original article

Oman Medical Journal [2020], Vol. 35, No. 3: e132 

Symptoms of Daytime Sleepiness and Sleep Apnea among Pregnant Women

Yassar Al-Jahdali1, Maliha Nasim2,4, Noha Mobeireek1, Anwar Ahmed2,4, Mohammad A Khan1,4,5, Adnan Al-Shaikh1,3, Yosra Ali1,4, Abdullah Al-Harbi1,4,5 and Hamdan Al-Jahdali1,4,5*

1King Saud bin Abdulaziz University for Health Sciences, College of Medicine, Riyadh, Saudi Arabia

2Statistics Division, King Saud bin Abdulaziz University for Health Sciences, College of Public Health, Riyadh, Saudi Arabia

3Department of Pediatrics, King Saud bin Abdulaziz University for Health Sciences, College of Medicine, Jeddah, Saudi Arabia

4King Abdullah International Medical Research Center, Riyadh, Saudi Arabia

5Department of Medicine, Pulmonary Division, Sleep Disorders Center, King Abdulaziz Medical City, King Saudi University for Health Sciences, Riyadh, Saudi Arabia

article info

Abstract

Objectives: Despite the fact that sleep disturbances have been associated with poor maternal and neonatal health outcomes in pregnancy, no studies have assessed excessive daytime sleepiness or the risk for sleep apnea among pregnant Saudi Arabian women. We sought to estimate the prevalence of excessive daytime sleepiness (EDS) and the high risk for sleep apnea (OSA) in a sample of pregnant Saudi women. Methods: An anonymous self-report questionnaire was completed by 517 pregnant women who attended obstetric outpatient clinics at King Abdulaziz Medical City, Riyadh, Saudi Arabia, for a routine pregnancy check. We collected demographic and clinical data for all patients and used the Berlin Questionnaire and the Epworth Sleepiness Scale to determine the primary outcomes. Results: A high risk of OSA was found in 37.1% of women (95% confidence interval (CI): 33.00%–41.50%), and EDS was found in 32.1% (95% CI: 28.10%–36.30%). The presence of both (EDS and a high risk of OSA) was found in 14.9% of women (95% CI: 11.90%–18.30%). We found increased odds of EDS in women who reported pain three times or more per week (adjusted odds ratio (aOR) = 2.59) and insomnia (aOR = 1.65). Older women (≥ 37 years) (aOR = 3.00), those who reported pain once a week (aOR = 1.99), pain twice a week (aOR = 2.75), three times or more a week (aOR = 2.57), and insomnia (aOR = 1.95) increased the odds of high risk for OSA. Conclusions: EDS and a high risk for OSA affected a large portion of the pregnant women included in the study, primarily those who reported pain and insomnia. Our study provides important information for gynecologists to help promote healthy sleep and manage the issues arising from sleep disturbances among pregnant women as part of their daily practice.

Sleep disturbances are a common occurrence in pregnant women.1–4 The National Sleep Foundation estimates that 78% of women experience sleep disturbances during pregnancy.5 Sleep disturbance issues occur in response to changes in normal sleep/wake patterns. Excessive daytime sleepiness (EDS), sleep deprivation, night waking, daytime napping, insomnia, and restless leg syndrome are the most common sleep disturbances reported by pregnant women.1–4

