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- hypokalemic alkalosis 缺鉀性鹼中毒
- hypokalemic alkalosis syndrome 低鉀血性礆中毒綜合征
- Alkalosis and potassium depletion may be pronounced. 可能有鹼中毒和缺鉀。
- Hypernatremia and metabolic alkalosis did not occur. 血尿素氮、肌酐等清除理想。
- Application of excessive hours, can cause metabolic alkalosis. 應用過量時,可致代謝性鹼中毒。
- The patients were hypokalemic during 6.5 years on the average. 這些患者低鉀血症的時間平均為6.;5年。
- Increased renal excretion occurs with both respiratory and metabolic alkalosis. 在呼吸性鹼中毒和代謝性鹼中毒中鉀離子的腎排泄增加。
- Status suggests a mixed metabolic acidosis and respiratory alkalosis. 病人的酸鹼平衡狀態提示混合性代謝性酸中毒和呼吸性鹼中毒。
- Metabolic acidosis had the same occurrence with metabolic alkalosis. 呼酸型>呼鹼型,代酸與代鹼基本相當;
- Thus, in alkalosis, the increased potassium ion excretion in exchange for sodium ion permits hydrogen ion conservation. 因此在鹼中毒中,鈉鉀交換的增加使氫離子保留。
- Of the total 168 patients , 121(72.0%) had TABD of respiratory alkalosis, 47(28.0%) had TABD of respiratory acidosis . 168例中呼吸性鹼中毒合併代謝性鹼中毒並代謝性酸中毒 (呼鹼型TABD) 12 1例 (72 0%25 ) ; 呼吸性酸中毒合併代謝性鹼中毒並代謝性酸中毒 (呼酸型TABD) 4 7例 (2 8 0%25 )。
- They have typical laboratory findings, including hypokalemia, metabolic alkalosis, hypomagnesemia, and hypocalciuria. 在此篇文章中,我們將報告三個病例:一是偶發性個案,另兩位是姐弟。
- Arterial blood gas (ABG) analysis demonstrates mild hypoxemia and respiratory alkalosis. 動脈血氣分析顯示輕度低氧血症和呼吸性鹼中毒。
- Kempf R,Wegmann D.Periodic hypokalemic paralysis in thyrotoxicosis[J].Schweiz Med Wochenschr,1993,123:1843. Kempf R,Wegmann D.甲狀腺功能亢進症伴低鉀周期性麻痹[J].Schweiz Med Wochenschr,1993,123:1843.
- Kempf R, Wegmann D. Periodic hypokalemic paralysis in thyrotoxicosis. S chweiz Med Wochenscher, 1993, 123:1843. 趙黨生.;甲狀腺機能亢進症併發周期性麻痹文獻複習(附7例報告)
- He seizured within fifteen minutes of his arrival and was found to have acute respiratory alkalosis. 在他抵達急診室后的十五分鐘時,忽然發生驚厥及呼吸性鹼中毒。
- Chronic respiratory alkalosis( CRA), CRA plus metabolic alkalosis and metabolic acidosis are seldom. 慢性呼吸性鹼中毒、性呼吸性鹼中毒並代謝性鹼中毒和代謝性酸中毒是少見的。
- Results 71.43% of rise in creatine phosphokinase of the idiopathic hypokalemic periodic paralysis. 結果原發性低鉀型周期性麻痹患者血清肌酸激酶增高佔71.;43%25;血清肌酸激酶改變呈現一定規律。
- Conclusion The heredity in hypokalemic periodic paralysis is of genetic heterogeneity. 結論低鉀性周期性麻痹的遺傳存在異質性。
- The outstanding laboratory features were hypochloremic alkalosis and severe hypokalemia. 實驗室檢查發現有代謝性鹼血症、低血鉀症及低血氯症。