Abstract
Background:
Stroke patients have sleep-wake disorders, mostly in form of insomnia, excessive daytime sleepiness/fatigue, or hypersomnia (increased sleep needs).
Objective:
The aim of this study was to analyze types of sleep disorder (SD) and their frequency in patients with sleep apnea and acute stroke in relation to the type of stroke and side of lesion.
Methods:
The study analyzed 110 patients with sleep apnea and acute stroke hospitalized in the Clinic of Neurology, University Clinical Centre Tuzla. Acute stroke has been verified either by computerized tomography or magnetic resonance imaging of the brain. SD was verified according to the Berlin Questionnaire Test, The Epworth Sleepiness Scale, The Stanford Sleepiness Scale and the General sleep questionnaire. Strokes were divided by: a) type, into hemorrhagic and ischemic, and b) the localization of the stroke, to right and left cerebral hemispheres.
Results:
Of the total number of respondents, all had some sleep disorder. 20% of respondents had severe level of SD, 35.4% moderate, 37.3% moderate- severe and 7.3% mild problems. There were no statistically significant differences in the frequency of SD among patients with ischemic and hemorrhagic stroke (p = 0.58). In relation to the side of lesion, there was more patient with SD and stroke in the both sides, but there were no statistically significant differences (X2=1.98, p=0.161). According Epworth Sleepiness Scale, Stanford Sleepiness Scale and Berlin Questionnaire test snoring was present in 81% and daytime sleepiness in all patients.
Conclusion:
SD as a neuropsychological disorder has a significant incidence in the acute phase of stroke in patients with sleep apnea. Sleep disorder is more common in ischemic stroke and stroke in the both hemisphere, but it is not statistically significant difference. Daytime sleepiness, fatigue and snoring are the most common sleep problems in patients with acute stroke and apnea, but it is not statistically significant.
Keywords: Stroke, Sleep Apnea, Sleep Disorders
1. BACKGROUND
Sleep apnea (SA) affects about 10% to 20% of middle to older aged adults (1), is characterized by the repeated obstruction of the upper airway during sleep that leads to complete cessation (apnea) or reduction (hyperpnea) of airflow, occurring irrespective of continued ventilatory effort. Before termination, these events lead to a decrease in blood oxygen saturation and an associated increase in carbon dioxide levels during longer events. The termination of the apnea is often preceded by an arousal, which leads to sleep fragmentation and activation of the sympathetic nervous system. The former is hypothesized to be involved in the neurocognitive sequelae, whereas the latter leads to cardiovascular dysfunction. This process is identified as the possible cause for the daytime sleepiness and cardiovascular health and functioning problems witnessed in these individuals (2, 3). Severe obstructive sleep apnea (OSA) has been linked to a 4- to 6-fold increased risk of mortality, irrespective of factors such as age, diabetes, or high cholesterol (4, 5).,Finally, rate of insomnia vary as a function of OSA severity. Supratentorial strokes have been linked to decreases in NREM sleep time, and to a lower sleep efficiency (6).
2. OBJECTIVE
The aim of this study was to analyze types of sleep disorder (SD) and their frequency in patients with sleep apnea and acute stroke in relation to the type of stroke and side of lesion.
3. PATIENTS AND METHODS
This prospective study was conducted at the Clinic of Neurology of the University Clinical Center in Tuzla. The examined group of 110 patients in the acute phase of stroke with SA was evaluated. The average age was 65.13 ± 9.27 years. Among them, it was 65 (59%) men. The study group included patients who meet the following criteria: confirmation of a diagnosis of ischemic stroke (IS) or a hemorrhagic stroke (HS) by computed tomography (CT) and/or magnetic resonance imaging (MR) of the brain, neuropsychiatric assessment of SA performed within seven days after stroke, Mini Mental test (MMT) > 23, Glasgow coma scale (GCS) > 8, written consent for participation in the research by the patients or a member of the patients immediate family. Patients with a GCS <8 on the day of neuropsychiatric examination were excluded from the study, as well as patients with epileptic seizures at the onset of stroke, with aphasia, with MMT< 23, with verified previous dementia/cognitive impairment (based on hetero anamnesis data from patients relatives, data from previous medical findings). Neurological tests were performed in all patients at five different periods: the first test–in the acute phase of stroke (first week of stroke), second test–one month after the stroke, third test- three months after stroke, fourth test–six months after stroke and fifth test–twelve months after stroke. In these periods, all patients were evaluated by: the Mini Mental Test (7), the Berlin Questionnaire Test (8), the Epworth Sleepiness Scale (9), the Stanford Sleepiness Scale (10) and the General Sleep questionnaire (11). The findings of CT of the brain and MR of the brain were interpreted by a radiologist who was not familiar with the goals and hypotheses of the research. Based on these interpretations, there were established: type of stroke, localization of the lesion, and lesion size. The study included also the data of the following socio-demographic characteristics: gender and age.
