10/05/2025 1
PREGNANCY INDUCED
HYPERTENSION
Prepaired by: ABIE ASCHALE
Modulator : Ephrem. (BSC, ECCN)
BY ABIE ASCHALE
DEPARTMENT OF EMERGENCY AND CRITICAL
CARE NURSING
10/05/2025
BY ABIE ASCHALE 2
CONTENT
Introduction
Risk factors
Pathophysiology
Classification
Diagnosis
Management
Complications
ICU admission criteria and management
10/05/2025
BY ABIE ASCHALE 3
OBJECTIVES Define hypertension and PIH
 state Risk factors for PIH
Diagnosis of PIH
Classification
Discuss Diagnosis
Discuss Management option for PIH
List the Complications of PIH
Identify ICU admission criteria and
management for PIH
At the end of this session students are expected
to:
10/05/2025
BY ABIE ASCHALE 4
INTRODUCTION
What is hypertension ?
Stages of hypertension ?
Types of hypertension?
10/05/2025
BY ABIE ASCHALE 5
INTRODUCTION CONTI………
(ACC/AHA) ; 2017
Normal blood pressure Systolic <120 mmHg and diastolic <80 mmHg
Elevated blood pressure – Systolic 120 to 129 mmHg and diastolic <80 mmHg
Hypertension:
•Stage 1 – Systolic 130 to 139 mmHg or diastolic 80 to 89 mmHg
•Stage 2 – Systolic at least 140 mmHg or diastolic at least 90 mmHg
If there is a disparity in category between the systolic and diastolic pressures,
the higher value determines the stage.
10/05/2025
BY ABIE ASCHALE 6
Isolated systolic hypertension vs Isolated diastolic hypertension
 White-coat hypertension - office/clinic BP (≥140/90 mmHg), but
normal at home or work.
 Masked hypertension - BP is normal at a clinic or office visit but
elevated at other times,
 more difficult to diagnose- WHY
 most typically diagnosed by 24-hour ABPM or automated home
BP monitoring
INTRODUCTION CONTI………
10/05/2025
BY ABIE ASCHALE 7
PIH
Pregnancy induced hypertension is defined as a rise in BP> 140/90 mmHg
after the 20th week of gestation measured twice at least six hours apart or a
single measurement of diastolic BP>110mmHg.
Exception
Gestational Trophoblastic diseases (GTD) and multiple pregnancy. Why ?
10/05/2025
BY ABIE ASCHALE 8
 unique to human pregnancy(PE)
 Complicates 7-10% of pregnancies
 70% Preeclampsia-eclampsia
 30% Chronic hypertension
 Eclampsia 0.05% incidence
 20% of Maternal Deaths
 Cause of 10% of Preterm birth
 Etiology unknown
INTRODUCTION CONTI………
10/05/2025
BY ABIE ASCHALE 9
RISK FACTORS
A past history of preeclampsia
Multifetal pregnancy - 20 percent
Nulliparity –
family history
Advanced maternal age < 18 or < 35 yrs.
Pre- existing medical conditions:
 Pregestational diabetes
 underlying kidney or vascular
disease
 Obesity
 abnormal lipid metabolism
 Chronic hypertension
10/05/2025
BY ABIE ASCHALE 10
PATHOPHYSIOLOGY
The pathophysiology of preeclampsia likely involves both maternal and
fetal/placental factors
 Abnormal development of the placenta
 Immunologic factors
 Genetic factors
 Environmental and maternal susceptibility factors
 Preexisting maternal vascular/metabolic/kidney/autoimmune disease
11
Anormal invasion of the spiral arterioles by the cytotrophoblast cells reduced
uteroplacental perfusion  placental ischemia (lack of oxygen and nutrients) release
of placental factors  endothelial dysfunction in the maternal circulation
Endothelial dysfunction  inner lining of the blood vessels becomes impaired and unable to
produce enough vasodilators (substances that relax the blood vessels) such as nitric
oxide and prostacyclin.  This results in increased vascular resistanceandhypertension
Endothelial dysfunction  to increased production of vasoconstrictors (substances that
narrow the blood vessels) such as endothelin and thromboxane  increase the sensitivity of
the blood vessels to angiotensin II, a hormone that regulates blood pressure and fluid
balance
10/05/2025
BY ABIE ASCHALE 12
10/05/2025
BY ABIE ASCHALE 13
• The increased vascular resistance and hypertension affect the renal
function and cause proteinuria (protein in the urine), edema (swelling),
and reduced glomerular filtration rate (GFR).
