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Stroke has a global incidence of 15 million people per year, is the third leading cause of death and is the most common cause of disability in the western world.1 High-blood pressure (BP) is the leading modifiable risk factor for both ischaemic and haemorrhagic stroke2 affecting 1 billion people worldwide.3 In acute stroke, 75% of patients have high BP and 50% of those have a prior history of hypertension.4 ,5 Although BP spontaneously falls in two-thirds of patients in the first week following stroke,4 one-third remain hypertensive and have an increased risk of a poor outcome.6 Data from the first International Stroke Trial demonstrated a U-shaped relationship between baseline systolic BP (SBP) and outcome, such that both high and low SBP were independently associated with increased early death and late death or dependency.7 In addition, high SBP is associated with an increased risk of early stroke recurrence.7 ,8 Post hoc analyses from several acute stroke clinical trials suggest that as well as increased SBP, other haemodynamic variables including higher peak SBP, mean arterial pressure (MAP), pulse pressure and increased SBP variability, are each associated with poor functional outcome,9 early neurological deterioration,10 recurrent stroke and death.11
The acute hypertensive response seen in stroke has numerous potential causes including: fluctuations in, or elevation of, pre-existing hypertension; infection; pain, for example, due to urinary retention; stress related to hospitalisation; activation of cortisol, natriuretic peptide, renin–angiotensin–aldosterone and sympathetic neuroendocrine systems; impaired cardiac baroreceptor sensitivity; and raised intracranial pressure (Cushing's reflex).12–15 Although low BP is far less common in acute stroke, it is associated with a poor outcome.7 Potential causes include sepsis, cardiac arrhythmias, heart failure and ischaemia, hypovolaemia and aortic dissection.16
Normal cerebral autoregulation, which maintains cerebral blood flow (CBF) despite fluctuations in cerebral perfusion pressure (CPP) between 50 and 150 mm Hg, is impaired in acute stroke resulting in cerebral perfusion having a linear relationship with CPP and therefore MAP.17 Rapid, large falls in BP could reduce CBF leading to extension of cerebral infarction,18 or perihaematomal ischaemia.19 Equally, with higher BP there is increased risk of haematoma expansion in intracerebral haemorrhage (ICH), haemorrhagic transformation in animal models of ischaemic stroke (IS) and cerebral oedema, in both types of stroke.6 ,20
The debate surrounding whether high BP should or should not be treated in the context of acute stroke started over 30 years ago21 ,22 and despite large clinical trials the answer remains largely unclear. In this review, we discuss the evidence for BP modulation in acute stroke, the challenges and issues raised, and look to on-going and future trials that may provide some clarity in this controversial area.
The α-2-adrenoreceptor agonist, clonidine, was tested in a small randomised controlled trial (RCT), which allocated 16 participants with middle cerebral artery infarction within 72 hours of onset and high baseline BP (SBP 170–220 mm Hg, diastolic BP (DBP) 95–120 mm Hg) to nicardipine 20 mg, captopril 12.5 mg, clonidine 0.1 mg, or placebo given every 8 hours for 3 days.24 BP fell in all groups but there was no significant difference in BP between the two main groups and no difference in stroke outcome, measured using the National Institutes of Health Stroke Scale (NIHSS), over the 3 days of treatment. To date, no large RCTs have assessed the use of α-2-adrenoreceptor agonists in acute stroke.
In three small RCTs of acute IS (AIS) oral perindopril,43 lisinopril44 and captopril24 independently reduced BP, while preserving CBF, although no differences in neurological impairment (NIHSS) or functional outcome (modified Rankin Scale (mRS)) were seen between groups.44
The Controlling Hypertension and Hypotension Immediately Post-Stroke (CHHIPS) trial25 randomised 179 patients with either IS or ICH within 36 hours of ictus and SBP >160 mm Hg to oral labetalol (50 mg), lisinopril (5 mg) or placebo in those without dysphagia, or intravenous labetalol (50 mg), sublingual lisinopril (5 mg), or placebo in those with dysphagia. Dose escalation occurred if participants did not reach target SBP (145–155 or 15 mm Hg reduction) at 4 and 8 hours postrandomisation. Lisinopril reduced mean BP by 14/7 mm Hg compared with placebo between randomisation and 24 hours. Following 14 days of treatment there was no difference in functional outcome (mRS >3) between treatment and control (relative risk (RR) 1.03, 95% CI 0.8 to 1.33, p=0.82), although lisinopril was safe with no increased reporting of serious adverse events.
