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1.
Ital J Pediatr ; 48(1): 165, 2022 Sep 06.
Article in English | MEDLINE | ID: mdl-36068631

ABSTRACT

Intraosseous (IO) access offers a fast and reliable route for administration of fluids and drugs when intravenous (IV) accesses like umbilical, peripheral, or peripherally inserted central lines fail in critically ill neonates. Several medications can be successfully administered via the IO route, however only limited information is available regarding IO administration of antiviral agents.We present the case of a 2-week-old neonate, admitted to the Neonatal Intensive Care Unit (NICU) due to suspected meningitis, who received acyclovir through IO infusion after the venous access was lost and a new one could not be established. No complications were reported within 12 months of follow up.This report highlights the feasibility of IO acyclovir infusion when IV accesses fail in a critically ill neonate.


Subject(s)
Critical Illness , Infusions, Intraosseous , Acyclovir , Humans , Infant, Newborn , Tibia
2.
Arch Ital Urol Androl ; 90(2): 127-129, 2018 Jun 30.
Article in English | MEDLINE | ID: mdl-29974730

ABSTRACT

BACKGROUND: The first-line drug therapy for patients with nocturnal enuresis (NE) associated with nocturnal polyuria and normal bladder function is desmopressin (dDAVP). OBJECTIVE: To evaluate if increasing dose of oral desmopressin lyophilisate (MELT) can improve response rates to dDAVP and is useful in enuretic children. MATERIALS AND METHODS: We enrolled a total of 260 children all diagnosed with NE. Enuretic children were treated with increasing MELT at a dose of 120, 180 and 240 mcg a day. RESULTS: We included in our study a total of 237 children, 164 males (69.2%) and 73 females (30.8%) aged between 5 and 18 years (mean age 10.32 ± 2.52 years). Of the 237 patients enrolled in the study and treated with MELT 120 mcg, a full response was achieved in 135 (56.9%). A partial response was achieved in 21 (8.9%) patients, therefore the dose was increased up to 180 mcg, with further improving symptoms (14.3%) or full response (9.5%), and up to 240 mcg, without usefulness. CONCLUSIONS: MELT at the dose of 120 mcg resulted efficacy and safety; the increased dose up to 180 mcg resulted poorly efficacy; finally, the further increase up to 240 mcg did not improve the symptoms with the increased risk of side effects.


Subject(s)
Deamino Arginine Vasopressin/administration & dosage , Deamino Arginine Vasopressin/therapeutic use , Nocturnal Enuresis/drug therapy , Renal Agents/administration & dosage , Renal Agents/therapeutic use , Administration, Oral , Adolescent , Child , Child, Preschool , Deamino Arginine Vasopressin/adverse effects , Dose-Response Relationship, Drug , Female , Humans , Male , Renal Agents/adverse effects , Treatment Outcome
3.
Scand J Urol Nephrol ; 43(5): 369-72, 2009.
Article in English | MEDLINE | ID: mdl-19921981

ABSTRACT

OBJECTIVE: This study compares the effects of daily cranberry juice to those of Lactobacillus in children with recurrent urinary tract infections (UTIs). MATERIAL AND METHODS: Eighty-four girls aged between 3 and 14 years were randomized to cranberry, Lactobacillus or control in three treatment arms: G1, cranberry juice 50 ml daily (n=28); G2, 100 ml of Lactobacillus GG drink on 5 days a month (n=27); and G3, controls (n=29). The study lasted for 6 months. RESULTS: Only four subjects withdrew: 1/28 (3.5%) from G1, 1/27 (3.7%) from G2 and 2/29 (6.8%) from G3, because of poor compliance to the established protocol. There were 34 episodes of UTIs in this cohort: 5/27 (18.5%) in G1, 11/26 (42.3%) in G2 and 18/27 (48.1%) in the G3, with at least one episode of infection (p<0.05). CONCLUSION: These data suggest that daily consumption of concentrated cranberry juice can significantly prevent the recurrence of symptomatic UTIs in children.


Subject(s)
Beverages , Fruit , Plant Preparations/therapeutic use , Urinary Tract Infections/prevention & control , Vaccinium macrocarpon , Adolescent , Bacteria/isolation & purification , Child, Preschool , Colony Count, Microbial , Female , Follow-Up Studies , Humans , Retrospective Studies , Secondary Prevention , Treatment Outcome , Urinary Tract Infections/microbiology
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