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Basics for Nonspecialists in Sleep Medicine for OSA

Basics for Nonspecialists in Sleep Medicine for OSA

Obstructive sleep apnea (OSA) occurs when there are repeated episodes of upper airway collapse and obstruction during sleep. Studies show that OSA is prevalent. However, it is highly underrecognized. It is estimated that 82% of men and 93% of women in the US with OSA are undiagnosed.

Symptoms

There are several common sleep and daytime symptoms linked with OSA.

Symptoms during sleep:

  • Snoring
  • Gasping
  • Snorting
  • Not breathing
  • Fragmented sleep
  • Insomnia
  • Bedwetting
  • Night sweats

Symptoms during the daytime:

  • Excessive sleepiness
  • Fatigue – feeling tired, low on energy and unmotivated
  • Morning headaches
  • Memory or concentration issues
  • Mood disturbances or irritability
  • Decreased libido

Risk Factors

There are 2 kinds of factors that influence the risk of OSA – unmodifiable and modifiable.

Unmodifiable risk factors are male sex, age, and race.

Modifiable risk factors are obesity, medications that cause muscle relaxation and narrowing of the airway, endocrine disorders, smoking, and nasal congestion or obstruction.

 

Sex

Men generally have a higher risk for OSA than women. But once women reach menopause, they also have a risk similar to men. Loss of hormones results in a greater risk of OSA in postmenopausal women. OSA tends to be less severe in women compared with men of similar body mass index (BMI). Symptoms vary in men and women: snoring and noticed apneas are more common in men. When it comes to women, insomnia and excessive daytime sleepiness are more common. This may lead to delayed diagnosis and higher mortality in women compared with men.

Age

Studies suggest that the risk of OSA increases with age. Ironically, older adults are less symptomatic, they report less daytime sleepiness and fatigue.

Race

Some studies show a slightly increased risk of moderate to severe OSA in blacks (20%) and American Indians (23%) compared with whites (17%). Other studies found no differences based on race in older patients. These differences among racial groups may be a result of variations in craniofacial anatomy.

Obesity

There is a link between increased risk of OSA and obesity.

Comorbidities

OSA is linked with the following comorbid conditions:

  • Stroke
  • Myocardial infarction
  • Hypertension
  • Hyperlipidemia
  • Glucose intolerance
  • Diabetes
  • Arrhythmias such as atrial fibrillation, pulmonary hypertension, congestive heart failure, and depression.

Screening

Screening patients for OSA begins with a good sleep history. It is used to identify symptoms, risk factors and comorbid conditions, and as a physical examination for OSA-related features.

Sleep history:  Sleep history starts with calculating the patient’s total sleep time, meaning time to bed, time to fall asleep, and time of wake-up. It includes difficulties in falling asleep, difficulties staying asleep or daytime naps.

Symptoms: Daytime naps indicate that there is a sleep deficit or sleep that is not refreshing enough. Examining sleep and daytime symptoms determine if excessive daytime sleepiness or unrefreshing sleep is disproportionate with the amount of sleep the patient is getting at night.

Some patients with OSA can have memory or concentration issues. They perhaps feel like they have attention deficit disorder. In fact, some patients are diagnosed with attention deficit disorder because of their OSA.

Drowsy driving is a major concern in patients with untreated OSA and sleep deprivation. Caffeine intake should be taken into account since people with OSA may use it to battle sleepiness during the day.

Screening tools: In addition to the Epworth Sleepiness Scale, the STOP-BANG questionnaire can help decide if a patient should be tested further for OSA.

The STOP-BANG questionnaire includes eight yes-no questions. More than two yes responses suggest the patient is at higher risk for moderate to severe OSA.

When it comes to diagnosing OSA, HSATs are available to confirm the diagnosis of OSA in patients at high risk for moderate to severe OSA.

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