check yoself Flashcards
causes of secondary hypertension
R - renal disease, renal artery stenosis
O - obesity
P - pregnancy / pre-eclampsia
E - endocrine, hyperaldosteronism (conns)
stage 2 + 3 hypertension
2
clinic = >160/100
AB = >150/95
3
clinic = >180/120
long term angina treatment
beta blocker - bisoprolol
CCB - amlodipine
others (not 1st line) long acting nitrates (isosorbide mononitrate) ivabradine nicorandil ranolazine
secondary prevention angina
aspirin
atorvastatin
acei
already on beta blocker
MI complications
D - death R - rupture of heart septum or papillary muscles E - edema (heart failure) A - aneurysm / arrhythmia D - Dresslers
AAA screening
men age 65-74
<3 normal
>3 monitored
homans sign
pain in calf on dorsiflexion of foot
DVT
common causes of AF
SMIRTH
S- sepsis / infection M - mitral / mechanical valve [athology I - intoxication (alcohol) R - rheumatic heart disease T- thyrotoxicosis H - Hypertension
AF rate control (first line)
BB (atenolol)
CCB (dil / vera)
** never together verapaKILLLLL !!!!
digoxin if fails - take a while to kick in, dangerous if hypokalaemic, slows AV conduction (more time to fill ventricle)
what anticoag if mitral stenosis associated AF
warfarin
when would you DC cardiovert in AF
if symptoms <48hrs or anticoagulated prior
do echo first to look for emboli
AF HR
300 - 600 bpm
irregularly irregular
atrial flutter HR
220-240bpm
regularly irregular
symptoms / causes of VT
dizziness / syncope
hypotension
usually triggered - hypoxia, electrolyte abnormalities
common in CHD or previous MI
mode of inheritance of brugada syndrome
autosomal dominant
ST elevation in RBBB in leads V1-3
cjanges may be seen after flecainide
2nd + 3rd heart block treatment
atropine IV
no improve - other inotropes = noradrenalin
defibrillate
long term = pacemaker
acute HF / oedema / cardiogenic shock
morphine
NIV / CPAP
inotropes - noradenalin infusion
dresslers pathophysio
AUTOIMMUNE response to cardiac damage - damaged heart muscle release previously encountered material that stimulates an immune response
HOCM management
high risj = ICD
low = amiodarone
genetic analysis
mode of inheritance of familial dilated cardiomyopathy
DCM
autosomal dominant
DCM can be sporadic - toxins, autoimmune
echo, CXR (cardiac enlargement)
same Mx as HF
drugs to close/open ductus arteriosus
open - prostaglandin E2
close - indomethacin
hereditary condition associated with coarctation of aorta
turner syndrome - monosomy X
corctation of aorta symptoms
headaches / nosebleeds - due to hypertension
claudication
delayed pulses
clinical features of tetralogoy of fallot
spasms of sub pulmonary muscles
episodes of severe cyanosis
cyanosis develops due to increased right sided pressure - right-to-left shunt
tetralogy of fallot conditions
VSD
overriding aorta
pulmonary stenosis
RV hypertrophy
tetralogoy of fallot treatment
treat each
spasms relieved by increasing systemic resitance using postural manoeuvres – squatting
marfans mode of inheritance
autosomal dominant - FBN1 mutation
50/50 - each child of one affected parent
marfans clinical features
heart - aortic aneurysm + dissection, mitral valve prolapse
eye - dislocated lenses, retinal detachment
tall, long arms, scoliosis
high arched palate
marfans management
BB (atenolol) - slows rate of dilation of aortic root
ARB
lifestyle - avoid long exercise, sedentary job
monitoring
genetic screening, counselling
normal ejection fraction
> 50%
ADH + angiotensin II - vasodilators/constrictors?
vasoconstrictors
chemical vasoconstrictors
serotonin
thromboxane A2
leukotrienes