1. Anaesthesia for Pregnant patient
with Mitral Stenosis
Speaker : Dr.Sushma,
Dr. Shiva krishna,
Moderator : Dr. Ananya
Dr.Gopinath
ESIC HOSPITAL ,SANATHNAGAR 1
2. TOPICS
ā¢ Mitral valve anatomy
ā¢ Mitral stenosis pathophysiology
ā¢ Physiological changes of pregnancy
ā¢ Pregnancy with MS
ļ¼Medical management
ļ¼Surgical management
ļ§ Management of PBMV
ļ§ Management of Cardiac surgery on CPB
ļ¼Case scenarios
4. Mitral stenosis
ā¢ Incidence : 25% of all rheumatic valvular lesions.
ā¢ Approximately 25% of women with mitral stenosis first experience symptoms
during pregnancy.
Etiology :
ā¢ Rheumatic fever
ā¢ congenital defects
ā¢ Atherosclerosis
ā¢ Lutembacher's syndrome
4
5. Mitral stenosisāPathology
Thickening and commissural fusion of the mitral valve leaflets.
Increased rigidity of the valve leaflets
Thickening, fusion and contracture of the chordae and papillary heads
Calcification of the valve apparatus
Obstruction at the level of the mitral valve
5
6. Mitral stenosis- pathophysiology
Obstruction at the level of the mitral valve
raised left atrial pressure enlargement of left atrium
pulmonary hypertension Atrial fibrilaltion
right heart failure
6
7.
8. Tricuspid Regurgitation
RA Enlargement
Hepatic Congestion
JVD
LA Enlargement, āLA
Pressure
LA Thrombi
Atrial Fib
,Ortners-RLN ,Lt bronchus
,Oesophagus
āPulmonary HTN
Pulmonary Congestion
RV Pressure Overload
RVH
RV Failure LV Filling
Fixed CO
9. Clinical features
Symptoms
ā¢ Dyspnea
ā¢ Paroxysmal nocturnal
dyspnea
ā¢ Orthopnea
ā¢ Palpitations
ā¢ Hemoptysis
ā¢ Chest pain
Signs
ā¢ Mitral facies
ā¢ Raised JVP
ā¢ Parasternal heave
ā¢ Tenderness right hypochondrium
ā¢ Ascites
ā¢ Diastolic murmur
ā¢ Accentuated 1st heart sound
(wide, loud, split first heart
sound, an S3 sound, and a soft
systolic ejection murmur in
pregnants)
ā¢ Opening snap
9
14. Prediction Of Mortality & Morbidity
ā¢ Correlate well with the NYHA functional classification.
ā¢ Cardiac complications occurs in 35% of the pregnancies.
ā¢ Maternal cardiac complications ā severity of the mitral
stenosis
ļ¶ As Pregnacy aggravates Mitral stenosis
o Mild MS in Non pregnant patient will become Moderate MS in
Pregnancy
o Moderate ļ Severe
o Severe ļ critical
18. Abnormal clinical findings in normal
pregnancy
ā¢ Palpitations (ā blood volume, displacement of heart)
ā¢ Loud S1 with exaggerated splitting of mitral & tricuspid components
ā¢ Systolic murmur in apex & pulmonary area
ā¢ Murmur in left 3rd & 4th ICS
ā¢ S3 ā rapid diastolic filling of left ventricle, S4
ECHO:
ā¢ LVH by 12 weeks gestation, with a 50% ā in mass at term.
ā¢ ā LV end diastolic diameters
ā¢ ā left and right atrial dimensions
18
19. Stroke volume & heart rate
Heart rate:
ļ¼ 1st trimester ļ ā15%
ļ¼ 2nd trimester ļ ā 25%
ļ¼ 3rd trimester ļ remains same as 2nd trimester
Stroke volume:
ļ¼ 5th to 8th week of gestationļ ā 20%
ļ¼ 2nd trimesterļ ā25% to 30%
ļ¼ until term ļ remains at that level
19
Clinical implication:-
āHR will ā diastolic
filling time will further
ā EDV
Implication :-āMS is fixed Cardiac outputācondition
20. Cardiac output
ā¢ 5 weeks ļ begins to increase
ā¢ 1st trimester of pregnancy ļ 35% to 40%
ā¢ 2nd trimester ļ ā50%
20
21. Blood pressure
ā¢ Systolic BP: not much effected
ā¢ Diastolic BP: early- to mid-gestational ā20%.
