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Wednesday, April 6, 2022

What is Juvenile Arthritis?

Article Part: 2 

Juvenile Arthritis Symptoms | Idiopathic Arthritis | Jia Arthritis | Juvenile Idiopathic Arthritis Treatment | Jia Symptoms

 Children with this disease may have serious complications, including infections and sometimes death, depending upon their age and severity of infection. Because of this rare form of IBD, most cases are diagnosed in infancy. According to the Centers for Disease Control & Prevention (CDC), there were just 7,831 reported cases of JIA diagnosed in January 2015 in children younger than 2 years old. Of these, only 3 affected infants died. Infections were reported in 1% of cases, with 8% developing acute forms of illness (such as pneumonia) and 19% developing chronic forms (such as arthritis) requiring long-term treatment, according to the American Health Information Center. Although not deadly, children with JIA may suffer from sepsis-like conditions called cytokine storm syndrome (CIS; see an article about CIS). The Centers for Disease Control & Prevention estimates there is a 6.5 death rate per 100 patient treated children 0-18 years, although those rates may be low because rates may be higher. After all, several large studies have not been completed. For example, a study published in June 2017 in BMJ Child & Adolescent Psychiatry found a 9% incidence of MIS among hospitalized children with JIA. The authors stated that they had difficulty finding data to prove that MIS was related to JIA because MIS occurred frequently enough to be considered incidental. They conclude, "The current evidence supports a link between MIS and MIS, which underscores the need for further investigation into this association." Another study was published in September 2018 in JAMA Pediatrics (Journal of the American Medical Association); this time, researchers found the 12-month mortality rate from MIS was 35% among people with the same health problems. The group of patients who did survive to 30 days of follow-up was 65 women and 49 men, with an average age of 15 years. Almost half of these patients were in the ICU, with the remainder hospitalized for their condition. Results showed that MIS may result from cytokine storms and that more aggressive treatments may reduce the risk of MIS or decrease clinical outcomes. Researchers suggest that future research could help identify interventions and better management practices to prevent and treat MIS from occurring. Overall, there are fewer than 5000 cases of MIS with JIA annually, though results are needed more closely to determine the risks and outcomes from these findings. As for MIS, the American Gastroenterological Association (AHA) does not recommend the use of antibiotics in infants with acute forms of inflammation or septic complications (such as MIS), although some researchers continue to support that recommendation due to concerns about the emergence of resistant organisms or poor nutrition, since these are typically a result of lack of proper care.

What Causes This Condition? As described above, JIA is primarily an inflammatory condition, and its severity can be varied. It is thought that there are possible causes for the initial infection itself, but there are no proven causes (other than a vaccination or maternal infection, which is uncommon). While the early infection is often associated with sepsis, infection with other respiratory viruses is more prevalent. In adults and young children, viral infections can cause a wide variety of conditions including pneumonia, sepsis, encephalitis, influenza and herpes, myocarditis, mononucleosis, and others. Since children cannot receive vaccinations and may develop weakened immune systems, the vaccines they receive in childhood may also cause autoimmune diseases. Other immune-compromised individuals may develop viral infections, such as measles, and even Hepatitis B and C, which can lead to hepatitis, liver cirrhosis, and liver cancer. Vaccines, whether developed for human use or animals, contain elements from viruses that are believed to be more likely to cause infection and/or immune diseases. In addition, other immune-compromised individuals may develop viral infections, such as measles, and even Hepatitis B and C, which can lead to hepatitis, liver cirrhosis, and liver cancer. The JIA virus that causes the condition has never been fully studied or analyzed using either human or animal models. All of the above risk factors would place vulnerable infants at higher risk as they develop and treat JIA. Although there are no known risk factors for JIA in newborns, these infants represent less than 1% of all infants with this condition. Therefore, any factor that increases the chance of developing JIA could lead to an increased number of infants with the condition, which would increase the overall burden on public health and healthcare systems. Furthermore, since each infant with JIA develops with a unique genetic makeup and is associated with a varied mix of genes that predispose them to various illnesses, there is no guarantee that a single child will develop the condition. The risk factors for JIA also vary based on age, sex, race, ethnicity, geographic location, and socioeconomic status. Given the wide varying risk factors and high mortality rates associated with JIA, a vaccine might be necessary to decrease the occurrence of this devastating condition. Unfortunately, although this condition is treated successfully, it is difficult to treat and requires close monitoring. A team of scientists was involved in finding a cure for JIA, including the University of Utah School of Medicine, the University of Cincinnati College of Medicine, and numerous pharmaceutical companies. They were able to create mRNA vaccines containing both the original, Japanese JIA virus and a version of Kawasaki Disease virus (a common pathogen, similar to the coronavirus that causes COVID-19), and have shown promising safety and efficacy in animal models. One of the key hurdles with the vaccine is that it must be injected intramuscularly, so it can’t be given intravenously. Even though it has been approved for use, this method has led to several complications and requires special equipment and staff trained in this area. Furthermore, the injection site is susceptible to local bleeding, causing a redness and tingling sensation in the injection site, which makes administering the vaccine extremely difficult. In addition, the Pfizer vaccine was recently found to have high levels of anti-inflammatory chemicals that can cause allergic reactions to the skin, hands, and eyes. Thus, the vaccination process poses significant challenges that limit its approval and use in humans. More importantly, the majority of JIA cases occur in babies and young children. This means that children in their developmental period of rapid growth and learning need the best care. Despite the availability of multiple therapies, there is a shortage of physicians specializing in JIA. Thus, there continues to be limited access to quality care, especially in rural areas where JIA infection is more common, resulting in less attention paid to the needs of infants and young