• The increased blood pressure and endothelial dysfunction also affect
the brain, the liver, and the coagulation system.
• The placental ischemia and the maternal hypertension also affect the fetal
growth and development. The reduced blood flow and oxygen delivery to the
placenta can cause intrauterine growth restriction (IUGR), fetal distress,
and premature birth image
10/05/2025
BY ABIE ASCHALE 14
PRE ECLAPSIA
GESTATION AL HTN
MILD
Pre existing HTN
ECLAPSIA
SEVER
10/05/2025
BY ABIE ASCHALE 15
CLASSIFICATION
10/05/2025
BY ABIE ASCHALE 16
1. GESTATIONAL HYPERTENSION
BP > 140/90 or more after the 20th week of gestation
without significant proteinuria.
Gestational hypertension may represent pre-eclampsia prior to
proteinuria or chronic hypertension previously unrecognized
10/05/2025
BY ABIE ASCHALE 17
2. PRE-ECLAMPSIA
Pre-eclampsia BP > 140/90mmHg
Presence of significant proteinuria of > 300 mg/24 hours urine
specimen OR > 1+ protein (equivalent to approximately 100mg/dl)
on dipstick in at least two randomly collected urine specimen at least 6
hours apart
Based on degree of hypertension or proteinuria and involvement of
other organ systems
10/05/2025
BY ABIE ASCHALE 18
1. Mild pre-eclampsia
The mild form of pre-eclampsia is diagnosed when the Systolic and
diastolic blood pressure is between 140-160 and 90-110mmHg respectively
without signs of severity.
10/05/2025
BY ABIE ASCHALE 19
2. Severe pre-eclampsia
Severe blood pressure elevation: BP > 110 ∕160mmHg measured twice at
least six hours apart OR A single measurement of diastolic BP
>120mmHg
Proteinuria > 5gm/24 hours or >3+ in randomly collected urine
Pulmonary edema
• Kidney function impairment- Serum creatinine >1.1 mg/Dl
• HELLP syndrome
10/05/2025
BY ABIE ASCHALE 20
10/05/2025
BY ABIE ASCHALE 21
Elevated Liver Enzymes (HELLP syndrome)
- Disseminated intravascular coagulation (DIC)
- Headache, visual disturbance and right upper abdominal pain
- Oliguria (<400ml in 24hours or 30ml/hour)
- Intrauterine growth restriction (IUGR)
- Cardiac decompensation, Pulmonary edema, cyanosis
10/05/2025
BY ABIE ASCHALE 22
3. ECLAMPSIA
 Eclampsia is the development of new-onset seizures (generalized tonic clonic type),
superimposed upon
 Preeclampsia, in a woman between 20 weeks of gestation and 4 weeks postpartum.
Eclampsia is the convulsive manifestation of preeclampsia
absence of other causative conditions (eg, epilepsy, cerebral arterial ischemia and
infarction, intracranial hemorrhage, drug use
Any convulsion occurring during pregnancy is eclampsia unless proven otherwise
.
10/05/2025
BY ABIE ASCHALE 23
DIAGNOSIS
History
Physical examination
laboratory
10/05/2025
BY ABIE ASCHALE 24
MANAGEMENT
objectives
1. Control hypertension
2. Prevent convulsion
3. Prevent complication
4. Deliver viable fetus
10/05/2025
BY ABIE ASCHALE 25
GENERAL PRENCIPLES
Stabilization of air way, breathing and circulation is the initial step.
Always anticipate difficult airway in pregnant patients.
Two large-bore intravenous cannula (14G or 16G) should be placed to
administer fluids.
The Foley catheter should be placed to monitor urine output.
Nurse in the left lateral position (30° wedge to the right hip) to prevent supine
hypotension syndrome
10/05/2025
BY ABIE ASCHALE 26
Non pharmacologic
- Bed rest at home in the lateral decubitus position.