EDS, a symptom of diverse disorders and causes, is a disabling condition frequently described by pregnant women. An estimated 52–65% of women are affected by EDS at some point during their pregnancy, and its prevalence is thought to increase as the pregnancy progresses.2,3,5,6 According to the American Academy of Sleep Medicine, people with EDS are unable to stay awake and alert during major waking episodes of the day, inappropriately dozing off at times when they should be awake. This behavior repeats daily for a minimum of three months.7 In addition, patients may report severe tiredness, fatigue, and lack of energy. EDS is a sleep disturbance known to impair daily functioning in all aspects of life (school, work, interpersonal relationships), and to negatively affect the quality of life.8 Studies have shown that EDS in pregnancy is associated with adverse maternal and obstetric health outcomes.8–10 Pregnant women with EDS and sleep apnea are more likely to develop gestational diabetes,2,11,12 suffer from clinical depression,13–15 postpartum depression,5,13,16,17 and undergo a cesarean section.8 The Epworth Sleepiness Scale (ESS), a self-reported questionnaire, is often used as an easy and reliable screening tool to assess daytime sleepiness in pregnant women.18 Studies have identified the following factors to be significantly associated with EDS in pregnant women: age (younger vs. older women), employment status (employed vs. unemployed), number of pregnancies (first pregnancy), restless leg syndrome,19,20 sleep-disordered breathing,9,10 and pre-eclampsia.21 EDS is frequently observed during all stages of pregnancy.2 However, some studies suggest its severity increases with pregnancy advancement and is more prevalent in the third trimester.1,22,23

Obstructive sleep apnea (OSA) is a major cause of EDS. OSA is characterized by partial or complete upper airway collapse leading to airflow obstruction and repetitive episodes of breathing pauses and/or shallow breathing. Predominant symptoms of EDS are associated with obstructive OSA, but not all patients with OSA suffer from EDS. The gold standard for diagnosing OSA is polysomnography. However, this test is time-consuming and expensive. The Berlin Questionnaire (BQ) is a more rapid and less costly method of screening for OSA.24 The self-reported questionnaire evaluates the symptoms of OSA and categorizes the respondent into either high- or low-risk groups for OSA.24 Positive BQ reporting represents a high risk of OSA development.25 The prevalence of pregnant women being in the high-risk group for OSA has been reported as 20% in one study26 and 32.2% in another.27 Furthermore, pregnant women who are overweight or obese may have pre-eclampsia or suffer from chronic diseases (diabetes, hypertension, and chronic inflammation) and have a significantly higher risk for OSA compared to healthy pregnant women.3,25,28–31 OSA in pregnancy is associated with increased maternal risk of gestational diabetes and hypertension,27,30,32,33 pre-eclampsia,32–34 and preterm and cesarean delivery.31,35 Furthermore, they are at higher risk of lowbirth weight, being small for gestational age, and are frequently admitted to intensive care units.31–34

In Saudi Arabia, to date, few studies are investigating the prevalence or correlates of EDS and OSA.36–38 In our previously published research about EDS and OSA among the general population, we found 31.9% at high risk of OSA when using the BQ. The risk of symptomatic OSA by combining BQ and EDS using ESS was 7.8%.39 To the best of our knowledge, no studies have assessed EDS and OSA among pregnant women in Saudi Arabia. EDS and OSA have been associated with poor maternal and neonatal health outcomes in pregnancy. Therefore, health care providers need to detect pregnant women at risk for these conditions early so that timely preventative interventions can be implemented. This is the first study to report the prevalence of OSA and EDS among pregnant women in Saudi Arabia. In addition, we hope to identify factors associated with the high risk for OSA and EDS using a validated Arabic version of the ESS and the BQ.40,41

Methods

We conducted a cross-sectional study between 1 June and 1 November 2014 in the department of Obstetrics and Gynecology (OB/GYN) at King Abdulaziz Medical City, Riyadh, Saudi Arabia. King Abdullah International Medical Research Center, Riyadh gave ethical approval for the study with protocol number RC13/106. The study sample was recruited from pregnant women who attended OB/GYN outpatient clinics for routine pregnancy checkups. Every year approximately 25 000 pregnant women visit the OB/GYN outpatient clinics, and this sample is calculated based on a confidence level of 95% with a margin of error of 5%, given a minimum sample size of 380 participants. We included all Saudi women who agreed to participate in the study, and we recruited an average of five participants every day during the study period. A consecutive sampling technique was performed on pregnant women who attended other obstetrics outpatient clinics at the hospital.

