Description
Actigraphy refers to the assessment of body movement activity patterns using devices, typically placed on the wrist or ankle, during sleep, which are interpreted by computer algorithms as periods of sleep and wake. Sleep-wake cycles may be altered in sleep disorders, including insomnia and circadian rhythm sleep disorders. Also, actigraphy could be used to assess sleep/wake disturbances associated with other disorders.

For individuals who have circadian sleep-wake rhythm disorders who receive actigraphy, the evidence includes an ancillary study within a randomized controlled trial. Relevant outcomes are test accuracy and test validity. Comparison with polysomnography (PSG) has shown that actigraphy is limited in differentiating between sleep and wake in more disturbed sleep. Actigraphy appears to reliably measure sleep onset and total sleep time in some patient populations. Comparisons with PSG and sleep diaries are limited. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population. The evidence is insufficient to determine the effects of the technology on health outcomes.

For children and adolescents with sleep-associated disorders, in children and adolescents who receive actigraphy, the evidence includes prospective and retrospective validation studies. Relevant outcomes are test accuracy and validity. Comparisons with PSG have shown that actigraphy can differ significantly in its estimations of wake and sleep times and sleep onset latency. Comparisons with sleep diaries have also failed to show satisfactory agreement, with greater discrepancies for more disturbed sleep. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population. The evidence is insufficient to determine the effects of the technology on health outcomes.

For individuals who have central disorders of hypersomnolence who receive actigraphy, the evidence includes a comparative observational study. Relevant outcomes are test accuracy and validity. Comparison with video-PSG has indicated that actigraphy has a sensitivity of 26.1% and specificity of 95.5%. General evidence has also revealed that the accuracy of actigraphy for differentiating between wake and sleep decreases as the level of sleep disturbance increases. Although actigraphy appears to provide reliable measures of sleep onset and wake time in some patient populations, its clinical utility compared with that of sleep diaries has not been demonstrated. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population. The complexity of the various syndromes as well as the potential for medical treatment with significant adverse events makes accurate diagnosis essential. The evidence is insufficient to determine the effects of the technology on health outcomes.

For individuals who have insomnia who receive actigraphy, the evidence includes prospective and retrospective validation studies. Relevant outcomes are test accuracy and validity. Comparisons with PSG have shown that actigraphy has poor agreement for reporting wake time and can overestimate sleep efficiency. Comparison with sleep diaries has indicated that actigraphy is less effective at differentiating between patients with insomnia and controls. General evidence has also revealed that the accuracy of actigraphy for differentiating between wake and sleep decreases as the level of sleep disturbance increases. Although actigraphy appears to provide reliable measures of sleep onset and wake time in some patient populations, its clinical utility compared with sleep diaries has not been demonstrated. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population. The evidence is insufficient to determine the effects of the technology on health outcomes. 

Background 
Sleep Disorders
Sleep disorders affect a large percentage of the U.S. population. For example, estimates suggest that 15% to 24% of the U.S. population suffers from insomnia.¹ Lack of sleep also contributes reduced cognitive functioning, susceptibility to heart disease, and workplace absenteeism.

Diagnosis
Actigraphy refers to the assessment of activity patterns (body movement) using devices, typically placed on the wrist or ankle, which are interpreted by computer algorithms as periods of sleep (absence of activity) and wake (activity). Actigraphy devices are usually placed on the nondominant wrist with a wristband and are worn continuously for at least 24 hours. Activity is usually recorded for a period of 3 days to 2 weeks but can be collected continuously over extended periods with regular downloading of data onto a computer. The activity monitors may also be placed on the ankle to assess restless legs syndrome or on the trunk to record movement in infants.

The algorithms for detecting movement vary across devices and may include “time above threshold,” the “zero crossing method” (the number of times per epoch that activity level crosses zero), or “digital integration” method, resulting in different sensitivities. Sensitivity settings (e.g., low, medium, high, automatic) can also be adjusted during data analysis. The most commonly used method (digital integration) reflects both acceleration and amplitude of movement.

Data on patient bedtimes (lights out) and rise times (lights on) are usually entered into the computer from daily patient sleep logs or by patient-activated event markers. Proprietary software is then used to calculate periods of sleep based on the absence of detectable movement, along with the movement-related level of activity and periods of wake. In addition to providing a graphic depiction of the activity pattern, the device-specific software can then analyze and report a variety of sleep parameters, including sleep onset, sleep offset, sleep latency, total sleep duration, and wake after sleep onset (actigraphy could also be used to measure the level of physical activity).

Actigraphy has been used for more than two decades as an outcome measure in sleep disorders research. For clinical applications, actigraphy is being evaluated as a measure of sleep-wake cycles in sleep disorders, including insomnia and circadian rhythm sleep disorders. Also, actigraphy is being investigated as a measure of sleep-wake disturbances associated with other diseases and disorders.

Regulatory Status
Numerous actigraphy devices have received FDA clearance for marketing through the 510(k) process. Some actigraphy devices are designed and marketed to measure sleep/wake states while others are designed and marketed to measure levels of physical activity. FDA product code: OLV.

Policy:
Actigraphy is investigational and/or unproven and therefore considered NOT MEDICALLY NECESSARY when used as the sole technique to record and analyze body movement, including but not limited to its use to evaluate sleep disorders. This does not include the use of actigraphy as a component of portable sleep monitoring (see Policy Guidelines section). When used as a component of portable sleep monitoring, actigraphy should not be separately reported.

Policy Guidelines
This policy does not address the use of actigraphy as a component of portable sleep monitoring under CPT codes 95800 or 95806 (see CAM 20118). When used as a component of portable sleep monitoring, actigraphy should not be separately reported.

Coding
Please see the Codes table for details.

Benefit Application
BlueCard^®/National Account Issues
State or federal mandates (e.g., FEP) may dictate that all devices approved by the U.S. Food and Drug Administration (FDA) may not be considered investigational, and thus these devices may be assessed only on the basis of their medical necessity.

Rationale  
Evidence reviews assess whether a medical test is clinically useful. A useful test provides information to make a clinical management decision that improves the net health outcome. That is, the balance of benefits and harms is better when the test is used to manage the condition than when another test or no test is used to manage the condition.

