肺炎马驹治疗期间血清淀粉样蛋白A的动力学

A. Lankenfeld, C. Weber, K. Rohn, M. Venner
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引用次数: 2

摘要

摘要:超声检查的马驹肺炎已被证明是成功的监测病程在治疗期间的疾病。然而,问题是另一个参数,如急性期蛋白血清淀粉样蛋白A (SAA),是否也适用于评估对治疗的反应、治疗期间的病程或决定终止肺炎马驹的治疗。在一项对52匹马驹进行的前瞻性研究中,通过几种诊断测试记录了中度或重度肺炎的病程。分别于诊断当日及治疗期间每周进行胸部临床及超声检查及血值(SAA、白细胞计数)测定。胸部超声检查肺脓肿评分15 ~ 19.5 cm(中度肺炎)的小马驹分为第1组(n = 31),给予利福平和图拉霉素治疗。脓肿评分为> ~ 20cm(重度肺炎)的马驹作为第二组(n = 21),给予利福平和阿奇霉素治疗。所有马驹在治疗期间均恢复正常。中度肺炎(1组)马驹胸部超声检查10天后无病理改变,重度肺炎(2组)马驹胸部超声检查11天后无病理改变。诊断时SAA值中位数为367 mg/L(中位数;25 /75: 23-937),中度肺炎的马驹和216 mg/L(中位数;25 /75: 16-690)。中度肺炎和重度肺炎马驹的SAA值分别在5天和4天后显著下降至正常值< 40 mg/L。中度肺炎的马驹从SAA达到正常值到肺部超声检查显示不再出现异常的时间为3天,重度肺炎的马驹为7天。SAA作为诊断方法在诊断当天对中度肺炎的敏感性为68%,对重度肺炎的敏感性为71%。如果只考虑肺炎和发烧的马驹,91%的马驹最初表现出SAA升高。在治疗过程中,SAA与脓肿评分、临床评分及诊断年龄相关,但与白细胞数量无关。总之,超声检查仍然是诊断马驹肺炎和跟踪其治疗进展的最精确工具。然而,SAA可以作为评估治疗成功的附加参数。特别是发烧的马驹和小马驹在肺炎患者中表现出较高的SAA值。通过观察患者SAA的动力学,该血液参数可以作为调整最终超声检查日期的支持。因此,治疗的持续时间可以单独调整。
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Kinetics of serum amyloid A during the treatment period of foals with pneumonia
Summary: The ultrasonographic examination of foals with pneumonia has been proven successful in monitoring the course of the disease during treatment. However, the question arises whether another parameter, such as the acute phase protein serum amyloid A (SAA), could also be suitable for evaluating the response to treatment, the course during treatment or the decision to terminate the treatment in foals with pneumonia. The course of moderate or severe pneumonia was recorded by several diagnostic tests in a prospective study performed on 52 foals. Clinical and ultrasonographical examination of the thorax and blood values (SAA, white blood cell count) of these foals were measured on the day of diagnosis and weekly during treatment. Foals with a pulmonary abscess score of 15–19.5 cm determined by sonography of the thorax (moderate pneumonia) were assigned to group 1 (n = 31) and received a treatment with rifampin and tulathromycin. If the abscess score was > 20 cm (severe pneumonia), the foals were included in group 2 (n = 21) and were treated with rifampin and azithromycin. All foals recovered during the treatment period. Sonography of the thorax of the foals with moderate pneumonia (group 1) showed no more pathologic findings after ten days, and the foals with severe pneumonia (group 2) after eleven days of treatment. At diagnosis the median SAA value at diagnosis was 367 mg/L (median; 25th/75th: 23–937) in foals with moderate pneumonia and 216 mg/L (median; 25th/75th: 16–690) in those with severe pneumonia. The SAA values of foals with initially elevated values decreased significantly until they reached normal values < 40 mg/L after five days in the foals with moderate pneumonia and four days in the those with severe pneumonia. The time between the day SAA reached normal values and ultrasonography of the lung revealed no more abnormalities was three days in foals with moderate pneumonia and seven days in those with severe pneumonia. The SAA as a diagnostic method had a sensitivity of 68 % in the case of moderate pneumonia and 71 % in the case of severe pneumonia on the day of diagnosis. If only the foals with pneumonia and fever were considered, 91 % showed an initially increased SAA. During treatment, the SAA correlated with the abscess score, the clinical score and the age at diagnosis, but not with the number of white blood cells. In conclusion, the ultrasonographic examination remains the most precise tool to diagnose pneumonia and follow its progress during treatment in foals. However, the SAA can be used as an additional parameter for evaluating the treatment success. Especially foals with fever and younger foals show high SAA values in patients with pneumonia. By observing the kinetics of SAA in a patient, this blood parameter could be a support to adjust the date of the final ultrasonographic examination. Thereby, the duration of treatment can be individually adapted.
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