Sentences with phrase «family members of the patients in»

Solid working experience in caring of elderly and handicapped people Wide knowledge of best sanitary practices and basic safety techniques Excellent skills in in - home care provision Strong ability to work closely with family members of the patients In depth ability to organize work and manage time

Not exact matches

Four family members of the first confirmed Ebola patient in the US have been ordered to stay at home as a precautionary measure.

In addition to hosting job fairs at the base, where 12,000 soldiers are stationed, Starbucks conducts regular plant tours for service members, maintains an Adopt a Unit program and supports the annual Fisher House Golf Tournament, which generates funds to aid families of patients receiving care at military and Veterans Administration medical centers.

Rather than the common policy of discharging such patients to nursing homes when family members insist on continued treatment or the insurance money runs out, Catholic institutions could develop sorely needed long «term rehabilitation facilities that could build on the encouraging work being done with such patients in England and Israel.

In fact, we believe that healthcare is most beneficial when it is delivered through a Patient — Family - Centered Care Model that views you and your child as integral members of the care team.

If an unruly, loud, smelly, rude or rambunctious family member of yours is disturbing you or the other patients that are within sight, smell, or earshot, that person will no longer be allowed in the delivery room.

Any infection that could have been avoided is one too many as the impact this has on patients and their families can be both debilitating and in some cases life changing, and sadly, as some members of MRSA Action UK know, can lead to loss of life.

ALBANY, NY (05/02/2018)(readMedia)-- Members of the New York State Public Employees Federation (PEF) will be joined by mental health experts and families of patients at the general meeting of the Orange County Legislature to advocate for state - operated mental health services in Orange County.

Many of us in the Legislature know family members, friends or neighbors who have been treated at the VA and were shocked to learn that more than 700 patients were potentially exposed to life - threatening viruses.

The legislators participated in protests with dozens, maybe hundreds, of patients, family members and mental health advocates and collected more than 17,000 signatures to deliver to the governor's office.

The law, named in honor of Ruth Murray, recognizes that nursing homes have a responsibility to notify family members or guardians when a patient has been badly injured as soon as possible.

The law, named in memory of Ruth Murray, recognizes that nursing homes have a responsibility to notify family members or guardians when a patient has been badly injured as soon as possible.

«Fibroblast growth factor receptor inhibitors are new therapies being developed in clinical trials for patients whose cancer cells have genetic alterations in this family of genes,» says Roychowdhury, a member of the OSUCCC — James Translational Therapeutics Program.

An associate professor of Neurology at Harvard Medical School, Talkowski adds, «Individuals in 10 countries — clinicians, investigators, patients and family members — helped us assemble the largest group of arhinia patients every studied, encompassing 24 percent of the previously reported 80 individuals and 21 newly identified patients.

Alzheimer's health care costs in have been estimated at $ 178 billion per year, including the value of unpaid care for patients provided by nearly 10 million family members and friends.

When patients like Godfrey Catanus in the study heard the voice of a family member calling their names out loud and reciting stories while they were in an MRI, their brains showed increased neural activity.

Louie's research team used filtration to capture the good bacteria from feces, which in most cases came from a family member of the patient.

«Patients, family members, and healthcare providers should work together to find solutions to the barriers preventing a patient from participating in a structured exercise programs, because exercise programs can help patients manage their condition,» said Lauren B. Cooper, M.D., lead author of the study and a fellow in cardiovascular diseases at the Duke University School of Medicine in Durham, North CPatients, family members, and healthcare providers should work together to find solutions to the barriers preventing a patient from participating in a structured exercise programs, because exercise programs can help patients manage their condition,» said Lauren B. Cooper, M.D., lead author of the study and a fellow in cardiovascular diseases at the Duke University School of Medicine in Durham, North Cpatients manage their condition,» said Lauren B. Cooper, M.D., lead author of the study and a fellow in cardiovascular diseases at the Duke University School of Medicine in Durham, North Carolina.

Shore is a Ph.D. scientist, and yet she and her lab members know most of the patients and families who come to Penn to see orthopedist Frederick Kaplan, one of the few clinicians who specializes in the diseases.