- Frequent evaluation of fetal well being
- Maternal well being i.e. BP, laboratory
- Advise patient to immediately report whenever they develop symptoms of severity such as
headache, epigastric pain, blurring of vision etc
- Plan termination of pregnancy at term.
- If the disease progresses to severe range, manage as severe case.
Management of mild pre-
eclampsia
Most patients are asymptomatic and can be managed conservatively. Such patients are
not candidates for urgent delivery.
10/05/2025 27
Pharmacologic
BY ABIE ASCHALE
BP control
 Arterial pressure not greater than 160/110 mmHg in preeclampsia can increase
the risk of complication, and it should be controlled.
 Goal of BP control is 15–25% reduction in the mean arterial pressure, and
 Reduction of pressure to normal levels (<140/90 mmHg) should be avoided as
it may compromise placental perfusion.
Methyldopa, 250-500mg P.O., 8 to 12 hourly
Nifedipine, 10-40mg P.O., BID OR slow release 30-60mg daily
N.B. Advise patient
10/05/2025
BY ABIE ASCHALE 28
PREECLAMPSIAAND ECLAMPSIA
B. BP CONTROL
10/05/2025
BY ABIE ASCHALE 29
1. Labetalol
 Dosage
 20 mg IV gradually over 2 minutes.
• If BP remains above target level at 10 minutes, give 40 mg IV over 2 minutes.
• If BP remains above target level at 20 minutes, give 80 mg IV over 2 minutes.
 Cumulative maximum dose is 300 mg. If target BP is not achieved, switch
to another class of agent. Hold dose if heart rate <60 beats per minute.
 A continuous IV infusion of 1 to 2 mg/minute can be used instead of
intermittent therapy or started after 20 mg IV dose.
10/05/2025
BY ABIE ASCHALE 30
2. HYDRALAZINE
Repeat BP measurement at 20-minute intervals:
•If BP remains above target level at 20 minutes, give 5 or 10 mg IV over 2
minutes, depending on the initial response.
Cumulative maximum dose is 20 to 30 mg per treatment event.
Initial dose - 5 mg IV gradually over 1 to 2 minutes.*
Less predictable than with IV labetalol.
10/05/2025
BY ABIE ASCHALE 31
3. NIFEDIPINE*
Immediate release- 10 mg orally.
• Repeat BP measurement at 20-minute intervals:
• If BP remains above target at 20 minutes, give 10 or 20 mg orally,
depending on the initial response.
• If BP remains above target at 40 minutes, give 10 or 20 mg orally,
depending on the previous response.
10/05/2025
BY ABIE ASCHALE 32
C. CONTROL SEIZURE
33
FIRST LINE - Magnesium sulphate
A loading dose
 4gm as 20% solution IV over 10-15 minutes followed by
10gm as 50% IM injection divided on two sides of the buttock,
Maintenance dose
5gm every 4 hours as 50% concentration over 2minutes,
2gm IV as 50% solution over 2minutes if convulsion recurs.
Reduce the maintenance dose by half if there are signs of renal derangement
during labor and for the first 24 hours postpartum
10/05/2025
BY ABIE ASCHALE 34
Monitor toxicity
 Loss of deep tendon reflexes
 Respiratory depression
 Loss of patellar reflex
If seizures recur while the patient is receiving magnesium, a repeat (2g)
bolus of magnesium may be given.
Infusion dose should be reduced in case of renal dysfunction.
Serum magnesium level should be monitored
Discontinue magnesium sulfate 24 h after delivery or after last seizer
10/05/2025
BY ABIE ASCHALE 35
D. DELIVERY
The definitive treatment for eclampsia is prompt delivery;
10/05/2025
BY ABIE ASCHALE 36
10/05/2025
BY ABIE ASCHALE 37
Maternal Complications
 DIC(3%),
 Renal failure (4%)
 Adult respiratory distress syndrome (3%).
