Vimala Colaco
Atropine
• Treatment of sinus 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.
Cautions: gastrointestinal obstruction,
 thyrotoxicosis, and tachycardia.
Adverse events: Tachycardia, palpitations, delirium,
 ataxia, dry hot skin, tremor, urinary retention
Epinephrine
Indications: Treatment of cardiac 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
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
Hydrocortisone
• Indications: Status asthmaticus, shock
  [50mg/kg/dose 4h],Treatment of adrenal
  insufficiency, congenital adrenal hyperplasia,
• Caution: Abrupt withdrawal -acute adrenal
  insufficiency.
• Adverse events: Hypertension, hyperglycemia,
  hypokalemia, euphoria, insomnia, headache, Cushing
  syndrome, peptic ulcer, cataracts,
  immunosuppression, skin and muscle atrophy, acne,
  edema.
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
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
Dopamine
• Indication: hypotension and shock
• 1–20μg/kg/min IV
• Adverse events: Tachycardia, ectopic beats,
 ventricular arrhythmias, tissue necrosis with
 extravasation, vasoconstriction, gangrene of
 extremities, excess urine output (doses <5μg/kg/min),
 oliguria (doses 10μg/kg/min).
Dose          microgm/kg/min

Strengthens             throughout dose    1-5
contractions            range


Increases renal blood   Low/intermediate   5-15
flow                    doses


Vasocontriction         High dose          15-25
Furosemide
Indications: Pulmonary edema-cardiac failure,
 SIADH, reduction of ICT in combination with
 mannitol, broncho-pulmonary dysplasia
Adverse events: Dehydration, electrolyte loss,
 hyperuricemia, photosensitivity, ischemic hepatitis,
 hypercalciuria, renal stones, ototoxicity (IV infusion
 rate >4mL/min), gastrointestinal intolerance
Heart failure. It inhibits 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
 Careful monitoring of 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
Digoxin
• Indications :Treatment of 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
The drug crosses the 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.
Digoxin in heart failure
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
Monitoring:
• Dosing should be 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.
Digoxin Immune Fab
Treatment of 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.
Naloxone
• Indication: opiate excess(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.
Phenytoin
• Indications: Anticonvulsant and 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
Cautions:
  Infuse slowly 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
• 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.
Phenobarbitone
Indications: anticonvulsant,sedative, hypnotic,
 anesthetic, hyperbillubinemia
Anticonvulsant
 loading dose Children:15 -20mg/kg PO, IV.
 Maintenance dose
         Neonates: 3–4mg/kg, Children: 5–
                  6mg/kg/24hr PO, IV, q12–24h.
• Cautions: Dose titrated 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.
.
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)
 Chloride responsive metabolic 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
Sodium bicarbonate
• Presence of 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
Alkali therapy may result 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
Calcium gluconate
Hyperkalemia- counteracts the 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.
Symptomatic hypocalcemia in neonates, 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

Medications in pediatrics

  • 1.
  • 2.
    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
  • 6.
    Hydrocortisone • Indications: Statusasthmaticus, shock [50mg/kg/dose 4h],Treatment of adrenal insufficiency, congenital adrenal hyperplasia, • Caution: Abrupt withdrawal -acute adrenal insufficiency. • Adverse events: Hypertension, hyperglycemia, hypokalemia, euphoria, insomnia, headache, Cushing syndrome, peptic ulcer, cataracts, immunosuppression, skin and muscle atrophy, acne, edema.
  • 7.
    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
  • 9.
    Dopamine • Indication: hypotensionand shock • 1–20μg/kg/min IV • Adverse events: Tachycardia, ectopic beats, ventricular arrhythmias, tissue necrosis with extravasation, vasoconstriction, gangrene of extremities, excess urine output (doses <5μg/kg/min), oliguria (doses 10μg/kg/min).
  • 10.
    Dose microgm/kg/min Strengthens throughout dose 1-5 contractions range Increases renal blood Low/intermediate 5-15 flow doses Vasocontriction High dose 15-25
  • 11.
    Furosemide Indications: Pulmonary edema-cardiacfailure, SIADH, reduction of ICT in combination with mannitol, broncho-pulmonary dysplasia Adverse events: Dehydration, electrolyte loss, hyperuricemia, photosensitivity, ischemic hepatitis, hypercalciuria, renal stones, ototoxicity (IV infusion rate >4mL/min), gastrointestinal intolerance
  • 12.
    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.
  • 23.
    Phenobarbitone Indications: anticonvulsant,sedative, hypnotic, anesthetic, hyperbillubinemia Anticonvulsant loading dose Children:15 -20mg/kg PO, IV. Maintenance dose Neonates: 3–4mg/kg, Children: 5– 6mg/kg/24hr PO, IV, q12–24h.
  • 24.
    • 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).
  • #21 Children 0.5–6 y:8–10mg/kg ;7–9 yr: 6–8mg/kg;10–16 yr: 6–7mg/kg/24hr PO, IVq12–24h
  • #22 Follows saturation (Michaelis-Menten) pharmacokinetics
  • #23 If necessary, measure free drug concentration: therapeutic 1–2?μg/mL
  • #25 Target serum concentrations: 15–40 μ g/mL coma (acute) &gt; 60 μ g/mL. Monitoring: Phenobarbital concentrations: sedation 15–40 μ g/mL; coma &gt;60?μ g/mL
  • #28 Low-dose 0.5–2?mEq/kg of sodium bicarbonate if not responding and pH &lt; 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.