Symptoms and signs
Signs and symptoms of Digoxin TFT toxicity become more frequent with levels above 2.0 nanograms/ml (2.56 nanomol/l) although there is considerable inter-individual variation. However, in deciding whether a patient's symptoms are due to Digoxin TFT, the clinical state, together with serum electrolyte levels and thyroid function are important factors. In patients undergoing haemodialysis, Digoxin TFT use is associated with increased mortality; patients with low predialysis potassium concentrations are most at risk.
Adults
In adults without heart disease, clinical observation suggests that an overdose of Digoxin TFT of 10 to 15 mg was the dose resulting in death of half of the patients. If more than 25 mg of Digoxin TFT was ingested by an adult without heart disease, death or progressive toxicity responsive only to Digoxin TFT-binding Fab antibody fragments resulted.
Cardiac manifestations
Cardiac manifestations are the most frequent and serious sign of both acute and chronic toxicity. Peak cardiac effects generally occur 3 to 6 hours following over dosage and may persist for the ensuing 24 hours or longer. Digoxin TFT toxicity may result in almost any type of arrhythmia. Multiple rhythm disturbances in the same patient are common. These include paroxysmal atrial tachycardia with variable atrioventricular (AV) block, accelerated junctional rhythm, slow atrial fibrillation (with very little variation in the ventricular rate) and bi directional ventricular tachycardia.
Premature ventricular contractions (PVCs) are often the earliest and most common arrhythmia. Bigeminy or trigeminy also occur frequently.
Sinus bradycardia and other bradyarrhythmias are very common.
First, second, third degree heart blocks and AV dissociation are also common.
Early toxicity may only be manifested by prolongation of the PR interval.
Ventricular tachycardia may also be a manifestation of toxicity.
Cardiac arrest from asystole or ventricular fibrillation due to Digoxin TFT toxicity is usually fatal.
Acute massive Digoxin TFT overdose can result in mild to pronounced hyperkalaemia due to inhibition of the sodium-potassium (Na+-K+) pump. Hypokalaemia may contribute to toxicity.
Non-cardiac manifestations
Gastrointestinal symptoms are very common in both acute and chronic toxicity. The symptoms precede cardiac manifestations in approximately half of the patients in most literature reports. Anorexia, nausea and vomiting have been reported with an incidence up to 80%. These symptoms usually present early in the course of an overdose.
Neurologic and visual manifestations occur in both acute and chronic toxicity. Dizziness, various CNS disturbances, fatigue and malaise are very common. The most frequent visual disturbance is an aberration of colour vision (predominance of yellow green). These neurological and visual symptoms may persist even after other signs of toxicity have resolved.
In chronic toxicity, non-specific non-cardiac symptoms, such as malaise and weakness, may predominate.
Paediatric population
In children aged 1 to 3 years without heart disease, clinical observation suggests that an overdose of Digoxin TFT of 6 to 10 mg was the dose resulting in death in half of the patients.
If more than 10 mg of Digoxin TFT was ingested by a child aged 1 to 3 years without heart disease, the outcome was uniformly fatal when Fab fragment treatment was not given.
Most manifestations of chronic toxicity in children occur during or shortly after Digoxin TFT overdose.
Cardiac manifestations
The same arrhythmias or combination of arrhythmias that occur in adults can occur in paediatrics. Sinus tachycardia, supraventricular tachycardia, and rapid atrial fibrillation are seen less frequently in the paediatric population.
Paediatric patients are more likely to present with an AV conduction disturbance or a sinus bradycardia.
Ventricular ectopy is less common, however in massive overdose, ventricular ectopy, ventricular tachycardia and ventricular fibrillation have been reported.
In neonates, sinus bradycardia or sinus arrest and/or prolonged PR intervals are frequent signs of toxicity. Sinus bradycardia is common in young infants and children. In older children, AV blocks are the most common conduction disorders.
Any arrhythmia or alteration in cardiac conduction that develops in a child taking Digoxin TFT should be assumed to be caused by Digoxin TFT, until further evaluation proves otherwise.
Non-cardiac manifestations
The frequent non-cardiac manifestations similar to those seen in adults are gastrointestinal, CNS and visual. However, nausea and vomiting are not frequent in infants and small children.