4. Methods / Instruments
Berlin Questionnaire Test
The Berlin Questionnaire included 10 questions on risk factors for SA, including body weight, snoring, breathing pauses, drowsiness on walking or during the day and hypertension. The ranking of the answers is gradual: 0 = never or almost never, 1 = 1 to 2 times a month, 2 = 1 to 2 times a week, 3 = 3 times a week and 4 = almost every day.
Epworth Sleepiness Scale
It consists of 4 parts that analyze drowsiness, sleep apnea/snoring, narcolepsy and other disorders. Scoring and analysis were performed according to the attached key. The ranking of the answers is gradual: 1 = rarely or never, 2 = sometimes, 3 = often, 4 = mostly.
Stanford Sleepiness Scale
The Stanford Sleepiness Scale is designed to self fatigue and measure drowsiness. It consists of 7 levels that describe the degree of drowsiness. If the patients score is above 3, he has serious sleep problems.
General Sleep Questionnaire
This questionnaire contains the following data: socio demographic (name, age, gender, and occupation), sleep pattern data, daytime sleepiness, chronic somatic diseases, and health data. The questionnaire has a total of 46 questions.
Statistical analysis
When testing the statistical significance of main differences, the standard Student T-test was used. Descriptive statistics were processed using the X2 (Hi–square test) and the proportional test. All calculations were performed using the Arcus Quickstadt Biomedical statistical data processing program as well as the long rank test with p < 0.05 considered significant. The research was approved by the Committee of the University Clinical Center Tuzla.
5. RESULTS
The study analyzed 500 patients with acute stroke (AS), and of those 110 (22%) were verified SA, with mean age 65.13 ± 9.27 years, and the majority were men 65 (59%). No statistically significant difference was found in the age of patients in either men or women (t = -0.16, p = 0.88). The largest number of patients with SA had an ischemic stroke (92 / 83.6%), while 18 (16.4%) had a HS, of whom 56 (86.2%) were men and 36 (80%) were women with IS and 9 (13.8 %) men and 9 (20%) women with HS. Of the patients with IS 92 (83.6%) had sleep disorders. According to the severity of the problem, 38 of them (41.3%) stated that they had a moderate-severe sleep problem, 34 (37%) moderate, 16 (17.4%) severe and 4 (4.34%) did not have a serious sleep problem. In patients with HS, 18 (16.4%) had sleep disturbance. According to the severity of the problem, 6 (33.3%) patients had severe sleep problem, 5 (27.7%) moderate, 3 (16.7%) moderate severe and 4 (22.3%) did not have a serious sleep problem. The X2 (Chi-square test) found that the presence of sleep disorders did not depend on the type of MU (X2= 0.31, p = 0.58). According to the ratio of sleep disorders, the incidence of sleep disorders is 1.41 times more common in the case of hemorrhagic stroke (95%, CI: 0.55-4.11), but the chances of sleep disorders in these two types of stroke do not differ statistically significantly (Tables 1).
Table 1. The severity of sleep problems in patients with ischemic and haemorrhagic stroke. Ischemic–hemorrhagic stroke X2= 0.31, p = 0.58.
