1 Flashcards

1
Q

what is the blood supply to external and internal oblique muscles

A

lower 6th thoracic nerves

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2
Q

what is the conjoint tendon made of

A

internal oblique and transversalis fascia

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3
Q

where does long head biceps attach

A

supraglenoid fossa

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4
Q

where does short head biceps attach

A

coracoid process

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5
Q

positions of appendix

A

retrocaecal, pelvic, subcaecal, pre and post ileal

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6
Q

what type of joint is atlanto-axial

A

pivot

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7
Q

what type of joint is carpal and first metacarpal of thumb

A

saddle joint

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8
Q

what type of joint is TMJ

A

modified hinge joint

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9
Q

what juvenile structure forms clivus

A

spheno-occipital

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10
Q

what runs in jugular foramen

A

IJV (continuation of sigmoid sinus), inferior petrosal sinus and CN 9,10,11

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11
Q

benign tumours of PCF

A

meningioma, acoustic neuroma, ependymoma, haemangioblastoma

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12
Q

which bone makes up middle ear

A

petrous part of temporal bone

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13
Q

what ia achalasia

A

motility disorder involving smooth muscle layer of oesophagus and lower oesophageal sphincter, resulting in incomplete LES relaxation, increased LES tone and lack of peristalsis of oesophagus

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14
Q

what is facial nerve intracranial course

A

origin between pons and medulla, internal acoustic meatus, facial canal (through petrous part of temporal bone), exit through stylomastoid foramen

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15
Q

what level is carotid bifurcation

A

C4

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16
Q

where does long and short head of biceps femoris originate

A

ischial tuberosity long
linea aspera of femur for short

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17
Q

what is adhesive capsulitis

A

chronic fibrosing condition characterised by insidious and progressive severe restriction of both active and passive shoulder range of motion

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18
Q

ligments attached to odontoid process

A

alar ligament
transverse atlantal ligament
apical odontoid ligament

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19
Q

ligaments between c1 and c2

A

anterior and posterior atlantoaxial and transverse ligament

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20
Q

layers to pass through for LP

A

skin, subcutaneous tissues, supraspinatous ligament, interspinatous ligament, ligamentum flavum, epidural space, dura mater, arachnoid mater

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21
Q

what type of joint is IV joint

A

secondary cartilaginous jointd

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22
Q

describe anatomy of IV disk

A

inner nucleus pulposus surrounded by annulus fibrosis

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23
Q

level of spinal cord in newborn and adult

A

L3 new born, L1/2 adult

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24
Q

how do spinal mets happen

A

direct arterial invasion
retrograde invasion through bartons venous plexus
direct invasion through intervertebral foramina

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25
Q

contents of epidural space

A

connective tissue
lymphatics
spinal nerve roots
fatty tissue
small arteries
network of internal venous plexuses

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26
Q

why cant you feel any spinous processess before C7

A

because they are short and bifid and are attached to nuchal ligament

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27
Q

what parts of the brain are supplied by the vertbero-basilar system

A

brainstem, cerebellum, thalamus, and occipital lobes

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28
Q

contents of carapl tunnel

A

Flexor pollicis longus, flexor digitorum superficialis and flexor digitorum profundus

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29
Q

what supplies supraspinatous muscle

A

suprascapular nerve

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30
Q

what supplies infraspinatous muscle

A

suprascapular nerve

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31
Q

what supplies teres minor

A

axillary nerve

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32
Q

what supplies subscapularis

A

subscapular artery

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33
Q

where do supraspinatous, infraspinatous and teres minor attach

A

greater tubercle humerus

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34
Q

what muscles insert into bicipital groove

A

teres major, lat dorsi and pec major

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35
Q

what are the boundaries of the quadrangular space

A

superior: teres minor
inferior: teres major
lateral: surgical neck of humerus
medial: long head triceps
anterior: subsapularis

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36
Q

what is contained in the quadrangular space

A

axillary nerve
circumflex humeral vessels

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37
Q

why does DIC happen

A

infections, burns, trauma, liver failure, massive transfusion, hypothermia, malignancy, obstetric causes (amniotic fluid emobolism)

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38
Q

what does APTT test

A

intrinsic/common pathway all factors except facotr VII

39
Q

what does PT test

A

extrinsic pathway-deficiencies in factors, 1,2,5,7,10

40
Q

causes of hypothyroidism

A

autoimmune-hashimotos
iodine deficiency
iatrogenic
drugs eg. lithium
transient thyroiditis