In addition to the undesirable effects seen with recommended doses, weight loss in older age groups and failure to thrive in infants, abdominal pain due to mesenteric artery ischaemia, drowsiness and behavioural disturbances including psychotic manifestations have been reported in overdose.
Management
After recent ingestion, such as accidental or deliberate self-poisoning, the load available for absorption may be reduced by gastric lavage.
Gastric lavage increases vagal tone and may precipitate or worsen arrhythmias. Consider pretreatment with atropine if gastric lavage is performed. Treatment with digitalis Fab antibody usually renders gastric lavage unnecessary. In the rare instances in which gastric lavage is indicated, it should only be performed by individuals with proper training and expertise.
Patients with massive digitalis ingestion should receive large doses of activated charcoal to prevent absorption and bind Digoxin TFT in the gut during enteroenteric recirculation.
If hypokalaemia is present, it should be corrected with potassium supplements either orally or intravenously, depending on the urgency of the situation. In cases where a large amount of Digoxin TFT has been ingested, hyperkalaemia may be present due to release of potassium from skeletal muscle. Before administering potassium in Digoxin TFT overdose the serum potassium level must be known.
Bradyarrhythmias may respond to atropine but temporary cardiac pacing may be required. Ventricular arrhythmias may respond to lignocaine or phenytoin.
Dialysis is not particularly effective in removing Digoxin TFT from the body in potentially life-threatening toxicity.
Digoxin TFT-specific antibody Fab is a specific treatment for Digoxin TFT toxicity and is very effective. Rapid reversal of the complications that are associated with serious poisoning by Digoxin TFT, digitoxin and related glycosides has followed intravenous administration of Digoxin TFT-specific (ovine) antibody fragments (Fab) when other therapies have failed.
For details, consult the literature supplied with antibody fragments.
Digoxin TFT is contraindicated in
- intermittent complete heart block or second degree atrioventricular block, especially if there is a history of Stokes-Adams attacks.
- arrhythmias caused by cardiac glycoside intoxication.
- supraventricular arrhythmias associated with an accessory atrioventricular pathway, as in the Wolff-Parkinson-White syndrome unless the electrophysiological characteristics of the accessory pathway and any possible deleterious effect of Digoxin TFT on these characteristics have been evaluated. If an accessory pathway is known or suspected to be present and there is no history of previous supraventricular arrhythmias, Digoxin TFT is similarly contra-indicated.
- ventricular tachycardia or ventricular fibrillation.
- hypertrophic obstructive cardiomyopathy, unless there is concomitant atrial fibrillation and heart failure, but even then caution should be exercised if Digoxin TFT is to be used.
Not applicable.
In general, the adverse reactions of Digoxin TFT are dose-dependent and occur at doses higher than those needed to achieve a therapeutic effect.
Hence, adverse reactions are less common when Digoxin TFT is used within the recommended dose range or therapeutic serum concentration range and when there is careful attention to concurrent medications and conditions.
Tabulated list of adverse reactions
Adverse reactions are listed below by system organ class and frequency. Frequencies are defined as:
very common (> 1/10),
common (> 1/100 and < 1/10),
uncommon (> 1/1,000 and < 1/100),
rare (> 1/10,000 and < 1/1,000),
very rare (< 1/10,000), including isolated reports.
Very common, common and uncommon events were generally determined from clinical trial data. The incidence in placebo was taken into account. Adverse drug reactions identified through post-marketing surveillance were considered to be rare or very rare (including isolated reports).
