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经皮椎间盘内注射高浓度富血小板血浆治疗慢性腰椎间盘源性疼痛的临床疗效。

Clinical outcomes following intradiscal injections of higher-concentration platelet-rich plasma in patients with chronic lumbar discogenic pain.

机构信息

Regenerative SportsCare Institute, New York, NY, USA.

Department of Physiatry, Hospital for Special Surgery, 535 E. 70th Street, New York, NY, 10021, USA.

出版信息

Int Orthop. 2022 Jun;46(6):1381-1385. doi: 10.1007/s00264-022-05389-y. Epub 2022 Mar 28.

Abstract

PURPOSE

This study aimed to assess clinical outcomes following intradiscal injections of higher-concentration (> 10 ×) platelet-rich plasma (PRP) in patients with chronic lumbar discogenic pain and to compare outcomes with a historical cohort.

METHODS

This retrospective study included 37 patients who received intradiscal injections of higher-concentration (> 10 ×) PRP and had post-procedure outcomes data (visual numerical scale pain score, Functional Rating Index [FRI], and NASS Patient Satisfaction Index). Outcomes were compared to a historical cohort of 29 patients who received intradiscal injections of < 5X PRP.

RESULTS

Pain and FRI scores significantly improved by 3.4 ± 2.5 and 46.4 ± 27.6, respectively, at 18.3 ± 13.3 months following intradiscal injections of > 10 × PRP (p < 0.001). These improvements were greater than those reported by the historical cohort (1.7 ± 1.6 and 33.7 ± 12.3; p = 0.004 and 0.016, respectively). Additionally, the satisfaction rate was higher in patients receiving > 10 × PRP compared to those receiving < 5 × PRP (81% vs. 55%; p = 0.032).

CONCLUSIONS

Findings from this study suggest that clinical outcomes can be optimized by using PRP preparations that contain a higher concentration of platelets. Further research is needed to continue to optimize the composition of PRP used to treat patients with lumbar disc disease.

摘要

目的

本研究旨在评估在慢性腰椎间盘源性疼痛患者中进行高浓度(> 10×)富含血小板血浆(PRP)椎间盘内注射的临床结果,并与历史队列进行比较。

方法

本回顾性研究纳入了 37 名接受高浓度(> 10×)PRP 椎间盘内注射且具有术后结局数据(视觉数字评分量表疼痛评分、功能评定指数[FRI]和 NASS 患者满意度指数)的患者。将结果与接受<5X PRP 椎间盘内注射的 29 名历史队列患者进行比较。

结果

在接受> 10×PRP 椎间盘内注射后 18.3±13.3 个月时,疼痛和 FRI 评分分别显著改善了 3.4±2.5 和 46.4±27.6(p<0.001)。这些改善明显大于历史队列的报道(1.7±1.6 和 33.7±12.3;p=0.004 和 0.016,分别)。此外,与接受<5X PRP 治疗的患者相比,接受> 10X PRP 治疗的患者的满意度更高(81% vs. 55%;p=0.032)。

结论

本研究结果表明,通过使用含有更高浓度血小板的 PRP 制剂可以优化临床结果。需要进一步的研究来继续优化用于治疗腰椎间盘疾病患者的 PRP 组成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a1/9117340/484e38093a78/264_2022_5389_Fig1_HTML.jpg

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