Monday, April 4, 2022

Juvenile Idiopathic Arthritis (JIA)

 Juvenile idiopathic arthritis (JIA) | TYPES | SYMPTOMS | TREATMENT 



There are many causes of arthritis in children, including some infectious diseases, such as influenza and rheumatoid arthritis (RA). However, one cause that is common in infants and children is the JIA type 1A (juvenile idiopathic arthritis [JIA]) virus, which is caused by a different strain of bacteria than another common disease, Kawasaki Disease (KD) (see article on the links below for more info about KD and its role in the development of arthritis in infants and children). Most commonly seen among infants with high-risk mothers, infantile RA is usually due to exposure to contaminated environments, such as hospitals, daycare centers, and nursing homes, or from immunosuppressive drugs, such as allopregnanolone. Infantile arthritis most often occurs two months after birth and may be accompanied by fever, rash, and swelling. These symptoms typically go away within a few days, but untreated, the condition can progress to juvenile idiopathic arthritis, in which no obvious signs of inflammation are seen, such as swelling and tenderness. Symptoms in young infants include pain, increased heart rate, sleep disturbance, fatigue, lethargy, and diarrhea, as well as fever and rash, with diarrhea being particularly severe. An estimated 10,000 infants in the U.S. are diagnosed with JIV annually, although numbers have been dramatically reduced over recent years. There is currently no cure for JIA, aside from the administration of corticosteroids and immunosuppressants. Vaccination against JIV, however, is available as an intervention. This article will discuss some of the causes, the epidemiology and risk factors, and the clinical manifestations of infection and complications with JIA, including the acute phase (a time when patients are not completely conscious or unconscious), the chronic phase (when symptoms are present and do not go away quickly) and the post-infection period while we wait for treatment and recovery to begin. The first section discusses the reasons why it's important to know that this illness does get better over time; we also talk about its causes and symptoms, as well as potential ways for doctors to treat and manage it. Next, we review the epidemiology of the JIA virus, how its spread impacts populations and populations, and other risk factors that may affect population health. Then we consider the clinical manifestations of this virus and how clinicians and parents should approach these challenges. Finally, we examine the post-infection syndrome and how practitioners and families should navigate this time, taking into consideration some information from the CDC regarding post-infection complications. At the end of this article, we also address some specific issues related to treating and managing JI in infants and children, providing links to articles written by medical professionals who specialize in this subject matter, and other resources that focus on treating and managing the condition. In the last sections, I will provide links to additional resources such as pediatrician societies that serve populations of infants and children, the American Academy of Pediatrics, National Institutes of Health, Joint Commission, FDA, NALC/CNSF, and others.

What Is It? A rare form of inflammatory bowel disease (IBD), JIA is known only as JIA when its symptoms have no obvious sign of inflammation or swelling. 

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Juvenile-Idiopathic-Arthritis

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