Studies | Source Population, No. Patients (% Women), Mean Age, Yrs | Definitions of Hand OA | Study Designs | Applied Instruments |
---|---|---|---|---|
Allen, et al23 | GOGO study (familial OA), 531 (80), 68 | Bony enlargement, KL ≥ 2 in ≥ 1 DIP | Observational, mean FU 4 yrs |
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Allen, et al24 | GOGO study, 878 (80), 69 | Bony enlargement, KL ≥ 2 in ≥ 1 DIP | Observational, cross-sectional |
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Altman, et al45 | Secondary care, 385 (77), 64 | ACR criteria | RCT (intervention > control)*, duration 8 weeks |
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Backman and Mackie18 | Secondary care, 26 (88), 67 | OA ≥ 2 joints, rheumatologist confirmed | Observational, test-retest after 2 weeks |
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Barthel, et al46 | Secondary care, 783 (80), 64 | ACR criteria, KL ≥ 1, symptoms ≥ 1 yr | RCT (intervention > control), duration 8 weeks |
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Bellamy, et al25 | Study 1: secondary care, 50 (80), 60. Study 2: secondary care, 44 (86), 60 | ACR criteria | Study 1: Observational, test-retest after 1 week. Study 2: Intervention, duration 6 weeks |
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Bijsterbosch, et al19 | GARP study (familial polyarticular OA), 260 (84), 65 | ACR criteria | Observational, cross-sectional |
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Bijsterbosch, et al82 | GARP study, 289 (83), 60 | ACR criteria | Observational, FU 6 yrs |
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Botha-Scheepers, et al83 | GARP study, 289 (83), 60 | ACR criteria | Observational, FU 2 yrs |
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Brosseau, et al47 | Secondary care, 88 (78), 65 | ACR criteria, radiographic OA | RCT (intervention = control)# duration 6 weeks |
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Dilek, et al48 | Secondary care, 56 (89), 59 | ACR criteria, bilateral | RCT (intervention > control), duration 3 weeks |
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Dreiser, et al49 | Secondary care, 60 (85), 59 | Radiographic OA | RCT (intervention > control), duration 2 weeks |
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Dreiser, et al13 | Secondary care, 200 (84), 66 | Radiographic OA | Observational, cross-sectional |
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Dreiser, et al26 | Not specified, 261 (92), 61 | ACR criteria, radiographic OA ≥ 2 joints bilateral, symptoms | RCT (effect not specified), duration 6 mos |
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Dziedzic, et al27 | Primary care, 55 (60), 67 | Hand problems (symptoms, nodes) | Observational, test-retest after 1 mo |
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Dziedzic, et al50 | Primary care, 257 (66), 66 | ACR criteria | RCT (intervention > control), duration 6 mos |
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Fernandes, et al28 | Secondary care, 211 (95), 63 | ACR criteria | Observational, FU 3 mos |
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Fioravanti, et al51 | Primary care, 60 (87), 71 | ACR criteria, symptomatic | RCT (intervention > control), duration 2 weeks |
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Flynn, et al52 | Secondary care, 26 (88), range 52–82 | ACR criteria | RCT (intervention > control), duration 2 mos |
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Gabay, et al53 | Secondary care, 162 (74), 63 | ACR criteria, radiographic OA ≥ 2 joints ≥ 2 flares finger OA | RCT (intervention > control), duration 6 mos |
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Garfinkel, et al54 | Not specified, 25 (56), range 52–79 | ACR criteria | RCT (intervention > control), duration 10 weeks |
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Grifka, et al55 | Secondary care, 594 (83), 62 | ACR criteria, symptomatic ≥ 3 mos | RCT (intervention > control), duration 4 weeks |
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Haugen, et al29 | Secondary care, 83 (93), 60 | ACR criteria, KL ≥ 2, ≥ 1 swollen/tender joint, VAS pain ≥ 30 | RCT (intervention > control), duration 42 days |
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Haugen, et al30 | Secondary care (Oslo hand OA cohort), 209 (91), 62 | ACR criteria | Observational, FU 7 yrs |
