A study by researchers from Hospital for Special Surgery has shown that platelet-rich plasma (PRP) holds great promise for treating patients with knee osteoarthritis. The treatment improved pain and function, and in up to 73% of patients, appeared to delay the progression of osteoarthritis, which is a progressive disease.
‘This is a very positive study,’ said Brian Halpern, M.D., chief of the Primary Care Sports Medicine Service at Hospital for Special Surgery, New York City, and lead author of the study.
Several treatments for osteoarthritis exist, including exercise, weight control, bracing, non-steroidal anti-inflammatories, Tylenol, cortisone shots and viscosupplementation, a procedure that involves injecting a gel-like substance into the knee to supplement the natural lubricant in the joint. A new treatment that is being studied by a small number of doctors is PRP injections. PRP, which is produced from a patient
Magnetic resonance imaging (MRI) measurements of atrophy in an important area of the brain are an accurate predictor of multiple sclerosis (MS). According to the researchers, these atrophy measurements offer an improvement over current methods for evaluating patients at risk for MS.
MS develops as the body’s immune system attacks and damages myelin, the protective layer of fatty tissue that surrounds nerve cells within the brain and spinal cord. Symptoms include visual disturbances, muscle weakness and trouble with co-ordination and balance. People with severe cases can lose the ability to speak or walk.
Approximately 85 percent of people with MS suffer an initial, short-term neurological episode known as clinically isolated syndrome (CIS). A definitive MS diagnosis is based on a combination of factors, including medical history, neurological exams, development of a second clinical attack and detection of new and enlarging lesions with contrast-enhanced or T2-weighted MRI.
‘For some time we’ve been trying to understand MRI biomarkers that predict MS development from the first onset of the disease,’ said Robert Zivadinov, M.D., Ph.D., FAAN, from the Buffalo Neuroimaging Analysis Center of the University at Buffalo in Buffalo, N.Y. ‘In the last couple of years, research has become much more focused on the thalamus.’
The thalamus is a structure of gray matter deep within the brain that acts as a kind of relay centre for nervous impulses. Recent studies found atrophy of the thalamus in all different MS disease types and detected thalamic volume loss in pediatric MS patients.
‘Thalamic atrophy may become a hallmark of how we look at the disease and how we develop drugs to treat it,’ Dr. Zivadinov said.
For this study, Dr. Zivadinov and colleagues investigated the association between the development of thalamic atrophy and conversion to clinically definite MS.
‘One of the most important reasons for the study was to understand which regions of the brain are most predictive of a second clinical attack,’ he said. ‘No one has really looked at this over the long term in a clinical trial.’
The researchers used contrast-enhanced MRI for initial assessment of 216 CIS patients. They performed follow-up scans at six months, one year and two years. Over two years, 92 of 216 patients, or 42.6 percent, converted to clinically definite MS. Decreases in thalamic volume and increase in lateral ventricle volumes were the only MRI measures independently associated with the development of clinically definite MS.
‘First, these results show that atrophy of the thalamus is associated with MS,’ Dr. Zivadinov said. ‘Second, they show that thalamic atrophy is a better predictor of clinically definite MS than accumulation of T2-weighted and contrast-enhanced lesions.’
The findings suggest that measurement of thalamic atrophy and increase in ventricular size may help identify patients at high risk for conversion to clinically definite MS in future clinical trials involving CIS patients.
‘Thalamic atrophy is an ideal MRI biomarker because it’s detectable at very early stage,’ Dr. Zivadinov said. ‘It has very good predictive value, and you will see it used more and more in the future.’
‘The next step is to look at where the lesions develop over two years with respect to the location of the atrophy,’ Dr. Zivadinov said. ‘Thalamic atrophy cannot be explained entirely by accumulation of lesions; there must be an independent component that leads to loss of thalamus.’
Radiological Society of North America
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A new computer tool to help reduce the risk of commonly made drug prescribing errors has been launched by a primary care research team and the PRIMIS business unit at The University of Nottingham.
