...Syllabus-MBA (Hospital Administration) PAPER – I: BASIC CONCEPT OF HEALTH -Code MHA 101 Concept of Health and Disease • Concept of health & disease and well being. • Natural history of disease and role of hospitals to offer various levels of care • Prevention aspect of diseases • Dynamics of disease transmission • Changing pattern of diseases • Concept of health indicators Preliminary Human anatomy and Physiology • Basic concepts of human anatomy • Basic concepts of human physiology Suggested Reading: Human Anatomy- Prof. Samar Mitra Human Anatomy- Prof. A. K. Dutta Text Book of Human Physiology- Dr. C. C. Chatterjee Common Pathological Conditions • Basic concepts of pathogenesis of common diseases • Basic concepts of interpretation of investigations reports Suggested Reading: Robbin’s Textbook of Pathology – Robbin, Cotran, Kumar Textbook of Microbiology – Ananantanarayan & Paniker Basic concepts of Pharmacology: Commonly used Medicine in a hospital, Narcotic drugs, use and abuse of drugs. Dispensing of medicine, Drugs store, drug stock / purchase of medicine, oxygen, I/V Fluid, Chemicals etc. Suggested Reading: Textbook of Pharmacology: Dr. K. D. Tripathi PAPER – 2: Hospital Based Healthcare & Its changing scenario-Code MHA 102 Overview of Hospital • Concept of Modern Hospital & Privatization in Health Sector • Public Sector Hospitals and Level of care / offered facilities ...
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... biological and chemical actions of drugs (Bryant & Knights, 2011). In the practice of medicine, drugs are used to diagnose, treat or prevent disease so for the registered nurse in a clinical setting, the knowledge of pharmacology plays a huge importance in their role of medication administration. Pharmacology knowledge allows the nurse to carry out safe medication administration, monitor medication actions, educate patients, and act legally and ethically within the pharmacological parameters. This knowledge is also vital for the nurse practititioner in their role of nurse prescribing. Pharmacology plays a huge part in these roles for the nurse. This essay below will elaborate on the importance of pharmacology for the five reasons of safe medication administration, monitoring of medication actions, patient education, legal and ethical aspects of pharmacology and the nurse practitioner. Firstly, safe medication administration. To administer drugs safely it is the nurse’s responsibility to have knowledge of the prescribed medications as well as their therapeutic and non therapeutic effects. Knowledge of the medications include, knowing its approved drug name and classification, correct dose and route of administration. A medication may have as many as three different names- a chemical name, a generic (proprietary) name and a trade name (Crisp & Taylor, 2011). A chemical name refers to the chemical makeup of a drug, a generic name is the drug name listed in official publications...
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...This assignment will discuss relevant issues surrounding the subject of safe administration of medicines. The assignment will outline both legal and professional standards that have been set out by government and professional bodies for nurses and other health care professionals to follow whilst administering medicines. It will then go onto analyse actual and potential problems that may occur when a professional is trying to achieve these standards. This assignment will be supported by literature findings. The conclusion will reflect what is written. The administration of drugs could be defined as the way in which drugs are selected, obtained, delivered, prescribed, administered and reviewed to make sure that the medicine is having the desired affect (Dougherty et al 2004). Drug administration is an integral part of a nurse’s role and as such responsibility for correct administration of drugs rests with the nurse (O’Shea 1999). It is stated that nurses spend up to 40% of their time administrating medicine (Armitage et al 2003) In order to perform this intervention safely a nurse needs to know about the drug its immediate effect and any side effects it may cause. This role involves safe handling and administration of medicines, the role also includes the nurse being responsible for the patients knowing what medicines they are taking and why. Legal, professional and cultural boundaries are changing in health care settings, which mean that a nurse’s role is now medicines management...
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...Ethical and Legal Issues in Healthcare Clinical Reasoning Table of Contents Introduction 2 Ethical and Legal Issues in Medication Administration 2 Ethical Issue in the Case 3 Application of Tools 3 Conclusion 4 References 5 Introduction Mr Joe Bloggers has been introduced as a new patient for the unit. His admission had been made at 8:30 AM in the department of emergency departed from another hospital. His case was that he ended up falling on the stairs, five days before he had been admitted. He has been going through a period of struggle due to an increase of pain in his back. As per the reports drafted based on his X- Ray and CT scan, it has been found that there is a damage in his soft tissue but there is no sign of a fracture. In addition to this, he has a number of large bruises and the pain increases when there is movement. This particular essay will be discussing certain ethical and legal issues involved in the medication chart that had been drafted in the case of Mr Blogges. Ethical and Legal Issues in Medication Administration Before the administration of...
