Management Of Excessive Sleepiness In Patients With Narcolepsy And OSA: Current Challenges And Future Prospects

Introduction

Excessive daytime sleepiness (EDS) is defined as unintentional sleepiness or inability to maintain wakefulness, thus impacting one’s functional ability.¹ Due to the subjectivity associated with self-reported EDS, prevalence in the general population is difficult to estimate. A recent population-based study showed that 33% of participants self-reported EDS at baseline and that 28% of participants without EDS at baseline developed EDS during the 5-year study period. Younger age and depression were independent predictors of incident EDS, and the degree of EDS fluctuated over time.² The term EDS is used interchangeably with hypersomnolence, though EDS is a symptom and hypersomnolence is a disease process.

EDS impacts quality of life and contributes to unsafe work and home environments, in addition to jeopardizing public safety on the roads.³ The most common cause of EDS is insufficient sleep syndrome. However, EDS is also a common symptom of medical disorders and a side effect of various prescription and over-the-counter medications. EDS can be a manifestation of sleep disorders, including obstructive sleep apnea (OSA), alveolar hypoventilation, restless leg syndrome, periodic limb movement disorder, circadian rhythm disorder, narcolepsy, idiopathic hypersomnia and Kleine-Levin syndrome. Other medical disorders in which EDS is a clinical symptom include hypothyroidism, renal/hepatic failure, neurodegenerative disorders such as Parkinsonism, stroke, myotonic dystrophy, multiple sclerosis, structural brain lesions, traumatic brain injury, and psychiatric disorders such as depression, anxiety, and substance abuse. Medications associated with EDS include sedative-hypnotics, beta blockers, antihistamines, anticonvulsants, antidepressants and opiates. The overlap of multiple risk factors in individual patients can present a diagnostic dilemma. Thus, alternative diagnoses for EDS should be considered if the patient does not respond to the primary management.⁴ Residual sleepiness in adequately treated patients with OSA can be multifactorial and requires further investigation and management.⁵

Epidemiology

Obstructive sleep apnea is a common disorder in North America. The estimated prevalence in the general adult population has been reported as 9% to 38%.⁶ The prevalence of narcolepsy is much lower in the general adult population and has been reported as 0.07% to 0.20%.⁷ The occurrence of OSA in the setting of narcolepsy is at best speculative. In a retrospective study of 133 patients with narcolepsy, 25% of patients had an apnea hypopnea index (AHI) ≥ 10. Thirty percent of patients with AHI ≥ 10 were initially diagnosed with OSA only, and there was a delay in the diagnosis of narcolepsy.⁴ Narcolepsy is associated with increased body mass index (BMI), which is a risk factor for OSA, again leading to under-diagnosis of narcolepsy.⁸ Additionally, two or more sleep onset REM periods (SOREMs) may be observed on the multiple sleep onset latency test (MSLT) in patients with untreated OSA, potentially confounding the true prevalence of either disorder.⁹

Pathophysiology

Narcolepsy

Breakthrough in the pathogenesis of narcolepsy occurred in 1998 when two groups of researchers identified the same gene in animal models. Lecea et al.¹⁰ named this new gene hypocretin and Sakurai et al.¹¹ referred to it as orexin. Hypocretin/orexin is a neuropeptide produced in the lateral posterior hypothalamus. It plays a crucial role in control of the sleep/wake cycle and of neurocognitive and metabolic functions. The pathophysiology of type 1 narcolepsy (NT1) is characterized by destruction of hypocretin/orexin-producing neurons and reduced levels of hypocretin/orexin in the cerebrospinal fluid (CSF). The destruction of these specific neurons is thought to be related to an autoimmune mechanism, though no direct evidence has been found. The arguments that support this theory are linked to a strong association between NT1 and the HLA-DQB1*0602 allele and polymorphisms. Seasonal variation in the incidence of NT1 suggests infectious etiologies, with an increased incidence of NT1 in Scandinavia after the Pandemrix vaccination for the H1N1 influenza virus was introduced. There is also a suggestion that NT1 is associated with Streptococcus infections with the finding of increased antibody titers to Streptococcus pyogenes when compared to controls.¹² In contrast to NT1, the pathophysiology of type 2 narcolepsy (NT2) is unknown, though it is thought to be due to less extensive damage to hypocretin/orexin. Most patients with NT2 have normal hypocretin levels; however, NT2 seems to be a heterogeneous disorder and subgroups may exist.¹

