Anemia LECTURE in INTERNAL MEDICINE for IV COURSE
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Tareq Al-Adaily Ibrahim Elhaj Ayah Fraihat Dana Alnasra Sheet
Anemia of decreased production II Sheet 3 – + Hemolytic anemia Dana Alnasra Ayah Fraihat Ibrahim Elhaj Tareq Al-adaily 0 **Flashback to previous lectures: − Anemia is the reduction of oxygen carrying capacity of blood secondary to a decrease in red cell mass. − We classified anemia according to cause into: 1. Anemia of blood loss (chronic and acute) 2. Anemia of decreased production 3. Hemolytic anemia − Then, we mentioned general causes for the anemia of decreased production, which are: nutritional deficiency, chronic inflammation, and bone marrow failure. We’ve already discussed the first two and now we will proceed to the last one. Anemias resulting from bone marrow failure: 1. Aplastic anemia 2. Pure red cell aplasia 3. Myelophthisic anemia 4. Myelodysplastic syndrome Other anemias of decreased production: 1. Anemia of renal failure 2. Anemia of liver disease 3. Anemia of hypothyroidism 00:00 1. Aplastic anemia Is a condition where the multipotent myeloid stem cells produced by the bone marrow are damaged. Remember: the bone marrow has stem cells called myeloid stem cells which eventually differentiate into erythrocytes, megakaryocytes (platelets), and myeloblasts (white blood cells). Notice that lymphocytes are not produced from the myeloid progenitor, therefore, they are not affected. depleted normal 1 | P a g e As a result, the bone marrow becomes depleted of hematopoietic cells. And this is reflected as peripheral blood pancytopenia (all blood cells -including reticulocytes- are decreased, with the exception of lymphocytes). Pathogenesis There are two forms of aplastic anemia according to pathogenesis: a. Acquired aplastic anemia It happens because of an extrinsic factor e.g. -
Dreaming in Patients with Temporal Lobe Epilepsy: a Focus on Bad Dreams and Nightmares Carmen Anderson Department of Psychology
1 Dreaming in Patients with Temporal Lobe Epilepsy: A Focus on Bad Dreams and Nightmares Carmen Anderson Department of Psychology University of Cape Town 29th October 2012 Supervisor: Prof. Mark Solms Co-supervisor: Warren King Word count: 7055 Abstract: 164 Main body: 6891 2 Abstract Nightmares and bad dreams occur more frequently in patients with temporal lobe epilepsy (TLE) than in normal individuals. This quantitative pilot study explored the relationship between seizure activity and dreaming in patients with TLE, compared to the dreams, bad dreams and nightmares of a control population. Groups were categorized by epilepsy variables (TLE and non-TLE) and gender. Patients with temporal lobe epilepsy completed self-report questionnaires concerning their epilepsy and dreaming, and this data was compared to dreaming data from the control group using ANCOVAs. The results showed that females have significantly higher scores than males on several variables, including dreams per week, bad dream distress and nightmare distress. However, no significant main effects or interactions were found for the variables bad dream frequency and nightmare frequency, which contradicts the study’s hypotheses. It is possible that this lack of differences was due to TLE patients being on antiepileptic drugs, which whilst controlling seizures, may have suppressed or eliminated the effects of bad dreams and nightmares. Keywords: temporal lobe epilepsy, dreaming, bad dreams, nightmares, gender differences. 3 Dreaming in Patients with Temporal Lobe Epilepsy: A Focus on Bad Dreams and Nightmares Nightmares and bad dreams occur more frequently in patients with temporal lobe epilepsy (TLE) than in normal individuals and in patients with generalized seizures (Silvestri & Bromfield, 2004). -
Anemias Supportive Module 4 "Essentials of Diagnosis, Treatment and Prevention of Major Hematologic Diseases"
