Feasibility of Conducting Comparative Effectiveness Research and Validation of a Clinical Disease Activity Score for Chronic Nonbacterial Osteomyelitis

被引:10
作者
Wu, Eveline Y. [1 ]
Oliver, Melissa [2 ]
Scheck, Joshua [3 ]
Lapidus, Sivia [4 ,5 ]
Akca, Ummusen Kaya [6 ]
Yasin, Shima [7 ]
Stern, Sara M. [8 ]
Insalaco, Antonella [9 ]
Pardeo, Manuela [9 ]
Simonini, Gabriele [10 ]
Marrani, Edoardo [10 ]
Wang, Xing [11 ]
Huang, Bin [12 ]
Kovalick, Leonard K. [1 ]
Rosenwasser, Natalie [3 ]
Casselman, Gabriel [3 ]
Liau, Adriel [3 ]
Shao, Yurong [3 ]
Yang, Claire [3 ]
Mosa, Doaa Mosad [13 ]
Tucker, Lori [14 ]
Girschick, Hermann [15 ]
Laxer, Ronald M. [16 ,17 ]
Akikusa, Jonathan D. [18 ]
Hedrich, Christian M. [19 ]
Onel, Karen [20 ]
Dedeoglu, Fatma [21 ]
Twilt, Marinka [22 ]
Ferguson, Polly J. [7 ]
Ozen, Seza [6 ]
Zhao, Yongdong [3 ]
机构
[1] Univ N Carolina, Div Rheumatol, Dept Pediat, Chapel Hill, NC 27515 USA
[2] Indiana Univ Sch Med, Div Pediat Rheumatol, Indianapolis, IN 46202 USA
[3] Univ Washington, Seattle Childrens Hosp, Div Pediat Rheumatol, Seattle, WA 98195 USA
[4] Hackensack Univ Med Ctr, Joseph M Sanzari Childrens Hosp, Dept Pediat, Div Rheumatol, Hackensack, NJ USA
[5] Hackensack Meridian Sch Med, Hackensack, NJ USA
[6] Hacettepe Univ, Dept Pediat, Div Rheumatol, Ankara, Turkiye
[7] Univ Iowa, Dept Pediat, Div Rheumatol Allergy & Immunol, Carver Coll Med, Iowa City, IA 52242 USA
[8] Univ Utah, Dept Pediat, Div Rheumatol, Salt Lake City, UT USA
[9] IRCCS Osped Pediatr Bambino Gesu, Div Rheumatol, ERN RITA Ctr, Rome, Italy
[10] Meyer Childrens Hosp IRCCS, ERN ReCONNET Ctr, Rheumatol Unit, Florence, Italy
[11] Seattle Childrens Res Inst, Biostat Epidemiol & Analyt Res, Seattle, WA USA
[12] Univ Cincinnati, Coll Med, Cincinnati Childrens Hosp Med Ctr, Div Biostat & Epidemiol, Cincinnati, OH USA
[13] Mansoura Univ, Mansoura Univ Hosp, Rheumatol & Rehabil Dept, Mansoura, Egypt
[14] Univ British Columbia, BC Childrens Hosp, Div Rheumatol, Vancouver, BC, Canada
[15] Vivantes Clin Friedrichshain, Dept Pediat, Berlin, Germany
[16] Hosp Sick Children, Toronto, ON, Canada
[17] Univ Toronto, Toronto, ON, Canada
[18] Royal Childrens Hosp, Melbourne, Vic, Australia
[19] Alder Hey Childrens NHS Fdn Trust, Eaton Rd, Liverpool, Merseyside, England
[20] Hosp Special Surg, Div Pediat Rheumatol, 535 E 70th St, New York, NY 10021 USA
[21] Harvard Med Sch, Boston Childrens Hosp, Div Immunol, Boston, MA 02115 USA
[22] Alberta Childrens Prov Gen Hosp, Dept Paediat, Div Rheumatol, Calgary, AB, Canada
基金
美国国家卫生研究院;
关键词
chronic nonbacterial osteomyelitis; chronic recurrent multifocal osteomyelitis; clinical disease activity score; comparative effectiveness research; consensus treatment plans; RECURRENT MULTIFOCAL OSTEOMYELITIS; WHOLE-BODY MRI; OSTEITIS; CHILDREN;
D O I
10.3899/jrheum.2022-1323
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1333 / 1340
页数:8
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