Laboratory of Veterinary Internal Medicine, Department of Clinical Sciences, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan.
Veterinary Teaching Hospital, Department of Veterinary Clinical Sciences, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan.
J Vet Med Sci. 2023 Jul 1;85(7):695-701. doi: 10.1292/jvms.23-0010. Epub 2023 May 29.
Dogs with precursor-targeted immune-mediated anemia (PIMA) are commonly treated with immunosuppressive therapy, but information on predictors of treatment response and response time is limited. Therefore, we retrospectively investigated predictive factors that influenced the treatment response and duration required to observe a response in dogs with PIMA receiving continuous immunosuppressive therapies for more than 105 days. Of 50 client-owned dogs that developed PIMA, 27 were included in this study, of which 18 were responders and 9 were non-responders to immunosuppressive therapies. Sixteen of the 18 responders responded to treatment within 60 days and the remaining 2 responded at 93 and 126 days, respectively. We found that an erythroid-maturation ratio of <0.17 may be a useful predictor for treatment response. In addition, complications of immunosuppressive therapies were investigated further in 50 dogs. Pancreatitis (n=4) and pneumonia (3) occurred over the entire treatment period, and infections such as abscesses (3) tended to be more common in dogs on an extended period of immunosuppressive therapy. These findings may be helpful when planning for the initial treatment and may provide evidence for informed consent about potential comorbidities throughout the treatment course.
患有前体靶向免疫介导性贫血(PIMA)的犬通常接受免疫抑制治疗,但关于治疗反应和观察反应所需时间的预测因素的信息有限。因此,我们回顾性地研究了影响接受持续免疫抑制治疗超过 105 天的 PIMA 犬治疗反应和所需反应时间的预测因素。在 50 只发生 PIMA 的患犬中,有 27 只被纳入本研究,其中 18 只为免疫抑制治疗的应答者,9 只为无应答者。18 名应答者中有 16 名在 60 天内对治疗有反应,其余 2 名分别在 93 天和 126 天有反应。我们发现,红细胞成熟比<0.17 可能是治疗反应的有用预测指标。此外,我们还进一步研究了 50 只犬的免疫抑制治疗并发症。整个治疗期间发生了胰腺炎(n=4)和肺炎(n=3),在接受长期免疫抑制治疗的犬中,脓肿等感染(n=3)往往更为常见。这些发现可能有助于初始治疗计划,并为整个治疗过程中的潜在合并症提供知情同意的证据。