-infective polyneuropathy

Aetiology:

Follows 1-3 weeks after infection (often trivial or campylobacter)

3 in 100 000 / year

Clinical Features:

Weakness of distal limbs +/- numbness

Weakness ascends over days for up to 3 weeks

Can affect respiratory and facial muscles in 30%

Investigations:

Clinical diagnosis

Nerve conduction studies

CSF - cell count normal, protein raised

Management:

Record respiratory function - ABG, vital capacity, FEV

Ventilate if required

High dose IV gamma-globulin

Plasmapharesis

SC heparin - prophylaxis

Prognosis:

Spontaneous gradual recovery

15% disability or death

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11
Q

IBS

A

Definition:

GI symptoms in the absence of structural pathology; abnormal autonomic reactivity, visceral hypersensitivity.

Aetiology:

Post-infective, stress, adverse life events, psychological problems: anxiety, depression.

Clinical Features:

Abdominal discomfort, relief with defaecation, alternating bowel habit, bloating

Investigations:

Patient
Patient >45, with short history or atypical symptoms – other pathologies should be ruled out

Management:

Supportive: explanation, reassurance, lifestyle advice

Medical: Aimed at specific symptoms – antispasmodics (Mebeverine), antidepressants, anti-diarrhoeals, constipation treatments

Dietary: Diary to discover causative foods & exclusion diet

Psychological: CBT

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12
Q

Bronchiectasis

A

Definition:

Abnormal & permanently dilated airways

Aetiology:

Congenital

Mechanical obstruction

Post-infective damage

Granuloma & fibrosis

Immunocological

Mucociliary clearence defects

Clinical Features:

Cough & excessive sputum

Recurrent chest infections

Halitosis

Haemoptysis

Clubbing

Coarse crackles

Hyperinflation

Investigations:

CXR - hyperinflation

CT

Sputum C&S

Immunoglobulins

Sweat electrolytes for CF

Mucociliary clearance

Management:

Postural drainage

Abx

Bronchodilators

Steroids

Tx

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12
Q

Peptic Ulcer Disease

A

Definition:

Break in the mucosal surface of the stomach or duodenum >5mm

Aetiology:

95% of duodenal ulcers & 70% of gastric ulcers are associated with H-pylori. Other associations are NSAIDs, smoking and alcohol.

Clinical Features:

Dyspepsia

Heartburn

Anorexia

Epigastric tenderness

Investigations:

OGD if >55 or red flag symptoms

Breath test if

Stool antigen test

Management:

PPI, amoxicillin, clarithromycin 500mg

or a PPI, metronidazole, clarithromycin 250 mg

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12
Q

Leukaemia

A

Definition:

Malignancy of the blood or bone marrow resulting in an abnormal increase of immature WBCs.

Acute - Rare (5 in 100 000) AML & ALL

Chronic - Usually older patients, changes to acute with a high 5-yr mortality CML & CLL

Aetiology:

Mostly unknown

Some genetic & environmental factors

Clinical Features:

Acute:

Bone marrow failure

Weakness and tiredness due to anaemia

Bruising due to thrombocytopenia

Repeated infections

Chronic Myeloid:

Anaemia

Night sweats & fever

Weight loss

Splenomegaly & pain

Chronic Lymphocytic:

Often incidental

Infections due to neutropenia

Anaemia

Lymphadenopathy

Hepatospenomegaly

Investigations:

Acute:

Blood count

Blood film - leukaemic blast cells

Bone marrow - blast cells

Chronic Myeloid:

Blood count - raised WCC

Multiple myeloid precursors

Bone marrow biopsy

Genetic testing for Philadelphia Chromosome 9:22 trans.

Chronic Lymphocytic:

Hb - low or normal

WCC - raised

40% lymphocytes

Plt - low or normal

Serum IG - low

Management:

Acute:

Correct anaemia & thrombocytopenia

Treat infections

Chemo to achieve remission

Bone marrow ablation

Chronic Myeloid:

Interferons - remission in 10%

Hydroxyurea reduced WCC

Myeloablation with BM Tx

Chronic Lymphocytic:

Nothing if asymptomatic

Steroids for haemolysis

Fludarabine or Chlorambucil

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12
Q

Delirium

A

Definition:

Impairment of consciousness associated with abnormalities of perception and mood

Aetiology:

Infection

Metabolic Disturbance

Hypoglycaemia

Intracranial - trauma, malig, abscess, haemorrhage

Drugs - anticonvulsants, anxiolytics, opiates, digoxin

Drug / alcohol withdrawal

Post-op

Vit Deficiency - Thiamine (wernicke-karsakoff), B12

Clinical Features:

Acute clears within days

Fluctuant with lucid periods

Worse at night

Visual hallucinations

Frightened, suspicious, restless & uncooperative

Investigations:

FBC, CRP, U&Es, LFTs, TFTs, B12

Cultures

ECG

CXR

CT Head

Management:

Treat underlying cause

Good nursing in well-lit environment

Good comms, include family

Hydration

Review drugs

Emergency Rx - Haloperidol 5mg IM, Lorazepam in withdrawal

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13
Q

Cor Pulmonale

A

Definition:

Right heart failure resulting from chronic pulmonary hypertension.

Aetiology:

COPD in most cases

Pulmonary Fibrosis

Recurrent PE

Clinical Features:

SoB
Wheeze
Chronic wet cough
Ascites
Peripheral oedema
Prominent neck and facial veins
Raised JVP
Hepatomegaly

Investigations:

Find cause

Management:

Treat cause

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14
Q

Neuropathy / Radiculopathy

A

Definition:

A pathological process that affects peripheral nerves (neuropathy) or roots (radiculopathy)

Pathology:

Demyelination

Axonal degeneration

Wallerian degeneration (after nerve section)

Compression

Infarction

Infiltration

Aetiology:

Mononeuropathies

Carpal tunnel syndrome

Ulnar nerve compression

Radial nerve compression (sat night palsy)

Mononeuritis multiplex

Polyneuropathies

Guillian-Barré syndrome

Wernicke-Korsakoff syndrome (Thiamin deficiency)

Vit B12 deficiency (subacute combined degeneration of the cord)

Peroneal Muscular Atrophy (Charcot - Marie - Tooth disease)

Autonomic Neuropathy

Caused by DM, G-B, Amyloidosis

Clinical Features:

Depends on cause

Investigations:

Depends on cause

Management:

Depends on cause

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14
Q

Nephrotic Syndrome

A

Definition:

A triad of:

  1. Proteinuria (>3g/24h)
  2. Hypoalbuminaemia (
  3. Oedema

Aetiology:

80% due to glomerulonephritis

membranous GN most common in adults

minimal change GN most common in children

Others:

DM, amyloidosis, SLE, drugs and allergies

Clinical Features:

Oedema - peri-orbital, face, arms

Frothy urine

Ascites

Normal JVP

Investigations:

Simple:

24hour urine, throat swab,

Bloods:

Albumin, U&Es (urea & Cr), Antibodies

Others:

CXR (pulmonary oedema)

Renal imaging (USS) +- biopsy

Management:

Sodium restriction

Diuretics

ACEi

Steroids

Cyclophosphamide

Complications:

DVT

Sepsis

Oliguric Renal Failure

Lipid Abnormalities

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15
Q

Glaucoma

A

Definition:

Raised intraoccular pressure

Disease of middle to late years and unioccular

Aetiology:

Blockage of drainage of aqueous from the anterior chamber via the canal of Schlemm

Clinical Features:

Pain

N&V

Corneal oedema

Fixed, dilated pupil

Investigations:

Opthalmoscopy

Management:

Refer to eye unit

Pilocarpine 2-4% drops hourly

Acetazolamide 500mg PO stat

Surgical - peripheral iridectomy

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15
Q

Red Eye

A

Definition:

Acute painful red eye

Aetiology:

Danger to vision - acute glaucoma, acute iritis, corneal ulcers)

Others - episcleritis, conjunctivitis, spontaneous conjunctival haemorrhage

Clinical Features:

Depends on location of irritation

Investigations:

Opthalmoscopy

Management:

Variable

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16
Q

Fibrosing Alviolitis

A

Definition:

Progressive idiopathic pulmonary fibrosis

Aetiology:

Idiopathic

Associations:

Autoimmune

Coeliac Disease

Ulcerative Colitis

Renal Tubular Acidosis

Clinical Features:

SoB

Cyanosis

Clubbing

Bilateral fine inspiratory crackles

Signs of respiratory failure, pulmonary HPT, RHF

Investigations:

CXR - reticulonodular shadowing

HiRes CT

Spirometry - restrictive pattern with reduced gas transfer

Bronchoalveolar lavage - hypercellular

Transbronchial biopsy

Management:

O2

Steroids

Immunosuppression

Single lung transplant

Complications:

Respiratory Failure

Median survival 5 years

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16
Q

Biliary Colic

A

Definition:

Pain caused by gallbladder contraction against a gallstone stuck in the neck or the cystic duct

Clinical Features:

Pain in the RUQ / Epigastrium - with radiation around costal margins to back
Sweaty
Pale
Tachycardia
Nausea / Vomiting

Patients often writhe around with pain, rather than sitting still

Attacks lasts < 6hrs

Examination is otherwise normal

Investigations:

FCB, U&Es, LFTs CRP, Urine Dipstix

USS gall bladder

Management:

Analgesia

Nil by mouth

Laprascopic Cholecystectomy

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16
Q

Psychosis

A

Definition:

Abnormal condition of the mind resulting in a loss of touch with reality

Aetiology:

Schizophrenia

Schizoaffective disorder

Bi-polar

PTSD

Drugs - alcohol, cannibis, meth

Clinical Features:

Schizophrenia:

First Rank Symptoms - auditory hallucinations, thought withdrawal, thought insertion, thought broadcasting, delusions, externally controlled emotions, somatic passivity and feelings

Investigations:

Clinical based on first rank symptoms

Management:

Neuroleptics - (SE)

Dopamine Antagonists (eg. Chlorpromazine, Haloperidol)

Atypical (eg. clozapine, risperidone, olanzaoine) less extrapyramidal SE

Psychosocial suppport and education

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18
Q

Melanoma

A

Incidence:

1 / 10000 per year

Median Age at Presentation 50

Risk Factors:

M:F = 1:2

FH

Acute Sunburn, esp. childhood

Number of pigmented moles

Previous Melanoma

Features:

Irregular pigment and edge

Increasing size in adult life

Occurs in young adults

Types:

Superficial Spreading

Nodular

Sites:

Males - back

Females - leg

Can occur anywhere on the body

Management:

Excise with wide margins - >1cm

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20
Q

Bundle Branch Block

A

Definition:

A disruption of conduction in the His / Purkinje system, either left or right. This causes the ‘blocked’ ventricle to receive the conduction impulse later.

