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Complication of pregnancy
Pregnancy Induced
Pregnancy(PIH)
Hypertensive Disorders of
Pregnancy
1. Chronic Hypertension (before pregnancy)
2. Gestational (in pregnancy) Hypertension
-

Pre-eclampsia
Severe pre-eclampsia
Eclampsia
HELLP syndrome
Hypertensive Disorders of
Pregnancy
• Most commonly reported disorder of
pregnancy
• May occur in 20% of all pregnancies
• One of the leading causes of maternal
morbidity and mortality worldwide
Pathophysiology/Etiology
1. Actual cause is unknown.
2. Theories of the etiology include the exposure to chorionic villi for the
first time, or in large amounts, along with
immunologic, genetic, and endocrine factors.
3. The disease is primarily seen in primagravidas.
4. Chronic hypertension, hydatidiform mole, multiple
gestation, polyhydramnios, and diabetes mellitus may
predispose to PIH.
5. Adolescents and women over 35 years of age are at higher risk.
6. Approximately 6% to 8% of pregnancies may be affected.
7. Vasospasms occur and result in increased resistance in vascular
flow, increasing the arterial blood pressure.
8. Increased sensitivity to angiotensin II occurs before the onset of
hypertension.
9. Hemoconcentration occurs due to the vasoconstriction or as a
result of increased vascular permeability or a combination of both.
Characteristics PIH
Three typical Symptoms:
• Hypertension(high blood pressure)
• Edema
• Protein urine
Pathophysiology:
1. Vasoconstriction
2. Vasospasm
3. Endothelial damage
Pathophysiology:
Damage to blood vessels
causes increased capillary
permeability and decreased
organ perfusion.
Clinical Manifestations
1. Hypertension, which is defined as a blood pressure of 140/90
mm Hg or greater on two occasions at least 6 hours apart
2. Proteinuria , +, ++, +++, ++++
3. Edema, nondependent, present after 8 to 12 hours of bed rest
,
4. Frequently, a sudden weight gain will occur, of 2 lb or more in
1 week, or 6 lb or more in 1 month. This often occurs before
the edema is present.
5. Altered level of consciousness, visual changes, headache
6. Oliguria
7. Epigastric pain, chest pressure
8. Hyperreflexia with or without clonus
Hypertensive Disorders of
Pregnancy

Preeclampsia

• Gestational Hypertension
PLUS
• Protein in the urine
PLUS
• Edema
Hypertensive Disorders of
Pregnancy
• Pre-eclampsia

Severe
Preeclampsia

PLUS one of the following:
1. Systolic BP > 160 mmHg
2. Diastolic BP > 110mmHg
3. Persistent headache, visual
changes or epigastric pain
4. Creatinine > 1.2 mg/dL
5. Platelets < 100,000
6. Increase liver function tests
eclampsia

• Gestational
Hypertension
PLUS
• Protein in the urine
PLUS
• Edema
PLUS
• Convulsion
Hypertensive Disorders of
Pregnancy
H = Hemolysis

HELLP
Syndrome

EL = Elevated
Liver
Enzymes

LP = Low Platelets
Hypertensive Disorders of
Pregnancy
• Risk factors
1.
2.
3.
4.
5.
6.

First pregnancy
More than one fetus
Pre-existing disease (diabetes, hypertension)
Obesity
Maternal age (< 20 years, > 40 years)
Family history
Diagnostic Evaluation
1. A 24-hour urine for protein of 300 mg or
greater
2. Serum BUN and creatine to evaluate
renal function
3. Sonogram, nonstress testing to evaluate
placenta and fetus
Management
1. Directed toward decreasing the maternal blood pressure through the
use of bed rest and antihypertensive medications along with
increase in dietary protein
2. Hospitalization and seizure
3. Medication
a. Magnesium sulfate (MgS04) may be given either IV or IM
Side effect, loss of knee reflex, should be given calcium gluconate
b. Antihypertensive drug; Hydralazine (Apresoline)
* Side effects include
tachycardia, palpitations, dizziness, faintness, headache.
c. Diazepam (Valium) and amobarbital sodium (Amytal Sodium) may
be used if convulsions occur that respond to MgS04.
4. If symptoms are uncontrollable, delivery is planned.
Complications
1. Abruptio placentae
2. DIC
3. HELLP syndrome
4. Prematurity
5. Intrauterine growth retardation (IUGR)
from decreased placental perfusion
6. Maternal/fetal death
Nursing Assessment
• Assessment of mother
1. Blood pressure
2. Protein in the urine

