The document discusses elements of professional gatekeeping including codes of ethics, scope of practice, dealing with impaired colleagues, and whistleblowing. It addresses obligations to protect patients and the profession by ensuring colleagues practice appropriately and addressing misconduct. Institutional ethics committees are presented as a resource to help navigate complex ethical issues.
DNS allows users to reference computer names via symbolic names like domain names instead of IP addresses. It works by translating these symbolic names to their associated IP addresses. DNS uses a hierarchical and distributed database across interconnected name servers to provide a global directory service for name resolution on the internet.
This document provides an overview of nursing codes of ethics, including their purpose and history. It discusses the International Council of Nurses, which was established in 1899 and has been a pioneer in developing nursing ethics codes. The first nursing ethics book was written in 1900. Nursing codes outline ethical standards and guidelines for nurses, inform the public of nursing standards, and provide direction for self-regulation. The document reviews the Code of Ethics for Filipino Nurses and the American Nurses Association Code of Ethics, noting updates made in 2001.
The document provides information on various public health programs and initiatives by the Department of Health in the Philippines. It includes the DOH health calendar for 2010 which lists important health awareness dates throughout the year focused on topics like cancer, kidney disease, tuberculosis, and more. It also discusses the maternal and child health program which aims to reduce maternal and child mortality rates through interventions like prenatal care, immunizations, nutrition supplementation, and clean and safe deliveries. Key aspects of family planning counseling are outlined as well, emphasizing the importance of informed choice and addressing clients' individual needs and circumstances.
Should America have dropped the Atomic Bomb PaperSchool_Seller
The document discusses whether the US was justified in dropping atomic bombs on Hiroshima and Nagasaki in 1945. It presents arguments on both sides of the issue. On one hand, the US claimed the bombs ended the war and saved American lives, as the Japanese refused to surrender. However, others argue the bombings killed thousands of innocent civilians, the US knew the power of the bombs from previous tests, and they may have been dropped more to prevent Soviet expansion than to end the war, as Japan had already asked for peace talks. The document concludes it was wrong to drop the bombs due to the immense devastation and deaths caused, but acknowledges the bombings did achieve a Japanese surrender and end the war.
The document discusses communication skills and tools that were covered in a useful course. It lists blogs, slideshare, podcasts, and vodcasts as different ways to communicate. It also mentions building skills like taking screenshots with Jing and using Evernote to organize information. In conclusion, it thanks the reader for allowing the author to take the course, which they found beneficial.
Superdome hurricane katrina power pointchuehuethao
The document discusses conditions in the Superdome and Convention Center in New Orleans during Hurricane Katrina, claiming the government did not provide adequate safety or living conditions. It notes both locations lacked water, air conditioning, lighting and authority figures. The Superdome roof was ripped off. Desperate people were dying there. The movie depicted the conditions as being like a live sewer with no running water and too much body heat. Others should care because if placed in the same situation, they would want better conditions and rescue from the governor.
Hurricanes form over warm ocean waters when strong winds blow off the Sahara and interact with tropical depressions. They generally move westward and can strike locations in the Caribbean Sea, Southeastern United States, and occasionally the Northeast. Some of the most damaging hurricanes have included the 1900 Galveston hurricane (Category 4, 8,000 deaths), the 1938 Long Island Express (Category 5, 600 deaths), Hurricane Camille in 1969 (Category 5, 256 deaths), and Hurricane Katrina in 2005 (Category 4, 1,200 deaths). The most dangerous aspects of hurricanes are their strong winds over 200 mph, heavy rainfall and flooding, and large storm surges that can produce walls of water over 20 feet high.
The document discusses elements of professional gatekeeping including codes of ethics, scope of practice, dealing with impaired colleagues, and whistleblowing. It addresses obligations to protect patients and the profession by ensuring colleagues practice appropriately and addressing misconduct. Institutional ethics committees are presented as a resource to help navigate complex ethical issues.
DNS allows users to reference computer names via symbolic names like domain names instead of IP addresses. It works by translating these symbolic names to their associated IP addresses. DNS uses a hierarchical and distributed database across interconnected name servers to provide a global directory service for name resolution on the internet.