Causes for ā DBP:
ļ¼ Low resistance intervillous space
ļ¼ Vasodilating effects of progesterone, estrogen &
prostacyclin
ā¢ MAP: not much effected
21
28. Incidence & Mortality
ā¢ Cardiac disease in pregnancy: 0.1-4%
ā¢ Rheumatic mitral stenosis forms 88% of the heart
diseases complicating pregnancy.
ā¢ The maternal mortality for parturients with MS
with NYHA class III & IV is 6.8% as compared to
0.4% for those in the NYHA class I and II
28
29. Why pregnancy aggravate the
symptoms of mitral stenosis?
ā¢ Pregnancy with severe MS do not tolerate the cardiovascular demands
ā¢ All the physiological changes of pregnancy are against the haemodynamic goals of
MS
ā¢ Heart rate ā 20-30 % ļ ā diastolic filling time of LV.
ā¢ ā SVR ļ peripheral pooling
ā¢ Caval compression āāvenous return (preload)
ā¢ ā Blood volume,autotransfusion ļ ā pulmonary capillary hydrostatic pressureļ
pulmonary edema
ā¢ ā O2 requirement
ā¢ Pregnancy+ MS+ AF ļ āAtrial thrombus
ļ¶ Convert the compensatory ļ decompensatory stage. 29
30. Labor & postpartum period
Labor:
ļ¼Pain ļ Sympathetic stimulation ļ tachycardia
ļ¼Uterine contractions ļ autotransfusion ļ ā
blood return to LA ļ pulmonary edema
Immediate post partum
ļ¼Autotransfusion & IVC de-compression ļ
sudden ā in the preloadļ flooding the central
circulationļ severe pulmonary oedema.
30
31. Autotransfusion:
ļ¼ Uterine involution ļ release of IVC compression
ļ¼ ā intervillous space ļ ā venous capacitance
ā¢ There continues to be autotransfusion of blood for 24ā72 hr after
deliveryļ The risk of pulmonary oedema extends for several days
after delivery.
ā¢ Risk of maternal death ļ greatest during labour & the immediate
post-partum period.
32. What are the risks to fetus ?
ā¢ Growth retardation
ā¢ Preterm delivery
ā¢ Low birth weight
ā¢ Respiratory distress
ā¢ fetal / neonatal death
32
33. Pre op optimization
ā¢ Bed rest in left lateral position
ā¢ Decrease pulmonary congestion: diuretics (Use of diuretics may be
reasonable for pregnant patients with MS and HF symptoms- AHA
2014)
ā¢ O2 therapy if patient had CHF- during decongestion therapy for
supportive care.
ā¢ Ī²-adrenergic receptor blockade is useful to prevent tachycardia during
pregnancy.
ā¢ Metoprolol has a lower incidence of fetal growth retardation than
atenolol and is the preferred beta blocker for use in pregnancy. (AHA
2014)
33
34. ā¢ Use of Ī² blockers as required for rate control is reasonable
for pregnant patients with MS in the absence of
contraindication .
ā¢ The use of Ī²- blockers with Ī²-1 selectivity is preferred
because the Ī²-2 effects on uterine relaxation are avoided.
(AHA 2014)
ā¢ Antibiotic prophylaxis for endocarditis is reserved only for
patients with a previous history of endocarditis / presence
of established infection.