The first step in assessing a medical test is to formulate the clinical context and purpose of the test. The test must be technically reliable, clinically valid, and clinically useful for that purpose. Evidence reviews assess the evidence on whether a test is clinically valid and clinically useful. Technical reliability is outside the scope of these reviews, and credible information on technical reliability is available from other sources.

Circadian Sleep-Wake Rhythm Disorders
Clinical Context and Test Purpose
The purpose of actigraphy is to provide a diagnostic option that is an alternative to or an improvement on existing tests in the assessment of patients with sleep disorders.

The question addressed in this evidence review is: Does the use of actigraphy in the diagnosis of sleep disorders improve the net health outcome?

The following PICO was used to select literature to inform this review.

Populations
The relevant population of interest is individuals with circadian sleep-wake rhythm disorders. The body's 24-hour internal physiologic systems, such as sleep, wakefulness, core temperature, and appetite are known as circadian rhythms. Disorders of circadian rhythms can be of the intrinsic system or precipitated by external factors (e.g., shift work). Clinical manifestations may be insomnia or excessive daytime sleepiness.

Interventions
The test being considered is actigraphy.

Actigraphy refers to the assessment of body movement activity patterns using devices, typically placed on the wrist or ankle, during sleep, which are interpreted by computer algorithms as periods of sleep and wake. Actigraphy data are generally recorded for periods between 3 days to 2 weeks but can be collected continuously over extended periods with regular downloading of data onto a computer.

Comparators
The following tests and tools are currently being used to make decisions about circadian sleep-wake rhythm disorders: polysomnography (PSG) and sleep diaries or logs. Polysomnography is the criterion standard for the evaluation of sleep-wake cycles. A sleep diary is a key component of sleep disorders evaluation and includes the patient's record of symptoms.

Outcomes
The general outcomes of interest are test validity and test accuracy. Measurement of movement (actigraph) is typically 3 types: zero crossing mode counts the number of times the waveform crosses 0 for each time period; proportional integral mode measures the area under the curve (AUC) and adds that size for each time period; and time above threshold uses a defined threshold and measures the length of time that the wave is above the threshold.

Study Selection Criteria
For the evaluation of clinical validity of actigraphy, studies that meet the following eligibility criteria were considered:

• Reported on the accuracy of the marketed version of the technology (including any algorithms used to calculate scores).
• Included a suitable reference standard.
• Patient/sample clinical characteristics were described.
• Patient/sample selection criteria were described.

Clinically Valid
A test must detect the presence or absence of a condition, the risk of developing a condition in the future, or treatment response (beneficial or adverse).

Review of Evidence
Actigraphy versus Polysomnography
Paquet et al. (2007) compared actigraphy assessment of sleep and wake with PSG under varying conditions of sleep disturbance (nighttime sleep, daytime sleep, daytime sleep with caffeine) in 23 healthy subjects.² This study was ancillary to another that evaluated the effects of caffeine on daytime recovery sleep. The experimental protocol involved 2 visits to the sleep laboratory, each including 1 night of nocturnal sleep, 1 night of sleep deprivation, and the next day of recovery sleep (once with placebo and once with caffeine 200 mg). Actigraphy monitoring used a specific device applied to the wrist (Actiwatch), which was synchronized with PSG equipment before recording. Assessments of sleep and wake for each 1-minute interval were compared for sensitivity, specificity, and accuracy of actigraphy with manually staged sleep from PSG recordings. Sensitivity was defined as the proportion of all epochs scored as sleep by PSG that were also scored as sleep by actigraphy. Specificity was the proportion of all epochs scored as wake by PSG that were also scored as wake by actigraphy. Accuracy was the proportion of all epochs correctly identified by actigraphy. Four sensitivity settings/scoring algorithms were compared. In general, as the threshold to detect movement increased, sensitivity to detect sleep increased, but the specificity to detect wake decreased. With the medium threshold algorithm, the sensitivity to detect sleep ranged between 95% and 96%. However, specificity or the ability to detect wake, was 54% for nighttime sleep, 45% for daytime recovery sleep, and 37% for daytime recovery sleep with caffeine. The main study finding was that the more disturbed the sleep, the less actigraphy could differentiate between true sleep and quiet wakefulness, with an accuracy of 72% for the most disrupted sleep condition. Through experimental manipulation of the level of sleep disturbance, this study provided information on the limitations of this technology for clinical populations with sleep disruption.

No specific studies were identified that compared actigraphy with sleep diaries in clinical populations.

Clinically Useful
A test is clinically useful if the use of the results informs management decisions that improve the net health outcome of care. The net health outcome can be improved if patients receive correct therapy, more effective therapy, or avoid unnecessary testing or therapy.

Direct Evidence
Direct evidence of clinical utility is provided by studies that have compared health outcomes for patients managed with and without the test. Because these are intervention studies, the preferred evidence would be from randomized controlled trials (RCTs).

No direct evidence for the use of actigraphy in the management of circadian rhythm disorders was identified.

Chain of Evidence
Indirect evidence on clinical utility rests on clinical validity. If the evidence is insufficient to demonstrate test performance, no inferences can be made about clinical utility.

Limited data indicated that actigraphy is comparable to PSG for detecting sleep, but is less specific for detecting wake activity in disturbed sleep conditions.

Section Summary: Circadian Sleep — Wake Rhythm Disorders
The diagnosis of circadian rhythm disorders in adults is made through a clinical evaluation that includes a review of sleep diaries or logs along with the use of PSG as necessary. For individuals who have circadian sleep-wake rhythm disorders who receive actigraphy, comparison with PSG has shown that actigraphy is limited in differentiating between sleep and wake in more disturbed sleep. Actigraphy appears to reliably measure sleep onset and total sleep time in some patient populations. Comparisons with PSG and sleep diaries are limited. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population.

Children or Adolescents with Sleep-Related Disorders
Clinical Context and Test Purpose
The purpose of actigraphy is to provide a diagnostic option that is an alternative to or an improvement on existing tests in the assessment of patients with sleep disorders.

The question addressed in this evidence review is: Does the use of actigraphy in the diagnosis of sleep disorders improve the net health outcome?

