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85% of COVID-19 patients and are often some       Material and Methods
          of  the  earliest  and  most  specific  indicators   Sample enrollment and evaluation
          of infection . Although initially assumed as      Patients who attended the Otorhinolaryngology
                      3
          transient by many authors  it is now known        Department's smell and taste clinic at Centro
                                     4,5
          that  about  15% of  infected  patients  do  not   Hospitalar Universitário de Santo António
          recover  for several months . Then, many          were evaluated for eligibility. Data related
                                       5,6
          COVID-19 patients may experience long-term        to anamnesis and physical examination
          changes in their smell and taste perception,      was collected according to the institutional
          which  adds  to  the  ongoing  burden  of         protocol described elsewhere .
                                                                                         1
          long COVID-19 .  Certainly, this underlooked      The inclusion criteria were: age ≥18 years, abrupt
                         7
          “olfactory pandemic” persists nowadays and        onset of olfactory impairment coincident with
          calls to be combated. With the former in mind,    SARSCoV-2  infection  verified  by  nasal  swab
          unravelling treatment solutions for long-lasting   and Polymerase Chain Reaction technique
          olfactory impairment has never seemed more        (PCR),  subjective  persistence  of  pCIOD  ≥
          urgent.  Various  therapeutic  modalities  have   12 months, objective olfactory perception
                1
          been suggested to  treat persistent COVID-19      threshold  (OPT)  ≤  7  at  the  time  of  PRP
          induced olfactory dysfunction (pCIOD) . These     injection, having performed olfactory training
                                               1,8
          include  topical nasal corticosteroids, intranasal   and adjuvant therapy without achieving
          vitamin A + E , vitamin B complex tablets,        substantial improvement (measured by at
          among others  . Nevertheless, besides olfactory   least two consecutive 3 months apart OPT
                        1
          training, no adjuvant therapy has unequivocally   evaluations)  and cognitive  ability to  sign
          shown  benefit .  Recently, a novel approach      informed consent. Exclusion criteria were
                        1,8
          for  treating  persistent  olfactory  dysfunction   as follows: Chronic rhinosinusitis, history of
          has been described : injection of platelet rich   head trauma with loss of consciousness,
          plasma (PRP) into the olfactory mucosa     9,10 .   documented       pre-existing      olfactory
          PRP is an autologous blood product                dysfunction before COVID-19, pregnancy,
          containing supraphysiologic levels of growth      previous  neurosurgery  or endoscopic nasal
          factors and cytokines 11,12 . It has been shown   surgery, known olfactory bulb lesions on
          to promote tissue  regeneration  and repair       imaging, known neurologic disease (Parkinson's,
          and has been medically used in various            Dementia, Epilepsy), major psychiatric disease,
          clinical scenarios, such as in osteoarticular     inability to tolerate nasal endoscopy, known
          pathology, skin rejuvenation, wound healing,      platelet or coagulation disorders, undergoing
          and hair regrowth   11,12 . PRP injection was     anti-inflammatory  or  anticoagulant  therapy,
          proposed as a potential new therapy for           and concurrent pathology presumably needing
          olfactory dysfunction treatment in 2019, when     anti-inflammatory treatment in the next 30 days
          Yan  et  al  brought  the  first  pilot  study    with   following injection.
          preliminary promising results . The same          A visual analog scale (VAS) was used to
                                          9
          group published the first randomized trial on     subjectively  assess  olfactory  impairment  on
          PRP  application  in  late  2022,  with  favorable   a scale from 0 to 10, with participants asked
          results  The main objective of this work is to    to rate their satisfaction with their smell
                10.
          describe the resulting olfactory outcomes of      and taste function (10 indicating a return to
          pCIOD patients submitted to PRP injection         normal). This measurement was taken at
          while addressing any possible ensuing             three time points: immediately before the
          complications. A distinctive, customized          injection, one month after, and three months
          protocol was developed at the smell and taste     after the injection. The olfactory perception
          consultation of Centro Hospitalar Universitário   threshold  (OPT)  was  measured  in  the  same
          de Santo António, and its implementation is       time  points  by  means  of  Burghart  Sniffin'
          outlined as follows.                              Sticks n-butanol threshold test with 16 levels



     346  Revista Portuguesa de Otorrinolaringologia - Cirurgia de Cabeça e Pescoço
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