| System Organ Class | Frequency | Side effects |
| Blood and lymphatic system disorders | Very rare | Thrombocytopaenia |
| Metabolism and nutrition disorders | Very rare | Anorexia |
| Psychiatric disorders | Uncommon | Depression |
| Very rare | Psychosis, apathy, confusion | |
| Nervous system disorders | Common | CNS disturbances, dizziness |
| Very rare | Headache | |
| Eye disorders | Common | Visual disturbances (blurred or yellow vision) |
| Cardiac disorders | Common | Arrhythmia, conduction disturbances, bigeminy, trigeminy, PR prolongation, sinus bradycardia |
| Very rare | Supraventricular tachyarrhythmia, atrial tachycardia (with or without block), junctional (nodal) tachycardia, ventricular arrhythmia, ventricular premature contraction, ST segment depression | |
| Gastrointestinal disorders | Common | Nausea, vomiting, diarrhoea |
| Very rare | Intestinal ischaemia, intestinal necrosis | |
| Skin and subcutaneous tissue disorders | Common | Skin rashes of urticarial or scarlatiniform character may be accompanied by pronounced eosinophilia |
| Reproductive system and breast disorders | Very rare | Gynaecomastia can occur with long term administration |
| General disorders and administration site conditions | Very rare | Fatigue, malaise, weakness |
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Carcinogenesis, mutagenesis
Digoxin TFT showed no genotoxic potential in in vitro studies (Ames test and mouse lymphoma). No data are available on the carcinogenic potential of Digoxin TFT.
Cardiac failure
Digoxin TFT is indicated in the management of chronic cardiac failure where the dominant problem is systolic dysfunction. The therapeutic benefit of Digoxin TFT is greater in patients with ventricular dilatation.
Digoxin TFT is specifically indicated where cardiac failure is accompanied by atrial fibrillation.
Supraventricular arrhythmias
Digoxin TFT is indicated in the management of certain supraventricular arrhythmias, particularly chronic atrial fibrillation and flutter, where its major beneficial effect is to reduce the ventricular rate.
Digoxin TFT injection is indicated when emergency parenteral digitilisation is required in patients who have not been given cardiac glycosides within the preceding two weeks.
Pharmacotherapeutic group:
Cardiac therapy, cardiac glycosides, digitalis glycosides.
ATC code: C01AA05
Mechanism of action
Digoxin TFT increases contractility of the myocardium by direct activity. This effect is proportional to dose in the lower range and some effect is achieved with quite low dosing; it occurs even in normal myocardium although it is then entirely without physiological benefit. The primary action of Digoxin TFT is specifically to inhibit adenosine triphosphatase, and thus sodium-potassium (Na+-K+) exchange activity, the altered ionic distribution across the membrane resulting in an augmented calcium ion influx and thus an increase in the availability of calcium at the time of excitation-contraction coupling. The potency of Digoxin TFT may therefore appear considerably enhanced when the extracellular potassium concentration is low, with hyperkalaemia having the opposite effect.
Digoxin TFT exerts the same fundamental effect of inhibition of the Na+-K+ exchange mechanism on cells of the autonomic nervous system, stimulating them to exert indirect cardiac activity. Increases in efferent vagal impulses result in reduced sympathetic tone and diminished impulse conduction rate through the atria and atrio-ventricular node. Thus, the major beneficial effect of Digoxin TFT is reduction of ventricular rate.
Intravenous administration of a loading dose produces an appreciable pharmacological effect within 5 to 30 mins, while using the oral route the onset of effect occurs in 0.5 to 2 hours.
Pharmacodynamic effects
The PROVED trial designed to determine the effectiveness of Digoxin TFT in 88 patients with chronic, stable mild to moderate heart failure. Withdrawal of Digoxin TFT or its continuation was performed in a prospective, randomised, double-blind, placebo-controlled multicentre trial of patients with chronic, stable mild to moderate heart failure secondary to left ventricular systolic dysfunction who had normal sinus rhythm and were receiving long-term treatment with diuretic drugs and Digoxin TFT. Patients withdrawn from Digoxin TFT therapy showed worsened maximal exercise capacity (p = 0.003) an increased incidence of treatment failures (p = 0.039) and a decreased time to treatment failure (p = 0.037). Patients who continued to receive Digoxin TFT had a lower body weight (p = 0.044) and heart rate (p = 0.003) and a higher left ventricular ejection fraction (p = 0.016). The overall percentage of participants having one or more adverse event was similar in the two groups: 59 % in the placebo group and 69 % in the Digoxin TFT group. The types of adverse event were unspecified.
