Endovascular therapy (EVT) is an effective treatment for ischemic stroke due to large vessel occlusion (LVO). Unlike intravenous thrombolysis, EVT enables visualization of the restoration of blood flow, also known as successful reperfusion in real time. However, until successful reperfusion is achieved, the survival of the ischemic brain is mainly dependent on blood flow from the leptomeningeal collaterals (LMC). It plays a critical role in maintaining tissue perfusion after LVO via pre-existing channels between the arborizing pial small arteries or arterioles overlying the cerebral hemispheres. In the ischemic territory where the physiologic cerebral autoregulation is impaired and the pial arteries are maximally dilated within their capacity, the direction and amount of LMC perfusion rely on the systemic perfusion, which can be estimated by measuring blood pressure (BP). After the EVT procedure, treatment focuses on mitigating the risk of hemorrhagic transformation, potentially via BP reduction. Thus, BP management may be a key component of acute care for patients with LVO stroke. However, the guidelines on BP management during and after EVT are limited, mostly due to the scarcity of high-level evidence on this issue. In this review, we aim to summarize the anatomical and physiological characteristics of LMC to maintain cerebral perfusion after acute LVO, along with a landscape summary of the literature on BP management in endovascular treatment. The objective of this review is to describe the mechanistic association between systemic BP and collateral perfusion after LVO and thus provide clinical and research perspectives on this topic.
The efficacy of intravenous thrombolysis (IVT) and endovascular therapy (EVT) for acute ischemic stroke patients after large vessel occlusion (LVO) has been established by large randomized clinical trials [
The fate of brain cells in the ischemic region beyond the LVO depends on perfusion through the leptomeningeal collateral (LMC) overlying the cerebral hemisphere. Inadequate LMCs, either due to anatomical paucity or physiological dysfunction, lead to rapid infarct growth and may contribute to the progression of ischemia after LVO [
This article outlines how knowledge of the anatomy and physiology of LMCs may be applied clinically and provides an overview of current evidence on BP management during and after endovascular treatment, as well as its influence on treatment outcomes. In the absence of randomized controlled trial evidence, the purpose of this review is to help stroke physicians develop an anatomo-physiological model-based approach to BP management while caring for patients with LVO stroke.
In a normal physiological state, blood flows from the heart to the brain via the anterior circulation, which comprises the internal carotid artery, the middle cerebral artery (MCA), which supplies the majority of this circulation, and the anterior cerebral artery (ACA). Blood also flows via the posterior circulation, which is formed by the vertebral artery, basilar artery, and posterior cerebral artery (PCA). The average diameter of the MCA at its origin is approximately 4 mm, roughly twice that of the ACA, which is approximately 2 mm [
On the surface of the cerebral hemisphere, the pial arteries lie within the subarachnoid space and provide perforating arteries into the brain parenchyma. The proximal part of the perforating arteries usually consists of an endothelium surrounded by a thick basement membrane material with embedded smooth muscle cells. However, at the capillary level, the vascular wall consists of a single layer of flattened endothelial cells with a very thin basement membrane and intermittent pericytes without smooth muscle cells [
LMC channels consist of small precapillary arterial conduits of varying sizes lying between the pial arteries and arterioles in the cerebral cortex. There are two types of precapillary links: a larger one that connects the surface pial arteries in an end-to-end manner, and a smaller one that bridges smaller perforating arterioles often near the point of cortical penetration. The diameter of these anastomoses shows a wide range (10 to 30 μm) in their resting state [
Perfusion through the arterial/arteriolar anastomoses described above is regulated by CA. CA is a normal physiological response that maintains constant blood flow in response to external and internal stimuli, such as changes in arterial BP between a mean arterial pressure (MAP) of 50 to 170 mm Hg [
As CA depends on the regulation of arteriolar diameters, the functional capacity of CA is determined by the structural and functional properties of the pial artery and arteriolar anastomoses. The normal physiological response of vasodilation to decreased perfusion pressure is altered in various pathological conditions such as aging, long-standing hypertension, and hyperglycemia [