2016/2017 Spring Semester Anemias Supportive module 4 "Essentials of diagnosis, treatment and prevention of major hematologic diseases" LECTURE IN INTERNAL MEDICINE FOR IV COURSE STUDENTS M. Yabluchansky, L. Bogun, L. Martymianova, O. Bychkova, N. Lysenko, N. Makienko V.N. Karazin National University Medical School’ Internal Medicine Dept. Plan of the lecture • Definition • Epidemiology • Etiology • Mechanisms • Adaptation to anemia • Classification • Clinical investigation • Diagnosis • Treatment • Prognosis • Prophylaxis • Abbreviations • Diagnostic guidelines http://anemiaofchronicdisease.com/wp-content/uploads/2012/08/anemia-of-chronic-disease1.jpg Definition Anemia is a disease and/or a clinical syndrome that consist in lowered ability of the blood to carry oxygen (hypoxia) due to decrease quantity and functional capacity and/or structural disturbances of red blood cells (RBCs) or decrease hemoglobin concentration or hematocrit in the blood A severe form of anemia, in which the hematocrit is below 10%, is called the hyperanemia WHO criteria is Hb < 13 g/dL in men and Hb < 12 g/dL in women (revised criteria for patient’s with malignancy Hb < 14 g/dL in men and Hb < 12g/dL in women) Epidemiology 1 https://www.k4health.org/sites/default/files/anemia-map_updated.png Epidemiology 2 http://img.medscape.com/fullsize/migrated/editorial/conferences/2006/4839/spivak.fig1.jpg Epidemiology 3 http://www.omicsonline.org/2161-1165/images/2161-1165-2-118-g001.gif Etiology 1 (basic forms) Basic forms • Blood loss • Deficient erythropoiesis • Excessive -
Predicting Chemotherapy-Induced Febrile Neutropenia Outcomes in Adult Cancer Patients: an Evidence-Based Prognostic Model
Predicting Chemotherapy-Induced Febrile Neutropenia Outcomes in Adult Cancer Patients: An Evidence-Based Prognostic Model Yee Mei, Lee Cert Nursing (S’pore), RN, Adv. Dip. (Oncology) in Nursing (S’pore), Bsc of Nursing (Monash), Master of Nursing (S’pore) Thesis submitted for the Doctor of Philosophy School of Translational Health Science The University of Adelaide Adelaide, South Australia Australia November 2013 Table of Contents TABLE OF CONTENTS -------------------------------------------------------------------- II LIST OF TABLES ------------------------------------------------------------------------ VII LIST OF FIGURES ---------------------------------------------------------------------- VIII LIST OF ABBREVIATIONS --------------------------------------------------------------- XI ABSTRACT ----------------------------------------------------------------------------- XII DECLARATION ----------------------------------------------------------------------- XIIII ACKNOWLEDGEMENTS-- ------------------------------------------------------------ IXV PUBLICATIONS ------------------------------------------------------------------------ XV 1 INTRODUCTION TO THE THESIS ---------------------------------------------------- 15 1.1 CLINICAL CONTEXT -------------------------------------------------------------------------------- 15 1.2 CLINICAL IMPACT OF CHEMOTHERAPY-INDUCED FEBRILE NEUTROPENIA -------------------- 16 1.3 ECONOMIC IMPLICATIONS OF CHEMOTHERAPY-INDUCED FEBRILE NEUTROPENIA ---------- 18 1.4 EVOLVING PRACTICE IN THE MANAGEMENT OF FEBRILE -
Download Dr. Qureshi's CV
Brief Synopsis Nazer H. Qureshi, M.D, D.Stat, M.Sc, DABNS, FAANS. Graduated from Medical School with top honors and first position in Anatomy and Histology in board examinations. Pursued surgical training in Europe including neurosurgery at the National Center for Neurosurgery affiliated with The Royal College of Surgeons of Ireland. In 1994 started as a junior faculty member at University of Dublin teaching medical students while pursuing his own research on “Interleukin-1 binding and expression in brain” towards Masters in Science. During that year also attained a Diploma in Statistics from University of Dublin. In summer of 1995 was a visiting fellow at University of Toronto working on use- dependent inhibitory depression in epilepsy models. In 1996 migrated to US and completed a research fellowship in gene therapy for brain tumors at Harvard Medical School/Massachusetts General Hospital. The work on gene therapy that included testing efficacy and toxicity of different viral vectors and & designing a novel method of gene delivery to human brain tumors culminated into a clinical trial. In 1999 completed a neurosurgery fellowship at University of Arizona. Completed 2 years of accredited General Surgery residency at Tuft’s University and Thomas Jefferson University followed by Neurosurgery Residency in June 2008 from University of Arkansas for Medical Sciences with “Prof. Iftikhar A. Raja Humanity in Medicine Award.” Diplomate American Board of Neurological Surgeons and Fellow of the American Board of Neurological Surgeons. Worked as an attending neurosurgeon at Baptist Hospital Medical Center in Little Rock the chief of brain and spine tumor service at Baptist Health Medical Center, North Little Rock. -
