Case 5

Dr Barik
A 35-year-old woman elder primi and has a 5-year history of
hypertension wants to become pregnant. She has stopped using
contraception. Her only medication is lisinopril at a dose of 10 mg
per day. Her blood pressure is 124/68 mm Hg,and her body-mass
index (the weight in kilograms divided by the square of the height
in meters) is 27.




        Pregnancy-related deaths(3201 in US,
        1991-1997-16%
Classification of Hypertension in Pregnancy
 From Gifford RW, August PA, Cunningham G, et al: Report of the National High Blood Pressure
 Education Program Working Group on High Blood Pressure in Pregnancy.
 Am J Obstet Gynecol 183:S1, 2000


                                                    Hypertension (blood pressure ≥140 mm Hg systolic or ≥90 mm
Chronic hypertension                                Hg diastolic) present before pregnancy or that is diagnosed
                                                    before the 20th week of gestation


                                                    New hypertension with a blood pressure of 140/90 mm Hg on
                                                    two separate occasions, without proteinuria, arising de novo
Gestational hypertension
                                                    after the 20th week of pregnancy. Blood pressure normalizes
                                                    by 12 weeks post partum.


                                                    Increased blood pressure above the patient's baseline, a
Preeclampsia superimposed on chronic hypertension
                                                    change in proteinuria, or evidence of end-organ dysfunction



                                                    Proteinuria (>0.3 g during 24 hours or ++ in two urine
                                                    samples) in addition to new hypertension. Edema is no longer
                                                    included in the diagnosis because of poor specificity. When
Preeclampsia-eclampsia
                                                    proteinuria is absent, suspect the disease when increased
                                                    blood pressure is associated with headache, blurred vision,
                                                    abdominal pain, low platelets, or abnormal liver enzymes.
Gestational
Hypertension – 3.7% in   Diagnosis
150,000 (National
Center for Health
Statics, 2001)




CHRONIC
HYPERTENSION
•BP ≥140/90 mmHg before pregnancy
   or diagnosed before 20weeks’
   gestation (not attributable to
   gestational trophoblastic disease)
               or
   •Hypertension first diagnosed after
   20weeks’ gestation and persistent after
   12weeks’ postpartum

Underlying hypertension-Essential familial hypertension (90%)
•BP≥ 140/90mmHg for first time during
pregnancy

•No proteinuria

•BP returns to normal < 12 weeks’ postpartum

•Final diagnosis made only postpartum

•May have other signs or symptoms of
preeclampsia, for example, epigastric discomfort
or thrombocytopenia
Essential familial hypertension (hypertensive vascular disease)
Obesity
Atrterial abnormalities
    Renovascular hypertension
    Coarctation of the aorta
Endocrine diorders
    Diabetes mellitus
    Cushing syndrome
    Primary aldosteronism
    Pheochromocytoma
    Thyrotoxicosis
Glomerulonephritis (acute and chronic)
Renoprival hypertension
    Chronic glomerulonephritis
    Chronic renal insufficiency
    Diabetic nephropathy
Connetive tissue disease
    Lupus erythematosus
    Systemic sclorosis
    Periarteritis nodosa
Polycystic kidney disease
Acute renal failure
INCIDENCE




Nulliparous women              BMI (Kg/m2)
Incidence : 5% (wide           Morbidity (%)
variation)                      <19.8
Influence by Parity, race,      4.3
ethnicity, genetic              >35
predisposition
Nulliparous                    13.3
    Total :7.6% / severe :     Gestation
    3.3% (Hauth, 2000)
Risk factor                     twin
    Chronic hypertension,      13
    multifetal gestation,       single
    maternal old age(>35        5
    yrs), obesity, African-
FACTOR                      RISK RATIO

Renal disease               20:1

Chronic hypertension        10:1

Antiphospholipid syndrome   10:1


Family history of PIH       5:1

Twin gestation              4:1
Nulliparity                 3:1

Age > 40                    3:1

Diabetes mellitus           2:1
African American            1.5:1
New-onset proteinuria≥ 300mg/24hours in
hypertensive women but no proteinuria
before 20 weeks’ gestation.