After LVO, a significant drop in local perfusion pressure occurs within the affected vascular territory, resulting in a mismatch between metabolic demand and oxygen/nutritional supply. In response to this, LMCs are recruited by vasodilation of the pial arteries and arteriolar anastomoses to their maximum available capacity. The average diameter of these anastomoses is less than 10 to 20 μm in the resting state, but when fully recruited after LVO, their diameter increases almost 6-fold (60 to 120 μm) [
Before successful recanalization is achieved after LVO, the objective of medical management is to prevent irreversible infarction of the ischemic penumbra. Cerebral autoregulatory mechanisms are unable to provide adequate regional CBF due to the severely depressed level of perfusion pressure [
After successful recanalization, the objective of BP management should be to mitigate the risk of hemorrhagic transformation. The prevailing belief is that lowering BP may prevent hemorrhagic transformation after EVT. However, this simple model does not consider the fact that angiographic recanalization does not always guarantee tissue reperfusion. Examples of such physiology include the “no-reflow” phenomenon and partial recanalization [
In the early EVT era, studies mainly focused on one parameter for BP management: BP at the time of hospital arrival (
The effect of procedural BP during EVT is mostly analyzed in conjunction with the type of anesthesia; therefore, the BP profile in such reports cannot be entirely distinguished from its influence (
BP measurements obtained after EVT received more attention only after the effectiveness of EVT was proven in clinical trials (
Due to the relatively regular interval of BP measurements during the post-EVT phase, the effect of BP variability post-EVT has also been investigated well, with multiple studies showing that higher BP variability is associated with larger infarct volume and poor functional recovery [
The BP management recommendations from current guidelines may be summarized as follows [
(1) Routine use of BP-lowering medication before recanalization treatment (thrombolysis and/or EVT) is not well established and is not recommended unless >220/110 mm Hg.
(2) For IVT alone, it is recommended to maintain a BP <185/110 mm Hg before, during, and 24 hours after treatment.
(3) For EVT, intensive BP lowering in the peri-EVT period lacks clear benefits. It is suggested that BP be maintained at <185/105 mm Hg during and after the procedure. This recommendation was based on recent clinical trial protocols.
The landscape review from the previous section can be summarized as follows:
(1) Admission BP has a J- or U-shaped association with clinical outcomes after EVT.
(2) Prolonged duration of low BP during EVT procedures is associated with unfavorable outcomes.
(3) BP variability after EVT correlates with a higher risk of poor functional recovery and/or increased rates of hemorrhagic complications.
(4) Relatively lower BP reductions after EVT are associated with poor functional recovery.
The objective of BP management during this period should be to maximize the viability of the ischemic penumbra. The recent literature is inconclusive, with both higher or lower levels of admission BPs reported to be correlated with poor outcomes. Current guidelines recommend that EVT candidates maintain an SBP <185 mm Hg. This BP threshold is a legacy from the eligibility criteria for the intravenous thrombolysis trial [
Most studies investigating procedural BP levels reported a higher likelihood of poor outcomes after a prolonged duration of lower or higher BP. However, these two points require further discussion. First, these were
Before recanalization, as in the pre-EVT period, the objective of BP management should be to ensure the viability of the ischemic penumbra. Prolonged exposure to low or high BP should be avoided. A mean arterial BP range between 70 and 90 mm Hg was suggested by one study [
The primary goal of BP management after successful recanalization is to mitigate the risk of hemorrhagic complications and stabilize ischemic tissues. Randomized clinical trials to test the efficacy of EVT for anterior circulation LVO have specified some BP management instructions. The Evaluation Study of Congestive Heart Failure and Pulmonary Artery Catheterization Effectiveness (ESCAPE) trial recommended SBP values ≥150 mm Hg while the artery remains occluded; controlling BP once reperfusion has been achieved while aiming for a normal BP in an individual is sensible [
Thus, the following rule of thumb may be considered until more evidence emerges.
(1) In the post-recanalization period, it is best to maintain the BP level of the patient.
(2) The practice of lowering SBP to less than 140 mm Hg after successful recanalization is not based on proven evidence.