The severity of sleep problems | Ischemic stroke N=92 | Percentage Hemorrhagic stroke Percentage % N=18 % |
---|---|---|
Mild | 4 | 4.3 4 22.3 |
Moderate | 38 | 41.3 3 16.7 |
Moderate–severe | 34 | 37.0 5 27.7 |
Severe | 16 | 17.4 6 33.3 |
Out of 50 (45.4.6%) patients had lesions in both hemispheres. Of these, 18 (36%) had moderate sleep problems, 17 (34%) moderate severe, 12 (24%) severe and 3 (6%) had no serious sleep problems. Of the 34 (31%) patients with right hemisphere stroke, 16 (47%) had moderate sleep problems, 10 (29%) had moderate-severe problems, 6 (18%) had severe problems, and 2 (6%) had no serious sleep problems. Lesions in the left hemisphere had 26 (23.6%) patients, of whom 12 (46%) had a moderately severe problem, 7 (27%) had a moderate problem, 4 (15%) had a severe problem and 3 (12%) had no serious sleep problem. Chi-square test found that the frequency of sleep problems in patients with stroke did not depend on the side of the lesion (X2 = 1.98, p = 0.161) (Table 2).
Table 2. The severity of sleep problems in relation to the side of the stroke. Left-right-both sides X2=1.98, p=0.161.
The severity of sleep problems | Left N=26 % | Right Both sides N=34 % N=50 % |
---|---|---|
Mild | 3 12.0 | 2 6.0 3 6.0 |
Moderate | 7 27.0 | 16 47.0 18 36.0 |
Moderate–severe | 12 46.0 | 10 29.0 17 34.0 |
Severe | 4 15.0 | 6 18.0 12 24.0 |
When examining the presence of sleep disorders according to the general questionnaire, sleep patterns were analyzed. In sleep patterns, the average time to go to sleep and the duration of sleep were analyzed. It was determined that the average time to go to sleep is 22h 34 ` ± 1h 52, and the length of sleep is 6h 23 ` ± 38 `. According to the length of sleep disorders in patients with SA, the average duration of the disorder was 28.6 months (12 to 120). The largest number of patients, 41 (37%), had sleep disturbances of 49-60 months, followed by 16 (15%) who had more than 72 months, 15 (14%) who had 61-72 months, 14 (13%) who had 25-36 months, 12 (11%) who had from 37–48 months and 12 (11%) who had less than 24 months (Table 3).
Table 3. Distribution of patients with sleep apnea in relation to the duration of sleep problems. Descriptive statistics: X med= 61.6 months; SD=28.6 months; X min=12 months; X max=120 months.
Duration months | Number of respondents N=110 | Percentage % |
---|---|---|
⩽24 | 12 | 10.91 |
25-36 | 14 | 12.73 |
37-48 | 12 | 10.91 |
49-60 | 41 | 37.27 |
61-72 | 15 | 13.64 |
>72 | 16 | 14.55 |
According to the severity of sleep problems, the largest number of patients with SA had a moderate problem 41 (37%) patients, 39 (35%) had a moderately severe problem, 22 (20%) severe problem and 8 (7.27%) not serious problem.
According to the Berlin Questionnaire, 89 (80.9%) patients reported snoring during sleep, and 21 (19%) denied snoring. Almost every day 51 (46.36%) patients snore, 25 (22.73%) snore 3-4 times a week, 8 (7.27%) snore 1-2 times a week and 5 (4.55%) snore 1-2 times a month (Table 4).
Table 4. Distribution of patients with sleep apnea in relation to the frequency of snoring.
Frequency of snoring | Number of respondents N=110 | Percentage % |
---|---|---|
Never | 21 | 19.09 |
(1-2) times per month | 5 | 4.55 |
(1-2) times a week | 8 | 7.27 |
(3-4) times a week | 25 | 22.73 |
Almost every day | 51 | 46.36 |
In the group of patients with stroke, 31 (28.18%) patients had SA almost every day, 39 (35.45%) 3-4 times a week, 40 (36.36%) 1-2 times a week and 1 (0.90%) 1-2 times a month (Table 5).
Table 5. Distribution of patients with sleep apnea in relation to the frequency of respiratory pauses p=0.082.
Frequency of pauses in breathing | Number of respondents N=110 | Percentage % |
---|---|---|
Never | 0 | 0.00 |
(1-2) times per month | 4 | 3.64 |
(1-2) times a week | 44 | 40.00 |
(3-4) times a week | 39 | 35.45 |
Almost every day | 23 | 28.0 |
Sleep fatigue was present in all patients with SA and stroke. Almost every day, 31 (28.18%) of patients had fatigue, 38 (34.55%) 3-4 times a week, 40 (36.36%) 1-2 times a week and 1 (1%) 1-2 times a month. There is no statistically significant difference (p = 0.082) between fatigue and sleep disturbances in patients with SA (Table 6).
