This document provides information on various medications including their indications, dosages, cautions, and adverse effects. It discusses drugs used to treat conditions like cardiac arrest, shock, seizures, and electrolyte abnormalities. The medications described include atropine, epinephrine, hydrocortisone, dopamine, furosemide, digoxin, phenytoin, phenobarbitone, potassium chloride, sodium bicarbonate, and calcium gluconate. Precise dosages are provided for neonatal and pediatric patients.
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Introduction of Vimala Colaco, who may be the presenter or a significant figure related to the discussed topics.
Atropine indications for heart conditions and organophosphate poisoning. Notable doses for neonatal use, cautions, and adverse events.
Epinephrine use in cardiac arrest and allergic reactions. Relevant dosage information and adverse events.
Hydrocortisone for adrenal insufficiency and shock management, including dosage guidelines and side effects.
Protocols for treating anaphylactic shock with epinephrine, antihistamines, and fluid resuscitation.
Dopamine's indication for shock and hypotension, dosage, and potential adverse events.
Furosemide's use in heart failure and other conditions, dosing strategies, and monitoring potassium levels.
Digoxin for heart failure treatment and its adjustments according to renal function. Dosing and toxicity management.
Naloxone's role in treating opiate overdoses, dosing in neonates and children, and monitoring adverse effects.
Phenytoin for status epilepticus, including dosing strategies for various age groups and cautions.
Phenobarbitone as an anticonvulsant and sedative, proper dosing, and monitoring for side effects.
Potassium chloride for hypokalemia and cardiac issues, dosing parameters, and possible adverse effects.
Indications for sodium bicarbonate in metabolic acidosis and potential complications of its use.
Calcium gluconate for hyperkalemia and hypocalcemia in neonates, dosing, and potential adverse events.
Atropine
• Treatment ofsinus pulseless electrical activity,
bradycardia, or asystole..
Neonates and children: 0.02mg/kg
intratracheal (max: 0.5mg); may repeat5min later, one
time
Cardiac pacing is required in neonates with ventricular
rates of 50 beats/min or experience heart failure after
birth. to increase the heart rate temporarily until
pacemaker placement can be arranged
Preoperative medication to inhibit secretions and
salivation
• Antidote to organophosphate poisoning.
0.02–0.05 mg/kg every 10–20min until atropine effect is seen
then q1–4h for at least 24hr.
3.
Cautions: gastrointestinal obstruction,
thyrotoxicosis, and tachycardia.
Adverse events: Tachycardia, palpitations, delirium,
ataxia, dry hot skin, tremor, urinary retention
4.
Epinephrine
Indications: Treatment ofcardiac arrest,
bronchospasm, anaphylactic reaction
For asystole or for failure Epinephrine (0.1–
0.3mL/kg of a 1:10,000 solution, intravenously or
intratracheally) is given to respond to 30sec of
combined resuscitation. The dose may be repeated
every 5 min
Routes- IV, intratracheal, continuous infusion and
nebulisation
5.
Adverse events:
Tachycardia, hypertension,nervousness, restlessness,
irritability, headache, tremor, weakness, nausea,
vomiting, acute urinary retention.
Peripheral soft tissue damage if they extravasate from
peripheral lines into the local tissues
Status asthmaticus
Oxygen inhalation+
adrenaline/terbutaline inj
inhalation salbutamol+ if not
ipratropium and loading dose theophylline
hydrocortisone (10mg/kg)
improve
continue terbutaline inj[20-
30min]
hydrocortisone 5mg/kg 6-8
hrly
8.
Anaphylactic shock
Consider when compatible history of severe allergic-type reaction with
respiratory difficulty and/or hypotension especially if skin changes present
Oxygen treatment when available
Stridor, wheeze, respiratory distress
or clinical signs of shock [1]
Adrenaline (epinephrine) [2,3] 1:1000 solution
0.5 mL (500 micrograms) IM
Repeat in 5 minutes if no clinical improvement
Antihistamine (chlorphenamine)
10-20 mg IM/or slow IV
IN ADDITION
For all severe or recurrent reactions and If clinical manifestations of shock do not
patients with asthma give respond to drug treatment give 1-2 litres IV
Hydrocortisone fluid. [4] Rapid infusion or one repeat dose
100-500 mg IM/or slowly IV may be necessary
Heart failure. Itinhibits the reabsorption of
sodium and chloride in the distal tubules and the
loop of Henle.
