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在存在感染、肿瘤和血液系统合并症的情况下,富血小板血浆注射治疗肌肉骨骼疾病的适应症和禁忌症:来自GRIIP(国际血小板注射研究组)的2025年正式共识

Indications and contraindications to platelet-rich plasma injections in musculoskeletal diseases in case of infectious, oncological and haematological comorbidities: A 2025 formal consensus from the GRIIP (International Research Group on Platelet Injections).

作者信息

Eymard Florent, Louati Karine, Noel Éric, Abouqal Redouane, Adam Philippe, Allali Fadoua, Antherieu Gabriel, Caers Jo, Cognasse Fabrice, Collado Hervé, Darrieutort-Laffite Christelle, Frère Corinne, Frey Alain, Gavillet Mathilde, Gremeaux Vincent, Heiblig Mael, Jerusalem Guy, Joly Charlotte, Kaux Jean-François, Lamontagne Martin, Leclerc Mathieu, Léonard Philippe, Lepeule Raphaël, Lopez-Trabada-Ataz Daniel, Magalon Jérémy, Michel Fabrice, Ornetti Paul, Oury Cécile, Pons-Tostivint Elvire, Real Fernando, Robert Ghislaine, Sanchez Mikel, Silvestre Alain, Bard Hervé

机构信息

Department of Rheumatology, Créteil, AP-HP Henri Mondor Hospital, Créteil, France.

Department of Rheumatology, AP-HP Saint Antoine Hospital, Paris, France.

出版信息

Knee Surg Sports Traumatol Arthrosc. 2025 Jun;33(6):2293-2306. doi: 10.1002/ksa.12682. Epub 2025 Apr 22.

Abstract

PURPOSE

Platelet-rich plasma (PRP) could be a vector for certain diseases, and its composition may vary by pathologic condition. The main comorbidities that could affect PRP composition are infectious, oncologic and haematologic. In addition to potential alteration of clinical response, these pathologies could have a significant impact on the local tolerance of PRP as well as a risk of disease dissemination to the injection site. To date, there are few specific recommendations related to these comorbidities to guide clinicians. Therefore, the International Research Group on Platelet Injections (GRIIP) supported a consensus project to develop these recommendations.

METHODS

Following the 'recommendations by formal consensus' methodology, a steering committee performed a literature review and drafted an initial set of recommendations. They were evaluated by an international rating group (15 specialists in musculoskeletal [MSK] diseases, five haematologists, four oncologists, three infectiologists and four scientists specialising in platelet physiology). From this rating, the first set of recommendations was discussed in a plenary meeting and then modified by the steering committee. Finally, four overarching principles and 23 recommendations were re-evaluated by the rating group. Recommendations were classified as appropriate or not, with strong or relative agreement, or uncertain.

RESULTS

From the 23 recommendations, 10 concerned infectious diseases (viral and bacterial infections; dialysis; immunosuppressive drugs; dental care…), five oncologic diseases (local tumour; cured, active or in remission cancer…) and eight haematologic diseases (cytopenia; cured, active or stabilised cured hemopathy; monoclonal gammopathy…). All were considered appropriate by the experts (median = 9; range = 8-9), with strong or relative agreement. Due to the paucity of literature data, the recommendations are mainly based on expert opinion (Grade D).

CONCLUSION

This consensus project provides four overarching principles and 23 recommendations related to contraindications of PRP injections in case of infectious, oncologic or hematologic diseases, validated by an international expert group.

LEVEL OF EVIDENCE

Level I.

摘要

目的

富血小板血浆(PRP)可能是某些疾病的传播媒介,其成分可能因病理状况而异。可能影响PRP成分的主要合并症包括感染性、肿瘤性和血液学方面的疾病。除了可能改变临床反应外,这些病理状况还可能对PRP的局部耐受性产生重大影响,并存在疾病传播至注射部位的风险。迄今为止,针对这些合并症的具体指导建议很少,难以指导临床医生。因此,国际血小板注射研究小组(GRIIP)支持开展一项共识项目以制定这些建议。

方法

按照“正式共识推荐”方法,一个指导委员会进行了文献综述并起草了一套初步建议。这些建议由一个国际评级小组(15名肌肉骨骼[MSK]疾病专家、5名血液学家、4名肿瘤学家、3名感染病学家和4名血小板生理学专家)进行评估。根据该评级,在全体会议上对第一套建议进行了讨论,然后由指导委员会进行修改。最后,评级小组对四项总体原则和23条建议进行了重新评估。建议被分类为适当或不适当,分为强烈或相对同意,或不确定。

结果

在23条建议中,10条涉及感染性疾病(病毒和细菌感染;透析;免疫抑制药物;牙科护理……),5条涉及肿瘤性疾病(局部肿瘤;治愈、活跃或缓解期癌症……),8条涉及血液学疾病(血细胞减少症;治愈、活跃或稳定的血液疾病;单克隆丙种球蛋白病……)。所有这些建议均被专家认为是适当的(中位数=9;范围=8-9),有强烈或相对同意。由于文献数据匮乏,这些建议主要基于专家意见(D级)。

结论

该共识项目提供了四项总体原则和23条与感染性、肿瘤性或血液学疾病情况下PRP注射禁忌相关的建议,经国际专家组验证。

证据水平

I级。

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