35. Management of Acute AF (<48 hrs)
ā¢ Anticoagulation should be given to all pregnant patients with MS &
AF. (AHA 2014)
ā¢ Rx atrial fibrillation:
ā Digoxin,Ī² blockers,cardioversion
ā¢ Haemodynamically unstable (Decompensated HF ):
hypotension/heart failure/chest pain/syncope
- DC Cardioversion ( with FHR monitoring), Digoxin
ā¢ Haemodynamically (compensated HF) stable :
ļ¼ Rate control - Ī² blockers
ļ¼ Anticoagulant
36. Standard anticoagulation therapy
during pregnancy
ļ¶SC/IV heparin/LMWH for up to 12 weeks antepartum (aPTT 1.5ā
2.5-times of normal)
ļ¶ Warfarin from 12 to 36 weeks (maintain INR 2.5ā3.0) ,
ļ¶SC/IV heparin,LMWH after 36 weeks
37. Pregnant patient with MS
Obstetric procedures Non Obstetric procedures
1.Termination of pregnancy
2.Labour & NVD
3.Caeserean section
Cardiac Non cardiac
1.BMV
2.CMC
3.OMC
4.MVR Emergency Non emergency
( appendicitis) (brain tumors)
37
41. Labor analgesia -1st Stage
ļ¼ Epidural analgesia with 0.125% bupivacaine + fentanyl 2mics/ml during
active labor & immediate postpartum period (to prevent tachycardia,
pulmonary edema)
or
ļ¼ Intrathecal opioid followed by epidural local anesthetic infusion
ā Avoid test dose
ā Avoid preloading
ā Phenylephrine for hypotension(1-2 mcg/kg)
ā Esmolol for rate control - 500 mcg/kg IV as a bolus dose over 1 min f/b maintenance
infusion of 50 mcg/kg/min IV for 4 minutes
41
42. 2nd stage of labour
ā¢ Assisted Vaginal Delivery
ā¢ only the uterine contractile force should be allowed rather
than the maternal expulsive effort that is always associated
with the valsalva maneuver
ā¢ Continue epidural infusion with S2- S4 as the desired level
ā¢ Pudendal nerve block.
ā¢ Avoid trendelenberg
42
43. ā¢ After delivery of the foetusļ slow infusion of oxytocin.
ā¢ Rapid infusion of oxytocin can ā SVR as well as ā PVR,
resulting in a drop in cardiac output.
ā¢ Methylergometrine / Carboprost , produces severe
hypertension, tachycardia and ā PVR
ā¢ Hemodynamic compromise & pulmonary edema during
the postpartum period mandates the need for intensive
care monitoring in the post partum period
43
44. Cesarean section
Advantages:
ā¢ Avoids hemodynamic consequences of labour.
ļ¶ Choice of anesthesia for CS depends on:
ļ± No controlled studies examining the best type of anaesthetic technique in these
patients and guidelines and standards are lacking.
ļ¼ Severity of MS
ļ¼ Emergency/Elective
ļ¼ Hospital facilities-Invasive monitors,Ventilator,ICU,cardiac facilities,Surgeons.
44
45. Neuraxial block
ā¢ A single-shot spinal anesthesia is contraindicated in severe stenosis
because of uncontrolled hypotension.
ā ā SVR
ā ā cardiac preload
ā reflex tachycardia
ā¢ In mild āmoderate cases spinal anesthesia with 1ml 0.5% bupivacaine
and 10-20mcg fentanyl along with epidural block or use of spinal
catheter .
ā¢ Small boluses of phenylephrine (25-50mcg) are effective in avoiding
precipitous hypotension.
45
46. Epidural block
ā¢ Epidural alone can be used in mild to moderate MS .
ā¢ A well-controlled, individualized epidural neuraxial block using
incremental graded dosing of local anesthetic in the hands of
experienced anesthesiologists with invasive monitoring of arterial
& CVP may be beneficial even for the most severe cardiac disease.
ā¢ Sensory level to be achieved with titrated doses of LA .
