Perinatal Sleep-Wake Cycles

Payne, G.S.; Bach, L.M.N.

doi:10.1159/000239965

Cited by 8 publications

(2 citation statements)

References 6 publications

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“…Up to 74% of all IM cases are present at birth; 89% of IM cases are diagnosed within the first 2 years of life. Rare cases of IM in older children and adults have been reported 8 . IM lesions are located in the skin, subcutaneous tissue, or muscles and include solitary (50%–74% of all cases) and multicentric manifestations 7,9,10 .…”

Section: Introductionmentioning

confidence: 99%

Infantile myofibromatosis: Excellent prognosis but also rare fatal progressive disease. Treatment results of five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry

Sparber‐Sauer

Vokuhl²,

Seitz³

et al. 2021

Pediatric Blood & Cancer

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Background Infantile myofibromatosis (IM) is a rare benign soft tissue tumor and often a self‐limiting disease but rarely includes life‐threatening complications. Little is known about optimal treatment of primary localized (LD) and multifocal disease (MFD). Methods Treatment and outcome of 95 children with IM registered within five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry (1981–2016) were evaluated. Results LD was diagnosed in 71 patients at a median age of 0.4 years (range 0.0–17.7). MFD was present in 24 patients. The mainstay of treatment was watch‐and‐wait strategy (w&w) after initial biopsy or resection. Low‐dose chemotherapy (CHT) was administered to 16/71 (23%) patients with LD and eight of 24 (33%) patients with MFD, imatinib was added in two. A delayed resection was possible in eight of 71 (11%) and five of 24 (21%) patients with LD and MFD, respectively. Overall, patients were alive in complete remission (n = 77) and partial remission (n = 10) at a median follow‐up time of 3.4 years after diagnosis (range 0.01–19.4); no data available (n = 5). Three patients died of progressive disease (PD) despite CHT. Gender, tumor size, and location correlated with a favorable event‐free survival (EFS) in patients with LD. The 5‐year EFS and overall survival of patients with LD were 73% (±12, confidence interval [CI] 95%) and 95% (±6, CI 95%), respectively; for MFD 51% (±22, CI 95%) and 95% (±10, CI 95%). Conclusion Prognosis is excellent in patients with LD and MFD. Targeted treatment needs to be evaluated for rare fatal PD.

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Section: Introductionmentioning

confidence: 99%

Infantile myofibromatosis: Excellent prognosis but also rare fatal progressive disease. Treatment results of five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry

Sparber‐Sauer

Vokuhl²,

Seitz³

et al. 2021

Pediatric Blood & Cancer

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“…Eye movements in relation to stage of sleep have been of interest since ASERINSKY and KLEITMAN (1953KLEITMAN ( , 1955 first reported the association between rapid eye movements and a characteristic cyclic variation in the EEG pattern during sleep in adults, and the same general pattern of cycling in infants (1955). Considerable research from many laboratories has served to define the characteristics of the sleep cycle of normal newborns, and the development of these sleep patterns from early prematurity to maturity (DREYFUS-BRISAC, 1962, 1964MONOD and DREYFUS-BRISAC, 1965;MONOD and PAJOT, 1965;PARMELEE et al, 1964PARMELEE et al, , 1967PARMELEE et al, a, 1967b; PAYNE and BACH, 1965;PRECHTL, 1968PRECHTL, , 1969PRECHTL et al, 1968PRECHTL et al, , 1969ROFFWARG, MUZIO andDEMENT, 1964, 1966;STERN et al, 1969;DREYFUS-BRISAC, MONOD, PAR-MELEE, PRECHTL and SCHULTE, 1970). Further, the presence of abnormal sleep patterns has been identified with a variety of disorders of infancy and early childhood, including head trauma (LENARD and PENNIGSTORF, 1970), hypoxia and other hazards of the neonatal period (DREYFUS-BRISAC, 1964;DREYFUS-BRISAC and MONOD, 1970;MONOD, ELIET-FLESCHER and DREYFUS-BRISAC, 1967;PRECHTL, WEINMANN and AKIYAMA, 1969); maternal diabetes (SCHULTE et al, 1969) hypothyroidism (SCHULTZ et al, 1968); mater-nal heroin addiction (SCHULMAN, 1969) and mental retardation (FEINBERG, 1968; PETRE-QUADENS, HARDY and DE LEE, 1971 ; ORNITZ et al, 1969ORNITZ et al, , 1971.…”

Section: Introductionmentioning

confidence: 99%

Eye Movements in Infants Using DC Recording

Schulman¹

1973

Neuropediatrics

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Ontogenesis of sleep in human prematures after 32 weeks of conceptional age

Dreyfus-Brisac

1970

Developmental Psychobiology

209

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Unite' de rech erches b io logiq u es n do-na tales (INSERM)Maternite ' Port-Royal, C The ontogenesis of sleep was studied in prematures from 32 t o 41 weeks of gestational age The characteristics of the EEG, the patterns and rate of respiration, the cardiac rate, body motility comprised of localized and diffuse movements, localized and diffuse jerks, clonic movements and electromyographic activity of the chin, as well as periods of total quietness were observed and correlated with the progressive organization of behavior in these infants. The data obtained at each gestational age, i.e., at 32-34 weeks, 35-37 weeks, and 38-41 weeks, were compared to those obtained in full-term newborns. The relationships between the different events and the features of the EEG and of the respiratory patterns were ascertained and compared to similar data obtained in the full-term newborn. This comparison shows that the premature at 40 weeks of gestational age has not attained a level of organization as high as that of the full-term newborn. An hypothesis suggesting a possible mechanism of this discrepancy is presented.premature infant ontogenesis sleep cycle polygraphic study

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Perinatal Sleep-Wake Cycles

Cited by 8 publications

References 6 publications

Infantile myofibromatosis: Excellent prognosis but also rare fatal progressive disease. Treatment results of five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry

Infantile myofibromatosis: Excellent prognosis but also rare fatal progressive disease. Treatment results of five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry

Eye Movements in Infants Using DC Recording

Ontogenesis of sleep in human prematures after 32 weeks of conceptional age

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