Alexandrov Anne W, Coleman Kisha C, Palazzo Paola, Shahripour Reza Bavarsad, Alexandrov Andrei V
Stroke Team and Mobile Stroke Unit, University of Tennessee Health Science Center & Australian Catholic University, Sydney, Australia. Address: UTHSC CON 920 Madison, Suite 532, Memphis, TN 38163, USA.
Blue Cross/Blue Shield of Alabama, Birmingham, Alabama.
Ther Adv Neurol Disord. 2016 Jul;9(4):304-9. doi: 10.1177/1756285616648061. Epub 2016 May 15.
In the USA, stable intravenous tissue plasminogen activator (IV tPA) patients have traditionally been cared for in an intensive care unit (ICU). We examined the safety of using an acuity-adaptable stroke unit (SU) to manage IV tPA patients.
We conducted an observational study of consecutive patients admitted to our acuity-adaptable SU over the first 3 years of operation. Safety was assessed by symptomatic intracerebral hemorrhage (sICH) rates, systemic hemorrhage (SH) rates, tPA-related deaths, and transfers from SU to ICU; cost savings and length of stay (LOS) were determined.
We admitted 333 IV tPA patients, of which 302 were admitted directly to the SU. A total of 31 (10%) patients had concurrent systemic hemodynamic or pulmonary compromise warranting direct ICU admission. There were no differences in admission National Institutes of Health Stroke Scale scores between SU and ICU patients (9.0 versus 9.5, respectively). Overall sICH rate was 3.3% (n = 10) and SH rate was 2.9 (n = 9), with no difference between SU and ICU patients. No tPA-related deaths occurred, and no SU patients required transfer to the ICU. Estimated hospital cost savings were US$362,400 for 'avoided' ICU days, and hospital LOS decreased significantly (p = 0.001) from 9.8 ± 15.6 days (median 5) in year 1, to 5.2 ± 4.8 days (median 3) by year 3.
IV tPA patients may be safely cared for in a SU when nurses undergo extensive education to ensure clinical competence. Use of the ICU solely for monitoring may constitute significant overuse of system resources at an expense that is not associated with additional safety benefit.
在美国,传统上一直是在重症监护病房(ICU)护理接受稳定静脉注射组织型纤溶酶原激活剂(IV tPA)治疗的患者。我们研究了使用适应病情严重程度的卒中单元(SU)管理接受IV tPA治疗患者的安全性。
我们对运营的前3年中连续入住我们适应病情严重程度的SU的患者进行了一项观察性研究。通过症状性脑出血(sICH)发生率、全身性出血(SH)发生率、与tPA相关的死亡以及从SU转至ICU的情况来评估安全性;确定成本节约和住院时间(LOS)。
我们收治了333例接受IV tPA治疗的患者,其中302例直接入住SU。共有31例(10%)患者同时存在全身性血流动力学或肺部功能不全,需要直接入住ICU。SU患者和ICU患者入院时的美国国立卫生研究院卒中量表评分无差异(分别为9.0和9.5)。总体sICH发生率为3.3%(n = 10),SH发生率为2.9%(n = 9),SU患者和ICU患者之间无差异。未发生与tPA相关的死亡,且没有SU患者需要转至ICU。“避免”的ICU天数估计节省医院成本362,400美元,医院住院时间显著缩短(p = 0.001),从第1年的9.8±15.6天(中位数5天)降至第3年的5.2±4.8天(中位数3天)。
当护士接受广泛教育以确保临床能力时,接受IV tPA治疗的患者可以在SU中得到安全护理。仅将ICU用于监测可能构成对系统资源的严重过度使用,且不会带来额外的安全益处。