A sudden increase in proteinuria or blood
pressure or platelet count <100,000/mm3 in
women with hypertension and roteinuria
before 20weeks’ gestation
Treatment of mild to moderate chronic hypertension
neither benefits the fetus nor prevents preeclampsia.
Excessively lowering blood pressure may result in
decreased placental perfusion and adverse perinatal
outcomes.
When BP is 150 to 180/100 to 110 mm Hg,
pharmacologic treatment is needed to prevent
maternal end-organ damage.
Antihypertensive Therapy Prior to
        and During Pregnancy

1. What is the proper management of young women
   with mild hypertension?
2. What are the benefits of treating mild
   hypertension in pregnancy?
3. Is pharmacological treatment of mild
   hypertension harmful to mothers, fetuses, and
   infants?
4. Are particular antihypertensive drugs more
   ffective or harmful than others?
What Are the Benefits of Treating
  Mild Hypertension in Pregnancy?

 Data are insufficient to either prove or
disprove effects in perinatal outcome
   • All trials had inadequate sample size
   • Most were unblinded
   • Few women enrolled in first trimester
   • 15 different drugs or combinations were
   studied
 Definite need for multicenter trials
What is the Proper Management of
  Young Women with Hypertension?
 No report that addressed the effect of blood
pressure control before conception on fetal
outcomes
 Women of reproductive age are excluded from
  randomized trials
 Only 3 trials in women aged 30-54 years
  • 8,565 studied
  • Little data in women < 40 years
16
Acute Medical Therapy

•   Hydralazine
•   Labetalol
•   Nifedipine
•   Nitroprusside
•   Clonidine
Hydralazine

• Dose: 5-10 mg every 20 minutes
• Onset: 10-20 minutes
• Duration: 3-8 hours
• Side effects: headache, flushing, tachycardia,
  lupus like symptoms
• Mechanism: peripheral vasodilator
Labetalol

• Dose: 20 mg, then 40, then 80 every 20
  minutes, for a total of 220mg
• Onset: 1-2 minutes
• Duration: 6-16 hours
• Side effects: hypotension
• Mechanism: Alpha and Beta blockade
Nifedipine

•   Dose: 10 mg po, not sublingual
•   Onset: 5-10 minutes
•   Duration: 4-8 hours
•   Side effects: chest pain, headache, tachycardia
•   Mechanism: CA channel blockade
Clonidine

• Dose: 1 mg po
• Onset: 10-20 minutes
• Duration: 4-6 hours
• Side effects: unpredictable, avoid rapid
  withdrawal
• Mechanism: Alpha agonist, works centrally
Nitroprusside

• Dose: 0.2 – 0.8 mg/min IV
• Onset: 1-2 minutes
• Duration: 3-5 minutes
• Side effects: cyanide accumulation,
  hypotension
• Mechanism: direct vasodilator
Seizure Prophylaxis

• Magnesium sulfate
• Loading dose of 4 to 6 g diluted in 100 mL of
  normal saline, given IV over 15 to 20 minutes,
  followed by a continuous infusion of 1-2 g per
  hour
• Monitor urine output, RR and DTR’s
• With renal dysfunction, may require a lower
  dose
• Low-dose aspirin (75 to 81 mg daily) has small to moderate
  benefits for the prevention of preeclampsia (NNT = 72), preterm
  delivery (NNT = 74), and fetal death (NNT = 243). The benefit of
  aspirin is greatest (NNT = 19) for prevention of preeclampsia in
  women at highest risk (previous severe preeclampsia, diabetes,
  chronic hypertension, renal disease, or autoimmune disease). –
  B

• For women with mild preeclampsia, delivery is generally not
  indicated until 37 to 38 weeks of gestation and should occur by
  40 weeks. – C
KEY RECOMMENDATIONS FOR PRACTICE

• In women without end-organ damage, chronic hypertension in
  pregnancy does not require treatment unless the patient's blood
  pressure is persistently greater than 150 to 180/100 to 110 mm
  Hg. – C

• Calcium supplementation decreases the incidence of
  hypertension and preeclampsia, respectively, among all women
  (NNT = 11 and NNT = 20), women at high risk of hypertensive
  disorders (NNT = 2 and NNT = 6), and women with low calcium
  intake (NNT = 6 and NNT = 13). – A
Chronic hypertension in pregrancy

