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      Reducing Door-to-Reperfusion Time for Mechanical Thrombectomy With a Multitiered Notification System for Acute Ischemic Stroke

      research-article
      , MD a , , , MBA b , , MSN, RN, ACNS-BC a , c , , BS, RHIA d , , BSN, RN-BC c , , RT e , f , , ARNP-CRNA g , , RT e , , RN, NE-BC c , , RN e , , MSN, RN, NE-BC a , c , , ARNP h , , ARNP h , , RN c , , MD a , i , , MD a , , DO j , , MD j , , MD k , , MD h , , MD i , , MD e , , MD, MSc a , , MD a
      Mayo Clinic Proceedings. Innovations, Quality & Outcomes
      Elsevier
      AIS, acute ischemic stroke, ASPECTS, Alberta Stroke Program Early CT Score, CT, computed tomography, DTR, door-to-angiographic reperfusion, ED, emergency department, IV, intravenous, LTR, last known normal time to angiographic reperfusion, LVO, large-vessel occlusion, mRS, modified Rankin Scale, MT, mechanical thrombectomy, NIHSS, National Institutes of Health Stroke Scale, NCC, neurocritical care service, rtPA, human recombinant tissue plasminogen activator

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          Abstract

          Objective

          To reduce door-to-angiographic reperfusion (DTR) time to 120 minutes for patients presenting with acute ischemic stroke attributed to anterior circulation large-vessel occlusion amenable to endovascular mechanical thrombectomy.

          Patients and Methods

          Patients treated with mechanical thrombectomy before (April 10, 2015, through April 11, 2016) and after (April 12, 2016, through May 10, 2017) implementation of a multitiered notification system were studied. Lean process mapping was used to assess inefficiencies with multidisciplinary triage. A 3-tiered paging platform, which rapidly alerts essential personnel of the acute ischemic stroke team at advancing decision points, was introduced.

          Results

          Sixty-two patients were analyzed before and after implementation (34 vs 28, respectively). Following intervention, DTR time was reduced by 43 minutes (mean DTR, 170 minutes vs 127 minutes; P=.02). At 90-day follow up, 5 of the 28 patients in the postintervention cohort (19%) had excellent neurologic outcomes, defined as a modified Rankin Scale score of 0, compared to 0 of 34 (0%) in the preintervention cohort ( P=.89). Reductions were also seen in the length of stay on the neurocritical care service (mean, 6 vs 3 days; P=.006), and total hospital charges for combined groups (mean, $100,083 vs $161,458; P<.001).

          Conclusion

          The multitiered notification system was a feasible solution for improving DTR within our institution, resulting in reductions of overall DTR time, neurocritical care service length of stay, and total hospital charges.

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          Most cited references6

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          Hemorrhagic transformation within 36 hours of a cerebral infarct: relationships with early clinical deterioration and 3-month outcome in the European Cooperative Acute Stroke Study I (ECASS I) cohort.

          The clinical correlates of the varying degrees of early hemorrhagic transformation of a cerebral infarct are unclear. We investigated the cohort of a randomized trial of thrombolysis to assess the early and late clinical course associated with different subtypes of hemorrhagic infarction (HI) and parenchymal hematoma (PH) detected within the first 36 hours of an ischemic stroke. We exploited the database of the European Cooperative Acute Stroke Study I (ECASS I), a randomized, placebo-controlled, phase III trial of intravenous recombinant tissue plasminogen activator in acute ischemic stroke. Findings on 24- to 36- hour CT were classified into 5 categories: no hemorrhagic transformation, HI types 1 and 2, and PH types 1 and 2. We assessed the risk of concomitant neurological deterioration and of 3-month death and disability associated with subtypes of hemorrhagic transformation, as opposed to no bleeding. Risks were adjusted for age and extent of ischemic damage on baseline CT. Compared with absence of hemorrhagic transformation, HI1, HI2, and PH1 did not modify the risk of early neurological deterioration, death, and disability, whereas, in both the placebo and the recombinant tissue plasminogen activator groups, PH2 had a devastating impact on early neurological course (odds ratio for deterioration, 32.3; 95% CI, 13. 4 to 77.7), and on 3-month death (odds ratio, 18.0; 95% CI, 8.05 to 40.1). Risk of disability was also higher, but not significantly, after PH2. Risk of early neurological deterioration and of 3-month death was severely increased after PH2, indicating that large hematoma is the only type of hemorrhagic transformation that may alter the clinical course of ischemic stroke.
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            Significance of large vessel intracranial occlusion causing acute ischemic stroke and TIA.