 HELLP syndrome3%,
 severe PE 4-12% with
 Uncontrolled Hypertension
 Risk of Cerebro-vascular Accident
 Liver failure (Liver rupture)
10/05/2025
BY ABIE ASCHALE 38
 Pulmonary oedema 2%(adult RDS)
 Pulmonary hemorrhage
 Placental abruption
 Eclampsia (risk of aspiration pneumonia)
10/05/2025
BY ABIE ASCHALE 39
Prematurity
IUGR
Utero-placental insufficiency
Oligohydramnios
Respiratory distress syndrome
Placental abruption
 Acute fetal distress
 IUFD
 Caesarean section,
 Admission to SCUBU/NICU
Fetal complications
10/05/2025
BY ABIE ASCHALE 40
ICU ADMISSION CRITERIA FOR SEVER CONDITIONS
The criteria for ICU admission for preeclampsia and depending on
 the severity of the condition,
 the availability of resources, and
 the clinical judgment of the obstetrician and the intensivist.
10/05/2025
BY ABIE ASCHALE 41
some common indicators may warrant ICU admission are
BP > 160/110 mmHg or higher, despite adequate antihypertensive therapy.
Severe proteinuria (> 4+ on dipstick or 5 g in 24 hours).
Oliguria (UO < 20-30 ml/hr) or AKI (cr. >1.3 mg/dl).
Signs of HELLP syndrome
Epigastric pain, headache, visual disturbances, or altered mental status (signs of
cerebral edema or ischemia).
Seizures or coma (eclampsia).
Pulmonary edema, signs of fluid overload or cardiopulmonary dysfunction.
Fetal distress or IUGR (signs of placental insufficiency or abruption).
10/05/2025
BY ABIE ASCHALE 42
GOAL OF ICU CARE AND ROLE OF NURSE
• Blood pressure control with intravenous antihypertensive a
• Magnesium sulfate infusion for seizure prophylaxis and treatment
• Fluid management with careful assessment of the fluid balance, urine
output, and hemodynamics.
• Fetal monitoring with continuous cardiotocography, ultrasound, and
biophysical profile
• Steroid administration for fetal lung maturation if the gestational age is
less than 34 weeks and delivery is anticipated within 7 days.
10/05/2025 43
SUMMERY
PIH) a condition where a pregnant woman develops high blood pressure after 20 weeks of
pregnancy.
It can affect the mother’s organs and the baby’s growth and development.
PIH can also lead to serious complications such as pre-eclampsia, eclampsia, and HELLP
syndrome.
PIH is diagnosed by measuring blood pressure and checking for protein in the urine.
Treatment options depend on the severity of the condition and the stage of pregnancy. Some
common treatments include bed rest, medication, and early delivery.
PIH usually goes away after childbirth
10/05/2025
BY ABIE ASCHALE 44
REFERENCES
Overview of pregnancy induced hypertension– UpToDate,2024
Protocol R. 3: Classification of hypertension in pregnancy. 2012;
Melkie DA, Internist, Teferra DE, Pediatrician, Assefa DM, Oncologist, et al. Food , Medicine and Healthcare Administration
and Control Authority of Ethiopia Standard Treatment Guidelines For General Hospital Diseases Investigations Good
Prescribing & Dispensing Practices for Better Health Outcomes. Fmhaca Addis Ababa. 2014;(3):360.
Brown MA, Magee LA, Kenny LC, Karumanchi SA, McCarthy FP, Saito S, et al. Hypertensive disorders of pregnancy: ISSHP
classification, diagnosis, and management recommendations for international practice. Hypertension. 2018;72(1):24–43.
Braunthal S, Brateanu A. Hypertension in pregnancy: Pathophysiology and treatment. SAGE Open Med. 2019;7.
 Gouveia, I., Costa, C., Cunha, P. et al. Pre-eclampsia in the intensive care unit: indicators of severity and hospital
outcome. Crit Care 9 (Suppl 1), P216 (2005). https://doi.org/10.1186/cc3279
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BY ABIE ASCHALE 45
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BY ABIE ASCHALE 46
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BY ABIE ASCHALE 47
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PIH.pptx best document for eccn students

  • 1.
    10/05/2025 1 PREGNANCY INDUCED HYPERTENSION Prepairedby: ABIE ASCHALE Modulator : Ephrem. (BSC, ECCN) BY ABIE ASCHALE DEPARTMENT OF EMERGENCY AND CRITICAL CARE NURSING
  • 2.
