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DOI 10.55563/clinexprheumatol/ycy3k7

Медицинская библиотека · Clinical and experimental rheumatology · 2023

Autologous fat or adipose-derived stem cell grafting in systemic sclerosis treatment: a systematic review and meta-analysis.

Cao Yang, Kan Haoxuan, Ma Xuda, Zhang Yuelun, Huang Jiuzuo, Long Xiao

МетаанализСистематический обзорСтатьяПеревод в очереди

Аннотация

OBJECTIVES

Systemic sclerosis (SSc) is characterised by vasculopathy and progressive fibrosis of the skin. The aim of this article is to analyse and summarise the efficacy and safety of autologous fat (AF), stromal vascular fraction (SVF) and adipose-derived stem cell (ADSC) grafting in the treatment of SSc, providing evidence for clinical application.

METHODS

The research involves the efficacy and safety of AF, SVF and ADSC grafting in the treatment of patients with SSc. The studies were screened and selected independently by two authors based on pre-specified criteria. The data extraction and quality assessment were also performed independently by two authors.

RESULTS

Fifteen studies were eligible for inclusion. Skin thickness reduced following SVF or AF therapy, but there was no significant difference. All measures used to assess fingertip symptoms revealed a significant improvement. Notably, SVF and AF were found to have the most impact on Raynaud's phenomenon improvement. The ADSC group improved the most in terms of finger pain alleviation. SVF reported the highest proportion of adverse events, accounting for approximately half of the cases.

CONCLUSIONS

AF, SVF, and ADSC all displayed therapeutic effects of improving SSc, but differences existed in the effects on different symptoms. Plastic surgeons should choose the most suitable treatment strategy after comprehensively evaluating the patient's clinical manifestations.

Для цитирования: Cao Yang, Kan Haoxuan, Ma Xuda, Zhang Yuelun, Huang Jiuzuo, Long Xiao. Autologous fat or adipose-derived stem cell grafting in systemic sclerosis treatment: a systematic review and meta-analysis.. Clinical and experimental rheumatology. 2023. DOI: 10.55563/clinexprheumatol/ycy3k7.

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