慢性肾病(CKD)患者睡眠障碍的研究

A. Hussein, A. E. hadidy, N. Gomaa, Y. Amin, T. El-Shabouny
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引用次数: 1

摘要

睡眠呼吸暂停是慢性肾脏疾病(CKD)患者的重要合并症。虽然CKD患者睡眠呼吸暂停的患病率增加已经得到证实,但很少有研究对肾功能进行全面检查。我们试图确定CKD患者睡眠呼吸暂停和相关夜间缺氧的患病率。我们假设睡眠呼吸暂停的患病率会随着肾功能的下降而逐渐增加。从门诊肾内科、肾内科和血液透析单位招募45例患者。所有患者均完成过夜住院多导睡眠图检查,以确定睡眠呼吸暂停(AHI≥5事件/小时)和夜间缺氧(血氧饱和度(SaO2)低于90%,夜间监测时间≥12%)的患病率。根据研究访问时估计的肾小球滤过率(eGFR)将患者分为三组:CKD 2期(eGFR 60至89 mL/min/1.73 m2)(对照组),CKD 3期和4期(eGFR 15至59 mL/min/1.73 m2)和CKD 5期(eGFR小于15 mL/min/1.73 m2)。eGFR采用慢性肾脏疾病流行病学合作(CKD-EPI)方程计算。在我们研究的45例肾功能全谱患者中,从eGFR 60 - 89 ml/min /1.73m2到eGFR小于15 ml/min /1.73m2, 15例(33.3%)有睡眠呼吸暂停(平均AHI;8.71±5.86)。我们的研究发现,睡眠呼吸暂停的患病率随着肾功能的下降而增加(I组,20%;II组,36.4%;III组,37.5%)。此外,睡眠呼吸暂停的严重程度随着肾功能的下降而增加(I组,平均AHI: 5.75±0.35;II组,平均AHI: 6±1.38;III组,平均AHI: 10.6±7.04)。我们还发现,与睡眠呼吸暂停相关的夜间缺氧在(II)和(III)组中的患病率(分别为27.3%和16.7%)高于(I)组(10%)。夜间缺氧的严重程度随着肾功能的下降而增加(I组,13%;II组:13.6±1.22%;III组,16.75±3.30%)。总体而言,45例CKD患者中有8例(17.8%)出现夜间缺氧(平均SaO2低于90%,夜间监测时间≥12%;15.1±2.87%)。我们的研究发现,随着肾功能的下降,呼吸暂停/低通气(AHI)指数升高,氧去饱和指数升高,最小外周毛细血管氧饱和度值降低,外周毛细血管氧饱和度小于90%的时间增加,打鼾指数升高。(II)组和(III)组呼吸窘迫指数(RDI)均高于(I)组。但只有呼吸窘迫事件、呼吸窘迫指数、打鼾事件和打鼾指数组间差异有统计学意义。这些结果表明,随着肾功能下降,睡眠期间一些呼吸参数也会恶化。此外,觉醒事件和指数以及睡眠阶段1(%)随着肾功能的恶化而增加。睡眠效率(%)在(I)组患者中最高,在(II)组和(III)组患者中较低;轻度睡眠(%)在(I)组患者中最低,在(II)组和(III)组患者中较高;深度睡眠(%)在(I)组患者中最高,在(II)组和(III)组患者中较低。从上述结果可以清楚地看出,随着肾功能下降,睡眠效率恶化,清醒指数增加,轻度睡眠(%)增加,深度睡眠(%)减少。我们得出结论,CKD患者睡眠呼吸暂停的患病率和严重程度随着肾功能下降而增加。几乎18%的CKD患者经历夜间缺氧,这可能导致肾功能丧失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Study of Sleep Disorders in Patients with Chronic Kidney Disease (CKD)
Sleep apnea is an important comorbidity in patients with chronic kidney disease (CKD). Although the increased prevalence of sleep apnea in patients with CKD is well established, few studies have examined the full spectrum of kidney function. We sought to determine the prevalence of sleep apnea and associated nocturnal hypoxia in patients with CKD. We hypothesized that the prevalence of sleep apnea would increase progressively as kidney function declines. 45 patients were recruited from outpatient nephrology clinics, nephrology department, and hemodialysis units. All patients completed an overnight inpatient polysomnograhy test to determine the prevalence of sleep apnea (AHI ≥ 5 events /h) and nocturnal hypoxia (oxygen saturation (SaO2) below 90% for ≥12% of the nocturnal monitoring time). Patients were stratified according to their estimated glomerular filtration rate (eGFR) at the time of the study visit into three groups as follows: CKD stage 2 (eGFR 60 to 89 mL/min/1.73 m2) (control group), CKD stages 3 and 4 (eGFR 15 to 59 mL/min/1.73 m2), and CKD stage 5 (eGFR less than 15 mL/min/1.73 m2). eGFR was calculated using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation. Out of the 45 patients included in our study with the full spectrum of kidney function, ranging from those with eGFR 60 to 89 ml/min./1.73m2 to patients with eGFR less than 15 ml/min./1.73m2, 15 (33.3%) had sleep apnea (Mean AHI; 8.71±5.86). Our study found that prevalence of sleep apnea increased as kidney function declined (Group (I), 20%; Group (II), 36.4%; Group (III), 37.5%). Furthermore, severity of sleep apnea increased as kidney function declined (Group (I), mean AHI: 5.75±0.35; Group (II), mean AHI: 6±1.38; Group (III), mean AHI: 10.6±7.04). We also found that prevalence of nocturnal hypoxia which is characteristically associated with sleep apnea was greater among groups (II) and (III) (27.3% and 16.7%, respectively) than in group (I) (10%). Severity of nocturnal hypoxia increased as kidney function declined (Group (I), 13%; Group (II), 13.6±1.22%; Group (III), 16.75±3.30%). Overall, 8 out of the 45 studied CKD patients (17.8%) had nocturnal hypoxia (Mean SaO2 below 90% for ≥12% of the nocturnal monitoring time; 15.1±2.87%). Our study revealed that as kidney function declined, Apnea/Hypopnea (AHI) indices increased, oxygen desaturation indices increased, minimal peripheral capillary oxygen saturation values decreased, peripheral capillary oxygen saturation time less than 90% increased, and snore indices increased. Also, respiratory distress index (RDI) was higher among groups (II) and (III) than in group (I). However, only differences between groups as regards respiratory distress events, respiratory distress indices, snore events, and snore indices were statistically significant. These results show that as kidney function declines, several respiratory parameters deteriorate during sleep. In addition, wake events and indices, and sleep stage 1 (%) increased as kidney function deteriorated. Sleep efficiency (%) was highest among group (I) patients and lower among groups (II) and (III), Light sleep (%) was lowest among group (I) patients and higher among groups (II) and (III), and deep sleep (%) was highest among group (I) patients and lower among groups (II) and (III). It is clear from the above results that as kidney function declines, sleep efficiency deteriorates, wake indices increase, light sleep (%) increases, and deep sleep (%) decreases. We concluded that prevalence and severity of sleep apnea in patients with CKD increase as kidney function declines. Almost 18% of patients with CKD experience nocturnal hypoxia, which may contribute to loss of kidney function.
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