Cardio Resp GI mix Flashcards
Budd-Chiari syndrome- causes?
caused by thrombosis of the hepatic vein:
hepatomegaly,
ascites
abdo pain.
liver metastases
history of breast cancer and nodular liver on examination
intraperitoneal organs
Some Drunk Japs Invented tequila shots
Stomach
Duodenum
Juojenum
Ilium
Transverse Colon
Sigmoid Colon
Coeliac trunk level
T12
Left renal artery level
L1
Testicular or ovarian arteries level
L2
Inferior mesenteric artery
L3
Bifurcation of the abdominal aorta
L4
Hesselbach triangle
M= R
L= I
I= I
Medial= Rectus Abdominis
Lateral= Inferior Epigastric Vessels
Inferior= Inguinal ligament
indirect inguinal hernia
deep inguinal ring
and
exits the inguinal canal at the superficial inguinal ring
where would you palpate the trachea?
Jugular notch at level of T2
Sternal angle at
level of 2nd rib// T4 -T5
Xiphoid process at level …
T10
Superior & inferior facets
articulate with the heads of the ribs
Costal facets
on transverse processes articulate with the tubercles of
the
ribs present on T1 T10
Trachea bifurcates to L&R main bronchi at the point of the
carina
T4/5
Larynx becomes trachea at level
of C6
vertebra
bucket handle
External, internal
and innermost intercostal muscles alter thoracic
dimensions
NVB (intercostal
vein, artery, nerve) runs …
in the costal groove
‘C3, 4, 5 keeps the …
diaphragm alive’
Phrenic nerve fires
diaphragm flattens
Type 2 hypersensitivity/cytotoxic
Generally Autoimmune conditions
IgM IgG
1) haemolytic anaemia
2) thyroid issue
overactivity of the thyroid gland
3) Goodpasture’s syndrome
Type 3/immune complex
hypersensitivity
1)Pneumonitis
IgG against inhaled antigens produced immune complexes formation –>
deposition in lung tissue
2) Lupus
3Local deposition of anti nuclear antibodies in complex with released
chromatin –> complement system activation –> inflammation
3)Serum sickness
antibody against foreign serum –> complex formation –> deposition anywhere in
the body (systemic inflammation)
Type 4/cell
mediated/delayed
type hypersensitivity
1) TB
2) IBD
- Sarcoidosis
T cell responses
against microbiota/self antigens
Pneumothorax
Small <2cm rim of air
Large >2cm rim of air
(measured at level of hilum)
Pneumothorax No SOB and < 2cm
No SOB and < 2cm
No treatment as usually spontaneous resolves
Follow up in 2 weeks
4 weeks of CXR to see if resolved
Primary Pneumothorax SOB or >2cm
Secondary Pneumothorax SOB or >2cm with lung disease
Primary
Aspiration
If aspiration fails twice
Chest drain
Secondary
Chest drain+admit straight up
Site of aspiration in tension
Ptx
2nd intercostal space mid clavicular line
Triangle of safety
*The 5th intercostal space (or the inferior nipple)
*The mid axillary line (or the lateral edge of the latissimus dorsi)
*The anterior axillary line (or the lateral edge of the pectoris major
*Insert just above the rib to avoid NV bundled that runs underneath
Excess ADH, name condition:
Condition SIADH (Hyponatremia).
Associated: SCLC
Small cell lung carcinoma - produces what? leads to what
produce ACTH
lead to cushing’s
Lambert
Eaton syndrome (LEAC)
muscle weakness as
antibodies against Ca2+ receptors.
Horner’s syndrome, which tumour
Pancoast tumour
-
Miosis = pupil constriction
-
Ptosis = eyelid drooping
-
Anhidrosis= lack of sweating
Community Acquired Pneumonia (CAP), which bacteria
Strep. Pneumonia
HAP bac
Gram -VE
MRSA
H. influenza
Klebsiella
Aspiration pneumonia which bacteria
enterococcus
Atypical pneumonia , what caused it
Birds/ Chlamydia
psittaci
Pneumocystis
jirovecii
GAYS/ FREDDIE MERCURY
Legionella
Hot tubs/ Air Con
Mycoplasma (3 points) youth
Infects younger people. “Walking pneumonia”
Less severe symptoms e.g. dry cough
PCR test
Mycobaterium tuberculosis bacteria. Cowboy
1) Rod shaped bacteria (bacillus).
2) Strict aerobes (require oxygen).
