| Literature DB >> 30886967 |
Samina A Turk1, Linda A Rasch2, Dirkjan van Schaardenburg1,3, Willem F Lems1,2, Marjolein Sanberg1, Lilian H D van Tuyl2, Marieke M Ter Wee2,4.
Abstract
BACKGROUND: Clinical response and remission are defined in multiple ways and measured with different instruments, resulting in substantial variation of the proportion of patients classified as being in remission. Therefore, the agreement between patient-perceived, physician-perceived remission and clinical response and remission definitions was determined in early rheumatoid arthritis (RA) patients. And secondly, differences in clinical and patient-reported outcomes, in patients in physician-perceived remission, between patients in and not in self-perceived remission were assessed.Entities:
Keywords: Disease-modifying antirheumatic drugs (Dmards); Fatigue; Patient reported outcomes; Physician agreement; Rheumatoid arthritis
Year: 2018 PMID: 30886967 PMCID: PMC6390551 DOI: 10.1186/s41927-018-0024-9
Source DB: PubMed Journal: BMC Rheumatol ISSN: 2520-1026
Demographics and outcomes at baseline and after 12 weeks of treatment
| Baseline values | Values after 12 weeks of treatment | |||||
|---|---|---|---|---|---|---|
| Total population | Patients in self-perceived remission at week 12, | Patients not in self-perceived remission at week 12, | Total population, | Patients in self-perceived remission at week 12, | Patients not in self-perceived remission at week 12, | |
| Demographics | ||||||
| Gender (female), | 56 (66.7) | 31 (69.9) | 25 (64.1) | |||
| Age (years) | 50.0 (12.4) | 50.4 (13.2) | 49.4 (11.5) | |||
| RF positive, | 70 (83.3) | 38 (84.4) | 32 (82.1) | |||
| ACPA positive, | 72 (85.7) | 39 (86.7) | 33 (84.6) | |||
| Symptom duration (months) | 8.0 [3.5–20.0] | 12.0 [4.0–22.0] | 7.0 [3.0–18.0] | |||
| Disease activity | ||||||
| DAS44 | 3.4 (1.2) | 3.2 (1.2) | 3.6 (1.1) | 1.4 (0.9)* | 1.0 (0.6) | 1.9 (0.9)‡ |
| VAS global (mm) | 62.0 [41.5–82.3] | 50.0 [29.5–73.5] | 70.0 [57.0–85.0]† | 12.0 [5.0–42.8] * | 5.0 [1.0–12.5] | 40.0 [13.0–50.0]‡ |
| TJC44ritchie | 7.0 [3.3–10.8] | 5.0 [3.0–10.0] | 7.0 [5.0–11.0] | 1.0 [0.0–2.0] * | 0.0 [0.0–1.0] | 2.0 [1.0–6.0]‡ |
| SJC44ritchie | 6.5 [3.0–13.0] | 7.0 [2.5–13.0] | 6.0 [3.0–12.0] | 0.0 [0.0–2.0] * | 0.0 [0.0–1.0] | 2.0 [0.0–4.0]‡ |
| ESR (mm/hour) | 20.0 [9.0–32.8] | 15.0 [7.0–30.0] | 23.0 [15.0–40.0]† | 7.0 [5.0–12.0] * | 7.0 [3.5–12.0] | 8.0 [5.0–12.0] |
| CRP (mg/l) | 7.7 [3.9–25.8] | 5.5 [3.5–24.0] | 8.3 [4.3–33.0] | 2.0 [1.1–3.6] * | 1.8 [1.1–3.9] | 2.0 [0.9–3.6] |
| Patient Reported Outcomes Measures | ||||||
| RAID pain (0–10) | 7.0 [5.8–8.0] | 7.0 [4.0–8.0] | 7.5 [6.0–8.3] | 2.0 [1.0–4.5] * | 1.0 [0.0–2.0] | 4.0 [2.5–6.0]‡ |
| RAID FDA (0–10) | 6.0 [4.0–8.0] | 5.5 [2.0–8.0] | 7.0 [5.0–8.3]† | 2.0 [0.0–4.5] * | 1.0 [0.0–2.0] | 5.0 [3.0–7.5]‡ |
| RAID fatigue (0–10) | 6.5 [3.0–8.0] | 5.5 [2.0–8.0] | 7.0 [4.8–9.0]† | 4.0 [2.0–7.0] * | 2.0 [0.0–5.8] | 5.0 [3.0–7.5]‡ |
| RAID sleep (0–10) | 7.0 [2.0–8.0] | 7.0 [2.0–8.0] | 6.5 [3.8–8.0] | 2.0 [0.0–6.0] * | 1.0 [0.0–4.0] | 5.0 [2.0–7.0]‡ |
| RAID physical well-being (0–10) | 4.0 [2.0–7.0] | 3.0 [1.3–6.0] | 5.0 [3.0–7.0]† | 3.0 [1.0–5.0] * | 1.0 [0.0–3.0] | 4.0 [2.0–5.0]‡ |
| RAID emotional well-being (0–10) | 5.0 [2.0–7.0] | 5.0 [1.3–6.8] | 6.0 [3.0–8.0] | 2.0 [0.0–5.0] * | 1.0 [0.0–3.0] | 4.0 [2.0–6.0]‡ |
| RAID coping (0–10) | 5.0 [2.0–7.0] | 3.0 [1.3–7.0] | 5.0 [3.0–7.3] | 2.0 [0.0–4.0] * | 0.5 [0.0–2.0] | 3.0 [2.0–5.0]‡ |
| HAQ (0–3) | 0.9 [0.5–1.5] | 0.8 [0.3–1.3] | 1.3 [0.6–0.8]† | 0.2 [0.0–0.6] * | 0.0 [0.0–0.3] | 0.5 [0.1–0.9]‡ |
Numbers are presented as mean (SD) or median [IQR] unless otherwise stated
ACPA anti-citrullinated protein, CRP C-reactive protein, DAS44 disease activity score of 44 joints, ESR erythrocyte sedimentation rate, FDA functional disability assessment, HAQ Health Assessment Questionnaire, IQR interquartile range, l liter, mg milligram, mm millimeter, n number, RAID Rheumatoid Arthritis Impact of Disease questionnaire, RF rheumatoid factor, SD standard deviation, SJC44 swollen joint count of 44 joints, TJC44 tender joint count of 44 joints, VAS visual analogue scale