Aetiology:

RBBB - congenital heart disease, cor pulmonale, PE, MI, cardiomyopathy, hyperkalaemia, normal

LBBB - AS, HPT, acute MI, severe coronary disease, cardiomyopathy

Clinical Features:

Investigations:

RBBB ECG - ‘RSR’ in v2 & slurred S in v5, v6

LBBB ECG - ‘RSR’ in I, AVL, v4-v6 & slurred S in v1, v2

Management:

Pacing in symptomatic patients

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20
Q

Tricuspid Regurgitation

A

Aetiology:

Infective Endocarditis in IV drug users

Chronic Lung Disease

Pulmonary HPT

Dilatation of Right Ventricle

Carcinoid Syndrome

Clinical Features:

Exersional SoB

GI upset due to congestion

Elevated JVP with giant V wave

Pulsatile Hepatomegaly

Peripheral Oedema

Ascites

Pleural effusions

Right Ventricular Impulse at Left Sternal Edge

Heart Sounds

Pansystolic Murmur at lower left sternal edge, louder in inspiration

Investigations:

Management:

Medical:

treat right ventricular failure

Surgical:

resection in infective EC

valve repair or replacement

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21
Q

Childhood UTI

A

Definition:

Commonest condition in childhood with E. Coli causing 95% of cases.

Clinical Features:

Fever

Poor Feeding

Irritability

Offensive Urine

Vomiting

Investigations:

Dipstix - leukocytes, blood, protein, nitrites

Clean Catch Sample - microscopy & culture

Management:

>3 months and not systemically unwell - treat at home with 3/7 Trimethoprim PO

Recurrent UTI - Trimethoprim low dose OD

Further Investigations:

Performed if UTI < 6months or recurrent >6months

USS - to detect structural abnormalities of kidneys or obstruction

DMSA - radio-isotope to give detailed anatomy of kidneys, shows renal scarring. Should be delayed by 2-3 months as recent infection affects validity.

Micturating Cysto-urethragram - detects reflux from bladder to ureters (vesico-ureteric reflux VUR)

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22
Q

Shock

A

Definition:

Circulatory failure resulting in inadequate organ perfusion. Generally systolic BP

Aetiology:

Pump Failure

Primary: Cardiogenic Shock

Secondary: PE, tension pneumothorax, cardiac tamponade

Peripheral Circulation Failure

Hypovolaemia

Bleeding: trauma, AAA, ruptured ectopic

Fluid Loss: Vomiting, diarrhoea, burns, ‘third spacing’

Anaphylaxis

Sepsis

Neurogenic

Endocrine Failure: Addison’s, Hypothyroidism

Iatrogenic: Drugs e.g. anaesthetics, antiHPT

Clinical Features:

Pallor

Inc. Pulse

Red. Capillary Return

Air Hunger

Oliguria

Investigations:

ABC approach

Simple: ECG, dipstix and culture, BM

Bloods: FBC, CRP, U&Es, TFTs, LFTs and clotting, Glucose, ABG + lactate, Cultures, X-Match

Radiology: CXR, ?echo, USS, abdo CT

Management:

ABC

Raise Foot of Bed

IV Access x2

Fluids Stat!

Identify Cause

Investigations as Above

Catheterise

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22
Q

Mitral Regurgitation

A

Aetiology:

Mitral Valve Prolapse
Rheumatic Fever
IHD
Dilated Cardiomyopathy
Infective Endocarditis

Clinical Features:

Palpitations
Exertional SoB
Fatigue
Cardiac Failure
Apex – laterally displaced, hyperdynamic, systolic thrill

Heart Sounds

Soft 1st heart sound
Loud pan-systolic @ apex with radiation to axilla
3rd heart sound

Investigations:

CXR
Echo
Cardiac Catheterisation

Management:

Medical:

Symptom management (ACEi, Diruretics)
 Endocarditis Prophylaxis

Surgical:

Valve replacement

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23
Q

Hernias

A

Definition:

The protrusion of a viscus through the walls of it’s containing cavity into an abnormal position

Aetiology:

Congenital hernias

Groin Hernias (most common 75%)

Inguinal - direct, enter inguinal canal through transversalis and emerge at superficial inguinal ring

  • indirect, enter inguinal canal through deep ring and often protrude into scrotum

Arise SUPERIOR & MEDIAL to pubic tubercle

Femoral - emerge through femoral canal, normally contains only fat & lymph nodes.

More prone to strangulation due to sharp edge of lacunar ligament

Arise INFERIOR & LATERAL to pubic tubercle

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24
Q

AV Block

First Degree

Second Degree

Mobitz Type 1 - Wenckebach or

Mobitz Type 2

2:1 or 3:1 Block

Third Degree (Complete Heart Block)

A

Definition:

1st - Prolonged PR interval

Mobitz 1 - Progressive elongation of PR until missed

Mobitz 2- Missed QRS without PR elongation

2:1 or 3:1 - Every 2nd or 3rd P conducts

3rd - No association of P waves & QRS

Aetiology:

IHD

Cardiac Surgery

Dilated Cardiomyopathy

Drugs

Clinical Features:

1st - Usually asymptomatic

Mobitz 1 - Usually asymptomatic

Mobitz 2 - Usually asymptomatic

2:1 or 3:1 - Asymptomatic or syncope, dizziness, HF, fatigue, lethargy

3rd - Asymptomatic or syncope, dizziness, HF, fatigue, lethargy

Investigations:

Management:

1st - Surveillance and v.rarely pacing

Mobitz 1 - Pacing if symptomatic (v.rare)

Mobitz 2- Pacing if symptomatic (v.rare)

2:1 or 3:1 - Pacing if symptomatic and consider without symptoms as can progress to 3rd degree

3rd - Rule out reversible causes (K, Mg, Ca), sepsis, other illness and bradycardic drugs

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25
Q

Aoritc Regurgitation

A

Aetiology:

Rheumatic Fever
Marfan’s
Syphilis
Connective Tissue Disorders
Aortic Dissection
HPT

Clinical Features:

Can be asymptomatic
Palpitations
Angina
LVF
Collapsing Pulse
Pistol Shot Femorals
Wide Pulse Pressure

Heart Sounds

Apex – displaced, diffuse, hyperdynamic
Soft, high-pitched early diastolic
Left sternal edge
Possible systolic aortic flow murmur
Visible Carotid or Head Nodding

Investigations:

Management:

Medical:

Nifedipine may prolong time before replacement

Surgical:

Valve replacement at the onset of ventricular dysfunction

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25
Q

Acute Abdomen

A

Definition:

Someone who becomes acutely ill and in whom symptoms and signs are chiefly related to the abdomen.

Aetiology:

Clinical Syndromes That Usually Require Laparotomy:

Rupture of an organ – spleen, aorta, ectopic pregnancy
Peritonitis – perforation of ulcer, diverticulum, appendix, bowel or gall bladder

Syndromes That May Not Require Laparotomy:

Local Peritonitis – diverticulitis, cholecystitis, salpingitis or appendicitis
Colic -

Clinical Features:

Rupture of an organ – shock, swelling, trauma
Peritonitis – prostration, shock, lying still, +ve cough test, tenderness +- rebound/percussion, rigid abdomen, guarding, absent bowel sounds
Local Peritonitis –
Colic – waxing & waning pain, restlessness

Investigations:

FBC
U&Es
Amylase
LFTs
CRP
Urinalysis
ABG (mesenteric ischaemia)

CXR (gas under diaphragm)

AbdoCT / USS

Management:

ABC approach
Fluid Resus
Pain relief
Nil by mouth
Find & treat cause

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26
Q

Hypocalcaemia

A

Definition:

Normal Range 2.12-2.65 mmol/L

Always check corrected calcium as hypoalbuminaemia may give falsely low serum calcium.