To elaborate on the genetic predisposition to narcolepsy, 86–98% of patients with NT1 are positive for the HLA-DQB1*0602 allele, though that is not sufficient to develop the disease. This allele is also reported in 5–38% of the general population. Some studies have reported a higher prevalence of this allele in NT2 than the general population, but the data are limited.¹³

In a small study of 26 patients, increased BMI in patients with narcolepsy/cataplexy was not correlated with their CSF hypocretin levels. This finding suggests that other metabolic mechanisms could explain the association of obesity with narcolepsy.¹⁴ In another study, higher BMI was associated with delayed diagnosis.¹⁵ Animal studies support the loss of hypocretin neurons rather than loss of hypocretin itself to be responsible for the weight gain. Some studies indicate that the food choices of patients with NT1 when compared to controls may also contribute to weight gain. This could indicate altered reward motivation and processing in patients with NT1 because binge eating, nocturnal eating, and carbohydrate craving have been reported in NT1.^16,17

OSA And Excessive Daytime Sleepiness

Repeated upper airway obstruction leading to arousals and sleep fragmentation is thought to result in EDS in patients with OSA.¹⁸ Variable results have been found linking intermittent nocturnal hypoxemia as well, but no clear correlation exists between the severity of sleep apnea and degree of EDS.^19,20 Chronic intermittent nocturnal hypoxemia could potentially injure wake-promoting neural networks with loss of dopaminergic and noradrenergic neurons, thus contributing to EDS. These effects were seen as early as two weeks in mice models.^21,22 A retrospective analysis in which untreated OSA was associated with two SOREMs on the MSLT found baseline minimal oxygen saturation to be an independent predictor, which raises the possibility of nocturnal hypoxemia as a promoter of SOREMs and EDS.²³ Autonomic dysregulation with increased sympathetic cardiac tone during autonomic arousals in patients with OSA may also contribute to EDS.^24,25 Additionally, obesity itself could be a contributing factor to EDS in patients with OSA via adipokines and chronic inflammation noted in obese patients.²⁶

Diagnosis And Current Diagnostic Challenges

EDS is the primary clinical symptom associated with narcolepsy. EDS is typically the first symptom to present and often has the greatest impact on daily life. Patients with narcolepsy experience generalized EDS in addition to involuntary lapses into sleep. Daily occurrence of EDS for at least three months is a required criterion for the diagnosis of narcolepsy.¹ EDS is also a common presenting symptom of OSA, but it does not occur universally and is not a required criterion for diagnosis.¹ EDS is often confused with fatigue, exhaustion, lethargy, tiredness, and lassitude.

Sleep deprivation is the most common cause of EDS. This could be behaviorally induced or related to circadian misalignment. Medication reconciliation needs to be done to ensure that the patient is not taking sedating medications. Although not an exhaustive list, these may include benzodiazepines, non-benzodiazepines, opiates, antihistamines, anti-epileptics, antidepressants, nonsteroidal anti-inflammatory drugs, digoxin, clonidine, prazosin, and beta-blockers. Substance abuse, including alcohol and marijuana, and endocrine disorders (especially hypothyroidism) should also be ruled out. Other pertinent history includes the presence of neurological lesions, stroke, traumatic brain injury, multiple sclerosis, neurodegenerative disorders, encephalopathies and neuromuscular disorders (Parkinson’s disease, myotonic dystrophy, amyotrophic lateral sclerosis, myasthenia gravis). In addition, other medical conditions such as heart failure, COPD, and rheumatological conditions should be evaluated. Psychiatric disorders including depression, PTSD, and anxiety need to be evaluated and treated. Other considerations include restless legs syndrome, periodic limb movement disorder of sleep, and parasomnias. A key tool for investigating EDS is an overnight polysomnogram (PSG) followed by a daytime MSLT to evaluate for sleep disorders that have no obvious etiologic basis.

