Brain scan 'can sort dementia by type'

Lead researcher Dr Corey McMillanThis could be used as a screening method and any borderline cases could follow up with the lumbar puncture or PET scan”
Annette MenzelTechnical University of MunichThe season of suffering for people with hay fever is getting more serious”
IVF has been linked to an increased risk of ovarian tumours in later life, according to a preliminary study.
Women given fertility drugs to produce eggs had more than triple the risk of an ovarian tumour that may turn cancerous, say Dutch researchers.
But the absolute risks are very low, they add.
A cancer charity said numbers involved in the study, published in the journal Human Reproduction, were too small to draw firm conclusions.
The study tracked more than 25,000 women attending IVF clinics in The Netherlands in the 80s and 90s.
Follow-up investigations revealed more cases than expected of ovarian tumours in women who had gone through IVF, which involves stimulating the ovaries to make eggs.
The biggest increase was in a type of growth, known as a borderline ovarian tumour, which can sometimes turn into cancer. It is less aggressive than other types of ovarian tumour, but requires surgery.
End Quote Prof Flora van Leeuwen Netherlands Cancer Institute, AmsterdamWomen should be informed about this but the risk should not be overstated”
It normally affects around one in 1,000 women in the general population, but was found in about 3.5 in 1,000 women who had gone through IVF, say the researchers.
A smaller increase in other types of ovarian tumour was also found. Overall, ovarian cancer rates were twice as high among women who had gone through fertility treatment, the experts said.
Prof Flora van Leeuwen, a co-author of the study, told the BBC: "The absolute risk of these tumours is very low. But there is an increased risk of a borderline malignant tumour that needs surgery.
"Women should be informed about this but the risk should not be overstated."
Another co-author, Prof Curt Burger added: "The main message is that women who have had IVF shouldn't be alarmed. The incidence of ovarian cancer was extremely low."
'Reassuring'Further research is planned to confirm the finding in a larger number of patients, and to look at whether some women are more at risk.
At present, the numbers involved are small. There were 61 women with ovarian tumours in the IVF treatment group; 31 had borderline ovarian tumours and 30 had ovarian cancer.
Commenting on the study, Prof Hani Gabra, of the Ovarian Cancer Action Research Centre at Imperial College London, said:
"Reassuringly, and in keeping with lots of previous research in this area, this study shows that the risks of invasive ovarian cancer are small in populations of patients receiving ovarian stimulation for IVF.
"Although this study shows that ovarian stimulation may increase the risk of much less aggressive borderline ovarian tumours, it underlines the fact that ovarian stimulation for IVF is not a major risk factor for invasive ovarian cancer."
Dr Claire Knight, senior health information officer at Cancer Research UK, said: "This interesting study suggests a possible link between ovarian stimulation for IVF and borderline ovarian tumours, but it certainly doesn't show that IVF causes invasive ovarian cancer.
"There were only a relatively small number of cases in this study, and the researchers didn't find that risk increased with the number of cycles a woman had, making conclusions hard to reach.
"Women can reduce their risk of ovarian cancer by being a non-smoker and keeping a healthy weight, and women who have taken the Pill or been pregnant are also at lower risk." Pill 'lowers ovarian cancer risk' Ovarian Cancer Action humrep.oxfordjournals.org
Hospitals are, by definition, buildings that are dedicated to health.
But in this week's Scrubbing Up, Dr Rachel Thompson, deputy head of science at World Cancer Research Fund, says that good work is being undermined by the contents of hospital vending machines.
Whenever I visit hospitals, I am always struck by how the efforts of the dedicated healthcare professionals who work in them are being undermined by what is happening in the waiting areas.
All too often, these waiting areas have vending machines that are filled with high-calorie foods and drinks such as chocolate bars, crisps and sugary drinks.
But because these foods are a cause of obesity, they are part of the reason many of the people will have ended up in hospital in the first place.
There is strong scientific evidence that excess body fat is a risk factor for cancer, as well as other non-communicable diseases such as heart disease and diabetes.
And yet hospital vending machines are selling products that are a cause of obesity at the same time as the health professionals working there are trying to cope with its consequences.
That is why hospitals should put an end to vending machines that sell high calorie foods and drinks.
Little focusIt is true that on its own this would be unlikely to have a serious impact on obesity levels.
