Deck 1 Flashcards

1
Q

Pathology of Psoriasis

A

Cytokines trigger keratinocyte hyperplasia. Leads to elongated club shaped rete ridges, paraketosis and mild spongiosis

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2
Q

Presentation of Psoriasis

A

Itchy, flaky layers of dead keratinocytes. Inflammation and rapidly dividing celss

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3
Q

Rx for Psoriasis

A

Topical steroids and photosystemic therapy. Adherence affected by work, side effects, cost, attitude etc.
Non-pharm: stress mgmt, increased sun exp, reduced weight, stop smoking and also moisturising.

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4
Q

Inflamm arthritis presentation

A

affects synovial membrane, tendon insertion poitns around joints (enthesitis) and also red, hot, swollen etc.

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5
Q

Cause of psoriatic arthropathy

A

degradation of synovial membrane. Similar to RA. Causes fatigue and stiffness. Need to start of DMARDs

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6
Q

Technique for IACI

A

Clean technique: informed consent, prep equipment and patient, be skilled, dispose of sharps and other hazardous waste post procedural advice.

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7
Q

Structure of synovial joints anxtrd normal synovial fluid

A

Synovial membrane, articular cartilage and joint capsule. Fluid should clear, viscous with no fibrin clots (-ve culture and normal WBC count)

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8
Q

Extra articular manifestations of RA

A

fatigue, weight loss, hair falling out and heart problems. Amyloidosis of kidney, scleritis of eye and fibrosis of lung.

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9
Q

Pharmacology of Rx for Ra

A

Increased proliferation of T-cells causes Ra and can either use methotrexate (blocks antigen presentation/activation of macrophages). Also TNF-a inhibitor

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10
Q

non-pharm mgmt of RA

A

weight control, OT, exercise, hydrotherapy

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11
Q

Diagnosis for RA

A

use anti-CCP AB (produced by inflammation of synovium) Also ultrasound for early RA

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12
Q

Describe feedback and feedforward control

A

Visual and somatosensory and vestibular input into central command. Feedforward accompany voluntary movements and feedback= reflex response evoked by sensory inputs following loss of balance

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13
Q

List the 6 ways fracture can be classified

A

anatomical location, direction of fracture( oblique or transverse), linear or comminuted, impacted, open or closed and if its pathological

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14
Q

5 factors for fracture healing

A

Immobilisation, Good reduction, good vascular supply, minimal necrosis and lack of infection

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15
Q

6 stages of bone healing

A

Haematoma–> inflammation–> granulation tissue–> Soft callus–> Hard callus–> Remodelling

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16
Q

What are the types of osteoporosis

A

Type 1: post-menopausal
Type 2: low peak bone mass, age related
Secondary: endocrine diseases, drugs, malabs, physical inactivity

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17
Q

Rx for osteoporosis

A

Bisphosphonates, bone strengthening exercise

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18
Q

What are the risk factors for falls

A

Age>80, peripheral neuropathy, postural hypertension, Poor footwear, hypoglycaemia, urinary incontinene
Prevention: balance, strength training, med review, hazard intervention

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19
Q

Depression DSM-V criteria

A

One of the first two and a total of 5 symptoms from the list below in the past few weeks:

1) Lack of interest in performing activities
2) Low mood
3) Changes in sleep patterns- disturbed sleep
4) Distressed/Impairment on social life
5) Psychomotor agitation/retardation
6) feelings of guilt/worthlessness
7) Appetite changes

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20
Q

What is the difference between an episode and a disorder

A

Episode= over a period of time and usually one or more of depressive, manic or hypomanic
Disorder: pattern of illness due to an abnormal mood

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21
Q

What disorder is this: Over 2 years, no high phases and lasts much longer than typical major depressive disorder. Not severe enough to be depression

A

Persistant depressive disorder or dysthymia

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22
Q

Name the disorder: Major depressive moods characterised by classic symptoms of severe depression. Awake early, feeling worse than they do later in the day, los appetite and weight, guilty

A

Major depression with melancholic features

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23
Q

Describe symptoms in major depression with psychotic features

A

Manic and major episodes can be accompanied by delusions which can be mood congruent or incongruent.