Screening Tools

The approach to a patient with EDS includes a subjective evaluation of EDS that can be done using a variety of validated scales. The Epworth Sleepiness Scale (ESS) is a self-administered questionnaire in which respondents rate their chances of falling asleep in eight situations that commonly occur in daily life.²⁷ Each situation is rated on a scale of 0–3 based on how likely the respondent is to fall asleep, with a score of greater than 10 being consistent with EDS.²⁸ The Epworth Sleepiness Scale for Children and Adolescents (ESS-CHAD) is a version of the ESS that has been modified to reflect the experiences of younger respondents.²⁹

Other scales that may be used include the Karolinska Sleepiness Scale (KSS), Stanford Sleepiness Scale (SSS), and Pittsburgh Sleep Quality Index (PSQI). The KSS and SSS are validated measures of subjective sleepiness at a particular time.^30,31 For the KSS, respondents rate their sleepiness in the preceding five minutes on a 9-point scale,³¹ and for the SSS, respondents rate their current sleepiness on a 7-point scale.³⁰ Because the KSS and SSS are both answered at one point in time, they may be useful to assess sleepiness as it relates to different activities, times of day, or levels of sleep. The PSQI is a validated tool that includes an evaluation of daytime dysfunction due to EDS as part of a global assessment of sleep quality.³² In addition to scales that evaluate EDS, the Swiss Narcolepsy Scale (SNS) is a 5-item, self-report scale that assesses for symptoms of narcolepsy with cataplexy. The SNS has a reported 96% sensitivity and 98% specificity for NT1 (narcolepsy with cataplexy).³³

Objective Testing

If narcolepsy is suspected following the clinical assessment, objective testing is the next step to confirming a diagnosis. The International Classification of Sleep Disorders – Third Edition (ICSD-3) has classified NT1 and NT2.¹ Both present with symptoms of EDS, sleep paralysis, and hypnagogic hallucinations, and the supportive criteria for objective testing is the same. An overnight PSG followed by next-day MSLT is the standard of care for objective testing.^1,34 Specific parameters that meet the diagnostic criteria for narcolepsy include a mean sleep latency of less than or equal to eight minutes and two or more SOREMs on the MSLT. Alternatively, a SOREM on the preceding night’s PSG should be counted in addition to any SOREM on the MSLT.¹ The PSG must be performed on the night immediately preceding MSLT to rule out other sleep disorders and evaluate for sleep disruptions that could influence the result of the MSLT. A sleep diary and/or actigraphy should be done 1–2 weeks prior to the PSG/MSLT to ensure that the sleep studies are completed during the patient’s usual sleep times.^34,35 Additional instructions prior to MSLT are presented in Table 1.

Table 1 Instructions For Multiple Sleep Latency Testing

MSLT measures the physiological tendency to fall asleep under standardized conditions. The MSLT begins 1.5 to 3 hrs after the PSG and consists of five nap opportunities at 2 hr intervals. The patient is allowed up to 20 mins to fall asleep and then up to 15 mins to enter REM sleep.³⁴ Sleep latency, defined as the time from lights out to the first epoch of any stage of sleep, is recorded for each nap. Sleep latency is considered an indicator of the level of sleepiness, and decreased mean sleep latency on the MSLT is associated with sleep disorders that cause EDS, including narcolepsy and OSA.³⁴ The presence of SOREMs is also evaluated during each nap, defined as the first epoch of REM sleep that occurs during the nap. Narcolepsy is a disorder of REM sleep, and these patients typically enter REM sleep earlier than expected, which is identified as a SOREM during the nap.³⁴

The MSLT must be performed under standardized conditions to maintain the validity of the results. The testing environment should be conducive to sleep and comfortable for the patient, and the test should be performed using a defined protocol.³⁴ Additionally, patients should not be taking any drugs that could affect sleep or cause sleepiness, such as stimulants, central nervous system depressants, or REM-suppressing medications. These medications should ideally be stopped two weeks prior to the MSLT, depending on the half-life of the drug, and confirmed with a urine drug screen prior to the MSLT.^1,34 Despite these recommendations, it is challenging to ensure an adequate washout period of each drug. This can be especially difficult in patients who are taking antidepressant medications and the nature of their psychiatric illness limits the safe taper of these medications. The diagnosis of narcolepsy by PSG/MSLT in such patients may be missed due to the REM-suppressing effects of these drugs. However, it can be difficult to wean off these medications in clinical practice and the interpretation should be done with this limitation in mind.

