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Showing posts with label Australia. Show all posts
Showing posts with label Australia. Show all posts

04 December 2014

World’s most comprehensive prostate cancer testing guidelines released for public consultation at 2014 World Cancer Congress

Leading cancer authorities in Australia today released for public consultation the world’s most robust set of clinical practice guidelines, aimed at maximising the benefits and reducing the harms associated with the Prostate Specific Antigen (PSA) test for prostate cancer; the second most common male cancer worldwide. If ratified, these new draft guidelines are expected to inform international opinion and clinical practice regarding PSA testing, where currently consensus is lacking and widespread confusion about best practice exists.

Professor Mary Gospodarowicz, President of the Union of International Cancer Control (UICC) welcomes the draft guidelines, saying: “The current PSA test is not accurate enough for population screening, yet it remains in widespread use. We need to focus on helping both patients and healthcare professionals understand the risks and benefits of this test to empower them to make more informed choices around screening. We applaud the Australian cancer authorities for taking the lead in developing the strongest set of clinical guidelines seen to date in prostate cancer; developed through a truly multisectoral approach. We expect the final recommendations of this review to clear the current confusions that exist around PSA testing.”

Approaches to prostate cancer testing differ across the world. Decision-making is complicated by the need to balance effective cancer detection and care, with concerns about over-diagnosis and prostate cancer treatment adverse side effects, including urinary incontinence, loss of sexual potency in men treated by radiotherapy and bowel problems.

The new draft guidelines, developed under the auspices of Cancer Council Australia’s guidelines unit with funding from Prostate Cancer Foundation of Australia (PCFA), address these risk/benefit concerns. Key recommendations include:

For men without a prostate cancer diagnosis or symptoms that might indicate prostate cancer
§  For men informed of the benefits and harms of screening who wish to undergo regular testing, offer PSA testing every two years from age 50 to age 69, and offer further investigation if the PSA is greater than 3.0 ng/mL.
§  In asymptomatic men interested in undergoing testing for early diagnosis of prostate cancer, digital rectal examination is not recommended as a routine test in the primary care setting.
§  Do not offer PSA testing to a man who is unlikely to live another seven years.
§  Offer evidence-based decisional support to men considering whether or not to have a PSA test, including the opportunity to discuss the potential benefits and risks of PSA testing before the decision to test is confirmed.
 
Active surveillance and watchful waiting
§  Offer active surveillance to men with prostate cancer who meet all the following criteria:
-    PSA ≤ 20 ng/mL, clinical stage T1-2 and Gleason score 6.
 
  • Advise men with potentially curable prostate cancer considering watchful waiting that their risk of developing more advanced prostate cancer and dying from it will be higher with watchful waiting than with immediate definitive treatment but that, in the medium to long term, watchful waiting is unlikely to diminish their wellbeing and quality of life.

Guidelines development panel member and leading cancer epidemiologist Emeritus Professor Bruce Armstrong AM, University of Sydney, noted that the draft guidelines did not recommend a national screening program, in keeping with health policy worldwide. “The draft guidelines are intended to inform the interactions between men and their doctors, when a man might request a PSA test or his doctor might offer one”, said Professor Armstrong AM.

Released today for public consultation via a globally-accessible wiki platform, the draft guidelines have been developed by a broad-based Australian Expert Advisory Panel, which included general practitioners, public health experts, urologists, pathologists, patient support groups and allied health professionals. This is the first time anywhere in the world that an expert advisory panel with all key stakeholders and varying perspectives has come together for such a systematic evidence-based review in this area of men’s health.

Associate Professor Anthony Lowe, PCFA CEO comments: “Crucial to the development of these new draft guidelines is that a wide variety of stakeholders worked collaboratively to gain consensus. It means we are able to make the most informed recommendations to date on the benefits and harms of PSA testing, and the optimum time to initiate treatment to save lives.”

Following today’s launch as part of the opening of the 2014 World Cancer Congress, health professionals and interested members of the public from around the world are invited to review and comment on the draft guidelines at: wiki.cancer.org.au/australia/Guidelines:PSATesting. Following the consultation phase, the draft guidelines will be submitted to the National Health and Medical Research Council of Australia for approval.

