Infants in the NICU were more likely to stay asleep during recordings of their mothers reading, finds new research. Babies who spend their first days or weeks of life in the Neonatal Intensive Care Unit may not sleep as soundly as those who go home. Now, researchers are examining whether one simple difference could help soothe these infants to sleep: the sound of their mother’s voice. When they were played recordings of their mothers reading children’s books, babies in the NICU slept better and woke up less often, according to a new abstract presented at the annual meeting for Sleep Medicine. “In the hospital, we take care of babies who are not in their usual environment, which can hinder their ability to have normal sleep,” says lead author Renée Shellhaas, M.D., M.S., a pediatric neurologist at University of Michigan C.S. Mott Children’s Hospital. “Even though we do our best to make the ICU as quiet an environment as possible, there are hospital disruptions that are unavoidable. Alarms, monitors, ventilators, bedside care and even just the building’s heating and cooling noises may be disruptive. We designed this study to see how the sound environment in the NICU potentially influences sleep and to see if there are relatively simple interventions that may make a difference.” “What we found was that babies in the NICU were more likely to stay asleep when the recordings of their mothers’ voices played than they were without them.” "If we can find simple tools to help babies in the unit get higher quality sleep, they could make a big difference to infants’ health and development, especially for those who must stay in the hospital for an extended time."
University of Michigan C.S. Mott Children’s Hospitallabblog.uofmhealth.org/rounds/moms-voice-may-help-babies-sleep-better-nicu
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The International Hospital Federation (IHF) announced in July the 27 finalists in the four categories of the 2018 IHF Awards which honors innovations and outstanding achievements in the healthcare industry.
The IHF awards program received a record number of 160 entries from 118 organizations in 33 countries for the IHF / Dr Kwang Tae Kim Grand Award and Excellence Awards in Leadership and Management in Healthcare, Quality & Safety and Patient-centered Care, and Corporate Social Responsibility. After an extensive review by the panel of judges composed of health leaders from around the globe, 27 top entries from the four categories have been selected as finalists from which the Gold, Silver, Bronze and Merit Awards will be chosen.
“With the number of entries vying for the IHF Awards this year, the judges had a very difficult time evaluating. I am happy and delighted to see that all 160 submitted entries are of high standards aiming at improving many different aspects of health care and service delivery,” said Dr Lawrence Lai, Chair of the IHF Awards Committee. “For the finalists this year, I am proud to say that their projects or programs are indeed most outstanding and impressive.”
IHF has been recognizing innovation, excellence, outstanding achievements and best practices of hospitals and healthcare organizations since 2015 when the Awards was first presented in Chicago, USA.
This year’s winners will be awarded in front of industry peers on 10 October 2018 during the 42nd World Hospital Congress at the Brisbane Convention and Exhibition Centre in Australia.
Gold Winners will be invited to speak at a special session during the World Hospital Congress to share their winning programs and projects while Silver, Bronze Winners and Merit Awardees will be displaying posters at the Congress exhibition.
For more information on the IHF Awards Finalists, go to: https://congress.ihf-fih.org/finalists
To attend the IHF Awards Ceremony and World Hospital Congress, go to: www.hospitalcongress2018.com
Infants with diabetes can drop insulin syringes. Researchers from Bergen and Exeter have been leading the work, which causes children worldwide to replace insulin syringes with tablets. "All infants diagnosed with diabetes before 6-7 months of age should be given a rapid gene test to change treatment as soon as possible from insulin to sulfonylurea tablets. They can expect a long and very good effect of the treatment of blood sugar control, and the treatment is safe," says Professor Pål Rasmus Njølstad at the University of Bergen. It was in 2004 discovered that relatively high doses of sulfonylurea tablets could be used to treat diabetes in infants. This principle has given a new life for children with this type of diabetes, because 90% can stop insulin injections and even achieve better blood sugar control, at least for one year without the same low blood sugar problem. However, it has been unknown whether this treatment can be maintained in the long term, especially as sulfonylureas fail in half of those with type 2 diabetes after five years of treatment. The results are now available from an international multi-center study from centers in Bergen, Exeter, Rome, Paris, and Krakow. This included 81 people who 10 years ago had changed the treatment from insulin to sulfonylurea tablets. It was found that the failure effect of treatment, which is often seen in type 2 diabetes, rarely exists in this type of infant diabetes. Sulfonylurea is safe in this treatment, even with the relatively high doses needed. An excellent control of blood glucose was retained after ten years of treatment. Some children initially experienced a certain recovery of neurological features, but most of them did not have any clear improvement in the problems. "These findings will give many children a new and better quality of life," says Njølstad. "This is one of the few examples of lasting effect of precision medicine."