Acute diuresis should be given intravenous or
intramuscular furosemide at an initial dose of 1–
2mg/kg, which usually results in rapid diuresis
.Chronic furosemide therapy is then prescribed at
a dose of 1–4mg/kg/24hr given between one and
four times a day
13.
Careful monitoringof electrolytes is necessary
with long-term furosemide therapy because of the
potential for significant loss of potassium.
Potassium chloride supplementation is usually
required unless the potassium-sparing diuretic
spironolactone is given concomitantly.
When furosemide is administered every other
day, dietary potassium supplementation may be
adequate to maintain normal serum potassium
levels
14.
Digoxin
• Indications :Treatmentof systolic heart failure and
supraventricular tachyarrhythmias
• Cautions: Contraindicated in AV block, idiopathic
hypertrophic subaortic stenosis,or constrictive
pericarditis
• Adverse events: Anorexia, nausea, vomiting,
diarrhea, feeding intolerance,bradycardia,
arrhythmias, lethargy, depression, vertigo, blurred
vision, diplopia, photophobia, yellow or green vision
15.
The drug crossesthe placenta, and therefore a fetus
with heart failure(secondary to arrhythmia) can be
treated by administering digoxin to the mother.
The kidney eliminates digoxin, so dosing must be
adjusted according to the patient'srenal function.
16.
Digoxin in heartfailure
Rapid digitalization of infants and children in heart
failure may be carried out intravenously. The
recommended schedule is to give half the total digitalizing
dose immediately and the succeeding two one-quarter
doses at 12hr intervals later.
Maintenance digitalis therapy is started approximately
12hr after full digitalization. The daily dosage is divided in
two and given at 12hr .The dosage is one quarter of the
total digitalizing dose
Slow digitalization –patient not critically ill or initiation
of a maintenance digoxin schedule without a previous
loading dose .full digitalization in 7–10 days
17.
Monitoring:
• Dosing shouldbe guided by measuring serum digoxin
concentrations: therapeutic: 0.8–2ng/mL; toxic: >2–
2.5ng/mL.
• DLIS - elevate digoxin levels, so pretreatment digoxin
levels can be obtained and subtracted from treatment
levels or samples can be run through a free-level filter to
remove DLIS before assay.
• Check post-distribution levels (drawn at least 6–8hr post
dose) at steady-state (2–4 wk) or if ECG or clinical signs of
toxicity. Check ECG, serum electrolytes, calcium, and
magnesium.
18.
Digoxin Immune Fab
Treatmentof digitalis intoxication from digoxin
Dose is based on amount of digoxin ingested or
estimated total body load based on post-distributive
serum concentration
Adverse events: Worsening of heart failure or atrial
fibrillation, hypokalemia, facial swelling, and redness.
19.
Naloxone
• Indication: opiateexcess(overdose, poisoning).
• Neonates and children: 0.1mg/kg IV (max dose: 2mg).
If no response, repeat q 2–3min until desired effect.
May give by continuous IV infusion
• Adverse effects May precipitate acute opiate
withdrawal. Duration of effect of many opiates may
be longer than naloxone requiring individualized
naloxone dosing.
20.
Phenytoin
• Indications: Anticonvulsantand antiarrhythmic.
• Status epilepticus:
mg/kg IV Loading dose Maintenance dose
Neonates 15-20 5
Children 15-18 .5-6yr 8-10
7-9yr 6-8
10-16yr 6-7
21.
Cautions:
Infuseslowly IV; variable oral bioavailability;
chewable tablet most consistent. Must shake oral
suspension very well before use.
Certain disease states (renal failure, acute head
trauma) may lead to imbalance between free and
protein-bound drug.
Fosphenytoin has advantages over the older
formulation - it is water soluble, less irritating after IV
injection, and well absorbed after intramuscular
injection
22.
