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Update Management of Hypertension
DR. MD. ABDUL MALEQUE
CLINICAL & INTERVENTIONAL CARDIOLOGIST
2020 ISH Global
Hypertension Practice
Guidelines
Definition of
Hypertension
2020 ISHGlobal
Hypertension PracticeGuidelines
Hypertension is diagonosed
when a person’s systolic
blood pressure (SBP) in the
office or clinic is ≥140 mm Hg
and/or their diastolic blood
pressure (DBP) is ≥90 mm Hg
following repeated
Examination.
Classification of Hypertension
Classification of hypertension
based on Office blood pressure (BP) measurement
Hypertension based on Office-, Ambulatory (ABPM)-
and Home Blood Pressure (HBPM) measurement
Classification of Hypertension
Definition of Hypertension- ESC
Optimal : <120/80 mmHg
Normal : <130/ 85 mmHg
High Normal : 130-139/85-89 mmHg
Hypertension:
Grade 1(mild): 140-159/90-99 mmHg
Grade 2 ( mod): 160-179/100-109 mmHg
Grade 3 ( severe): ≥180/110 mmHg
Isolated Systolic Hypertension:
Grade 1: 140-159/ <90 mmHg
Grade 2: ≥160/< 90 mmHg
Office Blood Pressure
Measurement
● 2-3 office visits at 1-4-week
intervals.
● Whenever possible, the
diagnosis should not be made
on a single visit (unless BP
≥180/110 mmHg and CVD).
● If possible and available the
diagnosis of hypertension
should be confirmed by out-
of-office measurement.
Blood Pressure Measurement and Diagnosis of Hypertension
Officebloodpressurelevels(mmHg)
<130/85 130-159/85-99 >160/100
• Confirm within a
few days/weeks.
• Remeasure within
3 years (1 year if
other risk factors).
• If possible confirm with
out-of-office measurement.
• Alternatively confirm with
repeated office visits.
BP Measurement Plan according to Office BP levels
Blood Pressure Measurement and Diagnosis of Hypertension
Treatment Overview
Goals of Therapy
▪Reduce Cardiac and renal morbidity and mortality.
▪Treat to BP <140/90 mmHg or BP <130/80 mmHg in
patients with diabetes or chronic kidney disease.
Non-Pharmacological Treatment
of Hypertension
2020 ISHGlobal
Hypertension PracticeGuidelines
Modification Approximate SBP reduction
(range)
Weight reduction 5–20 mmHg / 10 kg weight loss
Adopt DASH eating
plan
8–14 mmHg
Dietary sodium
reduction
2–8 mmHg
Physical activity 4–9 mmHg
Moderation of alcohol
consumption
2–4 mmHg
Lifestyle Modifications
• Healthy lifestyle choices can prevent or delay the
onset of high BP and can reduce cardiovascular risk.
• Lifestyle modification is also the first line of
antihypertensive treatment.
● Healthy lifestyle choices can prevent or delay
the onset of high BP and can reduce CV risk
● Lifestyle modification is often the first line of
antihypertensive treatment.
● Modifications in lifestyle can also enhance the
effects of antihypertensive treatment.
Non-pharmacological Treatment
Non-pharmacological Treatment - Diet
● Reducing salt added when preparing foods and at the
table. Avoid or limit consumption of high salt foods.
● Eating a diet rich in whole grains, fruits, vegetables, poly-
unsaturated fats and dairy products, such as DASH diet.
● Reducing food high in sugar, saturated fat and trans fats.
● Increasing intake of vegetables high in nitrates (leafy
vegetables and beetroot). Other beneficial foods and
nutrients include those high in magnesium, calcium and
potassium (avocados, nuts, seeds, legumes and tofu).
● Moderate consumption of healthy drinks (coffee,
green and black tea, Karkadé (Hibiscus) tea,
pomegranate juice, beetroot juice and cocoa.
● Moderation of alcohol consumption and
avoidance of binge drinking.
