Nothing Special   »   [go: up one dir, main page]

Hypertensive Diseases in Pregnancy: DR Lucio Pedro DM MD Facog

Download as ppt, pdf, or txt
Download as ppt, pdf, or txt
You are on page 1of 32

HYPERTENSIVE DISEASES

IN PREGNANCY
DR LUCIO PEDRO DM
MD FACOG

1
OUTLINE
• Classification
• Definition
• Pathophysiology
• Symptoms
• Prevention
• Risk Factors
• Management
• Risk of expectant management vs early delivery
• Complications
2
CLASSIFICATION
• Preeclampsia
– Without Severe features
– With Severe features
• Chronic Hypertension
• Chronic Hypertension with superimposed
preeclampsia
• Gestational Hypertension
• Eclampsia
3
DEFINITION
• Preeclampsia without severe features
– SBP >= 140 but <160 OR DBP >= 90 but < 110
on 2 occasions at least 4 hours apart after 20
weeks of gestation in a woman with previously
normal BP
– AND Proteinuria
• >= 300mg/24 hrs urine collection
• Protein/creatinine ratio >= 0.3
• Dipstick >= 1+

4
DEFINITION
• Preeclampsia with Severe Features (Any of
these findings)
– SBP>= 160 OR DBP>= 110 at least 4 hours apart (and
proteinuria)
– Thrombocytopenia (<100,000/mL)
– Impaired Liver Function (Twice Normal Transaminases)
– Severe persistent RUQ or Epigastric pain
– Progressive renal insufficiency (creatinine >1.1 mg/dl or
doubling serum creatinine concentration)
– Pulmonary edema
– New-onset cerebral or visual disturbances 5
DEFINITION
• Gestational Hypertension
– Same as PEC but without proteinuria or systemic
findings

6
DEFINITION
• Chronic Hypertension
– HTN that predates 20 weeks gestation

• Superimposed Preeclampsia
– Is CHTN in association with preeclampsia
• Without severe features
• With severe features

7
DEFINITION
• Eclampsia
– Is defined as the presence of new-onset Grand mal
seizures in a woman with preeclampsia

8
PATHOPHYSIOLOGY
• PEC is a multisystem disease that affects all
organ systems
• The placenta is evident as the root cause of
preeclampsia which is mainly due to poor
placentation
– Reduced trophoblast invasion results in fail
vascular remodelling of maternal spiral arteries

9
SYMPTOMS
• Preeclampsia
– Swelling of the face or hands
– Headache that will not go away
– Seeing spots or changes in eyesight
– Pain in upper right quadrant or stomach
– Nausea or vomiting (in second half of pregnancy)
– Sudden weight gain
– Difficulty breathing

10
PREVENTION
• Aspirin low dose (60-80mg) have been shown
to slightly reduce preeclampsia and adverse
perinatal outcomes.
• Calcium may be useful to reduce the severity
of preeclampsia in populations with low
calcium intake.

11
RISK FACTORS
• Primiparity
• Previous Preeclamptic pregnancy
• Chronic hypertension or chronic renal disease or both
• Multifetal pregnancy
• In vitro fertilization
• Family history of preeclampsia
• Type 1/2 DM
• Obesity
• System lupus erythematosus
• Advanced maternal age (older than 40 yrs)
12
MANAGEMENT
• GHTN / PEC without Severe Features
– Serial assessment of maternal symptoms
– Fetal movement & kick counts (Daily by mother)
– Serial BP (Twice Weekly)
– Assessment of Hb, Platelets, liver enzymes, and
Serum creatinine (Weekly)
– Assessment of Proteinuria once weekly
– Physician preference  however NO
antihypertensive maybe required
13
MANAGEMENT
• GHTN / PEC without Severe Features
– Ultrasonography to assess fetal growth (q 3 weeks) and
AFI (weekly)
– NST weekly for GHTN and twice weekly for PEC
without severe features
– BPP if NST is nonreactive
– If evidence of fetal growth restriction – assessment with
umbilical artery Doppler is recommended
– Expectant management with maternal and fetal
monitoring is suggested up to 37 0/7 weeks of gestation
and NOT beyond
14
MANAGEMENT
• PEC with Severe Features
– Inpatient Care
– Daily NST, Twice weekly AFI, USG q 2wks
– Delivery is suggested at 34 0/7 weeks
– Administration of corticosteriods for lung
maturity if GA <34 weeks
– Antihypertensive therapy is recommended
– Delivery decision should not be based on amount
of proteinuria or change in the amount of
proteinuria
15
MANAGEMENT
• PEC with Severe Features
– Pre viable pregnancy  delivery after maternal stabilization is
recommended
– It is suggested that corticosteriods be administered and delivery
deferred for 48hrs if maternal and fetal conditions remain stable with
a viable fetus at 33 6/7 wks or less and any of the following
• PPROM
• Labour
• Low platelet (<100,000)
• Persistently abnormal transaminases (>= twice normal)
• IUGR (<5%tile)
• Oligohydramnios (AFI<5)
• Reversed end-diastolic flow on umbilical doppler studies
• New-onset renal dysfunction or increasing renal dysfunction
• HELLP syndrome
16
MANAGEMENT
• PEC with Severe Features
– Recommended that corticosteriods be given if the fetus is
at 33 6/7 wks or less, but that delivery not be delayed
after initial maternal stabilization regardless of GA for
women complicated with any of the following
• Uncontrolled severe hypertension
• Eclampsia
• Pulmonary edema
• Abruptio placentae
• DIC
• NRFHRT