The following PICO was used to select literature to inform this review.

Populations
The relevant population of interest is children or adolescents with sleep disorders. Maturation of the sleep-wake cycle is a developmental process from the newborn period through the pubertal period. Premature infants are prone to sleep disturbances. Sleep disorders may be considered in children and adolescents presenting with irritability, behavioral problems, learning difficulties, and poor academic performance.

Interventions
The test being considered is actigraphy.

Actigraphy refers to the assessment of body movement activity patterns using devices, typically placed on the wrist or ankle, during sleep, which are interpreted by computer algorithms as periods of sleep and wake. Actigraphy data are generally recorded for periods between three days to two weeks but can be collected continuously over extended periods with regular downloading of data onto a computer.

Comparators
The following tests and tools are currently being used to make decisions about sleep-associated disorders in children and adolescents: PSG and sleep diaries or logs. Polysomnography is the criterion standard for the evaluation of sleep-wake cycles. A sleep diary is a key component of sleep disorders evaluation and includes the patient's record of symptoms.

Outcomes
The general outcomes of interest are test validity and test accuracy. Measurement of movement (actigraph) is typically three types: zero crossing mode counts the number of times the waveform crosses 0 for each time period; proportional integral mode measures the AUC and adds that size for each time period; and time above threshold uses a defined threshold and measures the length of time that the wave is above the threshold.

Study Selection Criteria
For the evaluation of clinical validity of actigraphy, studies that meet the following eligibility criteria were considered:

• Reported on the accuracy of the marketed version of the technology (including any algorithms used to calculate scores).
• Included a suitable reference standard.
• Patient/sample clinical characteristics were described.
• Patient/sample selection criteria were described.

Clinically Valid
A test must detect the presence or absence of a condition, the risk of developing a condition in the future, or treatment response (beneficial or adverse).

Review of Evidence
Actigraphy versus Polysomnography
Randomized Controlled Trials
Meltzer et al. (2016) compared actigraphy with concurrently worn comprehensive ambulatory home PSG among 148 children ages 5 to 12 born prematurely (Table 1).³ Subjects were participating in a larger study on the long-term effect of caffeine therapy for apnea of prematurity on sleep. After controlling for sleep disorders, compared with PSG, actigraphy underestimated total sleep by 30.1 minutes and overestimated sleep onset latency by 2.16 minutes (Table 2). The sensitivity and specificity of actigraphy were 88% and 84%, respectively; accuracy was 46%.

Table 1. Summary of Key RCT Characteristics

Study	Countries	Sites	Participants	Interventions
				Active	Comparator
Meltzer et al. (2016)3	U.S., Australia	50	148 (85 male, 63 female) children born preterm	Caffeine	Placebo

RCT: randomized controlled trials.

Table 2. Summary of Key RCT Results

Study	Mean PSG (SD)	Mean Actigraphy (SD)	Mean Difference (95% CI)	p
Meltzer et al. (2016)3
Total sleep time, min	535.9 (54.8)	505.7 (49.3)	-30.1 (-35.3 to -25.0)	.02
Sleep-onset latency, min	18.1 (18.8)	20.3 (23.0)	2.16 (-1.7 to 6.0)	.02
Sleep efficiency, %	89.6 (0.05)	84.6 (0.05)	-5.0 (-5.8 to -4.1)	.008

CI: confidence interval; PSG: polysomnography; RCT: randomized controlled trials; SD: standard deviation.
Tables 3 and 4 display notable limitations identified in each study.

Table 3. Study Relevance Limitations

Study	Populationa	Interventionb	Comparatorc	Outcomesd	Duration of Follow-Upe
Meltzer et al. (2016)3	3. Study population is unclear 4. Study population not representative of intended use	3. Not intervention of interest

The study limitations stated in this table are those notable in the current review; this is not a comprehensive gaps assessment.
a Population key: 1. Intended use population unclear; 2. Clinical context is unclear; 3. Study population is unclear; 4. Study population not representative of intended use.
b Intervention key: 1. Classification thresholds not defined; 2. Version used unclear; 3. Not intervention of interest.
c Comparator key: 1. Classification thresholds not defined; 2. Not compared to credible reference standard; 3. Not compared to other tests in use for same purpose.
d Outcomes key: 1. Study does not directly assess a key health outcome; 2. Evidence chain or decision model not explicated; 3. Key clinical validity outcomes not reported (sensitivity, specificity and predictive values); 4. Reclassification of diagnostic or risk categories not reported; 5. Adverse events of the test not described (excluding minor discomforts and inconvenience of venipuncture or noninvasive tests).
e Follow-Up key: 1. Follow-up duration not sufficient with respect to natural history of disease (true positives, true negatives, false positives, false negatives cannot be determined).

Table 4. Study Design and Conduct Limitations

Study	Populationa	Interventionb	Comparatorc	Outcomesd	Duration of Follow-Upe
Meltzer et al. (2016)3	3. Study population is unclear 4. Study population not representative of intended use	3. Not intervention of interest

            
The study limitations stated in this table are those notable in the current review; this is not a comprehensive gaps assessment.
a Selection key: 1. Selection not described; 2. Selection not random or consecutive (i.e., convenience).
b Blinding key: 1. Not blinded to results of reference or other comparator tests.
c Test Delivery key: 1. Timing of delivery of index or reference test not described; 2. Timing of index and comparator tests not same; 3. Procedure for interpreting tests not described; 4. Expertise of evaluators not described.
d Selective Reporting key: 1. Not registered; 2. Evidence of selective reporting; 3. Evidence of selective publication.
e Data Completeness key: 1. Inadequate description of indeterminate and missing samples; 2. High number of samples excluded; 3. High loss to follow-up or missing data.
f Statistical key: 1. Confidence intervals and/or p values not reported; 2. Comparison with other tests not reported.

Nonrandomized Studies
Yavuz-Kodat et al. (2019) evaluated the validity of actigraphy compared to PSG in 26 children (6 girls; 20 boys) with autism spectrum disorder.⁴ Per equivalence tests, the difference between actigraphy and PSG measures were clinically acceptable for total sleep time (< 30 minutes; p < .01), sleep latency (< 15 minutes; p < .001), and sleep efficiency (10%, p < .01), but not for wake after sleep onset ( < 15 minutes; p = .13). The study involved a sample size of only 26 subjects with high inter-individual variability, which may result in reduced statistical power. Additionally, the investigators only compared a single night of actigraphy to concurrent PSG readings versus the recommended collection of 5 to 7 nights of recordings.