3. Complaints of headache, liver pain,
or strange bruises or bleeding
Nursing Diagnoses
A. Fluid Volume Excess related to IV fluid
overload(edema)
B. Altered Tissue Perfusion, Fetal Cardiac
and Cerebral, related to altered placental
blood flow(fetal distress)
C. Risk for Injury related to convulsions
D. Anxiety related to concern for self and
fetus
A. Maintaining Fluid Balance
1. Control IV fluid intake using a continuous infusion
pump.
2. Monitor intake and output strictly; notify health
care provider if urine output is less than 30 mL/h.
4. Monitor hematocrit levels to evaluate intravascular
fluid status.
5. Monitor vital signs every hour.
6. Auscultate breath sounds every 2 hours and
report signs of pulmonary edema
(wheezing, crackles, shortness of
breath, increased pulse rate, increased respiratory
rate).
B. Promoting Adequate Tissue
Perfusion
1. Position on side, preferably the left side to
promote placental perfusion.
2. Monitor fetal activity.
3. Evaluate nonstress tests to determine
fetal status.
4. Increase protein intake to replace protein
lost through kidneys.
C. Preventing Injury
1. Instruct on the importance of reporting
headaches, visual changes, dizziness, and
epigastric pain.
2. Instruct to lie down on left side if symptoms are
present.
3. Keep the environment quiet and as calm as possible.
4. If hospitalized, side rails should be padded and
remain up to prevent injury if seizure occurs.
5. If hospitalized, have oxygen and suction setup, along
with a tongue blade and emergency medications
immediately available for treatment of seizures.
D. Decreasing Anxiety
1. Explain the disease process and
treatment plan.
2. Explain that PIH does not lead to chronic
hypertension.
3. Explain that PIH usually does not occur with
subsequent pregnancies.
4. Discuss the effects of all medications on the
mother and fetus.
5. Allow time to ask questions and discuss
feelings regarding the diagnosis and
treatment plan.
Patient Education/Health
Maintenance
1. Teach the woman the importance of bed rest in
helping to control symptoms.
2. Encourage the support of family and friends while
on bed rest.
3. Provide and suggest diversional activities while on
bed rest.
4. Provide information on tests and procedures to
evaluate maternal-fetal status, such as laboratory
tests, sonogram, nonstress tests.
5. Include support of the neonatal team for
discussion of fetal prognosis with the woman and
her family.
Evaluation
A. No evidence of pulmonary edema; urine
output adequate
B. Fetal heart rate within normal range;
reactivity present
C. No seizure activity
D. Expresses concern for self and the fetus

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13.pregnancy induced hypertention