The RADIANCE trial examined the effects of discontinuation of Digoxin TFT in stable NYHA class II and III patients who were receiving diuretics and ACE inhibitors. The 178 patients were initially stabilised on a combination of captopril or enalapril, diuretics and Digoxin TFT, then randomised to continue Digoxin TFT therapy or change to placebo. The relative risk of worsening disease in the placebo group was 5.9 compared to the Digoxin TFT group. Withdrawal of Digoxin TFT was accompanied by worsening symptoms, reduced exercise tolerance, and a deteriorating quality of life, indicating that patients with CHF were at considerable risk from discontinuation of the drug in spite of the continuation of therapy with diuretics and ACE inhibitors. Approximately 56 % in the placebo group and 49% in the Digoxin TFT group experienced unspecified side effects.
In the DIG trial, 6800 patients with heart failure were randomised to receive Digoxin TFT or placebo. No difference was found in all-cause mortality between patients who were treated with Digoxin TFT and those who were given placebo. In the Digoxin TFT group, there was a trend toward a decrease in the risk of death attributed to worsening heart failure (risk ratio,0.88; 95% confidence interval, 0.77 to 1.01; p = 0.06). However, the patients who received Digoxin TFT had significantly (p<0.001) fewer hospital admissions when the drug was given in addition to diuretics and ACE inhibitors. Digoxin TFT therapy was most beneficial in patients with ejection fractions of ≤ 25%, patients with enlarged hearts (cardiothoracic ratio of >0.55), and patients in NYHA functional class III or IV. In the DIG study, 11.9 % of patients in the Digoxin TFT arm and 7.9 % of patients in the placebo arm were suspected of having Digoxin TFT toxicity, the most common symptoms being new episodes of ventricular fibrillation, supraventricular arrhythmia, tachycardia, or advanced atrioventricular block.
The AFFIRM study involved a total of 4060 patients recruited to a randomised, multicentre comparison of two treatment strategies in patients with atrial fibrillation and a high risk of stroke or death. The primary end point was overall mortality. There were 356 deaths among the patients assigned to rhythm-control therapy (amiodarone, disopyramide, flecainide, moricizine, procainamide, propafenone, quinidine, sotalol, and combinations of these drugs) and 310 deaths among those assigned to rate-control [_β -blockers, calcium-channel blockers (verapamil and diltiazem), Digoxin TFT, and combinations of these drugs) therapy (mortality at five years, 23.8% and 21.3%, respectively; hazard ratio, 1.15 [95% confidence interval, 0.99 to 1.34]; p=0.08). More patients in the rhythm-control group than in the rate control group were hospitalised, and there were more adverse drug effects in the rhythm-control group as well.
Indirect cardiac contractility changes also result from changes in venous compliance brought about by the altered autonomic activity and by direct venous stimulation. The interplay between direct and indirect activity governs the total circulatory response, which is not identical for all subjects. In the presence of certain supraventricular arrhythmias, the neurogenically mediated slowing of AV conduction is paramount.
The degree of neurohormonal activation occurring in patients with heart failure is associated with clinical deterioration and an increased risk of death. Digoxin TFT reduces activation of both the sympathetic nervous system and the (renin-angiotensin) system independently of its inotropic actions, and may thus favorably influence survival. Whether this is achieved via direct sympathoinhibitory effects or by re-sensitising baroreflex mechanisms remains unclear.
Absorption
The Tmax following IV administration is approximately 1 to 5 hours, while the Tmax for oral administration is 2 to 6 hours. Upon oral administration, Digoxin TFT is absorbed from the stomach and upper part of the small intestine. When Digoxin TFT is taken after meals, the rate of absorption is slowed, but the total amount of Digoxin TFT absorbed is usually unchanged. When taken with meals high in fibre, however, the amount absorbed from an oral dose may be reduced.
The bioavailability of orally administered Digoxin TFT is approximately 63 % in tablet form and 75 % as oral solution.
