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Chemotherapy induced
Nausea and vomiting
CINV
Dr. SHEKH ABDULLAH AL MUKIT
Resident
MD(Oncology), BSMMU
Key Ideas:
• Most common side effect
• Most feared side-effect
• May be more distressing than future concerns of life expectancy
• Medical complications: dehydration, electrolyte imbalance, risk of
aspiration pneumonia.
• So Effective management of Nausea and Vomiting is essential
Definitions
Nausea is an unpleasant, diffuse sensation of unease and
discomfort, often perceived as an urge to vomit.
Vomiting is the involuntary, forceful expulsion of the contents of
one's stomach through the mouth and sometimes the nose.
Risk factors
• Female
• Younger age (less than 50 years)
• Genetic variation in metabolism of 5 HT3
• History of
o Motion sickness
o Nausea and vomiting associated with pregnancy
o CINV in prior CT
• Alcohol use
• Emesis prior to chemotherapy
• Emetogenic potential of drug
Centers involved in CINV
• Vomiting center in reticular formation of medulla activated by
stimuli from:
Chemoreceptor Trigger Zone (CTZ) in area postrema, floor of
the fourth ventricle which is outside blood-brain barrier
(fenestrated venules)
• Upper GI tract & pharynx
I. Vestibular apparatus
II. Higher cortical centers
Centers involved in CINV
Pathophysiology of vomiting
Mechanisms of Chemotherapy-Induced
Nausea and Vomiting (CINV)
Central mechanism:
• Chemotherapeutic agent activates the chemoreceptor trigger
zone (CTZ)
• Activated CTZ invokes release of various neurotransmitters,
which stimulate vomiting center
Peripheral mechanism:
• Chemotherapeutic agent causes irritation and damage to
gastrointestinal (GI) mucosa, resulting in the release of
neurotransmitters
• Activated receptors send signals to vomiting center via vagal
afferents
Types of Chemotherapy Induced Nausea
&Vomiting
Categories of CINV
Acute: Here patient will experience nausea and vomiting within 24 hours of chemotherapy
Delayed: Here patient will experience nausea and vomiting after 24 hours of
chemotherapy
Anticipated: Here patient will experience nausea and vomiting before starting of
chemotherapy
Break through: Even after giving prophylactic drugs to prevent nausea and
vomiting patients will have episodes of nausea and vomiting, which requires rescue
antiemetics
Refractory: Nausea and vomiting occurs when there is a poor response to multiple
antiemetic regimens
CINV: Classification
Anticipatory Acute Delayed
Chemo 16 - 24 hours
Post Chemotherapy Nausea and Vomiting
Definition of Risk for CINV
Minimal: <10%
Low:10-30%
Moderate 30-90%
High >90%
Emetic risk Agent
High (>90%) Cisplatin
Cyclophosphamide ≥1500mg/m2 Carmustine
Dacarbazine
Dactinomycin
Moderate (30–90%) Oxaliplatin
Cytarabine >1000mg/m2 Carboplatin
Ifosfamide
Cyclophosphamide Doxorubicin
Daunorubicin Epirubicin
Low (10–30%) Paclitaxel
Docetaxel
Mitoxantrone Topotecan Etoposide
Pemetrexed Methotrexate
Gemcitabine
Cytarabine ≤1000mg/m2 Fluorouracil
Trastuzumab
Minimal (<10%) Bevacizumab
Bleomycin
Busulfan Fludarabine Rituximab
Vincristine
WHY CINV is important?
How to manage children with CINV
• Pharmacological
• Non pharmacological
Principles of Management
Exclude the non chemotherapeutic causes
• bowel obstruction or dysmotility
• concomitant medications
• metabolic disturbances
• occult CNS metastasis
Patient counselling and education should be done promptly.
Selection of anti-emetics according to chemotherapy regimen
Non pharmacological
1. Counsil about:
• Eating frequent small foods served at room temperature.
• Drinking the liquid one hour before or after meals.
• Walking short distance outdoors and inhale air slowly.
• Keeping away from odor of foods, perfume and fume.
• Putting on comfortable clothes.
• Do not sleep immediately after dinner.
• Eating light foods (soup, yoghurt) after control of nausea &
vomiting.
Non pharmacological
• Acupuncture
• Acupressure
• Music therapy
• Progressive muscle relaxation
• Massage therapy
• Hypnosis
• Exercise
• Food habit change
Pharmacological Anti emetic classes:
• cyclazine
• Diphenhydramine
Antihistaminic
• Phenothiazine(chloropromazine)
• Butyrophenone(haloperidol)
• Benzamides(metaclopromide , domperdione )
antidopaminergic
• ondansetron
• Granisetron
• Palonosetron
Serotonin
antagonists
Neurokinin 1
antagonist
•Aprepitant
•Fosaprepitant
Pharmacological Anti emetic classes:
• Dexamethasone
Corticosteroides
• Aloprozolam
• Lorazepam
Benzodiazipens
• nabilone
• Dronabinol
Cannabinoids
Management Guidelines
Management of CINV with Highly Emetogenic
Agents
Management of CINV with Moderately
Emetogenic Agents
Management of CINV with Low Risk
Emetogenic Agents
Management of CINV with Minimal Risk
Emetogenic Agents
Complications
• Dehydration
• Electrolyte imbalance
• Metabolic alkalosis
• Oesophageal tear
• Under nutrition
• Weight loss
• Aspiration pneumonitis
THANK YOU

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Cancer induced nausea and vomiting.pptx

  • 1. Chemotherapy induced Nausea and vomiting CINV Dr. SHEKH ABDULLAH AL MUKIT Resident MD(Oncology), BSMMU
  • 2. Key Ideas: • Most common side effect • Most feared side-effect • May be more distressing than future concerns of life expectancy • Medical complications: dehydration, electrolyte imbalance, risk of aspiration pneumonia. • So Effective management of Nausea and Vomiting is essential
  • 3. Definitions Nausea is an unpleasant, diffuse sensation of unease and discomfort, often perceived as an urge to vomit. Vomiting is the involuntary, forceful expulsion of the contents of one's stomach through the mouth and sometimes the nose.
