Cardiac Flashcards
What are the risk factors of a cardiac condition?
- Pre existing medical problems
- Overweight
- 35 years old or more
- Socially deprived
- Smoking
- Congenital heart disease
- BAME
- Previous C/S
- Family history
- Assisted conceptions: comes with factors above
What are the red flags of CVD?
- Raised respiratory rate
- Severe chest pain spreading to the jaw, arm or back
- Tachycardia
- Severely breathless when resting, especially if it happens when laying flat (orthopnoea): Orthopnea is caused by increased pressure in the blood vessels of your lungs. When you lie down, blood flows from your legs back to the heart and then to your lungs. In healthy people, this redistribution of blood doesn’t cause any problems.
- Experience fainting while exercising/ exerting oneself (syncope)
What are the cardiac changes in pregnancy?
- The heart moves- Heart increases in size to keep up with demands, and moves upwards and to the left to make room for enlarging uterus.
- O2 consumption increased to give to baby, so RBC increase by 30%
- Plasma volume – haemodilution (40-50% above baseline by 32 weeks)
- Decreased resistance in circulation – increase in progesterone (muscle relaxant) causes the heart to compensate for it’s relaxed state which leads to increased cardiac output, increases by 10-20bpm.
- Increased stroke volume
- Cardiac output increase by 20% at 8 weeks, peak increase by 40% at 20-28 weeks
- At term, heart is physiologically dilated and myocardia contractility is increased
- BP drops in 2nd trimester (increased levels of progesterone leads to vasodilation of blood vessels) but will reach or exceed pregnancy levels by term
- CVP unchanged – haemodilution
- Colloid oncotic pressure falls by 10-15% (hydrostatic pressure pushes out), which makes pulmonary oedema more likely
- increase oedema of hands, feet and ankles
- Inferior Vena Cava pressure by the gravid uterus
- Pregnancy is a hypercoagulable state: increase in venous embolic event
- Changes in pharmacokinetics- what the body does to the drug: might not be as effective in pregnancy
What are the cardiac changed in labour?
- 15% increase in 1st stage as a result of pain/adrenaline which increases anxiety and HR. Women with cardiac conditions should be offered epidural as causes drop in BP due to vasodilation
- 50% increase in cardiac output in 2nd stage as woman pushes and holds breath (Valsalva manoeuvre) so need an increase to get O2 around the body. Women with cardiac disorders shouldn’t have c/s as more likely to bleed so use instrumentals for short 2nd stage
- Following delivery (3rd stage), relief of IVC compression and contraction of the uterus = autotransfusion of blood back into the maternal circulatory system, which increases cardiac output by 60-80%.
- This is the most risky time for pulmonary oedema as increased cardiac output as placenta delivered and the uterus contracts which is full of blood and blood is pushed back into the maternal circulation
What are the general principles of management of pregnancy in women with heart disease?
- Ideally all women with congenital or acquired heart disease should receive multi-disciplinary preconception counselling before pregnancy
- Termination of pregnancy is only beneficial under 16 weeks before significant increase in cardiac output has occurred.
- Guidance must be given early.
- Early review and risk assessment by MDT (obstetricians, anaesthetists & cardiologists) required.
- Optimise mother’s CV status during pregnancy
- Monitor for deterioration
- Careful fluid management
- Continuous ECG and continuous oxygen saturations.
- Address fetal issues (regular scans/ specialist cardiac fetal echo): stillbirth, IUD, IUGR
- Develop a clear, well documented and widely distributed plan for labour and the puerperium AND COMMUNICATE WITH THE WOMAN
- Avoid the supine position as associated caval compression reduces venous return and thus cardiac ouput by upto 25%
Effective pain relief important - Reduces rise in CO from pain and anxiety
- Low-dose regional anaesthesia
Limit maternal effort: - The managed second stage
- Assisted delivery (Ventouse/Forceps)
- Place of delivery: is a cardiac theatre appropriate
- Exercise caution with oxytocic drugs.
o Syntocinon infusion -> fluid retention
o Ergometrine -> contraindicated due to its vasoconstrictive and hypertensive disorders - Post labour HDU/ICU/CCU: usually 24 to 48 hours
- Senior post-partum obstetric and cardiology review important
- Early cardiology follow up (heart teams’ approach)
- Early discussion about risks of future pregnancy & robust contraception
What are the changes to an ECG in pregnancy?
- Ectopic beats
- Relative sinus tachycardia
- Ejection systolic murmur
- Loud first beat
- Peripheral oedema
- Q-wave (small) and inverted T-wave in lead III
- ST depression and T-wave inversion infero-lateral leads
- QRS axis leftward shift
What are the different cardiac heart disease?
- Congenital heart disease
- Acquired heart disease
- Cardiomyopathies: heart muscle failure
- Heart valves disease (prosthetics)
- Arrythmias
- Myocardial infarction/ acute coronary syndromes
- Dissection of the aorta
What are the different types of congenital heart disease?
- Atrial Septal Defect
- Ventricular Septal Defect
- Patent Ductus Arteriosus
- Coarctation of the aorta
- Pulmonary Hypertension
- Eisenmenger’s Syndrome
- Marfan syndrome
- Tetralogy of Fallot
What is atrial septal defect?
- An atrial septal defect is a birth defect of the heart in which there is a hole in the wall (septum) that divides the upper chambers (atria) of the heart.