In the prehospital environment the Paramedic Initiated Lisinopril For Acute Stroke Treatment (PIL-FAST) study randomised 14 patients with new unilateral arm weakness within 3 hours of onset and SBP >160 mm Hg to either sublingual lisinopril (5 mg) or placebo for a total of 7 days.26 BP fell in the lisinopril group compared to control by hospital admission and persisted for the duration of treatment. As a feasibility trial it was successful but was not powered to assess efficacy.
Angiotensin receptor antagonists
The Acute Candesartan Cilexetil Therapy in Stroke Survivors (ACCESS) study,27 randomised 339 participants with IS and elevated BP (≥180/105 mm Hg) to 7 days of oral candesartan or placebo within 36 hours of admission. Mortality at 12 months and cardiovascular events (secondary outcome) were significantly reduced in the candesartan arm, although there was no significant effect on functional outcome (Barthel index (BI), primary outcome) at 3 months, or on BP throughout the 12 months of the trial.
A post hoc subgroup analysis of the multinational Prevention Regimen for Effectively Avoiding Second Strokes (PRoFESS) trial28 examined the effect of adding telmisartan versus placebo to standard antihypertensive management in 1360 patients with mild IS recruited within 72 hours of ictus. Telmisartan lowered SBP and DBP by 6–7 and 2–4 mm Hg respectively compared with placebo and was safe with no excess of adverse events. However, telmisartan did not influence functional outcome (mRS at day 30, primary outcome) or death, stroke recurrence and cardiovascular events at days 7, 30 or 90. In contrast to the ACCESS study, PRoFESS participants had lower BP at randomisation, milder strokes, enhanced antihypertensive therapy, were recruited later (58 vs 29 hours) and had a longer period of treatment (30 months vs 7 days), which may account for the dissimilar findings between the trials.
Following ACCESS, the Scandinavian Candesartan Acute Stroke Trial (SCAST)29 recruited 2029 participants with acute stroke (IS and ICH) within 30 hours of onset and SBP ≥140 mm Hg. Patients were randomised to either candesartan 4 mg with dose escalation up to 16 mg, or placebo for 7 days. BP fell in both groups over the treatment period and was significantly lower in the candesartan arm compared to placebo (day 7 mean BP: 147/82 vs 152/84 mm Hg). Co-primary end points were measured at 6 months: a composite of vascular death, myocardial infarction and stroke was neutral; and functional outcome measured by a shift in mRS suggested a higher risk of poor outcome in those randomised to candesartan, but was not statistically significant given the two primary outcomes (adjusted common OR (acOR) 1.17, 95% CI 1.00 to 1.38, p=0.048). A prespecified subgroup analysis of those with ICH (n=274) also found that candesartan was associated with an increased risk of poor outcome (acOR 1.61, 95% CI 1.03 to 2.50, p=0.036).45
Several smaller, underpowered trials have assessed candesartan,46 irbesartan,47 telmisartan,30 and valsartan48 in AIS. Telmisartan did not alter CBF or BP acutely.30 The Valsartan Efficacy oN modesT blood pressUre Reduction in acute ischaemic stroke (VENTURE) trial,48 randomised 393 South Korean patients with AIS within 24 hours of onset and SBP 150–185 mm Hg to oral valsartan 80 mg daily with dose escalation, or placebo for 7 days. Valsartan significantly reduced mean DBP at day 7 compared with placebo (83.1 vs 84.8 mm Hg), while SBP was not significantly reduced. The primary outcome of death or dependency at 90 days (mRS >3) was neutral, but early neurological deterioration within 7 days was significantly higher in the valsartan group (16.6% vs 6%, OR 2.43, 95% CI 1.25 to 4.73, p=0.008); mainly due to stroke progression in those with large artery atherosclerosis as the cause of their stroke and angiographically confirmed large-artery stenosis or occlusion.
These neutral and negative findings may indicate that angiotensin receptor antagonists (ARAs) have undesirable properties in acute stroke or that gradual and late treatment of BP is ‘too little too late’, thus reducing cerebral perfusion and increasing brain injury.
