DISCHARGE SUMMARY Patient Name: Adela Torres Patient ID: 132463 DOB: Age: 57 Sex: Female Date of Admission: 6/22/---- Date of Discharge: 6/25/---- Admitting Physician: Liam Medina‚ MD Consultations: Sachi Kto‚ MD‚ Dermatology Procedures Performed: Intravenis Hydration Complications: None Discharge Diagnosis: 1. Methotrexate related dermatitis. 2. Rheumatoid arthritis class 3 stage 4 3. Osteoporosis
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ANAEMIA Anaemia is a reduction in the oxygen carrying capacity of the blood; this may be caused by a decrease in red blood cell (RBC) production‚ or reduction in haemoglobin (Hb) content of the blood. Sign and Symptoms • Pallor • Fatigue • Dizziness • Shortness of breathe on exertion • Pale mucous membranes • Fainting • Palpitations • Tachycardia Cause • Dietary deficiency • Numerous pregnancies • Menorrhage • Chronic infection • Antepartum haemorrhage • Postpartum haemorrhage
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(*) Tests|Patient Results &Date|Patient Results & Date|Normal|Possible causes for out of range result| Coagulation Tests:||||| Activated partial Thromboplastin time (PTT)|25.7||22.2-39.5|| Prothrombin time (PT)|11.6||9.9-14.7|| International Normalized Ratio (INR)|||1.0-3.5|| Clotting Factors||||| D-Dimer||||| Drug Therapeutic Levels:||||| Digoxin||||| Theophylline||||| Dilantin||||| Peak and Trough||||| Gentamicin||||| Vancomycin||||| Other||||| Arterial Blood Gases (ABGs):||||RA|
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_______________________________________ Part I—The Initial Physical Examination Scenario Mary and Bill adopted a three-year-old toddler named Sam two weeks ago. Sam is good-natured and very inquisitive. Typically‚ before the finalization of an adoption‚ children are required to undergo a routine examination by a physician. However‚ the required examination is not meant to be a complete health screening‚ and many conditions are not even checked. Therefore‚ Mary and Bill are bringing Sam to Trinity
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Brand name Dosage form composition Pack size Manufacturer importer prize FERROCARE CAPSULES DRIED FERROUS SULPHATE107.2MG‚FOLIC ACID 500MCG‚CYANOCOBALAMIN 300MCG 6x10s‚ 6s Softgel Health Care Pvt Ltd. Pharma Associates RARICAP L 200ML GLASS BOTTLES FERROUS CALCIUM CITRATE AND FOLIC ACID 25MG & 0.5MG Bafna Pharmaceuticals Ltd. