DAS28 măsoară activitatea bolii în artrita reumatoidă
Sixty-one patients with active RA participated in a double-blind, parallel group, randomized, multicenter methodology study receiving infliximab or placebo through 14 weeks.
This is an open access article distributed under the terms of the Creative Commons Attribution License das28 crp, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
The data are owned by Merck and Co. The data were accessed by the authors within regulated and controlled databases, either that of Merck or temporarily at the imaging companies, VirtualScopics and Spire Sciences, during the period das28 crp analysis. Final results are transferred to Merck. Interested researchers would make a request to EngageZone, a website controlled by Merck data management, which facilitates distribution of clinical data to credentialed researchers.
Requests for access to the study data can be submitted through the EngageZone Web site or via email to dataaccess merck. All authors, including Merck employees, participated in interpretation of data, writing or review of the manuscript, as well as the decision to submit the manuscript for publication. Spire Sciences, Inc. Competing interests: C. Beals, R. Baumgartner, A. Cheng, D. Feng, M. Vallee, and B. Peterfy and J.
DiCarlo are employees of Spire Sciences, Inc. Ashton is an employee of VirtualScopics, employed by Merck to analyze study results; A. Balanescu, G. Mirea, A. Das28 crp, and S. Popa claim no conflicts of interest. There are no additional declarations from the authors relevant to this research relating to employment, consultancy, products in development, patents, or revenues from marketed products to declare. Requests for data access can be submitted to: dataaccess merck.
Introduction Rheumatoid arthritis RA treatment options have expanded markedly over the past decade.
However, as these therapies have become available, the acceptable duration for placebo control has also shortened, with rescue therapy typically offered within 14—16 weeks.
The need to demonstrate both symptomatic and structure-modifying efficacy in randomized placebo controlled clinical trials RCT within this short time frame, along with growing difficulties recruiting RA patients into such studies, has made the use of radiography in RCTs impractical[ 1 ].
MRI has been shown to be more sensitive than radiography for detecting joint destruction in RA, and das28 crp able to evaluate the up-stream inflammatory drivers of bone erosion and articular cartilage loss, namely osteitis and synovitis.
One of the challenges of DCE-MRI is achieving sufficient imaging speed to capture the change das28 crp T1 signal within inflamed synovium, while maintaining sufficient spatial resolution and anatomical coverage to delimit the entire synovial tissue from adjacent joint fluid accurately.
The compromise of restricting enhancement measurements to small regions of interest ROIs within synovial tissue is confounded by the spatial heterogeneity of inflammation in RA.
In this study, we overcame these challenges by devising a DCE-MRI technique suitable for multicenter clinical trials that imaged the entire wrist and MCP joints simultaneously and with sufficient speed to measure kinetic synovial enhancement parameters accurately.
The baseline characteristics and inflammatory imaging endpoints from this study were previously used to derive a whole blood gene transcript signature that predicted a subsequent reduction in Ktrans with infliximab[ 11 ].
Both imaging methods similarly discriminated das28 crp treatment from placebo on measures related to synovial inflammation, yet remained stable during placebo treatment. Appropriate MRI techniques, along with clinical measures of RA activity, should improve the characterization of drug effects on inflammation and structural damage in RA. Materials and methods This was a week, randomized, double-blind, placebo-controlled, methodology study Study Protocol PO; S1 File conducted from April 6, to March das28 crp, in 3 clinical centers in Europe.
Medical Market - Atitudinea terapeutică actuală în poliartrita reumatoidă
The study was conducted in accordance with principles of Good Clinical Practice and was approved by the appropriate institutional review boards, the Comisia Nationala de Etica pentru Studiul Clinic al Medicamentului, Bucharest Romania and Comitetul National de Etica studiu clinic al medicamentelor si metodelor noi de tratament, Chisinau, Moldova. All subjects provided written informed consent. Key elements of the clinical protocol are available in supporting information S1 File.
- Tratamentul medicamentos al articulațiilor genunchiului
- - Мне кажется маловероятным, что Танкадо использовал непроизвольный набор знаков.
- Articulații și produse osoase
- Tratamente eficiente pentru articulațiile genunchiului
- Британского флага нигде не было .
- Articulațiile pot răni din cauza unei vânătăi
Patients had no contraindications to infliximab or MRI. Study medication was prepared by an unblinded trained person using the das28 crp code and without other involvement in study procedures, assessments, or data recording. Treatment allocation was blinded to investigators, study staff, and subjects. After 14 weeks of double-blinded therapy, participants in consultation with their physician could elect 3 months of open label infliximab treatment following the labeled dosing recommendations based on their previous randomized treatment assignment.
Joint counts were performed by examiners masked to treatment assignment who did not serve as study physicians. MRI assessments MRI of the most clinically severe hand and wrist was acquired at baseline and weeks 2, costul condroitinei cu glucozamina, and 14 using a 1.
An acrylic frame[ 10 ] was used to ensure fixed, reproducible positioning of the hand and wrist joints on serial MRI examinations.
Two small tubes containing solutions of copper sulfate sufficient to das28 crp T1 values of 90ms and ms were made in a single batch and distributed to all clinical sites.
Tubes were placed alongside the index and fifth fingers to serve as standards to verify appropriate T1 weighting, which is related to Gd concentrations for DCE-MRI measurements[ 1415 ].
Small ROIs were placed manually over volumes of enhancing synovium or enhancing tissue synovitis and osteitis without knowledge of the treatment or the order in which examinations were acquired. Das28 crp identified enhancing tissue by comparison of pre- and post-GBCA images.
- Scorul DAS28 în evaluarea artritei reumatoide | ghiduri medicale | breviar medical
- DAS28, care reprezintă "scorul activității bolii", se calculează folosind o formulă care include numărul de articulații sensibile și articulațiile umflate maxim 28 de articulații.
- Это вы убили Танкадо.
- Unguente pentru articulațiile phuket
- Balsam articular din
A trained technologist removed enhancing tissue that represented blood vessels or skin, and the resulting enhancing tissue map underwent radiologist review. Care was taken to ensure that identical locations were selected for each study visit of an individual subject. The rate of GBCA synovial leakage was measured using a pharmacokinetic compartment model[ 16 ] that quantifies the exchange of contrast agent between the plasma and tissue extracellular space synovium.
The model requires a measure of the rate of GBCA input into the plasma, and is derived using an automated method[ 1517 ] from T1 signal intensity in the radial artery over time. Outputs of the model include Ktrans sec-1a rate constant that reflects the flow and permeability surface area das28 crp enhancing synovium primary endpoint and volume of enhancing tissue synovitis and osteitis.
DAS28 măsoară activitatea bolii în artrita reumatoidă
One scan-rescan assessment of Ktrans reproducibility in RA patients using this exact technique was consistent with that identified in tumors Ashton, personal communication and with published reliability using a similar approach[ 18 ]. RAMRIS8 of synovitis, osteitis and bone erosion at the wrist and MCP were determined at baseline, 2, 4 and 14 weeks by two independent radiologists blinded to visit order and treatment assignments.
Statistical methods Ktrans of wrist synovium was the primary endpoint of the study.
The mean change from baseline to a given time point was estimated and tested from this model. Statistical significance of the dichotomous endpoints was determined using Fisher's exact test comparing placebo and treatment groups. All analyses were conducted on the changes from baseline to Weeks 2, 4 and Interpretation of the p-values for each endpoint was conducted in stepwise fashion using a closed stepwise procedure with p-values interpreted starting with Week Inter-reader agreement was assessed at baseline in terms of intra-class correlation coefficient ICC.
The primary method of comparisons amongst endpoints was comparison of treatment effect size.