ā¢ Optimize fluid status
ā¢ Avoid adrenaline in the epidural test dose
46
47. Advantages of graded epidural
analgesia
ā¢ Administered in incremental doses & total dose can be
titrated to the desired sensory level.
ā¢ Slower onset - allows the maternal CVS to compensate for
the occurrence of sympathetic blockade ļ Low risk of
hypotension & Low risk ofā uteroplacental perfusion .
ā¢ Segmental blockade spares the lower extremity āmuscle
pump,ā aiding in venous return.
ā¢ ā incidence of thrombo-embolic events.
47
48. General anaesthesia
ā¢ Modified rapid sequence induction using Etomidate, Remifentanyl & Sch is an
ideal choice in tight stenosis with pulmonary hypertension.
ā¢ Inhalational agents may be added to prevent awareness.
ā¢ A Ī²-blocker & opioids should be administered before / during the induction
of GA.
ā¢ Maintenance of anaesthesia with O2 & Air 50:50, sevoflurane, opioids &
vecuronium.
ā¢ Phenylephrine (0.5 -1 mcg/kg) boluses with restricted fluid therapy may be
used for management of hemodynamic instability.
ā¢ Invasive haemodynamic monitoring, FHR monitor
48
49. Avoid drugs that cause tachycardia
ļ¼ Atropine
ļ¼ Ketamine
ļ¼ Pancuronium
Treatment
ā¢ Esmolol has a rapid onset and short duration of action, it is
a better choice in controlling tachycardia.
ā¢ Fetal bradycardia has been reported after esmolol, foetal
heart rate should be monitored.
50. General anaesthesia- disadvantages
ā¢ Raises pulmonary arterial pressure
ā¢ Tachycardia during laryngoscopy and tracheal
intubation,extubation.
ā¢ Adverse effects of positive-pressure ventilation
on the venous return may ultimately lead to
cardiac failure.
ā¢ Risk of aspiration.
50
51. Surgical management
Non obstetric Options:
ļ¼ Percutaneous balloon mitral valvotomy (PBMV)
ļ¼ Closed mitral commissurotomy (CMV)
ļ¼ Open mitral commissurotomy (OMV)
ļ¼ Mitral valve replacement (MVR)
ā¢ PBMV is preferred over CMC / open procedure with CPB.
ā¢ PBMV is better than CMC in terms of valve area & long term
durability .
51
52.
53. PBMV
ā¢ Percutaneous mitral balloon commissurotomy is reasonable for
pregnant patients with severe MS (mitral valve area <1.5 cm2) with
valve morphology favorable for PBMV who remain symptomatic with
NYHA class III to IV HF symptoms despite medical therapy. (AHA 2014)
ā¢ Best performed after 20th week of gestation.
ā¢ Procedural time should be shortest possible .
ā¢ Abdominal shield to reduce radiation risk.
ā¢ Patient should be explained about the radiation risk to fetus.
ā¢ TEE guidance aids to reduce radiation
53
54. ā¢ Percutaneous mitral commisurotomy has edge over medical
management in patients with MVA < 1.0cm2
Decision to perform PBMV depends on (Wilkins score <8)
1. Valve area
2. Symptoms
3. Exercise tolerance
4. Adequate leaflet mobility with little calcification.
54
55. PBMV not preferred :
ļ¼ presence of clot in LA
ļ¼ severe leaflet calcification
ļ¼ leaflet thickening,
ļ¼ Immobility
ļ¼ subvalvular fusion
ļ¼ Commissural calcification
ā¢ Complication:
Mitral regurgitation represents the most common complication associated with
commissurotomy.
55
56. Anesthetic management of Balloon
valvuloplasty
ā¢ Best obtained in an awake state with minimal dose of opioids to
avoid fetal bradycardia & apnea in the pregnant patient.
ā¢ Intravenous sedation/ regional anesthesia is preferred over GA for
non-obstetrical procedures in pregnant patients because:
ļ¼ aspiration risk with GA
ļ¼ difficult airway management with difficult endotracheal intubation
can be avoided.