● Reduce weight and avoid obesity.
● Be careful with complementary, alternative or
traditional medicines – little/no evidence.
Non-pharmacological Treatment - Diet
● Smoking cessation.
● Engage in regular moderate intensity aerobic and
resistance exercise, 30 minutes on 5 – 7 days per
week or HIIT (High Intensity Interval Training).
● Reduce stress and introduce mindfulness.
● Reduce exposure to air pollution and cold temperature.
Non-pharmacological Treatment - Lifestyle
Drug Treatment ofHypertension
2020 ISHGlobal
Hypertension PracticeGuidelines
Drug Treatment
of Hypertension:
Thresholds
and Targets
Drug choice
& Sequencing
der the following strategies to improve medication adherence
ucing polypharmacy – use of single pill combinations
e-daily dosing over multiple times per day dosing
ng adherence behavior with daily habits
viding adherence feedback to patients
me BP monitoring
nder packaging of medications
powerment-based counseling for self-management
tronic adherence aids such as mobile phones or short messages ser
disciplinary healthcare team approach (ie, pharmacists) to improve m
herence
1.
Treatments should be evidence-based in relation to morbidity/mortality
prevention.
2. Use a once-daily regimen which provides 24-hour blood pressure control.
3. Treatment should be affordable and/or cost-effective relative to otheragents.
4. Treatments should be well-tolerated.
5.
Evidence of benefits of use of the medication in populations to which it is to be
applied.
Ideal Drug Characteristics
Drug Treatment of Hypertension
Drug Treatment of Hypertension
Drug Treatment Threshold
≥140/90 mmHg (raising to ≥160/100 mmHg
for those at lowest risk)
In established hypertension, uncontrolled by lifestyle measures:
Drug Treatment Target
Optimal: <65 years:
≥65 years:
<130/80 mmHg
<140/90 mmHg
: reduce BP by ≥20/10 mmHg
Class of drug Example Initiating dose Maintenance dose
Diuretics Hydrochlorothiazide 12.5 mg o.d. 12.5-25 mg o.d.
-blockers Atenolol 25-50 mg o.d. 50-100 mg o.d.
Calcium Amlodipine 2.5-5 mg o.d. 5-10 mg o.d.
channel
blockers
-blockers prazosin 2.5 mg o.d 2.5-10mg o.d.
ACE- inhibitors ramipril 1.25-5 mg o.d. 5-10 mg o.d.
Angiotensin-II Losartan 25-50 mg o.d. 50-100 mg o.d.
receptor blockers
Initial monotherapy
• mild primary hypertension
• whose blood pressures are less than 20/10mmHg
above goal.
• Black patients and older patients generally responding
better to monotherapy with a thiazide diuretic or
calcium channel blocker and relatively poorly to an
angiotensin-converting enzyme (ACE) inhibitor
• Younger < 55 yrs – ACE inhibitor
• Beta blockers are not commonly used for initial
monotherapy in the absence of a specific indication
Sequential monotherapy
• Who do not respond well to a moderate dose of
antihypertensive therapy
• Each of the recommended first-line agents will normalize
the blood pressure in 30 to 50 percent of patients with mild
hypertension.
• A patient who is relatively unresponsive to one drug has an
almost 50 percent likelihood of becoming normotensive on
a second drug.
• Thus, in a patient who has little or no fall in blood pressure
after an adequate dose of drug 1, switching to (rather than
adding) drug 2 and, if this is ineffective, switching to drug 3
may allow as many as 60 to 80 percent of patients with
stage 1 hypertension to initially be controlled with a single
agent.
Combination threapy
blood pressure is more than 20/10 mmHg above goal
Fixed-dose combination preparations are available that may
improve patient compliance, blood pressure control
Supine and standing pressures should be measured prior to
the initiation of combination therapy inpatients at increased
risk for orthostatic (postural) hypotension,
long-acting dihydropyridine calcium channel blocker plus a
long-acting angiotensin-converting enzyme
(ACE)inhibitor/ARB
Specific Circumstances:
Resistant Hypertension
Hypertension PracticeGuidelines
● Suspect resistant hypertension if office BP >140/90 mmHg
on treatment with at least 3 antihypertensives (in maximal
or maximally tolerated doses) including a diuretic.