Aetiology:

Vit D deficiency

Hypoparathyroid

Acute pancreatitis

Alkalosis

Alcoholism

Clinical Features:

spasm of hands and feet, twitching, tingling perioral, fatigue, depression, dry skin, coarse hair

Hyperreflexia, tetany, Trosseau’s, Chvosek’s

Worrying Features

Reduced GCS, chest pain, palpitations, low BP, abnormal ECG

Investigations:

ECG - prolonged QT, ST abnormalities, arrhythmias

Management:

Calcium Gluconate

?Vit D

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26
Q

Cholestasis

A

Definition:

Obstructive jaundice arising in the biliary tree

Aetiology:

Main
Gallstones
Pancreatic Cancer

Other
Cholangiocarcinoma
Chronic Pancreatitis
Enlarged lymph nodes in the porta-hepatitis

Clinical Features:

Yellow appearance of skin + mucous membranes (above 50 micromol/l)
Dark urine
Pale stools
Pruritis
Weight loss - due to inability to absorb fat

Investigations:

FBC
U&E
LFT - increased alk phos
Clotting
USS - gallbladder/biliary tree - is a stone or a tumour causing obstruction?
Chest X-ray

Management:

Gallstone

Laproscopic cholycystectomy + Laproscopic common bile duct exploration
or
ERCP with stone extraction + Laproscopic Cholycystectomy

Pancreatic Cancer

CT should be carried out too assess resectability
If it looks favourable then an endoscopic USS should be done:
Allow a closer look at head of pancreas
Allows cytology sample to be taken

If the endoscopic USS also suggests favourobility then Whipple’s should be done
If at surgery it’s decided the tumour is not removable, a biliary bypass should still be done

If the tumour is not treatable then a stent should be fitted via ERCP to provide symptomatic relief

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27
Q

Hepatic Failure

A

Definition:

Acute necrotizing hepatitis leading to cell destruction;

There are three types of acute liver failure:

  1. Hyperacute or fulminant liver failure – encephalopathy develops
  2. Acute liver failure – encephalopathy develops 2-4/52
  3. Subacute liver failure – encephalopathy develops 4-8/52

Aetiology:

viral hepatitis, infection, drugs, toxins, alcohol, ischaemia, complications of pregnancy, malignancy

Clinical Features:

Lethargy, weakness, nausea, anorexia, sleep disturbance, Jaundice, fever, fetor hepaticus, encephalopathy, cerebral oedema leading to bradycardia, hypertension, tachypnea

Investigations:

Liver Screen to identify cause

Poor prognostic indicators include: ⇑bilirubin, severe hyponatraemia, rising lactate, acidosis, rapid ⇓ transaminases, renal failure

Management:

Supportive in ITU, Liver Tx

Complications:

Renal failure, coagulopathy, respiratory failure, sepsis, circulatory failure, hypoglycaemia, pancreatitis

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28
Q

Migraine

A

Definition:

Recurrent headaches associated with visual and GI disturbance.

Aetiology:

Caused by the vasodilation and oedema of blood vessels and the release of vasoactive substances.

Clinical Features:

Prodrome:

Teichopsia (flashes)
Jagged Lines
Unilateral Patchy Scotoma
Lasts 15-60 mins
Headache (hemicranial or generalized)
N&V
Irritable
Preferance for the dark
Sleeping

Other Patterns:

Migraine without aura
Hemiplegic Migraine

Investigations:

Clinical

Management:

Avoid Precipitating Factors

During Attack:

Paracetamol
Antiemetics
Sumatripan (5HT agonist)
Ergotamine

Prophylaxis:

Pizotifen, Methylsergitide (5HT antagonist)
Propanolol
Amitriptyline (low-dose)

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30
Q

Orthostatic Hypotension

A

Definition:

A fall in systolic blood pressure of at least 20mm Hg and diastolic blood pressure of at least 10 mm Hg when a person assumes a standing position.

Aetiology:

The symptom is caused by blood pooling in the lower extremities upon a change in body position and reduction in venous return causing reduced cardiac output.

Hypovolaemia

Addison’s

Atherosclerosis

Clinical Features:

Dizziness
Euphoria or dysphoria
Bodily dissociation
Distortions in hearing
Lightheadedness
Nausea
Headache
Blurred or dimmed vision
Seizures

Investigations:

Management:

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30
Q

BCC

A

Incidence:

1 / 1000 per year

M:F 1.3:1.0

Risk Factors:

Skin Types 1&2

Sunburn in childhood

Immunosuppression

Old Age

Site:

Upper 2/3 of face

Features:

Pearly papule with telangectasia

Eroded centre

Slowly increasing in size

Management:

Surgical Excision

Mohs

Curettage & Cautery

Cryotherapy

Photodynamic Therapy

Topical 5-fluouracil

Superficial Radiotherapy

Prognosis:

Excellent - rarely local recurrence

50% 2nd BCC at 5 years

Does not metastasize

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31
Q

Mania

A

Definition:

A state of abnormally elevated or agitated mood

Aetiology:

Physical - genetic, reduced 5HT, hormonal, CNS abnormalities

Psychological - maternal deprivation, learned helplessness

Social - stressful life events, sexual abuse in childhood

Clinical Features:

Elevated mood, fast, pressured speech, flight of ideas, grandiose ideation, insomnia, disinhibition, increased libido, excessive drinking / spending

Investigations:

Rule out intoxication

Management:

Acute - Lithium, Neuroleptics (eg Haloperidol)

Prophylaxis - Lithium (monitor closely U&Es, TFTs), Carbamazepine, Valproate

Psychotherapy / CBT

Social

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31
Q

Rheumatoid Arthritis

A

Definition:

Systematic disease with chronic, symmetrical polyarthritis, synovitis and non-articular features

1-3% of population
Presents at all ages
Commonly presents 30-50 years
F > M before menopause
Familial or sporadic
HLA-DR4 in 50-70%

Aetiology:

Unexplained
T Cell Activation
Presence of rheumatoid factors

Clinical Features:

Slow onset but progressive
Symmetrical peripheral polyarthritis
Joint pain & morning stiffness
Eased by gentle activity
Joints warm and tender
Limitation of movement and deformity
Joint effusion
Muscle-wasting
Lethargy, malaise
Non-articular features

Investigations:

Anaemia
⇑ inflammatory markers
Rh factors in 70%
Xray – erosions

Management:

Explain diagnosis and reassure

MDT approach

NSAIDs & Analgesics

DMARDs
Sulphasalazine
Methotrexate
Leflunomide

Anti-TNF Drugs:
Entanercept
Infliximab
Adalimumab
Corticosteroids

Less commonly used:
Gold
Penicillamine
Hydroxychloroquine
Azathioprine
Ciclosporin
Anikinra

Joint Replacment / other surgery

Non-articular Manifestations of RA:

Hands:

Nail fold lesions of vasculitis
Tenosynovitis
Tendon sheath swelling
Carpal tunnel syndrome

Arms:

Bursitis / nodules

Eyes:

Scleritis
Scleromalacia
Dry - Sjögren’s Syndrome

Mouth:

Dry – Sjögren’s Syndrome

Neck:

Lymphadenopathy
Atlanto-axial subluxation
Rarely causing cervical cord compression

Lungs:

Pleural Effusion
Fibrosing Alviolitis
Caplan’s Syndrome
Small Airway Disease
Nodules

Heart:

Pericarditis
Splenomegaly
Renal:
Amyloidosis

Lower Limb:

Ulcers
Oedema
Sensorimotor Polyneuropathy

Anaemia

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32
Q

Atrial Flutter

A

Definition:

caused by a reentrant rhythm in either the right or left atrium. Typically initiated by a premature electrical impulse arising in the atria.

Aetiology:

IHD, Rheumatic heart disease, Thyrotoxicosis, Cardiomyopathy, W-P-W Syndrome, Pneumonia, ASD, Pericarditis, PE

Clinical Features:

Asymptomatic, reduced exercise tolerance, palpitations, HF, embolic events, completely irregular pulse

Investigations:

ECG - Sawtooth flutter waves between QRSs

Management:

Electrical Cardioversion

Class III Antiarrythmics (K) - Amioderone, Sotalol

33
Q

Sepsis

A

Definition:

SIRS + suspected infection

Severe Sepsis - sepsis + signs or organ hypoperfusion

Septic Shock - persistant hypotension despite fluid challenge

Aetiology:

Pneumonia, cellulitis, gangrene, endocarditis, perforation, UTI, pyelonephritis, wound infection, bowel leak

Clinical Features:

Symptoms of infection plus low BP, tachy, warm peripheries, low JVP, reduced GCS, oliguria

Investigations:

Determine severity using ‘sepsis 6’ protocol

Management:

Follow algorithm

Briefly:

  1. Give 15LO2
  2. Take blood cultures
  3. Give IV Abx (according to suspected source)
  4. Give IV fluids
  5. Take lactate & Hb
  6. Take urine for fluid balance (catherterise)
34
Q

Atrial Fibrillation

A

Definition:

Uncoordinated rapid continuous activation of atria from multiple foci. Fortunately only some of these are conducted to the ventricles due to the AV node.

Three Types

Paroxysmal

Persistent >48 hours

Permanent

Aetiology:

IHD, Rheumatic heart disease, Thyrotoxicosis, Cardiomyopathy, W-P-W Syndrome, Pneumonia, ASD, Pericarditis, PE

Clinical Features:

Spectrum - Asymptomatic > Palpitations > Dyspnoea > Chest Pain > Heart Failure > Syncope

Investigations:

ECG - irregularly irregular QRS, no P waves, irregular baseline

Rate may be fast, normal or slow

Management: (three principles)

Rate Control (if fast) - ß-blockers, Ca-blockers, Digoxin

Rhythm Control - ß-blockers, Flecanide (Na), Amioderone (K)

Stroke Prevention - Warfarin or Dabigatran/Rivaroxaban

CHA2Ds2VASc risk stratification for use of anti-coagulation

Consider DC Cardioversion

35
Q

Pancreatitis

A

Definition:

Inflammation of the pancreas, acute or chronic

Aetiology:

Alcohol

Gall Stones

Trauma

ERCP

Drugs - azathioprine, steroids, oral contraceptive

Infection - mumos, coxsackie, klebsiella

Metabolic - hypercalcaemia, hyperlipidaemia, renal failure

Other - hypothermia, malnutrition, scorpion bite

Clinical Features:

abdo pain radiating to back, N&V, anorexia, abdo tenderness & guarding, Grey-Turner sign, basal crackles

Investigations:

Abdo Xray

inc. neutrophils

U&Es - renal failure

Calcium & glucose

Amylase elevated

ABG - hypoxia & acidosis

LFTs

USS - gallstones

CT

Management:

GLASCOW SCORE

ABC

Analgesia

ERCP

HDU

37
Q

Psoriasis

A

Definition:

Common disorder characterized by red, scaly plaques.
2% of the population. M=F

Aetiology:

T-cell driven
Genetic

Environmental Triggers:
Infection
Drugs e.g. Lithium
UV light
Alcohol
Stress

Clinical Features:

Chronic Plaque Psoriasis:

Purplish / red scaly plaques, particularly on extensor surfaces
Scalp Involvement
Can occur in areas of skin trauma (Köbner Phenomenon)
50% Associated with nail changes

Flexural Psoriasis:

Occurs in older patients
Patches in groin, natal cleft, submammary

Guttate Psoriasis:

Raindrop lesions on trunk
Occurs in children / young adults 2 weeks post strep sore throat

Management:

Education & Explanation

Avoid irritants

Topical steroids

Calcipotriol (vit D analogue)

Coal tar

Phototherapy (PUVA)

Methotrexate if severe

39
Q

Pulmonary Oedema

A

Definition:

Fluid accumulation in the air spaces and paranchyma of the lungs.