The survey included four sections. The first section assessed demographic data: age, education level, and coffee and tea intake. The second section assessed clinical and sleep characteristics: trimester, history of abortion, diabetes, depression, anemia, pain (abdominal pain due to uterine contraction), sleep duration (average hours of sleep per day), and insomnia. The third section assessed daytime sleepiness as measured by the Arabic version of the ESS.40,42 ESS is a method to measure the chances of falling asleep while engaged in eight different activities. An ESS value of 11 is considered EDS. The fourth section assessed the high risk for sleep apnea, as measured by the Arabic version of the BQ.41 The BQ is comprised of 10 items, including wake time, snoring behavior, fatigue, history of obesity, hypertension, and obesity (body mass index > 30). A score of 2 or more was classified as a high risk for OSA. Verbal consent for participation was obtained from all subjects included in the study. A total of 630 anonymous surveys were distributed, and 517 pregnant women consented and completed the questionnaire giving a response rate of 82.1%.

Table 1: Sample characteristics.

Characteristics

n

%

Age, years

   

< 25

77

14.9

25–36

372

72.1

> 36

67

13.0

Third trimester

   

No

143

27.7

Yes

374

72.3

University

   

No

236

46.9

Yes

267

53.1

Coffee intake

   

No

128

24.8

Yes

389

75.2

Tea intake

   

No

268

51.8

Yes

249

48.2

History of abortion

   

No

234

55.2

Yes

190

44.8

Diabetes mellitus

   

No

482

93.2

Yes

35

6.8

Depression

   

No

502

97.1

Yes

15

2.9

Anemia

   

No

416

80.5

Yes

101

19.5

Bronchial asthma

   

No

462

89.4

Yes

55

10.6

Sleep duration, hours

   

< 7

302

60.0

7–9

154

30.6

> 9

47

9.3

Have pain per week

   

None

142

27.6

Once

113

21.9

Twice

121

23.5

Three times and above

139

27.0

Insomnia

   

No

371

71.8

Yes

146

28.2

EDS

   

No

351

67.9

Yes

166

32.1

High risk for OSA

   

No

325

62.9

Yes

192

37.1

EDS and OSA

   

No

440

85.1

EDS: excessive daytime sleepiness; OSA: obstructive sleep apnea.

The data analysis was performed by SPSS Statistics (IBM Corp. Released 2015. IBM SPSS Statistics for Windows, Version 23.0. Armonk, NY: IBM Corp.). The sample characteristics were summarized by percentages [Table 1]. The overall prevalence of EDS, high risk of OSA, and both EDS and high risk of OSA were reported by percentage and 95% confidence interval (CI). We used the chi-square test to assess the associations between the sample characteristics across EDS, the high risk of OSA, and both EDS and high risk of OSA [Table 2]. After adjusting for the sample characteristics in Table 2, we used multiple logistic regression models to determine the association between the sample characteristics and the presence of EDS, high risk of OSA, and both EDS and high risk of OSA in our sample [Table 3]. P-values < 0.050 were considered significant.

Table 2: EDS, high risk for OSA, and both EDS and high risk for OSA and their relation to the sample characteristics.

Factors

EDS

 

High risk for OSA

 

EDS and high risk for OSA

 

No

Yes

 

Low risk

High risk

 

No

Yes

 

n

%

n

%

p

n

%

n

%

p

n

%

n

%

p

Age, years

                             

< 25

49

63.6

28

36.4

0.097

54

70.1

23

29.9

0.028*

63

81.8

14

18.2

0.426

25–36

249

66.9

123

33.1

 

237

63.7

135

36.3

 

316

84.9

56

15.1

> 36

53

79.1

14

20.9

 

33

49.3

34

50.7

 

60

89.6

7

10.4

 

Third trimester

No

99

69.2

44

30.8

0.687

96

67.1

47

32.9

0.214

127

88.8

16

11.2

0.143

Yes

252

67.4

122

32.6

 

229

61.2

145

38.8

 

313

83.7

61

16.3

 

Coffee intake

No

82

64.1

46

35.9

0.285

85

66.4

43

33.6

0.339

107

83.6

21

16.4

0.579

Yes

269

69.2

120

30.8

 

240

61.7

149

38.3

 