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24
Q

Describe Bipolar disorder

A

manic and depressive episodes. Manic episodes for atleast one week

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25
Q

Name the suicide assesment tool

A
SAD PERSONS
S: Sex M>F
A: Age (teen and elderly)
D: Depression
P: Prev attempt
E: Ethanol abuse
R: Rationale thinking loss
S: Social support (none)
O: Organised plan
N: No spouse
S: sickness
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26
Q

What are the 2 types of headache

A

Tension type and migraine headache

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27
Q

What are the red flags of a headache

A

Exacerbated by coughing, provoked by postural hypertension, ass with eye movement, thunderclap, headache with stiff neck, general aches and pains.
Also dramatic change in quality and site as well as failure to response to appropriate therapy

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28
Q

What is the mechanism of SSRI

A

Blocks re-uptake, increasing serotonin (5-HT) in the synapse.

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29
Q

What are some things you need to warn patients about before placing them on SSRI?

A

Side effects ie they will get worse before they get better.

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30
Q

What are the 3 classic symptoms of Parkinson’s

A

Bradykinesia, Cogwheel rigidity and Tremor

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31
Q

What are the non-motor symp of PD

A

mood disturbance, neuropsychiatric symp, cognitive impairment, sense of smell altered, speech altered, acting out dreams in sleep.

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32
Q

What would you see on examination of PD

A

Gait, standing tests, tone. Also axial rigidity, mask face, increased tone, rapidly alternating movements, absence of humour.

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33
Q

Name 4 causes of an altered mental state

A

CNS ie trauma.
Physchological condition
drugs
non-CNS ie hypoglycaemia

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34
Q

Describe the GCS

A

Looks at Eye-opening, Verbal and Motor movements. 4,,5 and 6 scores.
Comatose is 8 or less. 3= totally unresponsive

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35
Q

What are some anatomical consequences of head trauma?

A

Haemorrhage, raised ICP, coma, loss of motor/sensory fn

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36
Q

What is the sequelae of traumatic brain injury

A

Confusion, collapse, coma and death

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37
Q

What are the classifications of seizure?

A

Partial (simple partial, complex partial or secondary) and generalised (grand mal)

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38
Q

What can ECG be used for?

A

Confirmation of brain death
spatial+ temporal resolution
investigating unexplained collapse
NOT to diagnose sleep abnormalities

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39
Q

What epileptic drugs would you give to:
Pregnant womn
Child
Someone with generalised seizures

A

Preg: NO valproate.
Child:Benzo
Generalised: Valproate

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40
Q

What are pros and cons of MMSE

A

Good: quick, no training req, can be done anywhere, cheap, way of communication
Bad: low sensitivity for fronto-temporal impairment. Lot of recall and NO cognition

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41
Q

What are functions of the frontal lobe

A

motor cortex: calling forth info and using it–> goal
working memory
exacerbation of though

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42
Q

Name the 4 ECG rhythms in order of most–> least alertness

A
Gamma: high cog state
B: normal everyday, alert and consious. Dreaming in REM
A; Eyes closed but awake and relaxed
D: Deep sleep
GBAD
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43
Q

What are the structures penetrated during a LP?

A

dura, skin, fat, supraspinatus lig, interspinous lig, lig flavum

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44
Q

Where would you inject an epipen in leg?

A

Inject at vastus lateralis away from femoral artery, vein and nerve

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45
Q

Where would you inject something in arm? Name a common condition due to incorrect technique

A

Deltoid muscles used for <2 y.o. In the deltoid triangle. Can hit the radial nerve.

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46
Q

Which subtypes of meningitis are common in neonates, kids and elderly

A

ALL have N.meningitidis and S.pneumoniae
Neonates: Group B strep, E.coli, protons, Pseudomonas, Listeria
Kids: HiB
Elderly: S.aureus, enterobact and listeria

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47
Q

What are some viral causes of meningitis?

A

Arbovirus (Murray, West Nile), mumps, measles, HIV

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48
Q

Clinical features of meningitis are?

A

fever, inflamm of meninges, headache, photophobia, neck stiffness, possible confusion. Can also cause seizures, infections in arachnoid and CF.

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49
Q

Hearing loss due to affect on vestibulo-chochlear nerve is due to what condition?

A

Meningitis. Ossicles are damaged in Otitis media

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50
Q

Name the 3 ligaments of the pelvis

A

Iliofemoral lig, catyloid lig and pubofemoral lig

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51
Q

Difference between ischaemia and infarction

A

Ischaemia is reduced bloody supply to the tissue. Infarction is death of tissue due to hypoxia.