You would have to spend a lot of time in hospital waiting rooms for the contents of the vending machines to make much of a difference to your weight.
End QuoteThere is no great mystery about what needs to happen”
But rather, the fact that hospital vending machines are filled with these kinds of foods and drinks is a symptom of how little meaningful focus there is on the obesity crisis.
Across society, big changes are needed if we are to address obesity and the preventable cases of cancer and other diseases that result from it.
The changes that we need are supported by common sense.
If you prioritise the needs of motorised transport when you plan a town, it is to be expected that people won't walk or cycle enough.
If you allow the food and drinks industry to market unhealthy products to children, then don't be surprised when children pester their parents to buy those products.
But the fact that hospital vending machines are still stocked with high-calorie foods and drinks illustrates that we are not recognising the problem.
There is no great mystery about what needs to happen.
There is already a large evidence base for what works and doesn't work when it comes to policy changes. What we need to see is political will and a change to the mindset where we tolerate the things that promote obesity.
This would not only mean the end of the kind of culture where the sale of unhealthy foods and drinks in hospital waiting rooms is seen as acceptable.
It could also mean fewer people end up in those waiting rooms in the first place.
Opportunities were missed to diagnose a 15-year-old girl who died of tuberculosis (TB), the BBC can reveal.
Alina Sarag, a pupil at Golden Hillock School in Sparkhill, Birmingham, died on 6 January.
A simple phlegm test which could have shown she had tuberculosis was never carried out at one West Midlands hospital, a clinical review of the case revealed.
A chest X-ray could also have indicated TB but the condition was not picked up.
The review, by Heart of Birmingham Teaching Primary Care Trust, concluded there must be a Birmingham-wide review of all standard procedures for TB after no-one considered the possibility in Alina's case, a high-risk patient.
Alina had been treated for TB and was seen at Birmingham Chest Clinic, in October 2009.
She was treated with antibiotics but the clinic failed to follow up her treatment.
After a visit to Pakistan in July 2010 she was sick upon her return.
Her mother, Farhat Mahmoode, said: "We took her to every hospital.
"If Heartlands Hospital didn't pick up something, maybe City Hospital.
"We took her to the Children's Hospital.
"We thought maybe another doctor would find out what was wrong, but we were failed at every turn."
After doctors at Heartland and City hospitals did not detect TB, Alina was admitted to Sandwell Hospital where she stayed for five days.
TB was picked up but no sputum test was carried out and a chest X-ray was thought to have found a chest infection.
She later saw a clinical psychologist at Birmingham Children's Hospital but was in such extreme pain that the psychologist could not complete the assessment.
A second appointment was arranged for 6 January, the day of her death.
The medical director of Sandwell and West Birmingham Hospitals, Donal O'Donahue, accepted there were mistakes with her care, but denied there was any need to change the systems.
'Clinicians devastated'Mr O'Donahue said TB was very difficult to diagnose and when the reader of the chest X-ray decided it was unlikely to be TB, the phlegm test was cancelled.
He said not diagnosing TB from the X-ray was reasonable.
"All the clinicians involved in Alina's case were devastated that we had missed an opportunity to diagnose TB.
"Other than the need to bear TB in mind, there is nothing in our systems that we felt that we needed to improve on the basis of Alina's care."
The review decided the chest clinic should have followed up her treatment and it should have ordered X-rays to ensure her treatment had been successful.
Heart of England NHS Foundation Trust (HEFT), which runs the chest clinic, said it had put an action plan in place.
It said: "HEFT is the centre of excellence for infectious diseases in the West Midlands and saw and treated over 350 patients last year with TB.
"We have completed an internal investigation into the care provided to Alina Sarag by Birmingham Chest Clinic and an action plan has been developed with our clinicians."
The review team has recommended training to increase awareness about TB for all Birmingham GPs and other clinicians.
The BBC is not responsible for the content of external Internet sites
End Quote Paul Bettison Local Government AssociationThere are many ways to make takeaways more healthy such as using lower fat oils, natural colourings and reducing salt. ”
Last reviewed: November 22, 2010.
Ventriculoperitoneal shunting is surgery to relieve increased pressure inside the skull due to excess cerebrospinal fluid (CSF) on the brain (hydrocephalus).
This article primarily discusses shunt placement in children.
See also: Intracranial pressure
This procedure is done in the operating room under general anesthesia. It takes about 1 1/2 hours.
