Treating Hypertension in Acute Stroke

Abstract

HomeHypertensionVol. 47, No. 6Treating Hypertension in Acute Stroke Free AccessEditorialPDF/EPUBAboutView PDFView EPUBSections ToolsAdd to favoritesDownload citationsTrack citationsPermissions ShareShare onFacebookTwitterLinked InMendeleyReddit Jump toFree AccessEditorialPDF/EPUBTreating Hypertension in Acute StrokeA Better Arrow for the Quiver J. David Spence J. David SpenceJ. David Spence From the Stroke Prevention and Atherosclerosis Research Centre, London, Ontario, Canada. Search for more papers by this author Originally published8 May 2006https://doi.org/10.1161/01.HYP.0000223025.17605.3cHypertension. 2006;47:1051Other version(s) of this articleYou are viewing the most recent version of this article. Previous versions: May 8, 2006: Previous Version 1 There has been a longstanding controversy about whether high blood pressure should be treated in the setting of acute stroke.1,2 Normally, cerebral blood flow is maintained through a wide range of systemic mean arterial blood pressure, from &50 to 150 mm Hg.3,4 In the setting of cerebral ischemia (and probably also in the zone of injury around intracerebral hemorrhages), the ischemic zone partially loses autoregulation, so cerebral blood flow in that region becomes dependent on perfusion pressure.5 Many experts, therefore, recommended that blood pressure elevation, which is common in the setting of acute stroke, not be treated for fear of exacerbating stroke by reducing perfusion pressure and thereby reducing flow in the compromised but viable ischemic penumbra.Because swelling in the region of ischemia raises tissue pressure, the cerebral perfusion pressure falls below systemic blood pressure, and it was thought that higher pressures might be beneficial. However, this is a double-edged sword, because pressures that are too high increase edema, leading to progressive infarction, causing tissue pressure to rise progressively, and reducing perfusion pressure farther and farther below systemic blood pressure. There is, therefore, a case for regulating blood pressure to an optimal level that maintains cerebral perfusion while minimizing exacerbation of edema. This may become possible through the recent development of methods to evaluate cerebral blood flow through widely available computerized tomography technology.6Furthermore, as Del Maestro and I pointed out in 1985,2 there are some circumstances in which the blood pressure must be treated, despite the occurrence of a recent cerebral infarction: in hypertensive encephalopathy, in patients whose cerebral infarction is because of embolization from a recent myocardial infarction, with pulmonary edema resulting from or aggravated by high pressure, or in patients whose stroke was because of aortic dissection picking off a carotid origin, there is simply no choice but to treat the blood pressure. The question then becomes how and how low? A key issue in that regard is that drugs that cannot be controlled, such as sublingual nifedipine, are contraindicated in this situation.4,7 In principle, therefore, it is best to use short-acting drugs that are administered by intravenous infusion so that blood pressure can be carefully titrated. Transdermal administration of drugs would fit with that principle, because they can be stopped by removing the patch and cleansing the skin underneath.With the recent widespread use of thrombolytic therapy for acute stroke, the need to control pressure to <185 mm Hg systolic and 110 mm Hg diastolic has become an imperative.8 The publication of the Acute Candesartan Cilexetil Therapy in Stroke Survivors (ACCESS) study,9 which showed improved outcomes with candesartan treatment between days 1 and 10 among patients with acute stroke and hypertension, has unfortunately not clarified this issue by much, because there was no blood pressure difference between patients treated with candesartan versus placebo. Furthermore, the administration of oral drugs, which cannot be retrieved if the pressure goes too low, is problematic.In that regard, the report by Wilmot et al10 in this issue of Hypertension lends strong support to the use of transdermal nitrates to treat hypertension