The single-centre β-blocker stroke (BEST) trial31 randomised 302 patients with clinically diagnosed strokes within 48 hours of onset to oral propranolol, atenolol or placebo. There was a greater fall in mean BP in the first 24 hours of treatment (6–9% vs 2%) and an increase in early and later death in those assigned to β-blockers compared to placebo. The negative inotropic effects of β-blockers may worsen cerebral perfusion in acute stroke and thus explain this finding, although pathophysiological trial data are lacking (table 2).
In those randomised to labetalol (a mixed α and β adrenergic antagonist) in the CHHIPS trial,25 SBP fell by 7 mm Hg at 24 hours. In contrast to the BEST trial, labetalol was safe with no increase in serious adverse events, early neurological deterioration or death. Overall, the active treatment group (labetalol and lisinopril combined) had reduced 90-day mortality compared to the placebo group (HR 0.40, 95% CI 0.2 to 1.0, p=0.05) but the study was not powered for this outcome.
Calcium channel antagonists
Early studies showed significant drops in BP in patients who received nimodipine66 or nicardipine,24 with the latter suggesting that large drops in BP due to nicardipine were associated with reduced regional CBF to infarcted tissue. Contrary to this, other small trials reported positive results of oral67 ,68 and intravenous nimodipine69 on long-term recovery in AIS, prompting the need for a larger RCT.
The Intravenous Nimodipine West European Stroke Trial (INWEST)32 randomised 295 patients with AIS within 24 hours of onset to intravenous nimodipine at 1 mg/hour (low dose) or 2 mg/hour (high dose) for 5 days then 120 mg daily (orally) for a total of 21 days, or placebo. Recruitment was stopped early due to statistically significant unfavourable functional outcomes (BI and Orgogozo neurological impairment scale) in the nimodipine groups compared with placebo at both 21 days and 6 months. Over the first 2 days, mean BP significantly fell from baseline in the treatment arms compared with placebo.70 In a subsequent analysis, DBP reduction in the high-dose treatment arm was associated with a poor functional outcome at day 21, while those who received high-dose nimodipine and had a large (≥20%) fall in DBP had an increased risk of death or dependency and death at day 21.70 A similar but unpublished trial in the USA had comparable results.71
A further trial of oral nimodipine recruited 454 patients within 6 hours of stroke ictus in primary care.33 At 24 hours there was no significant difference in BP between the nimodipine and control groups, and the primary outcome of death or dependency (mRS >3) at 3 months was neutral (RR 1.2, 95% CI 0.9 to 1.6). This trial was stopped early because a Cochrane systematic review involving 7665 patients from 29 trials of calcium channel antagonists (CCA) in AIS revealed no treatment effect on functional outcome or death at the end of follow-up.72 Interestingly, a subgroup analysis of unpublished and methodologically sound trials yielded a statistically significant unfavourable treatment effect indicative of publication bias (RR 1.14, CI 95% 1.0 to 1.3); overall, good quality trials produced a statistically significant negative treatment effect (RR 1.09, 95% CI 1.02 to 1.16).34 Unfortunately, much of the drive to test CCA, especially nimodipine, was driven by early positive data.67–69 ,73
There is limited data on diuretics in acute stroke.23 One small RCT randomised 37 hypertensive patients with AIS within 96 hours of onset to bendroflumethiazide (a thiazide-like diuretic) 2.5 mg daily or placebo for 7 days.35 Although mean SBP was lower in the treatment group compared with placebo within 70 hours of randomisation (156 vs 176 mm Hg), there was no difference in BP between the arms at day 7. Measures of CBF and cardiac baroreceptor sensitivity showed no significant change between groups at either time point in the trial, suggesting that bendroflumethiazide is an ineffective agent for use in acute patients with stroke.
A systematic review of several small pilot studies assessing magnesium in acute stroke reported a non-significant reduction in death or disability in patients treated with magnesium (OR 0.73, 95% CI 0.38 to 1.41).74 A large RCT allocated 2589 patients with AIS within 12 hours of onset to intravenous magnesium sulfate slow bolus (16 mmol) followed by infusion (65 mmol) over 24 hours, or placebo.36 Although BP fell by 4/3 mm Hg between baseline and 24 hours in the magnesium group compared with placebo, the only significant difference in BP was during the initial infusion. The primary outcome of death and disability at day 90 (BI <95 and mRS >1 combined) was neutral, but there was a trend towards increased mortality in the magnesium group (HR 1.18, 95% CI 0.97 to 1.42, p=0.098). In a prespecified subgroup of non-cortical strokes, magnesium significantly reduced death and disability (OR 0.75, 95% 0.58 to 0.97, p=0.011); a finding supported by a post-hoc analysis where those with lacunar stroke had reduced death and disability at day 90 (OR 0.7, 95% 0.53 to 0.92, p=0.0046). Patients who received magnesium within 3 hours of onset had a trend towards a better outcome (OR 0.66, 95% 0.25 to 1.7, p=0.46).
