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DOI 10.1093/rheumatology/keaa240

Медицинская библиотека · Rheumatology (Oxford, England) · 2020

Development and initial validation of a composite disease activity score for systemic juvenile idiopathic arthritis.

Tibaldi Jessica, Pistorio Angela, Aldera Elena, Puzone Laura, El Miedany Yasser, Pal Priyankar, Giri Prabhas Prasun, De Hriday, Khubchandani Raju, Chavan Pallavi Pimpale, Vilaiyuk Soamarat, Lerkvaleekul Butsabong, Yamsuwan Jutamas, Sabui Tapas K, Datta Pragati, Pardeo Manuela, Bracaglia Claudia, Sawhney Sujata, Mittal Sumidha, Hassan Waleed A, Elderiny Ghada Farouk, Abu-Zaid Mohammed Hassan, Eissa Mervat, Sztajnbok Flavio, das Neves Sztajnbok Fernanda C, Russo Ricardo, Katsicas María Martha, Cimaz Rolando, Marrani Edoardo, Alexeeva Ekaterina, Dvoryakovskaya Tatyana M, Alsuweiti Motasem O, Alzyoud Ra'ed M, Kostik Mikhail, Chikova Irina, Minoia Francesca, Filocamo Giovanni, Farag Yomna, Lotfy Hala, Nasef Samah Ismail, Al-Mayouf Sulaiman M, Maggio Maria Cristina, Magalhaes Claudia Saad, Gallizzi Romina, Conti Giovanni, Shimizu Masaki, Civino Adele, Felici Enrico, Giancane Gabriella, Ruperto Nicolino, Consolaro Alessandro, Ravelli Angelo

СтатьяВалидационное исследованиеПеревод в очереди

Аннотация

OBJECTIVE

To develop a composite disease activity score for systemic JIA (sJIA) and to provide preliminary evidence of its validity.

METHODS

The systemic Juvenile Arthritis Disease Activity Score (sJADAS) was constructed by adding to the four items of the original JADAS a fifth item that aimed to quantify the activity of systemic features. Validation analyses were conducted on patients with definite or probable/possible sJIA enrolled at first visit or at the time of a flare, who had active systemic manifestations, which should include fever. Patients were reassessed 2 weeks to 3 months after baseline. Three versions were examined, including ESR, CRP or no acute-phase reactant.

RESULTS

A total of 163 patients were included at 30 centres in 10 countries. The sJADAS was found to be feasible and to possess face and content validity, good construct validity, satisfactory internal consistency (Cronbach's alpha 0.64-0.65), fair ability to discriminate between patients with different disease activity states and between those whose parents were satisfied or not satisfied with illness outcome (P < 0.0001 for both), and strong responsiveness to change over time (standardized response mean 2.04-2.58). Overall, these properties were found to be better than those of the original JADAS and of DAS for RA and of Puchot score for adult-onset Still's disease.

CONCLUSION

The sJADAS showed good measurement properties and is therefore a valid instrument for the assessment of disease activity in children with sJIA. The performance of the new tool should be further examined in other patient cohorts that are evaluated prospectively.

Для цитирования: Tibaldi Jessica, Pistorio Angela, Aldera Elena, Puzone Laura, El Miedany Yasser, Pal Priyankar, Giri Prabhas Prasun, De Hriday, Khubchandani Raju, Chavan Pallavi Pimpale, Vilaiyuk Soamarat, Lerkvaleekul Butsabong, Yamsuwan Jutamas, Sabui Tapas K, Datta Pragati, Pardeo Manuela, Bracaglia Claudia, Sawhney Sujata, Mittal Sumidha, Hassan Waleed A, Elderiny Ghada Farouk, Abu-Zaid Mohammed Hassan, Eissa Mervat, Sztajnbok Flavio, das Neves Sztajnbok Fernanda C, Russo Ricardo, Katsicas María Martha, Cimaz Rolando, Marrani Edoardo, Alexeeva Ekaterina, Dvoryakovskaya Tatyana M, Alsuweiti Motasem O, Alzyoud Ra'ed M, Kostik Mikhail, Chikova Irina, Minoia Francesca, Filocamo Giovanni, Farag Yomna, Lotfy Hala, Nasef Samah Ismail, Al-Mayouf Sulaiman M, Maggio Maria Cristina, Magalhaes Claudia Saad, Gallizzi Romina, Conti Giovanni, Shimizu Masaki, Civino Adele, Felici Enrico, Giancane Gabriella, Ruperto Nicolino, Consolaro Alessandro, Ravelli Angelo. Development and initial validation of a composite disease activity score for systemic juvenile idiopathic arthritis.. Rheumatology (Oxford, England). 2020. DOI: 10.1093/rheumatology/keaa240.

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