            Acute ischemic stroke due to large vessel occlusion (LVO)-vertebral, basilar, carotid terminus, middle and anterior cerebral arteries-likely portends a worse prognosis than stroke unassociated with LVO. Because little prospective angiographic data have been reported on a cohort of unselected patients with stroke and with transient ischemic attack, the clinical impact of LVO has been difficult to quantify. The Screening Technology and Outcome Project in Stroke Study is a prospective imaging-based study of stroke outcomes performed at 2 academic medical centers. Patients with suspected acute stroke who presented within 24 hours of symptom onset and who underwent multimodality CT/CT angiography were approached for consent for collection of clinical data and 6-month assessment of outcome. Demographic and clinical variables and 6-month modified Rankin Scale scores were collected and combined with blinded interpretation of the CT angiography data. The OR of each variable, including occlusion of intracranial vascular segment in predicting good outcome and 6-month mortality, was calculated using univariate and multivariate logistic regression. Over a 33-month period, 735 patients with suspected stroke were enrolled. Of these, 578 were adjudicated as stroke and 97 as transient ischemic attack. Among patients with stroke, 267 (46%) had LVO accounting for the stroke and 13 (13%) of patients with transient ischemic attack had LVO accounting for transient ischemic attack symptoms. LVO predicted 6-month mortality (OR, 4.5; 95% CI, 2.7 to 7.3; P<0.001). Six-month good outcome (modified Rankin Scale score
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              Good clinical outcome after ischemic stroke with successful revascularization is time-dependent.

              Trials of IV recombinant tissue plasminogen activator (rt-PA) have demonstrated that longer times from ischemic stroke symptom onset to initiation of treatment are associated with progressively lower likelihoods of clinical benefit, and likely no benefit beyond 4.5 hours. How the timing of IV rt-PA initiation relates to timing of restoration of blood flow has been unclear. An understanding of the relationship between timing of angiographic reperfusion and clinical outcome is needed to establish time parameters for intraarterial (IA) therapies. The Interventional Management of Stroke pilot trials tested combined IV/IA therapy for moderate-to-severe ischemic strokes within 3 hours from symptom onset. To isolate the effect of time to angiographic reperfusion on clinical outcome, we analyzed only middle cerebral artery and distal internal carotid artery occlusions with successful reperfusion (Thrombolysis in Cerebral Infarction 2-3) during the interventional procedure (<7 hours). Time to angiographic reperfusion was defined as time from stroke onset to procedure termination. Good clinical outcome was defined as modified Rankin Score 0-2 at 3 months. Among the 54 cases, only time to angiographic reperfusion and age independently predicted good clinical outcome after angiographic reperfusion. The probability of good clinical outcome decreased as time to angiographic reperfusion increased (unadjusted p = 0.02, adjusted p = 0.01) and approached that of cases without angiographic reperfusion within 7 hours. We provide evidence that good clinical outcome following angiographically successful reperfusion is significantly time-dependent. At later times, angiographic reperfusion may be associated with a poor risk-benefit ratio in unselected patients.
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                Author and article information

                Contributors
                Journal
                Mayo Clin Proc Innov Qual Outcomes
                Mayo Clin Proc Innov Qual Outcomes
                Mayo Clinic Proceedings. Innovations, Quality & Outcomes
                Elsevier
                2542-4548
                24 May 2018
                June 2018
                24 May 2018
                : 2
                : 2
                : 119-128
                Affiliations
                [a ]Department of Neurology, Mayo Clinic, Jacksonville, FL
                [b ]Department of Management Engineering and Internal Consulting, Mayo Clinic, Jacksonville, FL
                [c ]Department of Nursing, Mayo Clinic, Jacksonville, FL
                [d ]Quality Data & Analysis, Mayo Clinic, Jacksonville, FL
                [e ]Department of Radiology, Mayo Clinic, Jacksonville, FL
                [f ]Telephone Office, Mayo Clinic, Jacksonville, FL
                [g ]Regulatory Compliance, Mayo Clinic, Jacksonville, FL
                [h ]Department of Neurologic Surgery, Mayo Clinic, Jacksonville, FL
                [i ]Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Jacksonville, FL
                [j ]Department of Anesthesiology, Mayo Clinic, Jacksonville, FL
                [k ]Department of Emergency Medicine, Mayo Clinic, Jacksonville, FL
                Author notes
                [] Correspondence: Address to Eric D. Goldstein, MD, Department of Neurology, Mayo Clinic, 4500 San Pablo Rd, Jacksonville, FL 32224. Goldstein.Eric@ 123456mayo.edu
                Article
                S2542-4548(18)30030-4
                10.1016/j.mayocpiqo.2018.04.001
                6124324
                55c45857-9b7a-47a8-b7bf-4a5d9c0586de
                © 2018 Mayo Foundation for Medical Education and Research. Published by Elsevier Inc.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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                Original Article

                ais, acute ischemic stroke,aspects, alberta stroke program early ct score,ct, computed tomography,dtr, door-to-angiographic reperfusion,ed, emergency department,iv, intravenous,ltr, last known normal time to angiographic reperfusion,lvo, large-vessel occlusion,mrs, modified rankin scale,mt, mechanical thrombectomy,nihss, national institutes of health stroke scale,ncc, neurocritical care service,rtpa, human recombinant tissue plasminogen activator

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