Distribution
The initial distribution of Digoxin TFT from the central to the peripheral compartment generally lasts from 6 to 8 hours. This is followed by a more gradual decline in serum Digoxin TFT concentration, which is dependent upon Digoxin TFT elimination from the body. The volume of distribution is large (Vdss = 510 litres in healthy volunteers), indicating Digoxin TFT to be extensively bound to body tissues. The highest Digoxin TFT concentrations are seen in the heart, liver and kidney that in the heart averaging 30- fold that in the systemic circulation. Although the concentration in skeletal muscle is far lower, this store cannot be overlooked since skeletal muscle represents 40% of total body weight. Of the small proportion of Digoxin TFT circulating in plasma, approximately 25% is bound to protein.
Biotransformation
The majority of Digoxin TFT is excreted by the kidneys as an intact drug, although a small fraction of the dose is metabolised to pharmacologically active and inactive metabolites. The main metabolites of Digoxin TFT are dihydroDigoxin TFT and digoxygenin.
Elimination
The major route of elimination is renal excretion of the unchanged drug.
Digoxin TFT is a substrate for P-glycoprotein. As an efflux protein on the apical membrane of enterocytes, P-glycoprotein may limit the absorption of Digoxin TFT. P-glycoprotein in renal proximal tubules appears to be an important factor in the renal elimination of Digoxin TFT.
Following intravenous administration to healthy volunteers, between 60 and 75% of a Digoxin TFT dose is recovered unchanged in the urine over a 6 day follow-up period. Total body clearance of Digoxin TFT has been shown to be directly related to renal function, and percent daily loss is thus a function of creatinine clearance, which in turn may be estimated from a stable serum creatinine. The total and renal clearances of Digoxin TFT have been found to be 193 ± 25 ml/min and 152 ± 24 ml/min in a healthy control population.
In a small percentage of individuals, orally administered Digoxin TFT is converted to cardioinactive reduction products (Digoxin TFT reduction products or DRPs) by colonic bacteria in the gastrointestinal tract. In these subjects over 40% of the dose may be excreted as DRPs in the urine. Renal clearances of the two main metabolites, dihydroDigoxin TFT and digoxygenin, have been found to be 79 ± 13 ml/min and 100 ± 26 ml/min respectively.
In the majority of cases however, the major route of Digoxin TFT elimination is renal excretion of the unchanged drug.
The terminal elimination half-life of Digoxin TFT in patients with normal renal function is 30 to 40 h.
Since most of the drug is bound to the tissues rather than circulating in the blood, Digoxin TFT is not effectively removed from the body during cardiopulmonary by-pass. Furthermore, only about 3% of a Digoxin TFT dose is removed from the body during five hours of haemodialysis.
Paediatric population
In the newborn period, renal clearance of Digoxin TFT is diminished and suitable dosage adjustments must be observed. This is especially pronounced in the premature infant since renal clearance reflects maturation of renal function. Digoxin TFT clearance has been found to be 65.6 ± 30 ml/min/1.73m2 at 3 months, compared to only 32 ± 7 ml/min/1.73 m2 at 1 week. By 12 months Digoxin TFT clearance of 88 ± 43 ml / min / 1.73m2 has been reported. Beyond the immediate newborn period, children generally require proportionally larger doses than adults on the basis of body weight and body surface area.
Renal impairment
The terminal elimination half-life of Digoxin TFT is prolonged in patients with impaired renal function, and in anuric patients will be of the order of 100 hours.
Hepatic impairment
Hepatic impairment has little effect on Digoxin TFT clearance.
Elderly
Age-related declines in renal function in elderly patients can result in a lower rates of Digoxin TFT clearance than in younger subjects, with reported Digoxin TFT clearance rates in the elderly of 53 ml/min/1.73m2.
Gender
Digoxin TFT clearance is 12% - 14% less in females than males and may need to be considered in dosing calculations.
Monitoring
Patients receiving Digoxin TFT should have their serum electrolytes and renal function (serum creatinine concentration) assessed periodically; the frequency of assessments will depend on the clinical setting.
Serum concentrations of Digoxin TFT may be expressed in Conventional Units of nanograms/ml or in SI units of nanomol/l. To convert nanograms/ml to nanomol/l, multiply nanograms/ml by 1.28.
The serum concentration of Digoxin TFT can be determined by radioimmunoassay.
Blood should be taken 6 hours or more after the last dose of Digoxin TFT.
