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10.1007/s40268-016-0152-x http://scihub22266oqcxt.onion/10.1007/s40268-016-0152-x C5318320!5318320!27838901     free     free     free Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 253.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 253.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 253.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 253.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 253.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Drugs+R+D 2017 ; 17 (1): 29-51 Nephropedia Template TP {{tp|p=27838901|t=2017. Efficacy of Immunobiologic and Small Molecule Inhibitor Drugs for Psoriasis: A Systematic Review and Meta-Analysis of Randomized Clinical Trials |pdf=|usr=}}{{27838901}} gab.com Text Efficacy of Immunobiologic and Small Molecule Inhibitor Drugs for Psoriasis: A Systematic Review and Meta-Analysis of Randomized Clinical Trials JO: Drugs R D http://www.kidney.de/pget.php?&tw=1&pmid=27838901 #FOAvip Background: Psoriasis is an immune-mediated inflammatory disease for which treatment has evolved over the past few years due to the introduction of immunobiologic and small molecule inhibitor medications. A better understanding of the comparative efficacies of drugs may help doctors to choose the most appropriate treatment for patients. Objective: The aim of this study was to conduct a systematic review and meta-analysis to assess the efficacy of immunobiologic and small molecule inhibitor drugs for patients with moderate to severe psoriasis. Data Sources: The EMBASE, PUBMED, LILACS, Web of Science and ClinicalTrials.org databases were searched for trials published to 21 July 2016. Study Selection: Only randomized, double-blind, placebo-controlled clinical trials that evaluated the efficacy of immunobiologics or small molecule inhibitors for moderate to severe plaque-type psoriasis were selected by two independent authors. No restrictions were used. Data Extraction and Synthesis: Two authors independently extracted the data and a random-effects model meta-analysis was performed. Main Outcomes and Measures: The Psoriasis Area and Severity Index (PASI) 75 was considered the primary outcome, measured at the primary endpoint of each study. Results: Thirty-eight studies were included in our analysis. The overall pooled effect favored biologics and small molecule inhibitors over placebo (risk difference [RD] 0.59, 95% confidence interval [CI] 0.58?0.60). Ixekizumab at a dose of 160 mg on week 0 and then every 2 weeks (RD 0.84, 95% CI 0.81?0.88), brodalumab 210 mg (RD 0.79, 95% CI 0.76?0.82), infliximab 5 mg/kg (RD 0.76, 95% CI 0.73?0.79), and secukinumab 300 mg (RD 0.76, 95% CI 0.71?0.81) showed a greater chance of response (PASI 75) when compared with placebo. Limitations: The methodology of a traditional meta-analysis does not allow for drugs to be ranked. Included studies used short-term endpoints (10?16 weeks) to evaluate the primary outcome, therefore long-term efficacy could not be determined. Conclusions and Relevance: The anti-IL-17 drugs brodalumab, ixekizumab and secukinumab showed an equal or greater chance of helping patients achieve a 75% improvement on PASI compared with other reviewed drugs. Electronic supplementary material: The online version of this article (doi:10.1007/s40268-016-0152-x) contains supplementary material, which is available to authorized users. Twit Text FOAVip Efficacy of Immunobiologic and Small Molecule Inhibitor Drugs for Psoriasis: A Systematic Review and Meta-Analysis of Randomized Clinical Trials ????Drugs R D http://www.kidney.de/pget.php?&tw=1&pmid=27838901 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27838901 #FOAvip English Wikipedia <ref>{{Cite pmid|27838901}}</ref> Efficacy of Immunobiologic and Small Molecule Inhibitor Drugs for Psoriasis: A Systematic Review and Meta-Analysis of Randomized Clinical Trials #MMPMID27838901 de Carvalho AVE; Duquia RP; Horta BL; Bonamigo RR Drugs R D 2017[Mar]; 17 (1): 29-51 PMID27838901show ga Background: Psoriasis is an immune-mediated inflammatory disease for which treatment has evolved over the past few years due to the introduction of immunobiologic and small molecule inhibitor medications. A better understanding of the comparative efficacies of drugs may help doctors to choose the most appropriate treatment for patients. Objective: The aim of this study was to conduct a systematic review and meta-analysis to assess the efficacy of immunobiologic and small molecule inhibitor drugs for patients with moderate to severe psoriasis. Data Sources: The EMBASE, PUBMED, LILACS, Web of Science and ClinicalTrials.org databases were searched for trials published to 21 July 2016. Study Selection: Only randomized, double-blind, placebo-controlled clinical trials that evaluated the efficacy of immunobiologics or small molecule inhibitors for moderate to severe plaque-type psoriasis were selected by two independent authors. No restrictions were used. Data Extraction and Synthesis: Two authors independently extracted the data and a random-effects model meta-analysis was performed. Main Outcomes and Measures: The Psoriasis Area and Severity Index (PASI) 75 was considered the primary outcome, measured at the primary endpoint of each study. Results: Thirty-eight studies were included in our analysis. The overall pooled effect favored biologics and small molecule inhibitors over placebo (risk difference [RD] 0.59, 95% confidence interval [CI] 0.58?0.60). Ixekizumab at a dose of 160 mg on week 0 and then every 2 weeks (RD 0.84, 95% CI 0.81?0.88), brodalumab 210 mg (RD 0.79, 95% CI 0.76?0.82), infliximab 5 mg/kg (RD 0.76, 95% CI 0.73?0.79), and secukinumab 300 mg (RD 0.76, 95% CI 0.71?0.81) showed a greater chance of response (PASI 75) when compared with placebo. Limitations: The methodology of a traditional meta-analysis does not allow for drugs to be ranked. Included studies used short-term endpoints (10?16 weeks) to evaluate the primary outcome, therefore long-term efficacy could not be determined. Conclusions and Relevance: The anti-IL-17 drugs brodalumab, ixekizumab and secukinumab showed an equal or greater chance of helping patients achieve a 75% improvement on PASI compared with other reviewed drugs. Electronic supplementary material: The online version of this article (doi:10.1007/s40268-016-0152-x) contains supplementary material, which is available to authorized users. äEfficacy of Immunobiologic and Small Molecule Inhibitor Drugs for Psor(epmc).pdf DeepDyve Pubget Overpricing