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...by Fred Sand Professor Newcomb, Legal – 500 February 27, 2014 compared The remainder of the document will discuss and examine law suites held against PharmaCARE and various ethical dilemmas the company may encounter. On August 17, 1997, executives around northern New Jersey’s drug corridor, where most of the international Pharmaceutical companies have their headquarters, mobilized for action” (Aitken & Holt, 2000, p. 82). According to Aitken and Holt (2000), this was the day that the US Food and Drug Administration issued temporary guidelines the, for the first time, permitting the drug makers to specify the uses of their prescription remedies in their radio and television advertisements (p. 82). Marketing and advertisement has been around almost since the beginning of time. One of the ethical dilemmas concerning television and radio advertisements for prescription drugs is the potential for the consumer to self-prescribe or evaluate their symptoms. According to the U.S. Food and Drug Administration (2013), doctors believe that patients understand that they need to consult a health care professional about appropriate treatment (p.1). On the other hand, it could be possible for the patient to adapt their own symptoms for the sake of obtaining a desired medication. “Intellectual property (IP) is the work product of the human mind. Novels, paintings, computer programs, songs and inventions are all examples” (Halbert & Ingulli, 2012, p. 316). “Activist...
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...Ethics is a set of moral principles. Principles that people tend to follow on an everyday basis, determining right from wrong. Research ethics is a system that incorporates ethical principles into research practice. Research ethics has three objectives, the first objective is to protect human and animal participants, the second objective is to make sure the research interests the people (individuals, groups and or society) and the third objective is to analyze particular research exercises and ventures for their moral soundness, taking a gander at issues, for example, the administration of hazard, assurance of classification and the procedure of educated assent. Generally, research ethics has customarily centered around issues in biomedical...
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...A system of medical practice that aims to combat disease by use of remedies (as drugs or surgery) producing effects different from or incompatible with those produced by the disease being treated. Allopathy is also called ‘modern’, ‘western’, or ‘scientific’ medicine. The term ‘biomedicine’, defined as the ‘application of the principles of natural science, especially biology and physiology to clinical medicine’, is also in use. ‘Clinical medicine’ is the medical practice involving and based on direct observation of patients or healthy volunteers who were given the drug that is being tested, to evaluate the drug’s curative potential, side effects, dosage levels, contra-indications, etc,, before recommending it for use. This concept is opposed to the earlier norms of medical practice based on theoretical study or laboratory investigation or class room teaching. Allopathy is now both biomedicine and clinical medicine. Nevertheless, a number of other systems like Homoeopathy and Ayurveda have also introduced the clinical element into their drug evaluation procedures. History The practice of medicine in both Europe and North America during the early 19th century is sometimes referred to as heroic medicine because of the extreme measures (such as bloodletting) sometimes employed in an effort to treat diseases.[6] The term allopath was used by Hahnemann and other early homeopaths to highlight the difference they perceived between homeopathy and the medicine of that time...
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...The Viewpoint of the Society on Medicinal Marijuana Everything in the society is changing, especially the laws. Legal and illegal drugs are everywhere in society. People, especially teens, know someone who has drugs and could easily get access to them. Drugs like marijuana are one of those easily accessible drugs. Marijuana is still one of the common drugs and is still considered illegal under the federal laws in the United States. Some states such as California have passed laws allowing marijuana legal to smoke and sell. The medical marijuana is to use for medicinal purposes and can only be prescribed by a doctor. Researchers and scientists support the use of marijuana as a medical drug. Some people like patients may view this positively, because the medical marijuana actually worked on them as they get a lot better. Despite some viewpoints in favor of the use of marijuana, it is still an unethical use of the drug, because there are still negative effects of using marijuana. Even though patients who are suffering from illness or disease and are using medical marijuana, patients viewed that it helps them feel better. With the increase of medical marijuana, the worldwide report estimates between 200 and 300 million people are now smoking marijuana (Earleywine 29). With 40% of the public using marijuana as medicine, it has changed the needs and values of our society. The use of medical marijuana can treat patients with many different ailments such as pain, nausea, vomiting,...