  • 1. Complication of pregnancy Pregnancy Induced Pregnancy(PIH)
  • 2. Hypertensive Disorders of Pregnancy 1. Chronic Hypertension (before pregnancy) 2. Gestational (in pregnancy) Hypertension - Pre-eclampsia Severe pre-eclampsia Eclampsia HELLP syndrome
  • 3. Hypertensive Disorders of Pregnancy • Most commonly reported disorder of pregnancy • May occur in 20% of all pregnancies • One of the leading causes of maternal morbidity and mortality worldwide
  • 4. Pathophysiology/Etiology 1. Actual cause is unknown. 2. Theories of the etiology include the exposure to chorionic villi for the first time, or in large amounts, along with immunologic, genetic, and endocrine factors. 3. The disease is primarily seen in primagravidas. 4. Chronic hypertension, hydatidiform mole, multiple gestation, polyhydramnios, and diabetes mellitus may predispose to PIH. 5. Adolescents and women over 35 years of age are at higher risk. 6. Approximately 6% to 8% of pregnancies may be affected. 7. Vasospasms occur and result in increased resistance in vascular flow, increasing the arterial blood pressure. 8. Increased sensitivity to angiotensin II occurs before the onset of hypertension. 9. Hemoconcentration occurs due to the vasoconstriction or as a result of increased vascular permeability or a combination of both.
  • 5. Characteristics PIH Three typical Symptoms: • Hypertension(high blood pressure) • Edema • Protein urine
  • 7. Pathophysiology: Damage to blood vessels causes increased capillary permeability and decreased organ perfusion.
  • 8.
  • 9. Clinical Manifestations 1. Hypertension, which is defined as a blood pressure of 140/90 mm Hg or greater on two occasions at least 6 hours apart 2. Proteinuria , +, ++, +++, ++++ 3. Edema, nondependent, present after 8 to 12 hours of bed rest , 4. Frequently, a sudden weight gain will occur, of 2 lb or more in 1 week, or 6 lb or more in 1 month. This often occurs before the edema is present. 5. Altered level of consciousness, visual changes, headache 6. Oliguria 7. Epigastric pain, chest pressure 8. Hyperreflexia with or without clonus
  • 10. Hypertensive Disorders of Pregnancy Preeclampsia • Gestational Hypertension PLUS • Protein in the urine PLUS • Edema
  • 11. Hypertensive Disorders of Pregnancy • Pre-eclampsia Severe Preeclampsia PLUS one of the following: 1. Systolic BP > 160 mmHg 2. Diastolic BP > 110mmHg 3. Persistent headache, visual changes or epigastric pain 4. Creatinine > 1.2 mg/dL 5. Platelets < 100,000 6. Increase liver function tests
  • 12. eclampsia • Gestational Hypertension PLUS • Protein in the urine PLUS • Edema PLUS • Convulsion
  • 13. Hypertensive Disorders of Pregnancy H = Hemolysis HELLP Syndrome EL = Elevated Liver Enzymes LP = Low Platelets
  • 14. Hypertensive Disorders of Pregnancy • Risk factors 1. 2. 3. 4. 5. 6. First pregnancy More than one fetus Pre-existing disease (diabetes, hypertension) Obesity Maternal age (< 20 years, > 40 years) Family history
  • 15. Diagnostic Evaluation 1. A 24-hour urine for protein of 300 mg or greater 2. Serum BUN and creatine to evaluate renal function 3. Sonogram, nonstress testing to evaluate placenta and fetus
  • 16. Management 1. Directed toward decreasing the maternal blood pressure through the use of bed rest and antihypertensive medications along with increase in dietary protein 2. Hospitalization and seizure 3. Medication a. Magnesium sulfate (MgS04) may be given either IV or IM Side effect, loss of knee reflex, should be given calcium gluconate b. Antihypertensive drug; Hydralazine (Apresoline) * Side effects include tachycardia, palpitations, dizziness, faintness, headache. c. Diazepam (Valium) and amobarbital sodium (Amytal Sodium) may be used if convulsions occur that respond to MgS04. 4. If symptoms are uncontrollable, delivery is planned.
  • 17. Complications 1. Abruptio placentae 2. DIC 3. HELLP syndrome 4. Prematurity 5. Intrauterine growth retardation (IUGR) from decreased placental perfusion 6. Maternal/fetal death
  • 18. Nursing Assessment • Assessment of mother 1. Blood pressure 2. Protein in the urine 3. Complaints of headache, liver pain, or strange bruises or bleeding
  • 19. Nursing Diagnoses A. Fluid Volume Excess related to IV fluid overload(edema) B. Altered Tissue Perfusion, Fetal Cardiac and Cerebral, related to altered placental blood flow(fetal distress) C. Risk for Injury related to convulsions D. Anxiety related to concern for self and fetus
  • 20. A. Maintaining Fluid Balance 1. Control IV fluid intake using a continuous infusion pump. 2. Monitor intake and output strictly; notify health care provider if urine output is less than 30 mL/h. 4. Monitor hematocrit levels to evaluate intravascular fluid status. 5. Monitor vital signs every hour. 6. Auscultate breath sounds every 2 hours and report signs of pulmonary edema (wheezing, crackles, shortness of breath, increased pulse rate, increased respiratory rate).
  • 21. B. Promoting Adequate Tissue Perfusion 1. Position on side, preferably the left side to promote placental perfusion. 2. Monitor fetal activity. 3. Evaluate nonstress tests to determine fetal status. 4. Increase protein intake to replace protein lost through kidneys.
  • 22. C. Preventing Injury 1. Instruct on the importance of reporting headaches, visual changes, dizziness, and epigastric pain. 2. Instruct to lie down on left side if symptoms are present. 3. Keep the environment quiet and as calm as possible. 4. If hospitalized, side rails should be padded and remain up to prevent injury if seizure occurs. 5. If hospitalized, have oxygen and suction setup, along with a tongue blade and emergency medications immediately available for treatment of seizures.
  • 23. D. Decreasing Anxiety 1. Explain the disease process and treatment plan. 2. Explain that PIH does not lead to chronic hypertension. 3. Explain that PIH usually does not occur with subsequent pregnancies. 4. Discuss the effects of all medications on the mother and fetus. 5. Allow time to ask questions and discuss feelings regarding the diagnosis and treatment plan.
  • 24. Patient Education/Health Maintenance 1. Teach the woman the importance of bed rest in helping to control symptoms. 2. Encourage the support of family and friends while on bed rest. 3. Provide and suggest diversional activities while on bed rest. 4. Provide information on tests and procedures to evaluate maternal-fetal status, such as laboratory tests, sonogram, nonstress tests. 5. Include support of the neonatal team for discussion of fetal prognosis with the woman and her family.
  • 25. Evaluation A. No evidence of pulmonary edema; urine output adequate B. Fetal heart rate within normal range; reactivity present C. No seizure activity D. Expresses concern for self and the fetus

Hinweis der Redaktion

  1. HELLP syndrome is a severe complication of pregnancy-induced hypertension. It is comprised of Hemolysis, Elevated Liver enzymes, and Low Platelets.1. These findings are frequently associated with DIC and in fact may be diagnosed as DIC.2. The hemolysis of erythrocytes is seen in the abnormal morphology of the cells.3. The elevated liver enzyme measurement is associated with the decreased blood flow to the liver as a result of fibrin thrombi.4. The low platelet count is related to vasospasm and platelet adhesions.5. Treatment is similar to treatment for PIH with close monitoring of liver function and bleeding.6. These women are at increased risk for postpartum hemorrhage
  2. Evaluate blood pressure with patient in a sitting position and in the left lateral position. 2. Check the protein level of a spot urine specimen. 3. Evaluate edema, carefully noting the presence after 12 hours or more of bed rest. Measure weight. 4. Evaluate deep tendon reflexes and clonus.