(3) We suggest monitoring BP levels after recanalization and treating only if BP levels are very high; for example, >185 mm Hg systolic when IVT has already been offered or when recanalization grade mTICI 2c or 3 has been achieved.
(4) Higher BP levels after recanalization may portend unfavorable treatment outcomes.
Despite a large body of literature, current clinical guidelines provide limited recommendations regarding BP management strategies in the peri-EVT period. One obvious reason is the retrospective and observational design of published studies. However, BP can be easily measured and readily controlled by parenteral medications. Owing to constant fluctuation in BP during this period, clinical inertia, that is, ignoring outlier BP values, may creep unintentionally. The discrepancy between a prespecified BP target and achieved BP levels is not infrequent in real-world clinical practice. In a recent clinical trial, the BP-Blood Pressure target in Acute Stroke to Reduce Hemorrhage after Endovascular Therapy (TARGET) study randomized 324 cases into an intensive SBP target (100 to 129 mm Hg) and a standard SBP target (130 to 185 mm Hg) during the 24 hours after EVT. The two groups were comparable in radiographic intraparenchymal hemorrhage at 24 to 36 hours, as well as functional recovery and safety outcomes. However, there was an unintended crossover between the assigned target group; patients in the intensive arm spent approximately a third of the duration in the SBP target range of the control arm [
Repeated measures of BP over time were obtained from a single patient. However, in clinical practice, these measurements are recorded over various time intervals, thus providing only a screenshot of the dynamic readings in time. Considering that every cardiac beat generates SBP and diastolic BP (
BP level, usually presented as mean BP over a specific duration, expresses the status of BP at a particular time point or period. This level is intuitive to physicians, and the change in the BP level may provide practical information (
As discussed in this review, regional tissue perfusion after LVO is maintained by the LMC channels. The recruitment of these LMC channels is determined by the pressure gradient between the arterial blood flow generated by cardiac contraction and venous blood flow. Based on this simple and linear model, it is intuitive to suppose that cerebral tissue perfusion after LVO may be regulated through systemic BP management.
However, the small arteries and arterioles of the brain have CA capacity, which modulates the vascular diameter to maintain almost constant CBF in response to local perfusion pressure changes. Therefore, the brain tissue that may receive increased local CBF from augmenting systemic BP is likely to be either the ischemic core or the ischemic penumbra without autoregulatory function. A long history of hypertension may indicate impaired autoregulatory function [
Based on the above, the following can be stated:
(1) The effect of systemic BP on blood flow distal to an LVO may vary based on the anatomic extent of the LMC channels and the remaining autoregulatory function.
(2) Ischemic brain injury may affect the vascular endothelium, pericytes, glia, and neuronal cells, and it prevents the maintenance of normal autoregulatory function. The autoregulatory function may also be affected by prior conditions, such as hypertension and diabetes mellitus.
(3) In general, LMC perfusion only provides inadequate blood flow that cannot sustain brain tissue viability for long.
(4) The BP management strategy for acute ischemic stroke patients may need to be personalized based on the individual assessment of the LMC channels and autoregulatory capacity.
Whether baseline hemodynamic status modifies the association between BP profiles and ischemic or functional outcomes is a fascinating research topic [
In current practice, stroke physicians use BP measurements as a proxy for brain perfusion pressure. Conceptually, the objective of BP management in the pre-recanalization phase is to maintain sufficient LMC perfusion. In the post-recanalization phase, the objective is to prevent hemorrhagic complications and stabilize the ischemic brain tissues. At present, the available research on BP management in EVT shows that higher BP on admission, lower BP levels post-recanalization, higher BP variability or variable trajectories, and prolonged durations of low BP during EVT are all associated with poor functional outcomes. However, the optimal BP level, variability, and trajectory for each phase are yet to be determined. Based on current anatomical and physiological knowledge, the ultimate goal is to directly gauge the amount and capacity of LMC perfusion after LVO to provide maximally available CBF to the ischemic brain until successful recanalization is achieved and to mitigate undesirable complications subsequent to ischemia and reperfusion. Given the heterogeneity of the anatomy and variability of the physiology of the LMC, understanding its behavior during stroke is now more pressing than ever. It is paramount that more novel mechanisms and parameters to assess regional brain perfusion and functioning CA capacity at the bedside are developed in order to individualize BP management in the periEVT period [
The authors have no financial conflicts of interest.
