xRead - Olfactory Disorders (September 2023)
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INTERNATIONAL CONSENSUS ON OLFACTION
TABLE IX.34 Use of vitamin A to treat OD Study Year LOE Study design
Study groups
Clinical end point Conclusions
Subjective olfactory improvement
Improvement in odor detection in 50 of 56 patients
Patients with olfactory disorders (eg, postinfectious, posttraumatic, idiopathic; n = 56) treated with high-dose systemic vitamin A therapy (injection, tablets, oral emulsion; 50,000 to 150,000 IU/day) for up to 12weeks Vitamin A–deficient patients (n = 27) treated with oral vitamin A (10,000 μ g/day) for 4weeks Patients with postinfectious or posttraumatic olfactory disorder (n = 52) receiving either oral vitamin A at a dose of 10,000 IU/day or placebo for 3 months Patients with acne (n = 33) treated with oral
Duncan and
1962 4
Case series over a
period of 15 years with differences in interventions
Briggs 1570
Garrett
1984 4
Descriptive
Pyridine detection and recognition threshold improvement
Significant improvement in olfactory threshold
Laster et al 1510
(noncontrolled)
SS-TDI
No significant difference between placebo and verum groups regarding the TDI change and subfunction (TDI) change after treatment
Reden
2012 2
Double-blind,
et al 456
improvement
placebo-controlled, randomized clinical
Kartal
2017 4
Descriptive
Improvement in SS-ID
Significant improvement in odor identification
et al 1571
(noncontrolled)
isotretinoin (0.5 to 0.8 mg/kg per day) for 3 months
Improvement in SS-TDI
OT + vitamin A produced significantly greater improvement compared with training alone, in discrimination score for all patients and in threshold and
Hummel et al 1572
2017 4
Retrospective cohort Patients with postinfectious (n = 102) or posttraumatic (n = 68) olfactory disorder (n = 170)
Treated with topical vitamin A 10,000 IU once daily, for 8 weeks and performing OT for 12 weeks Performing OT for 12 weeks only
discrimination in the postinfectious group
In the postinfectious group, significantly more patients showed improved general OF with combined therapy compared with training alone LOE level of evidence; OD = olfactory dysfunction; OF = olfactory function; OT = olfactory training; SS-ID = Sniffin’ Sticks identification only; SS-TDI = Sniffin’ Sticks threshold, discrimination, identification combination; TDI = threshold, discrimination, and identification.
reported that the improvement rate in patients with post– upper respiratory tract infection dysfunction, who received treatment with intranasal steroid treatment alone, TSS oral administration alone, or a combination of steroids and TSS, for 3 months, was 29%, 55%, and 60%, respectively. Most recently, Ogawa et al 1326 additionally reported on the time-course of olfactory recovery and the prognostic fac tors in patients with PIOD treated with TSS. They revealed that the recovery of OF often occurred during the early period, < 6 months from symptom onset, but the number of patients with recovery of OF increased for long-term symp toms 24 months after the first visit. This study also reported
that residual OF and younger age were prognostic factors for recovery of OF. 1326 Unfortunately, all of these studies are case series, with no placebo-control group and no tim ing restriction for enrollment, and therefore the potential for spontaneous resolution or other biases to confound these findings make these data currently inconclusive. Use of TSS for the treatment of OD Aggregate grade of evidence : C (Level 4: four studies). Benefit : Objective olfactory tests revealed the improve ment of OF by oral TSS administration. Lack of consid eration for spontaneous improvements, lack of control
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