O'Driscoll et al. (2010) compared actigraphy with PSG in 130 children referred for assessment of sleep-disordered breathing.⁵ The Arousal Index and Apnea-Hypopnea Index scores from PSG were compared with the number of wake bouts per hour and Fragmentation Index. Using a PSG-determined Apnea-Hypopnea Index of greater than 1 event per hour, the measure of wake bouts per hour had a sensitivity and specificity of 14.9% and 98.8%, respectively, and the Fragmentation Index had a sensitivity and specificity of 12.8% and 97.6%, respectively. Using a PSG-determined Arousal Index greater than 10 events per hour as the reference standard, the actigraphy measure of wake bouts per hour had a sensitivity and specificity of 78.1% and 52.6%, and the Fragmentation Index had a sensitivity and specificity of 82.2% and 50.9%, respectively. Based on receiver operating characteristic (ROC) curves, the ability of actigraphy to classify a child correctly as having an Apnea-Hypopnea Index of greater than 1 event per hour was considered poor.

Hyde et al. (2007) examined the validity of actigraphy for determining sleep and wake in children with sleep-disordered breathing using data analyzed over 4 separate activity threshold settings (low, medium, high, automatic).⁶ The low- and auto-activity thresholds were found to determine sleep adequately (relative to PSG) but to underestimate wake significantly, with a sensitivity of 97% and specificity of 39%. The medium- and high-activity thresholds significantly underestimated sleep time (sensitivity, 94%, and 90%) but did not differ significantly from the total PSG estimates of wake time (specificity, 59%, and 69%), respectively. Overall agreement rates between actigraphy and PSG (for both sleep and wake) ranged from 85% to 89%. Belanger et al. (2013) assessed the sensitivity and specificity of different scoring algorithms in healthy preschoolers.⁷ An algorithm designed specifically for children showed the highest accuracy (95.6%) in epoch-by-epoch comparison with PSG.

Insana et al. (2010) compared ankle actigraphy recording with PSG in 22 healthy infants (age range, 13 to 15 months).⁸ Actigraphy underestimated total sleep time by 72 minutes and overestimated wake after sleep onset by 14 minutes. In 55% of the infants, total sleep time was underestimated by 60 minutes or more. Sensitivity was calculated for total sleep time (92%), stages 1 and 2 combined (91%), slow wave sleep (96%), and rapid eye movement sleep (89%). Specificity for identifying wake was 59%, and accuracy was 90%. Overall, actigraphy identified sleep relatively well, but was unable to discriminate wake from sleep. A study by Spruyt et al. (2011) compared wrist actigraphy with PSG in 149 healthy school-aged children.⁹ Although sleep time did not differ significantly, actigraphy underestimated total sleep time by 32 minutes (p = .47) and overestimated wake after sleep onset by 26 minutes (p = .09). The authors concluded that actigraphy was relatively inaccurate for determining sleep quality in this population. Selected trial characteristics and results are provided in Tables 5 and 6.

Table 5. Summary of Key Nonrandomized Trial Characteristics

Study	Study Type	Country	Participants	Treatment	Comparator
Yavuz-Kodat et al. (2019)4	Cohort	France	26 children (mean age: 5.4 y)	Actigraphy	PSG
O'Driscoll et al. (2010)5	Cohort	Australia	130 children ages 2 to 18 y	Actigraphy	PSG
Hyde et al. (2007)6	Cohort	Australia	45 children ages 1 to 12 y	Actigraphy	PSG
Belanger et al. (2013)7	Cohort	Canada	12 children ages 2 to 5 y	Actigraphy algorithms	PSG
Insana et al. (2010)8	Cohort	U.S.	22 infants (14.1 mo)	Actigraphy	PSG

PSG: polysomnography.

Table 6. Summary of Key Nonrandomized Trial Results

Study	Sen, %	Spec, %	Accuracy	Total Sleep Time min
Yavuz-Kodat et al. (2019)4*	Mean (SD)	Mean (SD)	Mean (SD)
Low	0.94 ± 0.06	0.51 ± 0.20	0.87 ± 0.08	NA
Medium	0.90 ± 0.06	0.62 ± 0.19	0.86 ± 0.07	NA
High	0.86 ± 0.07	0.67 ± 0.18	0.83 ± 0.07	NA
Auto	0.94 ± 0.05	0.51 ± 0.15	0.86 ± 0.08	NA
O'Driscoll et al. (2010)5	82.2	50.9	-	-
Hyde et al. (2007)6	Median (IQR), %	Median (IQR), %		Median (IQR)
Low	96.5 (94.4 – 98.8)	39.4 (15.5 – 67.3)	NA	424 (397 – 453)
Median	93.9 (90.9 – 97.1)	59.0 (28.7 – 82.1)	NA	402 (376 – 433)
High	90.1 (85.3 – 94.6)	68.9 (40.6 – 92.6)	NA	388 (358 – 417)
Auto	97.7 (96.2 – 98.4)	39.4 (22.9 – 53.9)	NA	426 (404 – 459)
Belanger et al. (2013)7	Mean (SD)	Mean (SD)	Mean (SD), %	Mean (SD)
ACT40	87.9 (2.7)	500.7 (48.2)	87.5 (2.8)	500.7 (48.2)
ACT80	93.4 (1.6)	537.3 (50.0)	91.4 (2.1)	537.3 (50.0)
AlgoSmooth	97.7 (1.6)	565.1 (54.0)	95.0 (2.2)	565.1 (54.0)
Insana et al. (2010)8	Sens (Range), %	Spec (Range), %	Accuracy (Range), %
Stages 1 – 2	91.24 (79.6 – 97.9)	NA	NA	NA
Slow wave sleep	96.3 (73.1 – 100)	NA	NA	NA
REM sleep	88.9 (75.4 – 97.9)	NA	NA	NA
Total sleep time	92.4 (79.4 – 97.7)	NA	NA	NA
Wake	NA	58.9 (0 – 100)	NA	NA
Total sleep/total wake	NA	NA	89.6 (65.4 – 97.7)	NA

*Sensitivity, specificity, and accuracy values of epoch-by-epoch comparisons between actigraphy and polysomnography.
IQR: interquartile range: NA: not applicable; REM: rapid eye movement; SD: standard deviation; Sens: sensitivity; Spec: specificity.