Aetiology:

Cardiogenic - LVF, IHD

Non-cadiogenic - HPT crisis, upper airway obstruction

Clinical Features:

dyspnoea, orthopnoea, PND, frothy sputum

raised JVP, tachypnoea, fine crackles, wheeze, pitting, cold hands & feet

Investigations:

FBC - anaemia, infection, MI

CRP - infection

U&Es -

BNP

?ABG

ECG - exclude arrhythmias, STEMI, may show prev IHD

CXR - cardiomegaly, oedema

Echo - poor LVF

Management:

O2

Furosemide

Analgesia

?nitrates

39
Q

Gastroenteritis

A

Definition:

Diarrhoea with N&V +/- abdo pain.

Aetiology:

Usually due to viruses (inc. Norovirus) but other infectious agent important - Shigella, Campylobacter

Clinical Features:

Diarrhoea, N&V, abdo pain, fever, sweating

Investigations:

Stool culture

WCC inc.

CRP inc.

Management:

Fluid replacement

Antiemetics

Discuss with Micro

39
Q

Ulcerative Colitis

A

Definition:

Inflammatory bowel disease, affecting the colon only

Aetiology:

Mucosal inflammation of colon (transmural in crohn’s)

Clinical Features:

Weight loss
Bloody diarrhoea
Fever
Colicky abdominal pain
Tenesmus
Constipation

Tender abdomen
Distension
Abdominal mass

Extra-gastrointestinal signs

Erythema nodosum
Pyoderma gangrenosum
Ankylosing Spondylitis
Episcleritis
Primary Sclerosing Cholangitis

Investigations:

• Bloods
o FBC – anaemia
o CRP & ESR – disease severity
o Antibodies – p Anca
• Stool sample
o Blood
o Microscopy, Culture & Sensitivity
• Abdominal X-ray – signs of toxic megacolon
• Colonoscopy + Biopsy - diagnosis

Management:

Local – topical steroids in proctitis

Systemic
o Corticosteroids – Budesonide (induction of remission)
o Mesalazine – induction & maintinence of remission
o Azothiaprine – no response to steroids or >2 use of steroids in 1yr
o Infliximab – use when no response to azothiaprine (induction of remission)

Surgery
o Ileal pouch anal anastomoses (removal of colon)

40
Q

Goitre

A

Definition:

Swelling of the thyroid gland, may be associated with hypo / hyperthyroidism

Aetiology:

Aetiology in Euthyroid Patient:

Simple non-toxic goitre

  • Iodine Deficiency
  • Treated Grave’s disease
  • Puberty

Solitary Nodule

  • Thyroid adenoma
  • Thyroid cyst
  • Thyroid carcinoma

Aetiology in a Hypothyroid Patient:

Hashimoto’s Thyroiditis
Radioiodine-treated Grave’s

Aetiology in a Hyperthyroid Patient:

Grave’s Disease
Toxic Multinodular Goitre

Clinical Features:

Neck swelling and features of hyper / hypothyroidism

Management:

Treat cause

40
Q
A

Definition:

Aetiology:

Clinical Features:

Investigations:

Management:

41
Q

Parkinson’s / Parkinsonism

A

Definition:

Cell degeneration in the substantia nigra. Loss of dopamine in the extrapyramidal nuclei

Combination of tremor, rigidity and akinesia

Increases with age, 1:200 over 70

Less prevalent in smokers

Aetiology:

Idiopathic

Drug-induced eg. phenothiazides (chlorpromazine), antipsychotics

MPTP (illegal synthetic opiate)

Encephalitis lethargica

Clinical Features:

Tremor (pill-rolling)

Micrographia

Rigidity

Cogwheeling

Bradykinesia

Falls

Mask-like face

Reduced blinking

Festinant

Poor arm swing

Monotonous speech

Normal power

Brisk reflexes

Downgoing plantars

Cognitive function initially preserved, late dementia sometimes occurs

Investigations:

Clinical diagnosis

Management:

Levodopa plus decarboxylase inhibitor eg. Sinemet or Madopar (slow to reduce SE)

Dopaminergic agonists eg. bromocriptine

Selegeline - monoamine oxidase B inhibitor

Neurosurgery (occasional for intractable tremor)

Physiotherapy

Physical aids

SE of levodopa:

short - term:

N&V

Confusion

Visual hallucinations

Chorea

long-term:

End-of-dose dyskinesia

On-off syndrome

Chorea

Dystonic movements

42
Q

Respiratory Syncytial Virus

A

Definition:

Major cause of LRTI in children, most will have been infected by 2-3 years.

Causes bronchiolitis

Aetiology:

Clinical Features:

Flu-like illness, may lead to severe respiratory symptoms in some cases.

Investigations:

May do fluoroscopy

Management:

Supportive - fluids, O2, nebulsed saline

43
Q

SVT

A

Definition:

Two abnormal circuits produce this arrythmia, both passing through the AV node.

AVNRT - atrio-ventricular node re-entrant tachycardia (passes through and near to AV node)

AVRT - atrio-ventricular re-entrant tachycardia (electrical ‘hole’ in AV septum. This conducts the signal more rapidly - pre-excitation and shows as a delta wave on ECG

Aetiology:

Exertion

Caffeine

Alcohol

ß2-agonists

Congenital - W-P-W

Clinical Features:

Palpitations

Chest Pain

SoB

Syncope

Polyuria

Rapid Regular Pulse 140-280bpm

Investigations:

ECG - narrow complex tachycardia, P waves may be within or after the QRS

Management:

Vagotonic Manoeuvres

Carotid Sinus Massage

Occular Pressure

Valsalva Manoeuvre

Adenoseine (avoid in asthma)

Prophylaxis

Accessory Pathway Ablation

45
Q

Achalasia

A

Definition:

Aperistalsis in the oesophagus and failure of relaxation on the lower oesophageal sphincter.

Aetiology:

Unknown

Clinical Features:

Long history of dysphagia for both solids and liquids

Regurgitation

Severe retrosternal pain, particularly in younger patients

Investigations:

Barium Swallow - dilatation, aperistalsis, beak deformity

Gastroscopy to exclude malignancy

Oesophageal monometry - aperistalsis & failure of LOS to relax

CXR - dilated oesophagus with fluid level behind heart and no fundal gas shadow

Management:

Symptom relief

Dilatation or division of LOS

Botox or Ca-blockers also used

46
Q

Multiple Sclerosis

A

Definition:

Multiple plaques of demyelination in the brain and spinal cord disseminated in time and place

60-100 in 100 000 UK

Aetiology:

HLA linked

?viral infection

?dietary antigens

Clinical Features:

Optic - unilateral blurred vision, occular pain, optic neuritis, optic atrophy

Brainstem - double vision, vertigo, facial numbness, weakness, dysphagia, pyramidal, nystagmus, ataxia, CN defects, internuclear opthalmoplegia

Spinal Cord - difficult walking, sensory, Lhermitte’s Sign, GU, spastic paraparesis, inc tone, weakness, brisk reflexes, up-going plantars, sensory level

Others - epilepsy, trigeminal neuralgia, tonic spasms of hand, organic psychosis, dementia

Investigations:

Clinical diagnosis two neurological events separated in time and neurological location

MRI brain & spinal cord - plaques

CSF - oligoclonal bands in 80% & raised mononuclear cell count

Management:

Aimed at reducing frequency & intensity of relapses, long-term not affected.

Corticosteroids

ß interferon

Physio

Occupational Therapy

SALT

Counselling

Prognosis:

From grave disability to mild & benign

46
Q

Hyperkalaemia

A

Definition:

Normal Range 3.5-5.3 mmol/L

Aetiology:

Decreased Excretion:

Renal Failure

Drugs - spironolactone, ACEi, NSAIDs, Heparin

Addison’s

Acidosis

Increased Intake:

KCl administration

Blood Transfusion

Clinical Features:

Arrhythmias

Hypotension / bradycardia if severe

Kussmaul breathing (associated acidosis)

Widened QRS / tented T waves

Investigations:

ECG monitoring

Management:

Calcium Resonium

Dialysis

Treat Cause

47
Q

Pneumothorax

A

Definition:

Air in the pleural space leading to lung deflation

Aetiology:

Spontaneous (primary or secondary to lung disease)

Chest trauma

Ventilation

Clinical Features:

Pleuritic Chest Pain

SoB

Investigations:

CXR - lung markings not extending to the peripheries

Management:

If bilateral or haemodynamically unstable - chest drain

Primary + >2cm &/or SoB - aspirate (drain & admit if fails)

Primary with no SoB or

Secondary + >2cm - chest drain & admit

Secondary

48
Q

Ventricular Tachyarrythmias

A

Definition:

Ventricular Fibrillation - Irregular rhythm with irregular QRS voltage and width. Not compatible with life.