Polysomnography is the standard diagnostic test for OSA,³⁶ which can coexist with narcolepsy.⁴ OSA can be an independent cause of EDS, decreased sleep latency, and SOREMs, and should be treated prior to establishing a narcolepsy diagnosis.^34,35 A large retrospective study showed that male sex and extent of oxygen desaturation were some of the factors associated with SOREMs in OSA.²³ If OSA is identified on the PSG, continuous positive airway pressure (CPAP) is instituted. Re-evaluation of EDS by the Epworth Sleepiness Scale is done after adequate compliance (> 4 hrs of nightly use for > 70% of nights) is shown on the CPAP device for a stable duration of four weeks. Additionally, the absence of significant mask leak and an adequate CPAP pressure to control the AHI and nocturnal hypoxemia should be confirmed before pursuing alternate causes of EDS.^4,37 Other causes of EDS need to be ruled out prior to initiation of wake promoting drugs versus MSLT including suboptimal objective adherence, poor sleep hygiene, insufficient sleep, depression and/or restless legs syndrome.³⁸ If after careful consideration it is determined that the patient should undergo MSLT, the preceding PSG is performed with the patient’s CPAP device. The use of CPAP is necessary because untreated OSA can cause SOREMs.^9,23

OSA and narcolepsy both present with EDS, and the severity of EDS in patients with both conditions versus just narcolepsy has not been shown to be significantly different.^4,37 Narcolepsy can be missed, especially if cataplexy is not identified at the initial presentation, which leads to treatment delays. Therefore, diagnostic testing for narcolepsy should be considered in patients with residual EDS despite CPAP therapy.^4,37

EDS can also be objectively evaluated after treatment initiation with the maintenance of wakefulness test (MWT). Whereas the MSLT measures the tendency to fall asleep, the MWT measures the ability to stay awake.³⁴ The MWT must be performed using a standardized protocol. A preceding PSG is optional; however, optimal sleep and daytime alertness must be confirmed prior to the test, generally by sleep logs or self-report. The test begins 1.5 to 3 hrs after the typical wake time and consists of four trials at 2 hr intervals, during which the patient is seated in a room with minimal light and instructed to stay awake. Each trial ends after 40 mins of wakefulness or if sleep onset occurs during the trial, whichever comes first. Sleep latency is recorded for each trial, and the mean sleep latency is interpreted in the context of the clinical situation.³⁴ Clinical application of the MWT lies in the change in mean sleep latency that occurs in response to treatment for a disorder that is known to cause EDS, such as narcolepsy or OSA. This may be especially significant if the patient has an occupation that involves driving.³⁴

As outlined above, actigraphy or sleep logs are needed prior to the PSG/MSLT to ensure the test accuracy. However, challenges can arise because actigraphy is not universally available and sleep logs are a very subjective measure. Sleep deprivation or circadian rhythm disorder could therefore be missed during the clinical evaluation, and the patient could be falsely labeled as narcoleptic due to the effects of sleep deprivation/disruption on the PSG and MSLT.

Measurement of CSF hypocretin levels would be useful in a situation when the MSLT results are believed to be falsely negative, particularly when the patient is taking REM-suppressing medications. This test is now commercially available at the Mayo Clinic, Rochester, MN, USA.³⁹ However, this test is only useful in diagnosing NT1 and not NT2. One may argue that clinical judgment should be used to guide the management of narcolepsy rather than relying solely on the objective measures of PSG/MSLT. A trial of wake-promoting drugs such as modafinil or sodium oxybate for a short duration with close clinical follow-up may be a consideration. Additionally, patients with narcolepsy could be misdiagnosed and treated as attention deficit hyperactivity disorder (ADHD) due to overlap in the symptomatology. Therefore, screening patients with ADHD for hypersomnia should be encouraged, especially in children.^40,41