  • 4. Risk factors • Female • Younger age (less than 50 years) • Genetic variation in metabolism of 5 HT3 • History of o Motion sickness o Nausea and vomiting associated with pregnancy o CINV in prior CT • Alcohol use • Emesis prior to chemotherapy • Emetogenic potential of drug
  • 5. Centers involved in CINV • Vomiting center in reticular formation of medulla activated by stimuli from: Chemoreceptor Trigger Zone (CTZ) in area postrema, floor of the fourth ventricle which is outside blood-brain barrier (fenestrated venules) • Upper GI tract & pharynx I. Vestibular apparatus II. Higher cortical centers
  • 8. Mechanisms of Chemotherapy-Induced Nausea and Vomiting (CINV) Central mechanism: • Chemotherapeutic agent activates the chemoreceptor trigger zone (CTZ) • Activated CTZ invokes release of various neurotransmitters, which stimulate vomiting center Peripheral mechanism: • Chemotherapeutic agent causes irritation and damage to gastrointestinal (GI) mucosa, resulting in the release of neurotransmitters • Activated receptors send signals to vomiting center via vagal afferents
  • 9. Types of Chemotherapy Induced Nausea &Vomiting
  • 10. Categories of CINV Acute: Here patient will experience nausea and vomiting within 24 hours of chemotherapy Delayed: Here patient will experience nausea and vomiting after 24 hours of chemotherapy Anticipated: Here patient will experience nausea and vomiting before starting of chemotherapy Break through: Even after giving prophylactic drugs to prevent nausea and vomiting patients will have episodes of nausea and vomiting, which requires rescue antiemetics Refractory: Nausea and vomiting occurs when there is a poor response to multiple antiemetic regimens
  • 11. CINV: Classification Anticipatory Acute Delayed Chemo 16 - 24 hours
  • 12. Post Chemotherapy Nausea and Vomiting
  • 13. Definition of Risk for CINV Minimal: <10% Low:10-30% Moderate 30-90% High >90%
  • 14. Emetic risk Agent High (>90%) Cisplatin Cyclophosphamide ≥1500mg/m2 Carmustine Dacarbazine Dactinomycin Moderate (30–90%) Oxaliplatin Cytarabine >1000mg/m2 Carboplatin Ifosfamide Cyclophosphamide Doxorubicin Daunorubicin Epirubicin Low (10–30%) Paclitaxel Docetaxel Mitoxantrone Topotecan Etoposide Pemetrexed Methotrexate Gemcitabine Cytarabine ≤1000mg/m2 Fluorouracil Trastuzumab Minimal (<10%) Bevacizumab Bleomycin Busulfan Fludarabine Rituximab Vincristine
  • 15. WHY CINV is important?
  • 16. How to manage children with CINV • Pharmacological • Non pharmacological
  • 17. Principles of Management Exclude the non chemotherapeutic causes • bowel obstruction or dysmotility • concomitant medications • metabolic disturbances • occult CNS metastasis Patient counselling and education should be done promptly. Selection of anti-emetics according to chemotherapy regimen
  • 18. Non pharmacological 1. Counsil about: • Eating frequent small foods served at room temperature. • Drinking the liquid one hour before or after meals. • Walking short distance outdoors and inhale air slowly. • Keeping away from odor of foods, perfume and fume. • Putting on comfortable clothes. • Do not sleep immediately after dinner. • Eating light foods (soup, yoghurt) after control of nausea & vomiting.
  • 19. Non pharmacological • Acupuncture • Acupressure • Music therapy • Progressive muscle relaxation • Massage therapy • Hypnosis • Exercise • Food habit change
  • 20. Pharmacological Anti emetic classes: • cyclazine • Diphenhydramine Antihistaminic • Phenothiazine(chloropromazine) • Butyrophenone(haloperidol) • Benzamides(metaclopromide , domperdione ) antidopaminergic • ondansetron • Granisetron • Palonosetron Serotonin antagonists Neurokinin 1 antagonist •Aprepitant •Fosaprepitant
  • 21. Pharmacological Anti emetic classes: • Dexamethasone Corticosteroides • Aloprozolam • Lorazepam Benzodiazipens • nabilone • Dronabinol Cannabinoids
  • 23. Management of CINV with Highly Emetogenic Agents
  • 24. Management of CINV with Moderately Emetogenic Agents
  • 25. Management of CINV with Low Risk Emetogenic Agents
  • 26. Management of CINV with Minimal Risk Emetogenic Agents
  • 27. Complications • Dehydration • Electrolyte imbalance • Metabolic alkalosis • Oesophageal tear • Under nutrition • Weight loss • Aspiration pneumonitis