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Published on: December 6, 2016
Pediatric hypnic headache: a systematic review
Alessandro Ferretti1, Margherita Velardi2, Claudia Fanfoni1
1Pediatrics Unit, NESMOS Department, Faculty of Medicine and Psychology, Sapienza University, S. Andrea Hospital, Rome, Italy.
Insights
Hypnic headache (HH) is rare in children, presenting differently than in adults. This review highlights distinct pediatric features and suggests melatonin therapy may help manage this sleep-related headache.
Area of Science:
- Neurology
- Pediatrics
- Sleep Medicine
Background:
- Hypnic headache (HH) is a rare primary headache disorder, predominantly affecting adults, with poorly understood pediatric mechanisms.
- This systematic review focuses on characterizing the clinical presentation of pediatric HH and comparing it to adult cases.
Approach:
- A comprehensive systematic search identified and analyzed published case reports of HH in individuals under 18.
- Data extraction and analysis followed a standardized protocol across major medical databases from 1988 to April 2023.
Key Points:
- Seven pediatric HH cases revealed a mean age of onset at 10 years, with diagnostic delays averaging over 15 months.
- Pediatric HH features throbbing pain, lower attack frequency, and shorter duration compared to adults' dull/pressure pain.
- The International Classification of Headache Disorders, 3rd edition (ICHD-3) criteria demonstrated increased diagnostic sensitivity in children.
Conclusions:
- Pediatric HH exhibits unique clinical characteristics distinct from adult presentations.
- Further research and specific diagnostic criteria for pediatric HH are essential for improved diagnosis and management.
- Melatonin prophylactic therapy is a potential treatment option for children diagnosed with hypnic headache.
Introduction:
Hypnic headache (HH) is a primary headache, and it is considered a rare condition in children. The underlying mechanisms of HH are not yet fully understood. This systematic review aims to provide a comprehensive description of the clinical features of all published cases of pediatric HH. It will also discuss the differences in headache features between children and adults, the increased diagnostic sensitivity of the new diagnostic criteria (ICHD-3), potential pathophysiological hypotheses explaining the higher incidence in adults, differential diagnoses, and therapeutic options for children.
Methods:
A systematic search was conducted to identify and analyze articles reporting cases of HH in patients under the age of 18. The search was performed in major medical databases including Cochrane Library, EBSCO, Embase, Medline, PubMed, Science Direct, Scopus, and Web of Science. The search covered the period from 1988 to April 2023. Relevant studies were screened for eligibility, and data extraction was performed using a standardized approach.
Results:
Seven children with HH were included in the analysis. The mean age of onset for headache attacks was 10 ± 4.3 years (range 3-15 years). The average time from the start of headaches to diagnosis was 15.8 ± 25.0 months (range 1-60 months). Headache features in children differed from those observed in adult HH patients. Children experienced throbbing/pulsating pain, while adults reported dull/pressure-like pain. Children also had lower frequency and shorter duration of attacks compared to adults. The use of ICHD-3 criteria appeared to be more sensitive and inclusive for diagnosing HH in children compared to the previous ICHD-2 criteria. The association of headache attacks with sleep suggests that HH may be a primary disorder with a chronobiological origin. Hypothalamic dysfunction and melatonin dysregulation, which are more prevalent in older individuals, could potentially explain the higher incidence of HH in adults. Other primary headaches and secondary causes should be ruled out. Melatonin prophylactic therapy may be considered for pediatric patients.
Discussion:
Further evaluation of the clinical features of HH in children is needed. The development of specific diagnostic criteria for pediatric cases could improve diagnostic rates and enhance the management of children with HH.
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