TY - JOUR
T1 - Feasibility of Conducting Comparative Effectiveness Research and Validation of a Clinical Disease Activity Score for Chronic Nonbacterial Osteomyelitis
AU - Wu, Eveline Y.
AU - Oliver, Melissa
AU - Scheck, Joshua
AU - Lapidus, Sivia
AU - Akca, Ummusen Kaya
AU - Yasin, Shima
AU - Stern, Sara M.
AU - Insalaco, Antonella
AU - Pardeo, Manuela
AU - Simonini, Gabriele
AU - Marrani, Edoardo
AU - Wang, Xing
AU - Huang, Bin
AU - Kovalick, Leonard K.
AU - Rosenwasser, Natalie
AU - Casselman, Gabriel
AU - Liau, Adriel
AU - Shao, Yurong
AU - Yang, Claire
AU - Mosa, Doaa Mosad
AU - Tucker, Lori
AU - Girschick, Hermann
AU - Laxer, Ronald M.
AU - Akikusa, Jonathan D.
AU - Hedrich, Christian M.
AU - Onel, Karen
AU - Dedeoglu, Fatma
AU - Twilt, Marinka
AU - Ferguson, Polly J.
AU - Ozen, Seza
AU - Zhao, Yongdong
N1 - Publisher Copyright:
© 2023 The Journal of Rheumatology.
PY - 2023/10/1
Y1 - 2023/10/1
N2 - Objective. Prospective comparative effectiveness research (CER) in chronic nonbacterial osteomyelitis (CNO) is lacking. Our objectives were to (1) determine the use and safety of each consensus treatment plan (CTP) regimen for CNO, (2) assess the feasibility of using the Chronic Nonbacterial Osteomyelitis International Registry (CHOIR) data for CER, and (3) develop and validate a CNO clinical disease activity score (CDAS) using CHOIR. Methods. Consenting children or young adults with CNO were enrolled into CHOIR. Demographic, clinical, and imaging data were prospectively collected. The CNO CDAS was developed through a Delphi survey and nominal group technique. External validation surveys were administered to CHOIR participants. Results. One hundred forty (78.2%) CHOIR participants enrolled between August 2018 and September 2020 received at least 1 CTP regimen. Baseline characteristics from different CTP groups were well matched. Patient pain, patient global assessment, and clinical CNO lesion count were key variables included in the CNO CDAS. The CDAS showed a strong correlation with patient/parent report of difficulty using a limb, back, or jaw and patient/parent report of disease severity, but a weak correlation with patient/parent report of fatigue, sadness, and worry. The change in CDAS was significant in patients reporting disease worsening or improvement (P < 0.001). The CDAS significantly decreased after initiating second-line treatments from median 12.0 (IQR 8.0-15.5) to 5.0 (IQR 3.0-12.0; P = 0.002). Although second-line treatments were well tolerated, psoriasis was the most common adverse event. Conclusion. The CNO CDAS was developed and validated for disease monitoring and assessment of treatment effectiveness. CHOIR provided a comprehensive framework for future CER.
AB - Objective. Prospective comparative effectiveness research (CER) in chronic nonbacterial osteomyelitis (CNO) is lacking. Our objectives were to (1) determine the use and safety of each consensus treatment plan (CTP) regimen for CNO, (2) assess the feasibility of using the Chronic Nonbacterial Osteomyelitis International Registry (CHOIR) data for CER, and (3) develop and validate a CNO clinical disease activity score (CDAS) using CHOIR. Methods. Consenting children or young adults with CNO were enrolled into CHOIR. Demographic, clinical, and imaging data were prospectively collected. The CNO CDAS was developed through a Delphi survey and nominal group technique. External validation surveys were administered to CHOIR participants. Results. One hundred forty (78.2%) CHOIR participants enrolled between August 2018 and September 2020 received at least 1 CTP regimen. Baseline characteristics from different CTP groups were well matched. Patient pain, patient global assessment, and clinical CNO lesion count were key variables included in the CNO CDAS. The CDAS showed a strong correlation with patient/parent report of difficulty using a limb, back, or jaw and patient/parent report of disease severity, but a weak correlation with patient/parent report of fatigue, sadness, and worry. The change in CDAS was significant in patients reporting disease worsening or improvement (P < 0.001). The CDAS significantly decreased after initiating second-line treatments from median 12.0 (IQR 8.0-15.5) to 5.0 (IQR 3.0-12.0; P = 0.002). Although second-line treatments were well tolerated, psoriasis was the most common adverse event. Conclusion. The CNO CDAS was developed and validated for disease monitoring and assessment of treatment effectiveness. CHOIR provided a comprehensive framework for future CER.
KW - chronic nonbacterial osteomyelitis
KW - chronic recurrent multifocal osteomyelitis
KW - clinical disease activity score
KW - comparative effectiveness research
KW - consensus treatment plans
UR - https://www.scopus.com/pages/publications/85166774352
U2 - 10.3899/jrheum.2022-1323
DO - 10.3899/jrheum.2022-1323
M3 - Article
C2 - 37399459
AN - SCOPUS:85166774352
SN - 0315-162X
VL - 50
SP - 1333
EP - 1340
JO - Journal of Rheumatology
JF - Journal of Rheumatology
IS - 10
ER -