There are no rigid guidelines as to the range of serum concentrations that are most efficacious. Several post hoc analyses of heart failure patients in the Digitalis Investigation Group trial suggest that the optimal trough Digoxin TFT serum level may be 0.5 nanograms/ml (0.64 nanomol/l) to 1.0 nanograms/ml (1.28 nanomol/l).
Digoxin TFT toxicity is more commonly associated with serum Digoxin TFT concentration greater than 2 nanograms/ml. However, serum Digoxin TFT concentration should be interpreted in the clinical context. Toxicity may occur with lower Digoxin TFT serum concentrations. In deciding whether a patient's symptoms are due to Digoxin TFT, the clinical state together with the serum potassium level and thyroid function are important factors.
Determination of the serum Digoxin TFT concentration may be very helpful in making a decision to treat with further Digoxin TFT, but other glycosides and endogenous Digoxin TFT-like substances, including metabolites of Digoxin TFT, can interfere with the assays that are available and one should always be wary of values which do not seem commensurate with the clinical state of the patient. Observations while temporary withholding of Digoxin TFT might be more appropriate.
Arrhythmias
Arrhythmias may be precipitated by Digoxin TFT toxicity, some of which can resemble arrhythmias for which the drug could be advised. For example, atrial tachycardia with varying atrioventricular block requires particular care as clinically the rhythm resembles atrial fibrillation.
Many beneficial effects of Digoxin TFT on arrhythmias result from a degree of atrioventricular conduction blockade. However, when incomplete atrioventricular block already exists the effects of a rapid progression in the block should be anticipated. In complete heart block the idioventricular escape rhythm may be suppressed.
Sinoatrial disorder
In some cases of sinoatrial disorder (i.e. Sick Sinus Syndrome) Digoxin TFT may cause or exacerbate sinus bradycardia or cause sinoatrial block.
The administration of Digoxin TFT in the period immediately following myocardial infarction is not contraindicated. However, the use of inotropic drugs in some patients in this setting may result in undesirable increases in myocardial oxygen demand and ischaemia, and some retrospective follow-up studies have suggested Digoxin TFT to be associated with an increased risk of death. However, the possibility of arrhythmias arising in patients who may be hypokalaemic after myocardial infarction and are likely to be haemodynamically unstable must be borne in mind. The limitations imposed thereafter on direct current cardioversion must also be remembered.
Cardiac amyloidosis
Treatment with Digoxin TFT should generally be avoided in patients with heart failure associated with cardiac amyloidosis. However, if alternative treatments are not appropriate, Digoxin TFT can be used with caution to control the ventricular rate in patients with cardiac amyloidosis and atrial fibrillation.
Myocarditis
Digoxin TFT can rarely precipitate vasoconstriction and therefore should be avoided in patients with myocarditis.
Beri beri heart disease
Patients with beri beri heart disease may fail to respond adequately to Digoxin TFT if the underlying thiamine deficiency is not treated concomitantly. There is also some published information indicating that Digoxin TFT may inhibit the uptake of thiamine in myocytes in beri beri heart disease.
Constrictive pericarditis
Digoxin TFT should not be used in constrictive pericarditis unless it is used to control the ventricular rate in atrial fibrillation or to improve systolic dysfunction.
Exercise tolerance
Digoxin TFT improves exercise tolerance in patients with impaired left ventricular systolic dysfunction and normal sinus rhythm. This may or may not be associated with an improved haemodynamic profile. However, the benefit of Digoxin TFT in patients with supraventricular arrhythmias is most evident at rest, less evident with exercise.
Withdrawal
In patients receiving diuretics and an ACE inhibitor, or diuretics alone, the withdrawal of Digoxin TFT has been shown to result in clinical deterioration.
Electrocardiography
The use of therapeutic doses of Digoxin TFT may cause prolongation of the PR interval and depression of the ST segment on the electrocardiogram.
Digoxin TFT may produce false positive ST-T changes on the electrocardiogram during exercise testing. These electrophysiologic effects reflect an expected effect of the drug and are not indicative of toxicity.
Severe respiratory disease
Patients with severe respiratory disease may have an increased myocardial sensitivity to digitalis glycosides.