Iron Deficiency Anemia (Ida) Recommendations
IRON DEFICIENCY ANEMIA (IDA) Clinical Practice Guideline | March 2018 OBJECTIVE Alberta clinicians (specifically primary care and emergency department physicians) will be able to diagnose iron deficiency anemia (IDA), treat using oral and parenteral iron supplementation and provide ongoing management; will understand why red blood cell transfusion (RBC) may be harmful and is only occasionally required for the treatment of IDA. TARGET POPULATION Patients >5 years of age, hemodynamically stable, seen in emergency departments and primary care settings EXCLUSIONS Patients <5 years of age, all patients who are hemodynamically unstable, chronic kidney disease, rare genetic causes of and treatment of IDA, other types of iron deficiency, and the pre-latent stage of iron deficiency RECOMMENDATIONS ASSESSMENT INVESTIGATION FOR IDA Identify patients at risk for iron deficiency anemia Table 1: Possible Features, Signs and Symptoms of IDA ADULTS AND ADOLESCENTS Anticipated ongoing bleeding (e.g., menstruation, gastrointestinal) Head and neck manifestations including pallor (e.g., facial, conjunctival or palmar), blue sclerae, atrophic glossitis or loss of tongue papillae, angular cheilitis, alopecia Koilonychia (spoon nails) Restless leg syndrome Fatigue, shortness of breath, chest pain, lightheaded, syncope weakness, headache Irritability and/or depression Pica (craving/consumption of non-food substances e.g., dirt, clay, chalk) and pagophagia (ice craving) Decreased exercise tolerance Regular blood donors, particularly females donating more than twice a year and males donating more than three or four times a year SCHOOL-AGED CHILDREN (e.g., >5 to <18 years old) Tiredness, restlessness, irritability Pica and pagophagia Growth retardation Cognitive and intellectual impairment Signs of attention-deficit/hyperactivity disorder (ADHD) Breath-holding spells These recommendations are systematically developed statements to assist practitioner and patient decisions about appropriate health care for specific clinical circumstances. -
Local Anesthetic Agents Infiltration: Role of the Nurse
Doug Ducey Joey Ridenour Governor Executive Director Arizona State Board of Nursing 1740 W Adams Street, Suite 2000 Phoenix. AZ 85007 Phone (602) 771-7800 Home Page: http://www.azbn.gov OPINION: INFILTRATION OF LOCAL An advisory opinion adopted by AZBN is an interpretation of what the law requires. While an ANESTHETIC AGENTS: THE ROLE OF THE advisory opinion is not law, it is more than a recommendation. In other words, an advisory opinion NURSE is an official opinion of AZBN regarding the practice of nursing as it relates to the functions of APPROVED DATE: 3/2015 nursing. Facility policies may restrict practice further in their setting and/or require additional REVISED DATE: 7/2018 expectations related to competency, validation, training, and supervision to assure the safety of their patient population and or decrease risk. ORIGINATING COMMITTEE: SCOPE OF PRACTICE COMMITTEE Within the Scope of Practice of X RN x LPN ADVISORY OPINION LOCAL ANESTHETIC AGENTS INFILTRATION: ROLE OF THE NURSE It is within the scope of practice of a registered nurse (RN) and a licensed practical nurse (LPN) to administer certain local anesthetic agents intradermal, subcutaneous, and submucosal for the purposes of analgesia and/or anesthesia prior to potentially painful procedures. Tumescent lidocaine infiltration for ambulatory procedures, such as but not limited to, the treatment of hyperhidrosis, ambulatory phlebectomy and laser facial resurfacings would be within the RN scope under the direction of an licensed independent practitioner (LIP) and when certain criteria is met within this advisory opinion. The licensed nurse must meet the general requirements and course of instruction listed in parts I and II. -
Chapter 03- Diseases of the Blood and Certain Disorders Involving The