This document provides an overview of nursing codes of ethics, including their purpose and history. It discusses the International Council of Nurses, which was established in 1899 and has been a pioneer in developing nursing ethics codes. The first nursing ethics book was written in 1900. Nursing codes outline ethical standards and guidelines for nurses, inform the public of nursing standards, and provide direction for self-regulation. The document reviews the Code of Ethics for Filipino Nurses and the American Nurses Association Code of Ethics, noting updates made in 2001.
The document provides information on various public health programs and initiatives by the Department of Health in the Philippines. It includes the DOH health calendar for 2010 which lists important health awareness dates throughout the year focused on topics like cancer, kidney disease, tuberculosis, and more. It also discusses the maternal and child health program which aims to reduce maternal and child mortality rates through interventions like prenatal care, immunizations, nutrition supplementation, and clean and safe deliveries. Key aspects of family planning counseling are outlined as well, emphasizing the importance of informed choice and addressing clients' individual needs and circumstances.
Should America have dropped the Atomic Bomb PaperSchool_Seller
The document discusses whether the US was justified in dropping atomic bombs on Hiroshima and Nagasaki in 1945. It presents arguments on both sides of the issue. On one hand, the US claimed the bombs ended the war and saved American lives, as the Japanese refused to surrender. However, others argue the bombings killed thousands of innocent civilians, the US knew the power of the bombs from previous tests, and they may have been dropped more to prevent Soviet expansion than to end the war, as Japan had already asked for peace talks. The document concludes it was wrong to drop the bombs due to the immense devastation and deaths caused, but acknowledges the bombings did achieve a Japanese surrender and end the war.
The document discusses communication skills and tools that were covered in a useful course. It lists blogs, slideshare, podcasts, and vodcasts as different ways to communicate. It also mentions building skills like taking screenshots with Jing and using Evernote to organize information. In conclusion, it thanks the reader for allowing the author to take the course, which they found beneficial.
Superdome hurricane katrina power pointchuehuethao
The document discusses conditions in the Superdome and Convention Center in New Orleans during Hurricane Katrina, claiming the government did not provide adequate safety or living conditions. It notes both locations lacked water, air conditioning, lighting and authority figures. The Superdome roof was ripped off. Desperate people were dying there. The movie depicted the conditions as being like a live sewer with no running water and too much body heat. Others should care because if placed in the same situation, they would want better conditions and rescue from the governor.
Hurricanes form over warm ocean waters when strong winds blow off the Sahara and interact with tropical depressions. They generally move westward and can strike locations in the Caribbean Sea, Southeastern United States, and occasionally the Northeast. Some of the most damaging hurricanes have included the 1900 Galveston hurricane (Category 4, 8,000 deaths), the 1938 Long Island Express (Category 5, 600 deaths), Hurricane Camille in 1969 (Category 5, 256 deaths), and Hurricane Katrina in 2005 (Category 4, 1,200 deaths). The most dangerous aspects of hurricanes are their strong winds over 200 mph, heavy rainfall and flooding, and large storm surges that can produce walls of water over 20 feet high.
The document discusses an upcoming bone marrow donor drive hosted by the District in partnership with Be The Match Registry at City of Hope. The drive aims to register more donors to help patients find matches, including Steve Robbins, a District employee undergoing treatment. The registration process takes less than 15 minutes and involves providing contact information, a health history, and a DNA sample. Donors may later be contacted if matched to a patient and asked to donate bone marrow through a nonsurgical outpatient procedure. The District allows employees to participate in the drive during work hours without using sick or vacation time.
This annual report summarizes the activities of the Bone Marrow Donor Registry and Cancer Support Services organization in 2015. It highlights that the organization facilitated close to 9,000 donor-patient matches and over 2,000 life-saving stem cell transplants. It also details the organization's global reach, with transplants facilitated across 47 countries. The report emphasizes the growing need for stem cell transplants and calls for continued support to expand the donor registry and cancer support services.
Coping and Caring With Alzheimer's Disease and Dementia: Your Action Group In...Rotary International
This document discusses Alzheimer's disease and dementia. It provides statistics on the increasing prevalence and projected future impact of Alzheimer's disease. It discusses the burden on individuals, families, healthcare systems, and economies. The document outlines initiatives to make dementia a global health priority and increase awareness and funding for research toward treatment and prevention. It promotes lifestyle behaviors to potentially reduce risk and delay onset of Alzheimer's disease.
