Nebulized flunisolide in infants and young children with asthma: A pilot study

1996 ◽  
Vol 21 (5) ◽  
pp. 310-315 ◽  
Author(s):  
Fernando M. de Benedictis ◽  
Laura C. Martinati ◽  
Lucia F. Solinas ◽  
Gianluca Tuteri ◽  
Attilio L. Boner
Author(s):  
Samuel Crompton ◽  
Fabrizio Messina ◽  
Gillian Klafkowski ◽  
Christine Hall ◽  
Amaka C. Offiah

Abstract Background Recent studies have analysed birth-related clavicular fractures to propose time frames for healing that could be applied to dating of all fractures in cases of suspected child abuse. Objective To assess differences in healing rates between femoral fractures and birth-related clavicular fractures in infants and young children. Materials and methods A retrospective 5-year pilot study of femoral fractures in children younger than 3 years of age was performed. Anonymised radiographs were independently scored by two radiologists for stages of fracture healing. In cases of reader disagreement, radiographs were independently scored by a third radiologist. Results In total, 74 radiographs (30 children) met the inclusion criteria. Fracture healing evolved over time with subperiosteal new bone formation (SPNBF) appearing first, followed by callus then remodelling. A power calculation for a single proportion, with a level of confidence of 95% and a margin of error of 5%, showed that in a definitive study, 359 radiographs would be required. Conclusion Although the overall pattern of healing is similar, in this small pilot study, the earliest times for SPNBF and callus formation in femoral fractures appeared to lag behind healing of birth-related clavicular fractures. Remodelling appeared earlier than remodelling of clavicular fractures. A power calculation has determined numbers of femoral radiographs (359) required for a definitive study.


2018 ◽  
Vol 65 (4) ◽  
pp. 551-564 ◽  
Author(s):  
Audrone Muleviciene ◽  
Federica D’Amico ◽  
Silvia Turroni ◽  
Marco Candela ◽  
Augustina Jankauskiene

2019 ◽  
Vol 3 (1) ◽  
pp. e000382
Author(s):  
Sherna Marcus ◽  
Jeremy N Friedman ◽  
Ashley Lacombe-Duncan ◽  
Sanjay Mahant

ObjectivesTo describe the acceptability, safety and effectiveness of neuromuscular electrical stimulation (NMES) in infants and young children with neurological impairment (NI) who have severe dysphagia.DesignA prospective pilot study using a before and after study design.SettingThe Hospital for Sick Children, Toronto, Canada.PatientsTen infants and young children (0–24 months) with NI and severe dysphagia on videofluoroscopic swallow study (VFSS) who were referred to an occupational therapist (OT). Those with neurodegenerative conditions were excluded.InterventionNMES treatments lasting 20–45 min twice weekly for the duration of 2–4 months. The NMES was administered during feeding therapy sessions by a trained OT.Main outcome measuresImprovement in swallowing function as measured by VFSS and the need for tube feeding, adverse events and parental acceptability.ResultsSeven of 10 enrolled subjects (median age, 8.9 months) completed biweekly NMES treatments (median number of treatments per subject, 18). All of the seven (100%) subjects who completed treatment showed an improvement in swallow function on VFSS. Of the five patients who were not safe to orally feed on any consistency of liquid or puree at baseline, three established full oral feeding and two established partial oral feeding. At baseline, 5/7 children were completely fed by tube versus 0/7 at the end of treatment. No adverse events occurred other than mild skin irritation at the site of electrode placement. Five of seven caregivers felt that feeding was improved and were satisfied with the intervention.ConclusionsOur prospective pilot study of NMES in seven neurologically impaired infants and young children with severe dysphagia suggests that NMES is safe, acceptable to parents and has potential efficacy. Trials are needed to determine if any treatment benefit exists.Trial registrationClinicalTrials.gov NCT01723358.


2020 ◽  
Vol 31 (4) ◽  
pp. 698-700
Author(s):  
Valdir França de Macêdo Filho

Marcus S, Friedman JN, Lacombe Duncan A, Mahant S. Neuromuscular electrical stimulation for treatment of dysphagia in infants and young children with neurological impairment: a prospective pilot study. BMJ Paediatrics Open. 2019; 3(1): e000382.


2018 ◽  
Vol Volume 11 ◽  
pp. 233-243 ◽  
Author(s):  
Ahmed Alsuwaidi ◽  
Alia Alkalbani ◽  
Afaf Alblooshi ◽  
Junu George ◽  
Ghaya Albadi ◽  
...  

1993 ◽  
Vol 18 (1) ◽  
pp. 63-81 ◽  
Author(s):  
Sandra R. Wilson ◽  
Julia H. Mitchell ◽  
Sharon Rolnick ◽  
Lloyd Fish

2017 ◽  
Vol 23 (1) ◽  
pp. e1690 ◽  
Author(s):  
Lieselotte Corten ◽  
Jennifer Jelsma ◽  
Anri Human ◽  
Sameer Rahim ◽  
Brenda M. Morrow

PEDIATRICS ◽  
1987 ◽  
Vol 80 (6) ◽  
pp. 894-897
Author(s):  
Micha Aviram ◽  
Asher Tal ◽  
Zvi Ben-Zvi ◽  
Rafael Gorodischer

Saliva stimulation is required for measurement of drugs in saliva. Chewing on a piece of paraffin, which is the method usually used for saliva stimulation, requires cooperation of the patient and, thus, is inapplicable in infants and young children. To assess the value of determining theophylline concentrations from noninvasively obtained saliva in this age group, we studied the theophylline plasma to saliva concentration ratio in citric acid-stimulated saliva. Theophylline concentration was measured in 137 simultaneously obtained paired specimens of plasma and saliva from 68 patients 2½ months to 14 years of age treated with theophylline for asthma (dosage 20.8 ± 5.2 mg/kg/d, mean ± SD). Saliva secretion was stimulated by placing citric acid crystals on the tongue. A strong and highly significant correlation was observed between both determinations (r = .96; P < .01). The plasma to saliva ratio was 1.78 ± 0.22 (mean ± SD), with theophylline concentrations between 3.1 and 32.1 µg/mL of plasma. The ratio of estimated to actual plasma theophylline concentrations was 1.02 ± 0.12 (mean ± SD). Interindividual coefficient of variation of plasma to saliva theophylline concentrations ratios was 12.4%; mean intraindividual coefficient of variation was 5.3%. The use of citric acid for saliva stimulation is easily applicable to infants and young children. Compared with blood drawing, stimulation of saliva secretion by citric acid is painless and noninvasive, is more readily accepted to patients, is at least as clinically relevant for theophylline determination, and allows frequent measurements of drug levels for individualization of the dosage with samples taken at home. The therapeutic concentrations range of theophylline in saliva is estimated to be between 5.6 and 11.2 µg/mL (equivalent to plasma concentrations of 10 to 20 µg/mL) in our laboratory.


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