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1.
Curr Cardiol Rep ; 23(9): 128, 2021 07 28.
Article in English | MEDLINE | ID: mdl-34319478

ABSTRACT

PURPOSE OF THE REVIEW: The purpose of the review is to analyze the pathogenetic mechanisms that underlie acute pericarditis, with attention to autoimmune and autoinflammatory pericarditis, and, in addition, to review the available therapeutic armamentarium. RECENT FINDINGS: Several studies have been published on the use of anti-IL-1 drugs in recurrent pericarditis, including anakinra and rilonacept. The latest, the RHAPSODY study, based on the use of rilonacept in recurrent pericarditis, has recently reached phase 3 with promising results in terms of efficacy and safety. Alterations in the function of the inflammasome and the consequent overproduction of IL-1 play a pivotal role in the genesis of autoinflammatory pericarditis. Recent studies added evidence to the importance of anti-IL-1 drugs in the treatment of recurrent pericarditis with raised C-reactive protein. In the era of tailored medicine, anti-IL-1 agents may be very useful in the subset of patients with recurrent pericarditis and a clear inflammatory phenotype.


Subject(s)
Pericarditis , Humans , Interleukin 1 Receptor Antagonist Protein/therapeutic use , Pericarditis/drug therapy , Recurrence
2.
Horm Res Paediatr ; 88(3-4): 281-284, 2017.
Article in English | MEDLINE | ID: mdl-28898870

ABSTRACT

BACKGROUND/AIMS: Vitamin D deficiency is common in children with neurodisabilities. Oral vitamin D3 may not be absorbed appropriately due to dysphagia and tube feeding. The aim of this study was to compare efficacy of vitamin D3 buccal spray with that of oral drops. METHODS: Twenty-four children with neurodisabilities (5-17 years) and vitamin D deficiency (25(OH)D ≤20 ng/mL) were randomized to receive vitamin D3 buccal spray 800 IU/daily (n = 12) or oral drops 750 IU/daily (n = 12) for 3 months during winter. RESULTS: Both groups had a significant increase in 25(OH)D (z = 150; p < 0.0001). The differences between baseline and final parathyroid hormone measurements did not reach significance in both groups. Markers of bone formation and resorption did not change significantly in both groups. The satisfaction with the formulation was significantly higher in the patients using spray. CONCLUSION: Vitamin D3 supplementation with buccal spray and oral drops are equally effective in short-term treatment of vitamin D deficiency in children with neurodisabilities. Buccal spray may be more acceptable by the patients.


Subject(s)
Cerebral Palsy/complications , Cholecalciferol/therapeutic use , Epilepsy/complications , Vitamin D Deficiency/drug therapy , Adolescent , Child , Child, Preschool , Cholecalciferol/administration & dosage , Dietary Supplements , Drug Delivery Systems , Female , Humans , Male , Treatment Outcome , Vitamin D Deficiency/complications
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