17
MANAGEMENT
• PEC with Severe Features
– MgSO4 administration – up to 24 hrs postpartum
– BP monitoring is suggested in hospital for at least
72 hrs postpartum and again at 7-10 days after
delivery or earlier in women with symptoms
– Fluid therapy
• Fluid restrict: rate of 60 to max 125 ml per hour or
1ml/kg/hour

18
MANAGEMENT
• Chronic HTN
– Antihypertensive therapy is recommended for women
with persistent chronic HTN with SBP >= 160 or
DBP>= 105
– Patients on Antihypertensive, it is suggested that BP
levels be maintained between 120/80 and 160/105
– Delivery is recommended >= 38 wks if No additional
maternal or fetal complications
– Labetalol, Nifedipine, or Methyldopa are the
recommended antihypertensive

19
MANAGEMENT
• Chronic HTN
– For women who are at a great increased risk of
adverse pregnancy outcomes (Hx of early-onset
preeclampsia and preterm delivery at > 34 0/7
wks of gestation or preeclampsia in > one prior
pregnancy), initiating the administration of daily
low-dose aspirin (60-80mg) beginning in the late
first trimester is suggested to reduce the
incidence and morbidity of preeclampsia.

20
MANAGEMENT
• Chronic HTN and Superimposed
Preeclampsia
– Antenatal surveillance and management as
preeclampsia
– For women with superimposed preeclampsia with
severe features, administration of intrapartum-
postpartum parenteral MgSO4 to prevent
eclampsia is recommended

21
MANAGEMENT
• Chronic HTN and Superimposed
Preeclampsia
– For women with superimposed preeclampsia
without severe features and stable maternal and
fetal conditions, expectant management until 37
wks is suggested
– Superimposed preeclampsia with severe features,
delivery at 34 wks is recommended

22
MANAGEMENT
• Chronic HTN and Superimposed
Preeclampsia
– Delivery soon after maternal stabilization is
recommended irrespective of GA or full
corticosteriod benefit with any of the following
complications;
• Uncontrolled severe hypertension
• Eclampsia
• Abruptio placentae
• DIC
• NRFHRT 23
MANAGEMENT
• For women with preeclampsia in prior
pregnancy, preconception counselling and
assessment is suggested

24
MANAGEMENT
• Eclampsia
– Call for help
– Airway and Breathing – LLL, O2,
– Circulation – IV lines; labs; RBS
– MgSO4 – 4-6 g loading dose IV or IM
– Maintenance dose @ 1-2g/hr
– Foley catheter
– Multidisciplinary approach

25
MANAGEMENT
• Eclampsia
– If 2nd seizure
• Reload MgSO4 2g stat and increase maintenance dose
to 1.5 to 2g/hr
– If 3rd seizure despite 2 sets of MgSO4
• Give 10mg Diazepam IV slowly
– If continues to seize
• Call anesthesia; thiopentone infusion; intubate!

26
MANAGEMENT
• Eclampsia
– Control BP
• labetolol/nifedipine/methyldopa/hydralazine
– Assess Fetal wellbeing
– Give Corticosteriods if < 34 weeks GA
– DELIVER!
– Maintain MgSO4 for 24 hrs postpartum or last
seizure, whichever occurs last.
– Keep in hospital at least 4 days
– Monitor BP until 6 weeks postpartum 27
RISK
• Risk associated with Expectant management
include
– The development of severe hypertension (10-15%)
– Eclampsia (0.2-0.5%)
– HELLP syndrome (1-2%)
– Abruptio Placentae (0.5-2%)
– Fetal growth restriction (10-12%)
– Fetal Death (0.2-0.5%)

28
RISK
• Risk associated with immediate delivery
– Increased rates of admission to the neonatal ICU
– Neonatal respiratory complications
– Slight increase in neonatal death

29
COMPLICATIONS
• Placenta Abruption
• IUGR
• Oligohydramnios
• HELLP syndrome
• Intracranial bleeding and permanent neurologic damage
• Acute renal failure
• Hepatic damage, subcapsular hematoma, and rarely hepatic
rupture
• DIC
• Increased risk of recurrent preeclampsia/eclampsia with
subsequent pregnancy
• Maternal or fetal death 30
REFERENCE
• ACOG, Hypertension in Prenancy; Task
force, 2013
• Cunningham et.al, Williams Obstetrics 23rd
ed; Pregnancy Hypertension; 2010, pg 706-79

31
Thank You

Questions?

EMERGENCY NUMBER
647-6403
32

You might also like