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52
Q

What are causes and symptoms seen in Osteomylelitis

A

Causes: post trauma/surgery, haematogenous, continous with other infections.
Symp: fever, unexplained limp, trouble weight bearing on affected side

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53
Q

What are the causes of septic arthritis

A

> 70% haematogenous, surgery, spread from adjacent osteomyelitis

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54
Q

What are some causes of avascular necrosis of bone

A

Alcohol abuse, atherosclerosis, increased corticosteroid use, radiotherapy, sickle cell disease

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55
Q

How many vertebrae are in each section of the spine?

A
Cervical: 7
Thoracic:12
Lumbar: 5
Sacral:5
Cocys: fused
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56
Q

What are the primary and secondary curvatures of the spine

A

Kyphotic=primary. And Lordotic

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57
Q

What stimuli is carried by alpha-delta and C fibres?

A

Mechanical heat

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58
Q

What stimuli is carried by C fibres

A

Cold and chemicals

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59
Q

Difference between nociceptive and neuropathic pain?

A

Nociceptive is due to pain mediators and source of injury/damage. Neuropathic is due to membrane excitability/hypersensitivity to pain

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60
Q

What are the two types of NSAIDs

A

COX1: normal constituent and acts as gastric protector, renal sodium/water balance and platelet aggregation
COX2: More specific locations. Inducible constituent in pain, inflammation and pain.

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61
Q

What structures do the following supply: ACA, MCA and PCA

A

ACA: frontal and temporal mode (esp on the medial surface)
MCA: majority of cortex. inc Wernicke’s, Broca’s, Auditory area as well
PCA: Occipital and parietal

62
Q

Name the tract: arises in motor cortex and crosses at medulla. Control of skilled motor activity

A

Lateral corticospinal tract

63
Q

Name the tract: In motor area and uncrossed. Controls axial muscles

A

Anterior corticospinal tract

64
Q

Name the tract: Arises in contralateral red nucleus of the midbrain. Control of flexor tone

A

Rubrospinal tract

65
Q

Name the tract: Arses in the ipsilateral vestibular nucleus of the pons and controls extensor tone

A

Vestibulospinal tract

66
Q

What happens in an UMN lesion

A

contralateral increase in tone. Clonus and Babinski’s positive

67
Q

What happens in LMN lesion

A

Ipsilateral reduced tone

68
Q

Describe effect of UMN and LMN lesion of facial nerve

A

UMN: Affects only 1/4 of face
LMN: 1/2 of face ie Bell’s Palsy

69
Q

Name the stroke classifications

A

Haemorrhagic and Ischaemic. 85% Ischaemic

Haemorrhagic= bleed IN brain

70
Q

Risk factors for stroke

A

Non-modifiable: age>55, gender and fam Hx
Modifiable: Hypertension, CVD, smoking, alcohol, diet, overweight, physical inactivity
Medical condition related: prev episode of TIA, atrial fib, blood clotting disorder

71
Q

Steps in MGMT of stroke

A
  1. Rapid initial stroke screen
  2. Urgent CT/MRI
  3. Aspirin as soon as possible (if ischaemic)
  4. Monitor nuero status
72
Q

What is the ABCD2 score?

A

A: age>60, BP, Clinical features of TIA, Duration (TIA>60 mins) and DIabetes

73
Q

Describe the pathology of SLE

A

due to formation of immune complexes ( Type 3 hypersensitivity). These are usually broken down by complement activation but here can deposit at various sites. Complex deposition–>complement activation–> inflamm cell influx–> mediator release

74
Q

What investigations would you perform for SLE

A

Look for ANA AB and then diff tests conducted for the different symptoms present ie Coomb’s test for haemolytic anaemia

75
Q

What does the acronym VITAMIN CDEF stand for and what is its use

A
Used for formulating DDx/
V: vascular
I: infective
T: trauma
A: autoimmune
M: MSK
I: idiopathic
N: neural
C: congenital
D: Developmental
E: endocrine/environment
F: functional ie sleep
76
Q

What investigations would you perform for haemolytic anaemia

A

Looking for normocytic or macrocytic anaemia so look at blood smear.
Also positive DAT and increased bilirubin

77
Q

Name this test: RBC+ antigen placed in a solution. AB added and test for agglutination

A

Direct antigen test

78
Q

Name the test: AB and antigen RBC in solution, bind and then anti-AB added to bind the complexes