Actigraphy versus Sleep Diaries
Werner et al. (2008) assessed the agreement between actigraphy and parent diary or questionnaire to assess sleep patterns in 50 children, ages 4 to 7 years, recruited from kindergarten schools in Switzerland.¹⁰ Sixty-eight (10%) of 660 invited families participated. Each child was home-monitored with an actigraph for 6 to 8 consecutive nights, and parents were asked to complete a detailed sleep diary (15-minute intervals) during the monitoring days to indicate bedtime, estimated sleep start, wake periods during the night, and estimated sleep end. Parents' assessment of habitual wake time, get up time, bedtime, time of lights off, sleep latency, and nap duration was obtained through a questionnaire. The satisfactory agreement, defined a priori as differences smaller than 30 minutes, was achieved between actigraphy and diary for sleep start, sleep end, and assumed sleep. Actual sleep time and nocturnal wake time differed by an average of 72 minutes and 55 minutes, respectively. There was a lack of concordance between actigraphy and the questionnaire for any outcome parameter. Authors concluded that the diary was a cost-effective and valid source of information about children's sleep-schedule time, while actigraphy might provide additional information about nocturnal wake time or might be used if parents are unable to report in detail. Compliance and accuracy in the diaries were likely affected by parents' motivation, who self-selected into this study.

Sleep discrepancies between actigraphy and sleep diary measures in adolescents were reported by Short et al. (2012).¹¹ A total of 290 adolescents (age range, 13 to 18 years) completed 8 days of sleep diaries and actigraphy. Actigraphy estimates of total sleep time (median, 6 hours 57 minutes) were significantly lower than total sleep time recorded in the adolescent's sleep diaries (median, 8 hours 17 minutes) or parent reports (median, 8 hours 51 minutes). Wake after sleep onset averaged 7 minutes in sleep diaries and 74 minutes by actigraphy. Actigraphy estimated wake after sleep onset of up to 3 hours per night in the absence of any wakening from sleep diaries, suggesting an overestimation of wake in this population. The discrepancy between actigraphy and sleep diary estimates of sleep was greater for boys than for girls, consistent with PSG studies that have shown increased nocturnal motor behavior in boys.

Clinically Useful
A test is clinically useful if the use of the results informs management decisions that improve the net health outcome of care. The net health outcome can be improved if patients receive correct therapy, more effective therapy, or avoid unnecessary therapy or testing.

Direct Evidence
Direct evidence of clinical utility is provided by studies that have compared health outcomes for patients managed with and without the test. Because these are intervention studies, the preferred evidence would be from RCTs.

No direct evidence for the use of actigraphy in the management of sleep-related disorders in children and adolescents was identified.

Chain of Evidence
Indirect evidence on clinical utility rests on clinical validity. If the evidence is insufficient to demonstrate test performance, no inferences can be made about clinical utility.

A single ancillary study within an RCT, which compared actigraphy with PSG reported that accuracy was 46%. Nonrandomized comparator studies demonstrated low specificity for differentiating sleep-wake patterns.

Section Summary: Children or Adolescents with Sleep-Related Disorders
Comparisons with PSG have shown that actigraphy can differ significantly in its estimations of wake and sleep times and sleep onset latency. Comparisons with sleep diaries have also failed to show satisfactory agreement, with greater discrepancies for more disturbed sleep. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population.

Central Disorders of Hypersomnolence
Clinical Context and Test Purpose
The purpose of actigraphy is to provide a diagnostic option that is an alternative to or an improvement on existing tests in the assessment of patients with sleep disorders.

The question addressed in this evidence review is: Does the use of actigraphy in the diagnosis of sleep disorders improve the net health outcome?

The following PICO was used to select literature to inform this review.

Populations
The relevant population of interest is individuals with central disorders of hypersomnolence. Hypersomnolence is excessive sleepiness when wakefulness would be expected. Such disorders include narcolepsy, recurrent hypersomnia (Kleine-Levin syndrome), and idiopathic hypersomnia. Central nervous system tumors and neurodegenerative conditions may also present with hypersomnolence.

Interventions
The test being considered is actigraphy.

Actigraphy refers to the assessment of body movement activity patterns using devices, typically placed on the wrist or ankle, during sleep, which are interpreted by computer algorithms as periods of sleep and wake. Actigraphy data are generally recorded for periods between 3 days to 2 weeks but can be collected continuously over extended periods with regular downloading of data onto a computer.

Comparators
The following tests and tools are currently being used to make decisions about central disorders of hypersomnolence: PSG and sleep diaries or logs. Polysomnography is the criterion standard for the evaluation of sleep-wake cycles. A sleep diary is a key component of sleep disorders evaluation and includes the patient's record of symptoms.

Outcomes
The general outcomes of interest are test validity and test accuracy. Measurement of movement (actigraph) is typically 3 types: zero crossing mode counts the number of times the waveform crosses 0 for each time period; proportional integral mode measures the AUC and adds that size for each time period; and time above threshold uses a defined threshold and measures the length of time that the wave is above the threshold.

Study Selection Criteria
For the evaluation of clinical validity of actigraphy, studies that meet the following eligibility criteria were considered:

• Reported on the accuracy of the marketed version of the technology (including any algorithms used to calculate scores).
• Included a suitable reference standard.
• Patient/sample clinical characteristics were described.
• Patient/sample selection criteria were described.

Clinically Valid
A test must detect the presence or absence of a condition, the risk of developing a condition in the future, or treatment response (beneficial or adverse).