*Significant improvement (p < 0.05) for the total population, between baseline and 12 weeks after treatment
† Significant difference (p < 0.05) in baseline values between patient in and patient not in self-perceived remission after 12 weeks of treatment
‡ Significant difference (p < 0.05) in week 12 values between patients in and patient not in self-perceived remission after 12 weeks of treatment
Agreement between different definitions of response and remission
| Physician-perceived remission | Patient-perceived remission | DAS44 remission | EULAR good response | ACR70 response | Boolean remission | |
|---|---|---|---|---|---|---|
| Physician- perceived remission | x | 67% | 74% | 79% | 60% | 57% |
| Ƙ = 0.318 | Ƙ = 0.439 | Ƙ = 0.484 | Ƙ = 0.281 | Ƙ = 0.248 | ||
| Patient-perceived remission | 67% | x | 46% | 69% | 69% | 67% |
| Ƙ = 0.318 | Ƙ = 0.516 | Ƙ = 0.356 | Ƙ = 0.398 | Ƙ = 0.354 | ||
| DAS44 remission | 74% | 46% | x | 83% | 64% | 67% |
| Ƙ = 0.439 | Ƙ = 0.516 | Ƙ = 0.622 | Ƙ = 0.343 | Ƙ = 0.392 | ||
| EULAR good response | 79% | 69% | 83% | x | 52% | 50% |
| Ƙ = 0.484 | Ƙ = 0.356 | Ƙ = 0.622 | Ƙ = 0.220 | Ƙ = 0.199 | ||
| ACR70 response | 60% | 69% | 64% | 52% | x | 74% |
| Ƙ = 0.281 | Ƙ = 0.398 | Ƙ = 0.343 | Ƙ = 0.220 | Ƙ = 0.359 | ||
| Boolean remission | 57% | 67% | 67% | 50% | 74% | x |
| Ƙ = 0.248 | Ƙ = 0.354 | Ƙ = 0.392 | Ƙ = 0.199 | Ƙ = 0.359 | ||
Numbers are presented as level of agreement (%), kappa value (K) and p-value (P)
Physician-perceived remission was defined as a VAS of ≤10 mm as answer to the question: “How active do you think the rheumatoid arthritis of your patient is today?”
Patient-perceived remission was defined as “yes” or “no” as answer to the question: “Would you say that, at this moment, your disease activity is as good as gone?”
ACR70 American College of Rheumatology 70 response, DAS44 disease activity score of 44 joints, EULAR European League Against Rheumatism, mm millimeter
Fig. 1Comparison of improvement in patient-reported and clinical outcomes after 12 weeks of treatment, in patients in physician-perceived remission, who were in and not in patient-perceived remission
Differences in baseline values of patients in physician-perceived remission, stratified into patients in and not in self-perceived remission after 12 weeks of treatment
| In physician-perceived remission, | ||
|---|---|---|
| In patient-perceived remission, | Not in patient-perceived remission, | |
| DAS44 | 3.0 (1.1) | 3.2 (1.0) |
| VAS global (mm) | 47.5 [28.3–72.0] | 66.0 [50.0–76.0] |
| TJC44ritchie | 4.0 [3.0–9.0] | 6.0 [4.0–11.0] |
| SJC44ritchie | 6.0 [2.3–12.0] | 6.0 [3.0–12.0] |
| ESR (mm/hour) | 14.5 [8.0–31.0] | 20.0 [12.0–40.0] |
| CRP (mg/l) | 10.7 [4.2–24.8] | 7.2 [3.9–32.0] |
| RAID pain | 7.0 [3.0–8.0] | 7.0 [4.8–8.0] |
| RAID FDA | 6.0 [2.0–7.0] | 5.0 [4.0–8.0] |
| RAID fatigue | 5.0 [1.0–8.0] | 6.0 [3.0–8.0] |
| RAID sleep | 6.0 [2.0–8.0] | 5.5 [2.0–7.3] |
| RAID physical well-being | 3.0 [1.0–6.0] | 3.5 [3.0–6.8] |
| RAID emotional well-being | 3.0 [1.0–7.0] | 4.0 [2.5–7.0] |
| RAID coping | 3.0 [1.0–8.0] | 5.0 [2.5–8.0] |
| HAQ | 0.6 [0.1–1.1] | 0.8 [0.4–1.5] |
Numbers are presented as mean (SD) or median [IQR] where appropriate
CRP C-reactive protein, DAS44 disease activity score of 44 joints, ESR erythrocyte sedimentation rate, FDA functional disability assessment, HAQ Health Assessment Questionnaire, IQR interquartile range, l liter, mg milligram, mm millimeter, n number, RAID Rheumatoid Arthritis Impact of Disease questionnaire, SD standard deviation, SJC44 swollen joint count of 44 joints, TJC44 tender joint count of 44 joints, VAS visual analogue scale
*Significant difference (p < 0.05) in baseline values for patients in and not in self-perceived remission after 12 weeks of treatment