Table 6. Distribution of patients with sleep apnea in relation to the incidence of fatigue after sleep, p=0.082.
Incidence of fatigue after sleep | Number of respondents N=110 | Percentage % |
---|---|---|
Never | 0.0 | 0.00 |
(1-2) times per month | 1 | 0.91 |
(1-2) times a week | 40 | 36.36 |
(3-4) times a week | 38 | 34.55 |
Almost every day | 31 | 28.18 |
Analyzing sleep disorders according to the Epworth Sleepiness Scale, the results showed that the most common disorder was daytime sleepiness present in 110 (100%) patients of the study group, of which 75 (68.18%) had moderate sleepiness. 40 (36.36%) patients had moderate SA and 48 (43.6%) patients had moderate SA. Narcolepsy was not present in any patient. Other sleep disorders, which included periodic limb movements, restless legs syndrome, gnashing of teeth, walking, or speech during sleep, had 11 (10%) respondents.
According to the Stanford Sleepiness Scale, the results showed that daytime drowsiness was present in 110 (100%) patients, of which 69 (62.7%) had moderate drowsiness, 21 (19.1%) moderate severe and 20 (18.2%) patients severe drowsiness (Table 7).
Table 7. Distribution of patients in relation to sleep disorders according to the Stanford scale.
Sleepiness after sleep | Number of respondentsN=110 | Percentage % |
---|---|---|
Never | 0.0 | 0.00 |
Moderate | 69 | 62.7 |
Moderate-severe | 21 | 19.1 |
Severe | 20 | 18.2 |
6. DISCUSSION
Patients with stroke, primarily ischemic, may suffer from several types of sleep disorders, and their manifestation may depend on the severity of the neurological deficit (12). In this study, the presence of sleep problems was noted in all patients with stroke and SA. The majority of subjects 37% had a moderate degree, 35.4% moderately severe, 20% severe, and 7.3% of patients reported mild sleep disturbance. These results indicate that there is a high incidence of sleep disorders in patients with stroke. The largest number of surveyed patients with SA had an IS of 83.6% and all of them stated that they had more or less sleep problems, and the largest number of 41.3% had a moderately severe degree of sleep disorders. 16.4% of patients had HS, and the largest number, 33.3%, had a very serious sleep problem. The differences are not statistically significant. According to a prospective study conducted on 152 patients with acute IS, Bassetti et al. (13) confirmed that patients with acute IS have a high incidence of SD, it was 72%, and in a large number of cases SD precede stroke, including transient ischemic attack. In this study, relative to the lesion side, the largest number of patients had a stroke of 45.4% in both hemispheres. A chi-square test found that the frequency of sleep problems in patients with stroke did not depend on the side of the lesion, which supports the results of other studies. Wierzbick et al. (14) analyzed the influence of a foreign lesion on SD in 43 patients with stroke. Out of those, lesions were reported in one hemisphere for 35 patients, of whom 19 had lesions in the left and 16 in the right hemisphere, while other patients had lesions in both hemispheres. The results of this study also indicated that the side of the stroke lesion was not associated with SD. In this study in the SA group, the mean duration of sleep disorders was 61.6 ± 28.6 (range 12–120) months. The largest number of patients had sleep disturbances of 4-60 months (37%), followed by more than 72 months (14.5%). All patients had increased daytime sleepiness and difficulty sleeping at night. In the Pasic study, sleep problems were reported in 78% of patients with stroke and, for the most part, the problem was very severe, while 22% of patients denied sleep problems (15). The results of our study indicate that there is a high incidence of SD in patients with stroke and SA. According to a study with 190 patients with SA and stroke increased drowsiness was found in 47% of patients, which is lower than in this study (16). According to the Berlin Questionnaire, 81% of patients stated that they snore during sleep, and 19% denied snoring. Almost every day 46.4% snore and 22.7% snore 3-4 times a week. Similar results were found in the Pasic study that was conducted in 200 patients with stroke and sleep disturbances where it was stated that 82.5% snore during sleep, which is identical to our study (15). Similar results are reported by Dunai et al. (17), in a study conducted on 12.643 patients, where snoring was registered in 58% of cases almost every day, and confirmed that patients who snore have a 67% higher risk of stroke compared