More than 80 percent of radiation oncologists discuss the impact of cancer treatments on fertility with their patients of childbearing age, which can lead to improved quality of life for young cancer patients who are living much longer after their original diagnosis thanks to modern treatment options, according to a study.
In the past, the clinical focus for young cancer patients was strictly survival. With the success of today
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Hopes of at last controlling malaria in Africa could be dashed by the emergence of poor-quality and fraudulent anti-malarial medicines, warn experts. Unless urgent action is taken both within Africa and internationally, they argue, millions of lives could be put at risk. In a study published, an international team of researchers report that some cases of medicines on sale in Africa have been deliberately counterfeited by criminals or are of poor quality because of factory errors. Both types are not only potentially harmful to the patient but also risk promoting the emergence of drug resistance among the parasites that cause malaria.
According to the World Malaria Report 2010, malaria killed an estimated 781 000 people in 2009, mainly young children and pregnant women. It is caused by parasites that are injected into the bloodstream by infected mosquitoes.
The most effective anti-malarial drugs are the artemisinin derivatives, which have the advantages over other anti-malarial drugs (such as chloroquine and mefloquine) of having few side-effects but the fastest action. Although the drugs have been used on their own as monotherapy, fears over the development of resistance mean that they are recommended for use in conjunction with one or more other drugs as artemisinin-based combination therapies, now recommended by the WHO as the first-line treatment for uncomplicated falciparum malaria globally.
There has been a dramatic rise in reports of poor-quality and counterfeit anti-malarials in Africa. To find out more about the different types of medicines circulating and what they contain, and to look for evidence of where they might have come from, the researchers examined anti-malarials – collected in 11 African countries between 2002 and 2010 – that they believed to be either counterfeit or substandard.
Analysis of the medicines showed that some counterfeits contained a mixture of wrong active pharmaceutical ingredients, some of which might initially alleviate malaria symptoms but would not cure malaria. Worse still, these unexpected ingredients could cause potentially serious side-effects, particularly if they were to interact with other medication that a patient was currently taking, such as anti-retroviral therapies for HIV.
Some of the counterfeits also contained small amounts of artemisinin derivatives, perhaps to try to ensure that the drug would pass simple authenticity tests. Taken at such low levels, the drug is unlikely to rid the body of malaria parasites, leading to the emergence of strains of the parasite resistant to artemisinin.
The researchers identified pollen found in some of the tablets, which indicated that the counterfeit medicines originated in eastern Asia. Indeed, in 2001, police in Guangzhou, China, arrested Nigerian and Chinese men for production of counterfeits of the anti-malarial halofantrine. No evidence of counterfeit pharmaceutical production in Africa was found in the pollen analysis; however, production facilities for packaging materials for counterfeit anti-malarials have been seized in Nigeria.
Dr Paul Newton from the Wellcome Trust-Mahosot Hospital-Oxford University Tropical Medicine Research Collaboration in Laos, who led the research, says: ‘Public health organisations must take urgent, co-ordinated action to prevent the circulation of counterfeit and substandard medicines and improve the quality of the medicines that patients receive. We must move finally away from the use of single drugs and towards the exclusive use of combination therapies.
‘The enormous investment in the development, evaluation and deployment of anti-malarials is wasted if the medicines that patients actually take are, due to criminality or carelessness, of poor quality and do not cure. Malaria can be readily treated with the right drugs of good quality, but poor-quality medicines – as well as increasing mortality and morbidity – risk exacerbating the economic and social impact of malaria on societies that are already poor.
Wellcome Trust
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Abiraterone has been approved since September 2011 for men with metastatic prostate cancer that is no longer responsive to hormone therapy and progresses further during or after therapy with the cytostatic drug docetaxel. In an early benefit assessment pursuant to the ‘Act on the Reform of the Market for Medicinal Products’ (AMNOG), the German Institute for Quality and Efficiency in Health Care (IQWiG) examined whether abiraterone offers an added benefit compared with the present standard therapy.
IQWiG finds an indication of a considerable added benefit of abiraterone in patients who are not eligible for further treatment with docetaxel. In contrast, an added benefit is not proven in patients who can still be treated with docetaxel, as the dossier submitted by the drug manufacturer provides inadequate information for this group of patients.
In accordance with the specifications of the Federal Joint Committee (G-BA), IQWiG separately assessed abiraterone in two groups of patients. The G-BA has specified different appropriate comparator therapies for the two groups.