333

85.6

56

14.4

 

Tea intake

                             

No

179

66.8

89

33.2

0.578

161

60.1

107

39.9

0.173

220

82.1

48

17.9

0.046*

Yes

172

69.1

77

30.9

 

164

65.9

85

34.1

 

220

88.4

29

11.6

 

History of abortion

No

162

69.2

72

30.8

0.684

152

65.0

82

35.0

0.544

205

87.6

29

12.4

0.694

Yes

135

71.1

55

28.9

 

118

62.1

72

37.9

 

164

86.3

26

13.7

 

Diabetes mellitus

No

326

67.6

156

32.4

0.643

311

64.5

171

35.5

0.004*

412

85.5

70

14.5

0.380

Yes

25

71.4

10

28.6

 

14

40.0

21

60.0

 

28

80.0

7

20.0

 

Depression

No

341

67.9

161

32.1

1.000

317

63.1

185

36.9

0.431

428

85.3

74

14.7

0.477

Yes

10

66.7

5

33.3

 

8

53.3

7

46.7

 

12

80.0

3

20.0

 

Anemia

No

282

67.8

134

32.2

0.919

261

62.7

155

37.3

0.907

355

85.3

61

14.7

0.765

Yes

69

68.3

32

31.7

 

64

63.4

37

36.6

 

85

84.2

16

15.8

 

Bronchial asthma

No

313

67.7

149

32.3

0.840

299

64.7

163

35.3

0.011*

395

85.5

67

14.5

0.469

Yes

38

69.1

17

30.9

 

26

47.3

29

52.7

 

45

81.8

10

18.2

 

Sleep duration, hours

< 7

204

67.5

98

32.5

0.925

183

60.6

119

39.4

0.590

251

83.1

51

16.9

0.427

7–9

106

68.8

48

31.2

 

97

63.0

57

37.0

 

133

86.4

21

13.6

 

> 9

31

66.0

16

34.0

 

32

68.1

15

31.9

 

42

89.4

5

10.6

 

Have pain per week

None

110

77.5

32

22.5

0.001*

109

76.8

33

23.2

0.001*

129

90.8

13

9.2

0.058

Once

75

66.4

38

33.6

 

75

66.4

38

33.6

 

98

86.7

15

13.3

 

Twice

86

71.1

35

28.9

 

63

52.1

58

47.9

 

100

82.6

21

17.4

 

Three times and above

78

56.1

61

43.9

 

76

54.7

63

45.3

 

111

79.9

28

20.1

 

Insomnia

No

266

71.7

105

28.3

0.003*

251

67.7

120

32.3

0.001*

327

88.1

44

11.9

0.002*

EDS: excessive daytime sleepiness; OSA: obstructive sleep apnea.*Significant at p = 0.050.

Table 3: Multivariate factors associated with EDS, high risk for OSA, and EDS and high risk for OSA.

Factors

   

EDS

   

High risk for OSA

EDS and high risk for OSA

   

95% CI for OR

   

95% CI for OR

   

95% CI for OR

p

OR

Lower

Upper

p

OR

Lower

Upper

p

OR

Lower

Upper

Age, years

< 25

 

1.00

     

1.00

     

1.00

   

25–36

0.731

0.88

0.41

1.85

0.218

1.63

0.74

3.56

0.864

0.92

0.33

2.49

> 36

0.249

0.52

0.16

1.58

0.043*

3.00

1.03

8.68

0.325

0.47

0.10

2.12

Third trimester

No

 

1.00

     

1.00

     

1.00

   

Yes

0.656

0.89

0.52

1.50

0.905

0.97

0.57

1.62

0.776

1.11

0.53

2.31

University

No

                       

Yes

0.237

0.75

0.47

1.20

0.380

1.23

0.77

1.92

0.998

1.00

0.52

1.89

Coffee intake

No

 

1.00

     

1.00

     

1.00

   

Yes

0.490

0.83

0.48

1.41

0.655

0.89

0.52

1.50

0.380

0.73

0.36

1.47

Tea intake

No

 