Overview of leptomeningeal collaterals and cerebral autoregulation. (A) When a perfusion pressure gradient develops after large vessel occlusion, leptomeningeal collaterals are instantaneously recruited to provide cerebral perfusion to the ischemic territory within the functional capacity of cerebral autoregulation. (B) Microscopically, leptomeningeal collateral channels utilize pre-existing arterial tubular structures between the pial arteries, arterioles, or proximal branches. (C) The recruitment of leptomeningeal channels depends primarily on the myogenic dilatation of the pial arteries responsive to decreased local perfusion pressure (i.e., cerebral autoregulation).
Characteristics of blood pressure measurements and summary indices. Systolic and diastolic blood pressure (BP) is determined during every cardiac cycle. Intermittent measurements in routine clinical practice may capture only a fraction of the available BP measurements. BP measurements can be obtained repeatedly and exhibit constant fluctuations (A). The measurement density of BPs may be different throughout acute in-hospital care, that is, pre-endovascular treatment (EVT), during the procedure, as well as post-EVT. BP measurements can be summarized using means, as highlighted by the yellow line in the figure. The average BP level is intuitive and easy to calculate, but it does not reflect the variability and fluctuations in BP measurements that occur in a patient (B). Fluctuations of BP can be described by various variability measures, including standard deviations, coefficient of variations, maximum decrements, and average real variability, to name a few. In general, variability measures are calculated by taking the differences between each measurement or the differences between specific values (yellow lines). However, such variability measures do not provide information on the time intervals of the measurements. Thus, the absolute BP variability values may decrease during high measurement density periods such as during EVT procedures (C). The trajectory group describes the overall path (yellow line) of BP measurements over a certain period of time. By using a mixture model, clusters of patients with similar patterns of BP measurements over a period of time may be identified and grouped [
Admission BP and EVT outcomes
Study | Year | Study subjects | Major BP indices | Major findings |
---|---|---|---|---|
Nogueira et al. [ |
2009 | 305 LVO patients included in the MERCI and multi-MERCI trials | BP on admission | Higher SBP on admission associated with unfavorable outcomes but an independent predictor of successful recanalization |
Maier et al. [ |
2017 | 1,042 LVO patients with EVT from ETIS registry | BP on admission | Admission SBP showed J- or U-shaped association with mortality, with the inflection point at SBP 157 mm Hg |
Mulder et al. [ |
2017 | 500 LVO patients included in the MR CLEAN trial | BP at baseline, before EVT (for EVT group) or stroke unit admission (for the no-EVT group) | Baseline SBP showed U-shape association with functional outcome |
High SBP associated with mortality and symptomatic hemorrhage | ||||
No interaction between SBP level and EVT | ||||
Goyal et al. [ |
2017 | 116 LVO patients with EVT | SBP on admission | Admission SBP correlated with final infarct volume |
Higher admission SBP associated with mRS 0–2 | ||||
Schonenberger et al. [ |
2018 | 150 EVT cases randomized to GA or CS from the SIESTA trial | BP measurements were divided into 4 phases: pre-EVT, pre-recanalization, post- recanalization, and post-EVT | No association between the difference in SBP, DBP, and MAP from baseline to the different phases of intervention with 24-hour NIHSS |
No association of BP drop with a change in mRS | ||||
Anadani et al. [ |
2020 | 381 EVT cases from the ASTER trial | Baseline BP prior to randomization | No association between admission BP with mRS or successful revascularization |
van den Berg et al. [ |
2020 | 3180 EVT patients from the MR CLEAN registry | BP on admission | J-shaped association with mRS and mortality with inflection points at 150 and 81 mm Hg |
Higher SBP associated with poor mRS and mortality |
BP, blood pressure; EVT, endovascular treatment; LVO, large vessel occlusion; MERCI, Mechanical Embolus Removal in Cerebral Ischemia Trial; Multi-MERCI, Multi Mechanical Embolus Removal in Cerebral Ischemia Trial; SBP, systolic blood pressure; ETIS, endovascular treatment in ischemic stroke follow-up evaluation study; MR CLEAN, Multicenter Randomized Clinical Trial of Endovascular Treatment of Acute Ischemic Stroke in the Netherlands; mRS, modified Rankin Scale; GA, general anesthesia; CS, conscious sedation; SIESTA, Sedation vs. Intubation for Endovascular Stroke Treatment trial; DBP, diastolic blood pressure; MAP, mean arterial pressure; NIHSS, National Institutes of Health Stroke Scale; ASTER, Contact Aspiration vs. Stent Retriever For Successful Revascularization trial.