The ‘best supportive care population’ contains patients who are not eligible for further treatment with docetaxel. The appropriate comparator therapy for this group is palliative treatment with dexamethasone, prednisone, prednisolone or methylprednisolone, as well as ‘best supportive care’.
‘Best supportive care’ means the therapy that provides the patient with the best possible individually optimised supportive treatment to alleviate symptoms (e.g. adequate pain therapy) and improve quality of life.
The ‘docetaxel-retherapy population’ comprises patients who are still eligible for further treatment with docetaxel. The appropriate comparator therapy for this patient population is docetaxel in combination with prednisone or prednisolone.
Indication of increase in survival and delay in consequences of disease
One study (COU-AA-301), which considers patient-relevant outcomes and provides relevant data, was included in the assessment of added benefit in the ‘best supportive care population’. This study compared treatment with abiraterone versus placebo, in each case combined with prednisone and ‘best supportive care’.
IQWiG finds an indication of an added benefit in patients treated with abiraterone: the above study provides indications that abiraterone can prolong survival and delay consequences of prostate cancer, such as fractures or operations due to bone metastases. In addition, the ‘time to pain progression’ was prolonged in study participants receiving abiraterone.
IQWiG classifies the extent of this added benefit as ‘considerable’. The corresponding legal ordinance has specified three grades to determine the extent of added benefit: ‘minor’, ‘considerable’ and ‘major’.
The study data presented on health-related quality of life assessments cannot be used; an added benefit of abiraterone is therefore not proven for this outcome.
The indications of advantages for abiraterone are not accompanied by proof of greater harm.
Institute for Quality and Efficiency in Health Care
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People who are seriously injured in a car accident are more than 30 per cent more likely to survive at least 48 hours if they are taken directly to a trauma centre than those who are taken first to a non-trauma centre, new research has found.
However, fewer than half of people seriously injured in car accidents in Ontario are taken directly from the scene to a trauma centre. In addition, only half of those taken to the nearest hospital are later transferred to a trauma centre after being assessed and stabilise.
These findings are by Dr. Avery Nathens, trauma director at St. Michael’s Hospital in Toronto.
Ontario has nine Level 1 or Level 11 adult trauma centres. A trauma centre is a hospital with a trauma team that includes specially trained personnel available 24 hours a day, every day, to provide immediate treatment for the most critically injured patients. Higher levels of trauma centres also have the staff and highly sophisticated medical diagnostic equipment to provide specialised emergency care such as neurosurgery and orthopaedics.
Dr. Nathens and his team looked at data from 6,341 car accidents in Ontario from 2002 to 2010. Of those, 45 per cent were transported from the scene to a trauma centre. Of patients who were taken first to a non-trauma centre, only 57 per cent were transferred to a trauma centre.
Patients are taken to non-trauma centres for one of two reasons, Dr. Nathens said. First, the potential severity of their injuries might not be recognised by EMS personnel, so they might be transported to a non-trauma centre if it is the closest hospital. . Second, transport to a trauma centre might take too long, so patients are taken to a non-trauma centre unless air transportation is available.
When patients are taken first to a non-trauma centre, Dr. Nathens said it’s important that the emergency physician recognises the potential severity of their injuries and transfers them to a trauma centre as soon as possible.
Taken together, he said the findings point to the need to make sure all health care workers, especially EMS personnel and Emergency Department physicians, are trained to recognise who needs to be treated at a trauma centre. In addition, the health care system needs the resources to transport those patients quickly, he said.
‘Minutes matter and severely injured patients can’t advocate for themselves so we have the responsibility to ensure that the system works optimally,’ he said.
St. Michael
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The full ‘ESC Guidelines for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012’ will be available is online as of 14:30 hrs on Saturday 19 May 2012.
New recommendations on devices, drugs and diagnosis in heart failure were launched at the Heart Failure Congress 2012, 19-22 May, in Belgrade, Serbia.
The ESC Guidelines for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 were developed by the European Society of Cardiology (ESC) in collaboration with the Heart Failure Association (HFA) of the ESC. The Congress is the HFA
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About one baby is born every hour addicted to opiate drugs in the United States, according to new research from University of Michigan physicians.
In the research, U-M physicians found that diagnosis of neonatal abstinence syndrome, a drug withdrawal syndrome among new-borns, almost tripled between 2000 and 2009.
By 2009, the estimated number of new-borns with the syndrome was 13,539
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A cheap medical device can dramatically reduce the number of premature births in some at-risk women, according to a team of doctors in Spain. Being born before 34 weeks of pregnancy is linked to a host of health problems.
