医学
荟萃分析
随机对照试验
嗅觉缺失
严格标准化平均差
置信区间
鼻窦炎
内科学
梅德林
系统回顾
慢性鼻窦炎
相对风险
外科
法学
传染病(医学专业)
政治学
疾病
2019年冠状病毒病(COVID-19)
作者
Ebraheem Albazee,Hemail M. Alsubaie,Roaa Ali Alkanderi,Mubarak Althaidy,Husain Alsafar,Saad Alsaleh,Shawkat Abdulrahman
摘要
Abstract Introduction To comprehensively evaluate the reported clinical effectiveness of platelet‐rich plasma (PRP) in patients with chronic sinusitis undergoing endoscopic sinus surgery (ESS). Methods We performed a systematic review and meta‐analysis of randomised controlled trials (RCTs). Five digital online databases (PubMed, Scopus, Web of Science, Google Scholar and Cochrane CENTRAL) were searched from inception up to 1st May 2023. Our specific outcomes involved postoperative nasal endoscopy scores measured via Lund‐Kennedy score or Meltzer score, olfactory sensation scores and pre‐operative anosmia duration. All data were pooled as standardised mean difference (SMD) with a 95% confidence interval (CI), using the RevMan software. Results Six RCTs were included in this systematic review and meta‐analysis, with a total of 169 patients. The risk of bias in the included RCTs was low in three RCTs, some concerns in one RCT and high risk in two RCTs. The overall analysis of the postoperative nasal endoscopy scores showed that the PRP group had lower scores compared to the control group ( n = 3 RCTs, SMD = −1.19; 95% CI [−1.94, −0.44], p = .002). There was no significant difference between the PRP and control groups regarding anosmia duration ( n = 2 RCTs, SMD = 0.21; 95% CI [−0.17, 0.59], p = 0.28) or olfactory sensation scores, despite the PRP group having higher scores ( n = 2 RCTs, SMD = 0.53; 95% CI [−0.32, 1.39], p = 0.22). Conclusion This study highlights the potential advantages of using PRP as an additional treatment for individuals with chronic sinusitis undergoing ESS. The improvements associated with PRP include facilitating wound healing, reducing inflammation and enhancing surgical outcomes. To optimise the use of PRP in clinical settings, future research should focus on conducting larger trials with standardised protocols.
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