to patients who do not snore. According to other studies, there is a significant association between snoring and stroke (18). Snoring is significantly more common in patients who have suffered stroke (47.4%), and SA is present in 60% of patients with stroke and snoring in the post-acute period (19). Similar results as in our study were obtained by Sprigs et al. (20) in a study conducted in 400 patients with stroke and 400 control groups, adjusted by age and sex. Snoring was verified in 81.5% patients with stroke and 86.2% patients in the control group. The risk ratio for patients with stroke is 3.2 times higher for regular snorers, as opposed to those who did not snore regularly. Palomaki (21) states that the probability ratio of snoring as a risk factor for IS was greatly increased if snoring is accompanied by excessive daytime sleepiness and obesity, probably due to a higher incidence of SA in among snorers compared to non-snorers. In this study in the group of patients with stroke and SA, 28.18% had SA almost every day and 35.45% of patients 3-4 times a week. The Pasic study stated that the largest number of patients, 23.5%, have SA almost every day, and 15% of patients 3-4 times a week (15). Many researchers have shown that the association between stroke and SA is quite high, somewhere between 30% -90% in surviving patients (22, 23), which is support4ed by our study. In our study, sleep fatigue was present in almost every day in 28.18% and in 34.55% patients 3-4 times a week. There was no statistically significant difference (p = 0.082) between fatigue and sleep disturbances. Coleei et al. (24) claim that 37% of patients with stroke and SA experience sleep fatigue. Thurnheer et al. (16) reported energy deficiency in 62% and fatigue in 57% of patients with stroke and SA. According to the Epworth scale, the presence of daytime sleepiness was found in all patients with SA. Moderate daily drowsiness was present in 68% of patients, of whom 30% had severe drowsiness and 1.8% had moderate drowsiness. According to Guilleminault et al. (25) daytime sleepiness ranged from 30% -40% in patients with SA. Similar results were obtained in his study by Jha et al. (26) who reported a prevalence rate of excessive daytime sleepiness of 11% to 53% in patients with SA. The Epworth scale for daytime sleepiness was used, which confirmed the presence of this problem in 47% of milder patients, while 9% of patients had a more severe degree of daytime sleepiness. This study also indicates that the risk of stroke is 4.5 times higher in those patients who have a more severe degree of daytime sleepiness, while this risk is significantly reduced, to 2.6 times, in patients who have mild forms of the problem. Narcolepsy, as a form of sleep disorder, occurs in 20%-40% of patients after stroke; however in this study it was not observed in any patient with SA. Patients with a milder form of this disease often remain undiagnosed (27). According to the Stanford Sleepiness Scale, the results showed that daytime drowsiness was recorded in all patient patients with SA, of whom 62.7% had moderate drowsiness, 19.1% moderate severe and 18.2% had severe. According to Happe, excessive daytime sleepiness (EDS) occurs in 30% of the elderly and is defined by a subjective feeling of much-needed sleep at unusual times and in unusual places (28). It occurs far more frequently in stroke and primary sleep disorders such as SA, narcolepsy, and periodic limb movements during sleep (PLMS) (29-31). In the study of 190 patients with SA and stroke, lack of energy was found in 62%, fatigue in 57% and drowsiness in 47% of patients. When asked to choose the most significant symptom, 40% of patients said it was a loss of energy, and 22% said they were drowsy (16).
7. CONCLUSION
Sleep disturbance has a significant incidence in the acute phase of stroke in patients with sleep apnea. Sleep disorder is more common in ischemic stroke and stroke in the both hemisphere. Daytime sleepiness, fatigue and snoring are the most common sleep problems in patients with acute stroke and apnea.
Acknowledgements:
We would like to thank the participants for taking part in the study, as well as the staff of medical wards who participated in their treatment.
Author’s contribution:
Biljana Kojic contributed to the idea. Zikrija Dostovic, Mirjana Vidovic, Omer C. Ibrahimagic, Renata Hodzic and AmraIljazovic contributed to the critical revision of the paper. Final proof reading was made by the first author.
Conflict of interest:
None to declare.
Financial support and sponsorship:
Nil.
