Evidence map›Paper›PMID 35243362›Full record

ArticleThe Lancet. Rheumatology2022

The STAR care pathway for patients with pain at 3 months after total knee replacement: a multicentre, pragmatic, randomised, controlled trial.

Vikki Wylde, Wendy Bertram, Emily Sanderson, Sian Noble, Nicholas Howells, Tim J Peters, Andrew D Beswick, Ashley W Blom, Andrew J Moore, Julie Bruce and 8 more

Erratum issued Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in The Lancet. Rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT07629388 (Comparative Study Assessing the Efficacy of a Combined Distal Femoral Nerve Block for Postoperative Analgesia Following Total Knee Arthroplasty), which is not on this map. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 pooled it
10.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

NCT07629388 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

Comparative Study Assessing the Efficacy of a Combined Distal Femoral Nerve Block for Postoperative Analgesia Following Total Knee Arthroplasty (TKA)

TypeinterventionalSponsorGCS Ramsay Santé pour l'Enseignement et la RechercheRan2026 to 2027Enrolled240ConditionsPain After Total Knee Arthroplasty, Pain ManagementArmsCombined distal femoral nerve block, Saphenous nerve block alone, Standard perioperative care in both groups
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 3 syntheses or guidelines pooled it, 48 citations in OpenAlex.

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  12. Co-Designing the Early Pain Intervention After Knee Replacement (EPIK) Model of Care for People With Persistent Pain After Knee Replacement.Health expectations : an international journal of public participation in health care and health policy · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 9 institutions in 1 country.

Vikki WyldeBristol Medical School, University of Bristol, Bristol, UK.
Wendy BertramBristol Medical School, University of Bristol, Bristol, UK.
Emily SandersonBristol Trials Centre, University of Bristol, Bristol, UK.
Sian NobleBristol Medical School, University of Bristol, Bristol, UK.
Nicholas HowellsNorth Bristol NHS Trust, Bristol, UK.
Tim J PetersBristol Medical School, University of Bristol, Bristol, UK.
Andrew D BeswickBristol Medical School, University of Bristol, Bristol, UK.
Ashley W BlomBristol Medical School, University of Bristol, Bristol, UK.
Andrew J MooreBristol Medical School, University of Bristol, Bristol, UK.
Julie BruceWarwick Clinical Trials Unit, Division of Health Sciences, University of Warwick, Warwick, UK.
David A WalshPain Centre, Versus Arthritis/National Institute for Health Research Nottingham Biomedical Research Centre, University of Nottingham and Sherwood Forest Hospitals NHS Foundation Trust, Nottingham, UK.
Christopher EcclestonCentre for Pain Research, The University of Bath, Bath, UK.
Shaun HarrisBristol Trials Centre, University of Bristol, Bristol, UK.
Kirsty GarfieldBristol Trials Centre, University of Bristol, Bristol, UK.
Simon WhiteCardiff and Vale University Health Board, Cardiff, UK.
Andrew TomsRoyal Devon and Exeter NHS Foundation Trust, Exeter, UK.
Rachael Gooberman-HillBristol Medical School, University of Bristol, Bristol, UK.
STAR trial group
University of Bristol · GBNorth Bristol NHS Trust · GBCardiff and Vale University Health Board · GBNational Institute for Health Research · GBNottingham Biomedical Research Centre · GBRoyal Devon & Exeter NHS Foundation Trust · GBUniversity Hospitals Bristol NHS Foundation Trust · GBUniversity of Bath · GBUniversity of Warwick · GB

Funding

Medical Research Council MC_PC_19095
6 · The paper itself

Abstract

backgroundApproximately 20% of people experience chronic pain after total knee replacement, but effective treatments are not available. We aimed to evaluate the clinical effectiveness and cost-effectiveness of a new care pathway for chronic pain after total knee replacement.

methodsWe did an unmasked, parallel group, pragmatic, superiority, randomised, controlled trial at eight UK National Health Service (NHS) hospitals. People with chronic pain at 3 months after total knee replacement surgery were randomly assigned (2:1) to the Support and Treatment After Replacement (STAR) care pathway plus usual care, or to usual care alone. The STAR intervention aimed to identify underlying causes of chronic pain and enable onward referrals for targeted treatment through a 3-month post-surgery assessment with an extended scope practitioner and telephone follow-up over 12 months. Co-primary outcomes were self-reported pain severity and pain interference in the replaced knee, assessed with the Brief Pain Inventory (BPI) pain severity and interference scales at 12 months (scored 0-10, best to worst) and analysed on an as-randomised basis. Resource use, collected from electronic hospital records and participants, was valued with UK reference costs. Quality-adjusted life-years (QALYs) were calculated from EQ-5D-5L responses. This trial is registered with ISRCTN, ISRCTN92545361.

findingsBetween Sept 6, 2016, and May 31, 2019, 363 participants were randomly assigned to receive the intervention plus usual care (n=242) or to receive usual care alone (n=121). Participants had a median age of 67 years (IQR 61 to 73), 217 (60%) of 363 were female, and 335 (92%) were White. 313 (86%) patients provided follow-up data at 12 months after randomisation (213 assigned to the intervention plus usual care and 100 assigned to usual care alone). At 12 months, the mean between-group difference in the BPI severity score was -0·65 (95% CI -1·17 to -0·13; p=0·014) and the mean between-group difference in the BPI interference score was -0·68 (-1·29 to -0·08; p=0·026), both favouring the intervention. From an NHS and personal social services perspective, the intervention was cost-effective (greater improvement with lower cost), with an incremental net monetary benefit of £1256 (95% CI 164 to 2348) at £20 000 per QALY threshold. One adverse reaction of participant distress was reported in the intervention group.

interpretationSTAR is a clinically effective and cost-effective intervention to improve pain outcomes over 1 year for people with chronic pain at 3 months after total knee replacement surgery.

fundingNational Institute for Health Research.

Identifiers

PMID35243362
PMCPMC8873030
OpenAlexW4210782142

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.