CHEMOTHERAPY INDUCED NAUSEA AND VOMITING

Acute CINV, Delayed CINV, Anticipatory CINV, Enti emetics, seratonin receptor antagonists, corticosteroids, dopamine receptor antagonists, chemotherapy, side effects
continue reading these slides to know more about chemotherapy induced nausea and vomiting
 
Chemotherapy-Induced Nausea and Vomiting (CINV) 
Chemotherapy-induced nausea and vomiting (CINV) are significant side effects of cancer treatment that can severely impact a patient's quality of life and their ability to continue treatment. Effective management of CINV is crucial to ensure patient comfort and adherence to chemotherapy regimens.
 
Types of CINV
CINV can be categorized into several types based on the timing and triggers:

1. Acute CINV: Occurs within the first 24 hours after chemotherapy administration.
2. Delayed CINV: Occurs more than 24 hours after chemotherapy and can last for several days.
3. Anticipatory CINV: Triggered by the expectation of chemotherapy, often seen in patients who have previously experienced CINV.
4. Breakthrough CINV: Occurs despite prophylactic treatment and requires additional medication to control.
5. Refractory CINV: Persists despite prophylactic and breakthrough treatments.
 
Pathophysiology
The mechanisms underlying CINV involve complex interactions between the central nervous system (CNS) and the gastrointestinal (GI) tract. Key components include:

1. Chemoreceptor Trigger Zone (CTZ): Located in the area postrema of the brain, it detects emetogenic substances in the blood and cerebrospinal fluid and activates the vomiting center.
2. Vomiting Center: A neural network in the medulla oblongata that coordinates the act of vomiting.
3. Peripheral Pathways: Chemotherapy drugs can damage the GI tract lining, releasing serotonin (5-HT) and other neurotransmitters that activate vagal afferent nerves, sending signals to the vomiting center.

Risk Factors
Several factors influence the likelihood and severity of CINV:
Type of Chemotherapy: Certain drugs, such as cisplatin, are highly emetogenic.
Dosage and Schedule: Higher doses and certain administration schedules increase the risk.
Patient Characteristics: Younger age, female gender, history of motion sickness, and previous CINV episodes are associated with higher risk.
Lack of Prophylaxis: Inadequate preventive measures can lead to more severe CINV.

Management and Treatment
Effective management of CINV typically involves a combination of medications, lifestyle modifications, and supportive care:

1. Pharmacological Treatments:
   5-HT3 Receptor Antagonists: Drugs such as ondansetron, granisetron, and palonosetron block serotonin receptors and are effective for acute CINV.
   NK1 Receptor Antagonists: Aprepitant, fosaprepitant, and rolapitant block the neurokinin-1 receptor, reducing both acute and delayed CINV.
   Corticosteroids: Dexamethasone is commonly used in combination with other antiemetics to enhance efficacy.
   Dopamine Antagonists: Metoclopramide and prochlorperazine are used for breakthrough CINV.
   Benzodiazepines: Lorazepam and alprazolam can help with anticipatory CINV due to their anxiolytic properties.
   Cannabinoids: Dronabinol and nabilone are sometimes used for refractory CINV.

2. Non-Pharmacological Approaches:
   Dietary Modifications: Eating small, frequent meals and avoiding spicy, fatty, or very sweet foods can help.
   Hydration: Adequate fluid intake is crucial.
   Acupuncture and Acupressure: Some patients find relief with these techniques.
   Behavioral Therapy: Techniques such as relaxation and guided imagery can reduce anticipatory CINV.

3. Preventive Strategies:
   Prophylactic Medication: Administering antiemetics before chemotherapy can prevent CINV.
   Tailored Regimens: Individualizing antiemetic regimens based on patient-specific risk factors and chemotherapy regimen.

Monitoring and Follow-up
Regular assessment of CINV severity and the effectiveness of antiemetic therapy is essential. Tools such as the MASCC Antiemesis Tool (MAT) or patient diaries can help clinicians monitor and adjust treatment as needed.

Effective management of CINV improves patient outcomes by ensuring better adherence to chemotherapy, enhancing quality of life, and reducing the physical and emotional burden of cancer treatment.
Acute CINV, Delayed CINV, Anticipatory CINV, Enti emetics, seratonin receptor antagonists, corticosteroids, dopamine receptor antagonists, chemotherapy, side effects

Acute CINV, Delayed CINV, Anticipatory CINV, Enti emetics, seratonin receptor antagonists, corticosteroids, dopamine receptor antagonists, chemotherapy, side effects

Acute CINV, Delayed CINV, Anticipatory CINV, Enti emetics, seratonin receptor antagonists, corticosteroids, dopamine receptor antagonists, chemotherapy, side effects

Acute CINV, Delayed CINV, Anticipatory CINV, Enti emetics, seratonin receptor antagonists, corticosteroids, dopamine receptor antagonists, chemotherapy, side effects

Acute CINV, Delayed CINV, Anticipatory CINV, Enti emetics, seratonin receptor antagonists, corticosteroids, dopamine receptor antagonists, chemotherapy, side effects

Acute CINV, Delayed CINV, Anticipatory CINV, Enti emetics, seratonin receptor antagonists, corticosteroids, dopamine receptor antagonists, chemotherapy, side effects

 

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