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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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A proposed medication score for long-term trials of treatment of canine atopic dermatitis sensu lato

Thumbnail
Συγγραφέας
Saridomichelakis M.N., Favrot C., Jackson H.A., Bensignor E., Prost C., Mueller R.S.
Ημερομηνία
2021
Γλώσσα
en
DOI
10.1002/vetr.19
Λέξη-κλειδί
alimemazine
antifungal agent
antiinfective agent
barazone
budesonide
ceramide
cetirizine
chlorpheniramine maleate
cholesterol
cyclosporine
dimetindene
essential fatty acid
fexofenadine
genesis
hydrocortisone aceponate
hydroxyzine
lokivetmab
masitinib
methylprednisolone
oclacitinib
prednisolone
prednisone
recombinant gamma interferon
recombinant interferon
recombinant omega interferon
shampoo
tacrolimus
triamcinolone
unclassified drug
animal experiment
Article
atopic dermatitis
Canis
correlational study
Dermatophagoides
desensitization
long term care
medication score
nonhuman
scoring system
supplementation
treatment duration
treatment outcome
animal
atopic dermatitis
combination drug therapy
dog
dog disease
female
male
treatment outcome
veterinary medicine
Animals
Dermatitis, Atopic
Dog Diseases
Dogs
Drug Therapy, Combination
Female
Male
Treatment Outcome
John Wiley and Sons Inc
Εμφάνιση Μεταδεδομένων
Επιτομή
Background: The use of concurrent medications is necessary in trials of treatment of canine atopic dermatitis. Our aim was to use the best available evidence to construct and then to validate a medication score (MS) formula that will estimate the impact of concurrent medications on trial outcomes. Methods: Trials of 15 interventions were scrutinized to find those that were consistent in terms of specific medication, administration route and dosage regimen. A MS was constructed in five steps, starting from assigning a score of 1 for each day on oral prednisone, prednisolone or methylprednisolone at 0.5–1.0 mg/kg. The MS score was validated using the clinical records of 35 dogs with atopic dermatitis that had been treated for a period of 12 ± 2 weeks with six of these medications and compared with a previously published non-validated MS. Results: A MS could be assigned to eight treatments, six of which had been administered to the 35 dogs. A positive correlation was seen with the previously published MS and a negative correlation with changes in lesional and pruritus scores. Conclusion: This MS may be a useful tool in new studies evaluating the efficacy of treatments in canine atopic dermatitis. © 2021 British Veterinary Association
URI
http://hdl.handle.net/11615/78796
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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