The study showed that using a ‘cervical pessary’ reduced the rate in the at-risk group. Doctors said more studies were needed before the technique was used routinely.
The authors said 13 million babies were born prematurely every year.
In the trial, doctors were looking at women who had a cervix – part of the lower section of the uterus – which was shorter than 25mm. These pregnant women are thought to be at a higher risk of an early delivery.
The cervix was measured between 18 and 22 weeks into the pregnancy by an ultrasound scan. Of the 11,875 women who took part in the trial, 726 had a cervical length less than 25mm. Half of these women had a pessary, a small ring of silicone, inserted into their cervix.
In the group of women without the pessary, 27% of babies were born prematurely. The rate was six per cent among those fitted with a pessary.
Maria Goya, one of the researchers at the Vall d’Hebron Hospital, said: ‘Placement of a pessary is an affordable procedure, non-invasive, and easy to insert and remove as required.’
The study concluded the pessary was a ‘reliable alternative for prevention of preterm birth’ in a group of at-risk women.
Prof Steve Thornton of the University of Exeter, a spokesman for the Royal College of Obstetricians and Gynaecologists, said: ‘The difference in the two groups is pretty amazing.’
He said more research was needed to prove that it worked, and to find out if it could help other women at risk of a premature birth.
‘If this is borne out it could make a big difference,’ he added.
BBC
Researchers in New Zealand have developed a prototype Bluetooth-enabled medical monitoring device that can be connected wirelessly to your smart phone and keep track of various physiological parameters, such as body temperature, heart rate, blood pressure and movements. The prototype could be extended to include sensors for other factors such as blood glucose as well as markers for specific diseases. The connectivity would allow patients to send data directly to their healthcare provider and receive timely advice and medication suggestions.
Helen Zhou and Tim Roberts of the School of Electrical Engineering at Manukau Institute of Technology explain how they have developed a microcontroller-based personal health monitoring unit that can carry medical sensors and a positioning device. The unit can connect to other devices via the short-range wireless networking system known as Bluetooth and so could be readily connected to software on a smart mobile phone for health monitoring.
The team adds that the mobile phone can be used as a gateway to further relay patient health data to a remote database via the mobile network for remote diagnoses. ‘Any medical instructions can be sent back instantly to the mobile users,’ the team says. ‘The use of standard development tools makes it possible for patients to easily use everyday mobile devices for their personal health monitoring and assessment anytime anywhere.’ They add that, ‘Bluetooth and mobile networks enable wireless communications among mobile users, medical professionals and other healthcare givers in an easy, secure and efficient manner.’
The device software is based on the familiar cross-platform Java system and provides user with an easy to use graphical user interface (GUI) on their smart phone that uses the standard navigation buttons on mobile devices.
EurekAlert
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Healthcare imaging specialist Barco has signed an agreement to acquire UK-based JAOtech, a leading manufacturer of patient entertainment and point-of-care terminals for hospitals. The acquisition fits within Barco’s long-term vision of increasing healthcare efficiency and its growth strategy of expanding into multiple healthcare segments. With the JAOtech terminals and associated software, Barco builds a strong position in the fast growing point of care (POC) segment in healthcare.
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Children and young adults scanned multiple times by computed tomography (CT) have a small increased risk of leukaemia and brain tumours in the decade following their first scan.
The findings from a study of more than 175,000 children and young adults was led by researchers at Newcastle University and at the National Cancer Institute, part of the National Institutes of Health, USA.
The researchers emphasise that when a child suffers a major head injury or develops a life-threatening illness, the benefits of clinically appropriate CT scans should outweigh future cancer risks.
Lead author Dr Mark Pearce, Reader in Lifecourse Epidemiology at Newcastle University said: ‘CT scans are accurate and fast so they should be used when their immediate benefits outweigh the long-term risks. However, now we have shown that CT scans increase the risk of cancer, we must ensure that when they are used they are fully justified from a clinical perspective.’
The study represents the culmination of almost two decades of research in this area at Newcastle University, and is jointly funded by the UK Department of Health and NCI/NIH.
CT imaging is a vital and commonly used diagnostic technique and it is used more frequently in countries such as the USA and Japan. However, CT scans deliver a dose of ionising radiation to the body part being scanned and to nearby tissues. Even at relatively low doses, ionising radiation can break the chemical bonds in DNA, causing damage to genes that may increase a person
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