Review of Evidence
Nonrandomized Studies
Louter et al. (2014) reported on a study of actigraphy, compared with video-PSG, as a diagnostic aid for rapid eye movement sleep behavior disorder in 45 consecutive patients with Parkinson disease.¹² The study population included patients referred for a variety of reasons, including insomnia, restless legs syndrome, and sleep apnea. Following video-PSG, 23 patients were diagnosed with rapid eye movement sleep behavior disorder. There was no significant difference between groups for the presence of other sleep disorders. Using a cutoff of 95 wake bouts per night, actigraphy had a sensitivity of 26.1% and specificity of 95.5%, with a positive predictive value of 85.7%.

Clinically Useful
A test is clinically useful if the use of the results informs management decisions that improve the net health outcome of care. The net health outcome can be improved if patients receive correct therapy, more effective therapy, or avoid unnecessary therapy or testing.

Direct Evidence
Direct evidence of clinical utility is provided by studies that have compared health outcomes for patients managed with and without the test. Because these are intervention studies, the preferred evidence would be from RCTs.

No direct evidence for the use of actigraphy in the management of central hypersomnolence was identified.

Chain of Evidence
Indirect evidence on clinical utility rests on clinical validity. If the evidence is insufficient to demonstrate test performance, no inferences can be made about clinical utility.

There were insufficient data on clinical validity to establish clinical utility.

Section Summary: Central Disorders of Hypersomnolence
Comparison with video-PSG has indicated that actigraphy has a sensitivity of 26.1% and specificity of 95.5%. General evidence has also revealed that the accuracy of actigraphy for differentiating between wake and sleep decreases as the level of sleep disturbance increases. Although actigraphy appears to provide reliable measures of sleep onset and wake time in some patient populations, its clinical utility compared with that of sleep diaries has not been demonstrated. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population. The complexity of the various syndromes as well as the potential for medical treatment with significant adverse events makes accurate diagnosis essential.

Insomnia
Clinical Context and Test Purpose
The purpose of actigraphy is to provide a diagnostic option that is an alternative to or an improvement on existing tests in the assessment of patients with sleep disorders.

The question addressed in this evidence review is: Does the use of actigraphy in the diagnosis of sleep disorders improve the net health outcome?

The following PICO was used to select literature to inform this review.

Populations
The relevant population of interest is individuals with insomnia. The inability to fall asleep at an appropriate or desired time and to maintain sleep without excessive waking has multiple medical as well as psychosocial etiologies.

Interventions
The test being considered is actigraphy.

Actigraphy refers to the assessment of body movement activity patterns using devices, typically placed on the wrist or ankle, during sleep, which are interpreted by computer algorithms as periods of sleep and wake. Actigraphy data are generally recorded for periods between 3 days to 2 weeks but can be collected continuously over extended periods with regular downloading of data onto a computer.

Comparators
The following tests and tools are currently being used to make decisions about insomnia: PSG and sleep diaries or logs. Polysomnography is the criterion standard for the evaluation of sleep-wake cycles. A sleep diary is a key component of sleep disorders evaluation and includes the patient's record of symptoms.

Outcomes
The general outcomes of interest are test validity and test accuracy. Measurement of movement (actigraph) is typically 3 types: zero crossing mode counts the number of times the waveform crosses 0 for each time period; proportional integral mode measures the AUC and adds that size for each time period; and time above threshold uses a defined threshold and measures the length of time that the wave is above the threshold.

Study Selection Criteria
For the evaluation of clinical validity of actigraphy, studies that meet the following eligibility criteria were considered:

• Reported on the accuracy of the marketed version of the technology (including any algorithms used to calculate scores).
• Included a suitable reference standard.
• Patient/sample clinical characteristics were described.
• Patient/sample selection criteria were described.

Clinically Valid
A test must detect the presence or absence of a condition, the risk of developing a condition in the future, or treatment response (beneficial or adverse).

Review of Evidence
Nonrandomized Comparator and Observational Studies
Marino et al. (2013) assessed the clinical validity of wrist actigraphy to measure nighttime sleep using the Cole-Kripke algorithm in 54 young and older adults, either healthy or with insomnia, and in 23 night-workers during daytime sleep.¹³ Epoch-by-epoch comparison with PSG showed sensitivity (ability to detect sleep, 97%) and accuracy (86%) during the usual sleep/lights-out period to be high but specificity (ability to detect wake, 33%) was low. As the amount of wake after sleep onset time increased, the more actigraphy underestimated this parameter. Several other studies have assessed the clinical validity of patients with primary or secondary sleep disorders.

Taibi et al. (2013) found a sensitivity of 96.1% and specificity of 36.4% in a study of 16 older adults with insomnia who underwent 8 nights of concurrent actigraphy and PSG.¹⁴ Sleep efficiency (actual sleep as a percentage of total recording time) was overestimated by actigraphy (84.4%) compared with PSG (66.9%), and the accuracy of actigraphy declined as sleep efficiency declined. Actigraphy and PSG measures of total sleep time were highly correlated, but correlations were marginal for sleep-onset latency and wake after sleep onset. Sensitivity and specificity were not assessed.

Levenson et al. (2013) evaluated the utility of sleep diaries and actigraphy in differentiating older adults with insomnia (n = 79) from good sleeper controls (n = 40).¹⁵ Sensitivity and specificity were determined for sleep-onset latency, wake after sleep onset, sleep efficiency, and total sleep time; patients with insomnia completed PSG studies but controls did not. Using ROC curve analysis, sleep diary measurements produced AUC in the high range (0.84 to 0.97), whereas actigraphy performed less well at discriminating between those with insomnia and controls (AUC range, 0.58 to 0.61).

Kaplan et al. (2012) compared outcomes for actigraphy, PSG, and sleep diaries in 27 patients with bipolar disorder, who were between mood episodes, and in 27 age- and sex-matched controls.¹⁶ Blinded evaluation found no significant differences in sleep parameters between patients with bipolar disorder and controls. Sleep parameter estimates from actigraphy and PSG were highly correlated.

Dick et al. (2010) assessed actigraphy with a SOMNOwatch in 28 patients with sleep-disordered breathing and reported a sensitivity of 90%, a specificity of 95%, and overall accuracy of 86% compared with PSG.¹⁷ Pearson correlations were high for total sleep time (0.89), sleep period time (0.91), and sleep latency (0.89), and moderate for sleep efficiency (0.71) and sustained sleep efficiency (0.65).