3_ Has a waxy coating
4)
acid fast bacilli
Tuberculosis - 4 things about it
1)Granuloma
2) ‘Caseous necrosis’ / cheesy
3) Type IV hypersensitivity reaction.
4) South Asia/South Africa
Latent TB, ghost
Ghon Focus
Miliary TB
haematogenous spread throughout the body. Potentially life threatening.
TB prevention and test
BCG vaccine/ Mantoux test
Night sweats Weight loss?
TB
Test for TB
Ziehl Neelson stain
acid fast
bacilli Turns TB bacteria bright
red
Rifampicin
= red/orange discolouration of secretions
like urine and tears (red pissing)
Isoniazid
= peripheral tingling hands feet
Pyrazinamide tb drug
= hyperuricaemia (high uric acid levels)
resulting in gout.
Ethambutol
= colour blindness and reduced visual
acuity.
associated with hepatotoxicity? TB drugs
R.I.P
Interstitial Lung disease, R or O?
Restrictive:
FEV1% (FEV1/FVC) - normal or increased
Idiopathic pulmonary fibrosis.
** Amiodarone **
1) finger clubbing .
2) Bi basal fine inspiratory crackles,
3) breathlessness
4) dry cough
HONEYCOMB
HYPERSENSITIVITY PNEUMONITIS Lung
which Hypersensitivity, and what type of person gets smashed by this
1) Type 3 Hypersensitivity
2) farmer / birdworker
Chronic low
dose exposure can lead to a type 4 hypersensitivity transformation
Pneumoconioses (J.P)
‘Simple’ pneumoconiosis = asymptomatic
‘‘egg shell opacification’’ appearance on CXR at the lung hila.
‘Complicated’ pneumoconiosis (john prescott)
the same hilar egg shell opacification on CXR, but with symptoms a productive cough and breathlessness.
(Unlike other ILD where there is a dry cough, the cough with pneumoconiosis may be productive of sputum/mucus).
Sarcoidosis (six)
- Granulomas
- (CtX) bilateral hilar lymphadenopathy
- erythema nodosum
- lupus pernio
- Black ladies
- Raised serum ACE , raised calcium
RESTRICTIVE
Other extrinsic causes of a restrictive pattern on spirometry
Obesity
Kyphosis
Neuromuscular disorders
The parasympathetic nervous system which causes bronchoconstriction and
increases mucus secretion via which receptors?
M3
Non Atopic asthma
TH1/ IgG
Atopic asthma
- TH2 Secrete IL4 + IL13 -> B cells -> IgM to IgE
- Mast cells + eosinophils express
receptors for Fc region of IgE - release of
histamine
Chronic asthma
- Increased smooth muscle Oedema
- Increased mucus secretion
- Epithelial damage (exposing sensory nerve endings)
- Sub epithelial fibrosis
Peak Flow test Asthma- Obstructive
FEV1 - significantly reduced
1st line Asthma
SABA (Salbutomol)+ ICS (Beclo)
2nd line Asthma
SABA Salbutamol + ICS Beclometasone + LABA Salmeterol
- If no response consider
stopping LABA Salmeterol and increase ICS Beclometasone
2.If some response continue LABA Salmeterol
and increase ICS Beclometasone
3rd line Asthma
Add LTRA eg montelukast
or
Xanthines eg Theo
4th line Asthma
Add
oral steroid eg prednisalone
and
anti IgE Omalizumab
anti IL5 ?
anti IL4 alpha ?
LABA
Salmeterol/ Formoterol
1) Salmeterol Phosphodiesterase breaks down cAMP
2) formoterol binds B-2 receptors, leading to an increase in (cAMP) levels, which activates protein kinase A (PKA).
PKA then phosphorylates specific proteins, resulting in the relaxation of the smooth muscle in the bronchi and bronchioles.
LAMA for COPD
Tiotropuim (M3)
Aclindinium
Glycopyrronium
Blocks acetylcholine, Ach causes smooth muscle contraction in the airways
Inhaled ICS
Beclometasone,
Budesonide
glucocorticoid binds to GRα and enters the nucleus.
montelukast
cysLT1 receptors act competitively at the cysLT1 receptor derived from mast cells and infiltrating inflammatory cells cause smooth muscle contraction mucus secretion and oedema
antagonist .