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Machine learning using real-time symptom reports can accurately detect lymphedema, a distressing side effect of breast cancer treatment that is more easily treated when identified early, finds a new study led by NYU Rory Meyers College of Nursing. “Using a well-trained classification algorithm to detect lymphedema based on real-time symptom reports is a highly promising tool that may improve lymphedema outcomes,” said Mei R Fu, PhD, RN, FAAN, associate professor of nursing at NYU Meyers and the study’s lead author. Lymphedema is a build-up of lymph fluid that causes swelling in the arms or legs and is commonly caused by the removal of lymph nodes as part of cancer treatment. It can occur immediately after cancer surgery or as late as 20 years after surgery; a recent study found that more than 41 percent of breast cancer patients experienced lymphedema in their arms within 10 years of their surgery. Lymphedema is one of the most dreaded adverse effects from breast cancer treatment because of its chronic nature and debilitating symptoms, including arm swelling, heaviness, tightness, achiness, stiffness, burning, and decreased mobility. While there is no cure for lymphedema, early detection and intervention can reduce symptoms and keep it from worsening, although early detection remains a challenge. “Clinicians often detect or diagnose lymphedema based on their observation of swelling. However, by the time swelling can be observed or measured, lymphedema has typically occurred for some time, which may lead to poor clinical outcomes,” said Fu. “In our digital era, integrating technology into health care has led to advances in detecting and predicting various medical conditions,” said Yao Wang, PhD, professor of electrical and computer engineering at NYU Tandon School of Engineering and the study’s coauthor. A type of artificial intelligence, machine learning is of interest to researchers due to its ability to construct algorithms that continually improve predictions and generate automated knowledge through data-driven predictions or decisions with incoming data—in this case, symptom reports. Machine learning is particularly beneficial when there are many relevant factors that are not independent, which is true for lymphedema symptoms. In this study, the researchers used a web-based tool to collect information from 355 women who had undergone treatment for breast cancer, including surgery. In addition to sharing demographic and clinical information, including whether they had been diagnosed with lymphedema, participants were asked whether they were currently experiencing 26 different lymphedema symptoms. Statistical and machine learning procedures were performed for data analysis. Five different classification algorithms of machine learning were compared: Decision Tree of C4.5, Decision Tree of C5.0, gradient boosting model, artificial neural network, and support vector machine. The algorithms were also compared with a conventional statistical approach that determines the optimal threshold for the symptom count based on the receiver operating curve. The researchers found that all five machine learning approaches outperformed the standard statistical approach, and the artificial neural network achieved the best performance for detecting lymphedema. The artificial neural network was 93.75 percent accurate, correctly classifying patients to have true lymphedema cases or non-lymphedema cases based on the symptoms reported. “Such detection accuracy is significantly higher than that achievable by current and often used clinical methods,” said Fu. The researchers note that conducting such real-time lymphedema assessment encourages patients to monitor their lymphedema status without having to visit a healthcare professional. Based on patients’ symptoms and resulting risk for lymphedema, the assessment system could alert patients at risk to schedule in-person clinical visits for further evaluation. This may lessen the burden of unnecessary clinical visits on patients and the healthcare system. “This has the potential to reduce healthcare costs and optimize the use of healthcare resources through early lymphedema detection and intervention, which could reduce the risk of lymphedema progressing to more severe stages,” Fu said.
New York Universitywww.nyu.edu/about/news-publications/news/2018/june/machine-learning-helps-detect-lymphedema-among-breast-cancer-sur.html
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Researchers at Loma Linda University Health found that kidney transplantationcan be safely performed using organs testing positive for the hepatitis C virus (HCV) antibody but negative for active viral infection. Their findings, published July 24 in the American Journal of Transplantation, could expand the number of kidneys available for those in need. “One way of increasing the kidney donor pool is to utilize more organs from HCV positive donors,” said the study’s lead author, Michael E. de Vera, MD, director of Loma Linda University (LLU) Transplant Institute. “Currently, HCV positive donors are defined by donors that have previously had HCV even if they were cured. Now there has been a call to redefine the definition of an HCV positive donor in hopes that more organs can be used from these donors.” Co-author of the study, Michael Volk, MD, director of transplant hepatology at LLU Tansplant Institute, participated in a 2017 American Society of Transplantation consensus conference, which encouraged the use of organs testing positive for HCV — those with only a positive antibody, as well as those testing positive for the virus. This recommendation stems in part from the availability of newer and better medications to cure people of the virus.