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Haugen, et al84 | Oslo hand OA cohort, 209 (91), 62 | ACR criteria | Observational, FU 7 yrs |
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Hirsch, et al31 | Women’s Health and Aging Study, 919 (100), age ≥ 65 | ACR criteria | Observational, cross-sectional |
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Horvath, et al56 | Secondary care, 63 (81), 63 | ACR criteria, radiographic OA, pain ≥ 3 mos | RCT (intervention > control), duration 3 weeks |
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Kanat, et al57 | Not specified, 50 (100), 63 | ACR criteria | RCT (intervention > control), duration 10 days |
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Keen, et al58 | Secondary care, 36 (86), 58 | ACR criteria or radiographic OA | Intervention, FU 4 weeks (after injection) |
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Kjeken, et al59 | Secondary care, 70 (97), 61 | ACR criteria | RCT (intervention = control), duration 3 mos |
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Kovacs, et al60 | Secondary care, 45 (93), 59 | ACR criteria, KL ≥ 2 in ≥ 2 joints, VAS pain ≥ 30 | RCT (intervention > control), duration 3 weeks |
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Kvien, et al61 | Secondary care, 83 (93), 60 | ACR criteria, KL ≥ 2, ≥ 1 swollen/tender joint, VAS pain ≥ 30 | RCT (intervention > control), duration 42 days |
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Kwok, et al62 | Secondary care, 195 (87), 59 | Diagnosed by rheumatologist | Observational, FU 3 mos |
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MacIntyre and Wessel32 | Community-dwelling, 99 (80), 67 | ACR criteria (dominant hand) | Observational, cross-sectional |
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MacIntyre, et al33 | Community-dwelling, 104 (81), 68 | ACR criteria (dominant hand) | Observational, cross-sectional |
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Marshall, et al85 | Primary care, 1076 (60), 65 | Hand symptoms | Observational, FU 3 yrs |
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Moe, et al34 | Secondary care (Oslo hand OA cohort), 128 (91), 69 | ACR criteria | Observational, test-retest after 1 week |
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Moratz, et al63 | Population/secondary care, 77 (73), 69 | Not specified | Intervention, duration 12 weeks |
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Myers, et al35 | Primary care, 55 (60), 66 | Hand pain/problems | Observational, test-retest after 1 mo |
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Myrer, et al64 | Volunteers, 35 (77), 64 | ACR criteria, FIHOA > 5 | RCT (intervention > control), duration 4 weeks |
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Pastinen, et al65 | Secondary care, 29 (79), 58 | Clinical/radiographic finger OA | RCT (intervention > control), duration 14 weeks |
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Poiraudeau, et al36 | Secondary care, 89 (91), 63 | ACR criteria | Observational, FU 6 mos |
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Poole, et al37 | Population based (senior centers), 40 (60), 63 | Diagnosis of OA (not specified), symptoms | Observational, test-retest 1 week |
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Reeves and Hassanein66 | Not specified, 27 (59), 64 | Radiographic OA, pain | RCT (intervention > control), FU 6 mos (after injection) |
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Rintelen, et al38 | Secondary care, 71 (91), 60 | ACR criteria | Observational, cross-sectional |
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Rogers and Wilder67 | Secondary care, 55 (80), 72 | KL ≥ 2 | Intervention, duration 2 yrs |
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Rogers and Wilder68 | Community-based, 46 (87), 75 | KL ≥ 2 | RCT (intervention = control), duration 6 weeks |
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Romero-Cerecero, et al69 | Not specified, 113 (95), 62 | ACR criteria, radiographic OA ≥ 2 joints VAS ≥ 40, FIHOA ≥ 5 | RCT (intervention = control), duration 4 weeks |
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Rothacker, et al70 | Not specified, 49 (84), 66 | Physician/radiographic confirmed OA, symptoms | RCT (intervention > control), FU 45 min (after cream) |