REFERENCES
- 1.Vgontzas AN, Liao D, Pejovic S, et al. Insomnia with short sleep duration and mortality: the Penn State cohort. Sleep. 2010;33(9):1159–1164. doi: 10.1093/sleep/33.9.1159. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Marin JM, Agusti A, Villar I, et al. Association between treated and untreated obstructive sleep apnea and risk of hypertension. JAMA. 2012;307(20):2169–2176. doi: 10.1001/jama.2012.3418. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Nieto FJ, Young TB, Lind BK, et al. Association of sleep-disordered breathing, sleep apnea, and hypertension in a large community-based study. Sleep Heart Health Study. JAMA. 2000;283(14):1829–1836. doi: 10.1001/jama.283.14.1829. [DOI] [PubMed] [Google Scholar]
- 4.Marshall NS, Wong KK, Liu PY, et al. Sleep apnea as an independent risk factor for all-cause mortality: the Busselton Health Study. Sleep. 2008;31(8):1079–1085. [PMC free article] [PubMed] [Google Scholar]
- 5.Young T, Finn L, Peppard PE, et al. Sleep disordered breathing and mortality: eighteen-year follow-up of the Wisconsin sleep cohort. Sleep. 2008;31(8):1071–1078. [PMC free article] [PubMed] [Google Scholar]
- 6.Guilleminault C, Eldridge FL, Dement WC. Insomnia with sleep apnea: a new syndrome. Science. 1973;181(4102):856–858. doi: 10.1126/science.181.4102.856. [DOI] [PubMed] [Google Scholar]
- 7.Folstein MF, Folstein SE, Mc Hugh PR. Mini–Mental State: A practical method for grading the cognitive of patients for the clinical. J Psych Res. 1975;12:189–198. doi: 10.1016/0022-3956(75)90026-6. [DOI] [PubMed] [Google Scholar]
- 8.Netzer CM, Clark K, Strohl KP. Using the Berlin Questionnaire to identify patients at risk for the sleep apnea syndrome. Ann Intern Med. 1999;131:485–491. doi: 10.7326/0003-4819-131-7-199910050-00002. [DOI] [PubMed] [Google Scholar]
- 9.Johns MW. A new method for measuring daytime sleepiness, The Epworth Sleepiness Scale. Sleep. 1991;14:540–545. doi: 10.1093/sleep/14.6.540. [DOI] [PubMed] [Google Scholar]
- 10.Hoddes E, Zarcone V, Smythe H, Phillips R, Dement W. Quantification of sleepiness: a new approach. Phychophysiology. 1973;10:431–436. doi: 10.1111/j.1469-8986.1973.tb00801.x. [DOI] [PubMed] [Google Scholar]
- 11.Douglass AB, Bornstein R, Nino-Murcia G, Keenan S, Miles L, Zarcone VP, Guilleminault C, Dement WC. The Sleep Disorders Questionnaire. Sleep. 1994;17(2):160–167. doi: 10.1093/sleep/17.2.160. [DOI] [PubMed] [Google Scholar]
- 12.Harbison J, Ford G, James O, Gibson G. Nasal continuous positive airway pressure for sleep apnea following stroke. Eur Respir. 2002;19(6):1216–1217. [PubMed] [Google Scholar]
- 13.Bassetti C, Milanova M, Gugger M. Sleep-Disordered Breathing and Acute Ischemic Stroke. Stroke. 2006;37:967–972. doi: 10.1161/01.STR.0000208215.49243.c3. [DOI] [PubMed] [Google Scholar]
- 14.Wierzbicka A, Rola R, Wichniak A, Richter P, Ryglewicz D, Jernajczyk W. The incidence of sleep apnea in patients with stroke or transient ischemic attack. J Physiol Pharmacol. 2001;57(4):385–390. [PubMed] [Google Scholar]
- 15.Pasic Z. Sleep disorders in stroke patients. Master’s thesis. Faculty of Medicine, University of Tuzla. 2009 [Google Scholar]
- 16.Thurnheer R, Wraith PK, Douglas NJ. Influence of age and gender on upper airway resistance in NREM and REM sleep. J Appl Physiol. 2001;90(3):981–988. doi: 10.1152/jappl.2001.90.3.981. [DOI] [PubMed] [Google Scholar]