Broad Complex Tachycardia - VT until proven otherwise

Aetiology:

Shock

MI

Clinical Features:

VF - LOC

BCT - Palpitations, dizziness, syncope, angina

Investigations:

ECG VT - Irregular rhythm with irregular QRS voltage and width

ECG BCT - wide QRS, usually rapid >180bpm

Management:

VF - DC shock immediately

BCT - If haemodynamically stable try amioderone / lignocaine

If unstable DC shock as can progress to VF

50
Q

Osteoarthritis

A

Definition:

Pain & disability associated with joint space narrowing and altered cartilage osteophyte formation.

Aetiology:

Primary - Idiopathic

Secondary - trauma, chondrocalcinosis, haemochromatosis, acromegaly, haemophillia, AVN, sickle cell

Clinical Features:

Joint pain / swelling / instability
Morning Stiffness
Joint effusion & crepitus
Bony Swelling
Muscle Wasting
Limitation of movement & loss of function

Investigations:

Inflammatory markers not elevated
No autoantibodies
Xrays abnormal if severe damage
MRI can show early cartilage changes
Arthroscopy – early fissuring and cartilage surface erosion

Management:

Treat symptoms and disability, not xrays!
Explain diagnosis and reassure
Weight loss and exercise
Hydrotherapy
Heat / massage
Analgesia
Patients often use complimentary medicine
Joint replacements / other surgery

Clinical Subsets:

Nodal OA
Familial F >> M
Develops in late middle age
Poly articular involvement of the hand
Heberden’s Nodes
Generally good long-term functional outcome
Predisposes to OA of the knee, hip and spine
Xray – marginal osteophyte & joint space loss

Erosive OA
Rare
DIP & PIP joints
Poor functional outcome
Xray – marked subchondral cysts
May develop in to rheumatoid arthritis

Generalised OA
May occur in combination with nodal OA
Hands, knees, first MTP joints and hips
Familial
F > M
May be autoimmune
Large joint OA
Knees & Hips

Crystal-associated OA (Chondrocalcinosis)
Calcium Phosphate Crystal Deposition
Knees and wrists commonly affected
Xray – may show calcification in the cartilage

52
Q

Sinus Node Disease

A

Definition:

Variable combinations of fast & slow supraventricular rhythms.

Aetiology:

Ischaemia

Infarction

Degenerative Disease

Clinical Features:

Variable combinations of fast & slow supraventricular rhythms.

Investigations:

ECG - long interval between P waves >2 seconds

Management:

Permanent Pacemaker

Antiarrhythmics to reduce tachys

Anticoagulation

53
Q

Cellulitis

A

Clinical Features:

Hot, tender area of confluent erythema

Often on lower leg

Can affect face

Caused by streptococci

Risk Factors:

DM

Management:

Oral / IV Abx

54
Q

Paediatric Asthma

A

Definition:

Reversible airway obstruction +/- wheeze, dyspnoea & cough. Leading chronic disease of childhood.

Aetiology:

FH, bottle fed, atopy, pollution

Triggers - dust, pollen, animals, exercise, smoke

Clinical Features:

Wheeze

SoB

Cough

Investigations:

PEFR

CXR

Management:

Chronic-

Step 1 - occasional ß2-agonist via spacer

Step 2 - regular inhaled steroid

Step 3 - review diagnosis, check inhaler technique. Add LABA or aminophylline

Step 4 - refer to specialist & increase inhaled steroid

Step 5 - Prednisolone

54
Q

Diabetes

A

Definition:

Syndrome characterized by chronic hyperglycaemia due to relative insulin deficiency or resistance or both.

WHO Classification

Type 1:

β cell destruction usually leading to absolute insulin deficiency
Autoimmune or idiopathic

Type 2:

Variable combination of insulin resistance and defects in insulin secretion

Aetiology:

Autoimmune

Idiopathic

Genetic

Endocrine problems (e.g. Cushing’s)

Pancreatic trauma or disease

Drug-induced - corticosteroids, thiazides

Clinical Features:

Due to hyperglycaemia

Thirst
Polyuria
Weight loss
Ketoacidosis
⇓ Energy
Visual Blurring
Candida Infections

Due to Complications

Skin infections
Retinopathy - haemorrhages, exudates etc…
Polyneuropathy - ‘glove&stocking’, autonomic
Erectile Dysfunction
Arterial Disease - atheroma, stroke, MI, PVD
Renal Disease - glomerular sclerosis, pyelonephritis

Charcot’s Joints

Diabetic Foot

Investigations:

WHO Criteria For Diagnosis:

HbA1c >6.5% is diabetic

HbA1c 6.0-6.4% is high risk of developing diabetes
- lifestyle advice & yearly monitoring

Management:

Based on self-monitoring and management by the patient, helped and advised by specialists.

Requires good education and understanding of disease by the patient, including:

  • Monitoring blood sugar
  • Self-injection of insulin
  • Managing hypoglycaemic events
  • How to recognize complications
  • When to contact specialists for help

Type I Drugs

Insulin - fast, intermediate, long acting (pumps)

_Type II Drugs _

Oral Hypoglycaemics:

Biguanides - inc. insulin sensitivity (eg Metformin)

Sulfonylureas - inc. insulin secretion (eg Gliclazide)

Thiazolidinediones - inc. insuin sensitivity (eg Pioglitazone)

56
Q

Crohn’s Disease

A

Definition:

Inflammatory bowel disease which can affect anywhere from the mouth to the anus. It most commonly involves the terminal ileum, which can present as right iliac fossa pain. It affects patients between the ages of 18-30.

Aetiology:

Autoimmune attack against bowel wall. Causes full thickness infiltration and can therefore result in perforation, adhesions and fistula. It classically on colonscopy demonstrations skip lesions, which helps differentiate it from ulcerative colitis.

Clinical Features:

Fatigue
Weight loss
Fever
Abdominal pain (classically RIF)
Diarrhoea +/- blood
Episcleritis
Large joint arthropathy

Tender abdomen
Mass in RIF
Episcleritis
Erythema Nodosum
Episcleritis
Anal skin tags

Extra-intestinal Manifestations

Erythema Nodosum
Episcleritis
Large joint arthritis / Ankylosing spondylitis
Renal stones
Primary sclerosing cholangitis

Investigations:

FBC – Anaemia
CRP
Antibodies
- Anti-S cerevisiae antibodies (more common in crohns than UC)
Stool sample – culture & microscopy
Ilieo-colonoscopy + Biopsy – skip lesions, deep ulceration

Management:

Severe abdo pain, diarrhoea, bowel obstruction, or systemically unwell = admit

Mesalazine – prophylactic therapy

Budesonide – Fewer side effects than prednisolone, but may be less effective

Antibiotics for septic disease

Immunomodulators
Azothiaprine
Methotrexate

Biologics
Infliximab
Elemental diet

Surgery

Maintaining remission
Mesalazine – after surgery
Azothiaprine
Infliximab

56
Q

Osteoporosis

A

NOF

Definition:

Low bone mass & micro-architectural deterioration of bone. Mineralised normally but deficient in quantity & quality including structural integrity.

Aetiology:

Female, age, early menopause, smoking, FH, excess alcohol, nutrition, steroids, immunosuppression, endocrine disorders, RA, renal / liver failure

Clinical Features:

Back pain

Weight loss

Kyphosis

Colles’ #

Investigations:

Ca - ++, PO4 & alk phos normal

XRAYs

DXA -

Management:

Prevention

Identification & monitoring patients at risk

Diet rich in Ca & Vit D

Exercise

Stop smoking

Reduce risk of falls

Ca & Vit Supplements

Bisphosphonates

Raloxifene

Parathyroid hormone

Strontium

Androgens in hypogonadal men

57
Q

Syncope

A

Definition:

‘Blackouts’ with multiple clinical pictures and causes. May or may not involve LOC

Vasovagal Syncope: reflex bradycardia +/- vasodilation

Cough Syncope: weakness + LOC after coughing

Effort Syncope: on exercise, cardiac origin e.g. AS

Micturition Syncope: mostly men, at night

Carotid Sinus Syncope: carotid sinus hypersensitivity, headturning or shaving

Epilepsy: most likely Grand Mal presenting with LOC

Stokes-Adams Attacks: transient arrhythmias causing low cardiac output & LOC

Others: hypoglycaemia, orthostatic hypotension, drop attacks, anxiety

Clinical Features:

LOC with possible associated symptoms e.g. nausea, pallor, sweating, visual disturbance

Investigations:

Collateral History

CVS with sitting / standing BP

Neuro

BM

? 24hr ECG

Management:

Cause dependent

59
Q

Menorrhagia

A

Definition:

Increased menstrual blood loss for individual or change such as flooding, clots.

Aetiology:

IUCD

Fibroids

Endometriosis / Adenomyosis

PID

Polyps

Hypothyroidism

Dysfunctional Uterine Bleeding

Clinical Features:

As above

Investigations:

FBC

TFTs

Clotting

USS

Hysteroscopy

Laproscopy

Management:

1st Line - Mirena

2nd Line - Antifibrinolytics (Transexamic Acid), NSAIDs, COCP

3rd Line - oral prgesterone or injected pregesterone (Depo)

Surgical - Ablation (if family complete)

60
Q

Angina

A

Definition:

Transient symptoms of myocardial ischaemia due to exertion which is relieved by rest.

Risk Factors:

Age, Male Sex, FH, Hyperlipidaemia, Smoking, HPT, DM, COX 2 inhibitors (celecoxib)

Clinical Features:

Central Chest Pain - heavy, tight, gripping, radiation to arms and jaw

May be silent

Investigations:

Simple - ECG (normal or previous MI)

  • Exercise ECG (ST depression >1mm which reverts to normal)

Bloods - FBC, U&Es, TFTs

Radiology - Angiogram

                - Thallium Scan

Management:

GTN

ß-blocker or Ca-channel blocker, if not controlled….

Both ß-blocker & Ca-channel blocker

(*Nicorandil if not tolerated or cantraindicated*)

If not controlled…..

