Clinical Course of Acute Canine Polyradiculoneuritis Following Treatment with Human IV Immunoglobulin

Author:

Hirschvogel Katrin1,Jurina Konrad1,Steinberg Tanja A.1,Matiasek Lara A.1,Matiasek Kaspar1,Beltrán Elsa1,Fischer Andrea1

Affiliation:

1. Clinic of Small Animal Medicine, Ludwig-Maximilians University, Munich, Germany (K.H., L.M., A.F., T.S.); Tierklinik Haar, Haar, Germany (K.J.); Section of Clinical & Comparative Neuropathology, Institute of Veterinary Pathology, Ludwig-Maximilians University, Munich, Germany (K.M.); and Animal Health Trust, Lanwades Park, Kentford, Newmarket, England (E.B.).

Abstract

Treatment of dogs with acute canine polyradiculoneuritis (ACP) is restricted to physical rehabilitation and supportive care. In humans with Guillain-Barré syndrome, the counterpart of ACP, randomized trials show that IV immunoglobulin (IVIg) speeds recovery. The authors of the current study hypothesized that dogs with ACP would tolerate IVIg well and recover faster than dogs managed with supportive treatment only. Sixteen client-owned dogs with ACP were treated with IVIg, and 14 client-owned dogs served as a retrospective control group. Diagnosis was confirmed using clinical features, electrodiagnostics, cerebrospinal fluid analysis, and muscle/nerve biopsies. The duration of the initial progressive phase, the time from IVIg administration until the dogs were ambulating without assistance, and the duration of the complete episode were evaluated. Adverse reactions (anaphylaxis, mild hematuria) were observed in two dogs. Dogs treated with IVIg were ambulating without assistance after a median of 27.5 days (range, 15–127 days) from onset of clinical signs. The control group was ambulatory without assistance at a median of 75.5 days (range, 5–220 days). Even though this result is not statistically significant, there is a clear trend toward faster recovery in dogs treated with IVIg.

Publisher

American Animal Hospital Association

Subject

Small Animals

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