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Rothacker, et al71 | Secondary care, 81 (74), 61 | Physician confirmed OA, symptoms | RCT (intervention > control), FU 45 min (after cream) |
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Sautner, et al39 | Secondary care, 60 (73), 62 | ACR criteria | Observational, cross-sectional |
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Sautner, et al40 | Secondary care, 66 (77), 58 | ACR criteria | Observational, cross-sectional |
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Saviola, et al72 | Secondary care, 38 (95), 61 | Radiographic erosive OA ≥ 2 joints, VAS ≥ 40 | RCT (intervention 1 > intervention 2), duration 2 yrs (intervention 2 only 1 yr) |
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Schnitzer, et al73 | Not specified, 59 (68), 68 | Radiographic/ physical OA findings | RCT (intervention > control), duration 9 weeks |
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Seiler74 | Secondary care, 41 (90), median 63 | Radiographic OA, ≥ 3 painful/tender joints, ≥ 1 inflamed Heberden node | RCT (intervention > control), duration 4 weeks |
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Shin, et al75 | Secondary care, 86 (97), 58 | ACR criteria | RCT (intervention = control), duration 12 weeks |
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Stamm, et al41 | Secondary care, 100 (87), 61 | Bony swelling ≥ 1 DIP/PIP, pain/bony swelling ≥ 1 CMC1 | Observational, cross-sectional |
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Stamm, et al76 | Secondary care, 40 (88), 60 | ACR criteria | RCT (intervention > control), duration 3 mos |
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Stange-Rezende, et al77 | Secondary care, 45 (93), 60 | ACR criteria | RCT (intervention = control), duration 3 weeks |
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Stukstette, et al78 | Secondary care, 151 (83), 59 | ACR criteria | RCT (intervention = control), duration 3 mos |
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Tubach, et al42 | Secondary care, 249 (88), 64 | ACR criteria | Intervention, FU 4 weeks |
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Verbruggen, et al79 | Secondary care, 60 (85), 61 | ACR criteria | RCT (intervention = control), duration 1 yr |
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Wenham, et al80 | Not specified, 70 (81), 61 | ACR criteria | RCT (intervention = control), duration 4 weeks |
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Widrig, et al81 | Primary and secondary care, 204 (74), 64 | ACR criteria, radiographic OA ≥ 2 joints VAS ≥ 40, FIHOA ≥ 5 | RCT (intervention = control), duration 3 weeks |
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Wittoek, et al43 | Secondary care, 72 (89), 62 | ACR criteria | Observational, cross-sectional |
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Ziv, et al44 | Not specified, 32 (100), 70 | ACR criteria | Observational, test-retest after 1 week |
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↵* Intervention group performed better than control group, according to primary outcome measure.
↵# Intervention group did not perform better than control group, according to primary outcome measure. OA: osteoarthritis; GOGO: Genetics of Generalized OA; KL: Kellgren-Lawrence; DIP: distal interphalangeal joint; FU: followup; AUSCAN: Australian/Canadian Hand OA Index; ACR: American College of Rheumatology; RCT: randomized controlled trial; VAS: visual analog scale; OMFAQ: Older Americans’ Resources and Services Multidimensional Functional Assessment Questionnaire; AHFT: Arthritis Hand Function Test; FIHOA: Functional Index for Hand OA; HAQ: Health Assessment Questionnaire; GARP: Genetics osteoArthritis and Progression; ADL: activities of daily living; GAT: grip ability test; ASES: Arthritis Self Efficacy Scale; COPM: Canadian Occupational Performance Measure; MAP-hand: Measure of Activity Performance; AIMS-2: Arthritis Impact Measurement Scale-2; PRWHE: Patient-Rated Wrist/Hand Evaluation; MPUT: Moberg Pick-Up Test; MHQ: Michigan Hand Outcomes Questionnaire; HFI: hand functional index; HAMIS: Hand Mobility in Scleroderma Test; SACRAH: Score for Assessment and Quantification of Chronic Rheumatoid Affections of the Hands; PIP: proximal interphalangeal joint; CMC1: first carpometacarpal joint; JTHFT: Jebsen-Taylor Hand Function Test.