Chronic hypertension in pregrancy

  • 1.
  • 2.
    A 35-year-old womanelder primi and has a 5-year history of hypertension wants to become pregnant. She has stopped using contraception. Her only medication is lisinopril at a dose of 10 mg per day. Her blood pressure is 124/68 mm Hg,and her body-mass index (the weight in kilograms divided by the square of the height in meters) is 27. Pregnancy-related deaths(3201 in US, 1991-1997-16%
  • 3.
    Classification of Hypertensionin Pregnancy From Gifford RW, August PA, Cunningham G, et al: Report of the National High Blood Pressure Education Program Working Group on High Blood Pressure in Pregnancy. Am J Obstet Gynecol 183:S1, 2000 Hypertension (blood pressure ≥140 mm Hg systolic or ≥90 mm Chronic hypertension Hg diastolic) present before pregnancy or that is diagnosed before the 20th week of gestation New hypertension with a blood pressure of 140/90 mm Hg on two separate occasions, without proteinuria, arising de novo Gestational hypertension after the 20th week of pregnancy. Blood pressure normalizes by 12 weeks post partum. Increased blood pressure above the patient's baseline, a Preeclampsia superimposed on chronic hypertension change in proteinuria, or evidence of end-organ dysfunction Proteinuria (>0.3 g during 24 hours or ++ in two urine samples) in addition to new hypertension. Edema is no longer included in the diagnosis because of poor specificity. When Preeclampsia-eclampsia proteinuria is absent, suspect the disease when increased blood pressure is associated with headache, blurred vision, abdominal pain, low platelets, or abnormal liver enzymes.
  • 4.
    Gestational Hypertension – 3.7%in Diagnosis 150,000 (National Center for Health Statics, 2001) CHRONIC HYPERTENSION
  • 5.
    •BP ≥140/90 mmHgbefore pregnancy or diagnosed before 20weeks’ gestation (not attributable to gestational trophoblastic disease) or •Hypertension first diagnosed after 20weeks’ gestation and persistent after 12weeks’ postpartum Underlying hypertension-Essential familial hypertension (90%)
  • 6.
    •BP≥ 140/90mmHg forfirst time during pregnancy •No proteinuria •BP returns to normal < 12 weeks’ postpartum •Final diagnosis made only postpartum •May have other signs or symptoms of preeclampsia, for example, epigastric discomfort or thrombocytopenia
  • 7.
    Essential familial hypertension(hypertensive vascular disease) Obesity Atrterial abnormalities Renovascular hypertension Coarctation of the aorta Endocrine diorders Diabetes mellitus Cushing syndrome Primary aldosteronism Pheochromocytoma Thyrotoxicosis Glomerulonephritis (acute and chronic) Renoprival hypertension Chronic glomerulonephritis Chronic renal insufficiency Diabetic nephropathy Connetive tissue disease Lupus erythematosus Systemic sclorosis Periarteritis nodosa Polycystic kidney disease Acute renal failure
  • 8.
    INCIDENCE Nulliparous women BMI (Kg/m2) Incidence : 5% (wide Morbidity (%) variation) <19.8 Influence by Parity, race, 4.3 ethnicity, genetic >35 predisposition Nulliparous 13.3 Total :7.6% / severe : Gestation 3.3% (Hauth, 2000) Risk factor twin Chronic hypertension, 13 multifetal gestation, single maternal old age(>35 5 yrs), obesity, African-
  • 9.
    FACTOR RISK RATIO Renal disease 20:1 Chronic hypertension 10:1 Antiphospholipid syndrome 10:1 Family history of PIH 5:1 Twin gestation 4:1 Nulliparity 3:1 Age > 40 3:1 Diabetes mellitus 2:1 African American 1.5:1
  • 10.
    New-onset proteinuria≥ 300mg/24hoursin hypertensive women but no proteinuria before 20 weeks’ gestation. A sudden increase in proteinuria or blood pressure or platelet count <100,000/mm3 in women with hypertension and roteinuria before 20weeks’ gestation
  • 12.