The Field Administration of Stroke Therapy-Magnesium (FAST-MAG) trial37 sought to assess magnesium in this shorter time window by recruiting 1700 patients with presumed stroke within 2 hours of ictus to intravenous magnesium bolus followed by infusion, or placebo. SBP fell in both groups over the first 48 hours but those on treatment had a significantly lower SBP (∼3 mm Hg difference) at the end of the bolus dose and from 20 to 32 hours after starting the maintenance infusion. Although prehospital initiation of magnesium was safe, there was no significant shift in mRS at day 90 (primary outcome).
Nitric oxide donors
In three small RCTs in acute stroke, transdermal glyceryl trinitrate (GTN) lowered BP, pulse pressure and peak SBP while maintaining CBF and improving arterial compliance.65 ,76 ,77 A small ambulance-based feasibility trial of transdermal GTN administered within 4 hours of symptom onset revealed an improvement in functional outcome at 90 days, measured as a shift in mRS by 1 point (p=0.04).38 None of these trials were powered for functional outcome; this was assessed in the large Efficacy of Nitric Oxide in Stroke (ENOS) trial.39
ENOS randomised 4011 patients with AIS or ICH within 48 hours of onset and high SBP (140–220 mm Hg) to transdermal GTN 5 mg patches or placebo for 7 days. In addition, those participants on antihypertensive agents immediately prior to their stroke were randomised to stop or continue their medication, in a partial-factorial design.39 GTN significantly reduced both SBP and DBP day 1 after randomisation compared to placebo (mean difference: 7 and 3 mm Hg, respectively, p<0.001) but there was no statistically significant difference from day 3 onwards. Overall, GTN was safe in both IS and ICH. Although the primary outcome of mRS at day 90 was neutral (acOR 1.0, 95% CI 0.91 to 1.13, p=0.83), a prespecified subgroup analysis found that in those recruited in <6 hours from ictus, GTN was associated with a favourable shift in mRS (acOR 0.51, 95% 0.32 to 0.8, p=0.004), less death and improved cognition, disability, mood and quality of life.77 Beneficial effects were seen in patients with IS (including those receiving thrombolysis) and ICH.78
Several small studies have assessed the role of pressor therapy in AIS.23 ,79 One trial assessed intravenous phenylephrine versus conventional management in 15 patients with AIS within 1 week of ictus, >20% diffusion-perfusion mismatch on MRI and normotension (SBP <140 mm Hg).40 Phenylephrine was titrated to increase MAP by 10–20% and maintained for up to 72 hours. NIHSS and cognitive scores, and volume of hypoperfused tissue on MRI, improved in the treatment group with no significant adverse events, but there was no assessment of functional outcome. The aforementioned CHHIPS trial had a pressor arm, which sought to assess phenylephrine in hypotensive patients with IS, but grossly under-recruited (one participant only, who received placebo).80 Similarly, an unpublished trial of dobutamine only managed to recruit three patients.
Diaspirin cross-linked haemoglobin (DCLHb), a cell-free haemoglobin-based oxygen-carrying solution that scavenges NO,81 was compared with saline in 85 patients with AIS within 18 hours of onset.42 DCLHb caused a rapid rise in BP and more serious adverse events, disability (BI), death and poor functional outcome (mRS) at 3 months than control. In a small RCT of 33 patients within 1 month of IS,41 amphetamine raised BP and heart rate but had no impact on motor function or functional outcome. Although amphetamine was associated with a trend to improved motor function after IS in a systematic review, there was a non-significant increase in death, raising doubts over its safety.82 Other potential agents including norepinephrine (noradrenaline), epinephrine (adrenaline) and dopamine have no significant evidence base.79
Targetting BP in acute stroke
An alternative avenue of research has focused on whether aiming for a BP target in acute stroke, regardless of the agent(s) used, improves outcome.
