How to alleviate vomiting in Kawasaki disease

Written by Quan Xiang Mei
Pediatrics
Updated on December 04, 2024
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When children with Kawasaki disease experience vomiting, the first step is to refrain from eating and drinking, including water, for one to two hours after vomiting to avoid burdening the stomach and intestines.

If vomiting subsides after fasting, there is no need for medication temporarily. However, if there is no significant relief and bloating is evident, it is necessary to treat for bowel movement and gas release. At this time, oral medications that aid in digestion, such as digestive tonics, are acceptable. If relief is still not achieved, intravenous fluid supplementation and medications that enhance gastrointestinal motility can be administered. Parents can also keep the abdomen warm and, centering around the navel, perform clockwise abdominal massages to help alleviate the symptoms of vomiting.

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Causes of secondary recurrence of Kawasaki disease

Kawasaki disease, also known as mucocutaneous lymph node syndrome, commonly affects children and infants under five years old. It is an acute, systemic vasculitic disease. Clinically, it is primarily characterized by persistent fever, bilateral conjunctival congestion, cracked lips, strawberry tongue, rash, hard swelling of hands and feet, fingertip desquamation, and enlargement of cervical lymph nodes. In severe cases, it can lead to coronary artery dilation, coronary artery aneurysms, and thrombotic obstruction. The exact cause of Kawasaki disease is not very clear, but it is mainly believed to be related to infections. The probability of secondary recurrence of Kawasaki disease is about 2%, and its causes mainly have to do with infections, immune factors of the body, genetic factors, and so on.

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Does Kawasaki disease cause a runny nose?

Kawasaki disease, also known as mucocutaneous lymph node syndrome, primarily presents with repeated high fevers that do not respond to antibiotics, conjunctival congestion, diffuse oral congestion, chapped and congested lips, polymorphic erythema and scarlatiniform rashes on the skin, and unilateral or bilateral cervical lymphadenopathy. The cause of Kawasaki disease remains unclear, but studies suggest that respiratory or gastrointestinal infections may be common prodromal symptoms, indicating that the onset might be related to infections, though no contagious phenomena have been identified to date. Kawasaki disease might show prodromal signs such as upper respiratory infections, characterized by symptoms like a runny nose and cough, or gastrointestinal symptoms such as diarrhea and vomiting, which suggests that a runny nose might be a manifestation of Kawasaki disease.

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Why do children get Kawasaki disease?

Kawasaki disease has an unclear pathogenesis. It is speculated that it may be related to infections by microorganisms or other pathogens, familial genetic susceptibility, or autoimmune functions. Currently, the entire medical history is unclear, and there is no specific epidemiology identified for the onset of the disease; it can occur in any of the four seasons. The disease primarily affects infants and young children, with about 80% of cases occurring in children under five years of age. The ratio of male to female incidence is approximately 1.5:1. Thus, Kawasaki disease is most commonly seen in infants and young children. Currently, there is no definitive explanation for the mechanism of the disease.

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How is Kawasaki disease diagnosed?

Kawasaki disease, also known as mucocutaneous lymph node syndrome, is an acute febrile rash disease characterized primarily by inflammation of medium and small arteries throughout the body, with a self-limiting nature. Clinically, it mainly presents with fever, rash, mucosal lesions, conjunctival congestion, and non-suppurative enlargement of cervical lymph nodes. If untreated, 20% of cases can lead to coronary artery damage. To diagnose this disease, in addition to typical clinical manifestations, attention must also be paid to various tests such as blood tests, immunological tests, and ultrasound examinations for a comprehensive assessment. Although the clinical characteristics are largely indicative of the disease, ultrasound examination is crucial to check for any dilation of the coronary arteries.

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Is IgE high in Kawasaki disease?

Kawasaki disease, also known as mucocutaneous lymph node syndrome, has an unclear pathogenesis. It is speculated that certain components of infectious sources, such as superantigens, can activate CD30 T cells and CD40 ligand expression directly by binding with T cell antigen receptor fragments without going through mononuclear macrophages. Under the induction of carrier cells, there is polyclonal activation and reduced apoptosis of B08 cells, resulting in the production of large amounts of immunoglobulins such as IgG, IgM, IgA, and IgE, and cytokines. Therefore, the IgE levels in Kawasaki disease are elevated.