This article covers all peri-EVT periods.
BP during the EVT procedure and outcomes
Study | Year | Study subjects | Major BP indices | Major findings |
---|---|---|---|---|
Davis et al. [ |
2012 | 96 EVT cases (48 GA and 48 LA) | SBP, DBP, and MAP (minimum and maximum values for each) in LA and GA groups | Higher rates of mRS 0–2 in LA groups; lower SBP levels in GA group |
Hendén et al. [ |
2015 | 108 EVT cases | Fall in MAP of >40% compared to the baseline under GA | Fall in MAP of >40% from baseline associated with poor neurological recovery |
John et al. [ |
2015 | 147 EVT during 2008–2012 | Levels of BP during the EVT procedure under GA | Lower maximum intraprocedural SBP associated with mRS 0–2 |
Jagani et al. [ |
2016 | 99 EVT with CS or GA | Maximum or minimum values of SBP, DBP, and MAP | GA associated with lower BP levels and poor outcome |
Whalin et al. [ |
2017 | 255 Anterior circulation occlusions with mTICI ≥2b with monitored anesthesia care | MAP level during the procedure with monitored anesthesia care | 10% MAP drop associated with poor functional outcome |
Athiraman et al. [ |
2018 | 88 EVTs under GA | Episodes or durations of SBP lower than specific thresholds | Lower SBP levels associated with poor outcome |
Pikija et al. [ |
2018 | 164 EVT cases under GA | In-procedure SBP and MAP excursions to >120%/80% of the reference value and the reference BP/weighted in-procedure mean BP | High in-procedure SBP/MAP excursion to >120% associated with lower infarct volume and mRS 0–2 |
Higher in-procedure mean SBP/MAP associated with lower rates of hemorrhage | ||||
Rasmussen et al. [ |
2018 | 128 EVT patients randomized to GA or CS from the GOLIATH trial | Levels and durations of SBP or MAP lower than specific thresholds | Higher MAP or SBP levels in CS group |
No significant difference in the association between BP parameters and mRS | ||||
Schonenberger et al. [ |
2018 | 150 EVT cases randomized to GA or CS from the SIESTA trial | BP measurements were divided into 4 phases: pre-EVT, pre-recanalization, post-recanalization, and post-EVT | No association between the difference in SBP, DBP, and MAP from baseline to the different phases of intervention with 24 hours NIHSS |
No association of BP drop (magnitude of changes) with a change in mRS | ||||
Treurniet et al. [ |
2018 | 60 EVT under GA in the MR CLEAN trial | Levels and changes of SBP, DBP, and MAP during the procedure | Greater MAP reduction associated with worse functional outcome |
Petersen et al. [ |
2019 | 390 EVTs from two comprehensive stroke centers | Intraprocedural MAP, delta MAP (baseline MAP–lowest MAP during EVT procedures before recanalization) | MAP reduction noted in 87% of cases during EVT Delta-MAP associated with infarct growth and |
infarct volume; Delta-MAP correlated with higher mRS at discharge | ||||
Pikija et al. [ |
2019 | 39 BAO with EVT | BP levels and variability indices; difference of peak and trough values, SD, CV, ARV; reference SBP calculated as a median of the first five procedural measurements | Shorter procedural duration of SBP <140 associated with successful recanalization |
Higher SBP and longer duration of SBP over 180 mm Hg associated with hemorrhage | ||||
