Hypertension in Pregnancy: Difference between revisions

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!Adverse conditions (that increase the risk of severe complications)
!Adverse conditions (that increase the risk of severe complications)
!Severe complications (that warrant delivery)
!Severe complications (that warrant delivery)
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|CNS
|CNS
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* Eclampsia
* Eclampsia
;
* PRES
: PRES
* Cortical blindness or retinal detachment
;
* Glasgow coma scale < 13
: Cortical blindness or retinal detachment
* Stroke, TIA, or RIND
;
: Glasgow coma scale < 13
;
: Stroke, TIA, or RIND
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|Cardiorespiratory
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:* Chest pain/dyspnoea
:* Oxygen saturation < 97%
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:* Uncontrolled severe hypertension (over a period of 12hr despite use of three antihypertensive agents),
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:* Oxygen saturation < 90%, need for ⩾ 50% oxygen for > 1hr, intubation (other than for Caesarean section), pulmonary oedema
:* Positive inotropic support
:* Myocardial ischaemia or infarction
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|Haematological
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;  {| class="wikitable" !Organ system affected !Adverse conditions (that increase the risk of severe complications) !Severe complications (that warrant delivery) |- |CNS |
; ○
: Headache/visual symptoms |
; ○
: Eclampsia
; ○
: PRES
; ○
: Cortical blindness or retinal detachment
; ○
: Glasgow coma scale < 13
; ○
: Stroke, TIA, or RIND |- | colspan="3" | |- |Cardiorespiratory |
; ○
: Chest pain/dyspnoea
; ○
: Oxygen saturation < 97% [79] |
; ○
: Uncontrolled severe hypertension (over a period of 12hr despite use of three antihypertensive agents),
; ○
: Oxygen saturation < 90%, need for ⩾ 50% oxygen for > 1hr, intubation (other than for Caesarean section), pulmonary oedema
; ○
: Positive inotropic support
; ○
: Myocardial ischaemia or infarction |- | colspan="3" | |- |Haematological |
; ○
: Elevated WBC count
: Elevated WBC count
; ○
; ○
: Elevated INR or aPTT [80]
: Elevated INR or aPTT [80]
; ○
; ○
: Low platelet count |
: Low platelet count
; ○
|
: Platelet count < 50x109/L
: Platelet count < 50x109/L
; ○
; ○
: Transfusion of any blood product |- | colspan="3" | |- |Renal |
: Transfusion of any blood product
; ○
|-
|Renal
|
: Elevated serum creatinine [81]
: Elevated serum creatinine [81]
; ○
; ○
: Elevated serum uric acid |
: Elevated serum uric acid
; ○
|
: Acute kidney injury (creatinine > 150 μM with no prior renal disease)
: Acute kidney injury (creatinine > 150 μM with no prior renal disease)
; ○
; ○
: New indication for dialysis |- | colspan="3" | |- |Hepatic |
: New indication for dialysis
; ○
|-
|Hepatic
|
: Nausea or vomiting
: Nausea or vomiting
; ○
; ○
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: Elevated serum AST, ALT, LDH, or bilirubin
: Elevated serum AST, ALT, LDH, or bilirubin
; ○
; ○
: Low plasma albumin [82] |
: Low plasma albumin
; ○
|
: Hepatic dysfunction (INR > 2 in absence of DIC or warfarin)
: Hepatic dysfunction (INR > 2 in absence of DIC or warfarin)
; ○
; ○
: Hepatic haematoma or rupture |- | colspan="3" | |- |Feto-placental |
: Hepatic haematoma or rupture
; ○
|-
|Feto-placental
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: Non-reassuring FHR
: Non-reassuring FHR
; ○
; ○
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: Oligohydramnios
: Oligohydramnios
; ○
; ○
: Absent or reversed end-diastolic flow by Doppler velocimetry |
: Absent or reversed end-diastolic flow by Doppler velocimetry
|
: Non-reassuring FHR
; ○
; ○
: Abruption with evidence of maternal or fetal compromise
: IUGR [83], [84]
; ○
; ○
: Reverse ductus venosus A wave [85], [86]
: Oligohydramnios
; ○
; ○
: Stillbirth |} AST, aspartate aminotransferase; ALT, alanine aminotransferase; DIC, disseminated intravascular coagulation; FHR, fetal heart rate; LDH, lactate dehydrogenase; PRES, posterior reversible leukoencephalopathy syndrome; RIND, reversible neurological deficit < 48hr; RUQ, right upper quadrant; TIA, transient ischaemic attack. <ref name=":0" />
: Absent or reversed end-diastolic flow by Doppler velocimetry
|}
ST, aspartate aminotransferase; ALT, alanine aminotransferase; DIC, disseminated intravascular coagulation; FHR, fetal heart rate; LDH, lactate dehydrogenase; PRES, posterior reversible leukoencephalopathy syndrome; RIND, reversible neurological deficit < 48hr; RUQ, right upper quadrant; TIA, transient ischaemic attack.<ref name=":0" />
:


== Causes and Risk factor ==
== Causes and Risk factor ==

Revision as of 12:27, 27 August 2020

Introduction[edit | edit source]