The document encourages readers to join the Be The Match bone marrow registry by taking the first step of registering. It explains that registering is easy to do and by joining over 12 million people on the registry, one has the power to save a life by potentially being a match for a leukemia or cancer patient in need of a bone marrow transplant. The document provides information on the registration process, health guidelines for joining, the need for diversity on the registry, what to expect if identified as a match, and ways to donate bone marrow to help save a patient's life.
GeneBandhu is a nonprofit based in New Delhi that aims to build a repository of genetically matched stem cell donors for patients with blood disorders. It was founded in 1998 as the Safe Blood Organization and works with numerous stem cell registries globally. There is a great need for an Indian stem cell registry as the chances of finding a match for Indians is only 1 in 10,000, and the probability of a match within the family is only 25%. GeneBandhu helps patients find donors through its registry and connections to global databases, bringing hope to those diagnosed with blood cancer or disorders like Thalassemia Major.
Blood donation involves voluntarily donating blood which is then stored in blood banks for medical use by patients in need. A study assessed the awareness of blood donation among 71 medical students in 2010. It found that most students were aware of blood donation and its importance in saving lives, though some did not donate due to health issues or fear. The study concluded that students had generally good knowledge but should continue to be motivated to donate blood on a regular basis to help address shortages.
The document discusses the need for more bone marrow donors in South Africa. Leukemia and other illnesses can be treated through bone marrow stem cell transplants, but finding a matching donor is challenging. The South African Bone Marrow Registry calls for more people to register as potential donors to help patients, including children, fight illnesses like leukemia. While 70,000 donors are registered, more are still needed, especially from underrepresented ethnic groups.
This document discusses breast cancer and the efforts of Susan G. Komen for the Cure to fight the disease. It states that 900 women will be diagnosed with breast cancer in Greater Austin and 2,500 in Texas this year. It describes Komen's research, community programs, and advocacy work to improve screening, treatment and find cures. The document encourages donations to support Komen's continued efforts and invites organizations to volunteer at a water stop during Komen Austin's upcoming Race for the Cure event.
Fight Colorectal Cancer is a non-profit organization with 3 goals: patient support and awareness, advocacy, and funding research. They provide education and resources to patients and caregivers about colorectal cancer prevention, screening, treatment and living with the disease. Their services include an answer line, webinars, newsletters and social media community for patients. They also advocate for policy changes and research funding, and have awarded over $250,000 in research grants. Their mission is to demand a cure for colon and rectal cancers through supporting patients and survivors, and changing policies to increase research.
The Blood & Tissue Center Foundation raises funds and awareness to support the work of BioBridge Global and its subsidiaries. It is directed by a board of volunteer community leaders. Through contributions and fundraising events, the Foundation has raised nearly $10 million to purchase equipment and support programs that provide lifesaving services to patients worldwide. The Foundation supports patients like Jon Ugarte, who received a cord blood transplant to treat his leukemia, through involvement in cord blood collection and storage, marrow donor registration, and a bereavement program.
Alex Tabarrock on Using Incentives to Increase Organ Donation. More at http://www.marginalrevolution.com/marginalrevolution/2010/05/changing-views-on-organ-prohibition.html
Snapshot introduction to our chapter 2011Mike Brennan
The document provides information about the Kidney Foundation of Canada Windsor & District chapter. It discusses the chapter's vision, mission, goals, history since the 1960s, programs (including research, education, peer support), advocacy efforts, and ways to get involved through fundraising and volunteering. The chapter aims to support those with kidney disease and promote organ donation awareness.
Snapshot Introduction To Our Chapter 2011Mike Brennan
The document provides information about the Kidney Foundation of Canada Windsor & District chapter. It discusses the chapter's vision, mission, goals, history since the 1960s, programs (including research, education, support groups, camps), advocacy, events, and ways to get involved through volunteering or fundraising. The chapter aims to support those with kidney disease and promote organ donation through various community awareness and patient support initiatives.
This document summarizes the need for blood donations and promotes an upcoming blood donation camp at LSUHSC-S. It notes that someone needs blood every 2.5 seconds, 1 in 3 people will need a transfusion, and each unit donated can save up to 4 lives. The blood bank needs donations in advance to perform safety tests before use. The camp aims to increase donations from employees and students, though currently only 700 units are donated annually despite 20,000 being transfused to patients. Regular donations are encouraged, as it takes only 30 minutes and can be done every 56 days to help people in need.