“These organs testing positive for HCV are frequently discarded and often come from younger donors,” Volk said. “This approach has the potential to save lives by increasing the numbers of transplants.” Although there is a record number of deceased organ donors, de Vera said the gap between the number of kidney transplants performed and the number of patients on the waiting list remains substantial. There are now nearly 95,000 kidney patients on the waiting list, but less than 20,000 kidney transplants occurred in 2017, according to the United Network for Organ Sharing.
The problem is even wider in California, where nearly 2,300 people received a kidney in 2017, while nearly 19,000 remained on the waitlist.
HCV is tested in organ donors by checking for the presence of HCV antibodies (Ab) and HCV RNA, de Vera said. The presence of HCV antibodies shows that the virus at some point affected the host, but does not reveal if the host was cured. The presence of HCV RNA, on the other hand, indicates active infection. Many organ donors are HCV Ab positive but HCV RNA negative, and doctors have been reluctant to transplant kidneys from these donors for fear of transmitting HCV to the recipient. As a result, many of these kidneys have not been used in the past.
“Our hope is that this study will convince transplant doctors that the use of these donor kidneys is safe and does not lead to HCV transmission,” said de Vera. “And hopefully, more patients will receive these life-saving organs.” The study was titled, “Transplantation of hepatitis C virus (HCV) antibody positive, nucleic acid test negative donor kidneys to HCV negative patients frequently results in seroconversion but not HCV viremia.” The study looked at 32 patients who were transplanted with HCV Ab+/NAT- kidneys at Loma Linda University Medical Center from January 2017 to February 2018. All patients consented to the surgeries. Recipient ages ranged from early 40s to late 60s, and donor ages ranged from late 20s to mid 50s. All 32 patients are doing well without evidence of hepatitis C virus infection.
https://lluh.org/?rsource=lluhealth.org/
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Researchers at Okayama University report in The Journal of Vascular Access a supporting device for accurately placing hemodialysis catheters on kidney patients. The device was successfully used on a group of 10 patients and is expected to become an essential tool in situations where other, catheter-free hemodialysis approaches are not possible.
Patients with improperly functioning kidneys often need to undergo hemodialysis — the procedure of purifying blood in an artificial kidney outside the body — on a regular basis. Hemodialysis requires access to blood vessels, for the collection of blood and its re-introduction after purification. In this context, vascular access is commonly achieved with a so-called tunneled cuffed catheter (TCC). Accurate TCC placement is important; incorrect positioning can lead to blood clots and induce central vein thrombosis. Assistant Professor Toshiaki Ohara from Okayama University and colleagues have now developed a device enabling accurate TCC placement. The researchers’ insertion support device accommodates for individual body shape differences and is expected to decrease the rate of TCC replacements — typically ranging between 8.9% and 56%.
The device was made from a material called expanded polytetrafluoroethylene (ePTFE), having the property of maintained plasticity. It can be described as a bendable ribbon with holes (eyelets) spaced 1 cm apart; the holes allow making markings on the patient’s body with a felt-tip pen.
The insertion support device was tested on 10 Japanese adult hemodialysis patients (6 men and 4 women with a mean age of 71.3 years) treated at Shigei Medical Research Hospital. Placement of the device on the body took place with the help of X-ray imaging: the tip of the device, for marking the TCC entry site, was laid so that it overlaps with the right heart border. With the help of the markings made on the patient’s body, the physician could insert the TCC within an error of about 1 cm. The patients were observed for 2 months, during which there was no catheter replacement needed.