Long-acting nitrate (isosorbide) or Nicorandil

If not controlled……

Consider revascularisation

62
Q

SCC

A

Incidence:

1 / 4000 per year

Risk Factors:

Skin Type 1&2

Chronic Sun Exposure

Outdoor Work & Leisure Activities

Immunosuppression

Old Age

Chronic Skin Ulceration

Defects in DNA repair - xeroderma pigmentosum

Features:

Painful, firm, keratotic / eroded, indurated nodule

Increasing size over months

Sun exposed sites - scalp, ears, dorsa of hands, lower legs

Management:

Surgical Excision with 4mm margin

Prognosis:

More likely than BCC to recur or metastisize

Worse:

ear, lip, ulcers

size >2mm

depth >4mm

poorly differentiated

immunosuppressed

64
Q

Endometriosis

A

Definition:

Endometrial glandular tissue beyond the uterine cavity

Aetiology:

Long-term IUCD or tampon use

Retrograde menstrual flow

Clinical Features:

Pelvic pain at time of period

Dysmenorrhoea

Dyspareunia

Investigations:

PV exam

MRI

Laproscopy

Management:

Analgesia

COCP or IUCD to stop ovulation so patches atrophy

Excision

65
Q
A

Definition:

Aetiology:

Clinical Features:

Investigations:

Management:

67
Q

Alcoholic Liver Disease

A

Definition:

Steatosis > Fibrosis > Cirrhosis

Degree of liver damage dependent on genetic factors and coexisting liver disease; women progress to cirrhosis faster

Cage Questionnaire:

  • Have you ever felt the need to cut down?
  • Have you ever felt annoyed by criticism of your drinking?
  • Have you ever felt guilty about your drinnking?
  • Have you ever felt the need for an eye-opener?

Clinical Features:

lethargy, splenomegaly, jaundice, leuconychia, telangiectasia, spider naevi, gynaecomastia, xanthelasma/xanthoma, Dupuytren’s, clubbing, dilated chest/abdo wall veins, excoriations, fetor hepaticus (breath of the dead), palmar erythema

Investigations:

FBC - ⇑MCV, ⇓Platelets
LFTs - ⇑GGT, ⇑bilirubin
Coag - ⇑PT
Others: ⇑Albumin, ⇑cholesterol
Liver Screen: ⇑IgA
U&Es to check kidney function & provide baseline
USS +- biopsy

Management:

Abstinence

Nutrition

Vitamin replacement

Laxatives

Liver Tx

68
Q

TB

A

Definition:

Caseating granulomatous infection due to Mycobacterium tuberculosis in the lung

TB is a notifiable disease and contact tracing is important

Patients at Risk:

Those from developing countries

Immunosuppressed

HIV / Steroids / malignancy

Alcoholics / homeless / overcrowding

Clinical Features:

May be none

Malaise & Lethargy

Anorexia / Weight Loss

Fever

Cough

Haemoptysis

Pleural Effusion / Pneumonia / Fibrosis

Investigations:

CXR - affects upper zones mostly, +- calcification or cavitation

Sputum Microscopy - Ziehl-Nielsen and culture

Bronchial Lavarge / pleural biopsy

Management:

6/12 of combination Abx, usually:

Rifampicin & Isoniazaid

+ Pyrazinamide for 1st 2/12

Add Ethambutol if risk of resistance

Compliance Vital

70
Q

Gallstones

A

Definition:

Can be either:
Cholesterol stone - 75%
Pigment stone -
Mixed

90% are Radio-lucent (unable to see on X-ray)

Aetiology:

Female - 3x more common
Age - 10% of over 50’s have gall stones
Obesity
Hyperlipidaemia
Haemolytic anaemia
Crohn’s Disease

Clinical Features:

May Cause:

Gallbladder
Chronic cholecystitis
Biliary colic
Acute cholecystitis
Mucocele

Common bile duct
Obstructive jaundice
Cholangitis
Pancreatitis

Gut
Gallstone ileus

Investigations:

Urinalysis, ECG, CXR to rule out other diseases
FBC + CRP: infection
LFTs: pattern of cholecystitis - ⇑ALP & ⇑GGT
Amylase: pancreatitis
U&Es: baseline
USS to visualize stones
ERCP

Management:

Usually surgical: cholecystectomy

71
Q

Eczema

A

Definition:

Acute – inflamed weeping skin with vesicles
Subacute – erythema, dry / flaky skin, crusted
Chronic – lichinified skin

Aetiology:

40% of population have an episode associated with atopy

Atopic Individuals have a tendency to:
Asthma
Eczema
Hay Fever
Allergic Rhinitis

Genetic
Environmental – detergents, chemicals, infection, stress, animal fur, food

Clinical Features:

Itchy erythematous scaly patches
Often flexural
May be associated with nail pitting

Investigations:

May have raise IgE or eosinophils
Patch Testing

Management:

Education & Explanation
Avoid irritants
Emollients
Topical Steroids
Abx
Antihistamines

Second-line Agents:
UV
Oral Steroids
Ciclosporin / Azathioprine

73
Q

Depression

A

Definition:

Persistent low mood

Aetiology:

Physical - genetic, reduced 5HT, hormonal, CNS abnormalities

Psychological - maternal deprivation, learned helplessness

Social - stressful life events, sexual abuse in childhood

Clinical Features:

As you would expect plus hallucinations

Investigations:

Aimed at finding organic cause, endocrine, drugs etc

Management:

Stop depressing drugs

Exercise

SSRIs

Venlafaxine

?TCAs, MAOIs, ECT

Psychotherapy

CBT

Group / family support

75
Q

GI Malignancy

A

Definition:

Aetiology:

Clinical Features:

Investigations:

Management:

76
Q

Pneumonia

A

Definition:

Lung infection classified by site (lobar or bronchopneumonia) or by aetiology

Aetiology:

Bacterial - strep pneumoniae, mycoplasma pneumoniae

Viral - Influenza A, Haemophilus Influenzae

Opportunistic Infections

Chemical (eg aspiration of vomit)

Radiotherapy

Allergic

Clinical Features:

Cough

+/- purulent sputum

Fever

Pleuritic chest pain

SoB

Investigations:

CURB65

CXR

ABG

Blood & Sputum Culture

Microbiology

Management:

MIld - amoxicillin 500mg TDS (or Clarythromycin)

Moderate - IV amoxicillin 500mg TDS (or Claryth)

Severe - IV cefuroxime 1.5g QDS & Clarythromycin

Adjust according to C&S

O2

Supportive - fluids etc

Complications:

Respiratory Failure - type 1 (low paO2, low/norm. PaCO2)

Lung Abscess

Empyema

78
Q

Liver Cirrhosis

A

Definition:

Necrosis of hepatic parenchyma with connective tissue proliferation and nodular regeneration

Aetiology:

Alcoholism by far most common cause follwed by Hep c.

Others - Hep B, PSC, PBC, Drugs, NAFLD, AA hep, Wilson’s, Budd-Chiari

Clinical Features:

Related to underlying cause:

lethargy, splenomegaly, jaundice, leuconychia, telangiectasia, spider naevi, gynaecomastia, xanthelasma/xanthoma, Dupuytren’s, clubbing, dilated chest/abdo wall veins, excoriations, fetor hepaticus (breath of the dead), palmar erythema

Investigations:

Aimed at finding cause:
• LFTs
• FBC
• U&Es
• Albumin
• Coagulation
• Biopsy

Management:

Treat underlying cause

Complications of Cirrhosis:

Malnutrition

Hepatic Encephalopathy

Ascites / Oedema

Vitamin Deficiency

Coagulopathy

Impaired Immune System

Varices

Hepatorenal Syndrome

Hepatocellular Carcinoma

79
Q

Ovarian Cyst

A

Definition:

A collection of fluid within the ovary, usually during childbearing age.

Functional Cysts - follicular & corpus luteum (benign)

Non-functional - chocolate (endometreosis), dermoid

Aetiology:

Idiopathic

Clinical Features:

Fullness / aching in lower abdo

Urinary symptoms

Systemic symptoms

Disorders in menstruation

Investigations:

USS

Management:

95% benign so analgesia

Surgical excision

79
Q

Heart Failure

A

Definition:

Heart is unable to maintain sufficient tissue perfusion despite adequate venous filling pressures.

Aetiology:

Left HF - ischaemic heart disease, HPT, mitral / aortic valve disease, cardiomyopathy

Right HF - lung disease (cor pulmonale), PE, pulmonary HPT, L-R shunt, tricuspid regurgitation

Clinical Features:

Left HF - fatigue, exersional SoB, orthopnoea, PND, pulmonary oedema, tachy, enlarged heart, gallop rhythm, crackles

Right HF - Tiredness, anorexia, nausea, GI upset, raised JVP, pitting oedema, pleural effusion, hepatomegaly, ascites, tricuspid regurgitation

Investigations:

BNP

CXR

ECG

ECHO - LV ejection fraction

Angiography

Management:

If ejection fraction preserved then control comorbidities.