● Exclude pseudo-resistant hypertension (white-coat effect,
non-adherence to treatment, incorrect BP measurements,
errors in antihypertensive therapy) and substance-induced
hypertension as contributors.
● Optimise health behaviours and lifestyle.
Resistant Hypertension
● Consider changes in the diuretic-based treatment prior to
adding the fourth antihypertensive medication.
● Add a low dose of spironolactone (if serum potassium is <4.5
mmol/L and eGFR is >45 ml/min/1.73m2).
● Consider amiloride, doxazosin, eplerenone, clonidine and
beta-blockers as alternatives to spironolactone. If unavailable,
consider any antihypertensive class not already in use.
● Optimally, consider referring to a specialist centre with
sufficient expertise/resources.
Resistant Hypertension
Specific Circumstances:
Secondary Hypertension
Hypertension PracticeGuidelines
• Consider screening for secondary hypertension in:
early onset hypertension, resistant hypertension, sudden BP
control deterioration, hypertensive urgencies and emergencies,
high clinical probability of secondary hypertension.
• Exclude:
pseudo-resistant hypertension and drug/substance-induced
hypertension prior to investigations for secondary hypertension.
Secondary Hypertension
Basic screening for secondary hypertension
thorough history + physical examination (clinical clues) +
basic blood biochemistry (including serum sodium,
potassium, eGFR, TSH) + dipstick urine analysis.
Arrange other investigations for secondary hypertension
(additional biochemistry/imaging/others) based on information
from history, physical examination and basic clinical
investigations and/or if feasible refer to a specialist centre
Secondary Hypertension
Specific Circumstances:
Hypertension inPregnancy
2020 ISHGlobal
Hypertension PracticeGuidelines
● Pre-existing hypertension
● Gestational hypertension
● Pre-eclampsia
● Eclampsia
Hypertension in Pregnancy
Hypertension in Pregnancy
● Affects 5-10% of pregnancies worldwide.
● Maternal risks include placental abruption, stroke
and long term risk of cardiovascular disease.
● Fetal and newborn risks include fetal growth
restriction, pre-term delivery, increased fetal and
neonatal morbidity and mortality.
Prevention of Pre-eclampsia
In women at increased risk of pre-eclampsia:
• Aspirin (75-162 mg/day) and
• Oral calcium (1.5-2 g/day if low dietary intake)
• Increased Risk: 1st pregnancy >40 y age,
pregnancy interval >10 y, BMI >35 kg/m2, multiple
pregnancy, chronic hypertension, diabetes, CKD,
autoimmune disease, hypertension in previous
pregnancy or family history of pre-eclampsia
Hypertension in Pregnancy
Management (1)
Initiate Drug treatment if BP persistently:
• >150/95 mmHg in all women
• >140/90 mmHg if gestational hypertension or
subclinical HMOD
First Line Drug Therapy Options
Methyldopa, beta-blockers (labetalol), and
Dihydropyridine-Calcium Channel Blockers (DHP-CCBs)
Hypertension in Pregnancy
Hypertension in Pregnancy
Delivery in Gestational Hypertension or Pre-Eclampsia
• At 37 weeks if asymptomatic
• Expedite delivery in women with pre-eclampsia with
visual disturbances or haemostatic disorders or HELLP
syndrome.
ESSENTIAL
Post Partum
•
• OPTIMAL:
Lifestyle adjustment
Lifestyle adjustment with annual BP checks
Essential
Optimal
Investigation of Hypertension in Pregnancy
• Urinalysis, complete blood count, liver enzymes,
serum uric acid and serum creatinine.
• Test for proteinuria in early and the second half
of pregnancy. A positive urine dipstick should be
followed with a spot UACR.