Hypokalaemia
Hypokalaemia sensitises the myocardium to the actions of cardiac glycosides.
Hypoxia, hypomagnesaemia and hypercalcaemia
Hypoxia, Hypomagnesaemia and marked hypercalcaemia increase myocardial sensitivity to cardiac glycosides.
Thyroid disease
Administering Digoxin TFT to a patient with thyroid disease requires care. Initial and maintenance doses of Digoxin TFT should be reduced when thyroid function is subnormal. In hyperthyroidism there is relative Digoxin TFT resistance and the dose may have to be increased. During the course of treatment of thyrotoxicosis, dosage should be reduced as the thyrotoxicosis comes under control.
Malabsorption
Patients with malabsorption syndrome or gastro-intestinal reconstructions may require larger doses of Digoxin TFT.
Chronic congestive cardiac failure
Although many patients with chronic congestive cardiac failure benefit from acute administration of Digoxin TFT, there are some in whom it does not lead to constant, marked or lasting haemodynamic improvement. It is therefore important to evaluate the response of each patient individually when Digoxin TFT is continued long-term.
Direct current cardioversion
The risk of provoking dangerous arrhythmias with direct current cardioversion is greatly increased in the presence of digitalis toxicity and is in proportion to the cardioversion energy used.
For elective direct current cardioversion of a patient who is taking Digoxin TFT, the drug should be withheld for 24 hours before cardioversion is performed. In emergencies, such as cardiac arrest, when attempting cardioversion the lowest effective energy should be applied.
Direct current cardioversion is inappropriate in the treatment of arrhythmias thought to be caused by cardiac glycosides.
Since central nervous system and visual disturbances have been reported in patients receiving Digoxin TFT, patients should exercise caution before driving, using machinery or participating in dangerous activities.
Posology:
Digoxin TFT Injection is for administration by slow intravenous infusion (see Method of administration below).
The dose of Digoxin TFT for each patient has to be tailored individually according to age, lean body weight and renal function. Suggested doses are intended only as an initial guide.
If cases where cardiac glycosides have been taken in the preceding two weeks, the recommendations for initial dosing of a patient should be reconsidered and a reduced dose is advised.
The difference in bioavailability between injectable Digoxin TFT and oral formulations must be considered when changing from one dosage form to another. For example if patients are switched from oral to the I.V. formulation the dosage should be reduced by approximately 33%.
Emergency parenteral digitalisation (in patients who have not been given cardiac glycosides within the preceding two weeks):
Adults and paediatric populations over 10 years
Parenteral loading:
Parenteral loading should only be used in patients who have not been given cardiac glycosides within the preceding two weeks.
The total loading dose of parenteral Digoxin TFT is 500 to 1000 micrograms (0.5 to 1.0 mg) depending on age, lean body weight and renal function. The total loading dose should be administered in divided doses with approximately half of the total dose given as the first dose and further fractions of the total dose given at intervals of 4 - 8 hours. An assessment of clinical response should be performed before giving each additional dose.
Each dose should be given by intravenous infusion (see Method of administration) over a period of 10 - 20 minutes.
- Maintenance Dose:
The maintenance dosage should be based upon the percentage of the peak body stores lost each day through elimination. The following formula has had wide clinical use:
Ccr is creatinine clearance corrected to 70 kg body weight or 1.73 m2 body surface area.
If only serum creatinine (Scr) concentrations are available, a Ccr (corrected to 70 kg body weight) may be estimated in men as
NOTE: Where serum creatinine values are obtained in micromol/L these may be converted to mg/100 ml (mg %) as follows:
Where 113.12 is the molecular weight of creatinine.
For women, this result should be multiplied by 0.85.
NOTE: These formulae cannot be used for creatinine clearance in children.
In practice, this will mean that most patients with heart failure will be maintained on 125 to 250 micrograms (0.125 to 0.25 mg) Digoxin TFT daily; however in those who show increased sensitivity to the adverse effects of Digoxin TFT, a dosage of 62.5 microgram (0.0625 mg) daily or less may suffice. Conversely, some patients may require a higher dose.