LV dysfunction:

  1. ACEi (or ARB) + ß-blocker
  2. Add in spironolactone or ARB or hydralazine
  3. Consider CRT pacing and digoxin
81
Q

Oesophageal Disease

A

Definition:

Barrett’s Oesophagus - columnar epithelium with intestinal metaplasia replaces normal squamous mucosa

Oesophageal Carcinoma - 40% squamous, 60% adenocarcinoma

Achalasia - failure of relaxation of lower oesophageal sphincter

Aetiology:

Barrett’s Oesophagus - GORD

Oesophageal Carcinoma - Barrett’s, smoking

Achalasia -

Clinical Features:

_Barrett’s Oesophagu_s -

Oesophageal Carcinoma - dysphagia (solids-liquids), weight loss, anorexia, Virchow’s

Achalasia - dysphagia (solids-liquids)

Investigations:

Barrett’s Oesophagus - Endoscopy

Oesophageal Carcinoma - Endoscopy, USS, CT

Achalasia - Barium Swallow (Rat’s tail), endoscopy, manometry

Management:

Barrett’s Oesophagus - watchful waiting

Oesophageal Carcinoma - 10% 5 year survival, SCC (radio/chemo, surgery), Adeno (surgery, palliative, ablation, radio)

Achalasia - balloon dilatation, botox, Heller’s sphinctotomy

83
Q

Lymphadenopathy

A

Definition:

Palpable lymph nodes

Aetiology:

Isolated infection - EBV, CMV, hepatitis, HIV, TB

Malignancy - lymphoma, leukaemia, mets

Autoimmune - SLE, rheumatoid

Others - sarcoidosis, amyloidosis, drugs

Clinical Features:

Lump, usually in neck, axilla, groin

Worrying Features - non-tender, >3/52, >1cm, hard, irregular, tethering, weight loss, night sweats, fatigue, absence of infection

Investigations:

Determine infective cause if possible, or biopsy if concerned.

Management:

Watchful waiting or biopsy

84
Q

Stroke

A

Definition:

Stroke - a focal neurological deficit due to a vascular lesion lasting >24 hours (if the patient survives)

TIA - a focal neurological deficit lasting

Risk Factors:

HPT

Smoking

FH

Hyperlipidaemia

Afro-Caribbean

High-dose OCP

Clinical Features:

TIA

Carotid System - visual loss, asphasia, hemiparesis, hemianopic visual loss

Vertebrobasilar - diplopia, vertigo, vomiting, dysarthria, choking, ataxia, transient global ischaemia

Evidence of embolic source - AF, carotid bruit, valvular heart disease, subclavian stenosis

Cerebral Infarction

Initially flaccid, areflexic weakness followed by spastic tone, brisk reflexes and extensor plantars

Dysphasia - most probably left hemisphere, expressive - Broca’s area in frontal. Receptive - Wernicke’s area in temporal-parietal

Middle cerebral / internal carotid - hemiparesis, aphasia, hemianopic visual loss, dysarthria

Posterior inf cerebellar - coma, vertigo, vomiting, dysphagia, choking, ataxia, contralateral loss of pain on face

Management:

Acute:

CT Head to rule out haemorrhage

?Alteplase

Aspirin

Stroke unit

ABCD2 - risk of stroke following TIA

Find underlying cause - bloods, lipids, ECG, CXR, echo

Chronic:

SALT - swallowing assessment

Physio -

OT -

Risk Factor Modification

Anti HPT

Aspirin (300mg initially) / Clopidogrel

Anticoagulation - AF

Surgery (internal carotid)

Prognosis:

30-40% survival at 3 years

10% risk of further stroke within one year

85
Q

Myelopathy - Myasthenia Gravis

A

Definition:

Disorder of the neuromuscular junction

Aetiology:

Unknown - IgG antibodies to ACTH receptor leading to destruction. Thymic hyperplasia in 70%.

Associated with:

Thyroid disease

RA

Pernicious anaemia

SLE

Clinical Features:

Weakness and fatigability of muscles:

Proximal limb

Extraoccular

Speech

Facial expression

Mastication

Ptosis

Reflexes preserved but fatigable

Investigations:

Tensilon test

Serum ACTH receptor antibodies (+ve in 90%)

Mediastinal imaging for thymoma (CXR, CT, MRI)

Management:

Oral anticholinesterase eg. pyridostigmine

Thymectomy (improves prognosis)

Corticosteroids

Azathioprine

Plasmapheresis

86
Q

Paediatric Congenital Defects

A

Definition:

Aetiology:

Clinical Features:

Investigations:

Management:

87
Q

Peritonitis

A

Definition:

Inflammation of the peritoneum, locally (eg appendicitis) or generalised.

Aetiology:

Rupture of abdominal viscus eg perforated duodenal ulcer, perforated appendix.

Clinical Features:

Sudden onset abdominal pain

Shock

Still patient

Investigations:

AXR - air under diaphragm

Check amylase

Management:

Analgesia

Surgery

88
Q

Hypertension

A

Definition:

Chronically high BP

Stage 1 - >140/90 in clinic & ABPM average >135/85

Stage 2 - >160/100 in clinic & ABPM average >150/95

Severe - >180 systolic or >110 diasolic in clinic

Aetiology:

Primary - genetic, obesity, alcohol, sodium intake, stress

Secondary Renal - diabetic nephropathy, renovascular disease, adult polycystic disease, chronic glomerulonephritis

Secondary Endo - Conn’s, adrenal hyperplasia, phaeochromocytoma, Cushing’s, acromegaly

Secondary CVS - coaectation of aorta

Secondary Drugs - OCP, steroids, NSAIDs

Secondary Pregnancy - 2nd half of pregnancy, pre-eclampsia

Clinical Features:

Usually asymptomatic

Features of underlying cause

Headaches

Nose Bleeds

Nocturia

Elevated BP

Renal Artery Bruit

Radiofemoral Delay (coarctation)

Left Ventricular Hypertrophy

Retinal Changes

Grade 1 - tortuosity of retinal arteries & ‘silver wiring’

Grade 2 - G1 + arteriovenous nipping

Grade 3 - G2 + flame haemorrhages & soft “cotton wool” exudates

Grade 4 - G3 + papilloedema

Investigations:

Simple - Urinalysis - casts, protein & red cells

  • ECG - LV hypertrophy & strain

Bloods - Fasting BM & lipids

  • U&Es

Radiology - CXR

   - Echo - LV hyoertrophy

Management:

Step 1 - ACEi (or ARB)

Step 2 - Step 1 + Ca-channel Blocker

Step 3 - Step 2 + Diuretic (thiazide-like)

Step 4 - Consider Spironolactone or alpha-blocker or ß-blocker

>55 years or black

As above but start with Ca-channel Blocker

Lifestyle - weight loss, alcohol reduction, salt restriction, exercise, low fat diet

Complications:

Cerebrovascular Disease

Coronary Artery Disease

Retinopathy

Renal Disease

90
Q

Acute Coronary Syndrome

A

Definition:

ACS is ischaemia of the myocardium and includes STEMI, NSTEMI and angina

Aetiology:

It is usually due to atherosclerotic disease of the coronary vessels

Clinical Features:

Chest Pain - severe, sudden, at rest, >30mins

Not relieved by GTN

Sweating, SoB, N&V, Pale / grey, Tachy, HF, Hypotension, ‘Silent’ in 20%

Investigations:

Simple - ECG

Bloods - FBC, U&Es, Trop T/I, Lipids

Radiology - ?Angiography (see below)

Management:

O2 if hypoxic

Morphine + antiemetic

GTN

Aspirin 300mg and continue indefinitely

Fondaparinux if low bleeding risk & angio > 24 hours

or LMWH if angio

NSTEMI & Unstable Angina

GRACE score:

Lowest Risk - Conservative

Low Risk - 300mg loading then 12 months Clopidogrel

Intermediate to Highest Risk - As above but also consider GPI (Tirofiban) or Bivalirudin plus Angiography +/- PCI within 96 hours

STEMI

Cath lab for immediate PCI

Long-Term Drugs

Aspirin indefinitely

Clopidogrel 300mg for 12 months

ACEi

ß-blocker

Statins

Admin

Assess LVF

Follow -up clinic

Education

Cardiac Rehab

Lifestyle Modification

91
Q

Bronchitis

A

Definition:

LRTI worse in smokers & COPD

Aetiology:

Viral but may be complicated by bacterial infection

Clinical Features:

Cough

Wheeze

Retrosternal discomfort

Chest tightness

Investigations:

Rule out other or serious causes

Management:

Self limiting so supportive only 4-8 days

93
Q

Mechanical Back Pain

A

Definition:

Chronic back pain caused by a small injury leading to spasm of the back muscles and pain.

Aetiology:

Disc rupture - young

Vertebral # - old

Soft tissue tear - low back strain

Clinical Features:

Pain, usually self limiting

Red Flags - 50 years, trauma, CNS symptoms, infective symptoms, steroid use, bony tenderness

Investigations:

>3/52 - routine bloods to find cause

>4/52 &/or trauma &/or Red Flag - imaging

Management:

Get on with your life within limits of pain

Physio

Analgesia

Treat depression

Education

95
Q

Giant Cell Arteritis

A

Definition:

Inflammatory disease of the blood vessel

Aetiology:

Vasculitis

Clinical Features:

Headache

Pain on eating

Visual disturbance

Aching muscles

Tenderness

Pulseless or nodular vessel

Investigations:

ESR, CRP & Plts - raised

Hb - low

Biopsy diagnostic

Management:

Prednisolone

Analgesia

Urgent biopsy

Speak to opthalmology

96
Q

Hypothyridism

A

Definition:

A condition in which free T4 is reduced due to different potential causes.