1.00

             

1.00

   

Yes

0.533

0.87

0.55

1.36

0.124

0.71

0.45

1.09

0.029*

0.50

0.26

0.93

History of abortion

No

 

1.00

     

1.00

     

1.00

   

Yes

0.387

0.75

0.39

1.43

0.860

0.95

0.51

1.74

0.847

1.09

0.46

2.52

Diabetes mellitus

No

 

1.00

     

1.00

     

1.00

   

Yes

0.904

0.94

0.34

2.56

0.034

2.71

1.08

6.81

0.290

1.89

0.58

6.12

Depression

No

 

1.00

     

1.00

     

1.00

   

Yes

0.902

1.08

0.32

3.63

0.753

1.21

0.37

3.93

0.641

1.40

0.33

5.80

Anemia

No

 

1.00

     

1.00

     

1.00

   

Yes

0.381

1.29

0.72

2.29

0.300

1.34

0.76

2.34

0.152

1.71

0.82

3.55

Bronchial asthma

No

 

1.00

     

1.00

     

1.00

   

Yes

0.818

0.92

0.45

1.87

0.318

1.41

0.71

2.75

0.530

1.33

0.54

3.22

Sleep duration, hours

< 7

 

1.00

     

1.00

     

1.00

   

7–9

0.836

1.06

0.63

1.76

0.932

1.02

0.62

1.68

0.867

0.94

0.46

1.90

> 9

0.837

1.10

0.46

2.61

0.431

1.39

0.61

3.14

0.810

0.85

0.23

3.13

Have pain per week

None

 

1.00

     

1.00

     

1.00

   

Once

0.150

1.64

0.83

3.20

0.041*

1.99

1.02

3.87

0.648

1.25

0.48

3.21

Twice

0.995

1.00

0.49

2.02

0.003*

2.75

1.42

5.31

0.658

1.24

0.47

3.21

Three times and above

0.003*

2.59

1.38

4.83

0.003*

2.57

1.36

4.81

0.144

1.89

0.80

4.45

Insomnia

No

 

1.00

     

1.00

     

1.00

   

Yes

0.049*

1.65

1.00

2.71

0.006*

1.95

1.20

3.16

0.063

1.84

0.96

3.49

Gravida

0.378

1.11

0.88

1.38

0.355

1.11

0.89

1.37

0.563

1.09

0.81

1.45

EDS: excessive daytime sleepiness; OSA: obstructive sleep apnea.
*Significant at p = 0.050.

Results

A total of 517 pregnant Saudi women were included in the analysis. Of the sample, 72.3% were in the third trimester, 53.1% had university degrees, 44.8% had a history of abortion, and 6.8% had diabetes mellitus [Table 1]. The mean age of the sample studied was 30.1±5.4 years, with an age range of 17–47 years.

The overall prevalence of EDS was 32.1% (166 of 517) with 95% CI: 28.10%–36.30%. Of the pregnant women studied, 37.1% (192 of 517) had a high risk of OSA with 95% CI: 33.00%–41.50%. The presence of both (EDS and high risk of OSA) was 14.9% (77 of 517) with 95% CI: 11.90%–18.30%.

The overall prevalence of insomnia was 28.2%, while the prevalence of EDS was significantly higher in pregnant women with insomnia than in those without insomnia (41.8% vs. 28.3%, p = 0.003) [Table 2].

The prevalence of a high risk of OSA increases with age (29.9% in ≤ 24 years, 36.3% in 25–36 years, and 50.7% in ≥ 37 year olds, p = 0.028). The high risk of OSA was significantly higher in pregnant women with diabetes mellitus (60.0% vs. 35.5%, p = 0.004), bronchial asthma (52.7% vs. 35.3%, p = 0.011), and insomnia (49.3% vs. 32.3%, p = 0.001) than those without these issues. The prevalence of EDS and the high risk for OSA was significantly higher in pregnant women who did not consume tea (17.9% vs. 11.6%, p = 0.046) and those with insomnia (22.6% vs. 11.9%, p = 0.002).

