文章摘要
张海廷,王维,郭海晓,周红,张瑞云,李佳平.脑桥旁正中穿支动脉粥样硬化病临床特点分析[J].神经损伤功能重建,2025,(2):67-72
脑桥旁正中穿支动脉粥样硬化病临床特点分析
Analysis of Clinical Features of Paramedian Pontine Branch Atheromatous Disease
  
DOI:
中文关键词: 穿支动脉粥样硬化性病  脑桥旁正中动脉  静脉溶栓  替罗非班
英文关键词: paramedian pontine arteries  branch atheromatous disease  intravenous thrombolysis  tirofiban
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作者单位
张海廷,王维,郭海晓,周红,张瑞云,李佳平 民航总医院神经内 科 
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中文摘要:
      目的:探讨脑桥旁正中动脉(paramedian pontine arteries,PPA)穿支动脉粥样硬化病(branch atheromatous disease,BAD)所致脑梗死PPA-BAD的临床特点。方法:回顾性分析2018年至2024年在民航总医院神 经内科确诊PPA-BAD的患者221例,根据是否发生进展性运动功能缺损分为进展组(140例)和对照组(81 例);根据预后情况分为预后良好组(163例)和预后不良组(58例);根据是否接受重组组织型纤溶酶原激活 物(rt-PA)溶栓治疗分为治疗组(14例)和对照组(207例);对于进展组患者,根据是否使用替罗非班,分为替 罗非班治疗组(42例)和对照组(98例)。对各组人口统计学、临床及影像学资料进行比较,同时探讨rt-PA 静脉溶栓及替罗非班治疗的效果。结果:①起病6 h后进展140例(63.3%),提示PPA-BAD容易出现进展加 重;进展组患者高脂血症患者及以偏瘫症状起病者比例较高,起病、达峰、出院时的NIHSS评分较高(均P< 0.05);进展组预后较对照组差(P<0.05)。②Logistic多因素分析提示高龄、伴有陈旧性脑梗死、发生进展 性运动功能缺损、梗死面积大提示预后不良(均P<0.05);临床表现伴有头晕和共济失调的患者则更可能 呈现预后良好的趋势(P<0.05)。③rt-PA静脉溶栓和替罗非班安全性高;用药组和对照组的预后差异无统 计学意义(P>0.05)。结论:PPA-BAD患者容易发生进展性运动功能缺损;高龄、伴有陈旧性脑梗死、发生 进展性运动功能缺损、梗死面积大等因素易导致预后不良;目前尚缺乏有效的临床预测指标,需要针对个 体进行综合性治疗;推荐应用rt-PA静脉溶栓及替罗非班以提高疗效。
英文摘要:
      To explore the clinical characteristics of cerebral infarction caused by paramedian pontine arteries (PPA) branch atheromatous disease (BAD) - PPA-BAD. Methods: A retrospective analysis was conducted on 221 patients diagnosed with PPA-BAD in the Department of Neurology, Civil Aviation General Hospital from 2018 to 2024. According to the presence or absence of progressive motor deficits, patients were divided into a progressive group (140 cases) and a control group (81 cases); based on prognosis, they were classified into a good prognosis group (163 cases) and a poor prognosis group (58 cases); depending on whether they received recombinant tissue plasminogen activator (rt-PA) thrombolytic therapy, they were divided into a treatment group (14 cases) and a control group (207 cases); for patients in the progressive group, based on whether tirofiban was used, they were divided into a tirofiban treatment group (42 cases) and a control group (98 cases). Demographic, clinical, and imaging data of each group were compared, and the effects of rt-PA intravenous thrombolysis and tirofiban treatment were explored. Results: (1) 140 cases (63.3% ) progressed after 6 hours of onset, indicating that PPA-BAD tends to easily progress and worsen; the proportion of patients with hyperlipidemia and those presenting with hemiplegia symptoms was higher in the progressive group, and the NIHSS scores at onset, peak, and discharge were higher (all P<0.05); the prognosis of the progressive group was worse than that of the control group (P<0.05). (2) Logistic multivariate analysis indicated that advanced age, history of old cerebral infarction, occurrence of progressive motor deficits, and large infarct size suggested a poor prognosis (all P<0.05); clinical manifestations accompanied by dizziness and ataxia tended to show a trend of good prognosis (P<0.05). (3) rt-PA intravenous thrombolysis and tirofiban were safe; there was no statistically significant difference in prognosis between the medication group and the control group (P>0.05). Conclusion: Patients with PPA-BAD are prone to developing progressive motor deficits; factors such as advanced age, history of old cerebral infarction, occurrence of progressive motor deficits, and large infarct size can lead to poor prognosis; currently, there is a lack of effective clinical predictive indicators, necessitating comprehensive individualized treatment; the application of rt-PA intravenous thrombolysis and tirofiban is recommended to improve therapeutic efficacy.
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