Sivertsen et al. (2006) assessed the sensitivity and specificity of actigraphy and PSG in older adults treated for chronic primary insomnia.¹⁸ Visual scoring of PSG data was blinded, and actigraphy records were scored by proprietary software. The study found that actigraphy had a 95% sensitivity for the 30-second epochs, but only a 36% specificity for detecting wake time. The authors concluded that "the clinical utility of actigraphy" was "suboptimal in older adults treated for chronic primary insomnia."

Clinically Useful
A test is clinically useful if the use of the results informs management decisions that improve the net health outcome of care. The net health outcome can be improved if patients receive correct therapy, more effective therapy, or avoid unnecessary therapy or testing.

Direct Evidence
Direct evidence of clinical utility is provided by studies that have compared health outcomes for patients managed with and without the test. Because these are intervention studies, the preferred evidence would be from RCTs.

No direct evidence for the use of actigraphy in the management of chronic insomnia was identified.

Chain of Evidence
Indirect evidence on clinical utility rests on clinical validity. If the evidence is insufficient to demonstrate test performance, no inferences can be made about clinical utility.

Actigraphy accurately measured total sleep time but not other measures of sleep patterning.

Section Summary: Insomnia
Comparisons with PSG have shown that actigraphy has a poor agreement for reporting wake time and can overestimate sleep efficiency. Comparison with sleep diaries has indicated that actigraphy is less effective at differentiating between patients with insomnia and controls. General evidence has also revealed that the accuracy of actigraphy for differentiating between wake and sleep decreases as the level of sleep disturbance increases. Although actigraphy appears to provide reliable measures of sleep onset and wake time in some patient populations, its clinical utility compared with sleep diaries has not been demonstrated. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population.

Summary of Evidence
For individuals who have circadian sleep-wake rhythm disorders who receive actigraphy, the evidence includes a comparative study that selected subjects from another main study evaluating the effects of caffeine on daytime recovery sleep. Relevant outcomes are test accuracy and test validity. Comparison with PSG has shown that actigraphy is limited in differentiating between sleep and wake in more disturbed sleep. Actigraphy appears to reliably measure sleep onset and total sleep time in some patient populations. Comparisons with PSG and sleep diaries are limited. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population. The evidence is insufficient to determine that the technology results in an improvement in the net health outcome.

For children and adolescents with sleep-associated disorders, in children and adolescents who receive actigraphy, the evidence includes prospective and retrospective validation studies. Relevant outcomes are test accuracy and validity. Comparisons with PSG have shown that actigraphy can differ significantly in its estimations of wake and sleep times and sleep onset latency. Comparisons with sleep diaries have also failed to show satisfactory agreement, with greater discrepancies for more disturbed sleep. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population. The evidence is insufficient to determine that the technology results in an improvement in the net health outcome.

For individuals who have central disorders of hypersomnolence who receive actigraphy, the evidence includes a comparative observational study. Relevant outcomes are test accuracy and validity. Comparison with video-PSG has indicated that actigraphy has a sensitivity of 26.1% and specificity of 95.5%. General evidence has also revealed that the accuracy of actigraphy for differentiating between wake and sleep decreases as the level of sleep disturbance increases. Although actigraphy appears to provide reliable measures of sleep onset and wake time in some patient populations, its clinical utility compared with that of sleep diaries has not been demonstrated. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population. The complexity of the various syndromes as well as the potential for medical treatment with significant adverse events makes accurate diagnosis essential. The evidence is insufficient that the technology results in an improvement in the net health outcome.

For individuals who have insomnia who receive actigraphy, the evidence includes prospective and retrospective validation studies. Relevant outcomes are test accuracy and validity. Comparisons with PSG have shown that actigraphy has a poor agreement for reporting wake time and can overestimate sleep efficiency. Comparison with sleep diaries has indicated that actigraphy is less effective at differentiating between patients with insomnia and controls. General evidence has also revealed that the accuracy of actigraphy for differentiating between wake and sleep decreases as the level of sleep disturbance increases. Although actigraphy appears to provide reliable measures of sleep onset and wake time in some patient populations, its clinical utility compared with sleep diaries has not been demonstrated. Evidence has shown that actigraphy does not provide a reliable measure of sleep efficiency in this patient population. The evidence is insufficient to determine that the technology results in an improvement in the net health outcome.

The purpose of the following information is to provide reference material. Inclusion does not imply endorsement or alignment with the evidence review conclusions.

Practice Guidelines and Position Statements
Guidelines or position statements will be considered for inclusion in Supplemental Information if they were issued by, or jointly by, a U.S. professional society, an international society with U.S. representation, or National Institute for Health and Care Excellence (NICE). Priority will be given to guidelines that are informed by a systematic review, include strength of evidence ratings, and include a description of management of conflict of interest.

American Academy of Sleep Medicine
The American Academy of Sleep Medicine (2018) published practice guidelines for the use of actigraphy for the evaluation of sleep disorders and circadian rhythm sleep-wake disorders (Table 7).¹⁹

Table 7. Recommendations for Actigraphy

Condition	Use	Level of Recommendation
Insomnia disorder (adult)	To estimate sleep parameters	Conditional
Insomnia disorder (pediatric)	Assessment of patients	Conditional
Circadian rhythm sleep-wake disorder (adult)	Assessment of patients	Conditional
Circadian rhythm sleep-wake disorder (pediatric)	Assessment of patients	Conditional
Suspected sleep-disordered breathing (adult)	To estimate total sleep time during recording, integrated with home sleep apnea test devices and in the absence of alternative objective measurements of total sleep time	Conditional
Suspected central disorders of hypersomnolence (adult and pediatric)	To monitor total sleep time prior to testing with the Multiple Sleep Latency Test	Conditional
Suspected insufficient sleep syndrome (adult)	To estimate total sleep time	Conditional
Periodic limb movement disorder (adult and pediatric)	Recommendation to not use actigraphy in place of electromyography for diagnosis	Strong

Level of Recommendation: “Strong” recommendation is one that clinicians should follow under most circumstances. “Conditional” recommendation reflects a lower degree of certainty regarding the outcome and appropriateness of the patient-care strategy for all patients.

