Cyclic vomiting syndrome (NORD)

Cyclic vomiting syndrome (NORD)

Watch later

Watch later

Atrophy, aplasia, and hypoplasia
Metaplasia and dysplasia
Hyperplasia and hypertrophy
Enzyme function
Lipid-lowering medications: Statins
Miscellaneous lipid-lowering medications
Laxatives and cathartics
Protein synthesis inhibitors: Aminoglycosides
Antituberculosis medications
Protein synthesis inhibitors: Tetracyclines
Miscellaneous protein synthesis inhibitors
DNA synthesis inhibitors: Metronidazole
Mechanisms of antibiotic resistance
Antimetabolites: Sulfonamides and trimethoprim
Miscellaneous cell wall synthesis inhibitors
Cell wall synthesis inhibitors: Penicillins
Cell wall synthesis inhibitors: Cephalosporins
DNA synthesis inhibitors: Fluoroquinolones
Herpesvirus medications
Acetaminophen (Paracetamol)
Antihistamines for allergies
Anatomy of the pharynx and esophagus
Anatomy of the salivary glands
Gallbladder histology
Stomach histology
Colon histology
Pancreas histology
Esophagus histology
Small intestine histology
Liver histology
Gastrointestinal system anatomy and physiology
Liver anatomy and physiology
Anatomy and physiology of the teeth
Enteric nervous system
Gastric motility
Esophageal motility
Chewing and swallowing
Pancreatic secretion
Prebiotics and probiotics
Bile secretion and enterohepatic circulation
Eosinophilic esophagitis (NORD)
Gastric cancer
Celiac disease
Short bowel syndrome (NORD)
Ulcerative colitis
Crohn disease
Gallstone ileus
Familial adenomatous polyposis
Colorectal polyps
Irritable bowel syndrome
Diverticulosis and diverticulitis
Jaundice
Hemochromatosis
Cirrhosis
Cholestatic liver disease
Esophagitis: Clinical
Esophageal disorders: Pathology review
BRUE, ALTE, and SIDS: Clinical
MEN syndromes: Clinical
Abdominal pain: Clinical
Hypertensive disorders of pregnancy: Clinical
Cyclic vomiting syndrome (NORD)
Eating disorders: Clinical
Gastroesophageal reflux disease (GERD)
Gastroesophageal reflux disease (GERD): Clinical
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review
Esophageal disorders: Clinical
Acid reducing medications
Lipid-lowering medications: Fibrates
Minimal change disease
Non-alcoholic fatty liver disease
Fatty acid synthesis
Fatty acid oxidation
Deep vein thrombosis and pulmonary embolism: Pathology review
Childhood nutrition and obesity: Information for patients and families (The Primary School)
Hunger and satiety
Gallstones
Inflammatory bowel disease: Pathology review
Chronic pancreatitis
Glucagon
Cell membrane
Insulin
Niemann-Pick disease types A and B (NORD)
Metabolic acidosis
Ketone body metabolism
Chronic cholecystitis
Acute cholecystitis
Ascending cholangitis
Pancreatitis: Pathology review
Pancreatitis: Clinical
Bowel obstruction
Jaundice: Pathology review
Gallbladder disorders: Pathology review

Transcript

Watch video only

Cyclic vomiting syndrome, or CVS for short, is a disorder characterized by recurrent or cyclic episodes of severe nausea and vomiting. CVS can occur at any age, but is typically more common and severe in children.

Episodes of nausea and vomiting may last for a few hours to several days. They generally have sudden onset, resolve for a period of time, and are similar each time.

In some people, especially adults, nausea and vomiting may continue between episodes,but the intensity is far less severe than during episodes.

Episodes may occur a few times a year or as frequently as several times a month. Episodes may return like clockwork, and monthly episodes are common. They can occur at times of stress, or be apparently random.

During an episode, vomit can be bilious, appearing green or yellow. Children may experience bouts of projectile vomiting as frequently as four or more times per hour, which can potentially lead to dehydration and electrolyte imbalances, involving sodium and potassium.

Episodes can also be associated with severe abdominal pain, retching, and diarrhea, as well as decreased appetite and weight loss.

Some individuals may also experience migraine-like symptoms, like headaches and sensitivity to light and sound, as well as fever, dizziness, a lack of energy, and pallor.

In severe cases, an individual can become incapacitated and unable to walk or talk until the episode resolves. The exact cause of CVS is still unknown, but it seems to have many contributing factors.

The nervous system is thought to play a role. Nerves deliver messages throughout the body, including between the brain and gut, to coordinate functions.

Most individuals with CVS have migraines or a family history of migraines. In fact, CVS is sometimes called “abdominal migraine”.

Gastrointestinal motility may also have a role. The gastrointestinal tract has a layer of smooth muscles, which normally help push food, liquid, and gas from the esophagus down to the rectum.

In some individuals with CVS, gastrointestinal motility doesn’t function properly, which is known as dysmotility.

Dysmotility may also occur between vomiting episodes, resulting in conditions like gastroesophageal reflux, gastroparesis, and irritable bowel.

Other factors contributing to CVS may include changes or mutations in mitochondrial genes, as well as abnormal function of the autonomic nervous system called dysautonomia, and an overactive response to stress.

Key Takeaways

Cyclic vomiting syndrome (CVS) is a disorder characterized by recurrent, sudden episodes of severe nausea and vomiting. These episodes can last for hours, days, or weeks and are not associated with other illnesses or injuries. Between episodes, people with CVS feel entirely normal.

The cause of CVS is unknown, but it may be related to problems with the autonomic nervous system or changes in the levels of certain chemicals in the blood. Some people with CVS have a family history of the condition. CVS usually starts in childhood, mainly affecting children between the age of 3 to 7 years. It often resolves by adolescents, but it may persist in some individuals until adulthood.