首页> 外文期刊>Clinical toxicology: the official journal of the American Academy of Clinical Toxicology and European Association of Poisons Centres and Clinical Toxicologists >Efficacy and effectiveness of anti-digoxin antibodies in chronic digoxin poisonings from the DORA study (ATOM-1)
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Efficacy and effectiveness of anti-digoxin antibodies in chronic digoxin poisonings from the DORA study (ATOM-1)

机译:来自DORA研究(ATOM-1)的抗地高辛抗体在慢性地高辛中毒的功效和有效性

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Context: We hypothesized that in chronic digoxin toxicity, anti-digoxin antibodies (Fab) would be efficacious in binding digoxin, but this may not translate into improved clinical outcomes. Objective: This study aims to investigate changes in free digoxin concentrations and clinical effects on heart rate and potassium concentrations in chronic digoxin poisoning when anti-digoxin Fab are given. Materials and methods: This is a prospective observational study. Patients were recruited if they have been treated with anti-digoxin Fab for chronic digoxin poisoning. Data was entered into a standardised prospective form, supplemented with medical records. Their serum or plasma was collected, analysed for free and bound digoxin and free anti-digoxin Fab concentrations. Results: From September 2013 to February 2015, 36 patients (median age, 78 years; 22 females) were recruited from 18 hospitals. Median heart rate (HR) was 49 beats/min. Initial median digoxin and potassium concentrations were 4.7 nmol/L (3.6 mu g/L) (range: 2.3-11.2 nmol/L) and 5.3 mmol/L (range: 2.9-9.2 mmol/L) respectively. Beta-blockers (n = 18), calcium antagonists (n = 6), spironolactone and/or angiotensin blocking agents (n = 24) were also used concomitantly. Renal impairment and gastrointestinal symptoms were present in 31 (86%) and 22 (63%) patients respectively. Five patients died from conditions unrelated to digoxin toxicity. Median change in HR was 8 beats/min post-Fab with no effect on blood pressure; they were 4, 10 and 17 beats/min for the 1, 2 and >= 3 vials of anti-digoxin Fab groups respectively. Concomitant treatments with potassium lowering agents (12/36) and inotropic drugs (7/36) were used. Gastrointestinal effects resolved in all 22 patients. The median decrease for potassium was 0.3 mmol/L. Digoxin concentration reduced from 3.8 to 0 nmol/L post-Fab. There was a rebound observed in the free digoxin concentration in 25 patients but none had associated clinical deterioration. Conclusions: One to two vials of anti-digoxin Fab initially bound all free digoxin confirming Fab efficacy. However, this was associated with only a moderate improvement in HR and potassium, suggesting bradyarrhythmia and hyperkalaemia may be from other co-morbidities.
机译:背景:我们假设在地高辛的慢性毒性中,抗地高辛抗体(Fab)可以有效地结合地高辛,但这可能无法改善临床结果。目的:本研究旨在研究给予抗地高辛Fab时慢性地高辛中毒中游离地高辛浓度的变化以及对心率和钾浓度的临床影响。材料和方法:这是一项前瞻性观察研究。如果患者已接受抗地高辛Fab的慢性地高辛中毒治疗,则招募患者。数据以标准化的预期形式输入,并附有医疗记录。收集他们的血清或血浆,分析游离和结合的地高辛和游离抗地高辛Fab的浓度。结果:2013年9月至2015年2月,从18家医院招募了36例患者(中位年龄78岁;女性22位)。中位心率(HR)为49次/分钟。地高辛和钾的初始中值浓度分别为4.7 nmol / L(3.6μg / L)(范围:2.3-11.2 nmol / L)和5.3 mmol / L(范围:2.9-9.2 mmol / L)。还同时使用了β受体阻滞剂(n = 18),钙拮抗剂(n = 6),螺内酯和/或血管紧张素阻滞剂(n = 24)。分别有31例(86%)和22例(63%)患者出现肾功能不全和胃肠道症状。五例患者死于与地高辛毒性无关的疾病。 Fab后,HR的中值变化为8次/分钟,对血压无影响;对于1个,2个和> = 3个抗地高辛Fab组,它们分别为4、10和17次/分钟。与降钾药(12/36)和正性肌力药物(7/36)同时治疗。在所有22例患者中,胃肠道症状均得到缓解。钾的中位数下降为0.3 mmol / L。 Fab后地高辛的浓度从3.8降至0 nmol / L。在25名患者中观察到游离地高辛浓度出现反弹,但没有相关的临床恶化。结论:一到两个小瓶的抗地高辛Fab最初结合了所有游离的地高辛,从而确认了Fab的功效。但是,这仅与HR和钾的中度改善有关,表明缓慢性心律失常和高钾血症可能来自其他合并症。

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