U.S. Preventive Services Task Force Recommendations
Not applicable

Ongoing and Unpublished Clinical Trials
A search of ClinicalTrials.gov in April 2022 did not identify any ongoing or unpublished trials that would likely influence this review.

References 

1. Ford ES, Cunningham TJ, Giles WH, et al. Trends in insomnia and excessive daytime sleepiness among U.S. adults from 2002 to 2012. Sleep Med. Mar 2015; 16(3): 372-8. PMID 25747141
2. Paquet J, Kawinska A, Carrier J. Wake detection capacity of actigraphy during sleep. Sleep. Oct 2007; 30(10): 1362-9. PMID 17969470
3. Meltzer LJ, Wong P, Biggs SN, et al. Validation of Actigraphy in Middle Childhood. Sleep. Jun 01 2016; 39(6): 1219-24. PMID 27091520
4. Yavuz-Kodat E, Reynaud E, Geoffray MM, et al. Validity of Actigraphy Compared to Polysomnography for Sleep Assessment in Children With Autism Spectrum Disorder. Front Psychiatry. 2019; 10: 551. PMID 31428003
5. O'Driscoll DM, Foster AM, Davey MJ, et al. Can actigraphy measure sleep fragmentation in children?. Arch Dis Child. Dec 2010; 95(12): 1031-3. PMID 19850594
6. Hyde M, O'Driscoll DM, Binette S, et al. Validation of actigraphy for determining sleep and wake in children with sleep disordered breathing. J Sleep Res. Jun 2007; 16(2): 213-6. PMID 17542951
7. Belanger ME, Bernier A, Paquet J, et al. Validating actigraphy as a measure of sleep for preschool children. J Clin Sleep Med. Jul 15 2013; 9(7): 701-6. PMID 23853565
8. Insana SP, Gozal D, Montgomery-Downs HE. Invalidity of one actigraphy brand for identifying sleep and wake among infants. Sleep Med. Feb 2010; 11(2): 191-6. PMID 20083430
9. Spruyt K, Gozal D, Dayyat E, et al. Sleep assessments in healthy school-aged children using actigraphy: concordance with polysomnography. J Sleep Res. Mar 2011; 20(1 Pt 2): 223-32. PMID 20629939
10. Werner H, Molinari L, Guyer C, et al. Agreement rates between actigraphy, diary, and questionnaire for children's sleep patterns. Arch Pediatr Adolesc Med. Apr 2008; 162(4): 350-8. PMID 18391144
11. Short MA, Gradisar M, Lack LC, et al. The discrepancy between actigraphic and sleep diary measures of sleep in adolescents. Sleep Med. Apr 2012; 13(4): 378-84. PMID 22437142
12. Louter M, Arends JB, Bloem BR, et al. Actigraphy as a diagnostic aid for REM sleep behavior disorder in Parkinson's disease. BMC Neurol. Apr 06 2014; 14: 76. PMID 24708629
13. Marino M, Li Y, Rueschman MN, et al. Measuring sleep: accuracy, sensitivity, and specificity of wrist actigraphy compared to polysomnography. Sleep. Nov 01 2013; 36(11): 1747-55. PMID 24179309
14. Taibi DM, Landis CA, Vitiello MV. Concordance of polysomnographic and actigraphic measurement of sleep and wake in older women with insomnia. J Clin Sleep Med. Mar 15 2013; 9(3): 217-25. PMID 23493815
15. Levenson JC, Troxel WM, Begley A, et al. A quantitative approach to distinguishing older adults with insomnia from good sleeper controls. J Clin Sleep Med. Feb 01 2013; 9(2): 125-31. PMID 23372464
16. Kaplan KA, Talbot LS, Gruber J, et al. Evaluating sleep in bipolar disorder: comparison between actigraphy, polysomnography, and sleep diary. Bipolar Disord. Dec 2012; 14(8): 870-9. PMID 23167935
17. Dick R, Penzel T, Fietze I, et al. AASM standards of practice compliant validation of actigraphic sleep analysis from SOMNOwatch versus polysomnographic sleep diagnostics shows high conformity also among subjects with sleep disordered breathing. Physiol Meas. Dec 2010; 31(12): 1623-33. PMID 21071830
18. Sivertsen B, Omvik S, Havik OE, et al. A comparison of actigraphy and polysomnography in older adults treated for chronic primary insomnia. Sleep. Oct 2006; 29(10): 1353-8. PMID 17068990
19. Smith MT, McCrae CS, Cheung J, et al. Use of Actigraphy for the Evaluation of Sleep Disorders and Circadian Rhythm Sleep-Wake Disorders: An American Academy of Sleep Medicine Clinical Practice Guideline. J Clin Sleep Med. Jul 15 2018; 14(7): 1231-1237. PMID 29991437

Coding Section

Codes	Number	Description
CPT	95803	Actigraphy testing, recording, analysis, interpretation and report (minimum of 72 hours to 14 consecutive days of recording)
ICD-10-CM (effective 10/01/15)
	F51.01-F51.9	Sleep disorders not due to a substance or known physiological condition code range
	G25.81	Restless legs syndrome
	G47.00-G47.9	Sleep disorders code range
ICD-20-PCS (effective 10/01/15)		ICD-10-PCS codes are only for use on inpatient services. There is no specific ICD-10-PCS code for this procedure.
	4A1ZXQZ	Measuring & monitoring, physiological systems, monitoring, external, sleep
Type of Service	Medicine
Place of Service	Outpatient/Inpatent

Procedure and diagnosis codes on Medical Policy documents are included only as a general reference tool for each policy. They may not be all-inclusive.

This medical policy was developed through consideration of peer-reviewed medical literature generally recognized by the relevant medical community, U.S. FDA approval status, nationally accepted standards of medical practice and accepted standards of medical practice in this community, Blue Cross Blue Shield Association technology assessment program (TEC) and other nonaffiliated technology evaluation centers, reference to federal regulations, other plan medical policies, and accredited national guidelines.

"Current Procedural Terminology © American Medical Association. All Rights Reserved" 

History From 2024 Forward     

01/01/2024 NEW POLICY

04/17/2024 Annual review, no changes to policy intent.