in acute stroke. They showed that blood pressure could be lowered substantially, without reduction of cerebral perfusion in the ischemic region. Important advantages of the nitrate patch are that it is easy to implement, and, more importantly, it can be removed if the pressure is dropping too low. The results of their main trial, the Efficacy of Nitric Oxide in Stroke Trial (ENOS), to determine whether blood pressure reduction improves outcomes in patients with high blood pressure and acute stroke, are, therefore, to be eagerly anticipated.The opinions expressed in this editorial are not necessarily those of the editors or of the American Heart Association.FootnotesCorrespondence to David Spence, Stroke Prevention and Atherosclerosis Research Centre, 1400 Western Rd, London, Ontario, Canada N6G 2V2. E-mail [email protected] References 1 Yatsu FM, Zivin J. Hypertens in acute ischemic strokes. Not to treat. Arch Neurol. 1985; 42: 999–1000.CrossrefMedlineGoogle Scholar2 Spence JD, Del Maestro RF. Hypertension in acute ischemic strokes. Treat Arch Neurol. 1985; 42: 1000–1002.CrossrefMedlineGoogle Scholar3 Johansson B, Strandgaard S, Lassen NA. On the pathogenesis of hypertensive encephalopathy: the hypertensive “breakthrough” of autoregulation of cerebral blood flow with forced vasodilatation, flow increase, and blood brain barrier damage. Circ Res. 1974; 34 (suppl): 167–174.Google Scholar4 Spence JD, Paulson OB, Strandgaard S. Hypertension and Stroke. In: Messerli FH, ed. The ABCs of Antihypertensive Therapy. 2nd ed. New York, NY: Lippincott Williams & Wilkins; 2000: 279–296.Google Scholar5 Vorstrup S, Paulson OB, Lassen NA. Cerebral blood flow in acute and chronic ischemic stroke using xenon-133 inhalation tomography. Acta Neurol Scand. 1986; 74: 439–451.CrossrefMedlineGoogle Scholar6 Nabavi DG, Cenic A, Craen RA, Gelb AW, Bennett JD, Kozak R, Lee TY. CT assessment of cerebral perfusion: experimental validation and initial clinical experience. Radiology. 1999; 213: 141–149.CrossrefMedlineGoogle Scholar7 Spence JD, Zarnke KB. Stroke and Hypertension. In: Oparil S, Weber MA, eds. Hypertension: A Companion to Brenner and Rector’s The Kidney. Philadelphia, PA: W.B. Saunders; 2000: 266–286.Google Scholar8 Adams H, Adams R, Del ZG, Goldstein LB. Guidelines for the early management of patients with ischemic stroke: 2005 guidelines update a scientific statement from the Stroke Council of the Am Heart Association/Am Stroke Association. Stroke. 2005; 36: 916–923.LinkGoogle Scholar9 Schrader J, Luders S, Kulschewski A, Berger J, Zidek W, Treib J, Einhaupl K, Diener HC, Dominiak P. The ACCESS Study: evaluation of acute candesartan cilexetil therapy in stroke survivors. Stroke. 2003; 34: 1699–1703.LinkGoogle Scholar10 Wilmot M, Ghadami A, Whysall B, Clarke W, Wardlaw J, Bath PMW. Transdermal glyceryl trinitrate lowers blood pressure and maintains cerebral blood flow in recent stroke. Hypertension. 2006; 47: 1209–1215.LinkGoogle Scholar Previous Back to top Next FiguresReferencesRelatedDetailsCited By Spence J and Hammond R (2016) Hypertension and Stroke Hypertension and the Brain as an End-Organ Target, 10.1007/978-3-319-25616-0_3, (39-54), . Hocker S, Morales-Vidal S and Schneck M (2010) Management of Arterial Blood Pressure in Acute Ischemic and Hemorrhagic Stroke, Neurologic Clinics, 10.1016/j.ncl.2010.03.021, 28:4, (863-886), Online publication date: 1-Nov-2010. Spence J (2009) Treating Hypertension in Acute Ischemic Stroke, Hypertension, 54:4, (702-703), Online publication date: 1-Oct-2009. Spence J (2007) New treatment options for hypertension during acute ischemic or hemorrhagic stroke, Current Treatment Options in Cardiovascular Medicine, 10.1007/s11936-007-0019-0, 9:3, (242-246), Online publication date: 1-Jul-2007. Lakshminarayan K, Anderson D, Borbas C, Duval S and Luepker R (2007) Blood Pressure Management in Acute Ischemic Stroke, The Journal of Clinical Hypertension, 10.1111/j.1524-6175.2007.06567.x, 9:6, (444-453), Online publication date: 1-Jun-2007. June 2006Vol 47, Issue 6 Advertisement Article InformationMetrics https://doi.org/10.1161/01.HYP.0000223025.17605.3cPMID: 16682610 Originally publishedMay 8, 2006 PDF download Advertisement