Chapter 3 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50- D89) Excludes2: autoimmune disease (systemic) NOS (M35.9) certain conditions originating in the perinatal period (P00-P96) complications of pregnancy, childbirth and the puerperium (O00-O9A) congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) endocrine, nutritional and metabolic diseases (E00-E88) human immunodeficiency virus [HIV] disease (B20) injury, poisoning and certain other consequences of external causes (S00-T88) neoplasms (C00-D49) symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) This chapter contains the following blocks: D50-D53 Nutritional anemias D55-D59 Hemolytic anemias D60-D64 Aplastic and other anemias and other bone marrow failure syndromes D65-D69 Coagulation defects, purpura and other hemorrhagic conditions D70-D77 Other disorders of blood and blood-forming organs D78 Intraoperative and postprocedural complications of the spleen D80-D89 Certain disorders involving the immune mechanism Nutritional anemias (D50-D53) D50 Iron deficiency anemia Includes: asiderotic anemia hypochromic anemia D50.0 Iron deficiency anemia secondary to blood loss (chronic) Posthemorrhagic anemia (chronic) Excludes1: acute posthemorrhagic anemia (D62) congenital anemia from fetal blood loss (P61.3) D50.1 Sideropenic dysphagia Kelly-Paterson syndrome Plummer-Vinson syndrome D50.8 Other iron deficiency anemias Iron deficiency anemia due to inadequate dietary -
Guideline: Assessment and Treatment of Pressure Ulcers in Adults & Children
British Columbia Provincial Nursing Skin and Wound Committee Guideline: Assessment and Treatment of Pressure Ulcers in Adults & Children Developed by the BC Provincial Nursing Skin & Wound Committee in collaboration with Wound Clinicians from: / TITLE Guideline: Assessment and Treatment of Pressure Ulcers in Adults & Children1 Practice Level Nurses in accordance with health authority / agency policy. Care of clients 2 with pressure ulcers requires an interprofessional approach to provide comprehensive, evidence-based assessment and treatment. This clinical practice guideline focuses solely on the role of the nurse, as one member of the interprofessional team providing care to these clients. Background Researching existing data on pressure ulcer prevalence rates in Canada, Woodbury and Houghton (2004) found that mean pressure ulcer prevalence was 25.1% in acute care, 29.9% in non-acute care settings and 15.1% in community care with an overall mean prevalence rate of 26% across all settings.39 This prevalence data illustrates the significance of the problem and the need for consistent, evidence-based care. In pediatrics settings, a US multi-site national study found that the overall prevalence of skin breakdown was 18%, of which 4% was attributed to pressure ulcers.17 Pressure ulcers occur most commonly over bony prominences but can occur anywhere on the body when pressure, shearing force and friction are present and can lead to the death of underlying tissues. Heels and the sacrum are the two most common sites for pressure ulcers. Animal model studies have shown that a constant external pressure of 2 hours or longer can result in irreversible tissue damage.12 Populations at increased risk for pressure ulcers include those who have problems with peripheral circulation, are malnourished (overweight or underweight), have motor or sensory deficits, are incontinent, are immune compromised, have diabetes, renal failure, sepsis and/or cardiovascular problems or have had lower extremity surgery, especially hip replacements. -
Table of Contents
Table of Contents 09.06.02 - RULES GOVERNING MINIMUM MEDICAL\ AND HEALTH STANDARDS FOR PAID FIREMEN 000. LEGAL AUTHORITY. ........................................................................................ 3 001. TITLE AND SCOPE. ......................................................................................... 3 002. WRITTEN INTERPRETATIONS. ...................................................................... 3 003 ADMINISTRATIVE APPEALS. .......................................................................... 3 004.-- 010. (RESERVED). ......................................................................................... 3 Archive011. MINIMUM MEDICAL AND HEALTH STANDARDS FOR PAID FIREMEN. ...... 3 012. ABDOMINAL ORGANS AND GASTROINTESTINAL SYSTEM. ...................... 