Laboratory Evaluation

As an alternative to MSLT, NT1 could be diagnosed solely on reduced CSF hypocretin levels in the presence of EDS. Measurement of CSF hypocretin levels by radioimmunoassay (RIA) has been included in the recent ICSD-3 definition of NT1.¹ Levels of hypocretin ≤ 110 pg/mL are highly specific for the diagnosis of NT1.⁴² However, RIA lacks accuracy because it cross-reacts with various matrix constituents, which induces variability between batches. Low levels of hypocretin can also be found in patients with traumatic brain injury; therefore, interpretation should include the clinical context.⁴³ A recent study compared hypocretin/orexin A levels measured by RIA (Phoenix Pharmaceuticals, Burlingame, CA, USA) to ELISA (Wako Pure Chemical Industries, Osaka, Japan) and found reliable results in that the measurements were not equivalent (orexin A levels were much lower when measured by EILSA versus RIA).⁴⁴ CSF hypocretin testing has limited commercial availability, which limits its widespread use. However, per the ICSD-3 definition, patients with low hypocretin levels are diagnosed as NT1 even in the absence of cataplexy.¹ This is supported by prospective data that show patients with low hypocretin eventually develop cataplexy.⁴⁵

HLA testing may be used to support a diagnosis of narcolepsy, but it is not considered a diagnostic test.¹ HLA-DQB1*06:02 is a genetic marker that is strongly associated with NT1 but can also be present in healthy individuals. HLA testing may be a useful first step if CSF hypocretin testing is being considered because the hypocretin level is unlikely to be reduced if the HLA testing is negative.^1,46 Again, both CSF hypocretin testing and HLA testing should be interpreted within the clinical context.^42,46

Current Treatments

Narcolepsy

Non-Pharmacological Management

Non-pharmacological therapies are considered to be adjunctive in the management of narcolepsy. Scheduled daytime naps improve alertness and decrease unintended sleep periods.⁴⁷ Patients may take two 15- to 20 min regularly scheduled naps that are well-timed to facilitate optimal alertness when it is most needed during the day. They should also be encouraged to maintain an adequate and consistent nocturnal sleep schedule and practice good sleep hygiene to avoid exacerbation of symptoms that can occur with sleep deprivation.^47,48 Medications that cause insomnia or sleepiness should be avoided. Additionally, weight loss should be encouraged if patients are overweight or obese.¹⁴ Weight loss may be especially important if the patient has comorbid OSA.

Social support is an important element in the management of narcolepsy. Narcolepsy can have negative social, occupational, and economic consequences for the patient, partner, and family.⁴⁹ The social and occupational needs of the patient should be evaluated to determine if intervention is needed. Regular follow-up is important to identify supportive resources, monitor treatment response, and provide ongoing education. Safety must always be evaluated, and patients should be counseled to avoid driving or operating heavy machinery at home or at work while sleepy.⁴⁷ Lastly, regular screening for mood changes and hypertension is needed due to the side effects of simulant medications.^47,50

Pharmacological Management

To date, there is no cure for narcolepsy. Symptomatic relief is achieved through various medications. Wake-promoting drugs such as modafinil or sodium oxybate are the mainstay of therapy for EDS (Table 2). Additionally, stimulant medications may be used. The main side effects of stimulants are headaches, irritability, and agitation. These effects occur due to sympathetic stimulation and limit usage in certain patients. Caution should be exercised in patients who have uncontrolled hypertension or a previous cardiac history. Approximately one-third of patients develop tolerance, with the need to increase the dosage. Although these medications are effective, due to the potential for addiction and negative side effects, there is a need for newer, non-stimulating wake-promoting agents.⁵¹ Although abuse potential is a concern, a cross-sectional cohort study found an extremely low frequency of stimulant abuse among narcolepsy patients.⁵²

Table 2 Pharmacologic Management For Excessive Daytime Sleepiness

Stimulant Therapy Approved For Narcolepsy And OSA

Modafinil

Modafinil is a benzyhydrylsulfinylacetamide derivative and a non-amphetamine stimulant. It is considered the first-line treatment for EDS by the American Academy of Sleep Medicine (AASM).⁴⁷ The mechanism of action is not fully understood, but it is believed to be related to dopamine reuptake inhibition.^51,54 It is readily absorbed after oral administration, with maximum plasma concentration occurring within 2 to 4 hrs.⁵⁴ It is metabolized by the liver with renal elimination. The FDA published a maximum dosage of 400 mg, but dosages up to 600 mg have been studied with positive results.⁵³ The typical prescribed dosage varies from 100 mg to 400 mg administered once or twice per day.⁵¹ In 50–60% of adults with narcolepsy, modafinil is sufficient as a monotherapy, though it has no effect on cataplexy.⁵⁵ It has also been shown to improve objective and subjective sleepiness in patients with OSA with refractory sleepiness despite compliant use of CPAP. Additionally, it has been shown to improve behavioral alertness with reduction in functional impairment in OSA patients on CPAP.⁵⁶