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...the most current of series of pharmaceutical frustrations. A common pill which is VIOXX was taken down from the shelves from 2004 since it increased a danger from heart attacks and strokes. Several have disapproved the Food and Drug Administration from being too sloppy regarding examining drug protection. Whomever was too blame did have worth, there is an additional wrongdoer: those with of the exchange of continuous medical teaching keen to an initiative for drug marketing. The principle of coaching medical teams on how to observe medicine has been prearranged to the pharmaceutical business. Therefore, risky side effects have been left off the program. The states that describes for those doctors to acquire a least amount of credit hours of continuous medical teaching every twelve months to continue with their medical certificates. Here recently, most of those classes were constructed and rewarded for by colleges and association of medical. Although this has been misrepresented significantly over a decade. Nearly partly of the entire ongoing medical teaching classes in the United States are currently compensated by drug companies. Since pharmaceutical companies nowadays place a great amount of the program for what doctors study about drugs,...
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...O’Brien made against the company that contradict the code of ethics. O’Brien alleged the company violated federal law by under reporting complaints and problems patients were having with Amgen’s drugs. Since this was issue of legality, O’Brien sued because Amgen was not reporting to the Food and Drug Administration the patient’s complaints. O’Brien’s retaliation contradicted the code of ethics because his supervisor took him off the case and ? 2. Whistleblowing is when a person makes allegations to the public or someone in authority about illegal or fraudulent activities. In this case the whistleblower was Shawn O’Brien. Internal whistleblowing is when misconduct is reported within the company. For example, if an employee tells another employee or a superior about misconduct, that is internal. External whistleblowing is the opposite and occurs when someone reports the misconduct to a party that is apart of the company. For example, if employee tells an auditor, government agency, or the police about misconduct, that is external whistleblowing. I don’t think O’Brien too enough steps to report his concerns. He only reported the misconduct internally, but could have easily reported the misconduct externally. He could have taken his allegations to the Food and Drug Administration directly. 3. Integrity was the thing that motivated O’Brien to act as he did. Integrity is where someone has the courage to do what their character tells them even when others are pressuring...
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...that was written to propose set principles of providing health care insurance and services in Canada (Duckett, 2012, p. 10). There are five principles that make up the Canada Health Act and they are as follows: Public Administration, Comprehensiveness, Universality, Portability and Accessibility (Duckett, 2012, p. 11). The first principle of the Canada Health Act is Public Administration and the main elements of this principle are that it establishes rules for how a health care insurance plan can be formed, their responsibilities and how they will be reviewed (Duckett, 2012, p. 12). Public administration constrains the provincial governments as they have to appoint and audit insurance plans to make sure they are non-profit and providing the appropriate services (Duckett, 2012, p 12). The key issue with this principle is that only the insurer is written to be public, meaning that health care professionals can run their businesses privately forcing Canadians to pay extensive out of pocket expenses (Duckett, 2012, p. 12). The second principle of the Canada Health Act is Comprehensiveness and the main element of it is that health care insurance plans “must insure all insured health services provided by hospitals, medical practitioners or dentists” (Duckett, 2012, p. 12). Unfortunately a key issue with this principle is that it states “necessary services” is covered but this is a broad term so other aspects of health care such as prescription drugs or long term care are up in the...
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...Parle Milind et al. IRJP 2013, 4 (1) INTERNATIONAL RESEARCH JOURNAL OF PHARMACY www.irjponline.com ISSN 2230 – 8407 Review Article LABORATORY MODELS FOR SCREENING ANALGESICS Parle Milind* and Yadav Monu Pharmacology Division, Dept. Pharm. Sciences, Guru Jambheshwar University of Science and Technology, Hisar, Haryana, India Article Received on: 13/11/12 Revised on: 17/12/12 Approved for publication: 23/12/12 *Email: mparle@rediffmail.com ABSTRACT Pain is a complex unpleasant phenomenon composed of sensory experiences that include time, space, intensity, emotion, cognition and motivation. Analgesics are the agents, which selectively relieve pain by acting in the CNS or by peripheral pain mechanisms without significantly altering consciousness. Analgesics may be narcotic or non-narcotic. The study of pain in animals raises ethical, philosophical and technical problems. Philosophically, there is a problem that pain cannot be monitored directly in animals but can only be measured by examining their responses to nociceptive stimuli. The observed reactions are almost always motor responses ranging from spinal reflexes to complex behavior. The animal models employed for screening of analgesic agents, include Pain-state models based on the use of thermal stimuli, mechanical stimuli, electrical stimuli and chemical stimuli. The neuronal basis of most of the above laboratory models is poorly understood, however their application is profitable in predicting analgesic...