41
Q

difference in T3 and T4

A

t3 is x4 more potent than T4, peak effect within 24-48 hours, plasma protien binding capacity is less
active in vitro
thyroid gland only produces 20% of T3

42
Q

what is the Berlin criteria for ARDS

A

contains 3 must have criteria
1-timing withing 1 week of clinical insult
2-CXR shows bilateral opacities not fully explained by other pathollogy
3-respiratory failure-not fully explained by cardiac failure/fluid overload

43
Q

management of fluid overload

A

1-ABCDE
-high flow oxygen, IV furosemide, GTN
ITU review, CXR, ABG, ECG
pre-load reduction-nitrates
after-load reduction ACEI
inotropic support-dobutamine

44
Q

what is the purpose of fluid therapy

A

1-basal requirements of water and electrolytes
2-replace fluid and electrolytes lost eg vomiting, diarrhoea, pancreatic fistula
3-maintain arterial pressure incases of shock by increasing plasma volume and improving tissue perfusion

45
Q

what is the compensatory response to respiratory acidosis

A

1-initial response is small, cellular bufffering elevates bicarb slightly approx 1mEq/L for each 10mmg of PaCO2
1-renal compensaion that occurs over 3-5 days, renal excretion of carbonic acid and increased biocarb reabsoption

46
Q

how does the body sense hypercarbia

A

central chemoreceptors

47
Q

what is a consequence of this

A

increase respiratory rate to blow off more CO2

48
Q

what are the side effects of naloxone

A

sweating, nausea, vomiting, tachycardia, abdominal cramps

49
Q

ways to measure ICP

A

invasive-external ventricular drain, subdural catheter, ICP transducer
non-invasive, transcranial doppler can measure MCA velocity and derive a pulsality index correlating with ICP

50
Q

how and where is bilirubin conjugated

A

in liver, conjugates with glucouronic acid by enzyme glucuronyltransferase

51
Q

describe metabolism of bilirubin

A

most unconjugated bilirubin around 95% is reabsorbed in the terminal ileum
conjugated biliriubin passes into colon and is not absorbed, metabolised and deconjugated to urobilinogen (colourless) and oxidised to stercobilin (give stool brown colour)

52
Q

pre hepatic caused of jaundice

A

G6PD, hereditary spherocytosis, autoimmune haemolytic anaemia, gilberts syndrome

53
Q

causes of hepatic jaundice

A

hepatitis, drug induced, chronic autoimmune hepatitis

54
Q

causes of post hepatic jaundice

A

head of pancrease carcinoma, gallstones, sclerosing cholangitis, cholangiocarcinoma

55
Q

what is a fistula

A

an abnormal communication lined by granulation tissue between two epithelial or endothelial surfaces

56
Q

how to classify fistulas

A

congenital or acquired
cause-eg infection, malignancy
simple or complex
where the fistula is colovaginal, colovesciular
internal or external
physiology-low or high output

57
Q

management of fistula

A

SNAP, control sepsis, nutritional support, anatomical access/adequate fluid/electrolyte balance

58
Q

how does T4 come about

A

ATE ICE
-active transport of ioding into follicular cell
-thyroglobulin is formed in follicular ribosomes and placed into secretory vesicles
-exocytosis of thyroglobulin into follicle lumen where it is stored as colloid
-iodination of thyroglobulin
-coupling of MIT (monoiodotyrosine and diiodotyrosine) to form T3 and t3
-endocytosis of iodinated tyhroglobulin into follicular cell

59
Q

how is T4 converted to T3

A

deiodinase system D1,2,3 in multiple tissues and organs especially skeletal muscle, liver, brain and thyroid

60
Q

how to classify hyponatraemia

A

Depletional-burns, diretics, diarrhoea
dilutional-heart fialure, iatrogenic through too much IV fluids,
endocrine-addisons and hypothyroidism
pseudohyponatraemia-mulitple myeloma and SIADH

61
Q

how are BCC treated

A

curretage and elctrodissection, imiquimod, topical fluoracil, radiotherapy, photodynamic therapy

62
Q

lymphocytes, PMN, histiocytes and cells with bilobed nuclei

A

Reed Sternburg cells-lymphoma, Hogkins lymphoma

63
Q

familial MM

A

CDKN2A, CDK4, BRAC2

64
Q

encapusulated bacteria

A

strep pneumonia, e coli, klebsiella, neiserria menginitisi

65
Q

how does valve stenosis occur

A

lipid accumulation, calcification, stiffening and thickening of valve leading to stenosis