Neonates, infants & paediatric populations up to 10 years of age:
if cardiac glycosides have been given in the two weeks preceding commencement of Digoxin TFT therapy, it should be anticipated that optimum loading doses of Digoxin TFT will be less than those recommended below.
In the newborn, particularly in the premature infant, renal clearance of Digoxin TFT is diminished and suitable dose reductions must be observed, over and above general dosage instructions.
Beyond the immediate newborn period, children generally require proportionally larger doses than adults on the basis of body weight or body surface area, as indicated in the schedule below. Children over 10 years of age require adult dosages in proportion to their body weight.
Parenteral Loading dose:
The I.V. loading dose in the above groups should be administered in accordance with the following schedule:
| Pre- term neonates Less than 1.5kg | 20 micrograms/kg over 24 hours |
| Pre-term neonates 1.5 - 2.5kg | 30 micrograms/kg over 24 hours |
| Full-term neonates To age 2 years | 35 micrograms/kg over 24 hours |
| Age 2 - 5 years | 35 micrograms/kg over 24 hours |
| Age 5 - 10 years | 25 micrograms/kg over 24 hours |
The loading dose should be administered in divided doses with approximately half the total dose given as the first dose and further fractions of the total dose given at intervals of 4 - 8 hours, assessing the clinical response before giving each additional dose. Each dose should be given by intravenous infusion (see Method of Administration) over a period of 10 - 20 minutes.
Maintenance Dose:
The maintenance dose should be administered in accordance with the following schedule:
Preterm neonates:
daily dose = 20% of 24-hour loading dose (intravenous or oral)
Term neonates and children up to 10 years:
daily dose = 25% of 24-hour loading dose (intravenous or oral)
These dosage schedules are meant as guidelines and careful clinical observation and monitoring of serum Digoxin TFT levels should be used as a basis for adjustment of dosage in these paediatric patient groups.
Elderly.
The possibility of reduced renal function and lower lean body mass should be taken into account when dealing with elderly patients. If necessary, the dosage should be reduced and adjusted to the changed pharmacokinetics to prevent elevated serum Digoxin TFT levels and the risk of toxicity. The serum Digoxin TFT levels should be checked regularly and hypokalaemia should be avoided.
Renal impairment
The dosage recommendations should be reconsidered if patients are elderly or if there are other reasons for the renal clearance of Digoxin TFT being reduced. A reduction in both initial and maintenance doses should be considered.
Method of administration:
Dilution of Digoxin TFT injection:
Digoxin TFT injection can be administered undiluted or diluted with a 4-fold or greater volume of 0.9% Sodium Chloride Injection, 0.18 % Sodium Chloride/4% Glucose Injection or 5% Glucose Injection. A 4-fold volume of diluent equates to adding one 2 ml ampoule of Digoxin TFT to 6 ml of injection solution. The use of less than a 4-fold volume of diluent could lead to precipitation of Digoxin TFT.
Digoxin TFT Injection may be diluted with the following solutions:
Sodium Chloride Intravenous Infusion BP 0.9% w/v
Glucose Intravenous Infusion BP 5.0% w/v
Sodium Chloride (0.18% w/v) and Glucose (4% w/v) Intravenous Infusion BP
When diluted in the ratio of 1 to 250 (i.e. one 2ml ampoule containing 500 micrograms Digoxin TFT added to 500ml of infusion solution), Digoxin TFT Injection B.P. is known to be compatible with the above mentioned infusion solutions and stable for up to 48 hours at room temperature (20 - 25°C).
Dilution should be carried out either under full aseptic conditions or immediately prior to use. Any unused solution should be discarded.
Administration of Digoxin TFT injection:
Each dose should be given by intravenous infusion over of 10 - 20 minutes.
The total loading dose should be administered in divided doses with approximately half of the total dose given as the first dose and further fractions of the total dose given at intervals of 4 - 8 hours. An assessment of clinical response should be performed before giving each additional dose.
The intramuscular route is painful and is associated with muscle necrosis. This route cannot be recommended.
Rapid intravenous injection can cause vasoconstriction producing hypertension and/or reduced coronary flow. A slow injection rate is therefore important in hypertensive heart failure and acute myocardial infarction.
If only part used, discard the remaining solution.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements
