PMID- 24004561 OWN - NLM STAT- MEDLINE DCOM- 20140630 LR - 20211021 IS - 1746-6148 (Electronic) IS - 1746-6148 (Linking) VI - 9 DP - 2013 Sep 3 TI - Concurrent short-term use of prednisolone with cyclosporine A accelerates pruritus reduction and improvement in clinical scoring in dogs with atopic dermatitis. PG - 173 LID - 10.1186/1746-6148-9-173 [doi] AB - BACKGROUND: A randomized, unmasked, multicenter study was conducted to evaluate the rate of pruritus reduction and improvement in clinical scoring by cyclosporine A (5 mg/kg orally, once daily for 28 days) either alone (n = 25 dogs) or with concurrent prednisolone (1 mg/kg once daily for 7 days, followed by alternate dosing for 14 days; n = 23 dogs) for the treatment of atopic dermatitis in dogs. Dogs were included in the study after exclusion of other causes of pruritic dermatitis, and were assessed by dermatologists on days 0, 14 +/- 1 and 28 +/- 2. Assessments included: general physical examination, CADESI-03 lesion scoring, overall clinical response, evaluation of adverse events (AEs), body weight and clinical pathology (hematology, clinical chemistry and urinalysis). Owner assessments, including pruritus (visual analogue scale, VAS) and overall assessment of response were conducted every 3-4 days, either during visits to the clinic or at home. Owners reported AEs to the investigator throughout the study. RESULTS: By day 28 +/- 2 both treatment groups resulted in a significant improvement of the atopic dermatitis. Both investigators and owners agreed that concurrent therapy resulted in a quicker improvement of the dogs 'overall' skin condition and of pruritus (significant reduction of pruritus by day 3-4, 72.8% improvement by day 14 +/- 1), when compared to cyclosporine A alone (significant reduction of pruritus by day 7-8, 24.7% improvement by day 14 +/- 1). CADESI-03 scores significantly improved in both groups by day 14 +/- 1 onwards, and there were no significant differences in the scores between treatment groups at any time points. A total of 56 AEs (cyclosporine A alone = 34; concurrent therapy = 22) were reported in 33 dogs. No dogs died or stopped treatment due to an AE. The most commonly reported AEs in the cyclosporine A group were associated with the digestive tract, whilst systemic disorders were reported more frequently observed following concurrent therapy. Evaluation of body weight change and clinical pathology indices showed no overall clinically significant abnormalities. CONCLUSIONS: In dogs with atopic dermatitis, a short initiating course of prednisolone expedited the efficacy of cyclosporine A in resolving pruritus and associated clinical signs. The observed adverse events were consistent with those expected for the individual veterinary medicinal products. FAU - Dip, Ramiro AU - Dip R AD - Novartis Animal Health Inc,, Schwarzwaldallee 215, CH-4058 Basel, Switzerland. ramiro.dip@novartis.com. FAU - Carmichael, James AU - Carmichael J FAU - Letellier, Ingrid AU - Letellier I FAU - Strehlau, Guenther AU - Strehlau G FAU - Roberts, Elizabeth AU - Roberts E FAU - Bensignor, Emmanuel AU - Bensignor E FAU - Rosenkrantz, Wayne AU - Rosenkrantz W LA - eng PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't DEP - 20130903 PL - England TA - BMC Vet Res JT - BMC veterinary research JID - 101249759 RN - 0 (Anti-Inflammatory Agents) RN - 0 (Immunosuppressive Agents) RN - 83HN0GTJ6D (Cyclosporine) RN - 9PHQ9Y1OLM (Prednisolone) SB - IM MH - Animals MH - Anti-Inflammatory Agents/administration & dosage/adverse effects/therapeutic use MH - Cyclosporine/administration & dosage/adverse effects/*therapeutic use MH - Dermatitis, Atopic/drug therapy/*veterinary MH - Dog Diseases/*drug therapy MH - Dogs MH - Drug Administration Schedule MH - Drug Therapy, Combination MH - Female MH - Immunosuppressive Agents/administration & dosage/adverse effects/therapeutic use MH - Male MH - Prednisolone/administration & dosage/adverse effects/*therapeutic use MH - Pruritus/*drug therapy PMC - PMC3847128 EDAT- 2013/09/06 06:00 MHDA- 2014/07/01 06:00 PMCR- 2013/09/03 CRDT- 2013/09/06 06:00 PHST- 2013/05/14 00:00 [received] PHST- 2013/08/29 00:00 [accepted] PHST- 2013/09/06 06:00 [entrez] PHST- 2013/09/06 06:00 [pubmed] PHST- 2014/07/01 06:00 [medline] PHST- 2013/09/03 00:00 [pmc-release] AID - 1746-6148-9-173 [pii] AID - 10.1186/1746-6148-9-173 [doi] PST - epublish SO - BMC Vet Res. 2013 Sep 3;9:173. doi: 10.1186/1746-6148-9-173.