Baggot J D
Irish Equine Centre, Johnstown, County Kildare.
Vet Clin North Am Equine Pract. 1994 Apr;10(1):87-107. doi: 10.1016/s0749-0739(17)30370-x.
The neonatal period in foals refers to the first 7 days of postnatal life. The effects of drugs (pharmacologic agents) may be different in neonatal foals, particularly during the first 3 days of postnatal life, from those in older foals and adult horses. The changed drug effects decrease as the physiologic processes that affect absorption, distribution, and elimination (metabolism and excretion) of drugs mature. Dosage regimens should take into account the altered pharmacokinetic profiles of drugs, and because of wide individual variation, the response to therapy should be closely monitored for signs of toxicity. In conjunction with the prudent use of drugs, good nursing care and the provision of supportive therapy are critical in the management of neonatal foal diseases. Over-crowding imposes stress upon young foals and predisposes them to an increased incidence of bacterial and parasitic infections. The collection of specimens for precise microbiologic diagnosis and correction of deficits in serum immunoglobulins should precede antimicrobial therapy. Although E. coli is by far the most common cause of bacterial infections in neonatal foals, other bacterial pathogens of unpredictable susceptibility often cause infection. The selection of an antimicrobial drug for specific therapy should be based on both the microbiologic (quantitative susceptibility) and pharmacologic (pharmacokinetic) properties of the drug. The use of an antimicrobial drug or combination of drugs that will produce a bactericidal effect is highly desirable. Whenever possible, a parenteral preparation that can be administered intravenously should be chosen. The bioavailability and selectivity of action of pharmacologic agents are influenced by the dosage form and route of administration. Diazepam is the sedative drug of choice for neonatal foals. Cimetidine, an H2-receptor antagonist, may be indicated in foals diagnosed to have gastric ulcers; hepatic microsomal oxidative metabolism of drugs administered concurrently with cimetidine is decreased. Nonsteroidal anti-inflammatory drugs (flunixin, phenylbutazone) have a higher incidence of toxicity in foals and, when indicated, should be used at lower dosage than in adult horses. Even though it is highly important to maintain hydration status and electrolyte balance, intravenous infusion should always be performed slowly. Immature renal function decreases the ability of the neonatal animal to excrete excess fluid. The use of drugs in neonatal foals requires greater precision in dosage, more attention to the route and rate of administration, and close monitoring of pharmacologic effects.
驹的新生期是指出生后生命的前7天。药物(药理剂)对新生驹的影响可能与年龄较大的驹和成年马不同,尤其是在出生后的前3天。随着影响药物吸收、分布和消除(代谢和排泄)的生理过程成熟,药物效应的变化会减小。给药方案应考虑到药物改变的药代动力学特征,并且由于个体差异很大,应密切监测治疗反应以观察毒性迹象。在谨慎使用药物的同时,良好的护理和提供支持性治疗对于新生驹疾病的管理至关重要。过度拥挤会给幼驹带来压力,并使它们更容易发生细菌和寄生虫感染。在进行抗菌治疗之前,应采集标本进行精确的微生物学诊断并纠正血清免疫球蛋白的缺陷。虽然大肠杆菌是新生驹细菌感染最常见的原因,但其他具有不可预测易感性的细菌病原体也常引起感染。选择特定治疗的抗菌药物应基于药物的微生物学(定量敏感性)和药理学(药代动力学)特性。非常希望使用能产生杀菌作用的抗菌药物或药物组合。只要有可能,应选择可静脉注射的肠胃外制剂。药理剂的生物利用度和作用选择性受剂型和给药途径影响。地西泮是新生驹首选的镇静药物。西咪替丁,一种H2受体拮抗剂,可能适用于被诊断患有胃溃疡的驹;与西咪替丁同时给药的药物的肝微粒体氧化代谢会降低。非甾体抗炎药(氟尼辛、苯基丁氮酮)在驹中的毒性发生率较高,如有需要,应使用比成年马更低的剂量。尽管维持水合状态和电解质平衡非常重要,但静脉输液应始终缓慢进行。未成熟的肾功能会降低新生动物排泄多余液体的能力。在新生驹中使用药物需要在剂量上更加精确,更加注意给药途径和速度,并密切监测药理作用。