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Cooling therapy for cardiac arrest survivors is as cost-effective as accepted treatments for other conditions

Diane | August 11, 2009

Resource: American Heart Association

Cooling therapy for cardiac arrest survivors is as cost-effective as accepted treatments for other conditions

Study Highlights:

  • The cost effectiveness of post-resuscitation therapeutic hypothermia is comparable to widely accepted treatments for other medical conditions.
  • Lowering the body temperature of cardiac arrest patients can reduce death and disability if they survive out-of-hospital cardiac arrest due to ventricular fibrillation (VF), but hospitals have not widely adopted the treatment.
  • Researchers say from a societal perspective, the benefits of post-resuscitation hypothermia justify its costs.

DALLAS, Aug. 4, 2009 — Cooling unconscious cardiac arrest survivors can increase survival and has a cost effectiveness comparable to other widely accepted treatments in modern health care, researchers report in Circulation: Cardiovascular Quality and Outcomes.

Out-of-hospital cardiac arrest – in which the heart stops effectively pumping blood through the body – annually occurs in about 300,000 adults in the United States.

“Therapeutic hypothermia is the only post-resuscitation therapy shown to improve both survival and reduce disability after cardiac arrest,” said lead author Raina M. Merchant, M.D., M.S., a Robert Wood Johnson Foundation Clinical Scholar and emergency medicine physician at the University of Pennsylvania School of Medicine in Philadelphia.

“Since 2003, the American Heart Association has recommended that comatose (unconscious) patients with spontaneous circulation after out-of-hospital ventricular fibrillation (VF) cardiac arrest should receive therapeutic hypothermia,” Merchant said. “Despite repeating this recommendation in the 2005 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care, along with other studies that show its benefits, therapeutic hypothermia hasn’t been adopted as quickly as one would hope. We thought it would be a good idea to determine whether cost should be a barrier to its use.”

With therapeutic hypothermia, a patient’s body temperature is cooled and the patient is monitored so that their internal body temperature remains between 32 and 34 degrees centigrade (89.6 to 93.2 degrees Fahrenheit) for at least 12 to 24 hours. Cooling blankets, one of several technologies used to accomplish therapeutic cooling, were the focus of the current analysis.

Researchers used a complex mathematical design to measure quality-adjusted survival after cardiac arrest, cost of hypothermia treatment, cost of post-hospital discharge care and incremental cost-effectiveness ratios. Factors affecting costs included additional nursing care required during cooling treatment, extra time spent in the intensive care unit and post-discharge care required.

Merchant said, “Quality adjusted life year calculations were based on previous studies of patients with cardiac arrest.”

Quality adjusted life years (QALY) are a measurement of health outcomes that are calculated by combining quality of life and life expectancy.

The incremental cost-effectiveness ratio (ICER) for therapeutic hypothermia compared with conventional care (post-resuscitation care without hypothermia) was $47,168/ (QALY), Merchant said.
“We found that even at extreme estimates for costs, the cost-effectiveness of hypothermia remained less than $100,000/QALY in more than 91 percent of our simulations,” she said.

Researchers used data from two landmark papers published in 2002 by the Hypothermia After Cardiac Arrest (HACA) study group, which reported that therapeutic hypothermia improves survival and neurologic outcomes in comatose resuscitated cardiac arrest patients. In addition, researchers used information from cooling device companies and consultation with resuscitation experts.

In comparison, other studies estimated the ICER of kidney dialysis at $55,000/QALY. Public access defibrillation — the placement of automated external defibrillators (AEDs) in public places — has an ICER of $44,000/QALY. Placing AEDs on all U.S. commercial aircraft has an estimated cost of $94,700/QALY, researchers added.

“We showed that therapeutic hypothermia is a good value for the cost,” Merchant said. “In fact, even if a hospital had only one patient eligible for hypothermia therapy annually, and considerable post-resuscitation care costs resulted for survivors, the cost-effectiveness is consistent with many widely accepted healthcare interventions.”

One of the limitations of the current study is the lack of long-term outcomes data, which Merchant hopes will be overcome with future research.

Co-authors are Lance B. Becker, M.D.; Benjamin S. Abella, M.D., M.Phil.; David A. Asch, M.D., M.B.A. and Peter W. Groeneveld, M.D., M.S. Individual author disclosures are on the manuscript.

