Bala Keziban Aslı, Doğan Murat, Kaba Sultan, Akbayram Sinan, Aslan Oktay, Kocaman Selami, Bayhan Gülsüm İclal, Üstyol Lokman, Demir Nihat
Department of Pediatrics, Medical School, Yüzüncü Yil University, Van, Turkey.
Department of Pediatrics Division of Pediatric Infectious Diseases, Medical School, Yüzüncü Yil University, Van, Turkey.
Med Sci Monit. 2016 Sep 3;22:3129-34. doi: 10.12659/msm.899977.
BACKGROUND Our study aimed to demonstrate the frequency of the syndrome of inappropriate ADH secretion (SIADH) and associated factors during the course of brucellosis in children and adolescents. MATERIAL AND METHODS The study included children and adolescents aged 0-18 years old diagnosed with brucellosis between 2012 and 2014. The data were collected from patient charts. The diagnosis of brucellosis was made based on titrations >1:160 in standard Wright tube agglutination tests and/or positive culture tests. SIADH diagnosis was made based on the following criteria: euvolemic hyponatremia, serum Na+ <135 mmol/L, presence of serum hypoosmolarity (serum osmolarity <275 mOsm/L), increased urinary sodium (>25 mmol/L with normal dietary salt intake), low uric acid (<2 mg/dL), absence of kidney, thyroid or adrenal disease, and any anti-diuretic use. RESULTS The study included 160 children and adolescents with mean age of 9.58±3.95 years (range: 2-18 years) including 70 girls (43.8%) and 90 boys (56.2%). When the patients were stratified based on SIADH, it was found that SIADH was present in 35 patients (21.9%). SIADH was associated with elevated glucose (p<0.001), ALT (p<0.05), AST (p<0.05), LDH (p<0.001), CRP (p<0.001), and MPV (p<0.001); and decreased potassium (p<0.05), chloride (p<0.001), albumin (p<0.001), total protein (p<0.05), and hemoglobin (p<0.05) levels. CONCLUSIONS Our study reports on the frequency, clinical characteristics, predisposing factors, and management of SIADH that can develop in children and adolescents diagnosed with brucellosis.
背景 我们的研究旨在证明儿童和青少年布鲁氏菌病病程中抗利尿激素分泌不当综合征(SIADH)的发生率及相关因素。
材料与方法 该研究纳入了2012年至2014年间诊断为布鲁氏菌病的0至18岁儿童和青少年。数据从患者病历中收集。布鲁氏菌病的诊断基于标准Wright试管凝集试验中滴度>1:160和/或培养试验阳性。SIADH的诊断基于以下标准:血容量正常的低钠血症、血清钠+<135 mmol/L、血清低渗(血清渗透压<275 mOsm/L)、尿钠增加(正常饮食盐摄入时>25 mmol/L)、尿酸降低(<2 mg/dL)、无肾脏、甲状腺或肾上腺疾病以及未使用任何抗利尿药物。
结果 该研究纳入了160名儿童和青少年,平均年龄为9.58±3.95岁(范围:2至18岁),其中70名女孩(43.8%),90名男孩(56.2%)。当根据SIADH对患者进行分层时发现,35名患者(21.9%)存在SIADH。SIADH与血糖升高(p<0.001)、谷丙转氨酶(ALT,p<0.05)、谷草转氨酶(AST,p<0.05)、乳酸脱氢酶(LDH,p<0.001)、C反应蛋白(CRP,p<0.001)和平均血小板体积(MPV,p<0.001)相关;与血钾降低(p<0.05)、血氯降低(p<0.001)、白蛋白降低(p<0.001)、总蛋白降低(p<0.05)和血红蛋白降低(p<0.05)有关。
结论 我们的研究报告了诊断为布鲁氏菌病的儿童和青少年中可能发生的SIADH的发生率、临床特征、诱发因素及管理情况。