Study ID | Setting | n | Patient Characteristics (Median/Mean) | Treatments of Interest | Patient Experience with Treatments | Funding |
---|---|---|---|---|---|---|
Discrete choice experiments | ||||||
Fraenkel, et al52 | Online panel (self-reported RA), USA | 1101 | Age: 51 yrs; female: 90%; yrs RA: NR | csDMARD, bDMARD, tofacitinib | NR (all taking at least 1 DMARD) | Public |
Husni, et al53 | Patient registry, USA | 510 | Age: 56 yrs; female: 65%; yrs RA: 43% > 10 yrs | csDMARD, bDMARD, tofacitinib | 45% prior bDMARD | Industry |
Alten, et al54 | Outpatient clinics, Germany | 1588 | Age: 48% > 60 yrs; female: 74%; yrs RA: 44% > 10 yrs | bDMARD and tofacitinib | NR (all taking at least 1 DMARD) | Industry |
Hazlewood, et al14,55 | Outpatient clinics, Canada | 152 | Age: 53 yrs; female: 63%; yrs RA: 0.7 | csDMARD, anti-TNF | 97% csDMARD, 5% bDMARD | Public |
Louder, et al56 | Insurance database, USA | 380 | Age: 55 yrs; female: 82%; yrs RA: 9 | bDMARD and tofacitinib | Naive | Industry |
Nolla, et al57 | Outpatient clinics, Spain | 165 | Age: 56 yrs; female: 74%; yrs RA: 13 | bDMARD | 100% currently taking bDMARD | Industry |
Fraenkel, et al41 | Outpatient clinics, USA | 156 | Age: 59; female: 85%; yrs RA: 9 | bDMARD | 48% currently taking bDMARD | Public |
Poulos, et al58 | Online panel (self-reported RA), USA | 849 | Age: 61% ≥ 55 yrs; female: 74%; yrs RA: NR | bDMARD | NR (34% prior SC, 30% prior IV) | Industry |
Augustovski, et al40 | Outpatient clinics, Argentina | 240 | Age: 56 yrs; female: 87%; yrs RA: 9 | bDMARD | Naive | Industry |
Constantinescu, et al16,42 | Outpatient clinics, USA | 136 | Age: 55 yrs; female: 83%; yrs RA: 8 | Methotrexate, bDMARD | Median DMARD: 2 | Public |
Ozdemir, et al59 | Online panel (self-reported RA), USA | 463 | Age: 53 yrs; female: 64%; yrs RA: 8 | bDMARD | 16% receive SC or IV | Public |
Skjoldborg, et al39 | Outpatient clinic, Denmark | 178 | NR | Anti-TNF | Prior treatment not reported | Public |
Fraenkel, et al17 | Outpatient clinics, USA | 120 | Age: 70 yrs; female: 76% yrs RA: 8 | csDMARD, etanercept | 60% currently using a DMARD | Public |
Standard gamble (SG), time tradeoff (TTO), visual analog scale | ||||||
Chiou, et al18 | Outpatient clinics, USA | 484 | Age: 59 yrs, female: 79%, yrs RA: 13 | No specific Rx* | Prior treatment not reported | Industry |
Suarez-Almazor and Conner-Spady20 | Outpatient clinics, Canada | 51 | Age: 60 yrs; female: 72%; yrs RA: NR | No specific Rx* | Prior treatment not reported | NR |
Ferraz, et al19 | Outpatient clinic, Brazil | 25 | Age (range): 34–70 yrs; female: 20%; yrs RA: 8 | Prednisone | 95% ever taken steroids | NR |
Willingness to pay | ||||||
Tuominen, et al25 | Patient registry, Finland | 166 | Age: 64 yrs; female: 69%; yrs RA: NR | No specific Rx* | Prior treatment not reported | Partial industry |
Slothuus, et al23,24 | Outpatient clinic, Denmark | 115 | Age: 56 yrs; female: 71%; yrs RA: 15 | Anti-TNF (infliximab) | Naive | NR |
Willingness to accept risk | ||||||
Fraenkel, et al26,27 | Outpatient clinics, USA | 100 | Age: 68 yrs; female: 73%; yrs RA: NR | NSAID, prednisone, csDMARD | Current use: 39% NSAID; 68% prednisone; 81% csDMARD | Public |
Ho, et al28 | Outpatient clinic, UK | 67 | Age: 57 yrs; female: 73%; yrs RA: 10 | No specific Rx* | Prior treatment not reported | Public |
