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Enregistrement W4380852961 · doi:10.2106/jbjs.23.00496

In Knee OA, Adding Hyaluronic Acid (HA) Vs. Cross-Linked HA to Intra-Articular Platelet-Rich Plasma Did Not Differ for Pain at 6 Months

2023· letter· en· W4380852961 sur OpenAlexaboutno aff
Asheesh Bedi

Notice bibliographique

RevueJournal of Bone and Joint Surgery · 2023
Typeletter
Langueen
DomaineMedicine
ThématiqueOsteoarthritis Treatment and Mechanisms
Établissements canadiensnon disponible
Organismes subventionnairesnon disponible
Mots-clésHyaluronic acidPlatelet-rich plasmaIntra articularPlateletOsteoarthritisMedicineInternal medicinePathologyAnatomy

Résumé

récupéré en direct d'OpenAlex

Huang H-Y, Hsu C-W, Lin G-C, Lin H-S, Chou Y-J, Liou I-H, Sun S-F. Comparing efficacy of a single intraarticular injection of platelet-rich plasma (PRP) combined with different hyaluronans for knee osteoarthritis: a randomized-controlled clinical trial. BMC Musculoskelet Disord. 2022 Nov 4;23(1):954. Question: In patients with knee osteoarthritis (OA), what is the effect of adding hyaluronic acid (HA) versus a cross-linked HA to a single intra-articular injection of platelet-rich plasma (PRP) on pain? Design: Randomized (allocation concealed), blinded (patients and outcome assessors), controlled trial with 6 months of follow-up. Setting: Kaohsiung Veterans General Hospital, Taiwan. Patients: 99 patients aged 20 to 85 years (mean age, 61 years; 64% women) who had symptomatic knee OA (knee pain ≥30 mm on a 100-mm [worst pain] visual analog scale [VAS] for >6 months despite nonoperative treatment) and radiographs in the past 6 months showing Kellgren-Lawrence grade-2 knee OA. Exclusion criteria were orthopaedic surgery on the target knee, spine, or lower limb; disabling hip or foot OA; knee instability; joint effusion or marked valgus/varus deformity; intra-articular injections into the target knee in the past 6 months; or treatment with anticoagulants or antiaggregants. 96% of patients completed follow-up at 6 months. Intervention: Patients were allocated to a single intra-articular injection of HA, 2.5 mL (Artz; Seikagaku), followed immediately by a single intra-articular injection of PRP, 3 mL (n = 50); or cross-linked HA, 3 mL (HYAJOINT Plus; SciVision Biotech), followed by PRP, 3 mL (n = 49), using an anterolateral approach with the knee in 90° of flexion. Patients stopped analgesic or nonsteroidal anti-inflammatory drugs 7 days before baseline and were not to use analgesics, chondroprotective supplements, or physiotherapy during the trial. Acetaminophen, 4 g/day, was allowed as rescue treatment. Main outcome measures: The primary outcome was pain (VAS; score range 0 [no pain] to 100 [worst imaginable pain]). Secondary outcomes included the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), Lequesne index, single-leg stance test (SLS), and adverse events. Main results: Key efficacy outcomes at 6 months are reported in Table I. The groups did not differ for pain at 1, 3, or 6 months. At 6 months, the HA + PRP group had less knee stiffness and shorter SLS time compared with the cross-linked HA + PRP group. No serious adverse events were reported. TABLE I - Single intra-articular platelet-rich plasma (PRP) injection with hyaluronic acid (HA) versus a cross-linked HA in patients with knee osteoarthritis (intention-to-treat analysis)* Outcomes Mean Adjusted mean between-group difference at 6 months (95% CI) HA + PRP Cross-linked HA + PRP Pain† 11.9 8.7 2.8 (−3.0 to 8.6) WOMAC-total‡ 16.4 19.5 −2.5 (−7.4 to 2.3) WOMAC-pain‡ 3.2 3.9 −0.6 (−1.6 to 0.4) WOMAC-stiffness‡ 1.3 1.8 −0.6 (−0.1 to −1.0) WOMAC-function‡ 11.8 13.9 −1.4 (−5.0 to 2.2) Lequesne index§ 5.0 5.8 −0.8 (−2.1 to 0.5) Single-leg stance#(sec) 37.4 44.8 −13.8 (−23.0 to −4.6) *CI = confidence interval, WOMAC = Western Ontario and McMaster Universities Osteoarthritis Index.†Visual analog scale, score range 0 (no pain) to 100 (worst imaginable pain).