The China Antihypertensive Trial in Acute Ischaemic Stroke (CATIS)83 recruited 4071 patients with AIS with raised SBP (140–220 mm Hg) within 48 hours of onset and randomised them to either BP lowering (SBP 10–25% reduction within 24 hours and BP <140/90 mm Hg within 7 days) or control (no antihypertensive medication). Although a specific BP-lowering regimen was not being assessed they suggested first-line (intravenous ACEi), second-line (oral CCA) and third-line (oral diuretic) medications. Mean SBP fell by 13% within 24 hours of randomisation in the treatment group, compared with 7% in the control population. At 7 days, mean SBP in the treatment and control arms was 137 and 147 mm Hg respectively. The primary outcome of mRS ≥3 at 14 days or hospital discharge and secondary outcome of mRS at day 90 were neutral. A subgroup analysis of time to treatment found that those randomised to BP lowering 24 hours or longer after ictus had a significant reduction in death or dependency at 3 months (OR 0.73, 95% CI 0.55 to 0.97, p=0.03).83
There are several points to mention. First, the recruits had minor strokes (median NIHSS 4) resulting in 66% of the control population being independent at 2 weeks and therefore reducing the potential for the intervention to show benefit. Second, patients with large vessel carotid disease were omitted from the trial. And last, patients receiving thrombolysis were excluded, further limiting the trial's generalisability.83
In a small feasibility study of patients with ICH within 8 hours of symptom onset, aggressive BP lowering (MAP <110 mm Hg) was safe with no difference in rates of early neurological deterioration, haematoma expansion or cerebral oedema.84 The concern surrounding whether aggressive BP lowering compromises perihaematoma CBF was addressed in the Intracerebral Haemorrhage Acutely Decreasing Arterial Pressure Trial (ICH-ADAPT).85 Seventy-five patients with spontaneous ICH within 24 hours of onset and high BP (SBP ≥150 mm Hg) were randomised to a target SBP of <150 or <180 mm Hg within 1 hour of randomisation. Two hours after recruitment CT perfusion imaging revealed reduced CBF and cerebral blood volume within the perihaematoma region compared with the contralateral homologous area in all patients. There was no significant difference in relative CBF between the groups, indicating that aggressive BP reduction in ICH did not, at least in this study, precipitate perihaematomal ischaemia.85
Early BP lowering in the Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage Trial (INTERACT)86 involving 404 patients was safe, feasible and seemed to reduce haematoma growth. Similarly, BP reduction within 6 hours in the Antihypertensive Treatment of Acute Cerebral Haemorrhage (ATACH)87 study was safe. The magnitude of SBP lowering was associated with less haematoma expansion and improved functional outcome.88 The largest trial of intensive BP lowering in ICH, INTERACT2,89 recruited 2839 patients within 6 hours of onset with high SBP (150–220 mm Hg) and randomised them to guideline therapy (SBP <180 mm Hg) or intensive therapy (SBP <140 mm Hg within 1 hour) for 7 days using oral or intravenous agents at the discretion of the local investigator. At 1 hour, a third of patients in the intensive arm achieved the target SBP of <140 mm Hg with a mean SBP of 150 mm Hg, compared with 164 mm Hg in the guideline group. The primary outcome of death or major disability (mRS ≥3 at 90 days) was neutral, but a prespecified ordinal shift analysis of mRS revealed a favourable shift in those randomised to intensive BP lowering (OR 0.87, 95% CI 0.77 to 1.00, p=0.04). In addition, better outcomes were seen in those with larger BP reductions within 1 hour of randomisation.90 Intensive BP reduction was safe with no difference in death or other serious adverse events between groups.89
The use of mannitol in 62% of INTERACT2 participants is unclear given that the overall 24 hours median haematoma volume was 20 mL, making intracranial hypertension unlikely. The myriad combinations of antihypertensive agents used in the trial included one rarely used in the West (Urapidil) and others with potentially negative or harmful effects, which may have confounded the BP-lowering effect.91
While INTERACT2 did not show any change in haematoma expansion with aggressive BP lowering, a meta-analysis of four of the above trials84–86 ,89 found that intensive BP lowering in acute ICH appeared safe with a tendency towards improved functional outcome; an effect which may have been mediated through attenuation of haematoma expansion observed at 24 hours in both unadjusted and adjusted models.92 Furthermore, a post hoc analysis of INTERACT2 revealed that intensive BP lowering with greater SBP reduction prevented haematoma growth at 24 hours.93
To treat or not to treat?