3 013. BLOOD AND BLOOD-FORMING TISSUE DISEASES. ................................... 4 014. DENTAL. .......................................................................................................... 5 015. EARS. ............................................................................................................... 6 016. HEARING. ......................................................................................................... 6 017. ENDOCRINE AND METABOLIC DISORDERS. ............................................... 7 018. UPPER EXTREMITIES. .................................................................................... 7 019. LOWER EXTREMITIES. .................................................................................. -
Peripheral Edema with Hypoalbuminemia in a Nonhuman Primate Infected with Simian–Human Immunodeficiency Virus: a Case Report
Journal of the American Association for Laboratory Animal Science Vol 47, No 1 Copyright 2008 January 2008 by the American Association for Laboratory Animal Science Pages 42–48 Case Report Peripheral Edema with Hypoalbuminemia in a Nonhuman Primate Infected with Simian–Human Immunodeficiency Virus: A Case Report Carol L Clarke,1,* Michael A Eckhaus,2 Patricia M Zerfas,2 and William R Elkins1 A rhesus macaque (Macaca mulatta) infected with simian-human immunodeficiency virus (SHIV) while undergoing AIDS research, required a comprehensive physical examination when it presented with slight peripheral edema, hypoalbuminemia, and proteinuria. Many of the clinical findings were consistent with nephrotic syndrome, which is an indication of glomerular disease, but the possibility of concurrent disease needed to be considered because lentiviral induced immune deficiency dis- ease manifests multiple clinical syndromes. The animal was euthanized when its condition deteriorated despite supportive care that included colloidal fluid therapy. Histopathology confirmed membranoproliferative glomerulonephritis, the result of immune complex deposition most likely due to chronic SHIV infection. Clinical symptoms associated with this histopathol- ogy in SHIV-infected macaques have not previously been described. Here we offer suggestions for the medical management of this condition, which entails inhibition of the renin–angiotensin–aldosterone system and diet modifications. Abbreviations: ACE, angiotensin-converting enzyme; SHIV, simian–human immunodeficiency -
Myelophthisic Anemia in a Patient with Lobular Breast Carcinoma Metastasized to the Bone Marrow
Open Access Case Report DOI: 10.7759/cureus.3541 Myelophthisic Anemia in a Patient with Lobular Breast Carcinoma Metastasized to the Bone Marrow Muhammad H. Khan 1 , Abdurraoof Patel 1 , Purav Patel 1 , Poras Patel 2 , Elizabeth Guevara 2 1. Internal Medicine, The Brooklyn Hospital Center, Brooklyn, USA 2. Hematology / Oncology, The Brooklyn Hospital Center, Brooklyn, USA Corresponding author: Muhammad H. Khan, [email protected] Abstract Breast tumors have a predilection for metastasizing to the bone leading to cells being displaced by the cancer cells subsequently producing immature leukocytes and erythrocytes in the peripheral blood. We present a case of a 57-year-old female who was found to have myelophthisic anemia secondary to stage four lobular breast carcinoma metastasized to the bone marrow after being misdiagnosed as having thrombotic thrombocytopenia purpura. Diagnosis of myelophthisic anemia requires a thorough workup and treatment is based upon secondary management of the malignancy. Categories: Internal Medicine, Medical Education, Oncology Keywords: ttp, thrombotic thrombocytopenic purpura, adamst13, a disintegrin and metalloproteinase with a thrombospondin type 1 motif (member 13), er, estrogen receptor, pr, progesterone receptor, her2, human epidermal growth factor receptor 2 Introduction Approximately 252,710 new cases of invasive breast cancer were predicted to occur in the United States in 2017. From 2005 to 2014, the incidence of breast cancer among non-Hispanic blacks increased by 0.4% per year [1]. Breast tumors have a predilection for metastasizing to the bone. When metastasis to the bone marrow occurs, cells are displaced by the space-occupying cancer cells and this leads to immature leukocytes and erythrocytes in the peripheral blood [2-3].