Cardiac Disease in Pregnancy
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Transcript Cardiac Disease in Pregnancy
Cardiac Disease in
Pregnancy
Dr Jason Reidy
Cardiac Disease in Pregnancy
Why the interest?
Women consistently die form cardiac disease
associated with pregnancy
CEMACH Reports Cardiac Deaths
Congenital heart disease
Acquired heart disease
Cardiovascular Changes in
Pregnancy
Cardiovascular Changes in
Pregnancy
Pregnancy
SVR
Diastolic BP
Cardiac output
20% by 8/40
40% by 20-28/40
SV
Circulating volume
Physiological LVH
HR
Cardiovascular Changes in
Pregnancy
Labour
Cardiac output
1st stage ~15%
2nd stage ~50%
Sympathetic output
Uterine contractions
Autotransfusion
Cardiovascular Changes in
Pregnancy
Immediately Post-partum
Cardiac
output
60-80%
Rapid
decline to pre-labour levels
~2h
2 weeks post-partum
Back
to pre-pregnancy
Cardiovascular Changes in
Pregnancy
Cardiovascular disease can manifest or
worsen in pregnancy due to the
dynamic physiological demands placed
on the cardiovascular system
Maternal Deaths due to
Cardiac Disease
CEMACH 2003-2005
Cardiac Deaths
Commonest indirect and overall cause
48
deaths
Upward trend in deaths from IHD and
myocardial infarction
CEMACH 2003-2005
Cardiac Deaths
Triennium
Congenital
n(%)
Acquired
n(%)
Acquired
n(%)
Ischaemic
Other
Total
Rate
Per 100,00
Maternities
1985-1987
10 (43)
9 (39)
4 (17)
23
1.01
1988-1990
9 (50)
5 (28)
4 (22)
18
0.76
1991-1993
9 (24)
8 (22)
20 (54)
37
1.60
1994-1996
10 (26)
6 (15)
23 (59)
39
1.77
1997-1999
10 (29)
5 (14)
20 (57)
35
1.65
2000-2002
9 (20)
8 (18)
27 (61)
44
2.20
2003-2005
4 (8)
16 (33)
28 (58)
48
2.27
CEMACH 2003-2005
Cardiac Deaths
Triennium
Congenital
n(%)
Acquired
n(%)
Acquired
n(%)
Ischaemic
Other
Total
Rate
Per 100,00
Maternities
1985-1987
10 (43)
9 (39)
4 (17)
23
1.01
1988-1990
9 (50)
5 (28)
4 (22)
18
0.76
1991-1993
9 (24)
8 (22)
20 (54)
37
1.60
1994-1996
10 (26)
6 (15)
23 (59)
39
1.77
1997-1999
10 (29)
5 (14)
20 (57)
35
1.65
2000-2002
9 (20)
8 (18)
27 (61)
44
2.20
2003-2005
4 (8)
16 (33)
28 (58)
48
2.27
CEMACH 2003-2005
Cardiac Deaths
Triennium
Congenital
n(%)
Acquired
n(%)
Acquired
n(%)
Ischaemic
Other
Total
Rate
Per 100,00
Maternities
1985-1987
10 (43)
9 (39)
4 (17)
23
1.01
1988-1990
9 (50)
5 (28)
4 (22)
18
0.76
1991-1993
9 (24)
8 (22)
20 (54)
37
1.60
1994-1996
10 (26)
6 (15)
23 (59)
39
1.77
1997-1999
10 (29)
5 (14)
20 (57)
35
1.65
2000-2002
9 (20)
8 (18)
27 (61)
44
2.20
2003-2005
4 (8)
16 (33)
28 (58)
48
2.27
CEMACH 2003-2005
Cardiac Deaths
Triennium
Congenital
n(%)
Acquired
n(%)
Acquired
n(%)
Ischaemic
Other
Total
Rate
Per 100,00
Maternities
1985-1987
10 (43)
9 (39)
4 (17)
23
1.01
1988-1990
9 (50)
5 (28)
4 (22)
18
0.76
1991-1993
9 (24)
8 (22)
20 (54)
37
1.60
1994-1996
10 (26)
6 (15)
23 (59)
39
1.77
1997-1999
10 (29)
5 (14)
20 (57)
35
1.65
2000-2002
9 (20)
8 (18)
27 (61)
44
2.20
2003-2005
4 (8)
16 (33)
28 (58)
48
2.27
CEMACH 2003-2005
Cardiac Deaths
Indirect
Late
Aortic dissection
9
0
Myocardial infarction
12
4
Ischaemic heart disease
4
0
Sudden Adult Death Syndrome (SADS)
3
9
Peri-partum cardiomyopathy
0
12
Cardiomyopathy
1
4
Myocarditis or myocardial fibrosis
5
0
Mitral stenosis or valve disease
3
0
Infectious endocarditis
2
2
Right or left ventricular hypertrophy or hypertensive heart
failure
2
1
Pulmonary Hypertension
3
0
Congenital Heart Disease
3
2
47
34
Acquired
Congenital
Totals
CEMACH 2003-2005
Cardiac Deaths
Indirect
Late
9
0
12
4
Ischaemic heart disease
4
0
Sudden Adult Death Syndrome (SADS)
3
9
Peri-partum cardiomyopathy
0
12
Cardiomyopathy
1
4
Myocarditis or myocardial fibrosis
5
0
Mitral stenosis or valve disease
3
0
Infectious endocarditis
2
2
Right or left ventricular hypertrophy or hypertensive heart
failure
2
1
Pulmonary Hypertension
3
0
Congenital Heart Disease
3
2
47
34
Acquired
