Bassetti C, Aldrich M S, Chervin R D, Quint D
Department of Neurology, University of Michigan Hospitals, Ann Arbor 48109-0316, USA.
Neurology. 1996 Nov;47(5):1167-73. doi: 10.1212/wnl.47.5.1167.
Although sleep apnea (SA) appears to be a cardiovascular risk factor, little is known about its frequency in patients with transient ischemic attack (TIA) and stroke. We prospectively studied 59 subjects (26 women and 33 men; mean age, 62 years) with stroke (n = 36) or TIA (n = 23) with the use of a standard protocol that included assessment of snoring and daytime sleepiness (Epworth Sleepiness Score [ESS]), a validated SA score (Sleep Disorders Questionnaire [SDQ-SA]), and a severity of stroke score (Scandinavian Stroke Scale [SSS]). SA was considered clinically probable (P-SA) when habitual snoring was associated with an ESS of > 10 or when SDQ-SA score was > or = 32 in women and > or = 36 in men. Polysomnography (PSG) was obtained in 36 subjects (group 1) a mean of 12 days after TIA or stroke. In 23 subjects (group 2), PSG was not available (n = 11), refused (n = 10), or inadequate (n = 2). Clinical and PSG data were compared with those obtained in 19 age- and gender-matched control subjects. Groups 1 and 2 were similar in mean age (61 versus 64 years), type of event (36% versus 44% TIA), reported habitual snoring (58% versus 52%), and P-SA (58% versus 50%). PSG showed SA (Apnea-Hypopnea Index [AHI], > or = 10) in 25 of 36 subjects (69%). The proportion of subjects with SA was similar in the TIA and stroke groups (69% versus 70%) and was well above the frequency found in our control group (15%). An AHI of > or = 20 and a minimal oxygen saturation of < 85% were each found in 20 of 36 subjects (55%). Gender and age did not correlate with severity of SA. Subjects with habitual snoring, P-SA, or severe stroke (SSS of < 30) had a significantly higher AHI (p < 0.05). The sensitivity of P-SA for SA was 64%, and the specificity was 67%. We conclude that SA has a high frequency in patients in the acute phase of TIA and stroke and SA cannot be predicted reliably on clinical grounds alone but is more likely in patients with habitual snoring, abnormal SDQ-SA, or severe stroke.
尽管睡眠呼吸暂停(SA)似乎是一种心血管危险因素,但对于其在短暂性脑缺血发作(TIA)和中风患者中的发生率知之甚少。我们采用标准方案对59例中风(n = 36)或TIA(n = 23)患者(26例女性和33例男性;平均年龄62岁)进行了前瞻性研究,该方案包括评估打鼾情况和日间嗜睡程度(爱泼华嗜睡量表[ESS])、经过验证的SA评分(睡眠障碍问卷[SDQ-SA])以及中风严重程度评分(斯堪的纳维亚中风量表[SSS])。当习惯性打鼾与ESS>10相关,或女性SDQ-SA评分>或=32且男性SDQ-SA评分>或=36时,SA被认为临床上可能存在(P-SA)。36例受试者(第1组)在TIA或中风后平均12天进行了多导睡眠图(PSG)检查。在23例受试者(第2组)中,无法进行PSG检查(n = 11)、拒绝检查(n = 10)或检查不充分(n = 2)。将临床和PSG数据与19例年龄和性别匹配的对照受试者的数据进行比较。第1组和第2组在平均年龄(61岁对64岁)、事件类型(36%对44%为TIA)、报告的习惯性打鼾情况(58%对52%)以及P-SA(58%对50%)方面相似。PSG显示,36例受试者中有25例(69%)存在SA(呼吸暂停低通气指数[AHI],>或=10)。TIA组和中风组中SA患者的比例相似(69%对70%),且远高于我们对照组中的发生率(15%)。36例受试者中有20例(55%)的AHI>或=20且最低血氧饱和度<85%。性别和年龄与SA的严重程度无关。有习惯性打鼾、P-SA或严重中风(SSS<30)的受试者AHI显著更高(p<0.05)。P-SA对SA的敏感性为64%,特异性为67%。我们得出结论,SA在TIA和中风急性期患者中发生率较高,仅根据临床情况无法可靠预测SA,但习惯性打鼾、SDQ-SA异常或严重中风的患者更易发生SA。