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... Nelson March 2, 2013 RES 351 University of Phoenix Prof. Lara Lucas Unethical Research Two employees of Lee Research of Lenexa Kansas were indited for falsifying research information. The research company was contracted by Schering/Plough, a subsidiary of Mereck & C, to conduct clinical trails of a new allergy medication. The trials were conducted from January 2010 to May 2010. Dr. Wayne Spencer, a licensened physician and the principle investigator of the study, along with Lisa Sharp, the director of clinical trials at Lee Research Institute were named in the inditement.Dr. Spencer and Sharp were each charged with one case of conspiracy, three counts of mail fraud, and one count of falsifying information required by the Food and Drig Administration (Pharmalot.com, 2011). Dr. Spencer and Sharp were terminated by Lee Reasearch Institute following the inditements. Lee Research Institute immediately started an internal investigation of the alledged insedence in cooperation with the Food and Drug Administration and Schring/Plough (Kansas City Business Journal, 2011). The indictment accuses the two former employees of providing false information of the patients participating in the study trials. The study was to be conducted using subjects 50 years old or greater who suffer from ragweed allergies. Employees of the contracted research organization were prohibited from participation in the case study. Dr. Spencer and Sharp are accused of falsifying the information...
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...condition. The medicine is chosen on the basis of an evidencebased approach to clinical practice and assured to be compatible with any other medicines or alternative therapies the patient may be taking. The design of a dosage regimen is dependent on a basic understanding of the drug use process (DUP). When faced with a patient who shows specific clinical signs and symptoms, pharmacists must always ask a fundamental question: ‘Is this patient suffering from a drug-related problem?’ Once this issue is evaluated and a clinical diagnosis is available, the pharmacist can apply the DUP to ensure that the patient is prescribed an appropriate medication regimen, that the patient understands the therapy prescribed, and that an agreed concordance plan is achieved. Pharmacists using the DUP consider: ● ● ● ● ● ● Need for a drug Choice of a drug Goals of therapy Design of regimen – Route – Dose and frequency – Duration Monitoring and review Counselling Once a particular medicine is chosen, the principles of clinical pharmacokinetics are required to ensure the appropriate formulation of drug is chosen for an appropriate route of administration. On the basis of the patient’s drug handling parameters, which require an understanding of 2 Basic pharmacokinetics absorption, distribution, metabolism and excretion, the dosage regimen for the medicine in a particular patient can be developed. The pharmacist will then need to ensure that the appropriate...
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...TRIPARTITE GUIDELINE STABILITY TESTING FOR NEW DOSAGE FORMS Annex to the ICH Harmonised Tripartite Guideline on Stability Testing for New Drugs and Products Q1C Current Step 4 version dated 6 November 1996 This Guideline has been developed by the appropriate ICH Expert Working Group and has been subject to consultation by the regulatory parties, in accordance with the ICH Process. At Step 4 of the Process the final draft is recommended for adoption to the regulatory bodies of the European Union, Japan and USA. 1 Q1C Document History First Codification History Date New Codification November 2005 Q1C Q1C Approval by the Steering Committee under Step 2 and release for public consultation. 29 November 1995 Current Step 4 version Q1C Approval by the Steering Committee under Step 4 and recommendation for adoption to the three ICH regulatory bodies. 6 November 1996 Q1C 2 STABILITY TESTING FOR NEW DOSAGE FORMS Annex to the ICH Harmonised Tripartite Guideline on Stability Testing for New Drugs and Products ICH Harmonised Tripartite Guideline Having reached Step 4 of the ICH Process at the ICH Steering Committee meeting on 6 November 1996, this guideline is recommended for adoption to the three regulatory parties to ICH 1. GENERAL The ICH harmonised Tripartite Guideline on Stability Testing of New Drug Substances and Products was issued on October 27, 1993. This document is an annex to the ICH parent stability guideline and addresses the...
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