08 May 2012

Customers celebrate the launch of Tecan Australia


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Tecan recently invited customers from around Australasia to mark the inauguration of Tecan Australia as a fully owned Tecan subsidiary, with a series of launch events in Sydney, Brisbane and Melbourne. The creation of Tecan Australia reflects Tecan’s uniquely strong commitment to the Australasian market, and will provide customers in Australia, New Zealand and surrounding territories with an even better service, thanks to a new facility in Melbourne and local presence in several major cities. The launch events gave customers an opportunity to discuss their applications and automation issues with Tecan staff and their fellow scientists in a relaxed environment, and proved so successful that Tecan Australia will soon be establishing regular user group meetings to keep these valuable communication channels open.

The new Melbourne base houses a comprehensive sales and support organization – complete with a workshop and additional facilities for customer training and demonstrations – and provides additional warehouse facilities and stock levels to quickly support customers in need. Roland Durner, General Manager for Tecan Australia, said: “This is great news for our customers and employees alike. Our new facility, backed by strong operating procedures and with Tecan’s renowned emphasis on regulatory and quality requirements, will help us to improve every element of our business. Our existing team of highly trained sales and support staff will now be even better placed to provide a dedicated service to our customers in research, clinical diagnostics, forensics, and food and agriculture in the region.”

22 May 2010

Depresión postparto


Un estudio llevado a cabo en Australia y publicado en la revista "Physical Therapy", demuestra que acudir tras el parto a sesiones semanales de fisioterapia combinadas con charlas de de educación sanitaria sirve para mejorar el bienestar de las madres. De paso reduce el riesgo de sufrir depresión postparto en un 50%.

En estos casos de Australia las madres realizaban un programa de ejercicios en grupo y con sus bebés bajo la dirección de un fisioterapeuta. En el informe no se detalla hasta qué punto contribuyó el factor psicosocial a esos resultados positivos.

20 October 2009

El estudio ADVANCE revela nuevos avances en la lucha contra las complicaciones de la diabetes severa

Los nuevos resultados de ADVANCE (Action in Diabetes and Vascular Disease: Preterax y Diamicron evaluación) , el mayor ensayo clínico jamás realizado en pacientes con diabetes tipo 2 en todo el mundo, aportan ideas importantes sobre la estrategia terapéutica a adoptar para el control eficaz y seguro de la glucosa en sangre destinada a la reducción de la diabetes severa complications. Los nuevos datos de ADVANCE, presentado hoy en el Congreso de la Federación Internacional de Diabetes (FID), muestran que la eficacia y seguridad del control intensivo de la glucosa en sangre utilizando glicazida de liberación modificada (MR) (Diamicron MR)-basada en el tratamiento se mantiene a través de una amplia gama de settings.
Pacientes en diferentes clínicas ADVANCE han demostrado que el control intensivo de la glucosa con un MR gliclazida régimen basado en el tratamiento en personas con diabetes tipo 2 reduce el riesgo combinado de eventos microvasculares y macrovasculares, sobre todo a través de reducciones en el riesgo de diabetes nephropathy. "El control intensivo de la glucosa con un MR gliclazida régimen basado fue eficaz en reducir la HbA1c, independientemente de la edad, duración de la diabetes, sexo, índice de masa corporal, o HbA1c al inicio del estudio, y también con independencia de la glucosa inicial de reducción de tratamiento", dice Sophia Zoungas, investigadora del Instituto George de Salud Internacional, Australia. "El MR gliclazida régimen basado fue bien tolerado, con muy bajas tasas de hipoglucemia severa y sin aumento de peso."

ADVANCE mostró una tendencia positiva hacia la reducción de eventos cardiovasculares mayores en pacientes diabéticos que recibieron intensivo de la glucosa control. Este dato fue corroborado en un meta-análisis reciente de colaboración, de 4 de los ensayos de la glucosa en la reducción intensiva, incluidos los anticipos y el acuerdo, que demostró una significativa 9% de reducción de eventos cardiovasculares mayores, lo cual refleja principalmente una reducción del 15% en infarto de miocardio- Sobre la base de datos de observación, varios registros nacionales (incluidos los más de 70.000 pacientes con diabetes tipo 2), han informado recientemente de que la reducción de la glucosa regímenes que incluían gliclazida se asociaron con un menor riesgo de mortalidad en comparación con otros strategies terapéutico.
"Advance es una enorme reserva de la información clínica útil", concluyó el investigador principal ADVANCE el profesor John Chalmers, del Instituto George de Salud Internacional de Australia. "Por este motivo, tenemos previsto continuar con el seguimiento de los pacientes ADVANCE y creemos que este nuevo estudio-ADVANCE-ON6-jugará un papel fundamental en la definición de la gestión clínica en el futuro de las decenas de millones de personas con diabetes tipo 2 en todo el mundo. "

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