The study was funded by the Robert Wood Johnson Foundation’s Clinical Scholars program at the University of Pennsylvania (Dr. Merchant), and by a Career Development Transition Award from the Veterans Affairs Health Services Research and Development Service (Dr. Groeneveld).

###

Statements and conclusions of study authors published in American Heart Association scientific journals are solely those of the study authors and do not necessarily reflect the association’s policy or position. The association makes no representation or guarantee as to their accuracy or reliability. The association receives funding primarily from individuals; foundations and corporations (including pharmaceutical, device manufacturers and other companies) also make donations and fund specific association programs and events. The association has strict policies to prevent these relationships from influencing the science content. Revenues from pharmaceutical and device corporations are available at www.americanheart.org/corporatefunding.  

NR09-1095 (Circ Outcomes/Merchant)

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A little fun with social media and health

Diane | August 7, 2009

Enjoy this fun video and how hospitals are using social media as a way to communicate.

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Genetic link to increased risk of ovarian cancer found

Diane | August 6, 2009

Resource: University of Cambridge

  Scientists have located a region of DNA which – when altered – can increase the risk of ovarian cancer, according to research published in Nature Genetics over the weekend.

An international research group led by scientists based at the Cancer Research UK Genetic Epidemiology Unit at the University of Cambridge and UCL (University College London) searched through the genomes of 1,810 women with ovarian cancer and 2,535 women without the disease from across the UK. They analysed 2.5 million variations in DNA base pairs – the letters which spell out the genetic code – to identify common spelling ‘errors’ linked to ovarian cancer risk.

The scientists identified the genetic ‘letters’- called single nucleotide polymorphisms (SNPs) – which when spelt slightly differently increase ovarian cancer risk in some women. This is the first time scientists have found a SNP linked uniquely to risk of ovarian cancer and is the result of eight years of investigations. With the help of the international Ovarian Cancer Association Consortium (OCAC), they then looked at more than 7,000 additional women with ovarian cancer and 10,000 women without disease from around the world to confirm this finding.

The region of risk DNA is located on chromosome nine (there are 23 pairs of each chromosome in humans, one of each pair inherited from each parent). The scientists estimate that there is a 40 per cent increase in lifetime risk for women carrying the DNA variation on both copies of chromosome nine compared with someone who doesn’t carry it on either chromosome. The risk for women carrying the variation on both chromosomes is 14 in 1000 – compared with ten in 1000.

Approximately 15 per cent of women in the UK population carry two copies of the variant DNA.

The lifetime risk for a woman carrying the DNA variant on one copy of the chromosome is increased by 20 per cent from ten in 1000 to 12 in 1000. Approximately 40 per cent of women in the UK carry one copy.

Lead author, Professor Dr Paul Pharoah, a Cancer Research UK senior research fellow at the University of Cambridge, said: “We already know that people with mistakes in the BRCA1 and BRAC2 genes have a greater risk of ovarian cancer – but on their own they don’t account for all of the inherited risk of the disease.
“It is likely that the remaining risk is due to a combination of several unidentified genes – which individually carry a low to moderate risk. Now we have ticked one off, the hunt is on to find the rest.”

Senior author Dr Simon Gayther, whose work is supported by Cancer Research UK and The Eve Appeal charity which fundraises for the gynaecological cancer research team based at UCL, said: “The human DNA blueprint contains more than 10 million genetic variants. These are part and parcel of our characteristics and make-up – but a handful will also increase the chances of some women getting ovarian cancer and we have found the first one of these.

“There is now a genuine hope that as we find more, we can start to identify the women at greatest risk and this could help doctors to diagnose the disease earlier when treatment has a better chance of being successful.”

Ovarian cancer is the fifth most common cancer in women in the UK with around 6,800 new cases diagnosed each year in the UK – 130 women every week. It is the fourth most common cause of cancer death in women in the UK with around 4,300 deaths from the disease in the UK each year.

BRCA1 and BRCA2 are high risk genes which cause breast cancer and are already known to significantly increase the risk of ovarian cancer but faults in these genes are rare and probably cause less than five per cent of all cases of ovarian cancer.