‡24-item scale, score range 0 (best condition) to 96 (worst condition); subscales for pain (5 items, score range 0 to 20), stiffness (2 items, score range 0 to 8), and physical function (17 items, score range 0 to 68).§Knee pain severity in past week; score range 0 (no pain) to 24 (worst pain).#Static balance test of time standing on the study leg. Conclusion: In knee OA, adding HA versus cross-linked HA to a single intra-articular injection of PRP did not differ for pain at 6 months. Source of funding: Kaohsiung Veterans General Hospital Research Fund, Taiwan. For correspondence: Shu-Fen Sun, Department of Physical Medicine and Rehabilitation, Kaohsiung Veterans General Hospital, Taiwan. E-mail address: [email protected]. Commentary The randomized controlled trial by Huang and colleagues compared the efficacy of 2 viscosupplementation injections delivered with PRP in patients with moderate knee OA. Basic science studies have shown that both leukocyte-poor PRP and HA injections may have anti-inflammatory and chondroprotective effects that may ameliorate the symptoms of knee OA. Furthermore, studies have reported favorable outcomes with high-molecular-weight and biologically fermented HA compared with low-molecular-weight avian-derived formulations3. The results of the current trial suggest that delivery of PRP with either of these 2 HA formulations is safe and effective based on patient-reported outcomes (PROs). The cross-linked HA formulation with PRP improved static balance (SLS scores) for up to 6 months after injection, but the groups were largely equivalent in other PROs assessed through 6 months. The trial provides reasonable-quality evidence that PRP and HA treatment is an effective treatment option for patients with moderate OA of the knee (Kellgren-Lawrence grade 2), aligning with the results of Ciapini et al. of favorable outcomes for 6 months after PRP plus HA treatment1. It does not, however, provide any insights as to whether combined treatment with PRP and HA is more effective than either of these treatments alone. A recent systematic review by Belk et al. suggested that PRP or concentrated bone marrow aspirate is more effective in isolation than with HA injection2. The trial results are not broadly generalizable because patients with more severe radiographic arthritic changes were excluded, and all patients received 1 specific formulation of leukocyte-poor PRP with approximately 2.4 times the baseline platelet concentration. Future studies would benefit from additional treatment groups for each HA and PRP treatment alone, as well as corticosteroid injections, which are still frequently prescribed for patients with knee OA. In addition, assessment of structural changes based on serial radiographic and/or magnetic resonance imaging would be invaluable to assess if these treatments offer benefits beyond symptomatic relief. A recent randomized controlled trial by Küçükakkaş et al.3 reported greater knee femoral cartilage thickness with HA injection compared with PRP injection.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,004
score de la tête « metaresearch » (Gemma)0,005
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Essai randomisé · Signal consensuel: Essai randomisé
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,006
Score d'incertitude au seuil0,019

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0040,005
Méta-épidémiologie (sens strict)0,0020,001
Méta-épidémiologie (sens large)0,0050,004
Bibliométrie0,0010,001
Études des sciences et des technologies0,0010,001
Communication savante0,0010,001
Science ouverte0,0010,001
Intégrité de la recherche0,0030,003
Charge utile insuffisante (le modèle a refusé de juger)0,0060,001

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,028
Tête enseignante GPT0,259
Écart entre enseignants0,230 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeEssai randomisé
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations0
Publié2023
Routes d'admission1
Résumé présentoui

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