Aortic dissection
Myocardial infarction
Congenital
Totals
Trends in Cardiac Deaths
Malhotra & Yentis
IJOA
2006
288 maternal cardiac deaths in 30 year
period from CEMD/CEMACH
Trends in cardiac deaths with or without
known disease or risk factors
Trends in Cardiac Deaths
Deaths in women with diagnosed
disease
26%
Deaths in women with documented risk
factors
22%
De Novo deaths
52%
Congenital Heart Disease
Congenital Heart Disease
Improved survival with better surgery
Growing population
Good quality of life
Normal fertility
Pregnancy is a challenge for their repaired
CVS
They are not cured!
Estimates of the number of people with congenital heart disease (simple and complex), 2000 and 2010, United Kingdom
Complex congenital heart disease
(Incidence - 1.5/1,000 births)
Simple congenital heart disease
(Incidence - 4.5/1,000 births)
Date of birth
Number of births
in the UK
Number born with
congenital heart disease
First year
survival rate
Survivors at
18 year
12 months survival rate
Survivors at
18 years
1940-1960
16,620,000
24,930
20%
4,986
10%
2,493
1960-1980
17,260,000
25,890
50%
12,945
35%
9,062
11,555 in year 2000
1980-1990
7,550,000
11,325
70%
7,928
50%
5,663
17,218 in year 2010
1940-1960
16,620,000
74,790
90%
67,311
90%
67,311
1960-1980
17,260,000
77,680
90%
69,912
90%
69,912
137,223 in year 2000
1980-1990
7,550,000
33,980
90%
30,582
90%
30,582
167,805 in year 2010
All congenital heart disease
148,778 in the year 2000
185,023 in the year 2010
Congenital Heart Disease
Deaths are decreasing
Unplanned pregnancy
No
pre-pregnancy counselling
Ischaemic Heart Disease
What do we know?
Upward trends in deaths from IHD and
myocardial infarction
Maternal risk factors
Increasing maternal age
Obesity
Diabetes
Pre-existing hypertension
Higher parity
Smoking
Family history
Maternal Age
CEMACH
Percentages of maternities by age
<20
20-24
25-29
30-34
35-39
≥40
19971999
7.66
18.04
30.47
29.46
12.26
2.11
20002002
7.58
18.24
26.98
30.04
14.49
2.67
20032005
7.15
18.87
25.25
29.64
15.87
3.22
Maternal Age
CEMACH
Percentages of maternities by age
<20
20-24
25-29
30-34
35-39
≥40
19971999
7.66
18.04
30.47
29.46
12.26
2.11
20002002
7.58
18.24
26.98
30.04
14.49
2.67
20032005
7.15
18.87
25.25
29.64
15.87
3.22
Maternal Age
CEMACH
Death rates per 100,000 maternities by
age
20032005
Age
<20
20-24
25-29
30-34
35-39
≥40
9.9
9.8
12.4
14.5
19.1
29.4
Maternal Age
CEMACH
Death rates per 100,000 maternities by
age
20032005
Age
<20
20-24
25-29
30-34
35-39
≥40
9.9
9.8
12.4
14.5
19.1
29.4
Maternal Obesity
CEMACH
64% of women who died of cardiac
disease were overweight or obese
31%
had a BMI 25-30
33% had a BMI >30
60%
of these >35
33.3% of these >40
Maternal Obesity
CEMACH
BMI > 25
Direct
Thromboembolism
20(65%)
Pre-eclampsia/Eclampsia
9(50%)
Haemorrhage
7(47%)
AFE
6(43%)
Early Pregnancy
2(33%)
Sepsis
8(73%)
Anaesthetic
2(50%)
Indirect
Total
Cardiac
29(64%)
Other
27(39%)
Psychiatric
6(46%)
Malignancies
3(43%)
119(52%)
Maternal Obesity
CEMACH
BMI > 25
Direct
Thromboembolism
20(65%)
Preeclampsia/Eclampsia
9(50%)
Haemorrhage
7(47%)
AFE
6(43%)
Early Pregnancy
2(33%)
Sepsis
8(73%)
Anaesthetic
2(50%)
Indirect
Total
Cardiac
29(64%)
Other
27(39%)
Psychiatric
6(46%)
Malignancies
3(43%)
119(52%)
Maternal Obesity & Age
Percentage distribution of BMI by age
Health
Survey for England 2003
Percentage in
each age group
16-24
25-34
35-44
18.5 or under
7.4
1.0
1.0
18.6-25
61.2
51.8
43.5
25.1-30
18.3
28.3
33.3
30.1-40
11.1
15.1
18.6
Over 40
2.0
3.0
3.5
BMI
Maternal Obesity & Age
Percentage distribution of BMI by age
Health
Survey for England 2003
Percentage in
each age group
16-24
25-34
35-44
18.5 or under
7.4
1.0
1.0
18.6-25
61.2
51.8
43.5
25.1-30
18.3
28.3
33.3
30.1-40
11.1
15.1
18.6
Over 40
2.0
3.0
3.5
BMI
Cardiac Disease in Pregnancy
Who’s Going to Have a Problem?