Beclometasone,
Budesonide side affects (ICS, 2nd line part 2)
Oropharyngeal candidiasis (thrush)
Dysphonia (hoarse and weak voice)
Asthma mnemonic
Acute presentation (O SHITMAn)
●
Oxygen (at least 60%)
●
Salbutamol (neb)
●
Hydrocortisone (IV) OR oral prednisolone
●
Ipratropium (neb)
●
Theophylline (oral)
●
Magnesium sulphate (IV)
●
An anesthetist (to intubate)
Moderate Asthma attack
PEF = 50-75%
Severe Asthma attack
PEF= 33-50%
Resp rate above 25
Tachy
can’t complete sentences
Life threatening Asthma
Silent chest, PEF <33%, cyanosis / blue
Raised CO2 Ashtma
Near fatal
COPD ALPHA WHAT
alpha 1
antitrypsin deficiency
CHRONIC BRONCHITIS, secretion of what
hypersecretion of mucus by goblet cells
EMPHYSEMA
Inflammation neutrophils release proteases break down elastin walls of alveoli loss of elastic recoil
abnormally increased compliance
Obstructive lung disease
FEV1% (FEV1/FVC) - significanly reduced
EXAMPLE 3 O.L.D’s
Asthma
COPD
Bronchiectasis
Restrictive lung disease
FEV1% (FEV1/FVC) - normal or increased
EXAMPLE 3 R.L.D’s ,
Pulmonary fibrosis
Asbestosis
Sarcoidosis
HRCT for bronchiectasis screening. how to qualify?
Anyone with more than 3 exacerbations in 6 months should get
HRCT for bronchiectasis screening.
DLCO decreased or increase in emphysema
decrease
COPD home management
Oral prednisolone
●
Increase SABA/SAMA
●
Antibiotics if evidence of infection
COPD hospital Management
Hospital management
ISOAP
●Ipratropium
● Salbutamol
●Oxygen (target spO2 88 92%
●Amoxicillin (/doxycycline)
●Prednisolone
Virchow’s Triad
ChineSe Eat Humans
Hypercoagulable state - malignancy, pregnancy, peripartum period, IBD,
thrombophilia, sepsis.
Circulatory Stasis - LV dysfunction, immobility or paralysis, venous insufficiency
or varicose veins, obesity, pregnancy, venous obstruction from tumour.
Endothelial injury - venous disorders, venous valvular damage, trauma, surgery,
indwelling catheters
PE signs HTH
Signs
● Hypoxia
● Tachycardia
● May be hypotensive
PE investigation
Wells Score - >4 - do a CTPA. <4 - do a D-Dimer
Test for PE x 2
CTPA - can identify a large embolism.
V/Q scan sometimes used in pregnant
patients
PE management
High risk / unstable patient- thrombolysis (alteplase) then DOAC (Riva).
Intermediate or low risk / stable patient- DOAC ONLY.
Warfarin - not used as much. LMWH - still used in patients with active cancer and PE. NOT TO GIVE WHEN PREGNANT!!
Primary spontaneous pneumothorax:
patients without clinically apparent underlying lung disease
Secondary spontaneous pneumothorax, complication of which underlying lung disease
Cf,IPF,Marfan syndrome, Ehlers- Danlos
syndrome
Bronchiolitis, age? and which virus/
Under 18 months
tachypnoea
RSV Respiratory Syncytial Virus
● poor feeding
● irritating cough / grunting
● apnoea (in small babies)
Croup which virus
Symptoms:
Parainfluenza virus
● barking cough
● stridor
● difficulty breathing (fast onset)
● described as ‘already having a cold’
Treatment:
● oral or IM corticosteroids (eg dexamethasone)
Cystic Fibrosis, stats, gene , which chromosome, and what key indiciator
1 in 25
CFTR gene
chromosome 7.
Symptoms:
● salty sweat
Tetralogy of Fallot Boot shaped heart
1) VSD
2) RVH
3) Pulmonary stenosis
4)Over riding Aorta
Pneumotaxic center
Upper Pons. Fine tunes resp rate
Apneustic centre
Lower Pons
voluntary promoting inhalation and prolonging inspiratory duration
Apneusis= respiratory distress
DIVE
Dorsal= Inspiratory
Ventral= Expiratory
Negative chronotropic effect
Decrease H.R
Negative Inotropic effect
Decrease Contractibility
Baroreceptors
Aortic Arch + Carotid sinus
PR interval
Time period between Atrial and Ventricular Deporisation
1st Degree H.B
PR more than 0.2 secs
Mobitz type 1 (Wenky’s)
Lengthed PR, Missed QRS
Mobitz type 2 HB
Fixed PR, missed QRS
3rd degree HB
No relationship between PR and QRS
Tunica Intima
Endothelial