Alder Hey hospital warning after measles spike
Alder Hey Children's Hospital has reported the virus is on the rise in young people in the region and blamed the spike on a fall in uptake of the measles, mumps and rubella (MMR) vaccine.
Medical director Alfie Bass and chief nurse Nathan Askew said the symptoms can be severe and "are leading to increasing numbers of children being admitted to our hospital".
They said in a letter posted on social media that the "vaccine has been available for many years and is proven to be safe" and urged parents to get their children vaccinated.
Vaccine uptake in the UK has fallen over the last decade, leading to outbreaks of measles and whooping cough.
A recent report found parent obstacles such as difficulty booking appointments and a lack of reminders on what jabs are needed and when had prevented some from vaccinating their children.
The letter, which was co-signed by the public health directors of three Merseyside councils, said: "In rare cases, catching the disease can be fatal.
"Measles is particularly dangerous for some of our most vulnerable children and young people, including those under one year of age and those already battling other serious illnesses like cancer."
The letter urged parents and carers to get their children vaccinated, which is typically done when the child is aged 12 months, and then again at around three years and four months.
The hospital said two doses of the MMR vaccine was enough for "lifelong protection against measles, mumps and rubella".
Symptoms of measles usually start with a runny nose, sneezing, coughing and a high temperature, before the measles rash typically develops a few days later.
Listen to the best of BBC Radio Merseyside on Sounds and follow BBC Merseyside on Facebook, X, and Instagram. You can also send story ideas via Whatsapp to 0808 100 2230.
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The Company's range of immunotherapy and cell therapy platforms, alone and together, act to drive and sustain an immune response with the goal of creating durable and safe protection against disease. Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non-muscle invasive bladder cancer CIS that activates natural killer cells, T cells, and memory T cells for a long-duration response. The Company is applying its science and platforms to treating cancers, including the development of potential cancer vaccines, as well as developing immunotherapies and cell therapies that we believe sharply reduce or eliminate the need for standard high-dose chemotherapy. These platforms and their associated product candidates are designed to be more effective, accessible, and easily administered than current standards of care in oncology and infectious diseases. For more information, visit (Founder's Vision) and connect with us on X (Twitter), Facebook, LinkedIn, and Instagram. References: Action Bladder UK. Non-muscle invasive bladder cancer. May 2021. Available at: World Cancer Research Fund. Bladder Cancer Statistics. 2022. Available at: Aldousari S, Kassouf W. Update on the management of non-muscle invasive bladder cancer. Canadian Urological Association Journal, 4(1), 56–64. Holzbeierlein J, Bixler BR, Buckley DI, et al. Diagnosis and treatment of non-muscle invasive bladder cancer: AUA/SUO guideline: 2024 amendment. J Urol. 2024;10.1097/JU.0000000000003846. Grabe-Heyne, et al. Intermediate and high-risk non-muscle-invasive bladder cancer: an overview of epidemiology, burden, and unmet needs. Front Oncol. 2023 Jun 2;13:1170124. doi: 10.3389/fonc.2023.1170124. Kodera A, Mohammed M, Lim P, Abdalla O, Elhadi M. The Management of Bacillus Calmette-Guérin (BCG) Failure in High-Risk Non-muscle Invasive Bladder Cancer: A Review Article. 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