    10/05/2025 BY ABIE ASCHALE2 CONTENT Introduction Risk factors Pathophysiology Classification Diagnosis Management Complications ICU admission criteria and management
  • 3.
    10/05/2025 BY ABIE ASCHALE3 OBJECTIVES Define hypertension and PIH  state Risk factors for PIH Diagnosis of PIH Classification Discuss Diagnosis Discuss Management option for PIH List the Complications of PIH Identify ICU admission criteria and management for PIH At the end of this session students are expected to:
  • 4.
    10/05/2025 BY ABIE ASCHALE4 INTRODUCTION What is hypertension ? Stages of hypertension ? Types of hypertension?
  • 5.
    10/05/2025 BY ABIE ASCHALE5 INTRODUCTION CONTI……… (ACC/AHA) ; 2017 Normal blood pressure Systolic <120 mmHg and diastolic <80 mmHg Elevated blood pressure – Systolic 120 to 129 mmHg and diastolic <80 mmHg Hypertension: •Stage 1 – Systolic 130 to 139 mmHg or diastolic 80 to 89 mmHg •Stage 2 – Systolic at least 140 mmHg or diastolic at least 90 mmHg If there is a disparity in category between the systolic and diastolic pressures, the higher value determines the stage.
  • 6.
    10/05/2025 BY ABIE ASCHALE6 Isolated systolic hypertension vs Isolated diastolic hypertension  White-coat hypertension - office/clinic BP (≥140/90 mmHg), but normal at home or work.  Masked hypertension - BP is normal at a clinic or office visit but elevated at other times,  more difficult to diagnose- WHY  most typically diagnosed by 24-hour ABPM or automated home BP monitoring INTRODUCTION CONTI………
  • 7.
    10/05/2025 BY ABIE ASCHALE7 PIH Pregnancy induced hypertension is defined as a rise in BP> 140/90 mmHg after the 20th week of gestation measured twice at least six hours apart or a single measurement of diastolic BP>110mmHg. Exception Gestational Trophoblastic diseases (GTD) and multiple pregnancy. Why ?
  • 8.
    10/05/2025 BY ABIE ASCHALE8  unique to human pregnancy(PE)  Complicates 7-10% of pregnancies  70% Preeclampsia-eclampsia  30% Chronic hypertension  Eclampsia 0.05% incidence  20% of Maternal Deaths  Cause of 10% of Preterm birth  Etiology unknown INTRODUCTION CONTI………
  • 9.
    10/05/2025 BY ABIE ASCHALE9 RISK FACTORS A past history of preeclampsia Multifetal pregnancy - 20 percent Nulliparity – family history Advanced maternal age < 18 or < 35 yrs. Pre- existing medical conditions:  Pregestational diabetes  underlying kidney or vascular disease  Obesity  abnormal lipid metabolism  Chronic hypertension
  • 10.
    10/05/2025 BY ABIE ASCHALE10 PATHOPHYSIOLOGY The pathophysiology of preeclampsia likely involves both maternal and fetal/placental factors  Abnormal development of the placenta  Immunologic factors  Genetic factors  Environmental and maternal susceptibility factors  Preexisting maternal vascular/metabolic/kidney/autoimmune disease
  • 11.
    11 Anormal invasion ofthe spiral arterioles by the cytotrophoblast cells reduced uteroplacental perfusion  placental ischemia (lack of oxygen and nutrients) release of placental factors  endothelial dysfunction in the maternal circulation Endothelial dysfunction  inner lining of the blood vessels becomes impaired and unable to produce enough vasodilators (substances that relax the blood vessels) such as nitric oxide and prostacyclin.  This results in increased vascular resistanceandhypertension Endothelial dysfunction  to increased production of vasoconstrictors (substances that narrow the blood vessels) such as endothelin and thromboxane  increase the sensitivity of the blood vessels to angiotensin II, a hormone that regulates blood pressure and fluid balance
  • 12.
  • 13.