DKMS Saving Lives - Colin's Online VersionColin Hall
DKMS is the world's largest bone marrow donor center with over 3 million registered donors. It was founded in Germany in 1991 by Peter Harf, who lost his wife to blood cancer, to help patients find bone marrow donors. DKMS guides patients and families on bone marrow donation processes, helps organize donor drives, and registers donors at no cost to increase chances of finding matches for blood cancer patients in need of transplants. The document provides information on bone marrow and stem cell donations, the donation process, donor eligibility, common myths and facts, cancer statistics, and stories of cancer warriors and celebrity supporters of bone marrow donation.
This document summarizes upcoming webinars on transplant opportunities and increasing donor designation. It discusses a pilot program called Donate Life Voices that empowers transplant recipients and patients waiting for transplants to educate others about donation. A survey found that over 90% of those in the program said they impacted someone's decision to be a donor and over 75% of non-donors signed up to be donors after receiving an information kit. The document promotes using the materials in the kits to continue spreading awareness.
World Blood Donor Day is observed on June 14th every year to raise awareness about the importance of voluntary blood donation and to thank blood donors for their life-saving contributions. It serves as an opportunity to encourage more people to donate blood and to recognize the individuals who donate blood regularly without any monetary compensation.
The day was established by the World Health Organization (WHO) in collaboration with the International Federation of Red Cross and Red Crescent Societies (IFRC) to promote the availability and safety of blood and blood products for patients in need.
The theme for World Blood Donor Day varies each year, focusing on different aspects of blood donation. It aims to highlight the significant role of voluntary blood donors in saving lives and improving health care systems. Numerous events and activities are organized worldwide to celebrate this day, including blood donation drives, awareness campaigns, educational programs, and public discussions.
The document discusses an upcoming bone marrow donor drive hosted by the District in partnership with Be The Match Registry at City of Hope. The drive aims to register more donors to help patients find matches, including Steve Robbins, a District employee undergoing treatment. The registration process takes less than 15 minutes and involves providing contact information, a health history, and a DNA sample. Donors may later be contacted if matched to a patient and asked to donate bone marrow through a nonsurgical outpatient procedure. The District allows employees to participate in the drive during work hours without using sick or vacation time.
This annual report summarizes the activities of the Bone Marrow Donor Registry and Cancer Support Services organization in 2015. It highlights that the organization facilitated close to 9,000 donor-patient matches and over 2,000 life-saving stem cell transplants. It also details the organization's global reach, with transplants facilitated across 47 countries. The report emphasizes the growing need for stem cell transplants and calls for continued support to expand the donor registry and cancer support services.
Coping and Caring With Alzheimer's Disease and Dementia: Your Action Group In...Rotary International
This document discusses Alzheimer's disease and dementia. It provides statistics on the increasing prevalence and projected future impact of Alzheimer's disease. It discusses the burden on individuals, families, healthcare systems, and economies. The document outlines initiatives to make dementia a global health priority and increase awareness and funding for research toward treatment and prevention. It promotes lifestyle behaviors to potentially reduce risk and delay onset of Alzheimer's disease.
The document encourages readers to join the Be The Match bone marrow registry by taking the first step of registering. It explains that registering is easy to do and by joining over 12 million people on the registry, one has the power to save a life by potentially being a match for a leukemia or cancer patient in need of a bone marrow transplant. The document provides information on the registration process, health guidelines for joining, the need for diversity on the registry, what to expect if identified as a match, and ways to donate bone marrow to help save a patient's life.
GeneBandhu is a nonprofit based in New Delhi that aims to build a repository of genetically matched stem cell donors for patients with blood disorders. It was founded in 1998 as the Safe Blood Organization and works with numerous stem cell registries globally. There is a great need for an Indian stem cell registry as the chances of finding a match for Indians is only 1 in 10,000, and the probability of a match within the family is only 25%. GeneBandhu helps patients find donors through its registry and connections to global databases, bringing hope to those diagnosed with blood cancer or disorders like Thalassemia Major.
Blood donation involves voluntarily donating blood which is then stored in blood banks for medical use by patients in need. A study assessed the awareness of blood donation among 71 medical students in 2010. It found that most students were aware of blood donation and its importance in saving lives, though some did not donate due to health issues or fear. The study concluded that students had generally good knowledge but should continue to be motivated to donate blood on a regular basis to help address shortages.
