Efficacy of triptans for the treatment of acute migraines: a quantitative comparison based on the dose-effect and time-course characteristics

2019 ◽  
Vol 75 (10) ◽  
pp. 1369-1378
Author(s):  
Mengyuan Hou ◽  
Hongxia Liu ◽  
Yunfei Li ◽  
Ling Xu ◽  
Yingchun He ◽  
...  
2005 ◽  
Vol 141 (12) ◽  
Author(s):  
Paula E. Beattie ◽  
Robert S. Dawe ◽  
James Ferguson ◽  
Sally H. Ibbotson

1996 ◽  
Vol 83 (3) ◽  
pp. 600-605 ◽  
Author(s):  
Igor Kissin ◽  
Sandra S. Lee ◽  
G. Richard Arthur ◽  
Edwin L. Bradley

1996 ◽  
Vol 83 (3) ◽  
pp. 600-605 ◽  
Author(s):  
Igor Kissin ◽  
Sandra S. Lee ◽  
G. Richard Arthur ◽  
Edwin L. Bradley

1983 ◽  
Vol 55 (5) ◽  
pp. 1582-1592 ◽  
Author(s):  
N. M. Siafakas ◽  
M. Bonora ◽  
B. Duron ◽  
H. Gautier ◽  
J. Milic-Emili

The dose effect of pentobarbital sodium on integrated (“moving time average”) phrenic activity (EPHR), transdiaphragmatic pressure (Pdi), gastric pressure (Pga), changes in lung volume (V), and mechanical properties of the respiratory system was studied in six cats breathing room air. Increased pentobarbital dose from an initial value of 35 mg/kg ip, had no substantial effect on the relationship between EPHR and Pdi during both unoccluded and occluded inspirations, indicating that the diaphragmatic excitation-contraction coupling was not affected. Similarly, increased anesthetic dose had no effect on the relationship between EPHR and delta Pga during both occluded and unoccluded breaths, suggesting that the contribution of the diaphragm to the breathing movements did not change with increasing depth of anesthesia. Although the time course of phrenic activity showed substantial interanimal differences, the shape of the phrenic neurogram did not change substantially with increased pentobarbital dose in any of the cats studied. Increased anesthetic dose depressed, in the same proportion, the rate of rise of EPHR, Pdi, and V, but the mechanical properties of the respiratory system remained unchanged. The depression of ventilation with increased anesthetic dose was not proportional to the drop in central inspiratory activity, as quantified in terms of rate of rise of EPHR.


2019 ◽  
Vol 23 (2) ◽  
pp. 76-87 ◽  
Author(s):  
Qingqing Cheng ◽  
Jihan Huang ◽  
Ling Xu ◽  
Yunfei Li ◽  
Huafang Li ◽  
...  

Abstract Objective Model-based meta-analysis was used to describe the time-course and dose-effect relationships of antidepressants and also simultaneously investigate the impact of various factors on drug efficacy. Methods This study is a reanalysis of a published network meta-analysis. Only placebo-controlled trials were included in this study. The change rate in depression rating scale scores from baseline was used as an efficacy indicator because a continuous variable is more likely to reflect subtle differences in efficacy between drugs. Results A total 230 studies containing 64 346 patients were included in the analysis. The results showed that the number of study sites (single or multi-center) and the type of setting (inpatient or noninpatient) are important factors affecting the efficacy of antidepressants. After deducting the placebo effect, the maximum pure drug efficacy value of inpatients was 18.4% higher than that of noninpatients, and maximum pure drug efficacy value of single-center trials was 10.2% higher than that of multi-central trials. Amitriptyline showed the highest drug efficacy. The remaining 18 antidepressants were comparable or had little difference. Within the approved dose range, no significant dose-response relationship was observed. However, the time-course relationship is obvious for all antidepressants. In terms of safety, with the exception of amitriptyline, the dropout rate due to adverse events of other drugs was not more than 10% higher than that of the placebo group. Conclusion The number of study sites and the type of setting are significant impact factors for the efficacy of antidepressants. Except for amitriptyline, the other 18 antidepressants have little difference in efficacy and safety.


Sign in / Sign up

Export Citation Format

Share Document