Armodafinil

Armodafinil is the R-enantiomer of modafinil, which acts as a D2 receptor partial agonist.^53,57 Armodafinil is administered once daily at 100 mg to 250 mg and is FDA-approved for EDS in patients with OSA and narcolepsy.^3,57 Though the half-lives of modafinil and armodafinil are similar, differences in pharmacokinetics result in the plasma concentration of armodafinil being higher late in the day leading to improved wakefulness throughout the day.⁵⁸

Solriamfetol

Solriamfetol is a dopamine and norepinephrine reuptake inhibitor that received FDA approval in 2019 for EDS in OSA and narcolepsy. The approval was granted after publication of the results from the TONES studies (Treatment of Obstructive Sleep Apnea and Narcolepsy Excessive Sleepiness).^59,60 Solriamfetol is approved in 75 mg and 150 mg dosages for narcolepsy and 37.5 mg, 75 mg, and 150 mg dosages for OSA. The most common adverse effects are headaches, anxiety, decreased appetite, and nausea.

Other Stimulant Therapies For Narcolepsy

Methylphenidate

Methylphenidate is a derivative of amphetamines. It is a non-competitive dopamine reuptake blocker with some inhibiting action on serotonin-noradrenaline reuptake. In patients with narcolepsy, methylphenidate improves objective and subjective sleepiness but shows mixed results on performance tests.⁶¹ The starting dose is 10 mg per day, with a recommended maximum dose of 60 mg per day. Side effects include nausea, reduced appetite, headache, insomnia, and psychosis. Due to its adverse reactions and abuse potential, it is a second-line treatment or add-on therapy for more stressful situations.⁶²

Dextroamphetamine Sulfate (R-Amphetamine Sulfate Enantiomer)

Dextroamphetamine is a competitive dopamine transporter blocker and is considered third-line therapy due to abuse potential.

Pitolisant

Pitolisant is the first antagonist of the histamine H3 autoreceptor and increases histamine release in the hypothalamus and cortex.⁶² In contrast to the H1 receptor, H3 receptors are saturated in the CNS and therefore may not cause the same side effects that have limited the use of H1 receptor stimulators. In a double-blinded study in five European countries, pitolisant was found to be better tolerated than modafinil.⁶³ However, its efficacy is comparable to modafinil.⁵¹ The dosage ranges from 9 to 36 mg daily, and the half-life is about 10–12 hrs. Side effects include headache, insomnia, nausea, and anxiety. Pitolisant has been available in Europe for some time and received FDA approval in the United States for EDS in narcolepsy in 2019.

Sodium Oxybate (Xyrem^®)

Sodium oxybate is the sodium salt of g-hydroxybutyrate and considered a standard therapy for EDS with or without cataplexy by the AASM.⁴⁷ It has been shown to decrease attacks of cataplexy, increase sleep latency, and reduce sleep attacks.⁶⁴ The mechanism of action remains incompletely understood, but it is partially believed to act on the GABA-B receptors.^51,62

Sodium oxybate has a very short half-life; two doses are required nightly. The dosing starts with 2.25 grams twice per night and is titrated up according to the patient’s symptoms. The maximum recommended dose is 4.5 grams per dose with two doses per night (9 grams per night). The effectiveness of the medication is gradual and time-dependent, with symptom control achieved in 1 month or more. The most frequent side effects are nausea, dizziness, anxiety, and confusion, and the more disabling are enuresis, sleep walking, and mood disturbance.^51,62 The combination of Modafinil and sodium oxybate may have an additive effect on EDS.⁶⁵ A clinical trial is currently underway to assess the efficacy and safety of a once-nightly formulation of sodium oxybate.⁶⁶ REST-ON is a double-blind, randomized, placebo-controlled study of 264 patients to assess the efficacy and safety of a once-nightly formulation of sodium oxybate for the treatment of EDS and cataplexy in patients with narcolepsy.⁶⁶