When patients in the study heard the voice of a family member calling their names out loud and reciting stories while they were in an MRI, their brains showed increased neural activity.

As part of these ongoing research activities, the DNA of Dravet patients without SCN1A mutations was analyzed by trio exome sequencing, which searches across the active parts of the genome for de novo mutations that have arisen in these patients (de novo mutations are DNA copying errors that occur in the parents» gametes or in the fertilized egg or embryo, resulting in the afflicted family member being the first person in their family to have this genetic condition).

«While tumor profiling holds the promise of improved therapeutics through personalized medicine, it is important that both clinicians and patients discuss the possibilities of incidental findings prior to ordering the testing, as the findings can have serious implications for both the patient and their family members,» said Melinda Yushak, M.D., M.P.H., first author on the study and a medical oncology fellow in Yale School of Medicine.

While there were no significant differences in the responses of residents based on how far along they were in their training, the researchers were surprised to discover some significant differences among supervising physicians, with senior attendings being more likely than junior attendings — who could be fellows or attendings in practice less than five years — to prefer immediate notification for situations including patient falls, new or worsening pain, an angry parent or family member, or the need for restraints.

Some of the most striking differences were in logistical / social situations — such as an angry parent or family member, the need to put a patient in restraints, aggressive patient behavior or the inability to carry out a procedure for any reason.

«Understanding how patients vary in their inclusion of family members in decisions — by ethnicity, language spoken, marital status, sex, age, insurance status, and veteran status — may help physicians to better assess their patients» preferences for engaging family members in decisions,» said Dr. Hobbs.

«Our discovery of germline mutations in so many cases of Wilms tumor means that the children and family members of these patients may be at risk for tumor development,» said Perlman.

«Acute aortic dissections may be disguised as heart attacks, and we know that the genetic component of TAAD is strong — in about 20 % of patients, it is also found in family members.

In 2011, Vermeire's group published a study showing that healthy family members of Crohn's disease patients have a slight dysbiosis as well.

It is important for all patients (and family members of patients) with macular degeneration to know that although the disease can injure the central vision of both eyes severely enough to render one «legally blind,» it is extremely uncommon to cause complete blindness in even a single eye.

Now Cecilia Lai, Simon Fisher and colleagues, reporting in todays Nature, show that a gene on chromosome 7, which they call FOXP2, is mutated in the affected members of the KE family, as well as in an unrelated patient with a similar language deficit.

They compared the results with data from disease - free family members of the patients as well as healthy, unrelated controls to home in on CNVs unique to the cancer patients.

The same mutation was present in all members of the family who had Tourette but was absent in thousands of DNA samples from control subjects, who included unrelated people with similar ethnic backgrounds as well as a group of 720 Tourette patients, the researchers report today in The New England Journal of Medicine.

To nail down these evasive genes, teams led by human geneticist Jonathan Haines of Vanderbilt University in Nashville, Tennessee, and neurologist Jan Hillert of the Karolinska Institute in Stockholm, Sweden, compared several thousand MS patients from the United States and Europe with their family members and healthy controls.

Clark said Alberta is generally doing a good job in helping patients manage their health compared with parts of Europe or the United States, but more can be done to include family members in care decisions and integrate services between cardiologists, pharmacists, family physicians and primary care networks.

A voluntary program being spearheaded by Intermountain Healthcare that allows family members of hospitalized patients to participate in their care enhanced healing and reduced readmission rates, according to a new study published in the February issue of the medical journal, CHEST.

After doing a genetic epidemiology research project at McGill, looking at whether family members of head and neck cancer patients had an increased risk of the disease (and finding the topic fascinating), she went to the University of Washington (U.W.) in Seattle to earn a master's degree in epidemiology.

Via this system, the stroke specialists can not only view physical signs of a possible stroke in order to assess the patient's condition, but can speak to the patient, family members, nurses and attending physicians, as well as directly review CT scan images of the patient's brain.

It is very personalized and options, from traditional to investigational treatments, are carefully explained to the patient and family members, helping them in the decision making process of what is best for the patient.

