dc.creator | Krishnan K., Scutt P., Woodhouse L., Adami A., Becker J.L., Cala L.A., Casado A.M., Chen C., Dineen R.A., Gommans J., Koumellis P., Christensen H., Collins R., Czlonkowska A., Lees K.R., Ntaios G., Ozturk S., Phillips S.J., Sprigg N., Szatmari S., Wardlaw J.M., Bath P.M., ENOS Investigators | en |
dc.date.accessioned | 2023-01-31T08:47:10Z | |
dc.date.available | 2023-01-31T08:47:10Z | |
dc.date.issued | 2016 | |
dc.identifier | 10.1016/j.jstrokecerebrovasdis.2016.01.010 | |
dc.identifier.issn | 10523057 | |
dc.identifier.uri | http://hdl.handle.net/11615/75518 | |
dc.description.abstract | Background and purpose More than 50% of patients with acute intracerebral hemorrhage (ICH) are taking antihypertensive drugs before ictus. Although antihypertensive therapy should be given long term for secondary prevention, whether to continue or stop such treatment during the acute phase of ICH remains unclear, a question that was addressed in the Efficacy of Nitric Oxide in Stroke (ENOS) trial. Methods ENOS was an international multicenter, prospective, randomized, blinded endpoint trial. Among 629 patients with ICH and systolic blood pressure between 140 and 220 mmHg, 246 patients who were taking antihypertensive drugs were assigned to continue (n = 119) or to stop (n = 127) taking drugs temporarily for 7 days. The primary outcome was the modified Rankin Score at 90 days. Secondary outcomes included death, length of stay in hospital, discharge destination, activities of daily living, mood, cognition, and quality of life. Results Blood pressure level (baseline 171/92 mmHg) fell in both groups but was significantly lower at 7 days in those patients assigned to continue antihypertensive drugs (difference 9.4/3.5 mmHg, P <.01). At 90 days, the primary outcome did not differ between the groups; the adjusted common odds ratio (OR) for worse outcome with continue versus stop drugs was.92 (95% confidence interval,.45-1.89; P =.83). There was no difference between the treatment groups for any secondary outcome measure, or rates of death or serious adverse events. Conclusions Among patients with acute ICH, immediate continuation of antihypertensive drugs during the first week did not reduce death or major disability in comparison to stopping treatment temporarily. © 2016 The Authors. | en |
dc.language.iso | en | en |
dc.source | Journal of Stroke and Cerebrovascular Diseases | en |
dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957092952&doi=10.1016%2fj.jstrokecerebrovasdis.2016.01.010&partnerID=40&md5=b1f037b4350f009c7bce507de85db685 | |
dc.subject | alpha adrenergic receptor blocking agent | en |
dc.subject | antihypertensive agent | en |
dc.subject | beta adrenergic receptor blocking agent | en |
dc.subject | calcium channel blocking agent | en |
dc.subject | dipeptidyl carboxypeptidase inhibitor | en |
dc.subject | diuretic agent | en |
dc.subject | glyceryl trinitrate | en |
dc.subject | antihypertensive agent | en |
dc.subject | glyceryl trinitrate | en |
dc.subject | nitric oxide donor | en |
dc.subject | aged | en |
dc.subject | antihypertensive therapy | en |
dc.subject | Article | en |
dc.subject | brain hemorrhage | en |
dc.subject | cognition | en |
dc.subject | comparative study | en |
dc.subject | daily life activity | en |
dc.subject | disability | en |
dc.subject | drug efficacy | en |
dc.subject | drug withdrawal | en |
dc.subject | female | en |
dc.subject | human | en |
dc.subject | length of stay | en |
dc.subject | major clinical study | en |
dc.subject | male | en |
dc.subject | mood | en |
dc.subject | morning dosage | en |
dc.subject | multicenter study (topic) | en |
dc.subject | outcome assessment | en |
dc.subject | priority journal | en |
dc.subject | randomized controlled trial (topic) | en |
dc.subject | Rankin scale | en |
dc.subject | systolic blood pressure | en |
dc.subject | blood pressure | en |
dc.subject | clinical trial | en |
dc.subject | controlled study | en |
dc.subject | drug administration | en |
dc.subject | drug effects | en |
dc.subject | hypertension | en |
dc.subject | Intracranial Hemorrhage, Hypertensive | en |
dc.subject | middle aged | en |
dc.subject | mortality | en |
dc.subject | multicenter study | en |
dc.subject | multivariate analysis | en |
dc.subject | odds ratio | en |
dc.subject | pathophysiology | en |
dc.subject | proportional hazards model | en |
dc.subject | prospective study | en |
dc.subject | randomized controlled trial | en |
dc.subject | risk factor | en |
dc.subject | statistical model | en |
dc.subject | Stroke | en |
dc.subject | time factor | en |
dc.subject | treatment outcome | en |
dc.subject | very elderly | en |
dc.subject | Aged | en |
dc.subject | Aged, 80 and over | en |
dc.subject | Antihypertensive Agents | en |
dc.subject | Blood Pressure | en |
dc.subject | Disability Evaluation | en |
dc.subject | Drug Administration Schedule | en |
dc.subject | Female | en |
dc.subject | Humans | en |
dc.subject | Hypertension | en |
dc.subject | Intracranial Hemorrhage, Hypertensive | en |
dc.subject | Linear Models | en |
dc.subject | Logistic Models | en |
dc.subject | Male | en |
dc.subject | Middle Aged | en |
dc.subject | Multivariate Analysis | en |
dc.subject | Nitric Oxide Donors | en |
dc.subject | Nitroglycerin | en |
dc.subject | Odds Ratio | en |
dc.subject | Proportional Hazards Models | en |
dc.subject | Prospective Studies | en |
dc.subject | Risk Factors | en |
dc.subject | Stroke | en |
dc.subject | Time Factors | en |
dc.subject | Treatment Outcome | en |
dc.subject | W.B. Saunders | en |
dc.title | Continuing versus Stopping Prestroke Antihypertensive Therapy in Acute Intracerebral Hemorrhage: A Subgroup Analysis of the Efficacy of Nitric Oxide in Stroke Trial | en |
dc.type | journalArticle | en |