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SLEEP 2011 Abstract Supplement

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B. Clinical Sleep Science XI. Pediatrics<br />

Methods: To elicit an understanding of mother-child sleep patterns during<br />

ALL maintenance chemotherapy, a qualitative descriptive approach<br />

was chosen. This approach allows for the discovery of themes that are<br />

not identified in the literature, or may not be revealed through quantitative<br />

methods. The sample, obtained through The Children’s Hospital<br />

Denver (TCH) hematology practice included 23 dyads of mothers and<br />

children with ALL. The typical maternal participants were mid-thirties,<br />

married (76.9%), white (65%), 42% had a college education or higher,<br />

and 35% were employed. To the extent possible, patients from diverse<br />

cultural and socioeconomic backgrounds were included to provide<br />

broad perspectives. Participants shared audio recorded narratives (30-60<br />

minutes) pertaining to their sleep (e.g., quality, quantity) relative to their<br />

child’s ALL diagnosis.<br />

Results: Interviews were transcribed and independently analyzed by co-<br />

PIs and compared. Themes emerging from the data included:“ A Whole<br />

New Cancer World” and “I don’t remember what it is like to sleep.”<br />

Facets of the sleep theme included “sick at night,” “coping with exhaustion,”<br />

and “moving toward sleep.” Participants described the best and<br />

worst nights, and shared a wide variety of strategies to improve sleep.<br />

Conclusion: Even during maintenance chemotherapy, the quality and<br />

quantity of the child’s sleep had a major negative impact on maternal<br />

sleep and family sleeping arrangements. This study has implications<br />

for clinicians in assessing and implementing interventions for impaired<br />

sleep in parents, and children with ALL.<br />

Support (If Any): UC Denver Colorado Clinical Translational Science<br />

Institute (CCTSI) Pilot Award (1UL1RR014780)<br />

0881<br />

THE PREVALENCE AND PATTERNS OF <strong>SLEEP</strong> DISORDERS<br />

AND CIRCADIAN RHYTHM DISRUPTIONS IN CHILDREN<br />

WITH FETAL ALCOHOL SPECTRUMS DISORDERS (FASD)<br />

Goril S 2,3 , Shapiro CM 1,2<br />

1<br />

Psychiatry, Toronto Western Hospital, UHN, Toronto, ON, Canada,<br />

2<br />

Youthdale Child and Adolescent Sleep Centre, , Toronto, ON, Canada,<br />

3<br />

Collaborative Program in Neurosciences, University of Toronto,<br />

Toronto, ON, Canada<br />

Introduction: Sleep disorders have been poorly described in children<br />

and adolescents diagnosed with FASD. The objective of this study is<br />

to describe the sleep and circadian rhythm characteristics of children<br />

with FASD using 2 nights of overnight polysomnography, sleep questionnaires,<br />

and the Dim Light Melatonin Onset (DLMO) test. To our<br />

knowledge, no comprehensive study of this nature has been conducted.<br />

Methods: Children aged 5-18 years diagnosed with Fetal Alcohol Spectrum<br />

Disorder (FASD) were recruited from various FASD clinics to the<br />

Youthdale Child and Adolescent Sleep Centre in Toronto. After a medical<br />

consultation, each participant had 2 nights of overnight polysomnography,<br />

as well as an additional night of DLMO. Participants completed<br />

various sleep, alertness, and mood questionnaires. To date, objective<br />

sleep parameters, subjective questionnaire data were analyzed using<br />

SPSS for 9 study patients.<br />

Results: Descriptive pilot data shows the mean percentage values for<br />

stage 4 slow wave sleep (SWS) were slightly elevated compared to<br />

the normative values. The mean percentage values of REM sleep was<br />

slightly decreased. Mean percentage values of wakefulness were also increased,<br />

suggesting increased sleep fragmentation during the night. The<br />

DLMO results obtained to date in this group are all abnormal.<br />

Conclusion: Polysomnographic analysis supports disrupted sleep patterns<br />

in children with FASD including increased night awakenings, increased<br />

sleep fragmentation, and decreased REM sleep. The increased<br />

prevalence of sleep and circadian disturbances in this population suggests<br />

the need for a more proactive approach to sleep.<br />

0882<br />

POLYSOMNOGRAPHY AND ACTIGRAPHY CONCORDANCE<br />

IN JUVENILE IDIOPATHIC ARTHRITIS AND ASTHMA<br />

COMPARED TO HEALTHY CHILDREN<br />

Ward TM 1 , Lentz M 2 , Kieckhefer G 1 , Landis CA 2<br />

1<br />

Family & Child Nursing, University of Washington, Seattle, WA,<br />

USA, 2 Biobehavioral Nursing and Health Sciences, University of<br />

Washington, Seattle, WA, USA<br />

Introduction: Agreement between actigraphy and polysomnography<br />

(PSG) have been reported in healthy school-age children < 9 years old,<br />

but to our knowledge studies have not been reported in children with<br />

chronic illnesses such as arthritis or asthma. The purpose of this study<br />

was to evaluate sensitivity, specificity, and accuracy with an epoch-byepoch<br />

comparison between PSG and actigraphy, and to compare PSG<br />

derived sleep parameters to those derived from actigraphy in 9-to-11<br />

year-old children with juvenile idiopathic arthritis (JIA), asthma, and<br />

healthy children.<br />

Methods: Seventy-one children 9-11 years of age. Two consecutive<br />

nights of PSG and actigraphy were recorded and sensitivity, specificity,<br />

and accuracy were evaluated in an epoch-by-epoch comparison of PSG<br />

and actigraphy.<br />

Results: Overall, mean sensitivity and accuracy were higher than specificity<br />

but sensitivity was significantly higher for JIA on night 1, while<br />

specificity was significantly lower for JIA compared to asthma and controls<br />

for both nights at all three activity count thresholds evaluated. Total<br />

sleep time (TST), wake after sleep onset (WASO), and sleep efficiency<br />

(SE) derived from PSG were not different among the 3 groups, but TST<br />

and SE were higher and WASO was lower in JIA. Based on the Bland-<br />

Altman technique, actigraphy was more accurate in estimating TST and<br />

WASO at the medium sensitivity threshold.<br />

Conclusion: Compared to PSG, actigraphy was reasonably accurate in<br />

identifying sleep from wake in 9 to 11 year old children with JIA and<br />

asthma. However, actigraphy was less accurate in the identification of<br />

nocturnal wakefulness at all activity count thresholds tested in JIA. It<br />

is important for clinicians and researchers to understand the strengths<br />

and limitations of the various actigraphy devices, as actigraphy is not as<br />

sensitive for measuring nocturnal wakefulness in children with certain<br />

chronic illnesses.<br />

Support (If Any): National Institute of Nursing Research, T32<br />

NR00710, NR08136, NR08238, the Center for Women’s Health and<br />

Gender Research, NR04011, the National Center for Research Resources<br />

(NCRR), M01-RR-00037, the Center for Research on Management<br />

of Sleep Disturbances, NR011400, and Pulmonary Center Training<br />

grant, T72 MC 0007<br />

A301<br />

<strong>SLEEP</strong>, Volume 34, <strong>Abstract</strong> <strong>Supplement</strong>, <strong>2011</strong>

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