A

indirect DAT

79
Q

Describe the general scheme of iron transport around the body

A

oral iron in lumen–> blood–> either used or stored as ferritin. Can also be sent to macrophages for recycling

80
Q

What is ferroportin

A

Iron transporter. Allows iron to exit lumen and enter blood

81
Q

What is the fn of transferrin

A

Binds to iron which allows it to bind to transferrin receptor on erythroid progenitor cells

82
Q

What are the 3 types of anaemia and name one example of each

A

Macrocytic: B12 and Folate, hypothyroidism
Normocytic: renal failure, combined nutritional def
Microcytic: iron def, anaemic of chronic disease

83
Q

What are symptoms of IDA

A

tiredness, faitgue, PICA, pallor, hair loss, britlle nails, pallor of palmar creases, chest pain and tachycardia

84
Q

What are the 3 measurements that can be performed for IDA

A

Serum iron: iron in blood and reflective of intake
Ferritin: amount stored in body, usually low
Total iron binding capacity: measurement of the protein that carries iron

85
Q

What are the 3 factors affecting iron abs

A

concomitant consumption of inhibitors, GIT disorder and non-compliance

86
Q

What are the symptoms of iron OD

A

Nausea, abdominal discomfort, vomiting and diarrhoea

87
Q

What are haemantinics

A

Factors required to increased Red cell/blood cell productions ie EPO. Can be used in IDA but not recommended

88
Q

Name the 4 steps in primary haemostasis

A

Unstable platelet plug (at time of injury)–>Coagulation cascade–> fibrin formation–> fibrin stabilised platelet plug

89
Q

What is the role of vWF

A

Carrier of factor VIII and involved in primary haemostasis

90
Q

Symptoms of vWF disease?

A

Epitaxis, mucosal bleeding, menorrhagia and easy bruising

91
Q

What is the mgmt for vWF

A

IV infusion of desmopressin. Increased breakdown of vWF storing granules in platelets and endothelium
Biostate can be used for those that dont respond to desmopressin

92
Q

What is the function of the lymphatic system

A

aids the immune system in removing and destroying waste, debris, dead blood cells, toxin and cancer cells.

93
Q

What are the primary lymphoid organs and their fn

A

Bone marrow and thymus. They provide appropriate environment for development and maturation of lymphocytes

94
Q

What are secondary lymphocytes and their fn

A

Spleen, MALT, appendix, tonsils and lymph nodes. Trap antigens and site of antigen presentation. Generally from nearly tissues/fluids where lymphocytes can interact with antigens

95
Q

What are the developmental changes in the immune system

A

Start off with maternal AB protection and then after 6 months, innate and adaptive IS start to develop. Adaptive takes longer to develop with new exposures and vaccines

96
Q

What is the difference between innate and adaptive immunity

A

Innate: immediate and acts within 0-96 hours. No specific response. Includes neutrophils and complement system
Adaptive: more specialised response, tailored to the microorg after antigen presentation from APC. Divided into cell mediated and humoural immunity.

97
Q

Name the disease: fever, sore throat and runny nose. Begins on face and neck–> neck, trunk and extremities. Lasts 5 days. Behind ear and back of neck

98
Q

Name the disease: Itchy rash of red papules–> vesicles (blisters)–> other parts of body. Blisters can also arise in mouth. Others can get high fever, headache, cold like symp, vomitting and diarrhoea. Most experience cold-like symptoms before breaking out in a rash

A

Variecella!

99
Q

Name the disease: associated with splenomegaly, hepatitis and arthritis. Diffuse lymphadenopathy present and most common= faint, widespread, non-itchy rash for one week.

A

HHV or EBV

100
Q

Name the disease: Non-specific viral symp is mild fever and headache. Rash appears a few days later with red red cheeks. Lasts 2-4 days and causes polyarthropathy in adults

A

Parvovirus B19

101
Q

Name the disease: increased fever for 3-5 days and URT symptoms ie sore throat, cough, runny nose. Rash appears day 3-5 with small rose-pink raised spots that blanch when touches. Similar spots on uvula and soft palate

102
Q

What do you look for in an examination for severe lymphadenopathy

A

Tender? Enlarged? Growing? Symmetrical? mobile? Also look for systemic symptoms

103
Q

What are some signs of a serious illness in a child

A

reduced BP, high fever, unresponsive/ not eating. BP maintained in young children until last straw so any change= sig pathology

104
Q

What situations is safety netting important in?