The child's hair behind the ear is shaved off. A surgical cut in the shape of a horseshoe (U-shape) is made behind the ear. Another small surgical cut is made in the child's belly.
A small hole is drilled in the skull. A small thin tube called a catheter is passed into a ventricle of the brain.
Another catheter is placed under the skin behind the ear and moved down the neck and chest, and usually into the abdominal (peritoneal) cavity. Sometimes, it goes to the chest area. The doctor may make a small cut in the neck to help position the catheter.
A valve (fluid pump) is placed underneath the skin behind the ear. The valve is attached to both catheters. When extra pressure builds up around the brain, the valve opens, and excess fluid drains out of it into the belly or chest area. This helps decrease intracranial pressure.
The valves in newer shunts can be programmed to drain more or less fluid from the brain.
In hydrocephalus, there is a buildup of fluid of the brain and spinal cord (cerebrospinal fluid or CSF). This buildup of fluid causes higher than normal pressure on the brain. Too much pressure, or pressure that is present too long, will damage the brain tissue.
A shunt helps to drain the excess fluid and relieve the pressure in the brain. A shunt should be placed as soon as hydrocephalus is diagnosed.
Risks for any anesthesia are:
Reactions to medications
Problems breathing
Changes in blood pressure or breathing rate
Risks for any surgery are:
Bleeding
Infection
Possible risks of ventriculoperitoneal shunt placement are:
Blood clot or bleeding in the brain
Brain swelling
The shunt may stop working and fluid will begin to build up in the brain again.
The shunt may become infected.
Infection in the brain
Damage to brain tissue
Seizures
If the procedure is not an emergency (planned surgery):
Tell your doctor or nurse what drugs, supplements, vitamins, or herbs your child takes.
Give any drugs the doctor told you to give your child. It is okay if they take them with a small sip of water.
The doctor or nurse will tell you when to arrive at the hospital.
Ask your doctor or nurse about eating and drinking before the surgery. The general guidelines are:
Older children should not eat any food or drink any milk for 6 hours before surgery, but they can have clear fluids (juice or water) up until 4 hours before the operation.
Infants younger than 12 months can usually eat formula, cereal, or baby food until about 6 hours before surgery. They may have clear fluids up until 4 hours before the operation.
Your doctor may ask you to wash your child with a special soap on the morning of the surgery. Rinse well after using this soap.
Your child will need to lie flat for 24 hours the first time a shunt placed. After that your child will be helped to sit up.
The usual stay in the hospital is 3 to 4 days.The doctor will check vital signs and neurological status often. Your child may get medication for pain. Intravenous fluids and antibiotics are given. The shunt will be checked to make sure it is working properly.
Shunt placement is usually successful in reducing pressure in the brain. But if hydrocephalus is related to other conditions, such as spina bifida, brain tumor, meningitis, encephalitis, or hemorrhage, these conditions could affect the prognosis. The severity of hydrocephalus present before surgery will also affect the outcome.
Support groups for families of children with hydrocephalus or spina bifida are available in most areas.
The major complications to watch for are an infected shunt and a blocked shunt.
Review Date: 11/22/2010.
Reviewed by: Kevin Sheth, MD, Department of Neurology, University of Maryland School of Medicine, Baltimore, MD. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
Copyright © 2011, A.D.A.M., Inc
I wanted to write about my experience of having Jack and being pregnant. I have recently joined ASBAH's forum on Facebook and I realise how many other people with spina bifida are considering becoming a parent and thought it might be useful to share my experience.
I was 37 when, as a woman with spina bifida I became pregnant for the first time. Although it was a lovely surprise I have to admit it was also quite a shock having been told at the age of 20 I was infertile. Hence the pregnancy was unplanned as I had come to a point of acceptance years before that I wouldn't ever be a mum.
So there I was, standing in my bathroom in a state of disbelief staring at my pregnancy test as the word "pregnant" flashed up. I dropped the test stick in the sink and rushed in to my living room pacing the room. It was a mixture of elation and fear flooding through me all at once. Elation that once again the medical profession had got it wrong just like they told my mum I would probably never walk when I was two years old (I walked at 3 1/2). The realisation that I would in fact be a mum after so many years of believing I wouldn't. Then of course the fear. Fear for the baby as I hadn't been taking folic acid and fear for me. How would the pregnancy affect me and how could I physically cope with being a mum.