Hypertensive disorders of pregnancy is a leading cause of maternal and neonatal morbidity and mortality. Hypertension in pregnancy should be defined as a hospital systolic blood pressure (SBP) ⩾ 140 mmHg and/or dystolic blood pressure (DBP) ⩾ 90 mmHg, based on the average of at least two measurements, taken at least 15 min apart, using the same arm.[1]

Classification[edit | edit source]

A. Pre-existing (chronic) hypertension This is defined as hypertension that was present either pre-pregnancy or that develops at <20 weeks of gestation
• With comorbid condition(s) Comorbid conditions (e.g., pre-gestational type I or II diabetes mellitus or kidney disease) warrant tighter BP control outside of pregnancy because of their association with heightened cardiovascular risk
• With evidence of preeclampsia This is also known as ‘superimposed preeclampsia’ and is defined by the development of one or more of the following at ⩾ 20 weeks:
  • Resistant hypertension, or
  • New or worsening proteinuria, or
  • One/more adverse condition(s) or
  • One/more severe complication(s)

Severe preeclampsia is defined as preeclampsia with one or more severe complication(s)

B. Gestational hypertension This is defined as hypertension that develops for the first time at ⩾ 20 weeks of gestation.
• With comorbid condition(s) Comorbid conditions (e.g., pregestational type I or II diabetes mellitus or kidney disease) warrant tighter BP control outside of pregnancy because of their association with heightened cardiovascular risk
• With evidence of preeclampsia Evidence of preeclampsia may appear many weeks after the onset of gestational hypertension.
C. Preeclampsia Preeclampsia is defined by gestational hypertension and one or more of the following:
  • New proteinuria, or
  • One/more adverse conditions, or
  • One/more severe complication(s)
Severe preeclampsia is defined as preeclampsia with one or more severe complication(s)
’Other hypertensive effects’∗
Transient hypertensive effect Elevated BP may be due to environmental stimuli or the pain of labour, for example
White coat hypertensive effect BP that is elevated in the office (sBP ⩾ 140 mmHg or dBP ⩾ 90 mmHg) but is consistently normal outside of the office (<135/85 mmHg) by ABPM or HBPM
Masked hypertensive effect BP that is consistently normal in the office (sBP < 140 mmHg or dBP < 90 mmHg) but is elevated outside of the office (⩾135/85 mmHg) by ABPM or repeated HBPM

ABPM, ambulatory BP monitoring; BP, blood pressure; HBPM, home BP monitoring.[1]

Adverse conditions and severe complications of preeclampsia.[edit | edit source]

Organ system affected Adverse conditions (that increase the risk of severe complications) Severe complications (that warrant delivery)
CNS Headache/visual symptoms
  • Eclampsia
  • PRES
  • Cortical blindness or retinal detachment
  • Glasgow coma scale < 13
  • Stroke, TIA, or RIND
Cardiorespiratory
  • Chest pain/dyspnoea
  • Oxygen saturation < 97%
  • Uncontrolled severe hypertension (over a period of 12hr despite use of three antihypertensive agents),
  • Oxygen saturation < 90%, need for ⩾ 50% oxygen for > 1hr, intubation (other than for Caesarean section), pulmonary oedema
  • Positive inotropic support
  • Myocardial ischaemia or infarction
Haematological
Elevated WBC count
Elevated INR or aPTT [80]
Low platelet count
Platelet count < 50x109/L
Transfusion of any blood product
Renal
Elevated serum creatinine [81]
Elevated serum uric acid
Acute kidney injury (creatinine > 150 μM with no prior renal disease)
New indication for dialysis
Hepatic
Nausea or vomiting
RUQ or epigastric pain
Elevated serum AST, ALT, LDH, or bilirubin
Low plasma albumin
Hepatic dysfunction (INR > 2 in absence of DIC or warfarin)
Hepatic haematoma or rupture
Feto-placental
Non-reassuring FHR
IUGR [83], [84]
Oligohydramnios
Absent or reversed end-diastolic flow by Doppler velocimetry
Non-reassuring FHR
IUGR [83], [84]
Oligohydramnios
Absent or reversed end-diastolic flow by Doppler velocimetry

ST, aspartate aminotransferase; ALT, alanine aminotransferase; DIC, disseminated intravascular coagulation; FHR, fetal heart rate; LDH, lactate dehydrogenase; PRES, posterior reversible leukoencephalopathy syndrome; RIND, reversible neurological deficit < 48hr; RUQ, right upper quadrant; TIA, transient ischaemic attack.[1]

Causes and Risk factor[edit | edit source]

Pathological process[edit | edit source]

Epidemiology[edit | edit source]

Medical management[edit | edit source]

Physiotherapy intervention[edit | edit source]

Resources[edit | edit source]

  • bulleted list
  • x

or

  1. numbered list
  2. x

References[edit | edit source]

  1. 1.0 1.1 1.2 Magee LA, Pels A, Helewa M, Rey E, von Dadelszen P. Diagnosis, evaluation, and management of the hypertensive disorders of pregnancy. Pregnancy Hypertension: An International Journal of Women's Cardiovascular Health. 2014 Apr 1;4(2):105-45.