A

Case of missed/uncertainty of diagnosis, ruling out serious disease, parentral cancer, illness that can progress rapidly etc

105
Q

What are the steps of the Calgary Cambridge Framework

A

Open session–> Gather info–> physical exam–> explanation and planning–> close session. All the while providing structure and building rapport

106
Q

What are the valves of the heart and their location

A

A: aortic. Parasternal, 2nd intercostal space on the right
P: Pulmonary. Parasternal and 2nd intercostal space on the left
T: tricuspid valve. 5th intercostal space, parasternal
M: mittral. 5th intercostal space on the left

107
Q

What are the mechanical events of the heart during a cardiac cycle

A
Late systole
Atrial systole
Isovolumetric contraction
Ventricular ejection
Isovolumetric relaxation
108
Q

What happens in late diastole

A

both chambers relaxed and passive ventricular filling

109
Q

What happens in atrial systole

A

Atria contract, forcing a small amount of additional blood into the ventricles

110
Q

Isolvolumetric contration

A

First phase of ventricular contraction. Pressure in ventricle rises with the A-V valves closed but NOT enough to open the semilnar valves

111
Q

Ventricular ejection

A

Pressure eventually reaches high enough to open the semilunar valves–> ejection of blood

112
Q

Isovolumetric relaxation

A

The semilunar valves close as ventricles relax and pressure drops

113
Q

What are the major features of RHF

A

Subcutaneous nodules, erythema marginatum, Sydenham’s chorea, pancarditis and polyarthritis

114
Q

What are the minor symp of RHF

A

Raised CRP and ESR, fever, fatigue, athralgia

115
Q

Name the sequelae of RHF

A

Group A strep infection–> normal AB response–> develops into an autoAB response –> secondary infection–> exacerbates autoimmune response–> inflammation and effect on the heart

116
Q

What is the mgmt for RHF

A

single dose penicillin or oral erythromycin is allergic. [need monthly penicillin injections as prevention]

117
Q

Describe the compensatory mechanism of RHD

A

Chronic mittral regurg–> increased return to left atria-> left ventricular hypertrophy and increased stroke volume–> left atrial distension–> normal cardiac output and minimal pulmonary congestion

118
Q

Using the baroreceptor reflex, explain why atrial fib presents as head spins

A

Reduced blood outflow due to non-synchronous contraction of the heart–>sensed as a reduction in bp by receptors in the aortic arch– CV control centre–> increased output–> effectors which return homeostasis

119
Q

Explain presyncope from AF

A

AF–> rapid ventricualr response–> reduced diastolic duration–> reduced LV filling–> reduced CO–> baroreceptors cant compensate–> presyncope

120
Q

Why do you need anti-coagulants for patients with AF?

A

Turbulent blood flow one of the factors in Virchow’s triad for hypercoagulability

121
Q

What are the two ways to control AF and in what situation would you use either?

A

Can control rhythm or rate
Younger: rhythm
Older: rate

122
Q

What medication can be used to control heart rate in AF

A

Beta blockers, alpha blockers, diuretics, ACE inhibitors or ARBs

123
Q

Describe HF due to MR

A

Valvular insufficiency from MR–> volume overload of the heart–> heart working too hard and cant compensate–> failure. Results in SOB, tachycardia, cough etc

124
Q

What are 3 DDx for dizziness

A

HF, iron def, pulmonary hypotension, dehydration, heart attack

125
Q

What can be a cause of pain in calves in a patient with high cardiac risk factors?

A

Intermittent claudication–> MI

126
Q

Name this condition: set of signs and symptoms due to reduced blood flow meaning coronary part of heart muscle is unable to fn properly and dies

A

Acute coronary syndrome

127
Q

What are atypical and typical symptoms of MI

A

Typical: left arm pain, crushing pain
Atypical: pain in jaw, nausea, vomitting, back pain and discomfort, dysopnea

128
Q

Name the Rx for anyone with MI

A
First: aspirin ASAP unless contraindicated
Then ABCDE
A: ACE inhibitors
B: Beta blockers
C: Clopidogrel (anti-platelet, anti-ADP)
D: Diet (Statins)
E: exercise
129
Q

What are the 5 steps in the physiology of respiration

A

Ventilate lungs with air, diffusion of gases between air and blood, transfer of gases in blood, diffusion of gases from blood to tissues

130
Q

What are the physical barriers to protect the resp system

A

Nose hairs, cilia and mucus producing goblet cells. Cough reflex from the larynx. Upper airway branching (providing muco-cilliary clearance) Then alveolar macrophages and the innate IS

131
Q

What are the 3 ways an infection can develop in the RT

A

Haematogenous spread, aspirations, spread from adjacent site or inhalation from environment

132
Q

Pathophysiology of CAP

A

Inhalation of microrog, aspiration of oropharyngeal or gastric contents, haematogenous deposition or invasion of infection contigous structures, direct inoculation or reactivation

133
Q

Presentation of CAP?

