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Repetitive sleep starts: An important differential diagnosis of infantile spasms
Yuki Maki1, Hiroyuki Kidokoro1, Akihisa Okumura2
1Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Insights
Repetitive sleep starts (RSS) are non-epileptic movements during sleep onset. This study clarifies their characteristics to help distinguish them from epileptic spasms, preventing unnecessary treatments.
Area of Science:
- Neurology
- Sleep Medicine
- Pediatric Neurology
Background:
- Repetitive sleep starts (RSS) are characterized as nonepileptic, spasm-like movements during sleep onset.
- Detailed characteristics of RSS remain undefined, necessitating further clinical and electroencephalographic investigation.
Purpose of the Study:
- To define the detailed clinicoelectroencephalographic characteristics of repetitive sleep starts (RSS) in children.
- To differentiate RSS from epileptic spasms to guide appropriate clinical management.
Main Methods:
- A retrospective analysis of clinical information and video-electroencephalogram data was performed.
- Nine children meeting specific criteria for RSS (brief, simultaneous limb/trunk contractions, no EEG changes, occurring in sleep stages N1-N2) were included.
- Data analyzed included age at onset, frequency, duration, and interval of starts.
Main Results:
- The study identified background conditions including perinatal hypoxic-ischemic encephalopathy, West syndrome, and traumatic brain injury.
- Key parameters like age at onset, number of starts, interval, and duration of muscle activity were quantified.
- RSS resolved spontaneously in five out of nine children during a median follow-up of 33 months.
Conclusions:
- This is the largest case series to date defining RSS clinicoelectroencephalographic characteristics.
- Clinicians must be aware of RSS to differentiate it from epileptic spasms and other seizure disorders.
- Accurate differentiation can prevent unnecessary antiepileptic therapies.
Objective:
Repetitive sleep starts (RSS) are clusters of nonepileptic, spasm-like movements occurring during sleep onset. However, their characteristics have yet to be defined. We conducted a clinicoelectroencephalographic study of children with RSS to clarify their detailed characteristics.
Methods:
To differentiate starts from epileptic spasms, we recruited children with brief "crescendo-decrescendo" muscle contractions that simultaneously involved the limbs and trunk without electroencephalogram changes, and that fulfilled the following criteria: (1) repeated occurrence (five or more) and (2) manifestation during sleep stage N1-N2. A total of nine children met these criteria. Their clinical information and video-electroencephalogram data were analyzed retrospectively.
Results:
The background conditions observed at onset of RSS were perinatal hypoxic-ischemic encephalopathy (n = 4), West syndrome of unknown etiology (n = 1), and traumatic brain injury (n = 1). The age at onset of RSS, the number of starts in a given RSS cluster, the interval between starts, and the duration of surface electromyogram activity were between 3 and 46 months, 5 and 547, <1 and 60 s, and 0.3 and 5.4 s, respectively. None of the median value of these parameters differed between children with and without corticospinal tract injury. During the median follow-up period of 33 months, RSS disappeared spontaneously in five.
Conclusion:
This is the largest case series of RSS clarifying their clinicoelectroencephalographic characteristics reported to date. To avoid unnecessary antiepileptic therapies, clinicians should be aware of RSS and distinguish it from other disorders involving involuntary movements or seizures, especially epileptic spasms.
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