The document discusses the need for more bone marrow donors in South Africa. Leukemia and other illnesses can be treated through bone marrow stem cell transplants, but finding a matching donor is challenging. The South African Bone Marrow Registry calls for more people to register as potential donors to help patients, including children, fight illnesses like leukemia. While 70,000 donors are registered, more are still needed, especially from underrepresented ethnic groups.
This document discusses breast cancer and the efforts of Susan G. Komen for the Cure to fight the disease. It states that 900 women will be diagnosed with breast cancer in Greater Austin and 2,500 in Texas this year. It describes Komen's research, community programs, and advocacy work to improve screening, treatment and find cures. The document encourages donations to support Komen's continued efforts and invites organizations to volunteer at a water stop during Komen Austin's upcoming Race for the Cure event.
Fight Colorectal Cancer is a non-profit organization with 3 goals: patient support and awareness, advocacy, and funding research. They provide education and resources to patients and caregivers about colorectal cancer prevention, screening, treatment and living with the disease. Their services include an answer line, webinars, newsletters and social media community for patients. They also advocate for policy changes and research funding, and have awarded over $250,000 in research grants. Their mission is to demand a cure for colon and rectal cancers through supporting patients and survivors, and changing policies to increase research.
The Blood & Tissue Center Foundation raises funds and awareness to support the work of BioBridge Global and its subsidiaries. It is directed by a board of volunteer community leaders. Through contributions and fundraising events, the Foundation has raised nearly $10 million to purchase equipment and support programs that provide lifesaving services to patients worldwide. The Foundation supports patients like Jon Ugarte, who received a cord blood transplant to treat his leukemia, through involvement in cord blood collection and storage, marrow donor registration, and a bereavement program.
Alex Tabarrock on Using Incentives to Increase Organ Donation. More at http://www.marginalrevolution.com/marginalrevolution/2010/05/changing-views-on-organ-prohibition.html
Snapshot introduction to our chapter 2011Mike Brennan
The document provides information about the Kidney Foundation of Canada Windsor & District chapter. It discusses the chapter's vision, mission, goals, history since the 1960s, programs (including research, education, peer support), advocacy efforts, and ways to get involved through fundraising and volunteering. The chapter aims to support those with kidney disease and promote organ donation awareness.
Snapshot Introduction To Our Chapter 2011Mike Brennan
The document provides information about the Kidney Foundation of Canada Windsor & District chapter. It discusses the chapter's vision, mission, goals, history since the 1960s, programs (including research, education, support groups, camps), advocacy, events, and ways to get involved through volunteering or fundraising. The chapter aims to support those with kidney disease and promote organ donation through various community awareness and patient support initiatives.
This document summarizes the need for blood donations and promotes an upcoming blood donation camp at LSUHSC-S. It notes that someone needs blood every 2.5 seconds, 1 in 3 people will need a transfusion, and each unit donated can save up to 4 lives. The blood bank needs donations in advance to perform safety tests before use. The camp aims to increase donations from employees and students, though currently only 700 units are donated annually despite 20,000 being transfused to patients. Regular donations are encouraged, as it takes only 30 minutes and can be done every 56 days to help people in need.
DKMS Saving Lives - Colin's Online VersionColin Hall
DKMS is the world's largest bone marrow donor center with over 3 million registered donors. It was founded in Germany in 1991 by Peter Harf, who lost his wife to blood cancer, to help patients find bone marrow donors. DKMS guides patients and families on bone marrow donation processes, helps organize donor drives, and registers donors at no cost to increase chances of finding matches for blood cancer patients in need of transplants. The document provides information on bone marrow and stem cell donations, the donation process, donor eligibility, common myths and facts, cancer statistics, and stories of cancer warriors and celebrity supporters of bone marrow donation.
This document summarizes upcoming webinars on transplant opportunities and increasing donor designation. It discusses a pilot program called Donate Life Voices that empowers transplant recipients and patients waiting for transplants to educate others about donation. A survey found that over 90% of those in the program said they impacted someone's decision to be a donor and over 75% of non-donors signed up to be donors after receiving an information kit. The document promotes using the materials in the kits to continue spreading awareness.
