Doctors in England told not to start new patients on ADHD drugs due to shortage
Doctors in England told not to start new patients on ADHD drugs due to shortage
From the article: Henry Shelford, the CEO and a co-founder of ADHD UK, said: “ADHD is a disability and the sudden removal of medication is akin to removing a wheelchair from a disabled person that needs it.”
Ok, but you’re still refusing to let another disabled person have a wheelchair in the first place so…
Maybe not that way around, but in the EU the pharmaceutical companies take physicians out for dinner, take them on skiing trips etc. to accomplish the same result; push for more of this medication to be prescribed.
People downvoting me probably don’t work in healthcare and have no idea how these businesses work.
In the UK the NHS uses NICE guidelines for prescriptions. A doctor would be expected to justify prescribing outside of this.
Additionally, ADHD charities report that it is under diagnosed in people in the UK. With many parents suspicious of medicating children.
Your quote doesn’t say they calculate the result globally. It’s estimated based on the results in Carolina. They say estimate because the don’t have the data to say it is true.
ADHD administrative prevalence (based on rates of diagnosis and/or prescriptions) in children and adolescents in the UK has been estimated to fall between 0.2 and 0.9% since the mid-2000s (39). These rates remain below community prevalence estimates in the UK estimated at around 2.2% in 1999 and 2005 (55, 56), with more recent estimates of 1.6% in 2017, based on the more restrictive ICD-10 Hyperkinetic Disorder criteria (57). Administrative prevalence of adult ADHD in the UK stands at around 0.1% (40), far below even some of the lowest prevalence rates documented in adults (9).
This suggests about 1% of the UK population has ADHD and isn’t diagnosed. The would be more than 600,000 people.