• Ultrasound of kidneys, doppler ultrasound of
uterine arteries
Hypertension in Pregnancy
Management (2)
If SBP ≥170mmHg or DBP ≥110mmHg (Emergency):
• Immediately hospitalize
• Initiate IV labetalol (alternative i.v. nicardipine,
esmolol, hydralazine, urapidil), or oral methyldopa or
DHP-CCBs)
• Magnesium
• If pulmonary edema, IV nitroglycerin
Hypertension in Pregnancy
Specific Circumstances:
Hypertensive Emergencies
2020 ISHGlobal
Hypertension PracticeGuidelines
Emergency:
• Severely elevated BP associated with acute
hypertension mediated organ damage (HMOD).
• Requires immediate BP lowering, usually with IV
therapy.
Urgency:
• Severely elevated BP without acute HMOD.
• Can be managed with oral antihypertensive agents.
Hypertensive Emergencies
Hypertensive Emergencies
Assessment
Essential:
• Clinical exam: Evaluate for HMOD including fundoscopy
• Investigations: Hemoglobin, platelets, creatinine, sodium,
potassium, lactate dehydrogenase, haptoglobin,
urinalysis for protein, urine sediment, ECG.
Optimal:
Assessment
In addition, context specific testing:
• Troponins (chest pain or anginal equivalent)
• Chest x-ray (congestion/fluid overload)
• Transthoracic echocardiogram (cardiac structure and
function)
• CT/MRI brain (cerebral hemorrhage/stroke)
• CT-angiography thorax/abdomen (acute aortic disease)
Hypertensive Emergencies
Management
● Requires immediate BP lowering to prevent or
limit further HMOD
● Sparse evidence to guiding management –
recommendations largely consensus based.
● Time to lower BP and magnitude of BP
reduction depends on clinical context.
● IV Labetalol and nicardipine generally safe to
use in all hypertensive emergencies
Hypertensive Emergencies
Hypertensive
Emergencies
Hypertension Management
at aGlance
2020 ISHGlobal
Hypertension PracticeGuidelines
Hypertension
Management
at a Glance
Thank you

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Moins Lecture Collection(Update Management of Hypertension 3).pdf

  • 1. Update Management of Hypertension DR. MD. ABDUL MALEQUE CLINICAL & INTERVENTIONAL CARDIOLOGIST
  • 2. 2020 ISH Global Hypertension Practice Guidelines
  • 3. Definition of Hypertension 2020 ISHGlobal Hypertension PracticeGuidelines Hypertension is diagonosed when a person’s systolic blood pressure (SBP) in the office or clinic is ≥140 mm Hg and/or their diastolic blood pressure (DBP) is ≥90 mm Hg following repeated Examination.
  • 4. Classification of Hypertension Classification of hypertension based on Office blood pressure (BP) measurement
  • 5. Hypertension based on Office-, Ambulatory (ABPM)- and Home Blood Pressure (HBPM) measurement Classification of Hypertension
  • 6. Definition of Hypertension- ESC Optimal : <120/80 mmHg Normal : <130/ 85 mmHg High Normal : 130-139/85-89 mmHg Hypertension: Grade 1(mild): 140-159/90-99 mmHg Grade 2 ( mod): 160-179/100-109 mmHg Grade 3 ( severe): ≥180/110 mmHg Isolated Systolic Hypertension: Grade 1: 140-159/ <90 mmHg Grade 2: ≥160/< 90 mmHg
  • 7. Office Blood Pressure Measurement ● 2-3 office visits at 1-4-week intervals. ● Whenever possible, the diagnosis should not be made on a single visit (unless BP ≥180/110 mmHg and CVD). ● If possible and available the diagnosis of hypertension should be confirmed by out- of-office measurement. Blood Pressure Measurement and Diagnosis of Hypertension
  • 8. Officebloodpressurelevels(mmHg) <130/85 130-159/85-99 >160/100 • Confirm within a few days/weeks. • Remeasure within 3 years (1 year if other risk factors). • If possible confirm with out-of-office measurement. • Alternatively confirm with repeated office visits. BP Measurement Plan according to Office BP levels Blood Pressure Measurement and Diagnosis of Hypertension
  • 10. Goals of Therapy ▪Reduce Cardiac and renal morbidity and mortality. ▪Treat to BP <140/90 mmHg or BP <130/80 mmHg in patients with diabetes or chronic kidney disease.
