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1. Pathophysiology of Vomiting
2. Classification of drugs used in Vomiting
3. Explain Mechanism of action of antiemetic
drugs
Manikandan 3
Vomiting Centre
(medulla)
Cerebral cortex
Anticipatory emesis
Smell
Sight
Thought
Vestibular
nucleiMotion
sickness
Pharynx & GIT
Chemo & radio therapy
Gastroenteritis
Chemoreceptor
Trigger Zone
(CTZ)
(Outside BBB)
Cancer chemotherapy
Opioids
Muscarinic, 5 HT3 &
Histaminic H1
5 HT3 receptors
Dopamine D2
5 HT3,,Opioid
Receptors
Muscarinic
Histaminic H1
Pathophysiology of vomiting
Manikandan 4
Now answer this question
Which group of drugs can be used as antiemetics ?
 Muscarinic antagonis
 H1 Antagonist
 Serotonin 5 HT3 Antagonists
 Dopamine D2 Antagonist
 Cannabinoids
Manikandan 5
Classification of drugs used in
Vomiting
Manikandan 6
1. Anticholinergics
 Scopolamine (hyoscine) –
used as transdermal patch for motion sickness
 Useful in motion sickness
 Morning sickness
 Postoperative and other form of vomiting
 Their antiemetic action based on anticholinergic,
antihistaminic, and sedative property.
 Drugs- promethazine, Diphenhydramine,
cyclizine, meclizine, cinnarazine
Manikandan 7
2. H1 antagonist
Manikandan 8
3. 5 HT3 Antagonist
 Potent antiemetics
 Even though 5 HT3 receptors are present in
vomiting centre & CTZ, the antiemetic action is
restricted to emesis caused by vagal stimulation.
 High first pass metabolism
 Excreted by liver & kidney
 No dose reduction in renal insufficiency but needed
in hepatic insufficiency
 Given once or twice daily – orally or intravenously.
Manikandan 9
Drugs Available
 Ondansetron 32 mg / day
 Granisetron 10 mg / kg / day
 Dolasetron 1.8 mg / kg / day
Indications
 Chemotherapy induced nausea & vomiting – given
30 min. before chemotherapy.
 Postoperative & postradiation nausea & vomiting
Manikandan 10
Adverse Effects
 Excellent safety profile
 Headache & constipation
 All three drugs cause prolongation of QT interval,
but more pronounced with dolasetron.
Manikandan 11
4. D2 antagonist - Prokinetic drug
 MOA- Antagonise D2 receptors in CTZ.
 Drugs available
Metoclopramide 2.5 mg b.d
Domperidone 10 mg b.d
 Both drugs acts as antidopaminergic also
prokinetic agents due to their 5 HT4 agonist activity.
 Domperidone – oral ; Metoclopramide – oral & i.v
 Metoclopramide crosses BBB but domperidone
cannot.
 D2 antagonism – by blocking D2 receptor in GIT-
increasing gastric emptying, enhancing LES tone
by augmenting Ach release.
 5HT3 antagonism- seen only in high doses
 5-HT4 antagonism- metoclopramide acts in the
GIT to enhance Ach release from myenteric
motor neurons 5-HT4 receptor activation.
Manikandan 12
Manikandan 13
Now answer this question
Which is a better antiemetic – Metoclopramide or
Domperidone ?
 As CTZ is outside BBB both have antiemetic
effects.
 But as metoclopramide crosses BBB it has
adverse effects like extrapyramidal side effects..
 Domperidone is well tolerated.
 Antiemetic – metoclopramide effective in post-
operative, drug induced, diseased associated
vomiting.
 Gastrokinetic – to accelerate gastric emptying –
when emergency general anesthesia given, to,
relieve post vagotomy or diabetes associated
gastric stasis, to facilitate duodenal intubation
 Dyspepsia
 GERD
Manikandan 14
 Do not cross BBB
 DO NOT CAUSE EXTRAPYRAMIDAL SIDE
EFFECTS
 DOC FOR LEVODOPA INDUCED
VOMITING
 NO OTHER ACTION
Manikandan 15
Manikandan 18
Now answer this question
A physician prescribed Tab.Ondansetron
for prophylaxis of motion sickness. Even
though ondansetron is a potent antiemetic
it didn’t produce any effect in this patient.
Can you explain why ?
Manikandan 19
Explanation :
Vestibular nuclei has only
muscarinic and H1 histaminic receptors.
Manikandan 20
Points to Ponder
Manikandan 22
Extra-pyramidal effects
Dry mouth and blurred vision
Sedation
Tachycardia
Hypotension
Anti-emetic agents: Side effects
Manikandan 23
Postoperative
Chemotherapy
Travel sickness
Parkinson’s disease
(especially apomorphine)
Pregnancy
Anti-emetic agents: Choice
Manikandan 24