The device of Dr.Ohara and colleagues helps to reduce catheter waste and the overall cost of hemodialysis. In addition, as the attachment of a catheter requires exposure to X-rays, it reduces accumulated radiation doses for both patients and physicians. Although the study was only carried out for 10 patients in a short observation period, the scientists “anticipate that this new device … can be used for catheter intervention in many fields”.
http://www.okayama-u.ac.jp/index_e.html
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New NDT study shows that `normal´ pre-dialysis blood pressure measurement is not reliable. “Without performing extended ambulatory BP recordings (44h – 48h) we approvingly accept an error rate of about 30% in the diagnosis of hypertension in dialysis patients, a highly vulnerable patient group with a dramatically elevated cardiovascular risk. This is why EURECA-m recommends ambulatory blood pressure monitoring as gold standard for the diagnosis for hypertension in hemodialysis patient.”
There is a bidirectional relationship between high blood pressure and chronic kidney disease (CKD). Hypertension aggravates CKD progression. On the other hand, CKD can cause hypertension, because our kidneys do not only `detox´ our bodies, but also regulate the blood pressure. This is, why nephrologists are `core experts´ when it comes to uncontrolled or difficult-to-treat blood pressure.
In hemodialysis patients, hypertension is very common, because the kidneys – and with them the main blood pressure regulation mechanism – stopped working.
“High blood pressure is dangerous, also in dialysis patients. It can lead to severe complications like heart attacks and strokes”, explains Professor Carmine Zoccali, president of the ERA-EDTA. “The monitoring of blood pressure levels is therefore an essential part of the care of these patients. The European Cardiovascular and Renal Medicine (EURECA-m) recommends the 48-h ambulatory blood pressure monitoring (ABPM) in these patients. Our new data strongly support this recommendation.”
The EURECA-m working group has previously published a study, in which 396 hemodialysis patients underwent 48-h ABPM. It showed that the prevalence of hypertension in dialysis patient was very high (84.3%). Although similar rates have been seen when blood pressure levels were measured in the dialysis center before the dialysis treatment, the sensitivity and specificity of 48-h ABPM proved to be higher. Sensitivity means that patients with hypertension are reliably detected and specificity means that those who do not suffer from hypertension are also correctly identified. Obviously, the `normal´, pre-dialysis measurement does not have a sufficient sensitivity and specificity in dialysis patients. About 30% of the patients are misdiagnosed, when the blood pressure is measured in the dialysis center before each dialysis treatment.
Why is that the case? The new EURECA-m study showed that 18.2% of the patients suffered from “white coat hypertension”: They do not have hypertension in “real life”, but develop high blood pressure levels as soon as their blood pressure is measured by a doctor or nurse. Vice versa, 14.1% of the patients suffered from “masked hypertension”, in which high blood pressure values occur often during the nights, only. Therefore, this hypertension cannot be detected before the daily dialysis treatment. Only the 48-h ABPM can reliably detect a `masked hypertension´ as well as the `white coat hypertension´.
“If we do not perform a 48-h ABPM, there is the risk that we treat patients with `white coat hypertension´, who do not need any medication and that we do not treat those with a `masked hypertension´ or with nocturnal hypertension, who need the treatment. In short: Without performing extended ambulatory BP recordings (44h – 48h) we approvingly accept an error rate of about 30% in the diagnosis of hypertension in dialysis patients, a highly vulnerable patient group with a dramatically elevated cardiovascular risk”, explains Professor Zoccali, ERA-EDTA president and co-author of the new study. “This is why EURECA-m recommends 48-h ambulatory blood pressure monitoring as gold standard for the diagnosis for hypertension in hemodialysis patient.”
www.era-edta.org
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Common beliefs and misconceptions in the community about dementia are still proving obstacles to treatment despite a rise in public awareness campaigns, Researchers from Flinders University in South Australia pooled the results of 32 dementia surveys from around the world published between 2012 and 2017 and found that public awareness of the causes of dementia has not changed. Almost half of the total 36,519 respondents had the common misconception that dementia was a normal part of ageing and was not preventable. The importance of formal educational attainment and management of cardiovascular were acknowledged by less than half of respondents even though regular exercise has been proven as the single most powerful influencer of brain health. The public also tended to endorse poorly supported risk reduction strategies such as taking vitamin supplements, ahead of more effective but time consuming and energetic strategies, such as exercise regimes. “We were surprised to find that dementia literacy is still so poor, given how much effort has been put into improving understanding,” said lead researcher Monica Cations. “The view that dementia is a normal part of ageing with few treatment options is a demonstrated barrier to both preventive health behaviours and to help-seeking and diagnosis in the event that symptoms emerge.” The 32 surveys were sourced from Europe(12), the United States (11), Asia (7) and Australia (2). The findings and associated problems are outlined in the paper, What does the general public understand about prevention and treatment of dementia? A systematic review of population-based surveys, which has been published by PlosOne. There are about 47 million people living with dementia worldwide. While research has not yet discovered a cure, there is accumulating evidence about the potential to prevent approximately one third of cases of dementia with management of risk factors such as poor educational attainment, hypertension, and depression. The recently adopted World Health Organization (WHO) Global Action Plan on Dementia urges all countries to implement campaigns to raise awareness about dementia. The plan includes a global target that all member countries will have at least one public awareness campaign on dementia by 2025.