Fandler-Hofler et al. [ |
2020 | 115 Anterior circulation occlusion patients with EVT under GA | Peri-interventional BP levels and reduction | Single BP drop associated with poor outcome |
Maïer et al. [ |
2020 | 381 Patients from the ASTER trial | Dynamic BP parameter, CV; steady BP parameter, hypotension time of SBP <140 or MAP <90 | BP variability parameter associated with poor outcomes regardless of collateral status |
Hypotension time associated with poor outcomes only in patients with poor collaterals | ||||
Petersen et al. [ |
2020 | 90 EVTs for anterior circulation occlusions | Optimal ranges of MAP based on an autoregulatory index calculated by a real-time NIRS in response to changes in MAP | Percent time of MAP greater than the upper limit of the optimal range associated with worse 90- day outcomes and trends in hemorrhage |
Rasmussen et al. [ |
2020 | 368 EVT patient’s data from SIESTA, ANSTROKE, GOLIATH trials (CS vs. GA) | Levels and durations of MAP greater or less than thresholds | Cumulative hypo- (MABP <70 mm Hg for >10 minutes) and hypertension (MABP >90 mm Hg for >45 minutes) associated with poor functional outcomes |
Valent et al. [ |
2020 | 371 EVT cases under GA or CS | Baseline BP; BP measured in the interventional suite immediately before the induction | The time below 90% of the reference value associated with mRS ≥3 |
Duration of arterial hypotension (below the baseline BP) | ||||
Samuels et al. [ |
2021 | 440 EVT patients from the MR CLEAN registry, under CS or LA | Changes and duration of MAP levels | Lower MAP levels in CS; worse outcome in CS |
Xu et al. [ |
2021 | 131 EVT patients after LVO under GA | Delta MAP; MAP every 5 minutes–baseline MAP | Longer duration delta MAP associated with poor outcome, but only documented in mild reduction group |
Cumulated time and the longest continuous episode of delta MAP <10, 15, 20, 25, and 30 mm Hg | ||||
Chen et al. [ |
2021 | 139 EVT cases with successful recanalization | Procedural BPs categorized into baseline, pre-recanalization, postrecanalization, and post-intervention | High pre-recanalization BPs associated with poor outcomes; protocol-based BP lowering during EVT not associated with outcomes |
BP, blood pressure; EVT, endovascular treatment; GA, general anesthesia; LA, local anesthesia; SBP, systolic blood pressure; DBP, diastolic blood pressure; MAP, mean arterial pressure; mRS, modified Rankin Scale; CS, conscious sedation; mTICI, modified treatment in cerebral ischemia; GOLIATH, General or Local Anesthesia in Intra-arterial Therapy trial; SIESTA, Sedation vs. Intubation for Endovascular Stroke Treatment trial; NIHSS, National Institutes of Health Stroke Scale; MR CLEAN, Multicenter Randomized Clinical Trial of Endovascular Treatment of Acute Ischemic Stroke in the Netherlands; BAO, basilar artery occlusion; SD, standard deviation; CV, coefficient of variation; ARV, average real variation; ASTER, Contact Aspiration vs. Stent Retriever For Successful Revascularization trial; NIRS, near-infrared spectroscopy; ANSTROKE, Anesthesia During Stroke trial; MABP, mean arterial blood pressure; LVO, large vessel occlusion.
This article covers all peri-EVT periods.