Who’s going to have a problem?
Risk stratification
Traditional
assessment for non-cardiac
surgery
Probably not appropriate
Extrapolation from a physiologically
different population
Cardiac Disease in Pregnancy
How do we stratify risk in the
pregnant population?
Who’s going to have a
problem?
Siu et al, Circulation 2001
Prospective study
562 women with 599 pregnancies in
women with heart disease
Pregnancy & neonatal outcomes
Receiving comprehensive prenatal care
Who’s going to have a
problem?
Heart Disease
74% Congenital
22% Acquired
4% Arrhythmic
80 Cardiac Events (13%)
Pulmonary oedema
Arrhythmic
Stroke
Cardiac death (3)
Siu et al
Who’s going to have a
problem?
Siu et al
1.
4 Main predictors of adverse maternal
cardiac event
Prior history of
2.
Heart failure
TIA/Stroke
Arrhythmia
NYHA ≥ Class II or Cyanosis
Who’s going to have a
problem?
3.
Left Heart Obstruction
4.
Mitral valve < 2cm2
Aortic valve <1.5cm2
Gradient of >30mmHg
Reduced LV Function
EF<40%
Siu et al
Who’s going to have a
problem?
Siu et al
No RF, then < 5% risk of CVS event
1 RF, then >20% risk of CVS event
2 RF, then >60% risk of CVS event
Who’s going to have a
problem?
Lupton et al, Curr Opin Obst Gyn, 2002
More geared to congenital lesions
Aimed to stratify risk of mortality
Low
Intermediate
High
Low Risk
Lupton et al
Mortality 0.1-1.0%
Most
repaired lesions
Uncomplicated left-to-right shunts
Regurgitant valve lesions
Intermediate Risk
Lupton et al
Mortality 1-5%
Metal
valves
Single ventricles
Systemic right ventricle
Switch procedure
Unrepaired cyanotic lesions
Stenotic valve lesions
High Risk
Lupton et al
Mortality 5-30%
NYHA
III or IV
Severely impaired LV function
Severe aortic stenosis
Marfan’s Syndrome with aortic valve lesion
or dilated aortic root
Pulmonary hypertension
Mortality
30-50%
Management of Heart Disease in
Pregnancy
Management of Heart Disease in
Pregnancy
Pre-conception
Counselling
Start
essential
early
Discussion
of the effect of pregnancy on
the lesion
Discussion of risks for cardiac events/death
Drug regimen optimisation
CVS optimisation
Management of Heart Disease in
Pregnancy
Antenatally
Multidisciplinary
approach
Obstetrics
Midwifery
Cardiology/cardiothoracics
Anaesthesia
Multidisciplinary planning meetings are
helpful in forming plans for delivery
Management of Heart Disease in
Pregnancy
Antenatally
Regular
review in pregnancy
Including echocardiography
Low threshold for admission
Formal
assessment
Optimisation
Management of Heart Disease in
Pregnancy
Antenatally
Major
CVS changes in first 20 weeks
Cardiac decompensation
Watch for pre-eclampsia
Management of Heart Disease in
Pregnancy
Antenatal deterioration
Mother
or foetus
Optimise mother medically
Consider
Surgical
intervention
Termination
IOL or LSCS
Monitoring
Monitoring
Large CVS changes should be
anticipated perinatally
Degree of monitoring will depend on
nature and severity of the lesion
Monitoring
Continuous ECG
Consider
for all
Continuous SpO2
Consider
for all
Especially useful where shunting or
pulmonary oedema are a possibility
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Monitoring
Arterial line
Any
lesions associated with high risk of
mortality
Severe symptoms/impairment
Pre-eclampsia
High risk of haemorrhage
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Monitoring
Central Line
Useful in
Heart failure
Patients sensitive to hypovolaemia
Vasoactive substances
Drawbacks
What are you monitoring?
