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We read with interest Dr Turner's correspondence regarding our article.1 We completely agree with all the limitations raised, as we had already raised them in the discussion of our own investigation. As Dr Turner points out, the risk our specialty faces can be reduced with appropriate mitigation and use of personal protective equipment (PPE). Dr Turner has done an excellent job of summarizing the currently established risk for HCWs. [Extracted from the article]

Introduction: The current study evaluated the use of platelet‐rich plasma (PRP), an autologous blood product with supraphysiologic concentrations of growth factors, in the treatment of prolonged coronavirus disease 2019 (COVID‐19)–related smell loss. Methods: This multi‐institutional, randomized controlled trial recruited patients with COVID‐19 who had objectively measured smell loss (University of Pennsylvania Smell Identification Test [UPSIT] ≤ 33) between 6 and 12 months. Patients were randomized to three intranasal injections of either PRP or sterile saline into their olfactory clefts. The primary outcome measure was change in Sniffin' Sticks score (threshold, discrimination, and identification [TDI]) from baseline. The secondary end point measures included responder rate (achievement of a clinically significant improvement, ≥5.5 points TDI), change in individual TDI olfaction scores, and change in subjective olfaction via a visual analog scale. Results: A total of 35 patients were recruited and 26 completed the study. PRP treatment resulted in a 3.67‐point (95% CI: 0.05–7.29, p = 0.047) greater improvement in olfaction compared with the placebo group at 3 months and a higher response rate (57.1% vs 8.3%, odds ratio 12.5 [95% exact bootstrap confidence interval, 2.2–116.7]). There was a greater improvement in smell discrimination following PRP treatment compared with placebo but no difference in smell identification or threshold. There was no difference in subjective scores between PRP and placebo. No adverse effects were reported. Conclusion: Olfactory function following COVID‐19 can improve spontaneously after 6 months and can improve to a greater extent with PRP injection. These data build on the promise of PRP to be a safe potential treatment option for patients with COVID‐19–related smell loss, and larger‐powered studies will help further assess its efficacy. [ABSTRACT FROM AUTHOR]

A total of 69.8% (579/829) of responders with smell loss reported that their smell dysfunction had adversely impacted their quality of life (QoL). Keywords: olfaction; olfactory disorders; quality of life EN olfaction olfactory disorders quality of life 1558 1560 3 07/26/23 20230801 NES 230801 The coronavirus disease 2019 (COVID-19) pandemic has put unprecedented strains on healthcare systems across the globe and this is thought to continue with the advent of long COVID. High prevalence of persistent smell loss and qualitative smell dysfunction during the coronavirus disease 2019 (COVID-19) pandemic in the United States: Urgent need for clinical trials. [Extracted from the article]