  • 11. Non-Pharmacological Treatment of Hypertension 2020 ISHGlobal Hypertension PracticeGuidelines
  • 12. Modification Approximate SBP reduction (range) Weight reduction 5–20 mmHg / 10 kg weight loss Adopt DASH eating plan 8–14 mmHg Dietary sodium reduction 2–8 mmHg Physical activity 4–9 mmHg Moderation of alcohol consumption 2–4 mmHg
  • 13. Lifestyle Modifications • Healthy lifestyle choices can prevent or delay the onset of high BP and can reduce cardiovascular risk. • Lifestyle modification is also the first line of antihypertensive treatment.
  • 14.
  • 15. ● Healthy lifestyle choices can prevent or delay the onset of high BP and can reduce CV risk ● Lifestyle modification is often the first line of antihypertensive treatment. ● Modifications in lifestyle can also enhance the effects of antihypertensive treatment. Non-pharmacological Treatment
  • 16. Non-pharmacological Treatment - Diet ● Reducing salt added when preparing foods and at the table. Avoid or limit consumption of high salt foods. ● Eating a diet rich in whole grains, fruits, vegetables, poly- unsaturated fats and dairy products, such as DASH diet. ● Reducing food high in sugar, saturated fat and trans fats. ● Increasing intake of vegetables high in nitrates (leafy vegetables and beetroot). Other beneficial foods and nutrients include those high in magnesium, calcium and potassium (avocados, nuts, seeds, legumes and tofu).
  • 17. ● Moderate consumption of healthy drinks (coffee, green and black tea, Karkadé (Hibiscus) tea, pomegranate juice, beetroot juice and cocoa. ● Moderation of alcohol consumption and avoidance of binge drinking. ● Reduce weight and avoid obesity. ● Be careful with complementary, alternative or traditional medicines – little/no evidence. Non-pharmacological Treatment - Diet
  • 18. ● Smoking cessation. ● Engage in regular moderate intensity aerobic and resistance exercise, 30 minutes on 5 – 7 days per week or HIIT (High Intensity Interval Training). ● Reduce stress and introduce mindfulness. ● Reduce exposure to air pollution and cold temperature. Non-pharmacological Treatment - Lifestyle
  • 19. Drug Treatment ofHypertension 2020 ISHGlobal Hypertension PracticeGuidelines
  • 21.
  • 23. der the following strategies to improve medication adherence ucing polypharmacy – use of single pill combinations e-daily dosing over multiple times per day dosing ng adherence behavior with daily habits viding adherence feedback to patients me BP monitoring nder packaging of medications powerment-based counseling for self-management tronic adherence aids such as mobile phones or short messages ser disciplinary healthcare team approach (ie, pharmacists) to improve m herence
  • 24.
  • 25.
  • 26.
