J 2007

Radiographic progression of rheumatoid arthritis in patients from the Czech National Registry receiving infiiximab treatment

PAVELKA, K., J. GATTEROVA, D. TEGZOVA, K. JAROSOVA, J.T. STUDYNKOVA et. al.

Basic information

Original name

Radiographic progression of rheumatoid arthritis in patients from the Czech National Registry receiving infiiximab treatment

Name in Czech

Radiographic progression of rheumatoid arthritis in patients from the Czech National Registry receiving infiiximab treatment

Authors

PAVELKA, K. (203 Czech Republic), J. GATTEROVA (203 Czech Republic), D. TEGZOVA (203 Czech Republic), K. JAROSOVA (203 Czech Republic), J.T. STUDYNKOVA (203 Czech Republic), Adam SVOBODNÍK (203 Czech Republic), J. SVIHALEK (203 Czech Republic), Ladislav DUŠEK (203 Czech Republic, guarantor) and J. VENCOVSKY (203 Czech Republic)

Edition

Clinical and Experimental Rheumatology, 2007, 0392-856X

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30000 3. Medical and Health Sciences

Country of publisher

Italy

Confidentiality degree

není předmětem státního či obchodního tajemství

Impact factor

Impact factor: 2.270

RIV identification code

RIV/00216224:14110/07:00033158

Organization unit

Faculty of Medicine

UT WoS

000249556400006

Keywords in English

rheumatoid arthritis; biological treatment; radiographic progression
Změněno: 1/4/2010 08:42, prof. RNDr. Ladislav Dušek, Ph.D.

Abstract

V originále

Objective To evaluate the clinical status and radiographic progression in patients with rheamzatoid arthritis (RA) being followed by the Czech National Registry of biological treatments. Methods Patients who failed at least two disease-modifying antirheumatic drugs and had high disease activity (DAS28 > 5.1) were treated with infliximab. Radiographic progression was measured with a modified version of the Sharp score (TSS) after 54 weeks of treatment. Results Ninety-nine patients with an average disease duration of 13.7 years were enrolled. The DAS28 dropped from 6.66 to 4.07 (p < 0.001). Before treatment the mean TSS was 90.1 and the mean estimated yearly disease progression was 8.56. After 54 weeks of infliximab, radiographic progression was 4.15 times slower than the estimated rate before treatment and 63 patients did not show any radiographic progression at all. In the remaining 36 patients, the progression rate slowed to 3.8 +/- 0.9 from the estimated TSS of 10.9 +/- 6.9 before the initiation of treatment (p = 0.011). Conclusion Data derived from the Czech National Registry, which reflect general clinical practice, show a significant retardation of radiographic progression in patients treated with anti-TNF and the magnitude of the improvement seen is similar to results from clinical trials

In Czech

Objective To evaluate the clinical status and radiographic progression in patients with rheamzatoid arthritis (RA) being followed by the Czech National Registry of biological treatments. Methods Patients who failed at least two disease-modifying antirheumatic drugs and had high disease activity (DAS28 > 5.1) were treated with infliximab. Radiographic progression was measured with a modified version of the Sharp score (TSS) after 54 weeks of treatment. Results Ninety-nine patients with an average disease duration of 13.7 years were enrolled. The DAS28 dropped from 6.66 to 4.07 (p < 0.001). Before treatment the mean TSS was 90.1 and the mean estimated yearly disease progression was 8.56. After 54 weeks of infliximab, radiographic progression was 4.15 times slower than the estimated rate before treatment and 63 patients did not show any radiographic progression at all. In the remaining 36 patients, the progression rate slowed to 3.8 +/- 0.9 from the estimated TSS of 10.9 +/- 6.9 before the initiation of treatment (p = 0.011). Conclusion Data derived from the Czech National Registry, which reflect general clinical practice, show a significant retardation of radiographic progression in patients treated with anti-TNF and the magnitude of the improvement seen is similar to results from clinical trials

Links

1M0571, research and development project
Name: Bioindikace a revitalizace toxických antropogeních substrátů a vodních zdrojů: využití sinic, řas, půdních bakterií a symbiotických hub