Post-procedural BP and the recanalization treatment outcomes
Study | Year | Study subjects | Major BP indices | Major findings |
---|---|---|---|---|
Martins et al. [ |
2016 | 674 IVT or EVT cases | BP every 2 hours for 24 hours after admission | SBP showed J-shape in non-recanalized group but linear association in recanalized group |
Mistry et al. [ |
2017 | 228 EVT from three hospitals | BP (max, min, and average) in the first 24 hours after EVT | High peak SBP correlated with worse functional outcome and hemorrhagic complications |
Goyal et al. [ |
2017 | 217 LVO with EVT with hourly BP | BP goals post EVT; permissive hypertension (<220 or 185), moderate BP control (<160), intensive BP control (<140) | Higher SBPmax associated with mortality |
Intensive BP target (<140/90 mm Hg) associated with higher rates of mRS 0–2 | ||||
Bennett et al. [ |
2018 | 182 LVO patients with EVT | Post-procedural BP variability indices; SD, CV, and SV | High BPV associated with high mRS |
Chang et al. [ |
2018 | 303 LVO patients with EVT | Post-procedural BP variability indices; SD, CV, and VIM | High BPV associated with poor functional recovery and low successful recanalization |
Maier et al. [ |
2018 | 168 Anterior circulation occlusions with successful recanalization after EVT | Mean, max, and peak SBP for the first 24 hours after successful EVT | High mean SBP and maximum SBP associated with unfavorable outcome |
Martins et al. [ |
2018 | 674 IVT or EVT | Standard deviations of SBP and DBP during the first 24 hours after stroke | A differential effect from SD of SBP on mRS by recanalization status; significant only in non-recanalized patients |
Schonenberger et al. [ |
2018 | 150 EVT cases randomized to GA or CS from the SIESTA trial | BP measurements were divided into 4 phases: pre-EVT, pre-recanalization, post-recanalization, and post-EVT | No association between the difference in SBP, DBP, and MAP from baseline to the different phases of intervention and NIHSS change after 24 hours |
No association of BP drops with a change in mRS | ||||
Cernik et al. [ |
2019 | 690 EVT patients | Levels of SBP and DBP | Low BP levels associated with better functional recovery or recanalization |
Chang et al. [ |
2019 | 90 EVT with mTICI ≥2b | BP variability indices | BP variability associated with poor mRS only in patients with poor collaterals at baseline |
Cho et al. [ |
2019 | 378 EVTs | Levels and variability indices during the first 24 hours after admission | Higher mean SBP and SV of SBP associated with poor mRS; the effect of SV modified by recanalization status |
Choi et al. [ |
2019 | 1,540 AIS patients after IVT or EVT | BP ≤130/80 mm Hg | Lower BP levels associated with mRS 0–2 |
Kim et al. [ |
2019 | 211 EVT with mTICI ≥2b | Levels, excursions, variability indices, and time rate of BP variation | BP variability indices associated with higher rates of SICH |
Mistry et al. [ |
2019 | 485 Consecutive EVT patients from 12 centers | All SBP values within 24 hours post EVT | Peak SBP <158 mm Hg associated with good functional outcome |
Overall, SBP showed a U-shape association with outcome | ||||
Higher BP levels after EVT associated with poor outcome | ||||
Zhang et al. [ |
2019 | 72 LVOs with EVT | Post-procedural BP variability indices; SD, CV, and SV | Higher SV of SBP correlated with mRS at 3 months |
Anadani et al. [ |
2020 | 1,361 EVT cases from an international multicenter study | SBP reduction in the first 24 hours after EVT | SBP reduction associated with a good outcome only in patients with complete reperfusion (mTICI, 3) |
Anadani et al. [ |
2020 | 433 EVT cases from the BEST study [ |
SBP reduction, the absolute difference between admission SBP and mean SBP in the first 24 hours | No association between SBP with poor outcome or death |
Anadani et al. [ |
2020 | 1,019 Anterior circulation occlusion patients with EVT from eight comprehensive stroke centers | Post-EVT BP target, <140, <160, and <180 | Lower SBP goal (<140 or <160, compared to <180) associated with good outcome |
However, mean achieved SBP levels tended to overlap | ||||
