Actigraphy and Behavioral State in Premature Infants Exposed to Methylxanthines Presented By Chris Sherman.

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Presentation transcript:

Actigraphy and Behavioral State in Premature Infants Exposed to Methylxanthines Presented By Chris Sherman

Theophylline as a Treatment for Infant Sleep Apnea Common in VLBW (Very Low Birth Rate) infants Episodic (each lasting more than fifteen seconds) Symptoms include: Color/tonal change, loud breathing, limp musculature, heartrate <90bpm Premature Infant Sleep ApneaTreatment Standard U.S. treatment: Caffeine (P.O.) or Theophylline (I.V. or P.O.) Effectively bind more O 2 while decreasing C0 2 levels; leads to improved respiratory functioning Both bronchodilators produce autonomic side effects including tachycardia

Hypothesized effects of Methylxanthines on Sleep State Regulation Adenosine Sleep Onset Increased Adenosine build-up promotes sleep circadian cycling; binding of Adenosine promotes sleep Theophylline Result: Decreased Adenosine binding, increased Methylxanthine binding, decreased wakefulness Methylxanthines bind to the Adenosine receptor sites, blocking out Adenosine

General Procedure Control Group: N= 11 Theophylline Group: N=14 Caffeine Group N=14 Each infant was tested in the NICU of EMCC while in their home incubators Actigraphy: Piezo-electric sensors were placed under clothing along infant’s spine. These recordings were performed in-sync with video equipment recording at 4 readings/frames per second Data analyzed for overall motility during sleep; wake/sleep Waking periods over 1.5 min in length qualified as a “waking state”

Results/Discussion Note: A maturational hypothesis was offered in the event results were caused by a difference in PCA (all subjects were between weeks PCA) Prior exposure to Methylxanthines was substantially longer in the Caffeine group Actigraphy results showed that Methylxanthine exposure predicted an increase in wakefulness, suggesting an altered temporal organization of motor activity Exposure to Methylxanthines in a developing premature infant may negatively impact the sleep and arousal systems; this is associated with a greater risk of SIDS

Note: All of the findings/data presented in this slideshow originated from the unpublished work (as of January 2006) of the University of Maine’s Developmental Neuroscience Lab. The presenter had no involvement with the original study. Note: All of the findings/data presented in this slideshow originated from the unpublished work (as of January 2006) of the University of Maine’s Developmental Neuroscience Lab. The presenter had no involvement with the original study.