ļ¼ minimizes fetal exposure to the potent anesthetic agents.
56
57. Closed mitral commisurotomy
ā¢ Practiced mostly in developing countries
Disadvantages include :
ļUncontrolled procedure ( may cause MR)
ļSubvalvular deformity cannot be corrected
ļRisk of general anesthesia
57
58. Open commisurotomy
Advantages over MVR include :-
ā¢ Avoids risk of prosthetic valve
ā¢ Avoids need for anticoaguation
ā¢ Valve can be conserved
58
59. Mitral valve replacement
ā¢ Valve intervention is reasonable for pregnant patients with
severe MS (mitral valve area <1.5 cm2)
ā¢ valve morphology not favorable for PBMC ļ only if there
are refractory NYHA class IV HF symptoms. (AHA 2014)
ā¢ Valve operation should not be performed in pregnant
patients with valve stenosis in the absence of severe HF
symptoms. (AHA 2014)
59
60. APPENDICECTOMY
ā¢ Common in 2nd and 3rd trimester
ā¢ In pregnancy appendix lies above the iliac crest.
Concerns:
ļ¼ CO2 insufflation- hypercarbiaļ risk of pulmonary
hypertension
ļ¼ Elevated intraabdominal pressureļ lowers venous return
& uteroplacental blood flow
60
61. Laparoscopic surgery
Advantages
ā¢ Less post op pain
ā¢ Early mobilizationļ lesser
thromboembolic events.
ā¢ Lesser incidence of infection
ā¢ Decreased rate of fetal
depresion due to less
narcotic use
Disadvantages
ā¢ Technically difficult after 26
wks
ā¢ Trochar insertion
difficulty/Trauma
ā¢ āintra abdominal pressure ļ
utero placental blood flowā,
Fetal hypotension,
ā¢ Risk of uterine
irritationļ uterine
manipulation,cautery
ā¢ Fetal acidosis due to CO2
narcosis.
63. Cardiac surgery in Pregnancy
ā¢ Mortality in pregnant with MS is ā when compared
to non-pregnant patients with MS .
ā¢ Fetal mortality is 20-30%
ā¢ The period between the 20th and 28th weeks of
pregnancy appears to be safest for the fetus .(AHA
2014)
ā¢ CS should precede valvular surgery if fetus is viable.
63
64. Fetal risk in CPB is High because of ?
ā¢ Hypothermia ļ uterine contraction ā
ā¢ Hypothermia should be avoided
ā¢ Placental hypoperfusion ļ bradycardic response
in fetus
ā¢ CPB is avoided in 1st trimester due to high risk of
teratogenecity.
64
67. Uterine & Fetal Monitoring During CPB
Cardiotocography-Monitoring uterine activity & fetal heart
rate ļ information regarding placental blood flow &
perfusion.
ā¢Monitor fetal heart beats from the surface of maternal
abdominal wall.
Disadvantage :-Difficult to maintain in place during the
procedure.
ā¢Transvaginal probe to monitor fetal heart beats & umbilical
cord flow.
68. Pregnant with prosthetic valve
ā¢ TTE should be performed in all pregnant patients with a prosthetic valve if not
done before pregnancy.
ā¢ Also in ,patients who develop symptoms (prosthetic valve obstruction /
embolic event)
ā¢ Prosthetic valve thrombosis accounts for mortality of 1- 4 % in pregnants.
Anticoagulation:
ā¢ Therapeutic anticoagulation with frequent monitoring is recommended for all
pregnant patients with a mechanical prosthesis
ā¢ Asprin 75-100 mg reasonable in patients with bioprosthetic mitral valve
Matiasz R, Rigolin VH. 2017 Focused Update for Management of Patients With Valvular Heart Disease:
Summary of New Recommendations. J Am Heart Assoc
68
69.
