Efficacy and Safety of Budesonide Inhalation Suspension(Pulmicort Respules) in Young Children With Inhaled Steroid-Dependent,Persistent Asthma

PEDIATRICS ◽  
1999 ◽  
Vol 104 (2) ◽  
pp. 386-387
Author(s):  
M. I. Sachs
1998 ◽  
Vol 102 (5) ◽  
pp. 789-796 ◽  
Author(s):  
Gail Shapiro ◽  
Louis Mendelson ◽  
Michael J. Kraemer ◽  
Mario Cruz-Rivera ◽  
Karen Walton-Bowen ◽  
...  

2005 ◽  
Vol 99 (11) ◽  
pp. 1393-1402 ◽  
Author(s):  
Karin C. Lødrup Carlsen ◽  
Steve Stick ◽  
Wolfgang Kamin ◽  
Ieva Cirule ◽  
Sara Hughes ◽  
...  

PEDIATRICS ◽  
2002 ◽  
Vol 109 (Supplement_E1) ◽  
pp. 373-380
Author(s):  
David B. Allen

Although inhaled corticosteroids (ICS) have emerged as the preventive treatment of choice for persistent asthma, few studies have been conducted in infants and very young children that assess the benefits and risks of ICS therapy, particularly with regard to growth. Oral glucocorticoids inhibit growth at multiple levels by blunting pulsatile growth hormone (GH) secretion, decreasing insulin-like growth factor-1 bioactivity, and directly inhibiting new collagen synthesis. Normal childhood growth can be divided conceptually into 3 phases according to primary growth-supporting factors: nutrition-dependent growth of infancy, GH-dependent childhood growth, and sex steroid/GH stimulation of pubertal growth. Susceptibility to glucocorticoid-induced growth suppression appears to increase during periods of transition from one phase to another, particularly in the immediate prepubertal years. Studies using ICS at varying dosages demonstrate the possibility of short-term growth suppression, but long-term studies suggest a negligible effect, if any, on final adult height or bone mineral density. Although certain speculations regarding the safety of ICS use in infants and very young children can be made based on these data, age-specific studies are needed to account for effects of differences in oral versus airway deposition and growth axis resiliency, which may occur in these patients.


2002 ◽  
Vol 77 (5) ◽  
pp. 437-445 ◽  
Author(s):  
ELI O. MELTZER ◽  
RICHARD F. LOCKEY ◽  
BRUCE F. FRIEDMAN ◽  
CHRIS KALBERG ◽  
STACEY GOODE-SELLERSO ◽  
...  

Respirology ◽  
2009 ◽  
Vol 14 (8) ◽  
pp. 1156-1165 ◽  
Author(s):  
Ken OHTA ◽  
Terumasa MIYAMOTO ◽  
Taro AMAGASAKI ◽  
Manabu YAMAMOTO ◽  

2021 ◽  
Vol 9 ◽  
Author(s):  
Sidi Liu ◽  
Chuying Gui ◽  
Zhenzhen Lu ◽  
Huijie Li ◽  
Zhike Fu ◽  
...  

Objectives: Rituximab (RTX), a possible alternative treatment option, is recognized as a new therapeutic hope for the treatment of steroid-dependent nephrotic syndrome (SDNS) in children. However, the efficacy and safety of RTX in the treatment of childhood SDNS are still controversial. The objective of this study was to evaluate the efficacy and safety of RTX treatment in children with SDNS.Study Design: Six randomized controlled trials (RCTs) and one retrospective comparative control study data from studies, performed before January 2021 were collected, from PubMed, Cochrane Library, Embase, and Web of Science. The studies evaluating the efficacy and safety of RTX in childhood SDNS were included.Results: Six RCTs and one retrospective comparative control study were included in our analysis. Compared with the control group, the RTX treatment group achieved a higher complete remission rate (OR = 5.21; 95% CI, 3.18–8.54; p < 0.00001), and we found significant differences between the two groups on serum albumin level (MD = 0.88; 95% CI, 0.43–1.33; p = 0.0001) and estimated glomerular filtration rate (MD = 6.43; 95% CI, 2.68–10.19; p = 0.0008). However, RTX treatment did not significantly lower serum creatinine levels nor did it significantly reduce the occurrence of proteinuria. In addition, we found no advantages with RTX on treatment safety.Conclusions: RTX has shown satisfactory characteristics in terms of efficacy and may be a promising treatment method for SDNS in children. However, the long-term effects have not been fully evaluated and should be further studied through randomized clinical trials.


Sign in / Sign up

Export Citation Format

Share Document