Guidelines suggest that BP lowering in acute stroke should be postponed for days or even weeks unless BP is grossly elevated (>220/120 mm Hg), or >200/100 with concomitant evidence of acute kidney injury, aortic dissection, cardiac ischaemia, hypertensive encephalopathy or pulmonary oedema.94–96
Thrombolysis for hyper-acute ischaemic stroke
In the context of thrombolysis in AIS, BP must be <185/110 mm Hg prior to administration of alteplase, and <180/105 mm Hg for the following 24 hours; suggested methods involve using intravenous labetalol, nicardipine or nitroprusside.94 Unfortunately there is a paucity of evidence and this recommendation is based on expert opinion with extrapolation from trials of thrombolysis in myocardial infarction.97 ,98 Observational data from the Safe Implementation of Thrombolysis in Stroke (SITS) register99 ,100 revealed that a higher SBP post-thrombolysis is associated with symptomatic ICH and poor outcome. A U-shaped relationship was seen between SBP 2–24 hours after thrombolysis and major disability and death, with the most favourable outcomes occurring in those with SBP 141–150 mm Hg.100 The on-going Enhanced Control of Hypertension and Thrombolysis in Stroke Study (ENCHANTED)101 will provide insight into whether acute intensive lowering of BP (target SBP 130–140 mm Hg) has superior efficacy and lower risk of ICH than guideline management (SBP <180 mm Hg).
Race and ethnicity
Demographics are important and especially relevant in a cosmopolitan global community. For example, Chinese patients with stroke tend to be younger, smoke more, have increased intracranial atherosclerosis, less cervical atherosclerosis and a higher risk of ICH than their Caucasian counterparts.104 ,105 Hence, demographic similarities and differences should be considered in both future trials and individual patient data meta-analyses.
Time to treatment
In a recent Cochrane review, lowering BP in 15 432 patients with acute stroke did not improve outcome regardless of stroke type, or drug class and BP target used.23 However, in those who received treatment within 6 hours of stroke onset (INTERACT2 and RIGHT), there was a tendency towards a shift to less death or dependency, and improved quality of life.38 ,89 All drug classes described above lowered BP, with greater reductions seen in ICH than patients with AIS (−11.8/−5.1 vs −7/−3.1 mm Hg). Smaller BP changes occurred in patients recruited after 48 hours of onset, while the largest BP reduction was seen in those recruited earliest. Importantly, large falls in BP (>20%), especially in AIS, were associated with a poor outcome.23
A subsequent subgroup analysis of ENOS patients randomised to GTN within 6 hours adds weight to the argument for early treatment with reduced death or dependency, less death and improved cognition, disability, mood and quality of life.77 It is unclear whether this may represent a generic effect of early BP lowering or a specific effect of GTN. In contrast, other interventions namely ARA, β-blockers and CCA may be detrimental (table 2).29 ,31 ,34 ,45 ,72
Time is important: ultra-acute treatment of BP (intensive BP lowering or use of an appropriate agent) within the first few hours of symptoms in the prehospital setting is a vital avenue to explore further. Non-oral routes of administration, such as transdermal, sublingual and intravenous, would be preferable in this context, given the need for a swallowing assessment to rule out dysphagia. Of these, transdermal GTN,38 sublingual lisinopril,26 and intravenous magnesium,37 have been assessed in the prehospital environment and found to be safe. While transdermal preparations can be easily applied and removed according to clinical need, intravenous administration of BP-lowering agents require intensive monitoring. On-going (RIGHT-2: ISRCTN26986053) and planned trials of transdermal GTN in ultra-acute stroke will assess efficacy in the field.⇓
BP management in carotid disease and large vessel occlusion
High BP is commonly seen in patients with AIS due to carotid artery stenosis.106 Owing to dysfunctional cerebral autoregulation concerns are twofold: a higher systemic BP will result in a higher cerebral perfusion pressure increasing the risk of cerebral oedema and potential for haemorrhagic transformation; while lowering BP may reduce CBF resulting in infarct extension.6
A prespecified subgroup analysis from SCAST of patients with carotid imaging (n=993 (57%)), revealed that those with severe unilateral stenosis (≥70%) who received candesartan had a trend towards increased risk of stroke progression and poor functional outcome, although the CI were wide.107 Whether this was due to a specific effect of candesartan, or to BP lowering per se remains unclear. Of the 2038 participants in ENOS with carotid imaging data, GTN was safe with no evidence of harm across all levels of ipsilateral carotid stenosis.39
Patients with bilateral severe carotid stenosis pose another dilemma. A meta-analysis of three trials found that in patients with bilateral severe stenosis (≥70%), a lower BP was associated with higher stroke recurrence (SBP <130 mm Hg: HR 5.97, 95% CI 2.43 to 14.68, p<0.001).106 Although bilateral carotid stenosis is uncommon, caution regarding BP lowering in this group seems warranted pending further data.