  • 27. 1. Treatments should be evidence-based in relation to morbidity/mortality prevention. 2. Use a once-daily regimen which provides 24-hour blood pressure control. 3. Treatment should be affordable and/or cost-effective relative to otheragents. 4. Treatments should be well-tolerated. 5. Evidence of benefits of use of the medication in populations to which it is to be applied. Ideal Drug Characteristics Drug Treatment of Hypertension
  • 28. Drug Treatment of Hypertension Drug Treatment Threshold ≥140/90 mmHg (raising to ≥160/100 mmHg for those at lowest risk) In established hypertension, uncontrolled by lifestyle measures: Drug Treatment Target Optimal: <65 years: ≥65 years: <130/80 mmHg <140/90 mmHg : reduce BP by ≥20/10 mmHg
  • 29. Class of drug Example Initiating dose Maintenance dose Diuretics Hydrochlorothiazide 12.5 mg o.d. 12.5-25 mg o.d. -blockers Atenolol 25-50 mg o.d. 50-100 mg o.d. Calcium Amlodipine 2.5-5 mg o.d. 5-10 mg o.d. channel blockers -blockers prazosin 2.5 mg o.d 2.5-10mg o.d. ACE- inhibitors ramipril 1.25-5 mg o.d. 5-10 mg o.d. Angiotensin-II Losartan 25-50 mg o.d. 50-100 mg o.d. receptor blockers
  • 30. Initial monotherapy • mild primary hypertension • whose blood pressures are less than 20/10mmHg above goal. • Black patients and older patients generally responding better to monotherapy with a thiazide diuretic or calcium channel blocker and relatively poorly to an angiotensin-converting enzyme (ACE) inhibitor • Younger < 55 yrs – ACE inhibitor • Beta blockers are not commonly used for initial monotherapy in the absence of a specific indication
  • 31. Sequential monotherapy • Who do not respond well to a moderate dose of antihypertensive therapy • Each of the recommended first-line agents will normalize the blood pressure in 30 to 50 percent of patients with mild hypertension. • A patient who is relatively unresponsive to one drug has an almost 50 percent likelihood of becoming normotensive on a second drug. • Thus, in a patient who has little or no fall in blood pressure after an adequate dose of drug 1, switching to (rather than adding) drug 2 and, if this is ineffective, switching to drug 3 may allow as many as 60 to 80 percent of patients with stage 1 hypertension to initially be controlled with a single agent.
  • 32. Combination threapy blood pressure is more than 20/10 mmHg above goal Fixed-dose combination preparations are available that may improve patient compliance, blood pressure control Supine and standing pressures should be measured prior to the initiation of combination therapy inpatients at increased risk for orthostatic (postural) hypotension, long-acting dihydropyridine calcium channel blocker plus a long-acting angiotensin-converting enzyme (ACE)inhibitor/ARB
  • 34. ● Suspect resistant hypertension if office BP >140/90 mmHg on treatment with at least 3 antihypertensives (in maximal or maximally tolerated doses) including a diuretic. ● Exclude pseudo-resistant hypertension (white-coat effect, non-adherence to treatment, incorrect BP measurements, errors in antihypertensive therapy) and substance-induced hypertension as contributors. ● Optimise health behaviours and lifestyle. Resistant Hypertension
  • 35. ● Consider changes in the diuretic-based treatment prior to adding the fourth antihypertensive medication. ● Add a low dose of spironolactone (if serum potassium is <4.5 mmol/L and eGFR is >45 ml/min/1.73m2). ● Consider amiloride, doxazosin, eplerenone, clonidine and beta-blockers as alternatives to spironolactone. If unavailable, consider any antihypertensive class not already in use. ● Optimally, consider referring to a specialist centre with sufficient expertise/resources. Resistant Hypertension
  • 37. • Consider screening for secondary hypertension in: early onset hypertension, resistant hypertension, sudden BP control deterioration, hypertensive urgencies and emergencies, high clinical probability of secondary hypertension. • Exclude: pseudo-resistant hypertension and drug/substance-induced hypertension prior to investigations for secondary hypertension. Secondary Hypertension
  • 38. Basic screening for secondary hypertension thorough history + physical examination (clinical clues) + basic blood biochemistry (including serum sodium, potassium, eGFR, TSH) + dipstick urine analysis. Arrange other investigations for secondary hypertension (additional biochemistry/imaging/others) based on information from history, physical examination and basic clinical investigations and/or if feasible refer to a specialist centre Secondary Hypertension
  • 39. Specific Circumstances: Hypertension inPregnancy 2020 ISHGlobal Hypertension PracticeGuidelines
  • 40. ● Pre-existing hypertension ● Gestational hypertension ● Pre-eclampsia ● Eclampsia Hypertension in Pregnancy
  • 41. Hypertension in Pregnancy ● Affects 5-10% of pregnancies worldwide. ● Maternal risks include placental abruption, stroke and long term risk of cardiovascular disease. ● Fetal and newborn risks include fetal growth restriction, pre-term delivery, increased fetal and neonatal morbidity and mortality.