    10/05/2025 BY ABIE ASCHALE13 • The increased vascular resistance and hypertension affect the renal function and cause proteinuria (protein in the urine), edema (swelling), and reduced glomerular filtration rate (GFR). • The increased blood pressure and endothelial dysfunction also affect the brain, the liver, and the coagulation system. • The placental ischemia and the maternal hypertension also affect the fetal growth and development. The reduced blood flow and oxygen delivery to the placenta can cause intrauterine growth restriction (IUGR), fetal distress, and premature birth image
  • 14.
    10/05/2025 BY ABIE ASCHALE14 PRE ECLAPSIA GESTATION AL HTN MILD Pre existing HTN ECLAPSIA SEVER
  • 15.
    10/05/2025 BY ABIE ASCHALE15 CLASSIFICATION
  • 16.
    10/05/2025 BY ABIE ASCHALE16 1. GESTATIONAL HYPERTENSION BP > 140/90 or more after the 20th week of gestation without significant proteinuria. Gestational hypertension may represent pre-eclampsia prior to proteinuria or chronic hypertension previously unrecognized
  • 17.
    10/05/2025 BY ABIE ASCHALE17 2. PRE-ECLAMPSIA Pre-eclampsia BP > 140/90mmHg Presence of significant proteinuria of > 300 mg/24 hours urine specimen OR > 1+ protein (equivalent to approximately 100mg/dl) on dipstick in at least two randomly collected urine specimen at least 6 hours apart Based on degree of hypertension or proteinuria and involvement of other organ systems
  • 18.
    10/05/2025 BY ABIE ASCHALE18 1. Mild pre-eclampsia The mild form of pre-eclampsia is diagnosed when the Systolic and diastolic blood pressure is between 140-160 and 90-110mmHg respectively without signs of severity.
  • 19.
    10/05/2025 BY ABIE ASCHALE19 2. Severe pre-eclampsia Severe blood pressure elevation: BP > 110 ∕160mmHg measured twice at least six hours apart OR A single measurement of diastolic BP >120mmHg Proteinuria > 5gm/24 hours or >3+ in randomly collected urine Pulmonary edema • Kidney function impairment- Serum creatinine >1.1 mg/Dl • HELLP syndrome
  • 20.
  • 21.
    10/05/2025 BY ABIE ASCHALE21 Elevated Liver Enzymes (HELLP syndrome) - Disseminated intravascular coagulation (DIC) - Headache, visual disturbance and right upper abdominal pain - Oliguria (<400ml in 24hours or 30ml/hour) - Intrauterine growth restriction (IUGR) - Cardiac decompensation, Pulmonary edema, cyanosis
  • 22.
    10/05/2025 BY ABIE ASCHALE22 3. ECLAMPSIA  Eclampsia is the development of new-onset seizures (generalized tonic clonic type), superimposed upon  Preeclampsia, in a woman between 20 weeks of gestation and 4 weeks postpartum. Eclampsia is the convulsive manifestation of preeclampsia absence of other causative conditions (eg, epilepsy, cerebral arterial ischemia and infarction, intracranial hemorrhage, drug use Any convulsion occurring during pregnancy is eclampsia unless proven otherwise .
  • 23.
    10/05/2025 BY ABIE ASCHALE23 DIAGNOSIS History Physical examination laboratory
  • 24.
    10/05/2025 BY ABIE ASCHALE24 MANAGEMENT objectives 1. Control hypertension 2. Prevent convulsion 3. Prevent complication 4. Deliver viable fetus
  • 25.
    10/05/2025 BY ABIE ASCHALE25 GENERAL PRENCIPLES Stabilization of air way, breathing and circulation is the initial step. Always anticipate difficult airway in pregnant patients. Two large-bore intravenous cannula (14G or 16G) should be placed to administer fluids. The Foley catheter should be placed to monitor urine output. Nurse in the left lateral position (30° wedge to the right hip) to prevent supine hypotension syndrome
  • 26.
    10/05/2025 BY ABIE ASCHALE26 Non pharmacologic - Bed rest at home in the lateral decubitus position. - Frequent evaluation of fetal well being - Maternal well being i.e. BP, laboratory - Advise patient to immediately report whenever they develop symptoms of severity such as headache, epigastric pain, blurring of vision etc - Plan termination of pregnancy at term. - If the disease progresses to severe range, manage as severe case. Management of mild pre- eclampsia Most patients are asymptomatic and can be managed conservatively. Such patients are not candidates for urgent delivery.