70. Bhagra CJ, et al. Heart 2017;103:244ā252. doi:10.1136/heartjnl-2015-308199
71. ā¢ LMWH :
ļ¼Increased risk of valve thrombosis & embolic
events
ļ¼Require monitoring of anti-Xa levels
ā¢ Disadvantages of intravenous UFH
ļ¼Increased risk of serious infection due to IV
cannulation
ļ¼Osteoporosis .
72. Labor analgesia for pregnants on
anticoagulation
ļ¼Epidural, blocks ļ ā INR ļ Contraindicated
ļ¼Entonoxļ pulmonary pressures ā
ļ¼IV opioids ( remifentanyl) are the choice
73. Conclusion
Better understanding of the physiology of
pregnancy & its effect on mitral stenosis as a
whole is a prerequisite to achieve better
results.
76. Mild MS in labor
Plan of anaesthesia
ā¢ Epidural : 0.125% bupivacaine + fentanyl 25 mics (avoid adrenaline in test dose)
Level of Epidural placement ?
ā¢ L2-L3/L3-L4
Dermatomal level to be blocked by Epidural?
ļ¼ Stage1 : T10 to L1
ļ¼ Stage 2: S2 to S4
Precaution for 2nd stage of labour?
ā¢ Cut short stage 2 with forceps/ ventouse
76
77. Moderate MS for elective caesarean
section
ā¢ Graded epidural
ā¢ Epidural+GA
ā¢ CSE in experienced hands(mini spinal )
77
78. ā¢ 25 yrs female with 36 weeks of gestation with
Moderate MS with no signs of Heart Failure
for emergency caesarean section (fetal
distress) in tertiary care hospital .
ā¢ Plan of Anaesthesia?
ā¢ General anesthesia (no time for graded
epidural)
ā¢ Rapid sequence intubation
ā¢ TAP block/local infiltration
78
79. Cont..
ā¢ Sudden increase in airway pressure intraoperatively &
associated hypotension & tachycardia ?
ā¢ Pulmonary edema-pain,autotransfusion
ā¢ Rx :
ļ¼ Correct tachycardia to improve LV filling :
ļ§ Increase depth off anesthesia
ļ§ Iv esmolol
ļ§ Iv phenylephrine
ļ¼ PEEP
ļ¼ Loop diuretics
ļ¼ Head end elevation
80. Cont..
ā¢ Patient after successful LSCS under GA with TAP block ,
2hrs after extubation complaining of SOB Grade-IV with NO
pain .
ā¢ Vitals -BP-100/60mm Hg,
Hr-100/min.
Spo2-98% on Face mask,
RR-29/min.
ABG-pH-7.28,pCo2-50mmHg,pO2-58mm Hg?
Post delivery pulmonary edema
ā¢ Positive pressure ventilation-NIV
ā¢ Balloon mitral valvotomy/MVR
80
81. ā¢ 27yr female with 34 weeks of gestation S/P Mitral valvular
replacement (āmechanicalā)on vitamin K antagonist
,presented with decreased fetal movements (fetal distress)
in early stage of labour.On examination.....
ā¢ Hemodynamics-stable
ā¢ ECHO ānormal findings
ā¢ Plan of anaesthesia for Labour,LSCS?
81
82. ā¢ 20yr female patient with 20 weeks of gestaion with
moderate MS diagnosed to have acute cholilithiasis
,planned for laparoscopic cholicystectomy under GA
ā¢ Immediately after starting surgery patient developed
hypotension ,bradycardia ,airway pressures increased.
ā¢ Immediate Plan of management ?
83. ā¢ 24 yrs female with 20 weeks of gestation with
abdominal pain diagnosed to have acute
appendicitis.
ā¢ Hemodynamics-Stable
ā¢ Plan of anaesthesia?
Editor's Notes
The normal function of the mitral valve depends on its 6 components, which are (1) the left atrial wall, (2) the annulus, (3) the leaflets, (4) the chordae tendineae, (5) the papillary muscles, and (6) the left ventricular wall.