    Treatment of mildto moderate chronic hypertension neither benefits the fetus nor prevents preeclampsia. Excessively lowering blood pressure may result in decreased placental perfusion and adverse perinatal outcomes. When BP is 150 to 180/100 to 110 mm Hg, pharmacologic treatment is needed to prevent maternal end-organ damage.
  • 13.
    Antihypertensive Therapy Priorto and During Pregnancy 1. What is the proper management of young women with mild hypertension? 2. What are the benefits of treating mild hypertension in pregnancy? 3. Is pharmacological treatment of mild hypertension harmful to mothers, fetuses, and infants? 4. Are particular antihypertensive drugs more ffective or harmful than others?
  • 14.
    What Are theBenefits of Treating Mild Hypertension in Pregnancy?  Data are insufficient to either prove or disprove effects in perinatal outcome • All trials had inadequate sample size • Most were unblinded • Few women enrolled in first trimester • 15 different drugs or combinations were studied  Definite need for multicenter trials
  • 15.
    What is theProper Management of Young Women with Hypertension?  No report that addressed the effect of blood pressure control before conception on fetal outcomes  Women of reproductive age are excluded from randomized trials  Only 3 trials in women aged 30-54 years • 8,565 studied • Little data in women < 40 years
  • 16.
  • 19.
    Acute Medical Therapy • Hydralazine • Labetalol • Nifedipine • Nitroprusside • Clonidine
  • 20.
    Hydralazine • Dose: 5-10mg every 20 minutes • Onset: 10-20 minutes • Duration: 3-8 hours • Side effects: headache, flushing, tachycardia, lupus like symptoms • Mechanism: peripheral vasodilator
  • 21.
    Labetalol • Dose: 20mg, then 40, then 80 every 20 minutes, for a total of 220mg • Onset: 1-2 minutes • Duration: 6-16 hours • Side effects: hypotension • Mechanism: Alpha and Beta blockade
  • 22.
    Nifedipine • Dose: 10 mg po, not sublingual • Onset: 5-10 minutes • Duration: 4-8 hours • Side effects: chest pain, headache, tachycardia • Mechanism: CA channel blockade
  • 23.
    Clonidine • Dose: 1mg po • Onset: 10-20 minutes • Duration: 4-6 hours • Side effects: unpredictable, avoid rapid withdrawal • Mechanism: Alpha agonist, works centrally
  • 24.
    Nitroprusside • Dose: 0.2– 0.8 mg/min IV • Onset: 1-2 minutes • Duration: 3-5 minutes • Side effects: cyanide accumulation, hypotension • Mechanism: direct vasodilator
  • 25.
    Seizure Prophylaxis • Magnesiumsulfate • Loading dose of 4 to 6 g diluted in 100 mL of normal saline, given IV over 15 to 20 minutes, followed by a continuous infusion of 1-2 g per hour • Monitor urine output, RR and DTR’s • With renal dysfunction, may require a lower dose
  • 26.
    • Low-dose aspirin(75 to 81 mg daily) has small to moderate benefits for the prevention of preeclampsia (NNT = 72), preterm delivery (NNT = 74), and fetal death (NNT = 243). The benefit of aspirin is greatest (NNT = 19) for prevention of preeclampsia in women at highest risk (previous severe preeclampsia, diabetes, chronic hypertension, renal disease, or autoimmune disease). – B • For women with mild preeclampsia, delivery is generally not indicated until 37 to 38 weeks of gestation and should occur by 40 weeks. – C
  • 27.
    KEY RECOMMENDATIONS FORPRACTICE • In women without end-organ damage, chronic hypertension in pregnancy does not require treatment unless the patient's blood pressure is persistently greater than 150 to 180/100 to 110 mm Hg. – C • Calcium supplementation decreases the incidence of hypertension and preeclampsia, respectively, among all women (NNT = 11 and NNT = 20), women at high risk of hypertensive disorders (NNT = 2 and NNT = 6), and women with low calcium intake (NNT = 6 and NNT = 13). – A

Editor's Notes

  • #22 Note that labetalol therapy should not be used in women with asthma or congestive heart failure