Very Early Rehabilitation or Intensive Telemetry after Stroke: A Pilot Randomised Trial

被引:106
作者
Langhorne, Peter [1 ]
Stott, David [1 ]
Knight, Anne [2 ]
Bernhardt, Julie [5 ]
Barer, David [4 ]
Watkins, Caroline [3 ]
机构
[1] Univ Glasgow, Royal Infirm, Acad Sect Geriatr Med, Glasgow G4 0SF, Lanark, Scotland
[2] Royal Infirm, Stroke Unit, Glasgow G4 0SF, Lanark, Scotland
[3] Univ Cent Lancashire, Preston PR1 2HE, Lancs, England
[4] Univ Newcastle, Gateshead Hosp, Stroke Res Unit, Newcastle, NSW 2308, Australia
[5] Natl Stroke Res Inst, Melbourne, Vic, Australia
关键词
Stroke; Very Early Rehabilitation or Intensive Telemetry after Stroke trial; Early active mobilization; Automated monitoring; PHASE-II; AVERT; UNIT; CARE;
D O I
10.1159/000278931
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Stroke patients are more likely to make a good recovery if they receive care in a well-organised stroke unit. However, there are uncertainties about how best to provide such care. We studied 2 key aspects of early stroke unit care: early active mobilisation (EM) and automated monitoring (AM) for physiological complications such as hypoxia. Methods: This was an observer-blinded, factorial (2 x 2) pilot randomised controlled trial recruiting stroke patients within 36 h of symptom onset. The patients were randomised to 1 of 4 nurse-led treatment protocols: (a) standard stroke unit care, (b) EM, (c) AM or (d) combined EM and AM. The primary outcome was the Rankin score at 3 months. We also report the data on feasibility and safety. Results: We randomised 32 patients (mean age = 65 years; mean baseline modified NIH score = 6). On unadjusted comparisons, the EM patients were significantly (p < 0.05) more likely to mobilise very early (within 1 h of randomisation) and to achieve walking by day 5 and were less likely to develop complications of immobility. The AM group was significantly ( p < 0.05) more likely to have pre-defined physiological complication events detected. All these associations remained, but were less statistically significant, after correcting for age, baseline NIH score and co-interventions. There were no significant safety concerns. Discussion: We have demonstrated the feasibility of implementing EM and AM for physiological complications in a randomised controlled trial. Larger trials are warranted to determine whether these interventions have clinical benefits. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:352 / 360
页数:9
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