World Blood Donor Day is observed on June 14th every year to raise awareness about the importance of voluntary blood donation and to thank blood donors for their life-saving contributions. It serves as an opportunity to encourage more people to donate blood and to recognize the individuals who donate blood regularly without any monetary compensation.
The day was established by the World Health Organization (WHO) in collaboration with the International Federation of Red Cross and Red Crescent Societies (IFRC) to promote the availability and safety of blood and blood products for patients in need.
The theme for World Blood Donor Day varies each year, focusing on different aspects of blood donation. It aims to highlight the significant role of voluntary blood donors in saving lives and improving health care systems. Numerous events and activities are organized worldwide to celebrate this day, including blood donation drives, awareness campaigns, educational programs, and public discussions.
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by...Donc Test
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Adhd Medication Shortage Uk - trinexpharmacy.comreignlana06
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Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
2. • Donor registration process
• Who is Be The Match®
?
• Need for marrow donors
Learning Objectives
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
• Donation process
• How can I help?
• How we help patients
3. Who Is Be The Match®?
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
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4. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
d
Who Is Be The Match?
5. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
Be The Match® manages the
largest and most diverse marrow
registry in the world, saving lives
through transplant every day.
The National Registry
6. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
Robert Graves, DVM, was inspired
by his daughter’s leukemia to
create a national registry of
voluntary marrow donors.
Our Story
7. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
To facilitate marrow transplants
from volunteer donors as life-saving
therapy for patients of all racial and
socioeconomic backgrounds.
Our Mission
8. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
Every 4 minutes, one person is diagnosed with a
blood cancer.
Every 10 minutes, someone dies from a blood
cancer. That’s more than six people each hour, or
148 people each day.
Patients are searching for a cure. It could be YOU.
9. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
Transplant
Centers
Donor
Centers
Apheresis
Centers
Recruitment
Centers
Cooperative
Registries
Collection
Centers
Testing
Labs
Cord
Blood
Banks
Our Global
Network Of Care
49
20
92
40
174
26
100 44
10. How We Help Patients
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
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11. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
70% of patients have no match in their family
12. One Patient At A Time
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
• Grow the registry
• Connect patients to
donors
• Patients, caregivers,
families
• Clinical education
• Research
• Fundraising
13. The Need For Marrow Donors
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
d
14. How rare is my match?
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
African American
Hispanic & Latino
Asian & Pacific Islander
Native American
Caucasian & European
25% 50% 75% 100%
66%
72%
73%
82%
93%
15. Diversity is Crucial!
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
• Minority donors currently
represent only 28% of the
Be The Match Registry.
• Because tissue types are
inherited, patients are
more likely to match
someone who shares their
racial or ethnic heritage.
16. The Donor Registration Process
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
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17. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
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Step 1: Registry
Guidelines
•Are you between
18-44 years of age?
•Do you meet the
health guidelines?
•Are you committed
to donating to any
patient in need?
Step 2: Consent
Form
Step 3: Buccal
Swab
18. Steps To Donate
• Answer the call as a possible match
• Give another swab or blood sample
• Attend an info session
• Donate cells or marrow
• Receive follow-up
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
1
2
3
4
5
21. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
• Outpatient procedure
with anesthesia
• Marrow collected using
needles, syringes
• Collected from back of
the pelvic bone
• Donor receives
Filgrastim injections for
5 days
• Stem cells collected
through 2-arm apheresis
Two Ways To Donate
PBSCMarrow
22. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
Two Ways To Donate
PBSCMarrow
80%
20%
23. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
PBSCMarrow
Marrow or PBSC?
Donors give the source
best for the patient.
Marrow tends to
be best for child
patients
PBSC is preferred
for patients over
50 years
24. Do I Get To Meet My Recipient?
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
• Donors & patients may
correspond anonymously
for the first year
• After first year, both may
consent to meet
• International patients
may regulate contact
differently
25. What Do I Do Next?
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
d
26. Call to Action
• Join Be The Match today
• Become an advocate
• Keep your contact info current
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
Join • Give • Volunteer
27. The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
QUESTIONS?
28. Contact Us!
The NATIONAL MARROW DONOR PROGRAM® operates the Be The Match Registry®.
www.BeTheMatch.com
WEBSITE
EMAIL
marrowdonor@sw.org
PHONE
(979) 691-3261