Patients with MS and chronic AF are at increased risk for embolic stroke, at a rate of 7% to 15%
per year.Treatment may include anticoagulation with intravenous heparin or oral warfarin,
pharmacologic rate control, and pharmacologic or electrical cardioversion for hemodynamically
significant or acute-onset AF. In patients scheduled for cardioversion, TEE may need to be
performed first to rule out the presence of a left atrial thrombus.
[
Mitral stenosis prevents emptying of the left atrium and subsequent filling of the left ventricle - decreased stroke volume and decreased cardiac output - fixed cardiac output state - cannot cope up with situations warranting increased metabolic demand or increased blood volume -left atrium dilates and the left atrial pressure increases - back pressure leads to pulmonary congestion and, in severe cases, pulmonary oedema ā chronic cases pul HTN
The normal mitral valve orifice area is approximately 4 to 5 cm .Symptoms can occur with a valve area of less than 2.5 cm and can be precipitated by clinical events associated with increased cardiac output and consequent increased flow across the valve. Symptoms do not usually occur at rest unless the mitral valve area (MVA) has become less than 1.5 cm .Obstructed flow across the mitral valve is associated with a pressure differential or āgradientā
across the valve. The more severe the MS, the greater the gradient, as long as flow across the valve is held constant.
LV function or contractility is
assumed to be normal in most patients with MS. However, in a review of the literature, Klein
and Carroll
[335]
showed that the assumption of preserved LV contractility in patients with MS
is debatable. Instead, LV dysfunction may occur in as many as 30% of patients with MS.
Proposed mechanisms include reduced filling of the left ventricle, muscle atrophy,
inflammatory myocardial fibrosis leading to wall motion abnormalities, scarring of the
subvalvular apparatus, abnormal patterns of LV contraction, reduced LV compliance with
diastolic dysfunction, increased LV afterload leading to ventricular remodeling, right-to-left
septal shift secondary to the effect of pulmonary hypertension on the right ventricle, and
coexistent diseases such as systemic hypertension and coronary artery disease.
( The earliest change in cardiac output is attributed to an increase in heart rate, which occurs by the fourth to fifth week of pregnancy.)
Sbp : depends on stroke vol and aortic compliance..sv increases but aortic compliance increases so sbp decreases to some xtent in 8th wk...retrns to normal in term
Dbp : returns to normal at term due to aortic compression by the gravid uterus
The decreased systemic vascular resistance results from the development of a low resistance vascular bed (i.e., the intervillous space) as well as vasodilation caused by prostacyclin, estrogens, and progesterone
Reasons:
Increased sympathetic activity
Autotransfusion: 300- 500 ml
aortic compression due to uterine contractionsļ decreased uterine blood flow
Emptying of intervillous blood during uterine contractions into ovarian veins( unobstructed)
Hypercoagulable state: risk of thrombus if AF develops
Cardiac decompensation and pulmonary oedema may occur in pregnant women with overt or silent mitral valve stenosis during the second or third trimester.
Diuretics should be used with caution due to the
potential for reducing placental perfusion.
Stage 1: adequate analgesia (to avoid tachycardia)
Stage 2: cut short with forceps or vacuum (During the second stage of labour, only the uterine contractile force should be allowed rather than the maternal expulsive effort that is always associated with the valsalva maneuver.)
Oxytocin ā 1-2 units bolus f/b 5u infusion
Adr : reduces uterine bld flow
Unfortunately in deveoping countries ms is dx durig pregnancy
It is based on the surface detection of electrical activity, much like the conventional electrocardiography.
An abdominal belt contains two sets of electrodes, one to monitor the uterine activity and the other to monitor the fetal heart beats.
1st trimester:( fetal organogenesis)
Warfarin at term :(risk of fetal hemorrhage during delivery)
Dose-adjusted LMWH at least 2 times per day (with a target
anti-Xa level of 0.8 U/mL to 1.2 U/mL, 4 to 6 hours postdose)
during the first trimester is reasonable for pregnant
patients with a mechanical prosthesis