- 17.Dunai A, Keszei A, Kopp M, Shapiro C, Mucsi I, Novak M. Loud snoring associated with higher stroke and heart disease risk. Sleep. 2008;31(03):411–416. doi: 10.1093/sleep/31.3.411. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Harison J, Gibson G. Snoring, sleep apnea and stroke. Oxford Journals Medicine. 2000;93(10):647–654. doi: 10.1093/qjmed/93.10.647. [DOI] [PubMed] [Google Scholar]
- 19.Arzt M, Young T, Finn L, Skatrud JB, Bradley TD. Association of sleep-disordered breathing and the occurrence of stroke. Am J Respir Crit Care Med. 2005;172(11):1447–1451. doi: 10.1164/rccm.200505-702OC. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Sprigs DA, French JM, Murdy JM, Curless RH, Bates D, James OFW. Snoring increases the risk of stroke and adversely affects prognosis. Q J Med. 1992;84:555–562. [PubMed] [Google Scholar]
- 21.Palomaki H. Snoring and the risk of ischemic brain infarction. Stroke. 1991;22:1021–1025. doi: 10.1161/01.str.22.8.1021. [DOI] [PubMed] [Google Scholar]
- 22.Cadilhac DA, Thorpe RD, Pearce DC, Barnes M, Rochford PD, Tarquinio N, Davis SM, Donnan GA, Pierce RJ. Sleep disordered breathing in chronic stroke survivors. A study of the long term follow-up of the SCOPES cohort using home based polysomnography. J Clin Neurosci. 2005;12(6):632–637. doi: 10.1016/j.jocn.2004.08.014. [DOI] [PubMed] [Google Scholar]
- 23.Janssens JP, Pautex S, Hilleret H, Michel JP. Sleep disordered breathing in the elderly. Sleep. 2000;12(6):417–429. doi: 10.1007/BF03339872. [DOI] [PubMed] [Google Scholar]
- 24.Colle F, Bonan I, Gellez Leman M, Bradai N, Yelnik A. Fatigue after stroke. Ann Phys Rehabil Med. 2006;49(6):361–364. doi: 10.1016/j.annrmp.2006.04.009. [DOI] [PubMed] [Google Scholar]
- 25.Guillemninault C, Quera-Salva M, Partinen M, Jamieson A. Women and the obstructive sleep apnea syndrome. Chest. 1998;93:104–109. doi: 10.1378/chest.93.1.104. [DOI] [PubMed] [Google Scholar]
- 26.Jha A, Weintraub A, Allshouse A, Morey C, Cusick C, Kittelson J, Harrison-Felix C. A randomized trial of modafinil for the treatment of fatigue and excessive daytime sleepiness in individuals with chronic traumatic brain injury. J Head Trauma Rehabil. 2008;23(1):52–63. doi: 10.1097/01.HTR.0000308721.77911.ea. [DOI] [PubMed] [Google Scholar]
- 27.Hodoba D. Sleep disorders and wakefulness and their treatment. Medicus. 2002;11(2):193–205. [Google Scholar]
- 28.Happe S. Excessive daytime sleepiness and sleep disturbances in patients with neurological diseases: Epidemiology and management. Drugs. 2003;63(24):2725–2737. doi: 10.2165/00003495-200363240-00003. [DOI] [PubMed] [Google Scholar]
- 29.Kojic B, Dostovic Z, Ibrahimagic OC, Smajlovic Dz, Hodzic R, Iljazovic A, Salihovic D. Risk Factors in Acute Stroke Patients With and Without Sleep Apnea. Med Arch. 2021 Dec;75(6):444–450. doi: 10.5455/medarh.2021.6.444-450. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Kojic B, Dostovic Z, Ibrahimagic OC, Smajlovic Dz, Iljazovic A, Sehanovic A, Kunic K. Acute Stroke Patients with Sleep Apnea Acording to the Disability and Incidence of Relapse. Acta Informa Med. 2021 Oct;29(3):187–192. doi: 10.5455/aim.2021.3.187-192. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Cilovic-Lagarija S, Hasanica N, Radojicic M, Sokic-Begovic E, Mulic M, Mijovic B, Pilav A, Bardehle D, Musa S. All-Cause Mortality Trends in Federation of Bosnia and Herzegovina in Period 2011-2020 with Focus on the Leading Causes of Death in 2020. Int J Biomed Healthc. 2021;9(2):92–96. [Google Scholar]