Reference:
University of Cambridge. (August 3, 2009) Genetic link to increased risk of ovarian cancer found. Retrieved August 4, 2009 from http://www.admin.cam.ac.uk/news/dp/2009080301

 

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Cancer Research
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breast cancer, cancer, Cancer Research UK Genetic Epidemiology Unit, genetic code, Lead author, Nature Genetics, ovarian cancer, Paul Pharoah, Professor, Simon Gayther, SNP, United Kingdom, University College London, University of Cambridge
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Intensive Glucose Control Reduces Complications of Type 1 Diabetes

Diane | August 4, 2009

Resource: National Institutes of Health

Intensive Glucose Control Reduces Complications of Type 1 Diabetes
Near-normal control of glucose beginning as soon as possible after diagnosis greatly improves the long-term prognosis of type 1 diabetes, a new study found.

Nearly 24 million people nationwide have diabetes, with type 1 diabetes accounting for about 5-10% of confirmed cases. Formerly called juvenile-onset or insulin-dependent diabetes, type 1 diabetes develops when the body’s immune system destroys the cells that make the hormone insulin, which regulates blood glucose. Type 1 diabetes develops most often in children and young adults but can appear at any age.

The new study builds on the landmark Diabetes Control and Complications Trial (DCCT) and its follow-up study, the Epidemiology of Diabetes Interventions and Complications (EDIC). Both were funded by NIH. DCCT, conducted from 1983 to 1989, compared intensive management of blood glucose to conventional control. The intensive treatment group was asked to keep glucose levels as close to normal as possible, which requires at least 3 insulin injections a day or an insulin pump, guided by self-monitoring of blood glucose at least 4 times a day. At the time, conventional treatment consisted of 1 or 2 insulin injections a day with daily urine or blood glucose testing. DCCT found that intensive glucose control was superior to conventional control in delaying or preventing the complications of type 1 diabetes. EDIC continues to follow DCCT participants to track the long-term effects of the approaches.

In the new study, a team of researchers led by Dr. David M. Nathan of Massachusetts General Hospital and Dr. Trevor Orchard of the University of Pittsburgh looked at overall rates of eye, kidney and cardiovascular complications in people who were diagnosed with type 1 diabetes an average of 30 years earlier. The team looked at DCCT/EDIC participants as well as a subset of patients from another NIH-funded study of people diagnosed with type 1 diabetes from 1950 to 1980. The other study was observational, with the patients comparable to DCCT participants using conventional treatment.

In the July 27, 2009, issue of the Archives of Internal Medicine, the researchers reported that intensive glucose control significantly lowered rates of eye damage, kidney damage and cardiovascular disease events. Among DCCT participants, those randomly assigned to intensive glucose control had about half the rate of eye damage after 30 years of diabetes than those assigned to conventional glucose control (21% vs. 50%), less than half the rate of kidney damage (9% vs. 25%) and a lower rate of cardiovascular events (9% vs. 14%). Results from the other NIH-funded study were consistent with those from DCCT’s conventionally treated participants.

The researchers also found that, after 30 years of living with diabetes, less than 1% of those receiving intensive glucose control in the DCCT had significantly impaired vision or kidney failure or needed a limb amputation due to diabetes.

“Tight control is difficult to achieve and maintain, but its benefits have changed the course of diabetes,” says Dr. Saul Genuth of Case Western University, who co-chairs the EDIC study. Major technology improvements in the past decade, such as continuous glucose monitoring devices and improved insulin pump technology, are now helping patients control their blood glucose more precisely and conveniently.

Related Links:
Type 1 Diabetes:

http://health.nih.gov/result.asp?terms=diabetes&disease_id=379

DCCT and EDIC:
http://diabetes.niddk.nih.gov/dm/pubs/control/ Intensive Glucose Control Reduces Complications of Type 1 Diabetes
Near-normal control of glucose beginning as soon as possible after diagnosis greatly improves the long-term prognosis of type 1 diabetes, a new study found.

Nearly 24 million people nationwide have diabetes, with type 1 diabetes accounting for about 5-10% of confirmed cases. Formerly called juvenile-onset or insulin-dependent diabetes, type 1 diabetes develops when the body’s immune system destroys the cells that make the hormone insulin, which regulates blood glucose. Type 1 diabetes develops most often in children and young adults but can appear at any age.

