Citino Scott B, Munson Linda
White Oak Conservation Center, 581705 White Oak Road, Yulee, Florida 32097, USA.
J Zoo Wildl Med. 2005 Sep;36(3):401-16. doi: 10.1638/03-117.1.
A prospective clinical trial evaluating efficacy and long-term outcome of treatments for lymphoplasmacytic gastritis in cheetahs (Acinonyx jubatus) was conducted. The study evaluated efficacy of 11 different antibiotic and antiinflammatory treatment protocols in 32 cheetahs (19 male, 13 female) for reducing gastric inflammation and Helicobacter colonization and monitored the course of disease through histologic grading of gastric biopsies. All cheetahs were biopsied up to I wk before treatment and then rebiopsied within 1 mo after treatment. Most animals were reassigned to a second treatment regimen within 6 mo. Each animal received from one to three treatments during the study period. After the trial, gastric biopsies were obtained from each cheetah annually until death or transfer from the facility to assess disease progression. The trial and follow-up period spanned 10 yr. At onset of the trial, all 32 cheetahs had some degree of gastritis, and 26 cheetahs (81%) were colonized with Helicobacter. Inflammatory lesions worsened regardless of treatment or the presence of Helicobacter. No treatment had a significant effect on inflammatory changes except the lansoprazole/clarithromycin/amoxicillin treatment group, which produced a short-term decrease in inflammation when compared to controls. Prednisone had no effect on gastric inflammation. Overall, 65% of colonized cheetahs were initially cleared of histologic evidence of Helicobacter by treatment, with short-term eradication occurring in 100% of the animals treated with omeprazole/clarithromycin/amoxicillin or tetracycline/metronidazole/Pepto-Bismol for 28 days. Long-term follow-up of treated animals in this study clearly demonstrated that these treatments had little effect on life-long progression of gastritis or on Helicobacter burden in individual cheetahs, although some treatments provided short-term reduction in gastritis and Helicobacter. These results provide evidence that Helicobacter alone is not the cause of gastritis in cheetahs and do not support the use of antibacterial treatments in cheetahs unless significant clinical signs (e.g., frequent vomiting/regurgitation, weight loss) are apparent.
开展了一项前瞻性临床试验,评估猎豹(Acinonyx jubatus)淋巴浆细胞性胃炎治疗的疗效和长期结果。该研究评估了11种不同抗生素和抗炎治疗方案对32只猎豹(19只雄性,13只雌性)减轻胃部炎症和幽门螺杆菌定植的疗效,并通过胃活检的组织学分级监测疾病进程。所有猎豹在治疗前1周内进行活检,然后在治疗后1个月内再次活检。大多数动物在6个月内重新接受第二种治疗方案。在研究期间,每只动物接受一至三次治疗。试验结束后,每年从每只猎豹身上获取胃活检样本,直至死亡或从该机构转移,以评估疾病进展。试验和随访期长达10年。试验开始时,所有32只猎豹都有一定程度的胃炎,26只猎豹(81%)感染了幽门螺杆菌。无论治疗与否或是否存在幽门螺杆菌,炎症病变都会恶化。除兰索拉唑/克拉霉素/阿莫西林治疗组外,没有治疗对炎症变化有显著影响,与对照组相比,该治疗组炎症出现短期减轻。泼尼松对胃部炎症没有影响。总体而言,65%感染幽门螺杆菌的猎豹最初通过治疗清除了幽门螺杆菌的组织学证据,用奥美拉唑/克拉霉素/阿莫西林或四环素/甲硝唑/必奇治疗28天的动物中,100%出现短期根除。本研究中对接受治疗动物的长期随访清楚地表明,这些治疗对猎豹胃炎的终身进展或个体猎豹的幽门螺杆菌负荷几乎没有影响,尽管一些治疗能使胃炎和幽门螺杆菌短期内减少。这些结果证明,仅幽门螺杆菌不是猎豹胃炎的病因,并且不支持在猎豹中使用抗菌治疗,除非出现明显的临床症状(如频繁呕吐/反流、体重减轻)。