We help patients, family members, loved ones, and other physicians understand the benefits, risks, and limitations of treating cancer in older adults.

More than 1,500 patients and family members are now participating in genetic studies aimed at improving treatment through a better understanding of genetics.

On March 20th, just in advance of CORD's annual Rare Disease Day Conference, dozens of patients, family members and supporters will converge on Parliament Hill to meet with Members of Parliament to deliver one simple message, «National Pharmacare: Let's be fair to rare.members and supporters will converge on Parliament Hill to meet with Members of Parliament to deliver one simple message, «National Pharmacare: Let's be fair to rare.Members of Parliament to deliver one simple message, «National Pharmacare: Let's be fair to rare.»

As highlighted in the final print issue of Genome Technology, investigators leading clinical sequencing efforts have faced ethical dilemmas already, such as the return of genetic information to family members in the event that a patient dies.

A single member of the deceased patient's family (usually the executor of the estate) should receive the information in the family's behalf

In 2005, the identification of an activating mutation in JAK2 (the V617F mutation) as a STAT5 - activating and disease - causing genetic alteration in a significant proportion of patients with myeloproliferative neoplasms (MPNs) has emphasized the oncogenic role of the JAK tyrosine kinases in hematologic malignancies.2 — 5 JAK2 is a member of the Janus tyrosine kinase family comprising three other mammalian non-receptor tyrosine kinases (JAK1, JAK3 and TYK2) that associate with cytokine receptors lacking intrinsic kinase activity to mediate cytokine - induced signal transduction and activation of STAT transcription factors.6 All JAKs share a similar protein structure and contain a tyrosine kinase domain at the C - terminus flanked by a catalytically inactive pseudokinase domain with kinase - regulatory activity, by an atypical SH2 domain and by a FERM domain that mediates association to the membrane - proximal region of the cytokine receptors.7, 8 Soon after the discovery of JAK2 V617F, we and others described that activating JAK1 mutations are relatively common in adult patients with T - cell acute lymphoblastic leukemia (ALL) and participate in ALL development allowing for constitutive activation of STAT5.9 — 11 Several STAT5 - activating JAK1 mutations were also reported in AML and breast cancer patients.In 2005, the identification of an activating mutation in JAK2 (the V617F mutation) as a STAT5 - activating and disease - causing genetic alteration in a significant proportion of patients with myeloproliferative neoplasms (MPNs) has emphasized the oncogenic role of the JAK tyrosine kinases in hematologic malignancies.2 — 5 JAK2 is a member of the Janus tyrosine kinase family comprising three other mammalian non-receptor tyrosine kinases (JAK1, JAK3 and TYK2) that associate with cytokine receptors lacking intrinsic kinase activity to mediate cytokine - induced signal transduction and activation of STAT transcription factors.6 All JAKs share a similar protein structure and contain a tyrosine kinase domain at the C - terminus flanked by a catalytically inactive pseudokinase domain with kinase - regulatory activity, by an atypical SH2 domain and by a FERM domain that mediates association to the membrane - proximal region of the cytokine receptors.7, 8 Soon after the discovery of JAK2 V617F, we and others described that activating JAK1 mutations are relatively common in adult patients with T - cell acute lymphoblastic leukemia (ALL) and participate in ALL development allowing for constitutive activation of STAT5.9 — 11 Several STAT5 - activating JAK1 mutations were also reported in AML and breast cancer patients.in JAK2 (the V617F mutation) as a STAT5 - activating and disease - causing genetic alteration in a significant proportion of patients with myeloproliferative neoplasms (MPNs) has emphasized the oncogenic role of the JAK tyrosine kinases in hematologic malignancies.2 — 5 JAK2 is a member of the Janus tyrosine kinase family comprising three other mammalian non-receptor tyrosine kinases (JAK1, JAK3 and TYK2) that associate with cytokine receptors lacking intrinsic kinase activity to mediate cytokine - induced signal transduction and activation of STAT transcription factors.6 All JAKs share a similar protein structure and contain a tyrosine kinase domain at the C - terminus flanked by a catalytically inactive pseudokinase domain with kinase - regulatory activity, by an atypical SH2 