O’Brien, et al29 | Outpatient clinic and inpatients, UK | 50 | Age: 51 yrs; female: 84%; yrs RA: 13 | No specific Rx* | Prior treatment not reported | Public |
Rating or ranking of treatment outcomes | ||||||
Bacalao, et al60 | Outpatient clinic, USA | 119 | Age: 57 yrs, female: 91%; yrs RA: 11 | No specific Rx* | Prior treatment not reported | Public and industry |
van Tuyl, et al61 | Clinics and online panel in 5 countries | 274 | Age: 57 yrs; female: 75%; yrs RA: 12 | No specific Rx* | Prior treatment not reported | Public |
Buitinga, et al36 | Outpatient clinic, Netherlands | 74 | Age: 58 yrs; female: 62%; yrs RA: 7 | No specific Rx* | Current use: 70% csDMARD; 30% bDMARD | Public |
Sanderson, et al35 | Mix outpatient clinics and registries, UK | 254 | Age: 61% > 60 yrs; female: 76%; yrs RA: 76% > 5 | No specific Rx* | Current use: 52% csDMARD; 39% bDMARD | Public |
Da Silva, et al33 | Outpatient clinics (self-reported RA), Portugal | 667 | NR | No specific Rx* | Prior treatment not reported | Public |
Heiberg, et al34 | Patient registry, Norway | 1024 | Age: 63 yrs; female: 79%; yrs RA: 13 | No specific Rx* | Prior treatment not reported | Public |
Preference for different routes of delivery | ||||||
Desplats, et al62 | Outpatient clinics, France | 201 | Age: 58 yrs; female: 81%; yrs RA: 17 | bDMARD | 100% on IV bDMARD (ABA or TCZ) | Industry |
Bolge, et al30 | Online panel (self-reported RA), USA | 243 | Age: 53 yrs; female: 85%; yrs RA: 13 | bDMARD | Naive | Industry |
Navarro-Millan, et al31 | Patient registry, USA | 242 | Age: 54 yrs; female: 73%; yrs RA: 8 | Anti-TNF | 100% currently taking anti-TNF | Public |
Huynh, et al63 | Outpatient clinics, Denmark | 142 | Age: 57 yrs; female: 77%; yrs RA: NR | bDMARD | 75% taking bDMARD, 25% bDMARD-naive | Industry |
Scarpato, et al32 | Outpatient clinics, Italy | 802 | Age: 56 yrs; female: 77%; yrs RA: 9 | Anti-TNF | Naive | Industry |
Preference for different treatment options | ||||||
Martin, et al64 | Outpatient clinic, USA | 402 | Age: 64 yrs; female: 67%; yrs RA: 10.4 | Etanercept | Biologic-naive | Public and industry*** |
Van Overbeeke, et al38 | Broad recruitment including social media, Belgium | 121 | Age: 57% 40–60 yrs; female: 87%; yrs RA: NR | bDMARD and biosimilars | 55% prior DMARD, all naive to biosimilars | Public |
Fraenkel, et al37 | Patient panel, USA | 10 | Age: 38 yrs; female: 70%; yrs RA: 11 | All DMARD | Current use: 40% csDMARD only; 60% bDMARD | Public |
Goekoop-Ruiterman, et al15 | Patients enrolled in BeST RCT65 | 440 | Age: 55 yrs; female: 68%; yrs RA: 0.4 (at entry of BeST) | 4 arms of BeST** | All patients exposed to one of 4 trial arms | Industry |
↵* These studies valued health states relevant to DMARD treatment decisions, without a specific DMARD of interest.
↵** The 4 arms of the BeST trial were (1) Sequential csDMARD monotherapy; (2) Step-up csDMARD combination therapy; (3) Initial csDMARD combination therapy with prednisone; (4) Initial combination therapy with infliximab.
↵*** In-kind contribution from industry, who provided decision aid booklets at no cost. RA: rheumatoid arthritis; NR: not reported; DMARD: disease-modifying antirheumatic drug; csDMARD: conventional synthetic DMARD; bDMARD: biological DMARD; anti-TNF: antitumor necrosis factor; SC: subcutaneous; IV: intravenous; NSAID: nonsteroidal antiinflammatory drug; RCT: randomized controlled trial; ABA: abatacept; TCZ: tocilizumab.