66
Q

signs of aortic stenosis

A

slow rising pulse, spliting of S2, narrow pulse pressure, ejection systolic pulse, displaced apex beat

67
Q

what is rheumatic heart disease

A

a form of cardiac inflammation with scarring triggered by an autoimmune reaction to infection with Group A strep , type II hypersensitivity reaction occurs who antibodies react with bacterial M proteins
symptoms usually 1-3 weeks after strep pharyngiitis

68
Q

pathophysiology of RHD

A

recurren inflammation, narrowing and thickening of leaflets, retraction-thickening and calcifcation leads to scarring and fibrosis

69
Q

findings of valves with RHD

A

initially verucae-small deposits in valve
chronic-fusing of chordae tendinae and shortening, valve thickening stiffening and fibrosis

70
Q

microscopic findings in endocarditis

A

askoff bodies-granulomatous inflammation which consists of central zone of degenerating ECM infiltrated by lymphocytes, plasma cells and anitschkow cells-activated macrophages, found in all 3 layers of heart

71
Q

what to look for in ECHO

A

valvular regurgitation, leaflet prolapse, thickening, annular dilatation, chordae elongation/rupture, pericardial effusion, ventricular dilatation

72
Q

organisms cause endocarditis

A

staph aureus, strep viridians, coagulase negative staph, HACEK, enterococcus

73
Q

what are the Dukes criteria

A

2 major
1major and 3 minor
5 minor

74
Q

what are the major criterai

A

x2 blood cultures with endocarditis common organisms-staph aureus, strep viridans, coagulase negative staph, enterococcus or HACEK organisms and/or
echocardiogram positive for IE, abscess or new partial dehiscence of prostetic valve, new valvular regurgitation

75
Q

what are the minor cirteria

A

heart condition or IV drug use, vascular phenomena, microbiological evidence, fever, immunological phenomena-glomerulonephritis, osler’s nodes, roth spots and rheumatoid factor, echo findings

76
Q

how does heparin work

A

inhibits factor 9,10,11,12

77
Q

what are you looking for on ECHO in endocarditis

A

valvular regurigation
leafelt prolapse, coarptation failure, thickening
annular dilatation
chordal elongation/rupture
pericardial effusion
increased echogeneicity of subvavular apparatus

78
Q

complications of IE

A

abscess
arterial or septic emboli
aneursym
pericarditis
arrythmia
valvular insufficiency
-can cause glomerulonephritis
AKI, stroke, mesenteric abcess/infarct

79
Q

what are the pathological changes in osteoporosis

A

on DEXA scan 2.5sd below the mean
histologically normal bone that has reduced in quantity
in post menopausal women increased osteoclast activity, trabecular plates become perforate thinned and lose connections and get microfractures and vertebral collapse

80
Q

how do steroids cause osteoporosis

A

direct inhibition of osteoblast formation
stimulation of bone resorption
inhibition of GIT calcium absorption
stimulate renal calcium losses

81
Q

what is a pathological fracute

A

through abnormal or diseased bone, commonly occuring with little or no trauma

82
Q

how does fat embolilsm clinical present

A

SOB with petechiae

83
Q

stages of haematoma resolution

A

clot lysis by macrophages-1 week
growth of fibroblasts into haematoma, hyaline tissue

84
Q

what three things regulate bile flow

A

hepatic secretion, gall bladder contraction and sphincter of oddi resistance.

85
Q

what is the effect of immobility of bone

A

decreased bone mineral density and increased risk of osteoporosis

86
Q

what is contained in cryoprecipitate

A

factor VIII, XIII, fibrinogen and vWF

87
Q

what is contained in FFP

A

all clotting factors, fibrinofen, protein C&S, ATIII

88
Q

what malignancies are associated with immunosuppression

A

SCC, BCC, lymphoma (NHL from EBV), kaposi sarcoma, cervical

89
Q

conditions associated with PCKD

A

liver and pancreas cysts, brain anueusysms, mitral valve prolapse

90
Q

common organisms in NF name 4

A

staph aureus including MRSA, E coli, pseudomonas, clostridium, group A beta haemolytic strep

91
Q

mechanism of C diff infection

A

broad spectrum abx distrupt normal gut micro biome allowing for C diff to overgrow, release enterotoxin, bacteria secretes fibrin and pseudomembrane formation

92
Q

what cells do medullary thyroid come from

A

parafollicular C cells