  • 27.
    10/05/2025 27 Pharmacologic BY ABIEASCHALE BP control  Arterial pressure not greater than 160/110 mmHg in preeclampsia can increase the risk of complication, and it should be controlled.  Goal of BP control is 15–25% reduction in the mean arterial pressure, and  Reduction of pressure to normal levels (<140/90 mmHg) should be avoided as it may compromise placental perfusion. Methyldopa, 250-500mg P.O., 8 to 12 hourly Nifedipine, 10-40mg P.O., BID OR slow release 30-60mg daily N.B. Advise patient
  • 28.
    10/05/2025 BY ABIE ASCHALE28 PREECLAMPSIAAND ECLAMPSIA B. BP CONTROL
  • 29.
    10/05/2025 BY ABIE ASCHALE29 1. Labetalol  Dosage  20 mg IV gradually over 2 minutes. • If BP remains above target level at 10 minutes, give 40 mg IV over 2 minutes. • If BP remains above target level at 20 minutes, give 80 mg IV over 2 minutes.  Cumulative maximum dose is 300 mg. If target BP is not achieved, switch to another class of agent. Hold dose if heart rate <60 beats per minute.  A continuous IV infusion of 1 to 2 mg/minute can be used instead of intermittent therapy or started after 20 mg IV dose.
  • 30.
    10/05/2025 BY ABIE ASCHALE30 2. HYDRALAZINE Repeat BP measurement at 20-minute intervals: •If BP remains above target level at 20 minutes, give 5 or 10 mg IV over 2 minutes, depending on the initial response. Cumulative maximum dose is 20 to 30 mg per treatment event. Initial dose - 5 mg IV gradually over 1 to 2 minutes.* Less predictable than with IV labetalol.
  • 31.
    10/05/2025 BY ABIE ASCHALE31 3. NIFEDIPINE* Immediate release- 10 mg orally. • Repeat BP measurement at 20-minute intervals: • If BP remains above target at 20 minutes, give 10 or 20 mg orally, depending on the initial response. • If BP remains above target at 40 minutes, give 10 or 20 mg orally, depending on the previous response.
  • 32.
    10/05/2025 BY ABIE ASCHALE32 C. CONTROL SEIZURE
  • 33.
    33 FIRST LINE -Magnesium sulphate A loading dose  4gm as 20% solution IV over 10-15 minutes followed by 10gm as 50% IM injection divided on two sides of the buttock, Maintenance dose 5gm every 4 hours as 50% concentration over 2minutes, 2gm IV as 50% solution over 2minutes if convulsion recurs. Reduce the maintenance dose by half if there are signs of renal derangement during labor and for the first 24 hours postpartum
  • 34.
    10/05/2025 BY ABIE ASCHALE34 Monitor toxicity  Loss of deep tendon reflexes  Respiratory depression  Loss of patellar reflex If seizures recur while the patient is receiving magnesium, a repeat (2g) bolus of magnesium may be given. Infusion dose should be reduced in case of renal dysfunction. Serum magnesium level should be monitored Discontinue magnesium sulfate 24 h after delivery or after last seizer
  • 35.
    10/05/2025 BY ABIE ASCHALE35 D. DELIVERY The definitive treatment for eclampsia is prompt delivery;
  • 36.
  • 37.
    10/05/2025 BY ABIE ASCHALE37 Maternal Complications  DIC(3%),  Renal failure (4%)  Adult respiratory distress syndrome (3%).  HELLP syndrome3%,  severe PE 4-12% with  Uncontrolled Hypertension  Risk of Cerebro-vascular Accident  Liver failure (Liver rupture)
  • 38.
    10/05/2025 BY ABIE ASCHALE38  Pulmonary oedema 2%(adult RDS)  Pulmonary hemorrhage  Placental abruption  Eclampsia (risk of aspiration pneumonia)
  • 39.