• Adverse effects:Lethargy, dizziness, nystagmus,
hypotension, hirsutism, gingival hyperplasia, rash,
Stevens-Johnson syndrome, hepatitis, thrombophlebitis.
• Drug interactions:
May increase metabolism of certain hepatically cleared
drugs; griseofulvin, corticosteroids, cyclosporin;
Highly protein boundand may cause displacement
interaction.
• Monitoring: Phenytoin concentrations: therapeutic 8–
20μg/mL.
• Cautions: Dosetitrated to desired effect. Administer IV
=30mg/min
• Adverse effects: Hypotension, drowsiness, respiratory
depression, paradoxical hyperactivity
• Drug interactions:
May increase metabolism of many hepatically cleared
drugs; griseofulvin, corticosteroids.
Certain drugs may interfere with phenobarbital
metabolism: valproic acid, chloramphenicol, felbamate.
.
25.
Potassium chloride
Indications:
- Hypokalemia
< 2.5meq/l, cardiac rhythm disturbances
40mEq/L @ 0.6 mEq/kg/hr under continuous
EEG monitoring
- Tachyarrhythmias – chronic use of digoxin[max
100m mol)
26.
Chloride responsivemetabolic alkalosis , as a
component of mantainance fluids[10/20 meq/l],
bronchopulmonary dysplasia ( with
hydrochlorothiazide), supplementation (with
furosemide in heart failure with digoxin), nonketotic
hyperosmolar coma
Adverse effects : Hyperkalemia, gastritis
27.
Sodium bicarbonate
• Presenceof a severe metabolic acidosis(1mEq/kg,) as
documented by arterial blood gas analysis and during
a prolonged resuscitation when it may be given every
10 min during the arrest
• Symptomatic hyperkalemia(>7meq/L),
hypermagnesemia, tricyclic antidepressant drug
intoxications, or with adverse events due to sodium
channel blocking agents
• Alkalinization of urine with sodium bicarbonate
increases effectiveness of aminoglycosides against in
the urinary tract
28.
Alkali therapy mayresult in hypernatremia, skin
slough from infiltration, increased serum osmolarity,
hypocalcemia, hypokalemia,
Liver injury when oncentrated solutions are
administered rapidly through an umbilical vein
catheter wedged in the liver
29.
Calcium gluconate
Hyperkalemia- counteractsthe potassium-induced
increase in myocardial irritability Calcium
gluconate 10% solution, 1.0mL/kg IV, over 3–5 min
Neonatal tetany consists of intravenous injections of
5–10mL of a 10% solution of calcium gluconate at the
rate of 0.5–1mL/min while the heart rate is monitored.
30.
Symptomatic hypocalcemia inneonates, calcium
gluconate is given at a dose of 100–200mg/kg (1–
2mL/kg of a 10% solution).dose may be repeated
every 6–8hr until the calcium level stabilizes
Alternatively, intravenous infusion can be given
Adverse effects :hypercalcemia
Editor's Notes
#3 blocks action of acetylcholine and antagonizes histamine and serotonin).
#4 pulseless electrical activity (electrical-mechanical dissociation). These include hypothermia, hypoxia, hypovolemia, hyperkalemia, tension pneumothorax, pericardial tamponade, toxins, and pulmonary thromboembolism
#16 The rate of excretion is proportional to the glomerular filtration rate
#19 (binds with molecules of unbound digoxin or digitoxin and is renally cleared).
#28 Low-dose 0.5–2?mEq/kg of sodium bicarbonate if not responding and pH < 7.1 and ventilation (CO2 TREATMENT OF ARSENIC AND MERCURY INTOXICATION fluids, sodium bicarbonate, and mannitol to prevent renal failure secondary to the deposition of hemoglobin in the kidneys-- treat and prevent dysrhythmias elimination) is adequate
#31 Newborn infants with hypocalcemia usually do not have carpopedal spasm. Along with seizures, manifestations in newborns may include irritability, muscular twitching, jitteriness, and tremors. Alternatively, newborns with hypocalcemia may have symptoms suggestive of sepsis, such as poor feeding, vomiting, and lethargy.