Technicality of insertion
Complications
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Monitoring
Trans-oesophageal Echo/Doppler
?
Role
Not well tolerated at LSCS
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Mode of Delivery
Mode of Delivery in Cardiac
Disease
Low risk
Labour
with epidural
High risk
Elective
caesarean
Expert consensus document on management of cardiovascular diseases during pregnancy
European Heart journal (2003) 24, 761-81
Labour
Epidural analgesia for ALL
Including
Low
fixed output states
dose
Except
Therapeutic
anticoagulation
Clopidogrel ± Aspirin
Minimal pushing in 2nd stage!
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
LSCS
GA or Regional?
Either
done carefully is acceptable
Multifactorial
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
LSCS
Influences
Arrhthymias
SVR
Pulmonary hypertension
Anticoagulants/antiplatelets
Need for post-op ITU
Mortality & maternal attitude
Associated airway anomalies
Anaesthetist’s preference
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Peri-partum Problems
Peri-partum Problems
Haemorrhage
Some
lesions tolerate blood loss poorly
Aortic
stenosis
Fontan circulation
risk
due to anticoagulation
risk due to lack of uterotonics
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Peri-partum Problems
Uterotonics
Oxytocin
Tachycardia/hypotension
SVR,
CO
Ischaemic changes
Bolus Vs. infusion
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Peri-partum Problems
Uterotonics
Ergometrine
Hypertension
Pulmonary
vasoconstriction
Pulmonary hypertension
Safe i.m in less severe lesions in the
absence of hypertension
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Peri-partum Problems
Uterotonics
Carboprost
Hypertension
CVS
collapse
Pulmonary oedema
Largely unsuitable in cardiac disease
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Peri-partum Problems
Uterotonics
Misoprostol
Increasingly
used
Not evidence in cardiac disease
Good side effect profile
Uterotonic efficacy
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Peri-partum Problems
Pulmonary Oedema
Cardiac
Obstetric
Iatrogenic
Careful fluid balance in labour or at
LSCS
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Peri-partum Problems
Arrhythmias
Cardiac filling
Cardiac output
Coronary perfusion
Avoid precipitants
Oxytocin
Ephedrine
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Peri-partum Problems
Acute Pulmonary Hypertension
Severe/catastrophic
Even
in mild disease
Pulmonary hypertensive changes may
be accelerated
Adapted from Dob & Yentis, IJOA, 2006: 15(137-144)
Peri-partum Problems
Chest Pain
Aortic dissection
Acute surgical emergency
Bypass has 20% foetal mortality
Coronary ischaemia/myocardial infarction
Atheromatous changes
Coronary artery dissection
Peri-partum Problems
Management of AMI
Occur mostly peri-partum
Coronary dissection > atheroma
Thrombolysis contra-indicated in dissection
Important to exclude PPCM if heart failure present
Rx of choice
Immediate angiography
+/- coronary stenting
Normal coronaries in up to 47%
Beyond 2nd trimester safe for foetus
Thrombolysis is not contra-indicated in pregnancy
Expert consensus document on management of cardiovascular diseases during pregnancy
European Heart journal (2003) 24, 761-81
Peri-partum Problems
Management of AMI
Ongoing management to be directed jointly by cardiology and
obstetrics
Nitrates, aspirin, b-blockers, clopidogrel safe
ACE-I and statins not safe
Mortality
Estimated 37%
But up to 50% if delivery within 2 weeks of AMI
Expert consensus document on management of cardiovascular diseases during pregnancy
European Heart journal (2003) 24, 761-81
Post-Partum
Post-Partum
Fluid balance
Post-partum pre-eclampsia
Good analgesia
Thromboprophylaxis
Close monitoring should continue
How
long?
Summary
Cardiac deaths increasing
Congenital
Ischaemia
Maternal risk factors
Age
Obesity
Summary
What’s important
Close
supervision
High index of suspicion
Especially
More
for ischaemia
attention to risk factors
Summary
Management principles
Understand
the physiology of the lesion
Appropriate monitoring
Cardiovascular stability
Good
epidural analgesia in labour
Careful anaesthesia for LSCS
Awareness
that delivery is not the end of
the problem
Thank you