Effectiveness of Platelet‐Rich Plasma for COVID‐19‐Related Olfactory Dysfunction: A Controlled Study

Author:

Lechien Jerome R.1234,Saussez Sven24,Vaira Luigi A.5,De Riu Giacomo5,Boscolo‐Rizzo Paolo6,Tirelli Giancarlo6,Michel Justin7,Radulesco Thomas7

Affiliation:

1. Department of Otolaryngology Polyclinic of Poitiers, Elsan Poitiers France

2. Department of Human Anatomy and Experimental Oncology, Faculty of Medicine, UMONS Research Institute for Health Sciences and Technology University of Mons (UMons) Mons Belgium

3. Department of Otolaryngology–Head and Neck Surgery, Foch Hospital, School of Medicine, UFR Simone Veil Université Versailles Saint‐Quentin‐en‐Yvelines (Paris Saclay University) Paris France

4. Department of Otorhinolaryngology and Head and Neck Surgery CHU Saint‐Pierre Brussels Belgium

5. Maxillofacial Surgery Operative Unit, Department of Medicine, Surgery and Pharmacy University of Sassari Sassari Italy

6. Department of Medical, Surgical and Health Sciences, Section of Otolaryngology University of Trieste Trieste Italy

7. Department of Otorhinolaryngology and Head and Neck Surgery, APHM, IUSTI, CNRS, La Conception University Hospital Aix Marseille University Marseille France

Abstract

AbstractObjectiveTo investigate the effectiveness of platelet‐rich plasma (PRP) injection into the olfactory clefts of coronavirus disease 2019 (COVID‐19) patients with persistent olfactory dysfunction (OD).Study DesignControlled study.SettingMulticenter study.MethodsFrom March 2022 to November 2022, COVID‐19 patients with persistent OD were recruited from three European hospitals to undergo PRP injections into the olfactory clefts. Olfactory function was evaluated at baseline and 10 weeks postinjection with the Olfactory Disorder Questionnaire (ODQ) and threshold, discrimination, and identification (TDI) test. Data were compared with a control group of untreated patients.ResultsEighty‐one patients who underwent PRP injection and 78 controls were included. Sixty‐five PRP patients (80.3%) experienced subjective smell improvement after a mean duration of 3.4 ± 1.9 weeks. The parosmia, life quality statement, and ODQ sub‐ and total scores significantly decreased from pre‐ to 10‐week postinjection in the PRP group. The TDI sub‐ and total scores significantly increased 10 weeks postinjection. In controls, the ODQ score did not change over time, while the discrimination, identification, and total TDI scores significantly increase after 10 weeks of follow‐up. The 10‐week TDI and ODQ scores were significantly better in the PRP group compared with the controls.ConclusionPatients who underwent PRP injection reported better 10‐week subjective and objective smell outcomes than controls. Future randomized‐controlled studies using saline injection into the olfactory cleft of controls are needed to determine the superiority of PRP over placebo.

Publisher

Wiley

Subject

Otorhinolaryngology,Surgery

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