domain and by a FERM domain that mediates association to the membrane - proximal region of the cytokine receptors.7, 8 Soon after the discovery of JAK2 V617F, we and others described that activating JAK1 mutations are relatively common in adult patients with T - cell acute lymphoblastic leukemia (ALL) and participate in ALL development allowing for constitutive activation of STAT5.9 — 11 Several STAT5 - activating JAK1 mutations were also reported in AML and breast cancer patients.in a significant proportion of patients with myeloproliferative neoplasms (MPNs) has emphasized the oncogenic role of the JAK tyrosine kinases in hematologic malignancies.2 — 5 JAK2 is a member of the Janus tyrosine kinase family comprising three other mammalian non-receptor tyrosine kinases (JAK1, JAK3 and TYK2) that associate with cytokine receptors lacking intrinsic kinase activity to mediate cytokine - induced signal transduction and activation of STAT transcription factors.6 All JAKs share a similar protein structure and contain a tyrosine kinase domain at the C - terminus flanked by a catalytically inactive pseudokinase domain with kinase - regulatory activity, by an atypical SH2 domain and by a FERM domain that mediates association to the membrane - proximal region of the cytokine receptors.7, 8 Soon after the discovery of JAK2 V617F, we and others described that activating JAK1 mutations are relatively common in adult patients with T - cell acute lymphoblastic leukemia (ALL) and participate in ALL development allowing for constitutive activation of STAT5.9 — 11 Several STAT5 - activating JAK1 mutations were also reported in AML and breast cancer patients.in hematologic malignancies.2 — 5 JAK2 is a member of the Janus tyrosine kinase family comprising three other mammalian non-receptor tyrosine kinases (JAK1, JAK3 and TYK2) that associate with cytokine receptors lacking intrinsic kinase activity to mediate cytokine - induced signal transduction and activation of STAT transcription factors.6 All JAKs share a similar protein structure and contain a tyrosine kinase domain at the C - terminus flanked by a catalytically inactive pseudokinase domain with kinase - regulatory activity, by an atypical SH2 domain and by a FERM domain that mediates association to the membrane - proximal region of the cytokine receptors.7, 8 Soon after the discovery of JAK2 V617F, we and others described that activating JAK1 mutations are relatively common in adult patients with T - cell acute lymphoblastic leukemia (ALL) and participate in ALL development allowing for constitutive activation of STAT5.9 — 11 Several STAT5 - activating JAK1 mutations were also reported in AML and breast cancer patients.in adult patients with T - cell acute lymphoblastic leukemia (ALL) and participate in ALL development allowing for constitutive activation of STAT5.9 — 11 Several STAT5 - activating JAK1 mutations were also reported in AML and breast cancer patients.in ALL development allowing for constitutive activation of STAT5.9 — 11 Several STAT5 - activating JAK1 mutations were also reported in AML and breast cancer patients.in AML and breast cancer patients.10

«Health officials in Dallas were assessing about 100 people for possible contact with the Ebola virus Thursday, while four family members of the Texas hospital patient diagnosed with the disease were placed under quarantine Wednesday night to stem its potential spread.»

That was what happened with Marge Benham - Hutchins, 61, of San Antonio, Texas, a patient and family advisory council member at Beyond Celiac who was diagnosed in her early 50s.

The day - to - day workings of hospital dwellers — doctors, nurses, patients and family members — who have to make incredibly difficult end - of - life decisions might seem like a parody of documentary short nominations, but it is an incredibly powerful and sensitive portrait of people in incredibly tough circumstances.

She can often be found on the floor of an exam room with a treat in her hand, gently greeting a nervous patient or getting chin kisses from an exuberant pet.At the core of her practice philosophy is the belief that pet owners are key members of their pet's health care team and that decision making should be a collaborative effort based on client education and each family's unique circumstances.

We value all our staff members for their individuality as well as for what they bring to the team, and stress patient comfort and family involvement in all aspects of our practice.

We aim to keep our clients involved in the decision making process with regards to their pets, remembering that clients and patients are members of our extended family.