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Drugs for vomiting

  • 1.
  • 2. 1. Pathophysiology of Vomiting 2. Classification of drugs used in Vomiting 3. Explain Mechanism of action of antiemetic drugs
  • 3. Manikandan 3 Vomiting Centre (medulla) Cerebral cortex Anticipatory emesis Smell Sight Thought Vestibular nucleiMotion sickness Pharynx & GIT Chemo & radio therapy Gastroenteritis Chemoreceptor Trigger Zone (CTZ) (Outside BBB) Cancer chemotherapy Opioids Muscarinic, 5 HT3 & Histaminic H1 5 HT3 receptors Dopamine D2 5 HT3,,Opioid Receptors Muscarinic Histaminic H1 Pathophysiology of vomiting
  • 4. Manikandan 4 Now answer this question Which group of drugs can be used as antiemetics ?  Muscarinic antagonis  H1 Antagonist  Serotonin 5 HT3 Antagonists  Dopamine D2 Antagonist  Cannabinoids
  • 5. Manikandan 5 Classification of drugs used in Vomiting
  • 6. Manikandan 6 1. Anticholinergics  Scopolamine (hyoscine) – used as transdermal patch for motion sickness
  • 7.  Useful in motion sickness  Morning sickness  Postoperative and other form of vomiting  Their antiemetic action based on anticholinergic, antihistaminic, and sedative property.  Drugs- promethazine, Diphenhydramine, cyclizine, meclizine, cinnarazine Manikandan 7 2. H1 antagonist
  • 8. Manikandan 8 3. 5 HT3 Antagonist  Potent antiemetics  Even though 5 HT3 receptors are present in vomiting centre & CTZ, the antiemetic action is restricted to emesis caused by vagal stimulation.  High first pass metabolism  Excreted by liver & kidney  No dose reduction in renal insufficiency but needed in hepatic insufficiency  Given once or twice daily – orally or intravenously.
  • 9. Manikandan 9 Drugs Available  Ondansetron 32 mg / day  Granisetron 10 mg / kg / day  Dolasetron 1.8 mg / kg / day Indications  Chemotherapy induced nausea & vomiting – given 30 min. before chemotherapy.  Postoperative & postradiation nausea & vomiting
  • 10. Manikandan 10 Adverse Effects  Excellent safety profile  Headache & constipation  All three drugs cause prolongation of QT interval, but more pronounced with dolasetron.
  • 11. Manikandan 11 4. D2 antagonist - Prokinetic drug  MOA- Antagonise D2 receptors in CTZ.  Drugs available Metoclopramide 2.5 mg b.d Domperidone 10 mg b.d  Both drugs acts as antidopaminergic also prokinetic agents due to their 5 HT4 agonist activity.  Domperidone – oral ; Metoclopramide – oral & i.v  Metoclopramide crosses BBB but domperidone cannot.
  • 12.  D2 antagonism – by blocking D2 receptor in GIT- increasing gastric emptying, enhancing LES tone by augmenting Ach release.  5HT3 antagonism- seen only in high doses  5-HT4 antagonism- metoclopramide acts in the GIT to enhance Ach release from myenteric motor neurons 5-HT4 receptor activation. Manikandan 12
  • 13. Manikandan 13 Now answer this question Which is a better antiemetic – Metoclopramide or Domperidone ?  As CTZ is outside BBB both have antiemetic effects.  But as metoclopramide crosses BBB it has adverse effects like extrapyramidal side effects..  Domperidone is well tolerated.
  • 14.  Antiemetic – metoclopramide effective in post- operative, drug induced, diseased associated vomiting.  Gastrokinetic – to accelerate gastric emptying – when emergency general anesthesia given, to, relieve post vagotomy or diabetes associated gastric stasis, to facilitate duodenal intubation  Dyspepsia  GERD Manikandan 14
  • 15.  Do not cross BBB  DO NOT CAUSE EXTRAPYRAMIDAL SIDE EFFECTS  DOC FOR LEVODOPA INDUCED VOMITING  NO OTHER ACTION Manikandan 15
  • 16. Manikandan 18 Now answer this question A physician prescribed Tab.Ondansetron for prophylaxis of motion sickness. Even though ondansetron is a potent antiemetic it didn’t produce any effect in this patient. Can you explain why ?
  • 17. Manikandan 19 Explanation : Vestibular nuclei has only muscarinic and H1 histaminic receptors.
  • 19. Manikandan 22 Extra-pyramidal effects Dry mouth and blurred vision Sedation Tachycardia Hypotension Anti-emetic agents: Side effects
  • 20. Manikandan 23 Postoperative Chemotherapy Travel sickness Parkinson’s disease (especially apomorphine) Pregnancy Anti-emetic agents: Choice

Editor's Notes

  1. Explain Clinical Profile of Drugs used for Vomiting
  2. enhances gastrointestinal motility by increasing the frequency or strength of contractions, but without disrupting their rhythm
  3.  dystonia (continuous spasms and muscle contractions), akathisia (may manifest as motor restlessness),[1] parkinsonism (characteristic symptoms such as rigidity), bradykinesia (slowness of movement), tremor, and tardive dyskinesia (irregular, jerky movements)