The PINCER Query Library Tool has been developed after a clinical trial showed that an innovative pharmacist-led computer-based prescription checking and GP feedback system led to significantly fewer prescribing errors than traditional computerised feedback alone.
The PRIMIS unit within the Division of Primary Care specialises in health informatics and training and has been working with the PINCER trial research team to develop the tool based on the results of the trial.
The PINCER study involved at-risk patients in 72 general practices taking the drugs that are most commonly and consistently associated with medication errors. The general practices were randomly allocated to receive either computerised feedback on patients at risk, or computerised feedback with support from a pharmacist to correct any errors detected. When followed up six months later the general practices receiving pharmacist support had significantly fewer prescribing errors.
The new PINCER tool is an extension of the PRIMIS CHART Query Library and is now available free to all GP practices in England. CHART helps GPs improve patient care by analysing the data held on their clinical computer systems. GP practices access the library through membership of the PRIMIS Hub scheme.
Professor of Primary Health Care, Tony Avery, in the University
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Identifying the "smell" of different types of lung bacteria could lead to a simple breath test to diagnose infections, a study on mice suggests. Breath analysis could reduce lung infection diagnosis times from weeks to minutes, the Vermont researchers said. Scientists have already researched breath tests to diagnose asthma and cancer. An expert said breath analysis was "an important and emerging field".
Diagnosing bacterial infections traditionally means collecting a sample that is used to grow bacteria in the lab. This bacteria is then tested to classify it and see how it responds to antibiotics, which can take time. Doctors see breath analysis, in contrast, as a fast and non-invasive method of diagnosing diseases. For the study, researchers from the University of Vermont analysed volatile organic compounds (VOCs) given off in exhaled breath by different bacteria as well as different strains of the same bacterium.
They infected mice with two bacteria that are both common in lung infections – Pseudomonas aeruginosa and Staphylococcus aureus – and sampled their breath after 24 hours. The compounds in their breath were analysed using a technique called secondary electrospray ionisation mass spectrometry (SESI-MS), which is capable of detecting extremely small elements of the chemicals present in their breath.
The researchers said they found a "statistically significant" difference between the breath profiles of the mice infected with the bacteria and the mice that were uninfected. They also said they were able to differentiate between two species of bacteria and two different strains of the same P. aeruginosa bacterium.
But Jane Hill, co-author of the study, from the University of Vermont College of Medicine, said there were still some challenges to overcome with "breath-prints".
"We are now collaborating with colleagues to sample patients in order to demonstrate the strengths, as well as limitations, of breath analysis more comprehensively," she said.
Richard Hubbard, professor of respiratory epidemiology at Nottingham City Hospital and a spokesman for the British Lung Foundation, said breath analysis was already being used to diagnose children with asthma.
"Breath analysis is an emerging field and is likely to take off across the board. It could be a very useful tool for children with cystic fibrosis, for example, as a guide on how to treat them," he said. BBC
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A new pacemaker has been built inside a heart by converting beating muscle into cells which can organise the organ’s rhythm, US researchers report. The heartbeat is controlled by electrical signals and if these go awry the consequences can be fatal.
Scientists injected a genetically-modified virus into guinea pigs to turn part of their heart into a new, working pacemaker.
A human heart is made up of billions of cells, but researchers say fewer than 10,000 are responsible for controlling the heartbeat. Age and disease can lead to problems such as the heart pumping too fast or too slow – and it can even stop completely, in what is known as a cardiac arrest.
The solution is an implanted battery-powered pacemaker which will jolt the heart to keep it in line.
Instead a team of researchers at the Cedars-Sinai Heart Institute tried to restore the heart’s own ability to dictate the beat by creating new pacemaker cells. They used a virus to infect heart muscle cells with a gene, called Tbx18, which is normally active when pacemaker cells are formed during normal development in an embryo.
When heart cells were infected with the virus they became smaller, thin and tapered as they acquired the ‘distinctive features of pacemaker cells’, the report said.