My pregnancy was full of professionals who although monitored me as a high risk "mum to be" appeared to have no specialist knowledge of spina bifida. Thank God for ASBAH and the medical advisers who I was really able to talk to and discuss and prepare myself for the way ahead.
My pregnancy wasn't easy. I went from walking without aids to being on crutches and barely able to dress myself at the end and other problems related to my disability worsened. Having said that I look back on the experience fondly and still remember the first time my unborn baby kicked me. It was Boxing Day and it was the best Christmas present I could ever have.
At 20 weeks pregnancy came a bit of a blow. My scan showed that my baby had talipes. They had been looking for spina bifida and had ruled it out up to then but since I too have talipes (clubfoot) and it can be associated with spina bifida I was told that they had to suspect that the baby could have some form of spina bifida even though they couldn't see it. Again I was fearful. Having a baby was going to be physically demanding enough for me but having a baby who also had physical problems to deal with seemed overwhelming. From then on I was scanned regularly until 30 weeks.
On 11th June 2008 I gave birth to my beautiful son Jack. He was born by emergency caesarean nearly 2 weeks overdue after I had been induced and he had gone into distress during labour. I have to say that one of the positive aspects of being a spina bifida mum in labour was that pain didn't scare me nor did medical intervention. The big disappointment was that my spina bifida meant that my caesarean had to be performed under general anaesthetic rather than a spinal anaesthetic so I wasn't awake to see him come into the world.
When I woke up I peered across the room to see my partner Michael holding this bundle in his arms. He brought him over to me and the midwife put him straight to my breast. It was love at first sight. I soon discovered why my labour hadn't progressed so well. He weighed in at 8 pound 14 oz and I'm only 4 ft 9 inches tall! My advice to other mums to be in my position is to push for a 36-week scan to estimate the baby’s size. I was offered one but was told it was optional and therefore didn’t have one as I’d had so many during my pregnancy. I think if I'd had one at that point they wouldn't have let me go overdue and the birth would have been a lot less traumatic for all of us whether it had been a planned Caesarean or a pre term vaginal delivery.
Jack started treatment for his clubfoot at 13 days old when he was put in plaster. His foot was gradually straightened using a series of weekly plasters, a small op and the boots and bars. He will have to wear them at night until he is 4 years old.
Jack doesn't have spina bifida. He was 10 weeks old before they finally ruled it out. I was relieved because even though I've achieved everything I have wanted to in life I'm glad he won't have to go through the operations and pain I had to put up with. And when he is 4 years old his foot will be completely corrected.
Caring for Jack through his treatment has been emotionally hard for me. Going to Great Ormond Street, albeit a fantastic hospital, bought back memories of my childhood that I would have rather left behind me. It's also been physically very challenging for me, as Jack is very tall and heavy for his age. My initial reservations about asking for help have subsided and I have managed to get some good support from occupational therapy in looking for equipment that will help me and strategies in helping me to get Jack be a bit more cooperative during change times so he doesn't fight and run away from me but gets rewarded for sitting still. I think though that asking for help has been the hardest aspect of being a new mum as I've fought all my life for maximum independence. You have to remember though that all new mums need help and not feel as though it's the disability getting the better of you.
A positive aspect of being a disabled mum is that I feel I am so much more used to assessing the risks that could be present for Jack. When you have a disability you have to plan ahead when you are going out and know your limitations. These become a way of life for a physically disabled person and they are excellent attributes to have as a mum. Also I've noticed how much of a shock it is to new able-bodied mums: having to think about ramps and access for buggies. Even though I walk independently I'm used to looking for lifts, handrails and ramps so a new pram didn't feel like a new obstacle; in fact it helped me get back on my feet by offering me something to hold on to... The best walking aid ever.... a pram with your new baby in it.
There are days when Jack is having tantrums that he makes me feel very physically inadequate. If he decides to run off and lie down on the ground in a temper there is nothing I can do to stop him. But I think every mum goes through these feelings so I try not to let it get to me. I know that all Jack really needs is love and affection. My disability is as insignificant to him as his foot problems are to me. They are just part of who we are and if anything add to the bond we have with each other.
Alison has spina bifida and is mum to Jack who is 2 years old.
More patients in Scotland given antidepressants 13 October 2015 From the section Scotland Image copyright Thinkstock Image ca...