    10/05/2025 BY ABIE ASCHALE39 Prematurity IUGR Utero-placental insufficiency Oligohydramnios Respiratory distress syndrome Placental abruption  Acute fetal distress  IUFD  Caesarean section,  Admission to SCUBU/NICU Fetal complications
  • 40.
    10/05/2025 BY ABIE ASCHALE40 ICU ADMISSION CRITERIA FOR SEVER CONDITIONS The criteria for ICU admission for preeclampsia and depending on  the severity of the condition,  the availability of resources, and  the clinical judgment of the obstetrician and the intensivist.
  • 41.
    10/05/2025 BY ABIE ASCHALE41 some common indicators may warrant ICU admission are BP > 160/110 mmHg or higher, despite adequate antihypertensive therapy. Severe proteinuria (> 4+ on dipstick or 5 g in 24 hours). Oliguria (UO < 20-30 ml/hr) or AKI (cr. >1.3 mg/dl). Signs of HELLP syndrome Epigastric pain, headache, visual disturbances, or altered mental status (signs of cerebral edema or ischemia). Seizures or coma (eclampsia). Pulmonary edema, signs of fluid overload or cardiopulmonary dysfunction. Fetal distress or IUGR (signs of placental insufficiency or abruption).
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    10/05/2025 BY ABIE ASCHALE42 GOAL OF ICU CARE AND ROLE OF NURSE • Blood pressure control with intravenous antihypertensive a • Magnesium sulfate infusion for seizure prophylaxis and treatment • Fluid management with careful assessment of the fluid balance, urine output, and hemodynamics. • Fetal monitoring with continuous cardiotocography, ultrasound, and biophysical profile • Steroid administration for fetal lung maturation if the gestational age is less than 34 weeks and delivery is anticipated within 7 days.
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    10/05/2025 43 SUMMERY PIH) acondition where a pregnant woman develops high blood pressure after 20 weeks of pregnancy. It can affect the mother’s organs and the baby’s growth and development. PIH can also lead to serious complications such as pre-eclampsia, eclampsia, and HELLP syndrome. PIH is diagnosed by measuring blood pressure and checking for protein in the urine. Treatment options depend on the severity of the condition and the stage of pregnancy. Some common treatments include bed rest, medication, and early delivery. PIH usually goes away after childbirth
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    10/05/2025 BY ABIE ASCHALE44 REFERENCES Overview of pregnancy induced hypertension– UpToDate,2024 Protocol R. 3: Classification of hypertension in pregnancy. 2012; Melkie DA, Internist, Teferra DE, Pediatrician, Assefa DM, Oncologist, et al. Food , Medicine and Healthcare Administration and Control Authority of Ethiopia Standard Treatment Guidelines For General Hospital Diseases Investigations Good Prescribing & Dispensing Practices for Better Health Outcomes. Fmhaca Addis Ababa. 2014;(3):360. Brown MA, Magee LA, Kenny LC, Karumanchi SA, McCarthy FP, Saito S, et al. Hypertensive disorders of pregnancy: ISSHP classification, diagnosis, and management recommendations for international practice. Hypertension. 2018;72(1):24–43. Braunthal S, Brateanu A. Hypertension in pregnancy: Pathophysiology and treatment. SAGE Open Med. 2019;7.  Gouveia, I., Costa, C., Cunha, P. et al. Pre-eclampsia in the intensive care unit: indicators of severity and hospital outcome. Crit Care 9 (Suppl 1), P216 (2005). https://doi.org/10.1186/cc3279
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Editor's Notes

  • #7 2014 EGHTG
  • #22 There could also be atypical eclampsia.
  • #31 * We caution against use of immediate-release oral nifedipine, although some obstetric guidelines have endorsed its use as a first-line option for emergency treatment of acute, severe hypertension in pregnancy or postpartum (other options were labetalol and hydralazine), particularly when IV access is not in place. In most cases, use of immediate-release oral nifedipine will be safe and well tolerated; however, there is a risk of an acute, precipitous fall in blood pressure, which may result in a reduction in uteroplacental perfusion. The immediate-release preparations are also associated with a higher incidence of headache and tachycardia. In nonpregnant adults, the package insert states that "nifedipine capsules should not be used for the acute reduction of blood pressure.