The new study builds on the landmark Diabetes Control and Complications Trial (DCCT) and its follow-up study, the Epidemiology of Diabetes Interventions and Complications (EDIC). Both were funded by NIH. DCCT, conducted from 1983 to 1989, compared intensive management of blood glucose to conventional control. The intensive treatment group was asked to keep glucose levels as close to normal as possible, which requires at least 3 insulin injections a day or an insulin pump, guided by self-monitoring of blood glucose at least 4 times a day. At the time, conventional treatment consisted of 1 or 2 insulin injections a day with daily urine or blood glucose testing. DCCT found that intensive glucose control was superior to conventional control in delaying or preventing the complications of type 1 diabetes. EDIC continues to follow DCCT participants to track the long-term effects of the approaches.

In the new study, a team of researchers led by Dr. David M. Nathan of Massachusetts General Hospital and Dr. Trevor Orchard of the University of Pittsburgh looked at overall rates of eye, kidney and cardiovascular complications in people who were diagnosed with type 1 diabetes an average of 30 years earlier. The team looked at DCCT/EDIC participants as well as a subset of patients from another NIH-funded study of people diagnosed with type 1 diabetes from 1950 to 1980. The other study was observational, with the patients comparable to DCCT participants using conventional treatment.

In the July 27, 2009, issue of the Archives of Internal Medicine, the researchers reported that intensive glucose control significantly lowered rates of eye damage, kidney damage and cardiovascular disease events. Among DCCT participants, those randomly assigned to intensive glucose control had about half the rate of eye damage after 30 years of diabetes than those assigned to conventional glucose control (21% vs. 50%), less than half the rate of kidney damage (9% vs. 25%) and a lower rate of cardiovascular events (9% vs. 14%). Results from the other NIH-funded study were consistent with those from DCCT’s conventionally treated participants.

The researchers also found that, after 30 years of living with diabetes, less than 1% of those receiving intensive glucose control in the DCCT had significantly impaired vision or kidney failure or needed a limb amputation due to diabetes.

“Tight control is difficult to achieve and maintain, but its benefits have changed the course of diabetes,” says Dr. Saul Genuth of Case Western University, who co-chairs the EDIC study. Major technology improvements in the past decade, such as continuous glucose monitoring devices and improved insulin pump technology, are now helping patients control their blood glucose more precisely and conveniently.

Related Links:
Type 1 Diabetes:

http://health.nih.gov/result.asp?terms=diabetes&disease_id=379

DCCT and EDIC:
http://diabetes.niddk.nih.gov/dm/pubs/control/

Reference:
NIH.gov (2009). Intensive glucose control reduces complications of type 1 diabetes.  Retrieved August 3, 2009, from http://www.nih.gov/news/research_matters/august2009/08032009diabetes.htm

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Diabetes Research
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amputation, cardiovascular disease, Case Western University, continuous glucose monitoring devices, David M. Nathan, diabetes, diabetes accounting, improved insulin pump technology, insulin injections, insulin pump, kidney failure, Massachusetts General Hospital, National Institute of Health, Saul Genuth, technology improvements, the Archives of Internal Medicine, Trevor Orchard, University of Pittsburgh
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Healthcare Reform Bill, H.R. 3200 before the 11th Congress.

Diane | August 3, 2009

For your reference here is a link to the actual Healthcare Reform Bill, H.R. 3200 before the 11th Congress.

Healthcare Reform Bill, H.R. 3200

“To provide affordable, quality health care for all Americans and reduce
the growth in health care spending, and for other purposes.”

http://frwebgate.access.gpo.gov/cgi-bin/getdoc.cgi?

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Resources for Medical Information United States

Diane |

Resource: PubMed Central

PubMed Central (PMC)
is the U.S. National Institutes of Health (NIH) free digital archive of biomedical and life sciences journal literature.


All the articles in PMC are free (sometimes on a delayed basis). Some journals go beyond free, to Open Access. PMC’s utilities include an OAI service that provides XML of the full-text of some articles, functions for scripting PMC searches and linking to specific PMC articles from your site, and more.  Looking for a modern journal article DTD? Take a look at NLM’s Journal Publishing XML DTD and schema. It’s about preservation and access: digitizing the complete run of back issues of many of the journals in PMC.

Pub Med Central News Feed

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