Both frequent pain (abdominal pain due to contractions) (aOR = 2.59; 95% CI: 1.38–4.83) and insomnia (aOR = 1.65; 95% CI: 1.00–2.71) increased the odds of EDS [Table 3].

Older age (≥ 37 years) (aOR = 3.00; 95% CI: 1.03–8.68), pain once a week (aOR = 1.99; 95% CI: 1.02–3.87), pain twice a week (aOR = 2.75; 95% CI: 1.42–5.31), and pain three times or more a week (aOR = 2.57; 95% CI: 1.36–4.81), and insomnia (aOR = 1.95; 95% CI: 1.20–3.16) increased the odds of a high risk of OSA.

Discussion

Our study investigated the important issue of EDS and the risk of OSA based on ESS and BQ, respectively, in a cohort of pregnant Saudi women attending a tertiary care facility in Riyadh, Saudi Arabia. There is sparse data in this area of research, and our study has highlighted the prevalence and likely factors associated with EDS and the risk of OSA. To date, sleep disturbances have been associated with poor pregnancy outcomes.30,32 Our study reported a high prevalence of OSA and EDS during the pregnancy term. There is a need to establish proper management options to prevent OSA and EDS during pregnancy.

The gold standard for the diagnosis of sleep breathing disorders is polysomnography. However, it is more expensive, time-consuming, and needs more logistics when used as a screening tool in general populations. ESS and BQ are well-validated tools in identifying EDS and patients at high risk of OSA. A recent meta-analysis has shown the sensitivity and specificity of ESS (54% and 65%) and BQ (76% and 59%), respectively, for identifying the risk of OSA.43 A study by Signal et al,44 revealed that the prevalence of EDS in their cohort of pregnant women was 1.8-times higher than in the general population. Another study reported an EDS prevalence of 12.7% in their study cohort in middle- to low-income countries.45 The risk of OSA in pregnant women has a prevalence of 20–32% reported in the literature.3,25,27 In our study, almost one in three women had either EDS or the risk of OSA based on the questionnaire survey, and 14.9% have both disorders, which is similar to published studies.2,3,5,6,26,27 However, the prevalence of OSA and EDS is much higher than the prevalence among the general Saudi population, which was 7.8%.39 It will be useful to see, in the future, whether other countries in the region have a similarly high prevalence of OSA in the
pregnant cohorts.

The important factors identified in this study that are associated with EDS and the risk of OSA are insomnia, pain-related issues, increasing age, and medical comorbidities. Sleep disturbances, including insomnia, was 28.2% in our study. This is a well-known phenomenon in pregnancy and the incidence of insomnia increases as the pregnancy advances with reported incidences of 12% to 73.5%.46–49 Our finding of pain as a contributor to sleep fragmentation, and therefore EDS with the risk of OSA, has been recently published in a large-scale US study involving more than 2400 participants.29 Low education level, increasing maternal age, and the number of previous abortions were also important risk factors associated with EDS and risk of OSA as factors in other studies.2,29

There are many limitations for our study, first, it uses a questionnaire, which may overestimate the prevalence of OSA. Second, it is a cross-sectional study with known limitations. For example, we could not measure the outcome of pregnancy among those with a high risk of OSA. Furthermore, there are many causes of EDS among pregnant women, which we did not address directly. These factors include poor sleep hygiene, medical problems, and psychosocial issues. The strength of our study is that it is a reasonably large sample and is the first study using validated tools among our population, which addresses major issues about sleep disorders among pregnant women.

Conclusions

Our study identified, for the first time in a cohort of pregnant Saudi women, the prevalence of EDS and the risk of OSA using validated tools. The results of this study would help health care professionals in looking actively for the presence of EDS and OSA in the care of these subjects. They should be diligent in seeking the right involvement of the teams in education and identification of these symptoms in pregnant women so that the adverse effects of EDS and OSA on pregnancy can be averted.

Disclosure

The authors declared no conflict of interest. No funding was received for this study.

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