Cheng et al. [ |
2020 | 124 Anterior circulation occlusion patients with EVT | Two BP measurements immediately after successful recanalization | Higher BP associated with PH2 hemorrhagic transformation |
Chu et al. [ |
2019 | 166 EVT patients | Hourly BP after EVT, by 1–6, 7–12, 13–18, and 19–24 hours | Lower mean, max, SD of SBP, and DBP associated with functional independence, in <6 hours |
Dias et al. [ |
2020 | 458 EVT cases | Median SBP within the first hour after EVT | Lower median SBP associated with NIHSS reduction by 8 or ≤2 at 24 hours |
Ding et al. [ |
2020 | 262 EVT cases | Maximum SBP and DBP for 24 hours after the EVT | Max SBP associated with poor mRS and parenchymal hemorrhage (hyper attenuated lesion on immediate CT, cannot distinguish from contrast staining) |
Matusevicius et al. [ |
2020 | 3,631 EVT cases from the SITS-ISTR | Mean 24-hour SBP after EVT | Higher SBP associated with poor functional recovery in successful recanalization patients and with SICH in all recanalization |
McCarthy et al. [ |
2020 | 212 EVT patients | Daily peak SBP and DBP | Higher peak 24-hour SBP associated with SICH and poor outcome |
Higher peak SBP at day 2 and day 3 associated with poor outcome | ||||
Mistry et al. [ |
2020 | 443 EVT cases from the BEST study [ |
Systolic BPV (SD, CV, ARV, SV, and rSD) during 24 hours after EVT | Higher BP variability associated with poor outcome and mortality |
Anadani et al. [ |
2021 | 5,835 EVT patients from the SITS-ISTR registry | Delta SBP (SBP–baseline SBP) 0–2/2–4/4–12/12–24 hours | SBP elevation after EVT associated with poor functional outcome |
Gigliotti et al. [ |
2021 | 117 EVT cases | SBP for 24 hours after EVT | SBP ≥180 associated with poor function at discharge but not at 3 months |
SBP ≥160 associated with malignant cerebral edema with lower symptomatic hemorrhage | ||||
Han et al. [ |
2021 | 187 BAO with EVT | Levels of SBP, MAP, and DBP | Maximum SBP and maximum MAP associated with mortality |
Huang et al. [ |
2021 | 502 Anterior circulation LVO patients with EVT | Levels and variability indices of SBP and DBP | High BP variability associated with poor functional recovery and hemorrhagic complications, differentiated by recanalization status, not by baseline collaterals |
Liu et al. [ |
2021 | 596 LVO patients with EVT (GA in 37%) | BP for 24 hours after EVT | Higher mean SBP levels, mean SBP >140, and SD of SBP associated with the unfavorable outcome only in poor collaterals subgroup |
Mazighi et al. [ |
2021 | 324 LVO patients with EVT (BP-TARGET trial) | Randomized to intensive SBP target (100–129) vs. standard SBP target (130–185) for 24 hours | No difference in the primary outcome (any hemorrhage or hypotensive event) |
Castro et al. [ |
2021 | 146 Anterior circulation LVO with successful recanalization | Spectral analysis of 5-minute recordings of beat-to-beat BP | High frequency BP variability associated with cerebral edema and unfavorable functional outcomes |
BP, blood pressure; IVT, intravenous thrombolysis; EVT, endovascular treatment; SBP, systolic blood pressure; LVO, large vessel occlusion; mRS, modified Rankin Scale; SD, standard deviation; CV, coefficient of variation; SV, successive variation; BPV, BP variability; VIM, variation independent of the mean; GA, general anesthesia; CS, conscious sedation; SIESTA, Sedation vs. Intubation for Endovascular Stroke Treatment trial; DBP, diastolic blood pressure; MAP, mean arterial pressure; NIHSS, National Institutes of Health Stroke Scale; mTICI, modified treatment in cerebral ischemia; AIS, acute ischemic stroke; SICH, symptomatic intracranial hemorrhage; BEST, Blood Pressure after Endovascular Therapy for Ischemic Stroke study; CT, computed tomography; PH2, parenchymal hemorrhage type 2; SITS-ISTR, Safe Implementation of Thrombolysis in Stroke International Stroke Thrombolysis Registry; ARV, average real variation; rSD, residual standard deviation; BAO, basilar artery occlusion; BP-TARGET, Blood Pressure target in Acute Stroke to Reduce Hemorrhage after Endovascular Therapy trial.
This article covers all peri-EVT periods.