- Common CVD in women
Signs and symptoms
- Shortness of breath, especially when exercising
- Fatigue, migraine
- Swelling of legs, feet or abdomen
- Heart palpitations or skipped beats
- Heart murmur, a whooshing sound that can be heard through a stethoscope
- Stroke
Impact on pregnancy
- Usually well tolerated in pregnancy
- PET, IUGR, Atrial arrhythmias can occur in unrepaired ASD
Coarctation of the aorta?
- Constriction of the aorta = marked hypertension
- Usually repaired surgically in infancy but some women may present with undetected CA
- Can be associated with aneurysm of the circle of Willis
- Risks of uncorrected CA in pregnancy = angina, hypertension, congestive heart failure, aortic rupture or dissection
What is pulmonary hypertension?
- Unknown (idiopathic)- often first manifested in pregnancy
- Defined by an elevation in mean pulmonary arterial pressure (PAP) >_25 mmHg at right heart catheterisation
- Lung disease e.g. cystic fibrosis
- Congenital heart disease - Eisenmenger’s syndrome
Impact on pregnancy
- Pulmonary hypertension of whatever cause has a maternal mortality of 30-50% (16-30% with treatment)
- The greatest period of risk is the puerperium, especially the early post-partum period
- Avoid pregnancy or offer termination
- Increased fetal and neonatal mortality
- Increased risk of VTE
What is Eisenmenger’s Syndrome?
- This refers to a shunt in the heart with blood going from left to right (note reversal of direction)
- Usually as a result of an unrepaired septal defect
- Results in the mixing of de-oxgenated and oxygenated blood causing cyanosis and increased pulmonary vascular resistance
- R-to-L shunting increases in pregnancy because SVR falls
Pregnancy
- Offer termination (also carries risks)
If continues
- High risk of VTE
- May get paradoxical emboli = anticoagulation
- Risk of bleeding, Vit-k deficiency, clotting factors, thrombocytopenia
- Hospital admission likely with activity restriction or bed rest
- Oxygen therapy guided by saturation monitoring
- Any congestive heart failure = diuretics but difficult as they do not tolerate rapid fluid fluctuations
- Intensive fetal monitoring as IUGR common
- 7 days stay in ICU after birth.
What is Marfan syndrome?
- Rare genetic (autosomal dominant) disorder of the connective
- Inherited disorder
- Increased height with arm span greater than height
- Arachnodactyly (very long, slender digits)
- Pectus excavatum (dip at sternum)
- High arched palate, large bulging eyes
- Joint laxity
- Aortic root dilatation and risk of rupture
In pregnancy
- Pregnancy contraindicated if aortic root is less than 4.0cm (measure with echo)
- If dilated surgical replacement prior to pregnancy
- When a woman with known aortic dilatation (history of) dissection or genetic predisposition for dissection becomes pregnant, strict blood pressure control is recommended
- Repeated ECG imaging every 4–12 weeks (depending on diagnosis and severity of dilatation) is recommended during pregnancy and 6 months post-partum in patients with ascending aorta dilatation
- It is recommended to deliver all women with aortic dilatation or (history of) aortic dissection in an experienced centre with a pregnancy heart team.
- In patients with an ascending aorta <40 mm, vaginal delivery is recommended; In patients with an ascending aorta >45 mm, caesarean delivery should be considered (same with h/o dissection)
- In patients with an aorta 40–45 mm, vaginal delivery with epidural anaesthesia and an expedited second stage should be considered.
- When possible, the use of ergometrine is not recommended in women with aortic disease= the heart is a smooth muscle so ergometrine will effect it.
Management of Marfan’s
- ß-blockers have been shown to reduce rate of aortic dilatation
What is tetralogy of fallot?
- Tetralogy of Fallot is a combination of four congenital abnormalities. The four defects include a ventricular septal defect (VSD), pulmonary valve stenosis, a misplaced aorta and a thickened right ventricular wall (right ventricular hypertrophy).
- A bluish coloration of the skin caused by blood low in oxygen (cyanosis)
- Shortness of breath and rapid breathing, especially during feeding or exercise
- Loss of consciousness (fainting)
- Clubbing of fingers and toes — an abnormal, rounded shape of the nail bed
- Poor weight gain
- Tiring easily during play or exercise
- Irritability
- A heart murmur
Risk factors of TF
- A viral illness during pregnancy, such as rubella (German measles)
- Alcoholism during pregnancy
- Poor nutrition during pregnancy
- A mother older than age 40
- A parent who has tetralogy of Fallot
- The presence of Down syndrome or DiGeorge syndrome
Pregnancy
- Women with repaired tetralogy of Fallot usually tolerate pregnancy well (WHO risk class II).
- Cardiac complications have been reported in 8% of repaired patients, especially in those taking cardiac medication prior to pregnancy.
- Arrhythmias and HF are the most common complications. Thrombo-embolism and endocarditis are rarer.
- The risk of offspring complications is increased, in particular fetal growth restriction (FGR).
- Maternal screening for 22q11 deletion should be undertaken prior to pregnancy.
- Follow-up every trimester is sufficient in most patients. In women with severe pulmonary regurgitation, monthly or bimonthly cardiac evaluation is indicated.
- If RV failure occurs during pregnancy, treatment with diuretics should be started and bed rest advised. avoid pulmonary oedema
- Early delivery or, rarely, transcatheter valve implantation could be considered in those who do not respond to conservative treatment.
What are the different acquired CVD related to Rheumatic Heart Disease?
- Mitral valve stenosis
- Aortic Stenosis
- Artificial/Prosthetic Heart Valves