  • 42. Prevention of Pre-eclampsia In women at increased risk of pre-eclampsia: • Aspirin (75-162 mg/day) and • Oral calcium (1.5-2 g/day if low dietary intake) • Increased Risk: 1st pregnancy >40 y age, pregnancy interval >10 y, BMI >35 kg/m2, multiple pregnancy, chronic hypertension, diabetes, CKD, autoimmune disease, hypertension in previous pregnancy or family history of pre-eclampsia Hypertension in Pregnancy
  • 43. Management (1) Initiate Drug treatment if BP persistently: • >150/95 mmHg in all women • >140/90 mmHg if gestational hypertension or subclinical HMOD First Line Drug Therapy Options Methyldopa, beta-blockers (labetalol), and Dihydropyridine-Calcium Channel Blockers (DHP-CCBs) Hypertension in Pregnancy
  • 44. Hypertension in Pregnancy Delivery in Gestational Hypertension or Pre-Eclampsia • At 37 weeks if asymptomatic • Expedite delivery in women with pre-eclampsia with visual disturbances or haemostatic disorders or HELLP syndrome. ESSENTIAL Post Partum • • OPTIMAL: Lifestyle adjustment Lifestyle adjustment with annual BP checks
  • 45. Essential Optimal Investigation of Hypertension in Pregnancy • Urinalysis, complete blood count, liver enzymes, serum uric acid and serum creatinine. • Test for proteinuria in early and the second half of pregnancy. A positive urine dipstick should be followed with a spot UACR. • Ultrasound of kidneys, doppler ultrasound of uterine arteries Hypertension in Pregnancy
  • 46. Management (2) If SBP ≥170mmHg or DBP ≥110mmHg (Emergency): • Immediately hospitalize • Initiate IV labetalol (alternative i.v. nicardipine, esmolol, hydralazine, urapidil), or oral methyldopa or DHP-CCBs) • Magnesium • If pulmonary edema, IV nitroglycerin Hypertension in Pregnancy
  • 47. Specific Circumstances: Hypertensive Emergencies 2020 ISHGlobal Hypertension PracticeGuidelines
  • 48. Emergency: • Severely elevated BP associated with acute hypertension mediated organ damage (HMOD). • Requires immediate BP lowering, usually with IV therapy. Urgency: • Severely elevated BP without acute HMOD. • Can be managed with oral antihypertensive agents. Hypertensive Emergencies
  • 49. Hypertensive Emergencies Assessment Essential: • Clinical exam: Evaluate for HMOD including fundoscopy • Investigations: Hemoglobin, platelets, creatinine, sodium, potassium, lactate dehydrogenase, haptoglobin, urinalysis for protein, urine sediment, ECG.
  • 50. Optimal: Assessment In addition, context specific testing: • Troponins (chest pain or anginal equivalent) • Chest x-ray (congestion/fluid overload) • Transthoracic echocardiogram (cardiac structure and function) • CT/MRI brain (cerebral hemorrhage/stroke) • CT-angiography thorax/abdomen (acute aortic disease) Hypertensive Emergencies
  • 51. Management ● Requires immediate BP lowering to prevent or limit further HMOD ● Sparse evidence to guiding management – recommendations largely consensus based. ● Time to lower BP and magnitude of BP reduction depends on clinical context. ● IV Labetalol and nicardipine generally safe to use in all hypertensive emergencies Hypertensive Emergencies
  • 53. Hypertension Management at aGlance 2020 ISHGlobal Hypertension PracticeGuidelines