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0196085http://theleadsouthaustralia.com.au/category/industries/health/
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Abington Hospital – Jefferson Health has been recognized as a Baby-Friendly hospital by Baby-Friendly USA, Inc. This designation recognizes Abington Hospital for the optimal level of care it provides breastfeeding mothers and their babies.
The World Health Organization (WHO) and the United Nations Children’s Fund (UNICEF) launched the Baby-Friendly Hospital Initiative (BFHI) in 1991. This initiative is centered around the Ten Steps to Successful Breastfeeding; a plan developed by global experts. Hospitals that provide mothers with the information, skills and confidence they need to successfully initiate and continue breastfeeding are recognized as Baby-Friendly. The World Alliance for Breastfeeding Action (WABA) coordinates World Breastfeeding Week, which is recognized annually August 1 to 7, to protect, promote and support breastfeeding mothers worldwide.
“We are committed to providing new mothers with the information and skills needed to confidently feed their babies,” says Dr. Steven Shapiro, Chair, Department of Pediatrics. “Abington Hospital is so proud to have achieved this designation which reflects the great efforts of our doctors, nurses and staff.”
In order to be considered for designation, Abington Hospital completed a rigorous on-site survey. The award will be maintained by upholding the practice of the Ten Steps to Successful Breastfeeding.
The BFHI continues to grow with Baby-Friendly hospitals now in all 50 states and 24 percent of births taking place in the more than 500 Baby-Friendly designated facilities. Nearly 5,000 babies are delivered per year at Abington Hospital. The BFHI initiative used in Abington Hospital encourages the use of evidence-based care and has seen tremendous success in helping mothers reach their breastfeeding goals.
https://www.abingtonhealth.org/
A new Antimicrobial Resistance (AMR) Accelerator Programme as part of new Calls for proposals was launched in July by the Innovative Medicines Initiative (IMI). Of the other topics launched in the Calls, many address brain disorders (e.g. Alzheimer’s disease, Parkinson’s disease, Huntington’s disease, major depression) and immune-mediated diseases (e.g. rheumatoid arthritis and lupus as well as inflammatory bowel diseases such as Crohn’s and colitis, and skin diseases like dermatitis and psoriasis). Among other things, the topics aim to make clinical trials more patient-centric, contribute to medicines safety, and apply blockchain technologies to the drug development and health sectors. The Calls for proposals launched in July (IMI2 – Calls 15 and 16) have a total budget of EUR 434 million. Around half of this comes from Horizon 2020, the EU’s framework programme for research and innovation. The other half comes from EFPIA companies and IMI Associated Partners; these do not receive any funding from IMI but contribute to projects, mainly through ‘in-kind’ contributions (e.g. researchers’ time). The aim of the new IMI AMR Accelerator is to progress the development of new medicines to treat or even prevent resistant bacterial infections in Europe and worldwide. The programme comprises three pillars. A Capability Building Network will coordinate the programme and carry out research to strengthen the scientific basis in the AMR field, while the Tuberculosis Drug Development Network will work to accelerate the discovery of new combinations of drugs to treat TB. Finally, Portfolio Building Networks will support collaborative efforts to discover, develop and advance new and innovative agents to prevent or treat AMR. The scope of the AMR Accelerator is broad; under one structure, it will address many of the scientific challenges of AMR, and it will support the development of new ways to prevent AMR (including vaccines) and treatments (including new antibiotics). More broadly, the IMI AMR Accelerator also contributes to the European action plan on AMR, which includes a chapter on boosting research, development and innovation for AMR.
www.imi.europa.eu
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