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1.
Eur J Pediatr ; 183(5): 2091-2099, 2024 May.
Article in English | MEDLINE | ID: mdl-38347262

ABSTRACT

Functional gastrointestinal disorders (FGIDs) are characterized by a variety of symptoms that are frequently age-dependent, chronic, or recurrent and are not explained by structural or biochemical abnormalities. There are studies in the literature reporting different results regarding the relationship between prematurity and FGIDs. The main objective of this study was to compare the frequency of FGIDs between preterm and term infants. The secondary objective was to evaluate whether there was any association between neonatal characteristics and development of FGIDs. A multicenter prospective cohort study that included preterm infants born before 37 weeks of gestation and healthy term infants was carried out. At 1, 2, 4, 6, 9, and 12 months of age, infants were assessed for the presence of FGIDs using the Rome IV criteria. In preterm infants, an additional follow-up visit was made at 12 months corrected age. 134 preterm and 104 term infants were enrolled in the study. Infantile colic, rumination syndrome, functional constipation, and infant dyschezia were more common in preterm infants. Incidence of other FGIDs (infant regurgitation, functional diarrhea and cyclic vomiting syndrome) were similar among preterm and term infants. Preterm infants who are exclusively breastfeed in the first 6 months of life have a lower incidence of infantile colic (18.8% vs 52.1%, p = 0.025). In terms of chronological age, FGIDs symptoms started later in preterm infants; this difference was statistically significant for infantile colic and regurgitation (median age 2 months vs 1 month, p < 0.001).   Conclusions: Preterm infants have a higher prevalence of FGIDs compared with term controls. Therefore, especially if they have gastrointestinal complaints, they should be screened for FGIDs. Possibly due to maturational differences, the time of occurrence of FGIDs may differ in preterm infants. Infantile colic incidence decreases with exclusive breastfeeding. What is Known: • The functional gastrointestinal disorders are a very common in infancy. • Data on preterm infants with FGIDs are currently very limited. What is New: • Preterm infants have a higher incidence of infantile colic, rumination syndrome, functional constipation and infant dyschezia when compared to term infants. • Preterm infants who are exclusively breastfed during the first 6 months of life experience a lower incidence of infantile colic.


Subject(s)
Gastrointestinal Diseases , Infant, Premature, Diseases , Infant, Premature , Humans , Prospective Studies , Gastrointestinal Diseases/epidemiology , Gastrointestinal Diseases/diagnosis , Female , Infant, Newborn , Male , Infant , Infant, Premature, Diseases/epidemiology , Infant, Premature, Diseases/diagnosis , Incidence , Neonatal Screening/methods , Follow-Up Studies
2.
J Pediatr Endocrinol Metab ; 28(11-12): 1383-5, 2015 Nov 01.
Article in English | MEDLINE | ID: mdl-26181046

ABSTRACT

Association of Kocher-Debré-Semelaigne syndrome-a myopathy of hypothyroidism in childhood characterized by muscular hypertrophy, with rhabdomyolysis is very rare. We present a case of Kocher-Debré-Semelaigne syndrome with rhabdomyolysis secondary to Hashimoto's thyroiditis. He had muscular symptoms simulating poly/dermatomyositis, massively elevated creatine kinase (CK) levels and high creatinine levels. All of the findings reversed on treatment of hypothyroidism. The response to the therapy strongly suggested that Kocher-Debré-Semelaigne (KDS) syndrome was the underlying etiology. Serum thyroid- stimulating hormone levels should be routinely determined in all patients with muscular symptoms and/or elevation of CK and creatinine, keeping KDS syndrome in mind.


Subject(s)
Congenital Hypothyroidism/complications , Creatinine/blood , Hashimoto Disease/complications , Hypertrophy/complications , Muscle, Skeletal/pathology , Muscular Diseases/complications , Rhabdomyolysis/etiology , Adolescent , Congenital Hypothyroidism/blood , Creatine Kinase/blood , Hashimoto Disease/blood , Hashimoto Disease/drug therapy , Humans , Hypertrophy/blood , Male , Muscular Diseases/blood , Rhabdomyolysis/blood , Thyroxine/therapeutic use , Treatment Outcome
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