Pacemakers are implanted into the chest to regulate the heartbeat When the virus was injected into a region of the hearts of seven guinea pigs, five later had heartbeats which originated from their new pacemaker.
One of the researchers Dr Hee Cheol Cho, from Cedars-Sinai, told that he expected the same method to work in the human heart as they used a human gene, Tbx18, to generate the effect. However, far more animal testing would be needed before the technique would ever be considered in people.
Dr Cho added: ‘Electronic devices are limited to their finite battery life, requiring battery changes. Complications such as displacement, breakage, entanglement of the leads are not uncommon and could be catastrophic, the incidence of devices with bacterial infection keeps going up and, for paediatric patients, the device does not ‘grow’ with the patients. All these problems could be solved by a biological pacemaker.’
BBC
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A new functional magnetic resonance imaging (fMRI) technique may provide neurosurgeons with a non-invasive tool to help in mapping critical areas of the brain before surgery.
Evaluating brain fMRI responses to a ‘single, short auditory language task’ can reliably localise critical language areas of the brain
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Using functional magnetic resonance imaging (fMRI) for before-and-after analysis, a team of researchers including a UC Santa Barbara graduate student discovered positive changes in brain activity in children with autism who received a particular type of behavioural therapy.
Work completed at Yale University’s Child Study Center used fMRI as the tool for measuring the impact of Pivotal Response Treatment (PRT)
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Hearts previously rejected due to donors’ age or other risk factors can now be declared viable for transplantation using pharmacological stress echo, according to research presented at EUROECHO and other Imaging Modalities 2012. The study was presented by Dr Tonino Bombardini from Pisa, Italy.
Heart transplantation is an established procedure in patients with end-stage heart failure but it is limited by a severe donor organ shortage. The average age of organ donors has increased and the donor is frequently a patient who died of a stroke. Every year in Europe a pool of
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A tiny, EPFL-designed implantable device that can be positioned within the eye and controlled remotely may well revolutionise the treatment of glaucoma. The device should be through testing this year and on its way to the market in 2014 via Rheon Medical, an EPFL spin-off.
Glaucoma is the second leading cause of blindness globally, after cataracts. It is characterised by the presence of too much liquid between the cornea and the iris. This leads to a build-up of pressure within the eye, a situation that can destroy the optic nerve if it is not handled correctly.
Professor Nikos Stergiopulos’s team at the EPFL’s Laboratory of Hemodynamics and Cardiovascular Technology (LHTC) has developed an adjustable implantable ‘micro-tap’ that can drain surplus fluid in the eye. Clinical trials on this glaucoma drainage device should be starting before the end of the year and will be co-ordinated by Rheon Medical, an EPFL start-up. In addition to Prof. Stergiopulos, the project team is composed of LHTC members St
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Why does training in mindfulness meditation help patients manage chronic pain and depression? In a newly published neurophysiological review, Brown University scientists propose that mindfulness practitioners gain enhanced control over sensory cortical alpha rhythms that help regulate how the brain processes and filters sensations, including pain, and memories such as depressive cognitions.
The proposal, based on published experimental results and a validated computer simulation of neural networks, derives its mechanistic framework from the intimate connection in mindfulness between mind and body, since standardised mindfulness meditation training begins with a highly localised focus on body and breath sensations. This repeated localised sensory focus, the scientists write, enhances control over localised alpha rhythms in the primary somatosensory cortex where sensations from different body are ‘mapped’ by the brain.
In effect, what the researchers propose in their paper, is that by learning to control their focus on the present somatic moment, mindfulness meditators develop a more sensitive ‘volume knob’ for controlling spatially specific, localised sensory cortical alpha rhythms. Efficient modulation of cortical alpha rhythms in turn enables optimal filtering of sensory information. Meditators learn not only to control what specific body sensations they pay attention to, but also how to regulate attention so that it does not become biased toward negative physical sensations such as chronic pain. The localised attentional control of somatosensory alpha rhythms becomes generalised to better regulate bias toward internally focused negative thoughts, as in depression.
‘We think we
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