Aetiology:

Hashimoto’s - autoimmune Thyroid destruction
Radioiodine-treated hyperthyroidism
Thyroidectomy

Clinical Features:

Weight gain
Lethargy
Depression
Patient feels cold
Constipation
Poor appetite
Menstrual disturbances
Myxoedema facies; thickened skin
Brittle hair
Periorbital puffiness
Bradycardia
Slow relaxing reflexes

Investigations:

Biochemistry
Haemotology – macrocytosis, anaemia
Anti-thyroid antibodies

Management:

Thyroxine
Caution in cardiac disease
Monitor TSH

98
Q

Anaemia

A

Definition:

Reduced Hb concentration (Normal Range 13M, 11.5F)

Aetiology:

Reduced production - aplastic, pernicious, iron deficiency

Increased destruction - congenital, sickle cell, AA, DIC

RBC loss - haemorrhage, menstruation

Clinical Features:

Fatigue

SoB

Exertional angina

Palpitations

Pallor

Tachy

Koilonychia

Angular stomatits / glossitis

Investigations:

WCC may be low in bone marrow failure

Reticulocytes - measures bone marrow activity

Blood film - shows erythrocyte morphology

Management:

Treat underlying cause eg iron supplements

99
Q

Stridor

A

Definition:

Upper airway obstruction which produces a high-pitched wheeze

Aetiology:

Infection (epiglottitis, abscess)

Tumour

Foreign Body

Trauma

Post-op

Analphylaxis

Management:

ABC approach

Anaesthetic & ENT urgently

DO NOT LOOK IN MOUTH

O2

Adrenaline Nebs (5mL of 1:1000)

Look for signs of anaphylaxis

Urgent portable CXR

100
Q

Hypokalaemia

A

Definition:

Normal Range 3.5-5.3 mmol/L

Determined by cellualr uptake, renal excretion and extra renal losses (GI)

Aetiology:

Renal - diuretics (thiazide & loop)

Increased aldosterone - liver / heart failure, nephrotic syndrome, Cushing’s, Conn’s, ACTH tumours

Steroids

Renal Disease

Dietary Deficiency

GI Losses

Clinical Features:

Muscle paralysis if severe

Arrhythmias in abnormal hearts

Potentiation of Digoxin toxicity

Investigations:

ECG

Management:

K+ supplements

K+- sparing drugs

Treat underlying cause

102
Q

Venous Thromboembolism (DVT)

A

Definition:

Occur in 25-50% of surgical patients, and many none surgical patients. 65% of below knee DVTs are asymptomatic and rarely embolize to the lungs.

Risk Factors:

Age, pregnancy, synthetic oestrogen, surgery, prev. DVT, malignancy, obesity, immobility, thrombophillia

Clinical Features:

Calf warmth / swelling / tenderness / erythema

Mild Fever

Pitting Oedema

Investigations:

Wells Score

>3 - High probability, treat as suspected DVT & USS

1-2 - Intermediate probability, treat as suspected DVT & USS

0 - Low probability, perform D-dimer….

If +ve treat as suspected DVT & USS

If -ve DVT is reliably excluded

Management:

Enoxaparin and Warfarin for ~48 hours and stop Enoxaparin when INR = 2-3

Continue Warfarin for 3/12 post-op, 6/12 if no cause, lifelong if recurrent DVTs

IVC filters may be considered later

103
Q

Cataract

A

Definition:

Opacification of the lens by lens proteins

Aetiology:

Age
Trauma
Radiation
Genetics
Skin diseases
Drug use
Medications

Clinical Features:

Blurred vision

Investigations:

Management:

Surgery

104
Q

Aortic Stenosis

A

Aetiology:

Congenital
Rheumatic Fever
Clacific

Clinical Features:

Often None
Exertional angina, syncope, SoB
Small volume, slow-rising pulse
Sustained apex beat
Systolic Thrill in aortic region
Sudden Death

Heart Sounds

Ejection systolic murmur @ aortic area
Radiation to carotids
Ejection Click
Soft 2nd heart sound

Investigations:

CXR

Echo

Management:

Conservative:

Avoid strenuous exercise
Avoid vasodilators

Medical:

β-blocker for angina

Surgical:

Valve replacement (mandatory in symptomatic patients)

105
Q

Adrenal Insufficiency

A

Definition:

Primary Hypoadrenalism (Addison’s)

Destruction of adrenal cortex causing reduced production of glucocorticoid, mineralocorticoid and sex steroids.

Aetiology:

Common:

Autoimmune disease ~90%
TB
Surgical removal

Uncommon:

Haemorrhage / infarction
Meningococcal septicaemia
Venography
Malignancy
Amyloid

Clinical Features:

Tiredness
Debility
N&V
Anorexia / weight loss
Abdo pain
Diarrhoea
Depression
Menstrual disturbance
Pigmentation – mouth, palmar creases
Postural hypotension
Dehydration
Loss of body hair

Investigations:

Reduced 9am Cortisol

Reduced Synacthen Test

Management:

Replacement of glucocorticoids and mineralocorticoids with oral hydrocortisone and fludrocortisone

106
Q

Hypercalcaemia

A

Definition:

Normal Range 2.12-2.65 mmol/L

Aetiology:

Hyperparathyroidism, malignancy, excess Vit D

Clinical Features:

Bones (pain / #), Stones (renal), Moans (depressed), Groans (abdo pain). Also: vomiting, const, weakness, thirst, polyuria, weight loss

hypertension, arrhythmias, dehydrated, cachexia, bony tenderness

Worrying Features

Reduced GCS, chest pain, palpitations, inc HR, low BP, abnormal ECG

Investigations:

ECG - short QT, arrhythmias

CXR; Bone scan

Management:

Correct fluid deficit

Furosemide

Catheterisation

Bisphosphonates

107
Q

Macular Degeneration

A

Definition:

Wet or Dry subtypes which are retinal damage causing blindness in the centre of the visual field.

Aetiology:

Dry (nonexudative) form, cellular debris called drusen accumulates between the retina and the choroid, and the retina can become detached

Wet (exudative) form, which is more severe, blood vessels grow up from the choroid behind the retina, and the retina can also become detached

Clinical Features:

Deterioration of central vision, loss of acuity but fields intact

Pigment, fine exudate and bleeding at the macula

Drusen

Investigations:

Opthalmoscopy

Management:

Laser photocoagulation

Screenin initiated if Drusen are seen

108
Q

PID

A

Definition:

Inflammation of the fallopian tubes or uterus, ovaries caused by infection. It may lead to adhesions and potentially infertility.

Aetiology:

90% STI - usually chlamydia

Clinical Features:

Pain

Fever

Lower abdo muscle spasm

Cervicitis with purulent, bloody discharge

Investigations:

Endocervical & urethral swabs

Blood cultures

Management:

IV Abx (cefriaxone & doxycycline)

Contact tracing

109
Q

Hypernatraemia

A

Definition:

Normal Range 135-145 mmol/L

Nearly always due to inadequate water intake

Aetiology:

Inadequate water intake plus:

ADH deficiency (diabetes insipidus)

Insensitivity to ADH (drugs, ATN)

Osmotic Diuresis (diabetic coma, TPN)

Clinical Features:

Volume depletion

Confusion / convulsions

Fever

Features of underlying cause

Investigations:

Plasma osmolality high

Low urine osmolality indicates diabetes insipidus

Management:

Replace fluid

Treat underlying cause

110
Q

Anxiety

A

Definition:

A displeasing feeling of fear and concern

Aetiology:

“biological vunerability”

Clinical Features:

GI - dry mouth, dysphagia, epigastric pain, diarrhoea

Resp - chest constriction, difficulty inhaling, overbreathing

CVS - palpitations, chest pain

GU - frequency, erection failure, reduced libido

Neuro - fatigue, blurred vision, dizziness, headache, poor sleep

Psychological - Apprehension & fear, irritability, poor concentration, distractibility, restlessness, sensitivity to noise, depression, depersonalisation, derealisation

Investigations:

Clinical diagnosis

Management:

Reassurance, relaxation techniques, anxiety management, CBT

SSRIs - citalopram, fluoxetine, sertraline

ß-blockers for physical symptoms

Short course of benzodiazepines - diazepam, temazepam

111
Q

Cholecystitis

A

Definition:

Inflammation of the gall bladder

Aetiology:

Caused by chemical irritation within an obstructed gallbladder. Often begins with simple Biliary Colic

Clinical Features:

Severe RUQ pain
Fever
Tachycardia
Nausea / Vomiting

Murphy’s sign +ve - ask patient to take deep breath pressing RUQ under costal margin

Patients tend to lay still & take shallow breaths as this is a local peritonitis

Investigations:

WCC - increased
USS - Gallbladder - thickened gallbladder
Plain Abdominal X-ray - only show 10% of stones

Management:

IV Fluid resuscitation
IV Antibiotics - Cefuroxime
Keep patient NBM

Cholecystectomy
Time frame is controversial
Increasingly surgeons carry out procedure early in the acute phase
Some say it’s better to wait until 6-8 weeks later

80-90% of cases of acute cholecystitis will spontaneously resolve over 24-48hrs

112
Q

Carpal Tunnel

A

Aetiology:

Compression of the median nerve as it passes depp to the flexor retinaculum. F>M

Idiopathic

DM

Hypothyroidism

Pregnancy

RA

Obesity

Clinical Features:

Tingling or pain in thumb, index & middle fingers

Worse at night

Shake or flick wrist for relief

Later: wasting of thenar eminence

Investigations:

Phalen’s (inverted prayer for 1-2mins)

Tinel’s (tapping over tunnel)

USS

Management:

Pain relief

Splints at night

Retinaculum division

113
Q

Motor Neurone Disease

A

Definition:

Progressive degeneration of lower motor neurons and upper motor neurons of the cortex, cranial nerve nuclei and spinal cord.

2:100 000 pa

Slight Male predominance

Clinical Patterns:

Progressive muscular atrophy – progressive weakness and wasting of arm and hand muscles

Amyotrophic Lateral Sclerosis – progressive spastic tetraparesis or paraparesis with wasting and fasciculation

Progressive Bulbar Palsy – degeneration of lower cranial nerve nuclei

Clinical Features:

Muscle Wasting
Fasciculation
Areflexia or hypereflexia
Dysarthria
Dysphagia
Nasal Regurgitation of fluids
Choking
Bulbar & Pseudobulbar palsy
Occular Movements not affected
Cerebellar or extrapyramidal signs do not occur
Dementia is unusual
Sphincter function is usually preserved
No sensory signs

Investigations:

Clinical diagnosis

Electromyography (EMG) – denervation of muscles with preserved motor conduction velocity

Management:

Riluzole – sodium channel blocker slows progress

Nothing affects outcome

Relentlessly Progressive with death in 3 years