Evidence map›Paper›PMID 30608614›Full record

ArticleRheumatology (Oxford, England)2019

Responsiveness of clinical and ultrasound outcome measures in musculoskeletal systemic lupus erythematosus.

Khaled Mahmoud, Ahmed S Zayat, Yuzaiful Yusof, Elizabeth Hensor, Philip G Conaghan, Paul Emery, Edward M Vital

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Review
  4. Improving the arthritis component of the SLEDAI-2K.Rheumatology (Oxford, England) · 2025
    Observational
  5. Article
  6. A glimpse into the future of systemic lupus erythematosus.Therapeutic advances in musculoskeletal disease · 2022
    Review
  7. Article
  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Khaled MahmoudLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds.
Ahmed S ZayatLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds.
Yuzaiful YusofLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds.
Elizabeth HensorLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds.
Philip G ConaghanLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds.
Paul EmeryLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds.
Edward M VitalLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds.

Funding

Department of Health CS-2013-13-032Department of Health DRF-2014-07-155Department of Health RTF/01/097Medical Research Council MR/M01665X/1MRF_ MRF-159-0003-ELP-VITAL
6 · The paper itself

Abstract

objectiveTo assess the responsiveness of clinical outcome measures in musculoskeletal SLE compared with US.

methodsA prospective pilot study was conducted in consecutive SLE patients with inflammatory musculoskeletal symptoms. Clinical assessments including SLEDAI, BILAG, 28 tender and swollen joint counts, physician and patient visual analogue scales (VAS), and US were performed at 0, 2 and 4 weeks following 120 mg i.m. methylprednisolone acetate. Responsiveness was analysed using changes and effect sizes using Cohen's criteria.

resultsTwenty patients were recruited. Fifteen out of 20 had clinical swelling at baseline. All clinical and US parameters were significantly improved at week 4 (all P ⩽ 0.01). Musculoskeletal-BILAG score improved in 16/20. Musculoskeletal-SLEDAI improved in 7/20. SLE responder index 4 criteria were assessed in 19 patients with SLEDAI ⩾4 at baseline and were met in 9/19 at 4 weeks. Effect sizes at 4 weeks were large (>0.5) for US, physician VAS and BILAG, and medium (>0.3) for joint counts and SLEDAI. Large effect sizes for improvement in US grey-scale and power Doppler were observed in both SLE responder index 4 responders (r = -0.51 and -0.56, respectively) and non-responders (r = -0.62 and -0.59, respectively) at 4 weeks.

conclusionThis is the first study to measure the responsiveness of clinical outcome measures in musculoskeletal SLE against an objective inflammation measure. BILAG and physician VAS were the most responsive clinical instruments. US was highly responsive in musculoskeletal SLE, while SLEDAI and joint counts appeared suboptimal for detection of improvement. These results suggest that clinical trials based on the SLEDAI and SLE responder index 4 may underestimate the efficacy of therapy in SLE.

Identifiers

PMID30608614
PMCPMC6649792

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.