Sodium oxybate carries a black box warning for abuse and is only dispensed by a central pharmacy per FDA guidelines. Caution is advised for patients with an existing history of depression or untreated sleep apnea. Given that sodium oxybate is a sedating medication, there is a strong warning against taking other sedating medications concurrently due to the risk of respiratory depression. The risk of rebound cataplexy or status cataplecticus is low with withdrawal or disruption of the medication.⁶⁷

Cardiovascular Risk Assessment Prior To Initiation Of Stimulants

A large retrospective study showed no evidence of increased serious cardiovascular events in patients with ADHD aged 2 to 24 years receiving stimulant medicaitons.⁶⁸ Similar results were seen in another retrospective cohort study in patients with ADHD aged 25 to 64 years.⁶⁹ Based on the aforementioned trials, the FDA concluded that there was no strong association between ADHD pharmacotherapy and adverse cardiovascular events.⁷⁰ Nonetheless, patients should be cautioned about potential changes in heart rate and blood pressure. In general, stimulants should be avoided in patients with cardiovascular disease; if needed, they should be prescribed in consultation with a cardiologist. The American Academy of Pediatrics, American Heart Association, and American College of Cardiology recommend a cardiovascular evaluation (history, family history, and examination) in children prior to the initiation of stimulants.⁷¹

Clinical Dilemma

Clinicians are faced with challenging questions because studies of stimulant medications and cardiovascular risk did not include patients above 65 years; thus, the effect of pre-existing cardiac conditions in the elderly population is unclear. These studies are also confounded by healthy user bias, which limits generalizability. There is a need for further research on use of stimulants in the elderly population, especially in patients with OSA on CPAP with residual daytime sleepiness.

Excessive Daytime Sleepiness In OSA

CPAP has been shown to reduce daytime sleepiness and therefore is considered the gold standard for treating patients with OSA.⁷² The efficacy of CPAP therapy depends significantly on the compliance and hours of usage. A multicenter, quasi-experimental study in patients with severe sleep apnea showed that at least 4 hrs, 6 hrs, and 7.5 hrs of nightly CPAP usage were needed to show an improvement in the ESS score, MSLT, and Functional Outcomes of Sleep Questionnaire, respectively. The authors concluded that more hours of CPAP use is associated with greater improvement in sleepiness. However, there is variation in the amount of CPAP use required to normalize sleepiness, so nightly use recommendations may be individualized and considered in terms of desired treatment outcomes.⁷³ If there is persistence of residual daytime sleepiness after adequate CPAP use, clinical assessment as mentioned above should be performed. If no modifiable factors are identified and the patient is compliant with CPAP, MSLT could be considered. Alternatively, a trial of stimulant therapy may be considered.

Clinical Challenge

Meticulous stepwise screening for comorbidities contributing to EDS in OSA patients is warranted. Achieving the above-mentioned CPAP usage parameters is a significant challenge in the management of EDS. As a result, patients are prematurely started on stimulant therapy for clinical improvement and patient satisfaction, potentially exposing them to adverse effects.

Co-Management Of OSA In Narcolepsy

Although sleepiness improves with CPAP therapy in patients with comorbid narcolepsy and OSA, narcolepsy-related EDS is not expected to respond to CPAP. Therefore, the mainstay of therapy for narcolepsy should be medications. CPAP in narcoleptics with OSA should remain a second-line, adjunctive therapy to standard pharmacological treatments.³⁷

Pediatric Population

EDS is required for the diagnosis of narcolepsy in the pediatric population. In younger children, EDS may be vague and present as behavior problems or concentration difficulties.⁷⁴ Treatment of narcolepsy in the pediatric population is similar to the treatment in adults.⁵¹ Sodium oxybate has recently been approved for use in children ages 7 and older and is the only FDA approved medication for the treatment of EDS and cataplexy in the pediatric population. The dosing for sodium oxybate in children is weight based, and the most common side effects include enuresis, nausea/vomiting, headache, decreased weight/appetite and dizziness.⁷⁵ Children with both narcolepsy and mild to moderate OSA have shown improvement in daytime sleepiness following adenotonsillectomy.⁷⁶

