Platelet‐rich plasma following endoscopic sinus surgery in patients with chronic sinusitis: A systematic review and meta‐analysis of randomised controlled trials

Author:

Albazee Ebraheem1ORCID,Alsubaie Hemail M.2ORCID,Alkanderi Roaa1ORCID,Althaidy Mubarak1ORCID,Alsafar Husain1ORCID,Alsaleh Saad3ORCID,Abdulrahman Shawkat4ORCID

Affiliation:

1. Kuwait Institute for Medical Specializations (KIMS) Kuwait City Kuwait

2. Otorhinolaryngology‐Head and Neck Surgery and Communication Sciences Department King Faisal Specialist Hospital and Research Center Riyadh Saudi Arabia

3. Department of Otolaryngology‐Head & Neck Surgery College of Medicine, King Saud University Riyadh Saudi Arabia

4. Department of Otolaryngology‐Head & Neck Surgery Tallaght University Hospital Dublin Ireland

Abstract

AbstractIntroductionTo comprehensively evaluate the reported clinical effectiveness of platelet‐rich plasma (PRP) in patients with chronic sinusitis undergoing endoscopic sinus surgery (ESS).MethodsWe 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.ResultsSix 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).ConclusionThis 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.

Publisher

Wiley

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