With the advent and proven effectiveness of endovascular intervention for proximal anterior circulation vessel occlusions in AIS,108 numerous questions remain unanswered, including how BP should be managed before, during and after thrombectomy. At present this is an evidence-free zone. Retrospective data comparing general with local anaesthesia during the procedure found that general anaesthesia, which was often associated with SBP <140 mm Hg, was associated with a poor functional outcome (mRS >2) at 90 days.109 Prospective research in this area should prove illuminating.
Continue or stop pre-stroke antihypertensives
Whether to temporarily stop or continue existing antihypertensive agents early after a patient's stroke is a common clinical question. The Continue or Stop Post-Stroke Antihypertensives Collaborative Study (COSSACS)110 randomised 763 patients within 48 hours of stroke to either stop or continue their pre-existing antihypertensive medication for 2 weeks. Those who continued their medication had a lower BP at 2 weeks compared with those who stopped (mean difference 13 / 8 mm Hg). Death or dependency at 2 weeks (mRS >3, primary outcome), death, major cardiovascular events and serious adverse events at 6 months did not differ between the two arms.110
The partial-factorial ENOS trial39 enrolled 2097 patients within 48 hours of stroke onset to continue or stop their pre-stroke antihypertensive drugs for 7 days. Although there was no effect on functional outcome (mRS) at day 90, continuation of pre-stroke BP drugs increased the risk of pneumonia (perhaps due to aspiration), worsened BI and increased cognitive impairment at 90 days.
When pooled data from COSSACS and ENOS were reviewed, continuation of antihypertensives was associated with worse disability (BI) and quality of life but no change in functional outcome (mRS).23 This incongruity is perplexing, but may represent chance, outcome bias or indeed be real. If the latter is true and continuing medication is detrimental, what is the mechanism? First, giving medication to dysphagic patients without appropriate enteral access could lead to aspiration and resultant pneumonia.39 Second, as ACEi, ARA and β-blocker drugs attenuate stress hormones, are common preparations used prior to stroke, and are associated with harm when given acutely after stroke (ARA and β-blockers),29 ,31 it may be that continuing them in the acute phase is potentially hazardous.23 It therefore seems reasonable to pause existing antihypertensive medication during the acute phase of stroke until patients have suitable enteral access and are medically and neurologically stable.23
Despite the recent publication of several large clinical trials and systematic reviews, there are no definitive recommendations that can be drawn regarding BP modulation in AIS. BP should be lowered rapidly in patients with ICH. Although stroke is more common in the older population, trials to date have mostly involved patients with a mean age of ≤75 years. Despite this, there is no suggestion that older patients should not have their BP lowered.89 In addition to age, further evidence is needed on whether time of onset, stroke subtype, severity, drug choice (dose, route and timing), and BP variability influence response to changes in BP. Individual patient data meta-analysis is warranted to aid patient selection by identifying groups who are more or less likely to benefit and to establish whether a certain drug class, dose, route or BP target is optimal.23
In summary, antihypertensives should be withheld after stroke until they can be given safely in patients who are neurologically stable. Both early intensive lowering of BP in ICH and early nitrate use in all stroke subtypes are safe and associated with improved functional outcome. Whether these effects are mediated through BP reduction or specific pharmacological effects incorporating neuroprotection and/or reperfusion is unclear. Time seems to be a key factor and so on-going and future hyper-acute and ultra-acute trials are pivotal in testing this hypothesis.
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