Future Trends

Availability of CSF hypocretin testing is forthcoming in the United States, but the cost of testing and performing the lumbar puncture is unknown and there are risks associated with the procedure itself. To date, there is no cure for narcolepsy, and management focuses on symptomatic relief with medications. Orexin supplementation is a novel therapy that has a potential role in treating the disease. Various modalities have been proposed, including orexin agonists, gene therapy, and cell transplantation. Recent experiments in mice showed that central administration of orexin in orexin-cell-ablated mice improved wakefulness and reduced cataplexy.⁷⁷ Other studies showed amelioration of narcolepsy symptoms with peripherally administered YNT-185 (non-peptide selective orexin type-2 receptor agonist)⁷⁸ and TAK-925 (orexin 2 receptor selective agonist)⁷⁹ in mice models, providing further proof of concept. Human studies with oral formulations of orexin agonists are in the beginning stages.

Clinical Case 1

30-year-old male with no significant past medical history came to the sleep clinic for evaluation of snoring. His wife was having difficulty sharing the bedroom with him due to loud snoring. His Epworth Sleepiness Scale (ESS) score was 15/24. Additionally, he reported dry mouth and morning headaches upon waking up. Infrequently, he felt “trapped in his body” due to the inability to move his body while trying to initiate sleep. He had good sleep hygiene with an average total sleep time of 7.5 hrs. Physical exam revealed BMI of 36, Modified Mallampati score of III, macroglossia, and neck circumference of 17 inches. The rest of the exam was unremarkable, and the patient was on no medications. The patient underwent attended polysomnography (PSG) in the sleep laboratory. The sleep architecture was normal, and the apnea hypopnea index (AHI) was 20/hour. He was titrated to CPAP of 12 cm H₂O. He returned for his compliance visit in 3 months and felt more refreshed but still sleepy. The download from the CPAP showed 80% compliance (> 4 hrs usage) with minimal leaks and residual AHI of 0.1/hr. His ESS score was 12/24. In the following clinic visit, the patient did not feel any different and was still sleepy despite 100% compliance on his CPAP machine. On further questioning, he still had the feeling of inability to move his body while initiating sleep but denied feeling weak with strong emotions. He also endorsed occasional hypnogogic hallucinations. The patient underwent PSG with the CPAP of 12 H₂O, followed by MSLT. The AHI on the PSG with CPAP was 1/hr. MSLT showed 2 SOREMs with mean sleep onset latency of 6 mins. On retrospective review, the first PSG also revealed a REM sleep onset latency of 15 mins. The patient was diagnosed with OSA and narcolepsy and responded to modafinil. This case highlights the fact that narcolepsy could be a missed diagnosis because the signs and symptoms of OSA and narcolepsy may have significant overlap. Note: This case is a mock case used to highlight points raised in the review.

Clinical Case 2

25-year-old female with a previous diagnosis of NT1 presented with worsening EDS. She was previously well controlled on modafinil 100 mg twice daily. Her cataplexy episodes had already reduced in frequency and she did not require any specific treatment for it. Recently, she started working in the corporate sector and living independently. In the interim, she was diagnosed with depression and started on fluoxetine. Since then, her EDS had worsened. She also gained 10 pounds in the past 2 years. Her sleep routine was consistent, with 7 to 8 hrs of sleep, though she was unable to nap now. Her caffeine intake had also increased, and her ESS during the clinic visit was 14/24 which was up from 9/24 one year ago. On further questioning, the patient had been told that she started snoring. On physical exam, her BMI was 30 and her Modified Mallampati score was III with 2+ tonsils. The rest of the exam was unremarkable. The patient was screened for OSA with a PSG. She was diagnosed with moderate OSA and was initiated on CPAP while she continued on modafinil. After 3 months of CPAP usage, she returned to clinic for re-evaluation. She had excellent compliance with > 4 hrs usage of 90% and residual AHI of 1/hr. Her EDS had improved and her ESS was 8/24. This case demonstrates that other causes of EDS should be re-evaluated in patients presenting with worsening of the previously well-controlled symptoms of narcolepsy. Note: This case is a mock case used to highlight points raised in the review.