Table 2.
Hypertensive states and suggested plan of action | Pharmacotherapy choices |
---|---|
Acute severe hypertension Confirm hypertension, re-assess in 7 days, undertake secondary screen if applicable. Confirm adherence in known hypertension. Aim to achieve target BP in 6–12 weeks |
Confirmed new hypertension: angiotensin-converting enzyme inhibitor/angiotensin receptor blocker or calcium channel blocker as per NG 136 Pre-existing hypertension: increase doses of current medications, consider adding medications as per NG 136 |
Malignant hypertension/accelerated hypertension (eye changes only) Start oral therapy, monitor response, arrange frequent follow up Aim to achieve target BP in days to weeks (preferably by 6 weeks, at the least by 12 weeks) |
Oral atenolol 25 mg OR Oral amlodipine 5 mg/Or oral long acting nifedipine 30 mga |
Hypertensive encephalopathy Invasive BP monitoring Reduce mean arterial pressure (MAP) by no more than 20–25% over few hours and/or Reduce diastolic BP (DBP) to 100–110 mmHg |
IV labetalol bolus 0.25–0.5 mg/kg (usually 50 mg bolus given 1–2 min, repeated within 5 min if necessary, not exceeding 200 mg), or can be administered as 15–20 mg/h continuous infusion, adjusting every 15 mins OR IV nicardipine 3–5 mg/h for 15 min, adjust with increments of 0.5 or 1 mg every 15 min, not exceeding 15 mg/h overall |
Intracerebral haemorrhage Invasive BP monitoring Reduce systolic BP (SBP) by 20–25% BP targets in the range of 140–180 mmHg SBP and 90–110 mmHg DBP |
IV labetalol bolus 0.25–0.5 mg/kg (usually 50 mg bolus given over 1–2 min, repeated within 5 min if necessary, not exceeding 200 mg), or can be administered as 15–20 mg/hr continuous infusion, adjusting every 15 min OR IV nicardipine 3–5 mg/h for 15 min, adjust with increments of 0.5 or 1 mg every 15 mins, not exceeding 15 mg/h overall |
Ischaemic stroke Reduce BP only if specific criteria met δ. Reduce MAP by no more than 15% in patients with BP ≥ 220/120 mmHg |
IV labetalol bolus 0.25–0.5 mg/kg (usually 50 mg bolus given over a minute, repeated within 5 min if necessary, not exceeding 200 mg), or can be administered as 15–20 mg/hr continuous infusion, adjusting every 15 min OR IV nicardipine 3-5 mg/h for 15 min, adjust with increments of 0.5 or 1 mg every 15 mins, not exceeding 15 mg/h overall |
Subarachnoid haemorrhage Pain control is essential Weigh benefits and risks of reduction in BP considering cerebral vasospasm and hypoperfusion Target SBP range 140–180 mmHg |
Nimodipine 60 mg orally, nasogastric, or gastric tube every 4 h, usually started within 96 h of onset of subarachnoid haemorrhage and continued for 21 days. Oral therapy preferred over other routes. |
Acute aortic syndromes Pain, and anxiety control is crucial Invasive BP monitoring Reduce HR to <60 bpm, and Reduce SBP to 120 mmHg while monitoring for adequate perfusion through the false lumen |
IV labetalol bolus 0.25–0.5 mg/kg (usually 50 mg bolus given over 1–2 min, repeated within 5 min if necessary, not exceeding 200 mg), or can be administered as 15–20 mg/h continuous infusion, adjusting every 15 min OR IV nicardipine 3–5 mg/h for 15 min, adjust with increments of 0.5 or 1 mg every 15 mins, not exceeding 15 mg/h overall OR IV nitroprusside initially started at 0.5–1.5 mcg/kg/min increased every 5 min by 0.5 mcg/kg/min if necessary, usual maintenance dose 10–200 mcg/min. |
Acute coronary syndrome Prioritise revascularisation treatment strategy, pain and anxiety management Reduce SBP/ MAP by no more than 20–25% and avoid DBP < 70 mmHg |
IV Glyceryl Trinitrate (GTN) started at 15–20 mcg/min, can increase/decrease by 5–10 mcg/min every 15–30 min, overall dose adjustment as per individual needs are met. OR IV labetalol 20 mg/h infusion, adjust every 15 min, can be administered in intermittent boluses |
Left ventricular failure/Pulmonary oedema Reduce SBP/ MAP by not more than 20–25% |
IV GTN 5-200 mcg/min (starting doses can start from 20–25 mcg/min), can increase/decrease by 10–15 mcg/min subsequently until required effect achieved. IV furosemide 40–80 mg (0.5–2 mg/kg) for relief of congestive symptoms (can be administered as infusion or IV boluses, subsequently oral) |
Severe pre-eclampsia/eclampsia Reduce to target BP of pre-pregnancy level or ≤140/90 mm Hg in hypertension-naïve patients, reduce SBP by not more than 20% MAP in patients with very high BP values (>200/120 mmHg). Consider benefits and risks of delivery versus expectant management (NG133) Monitor maternal and foetal parameters closely. |
IV magnesium, loading dose 4 g over 5–15 min followed by infusion of 1 g/h for 24 h, further dose of 2–4 g given over 5–15 min if recurrent seizures. Labetalol 200 mg oral stat or slow IV bolus injection 50 mg (over 1–2 min) which can be repeated. If IV infusion is required, at ~20–40 mg/h, up titrate as necessary. Consider addition of oral long acting nifedipine. Consider IV hydralazine slow IV injection 5–10 mg which maybe repeated or IV infusion 200–300 mcg/min: usual maintenance 50–150 mcg/min. monitor for fluid and volume status. |
Phaeochromocytoma/ adrenergic crisis Maintain adequate hydration |
Alpha blockade with phenoxybenzamine starting at 10 mg/day, with volume expansion using fluid and salt. Phentolamine may be used where available. Doxazosin 1–2 mg starting doses may be a suitable alternative. Beta-blockers are employed only if tachycardia ensues |
BP blood pressure, MAP mean arterial pressure, SBP systolic blood pressure, DBP diastolic blood pressure, NG- NICE guidelines, EOD end organ damage, GTN glyceryl trinitrate
aLong-acting calcium channel blocker such as Adalat La 30 mg may be considered when available. Do not use short-acting nifedipine. δ1. If BP is greater than >220/120 mmHg in the acute phase. Lower MAP by no more than 15% over 24 h. 2. Reduce BP to 185/110 mmHg if patient is a candidate for thrombolysis 3. Reduce BP according to the concomitant emergency state as indicated. Please consult local guidelines, when available. Specialist advise should be sought for each hypertensive state, such as in the presence of renal dysfunction seek renal specialist/team advice.