A

Fevers, rigors, dysopnea, cough, haemoptysis, pleuritic chest pain

134
Q

What does CURB-65 stand for

A
C: Confusion
U: urinary fn
R: resp rate (>30bpm)
B: BP (<90 systolic and <60 diastolic)
Age>65
135
Q

What does CORB stand for

A

C: Confusion, O:Oxy sat 90% , R: Resp rate (>30) and B: BP

136
Q

What appears white on an x-ray

A

Consolidation, Fluid, solid tumour or foriegn body and collapsed lung

137
Q

Name the 4 divisions of the resp tract and the histological features of each

A

Trachea: Psuedostrat epithelium and C-shaped cartilage
Bronchi: More elastic, less smooth muscle. Patchy cartialge
Bronchioles: more smooth muscle, less elastic
Alveoli: Simple squamous epithelium with no cartilage

138
Q

What is the pathophysiology of asthma

A

antigen–> APC–> Th2 cells–> IL-4–> B cells–> plasma cells IgE production–> IgE–> mast cells and binding via epsilon receptors–> release of histamine, leukotrines. Then cytokines, chemokines and enzymes.

139
Q

What is the result of the immune response in asthma

A

Smooth muscle contraction, sneezing, nasal discharge, redness. Oedema and bronchoconstriction as well as remodelling

140
Q

Lists the steps in the cough reflex

A

irritant–> mechanoreceptors in the throat–> vagus nerve–> medulla–> cough reflex (closure of epiglottis and pressure builds up in the lungs as expiratory muscles contract. Then the epiglottis opens and the irritant is violently expelled

141
Q

What is the mechanism of a wheeze

A

Contraction of smooth muscles reduces the diametre of airways (from the larynx to small bronchi) hence making it harder for air to leave the lungs. This produces a wheezing sound as the air travels through the resp tract

142
Q

List the 4 causes of airway narrowing

A

Smooth muscle contraction, mucosal oedema, abnormal mass or external compression

143
Q

What are some precipitating factors for asthma

A

Smoking, allergies.

144
Q

What are the signs and symptoms of poorly controlled asthma

A

Daytime symp for >2days/week which can be partially or fully relived by a bronchodilator.
>3 symp of partial control in the same week ie limitation of activity, symp during the night and when they wake up

145
Q

What are the clinical features of astham

A

Wheeze, cough, SOB, tight chest. Reduced FEV1

146
Q

What is the Rx for asthma?

A

Short term: bronchodilators ie SABAs (salbutamol). Work for 4-6 hours
Long term: need LABAs and inhaled corticosteroids. Inhaled corticosteroids are the number one controllers and often combined with LABAs. These are preventors!!!

147
Q

What education advice can you give to an adult about spacers? Should they use them?

A

Yes! Spacers dilute the dose in the container and increase the delivery of the medication to the lungs hence more effective! Young children use it due to lack of co-ordination but highly recommended in older individuals as well. Reduces the amount of medication stuck at the back of the throat (sore throat)

148
Q

Why is an action plan neecesary for asthma?

A

To be able to recognise deterioration and respond properly. Also aims to enable early intervention and prevent severity of attack

149
Q

What happens to FEV1/FVC, lung volumes, resp rate and gas transfer in intersitial lung disease?

A
FEV1/FVC usually maintained
Lung volumes reduced
Impaired gas transfer
Increased resp rate
also worsening breathlessness
150
Q

What happens to FEV1/FVC in obstructive vs restrictive disease?

A

Obstructive: reduced
Rest: increased or normal because BOTH parameters change

151
Q

What are the goals and risks of oxygen therapy

A

Goal is tor relive hypoxaemia

Risks: fire, reduced resp drive and not enough oxygen

152
Q

List 5 aspects of a good death

A

Patient should know and understand what’s coming
It should be in a location of their choice
Offer digniity and privacy
Available expertise on whatever info required
They should be able to retain control of what happens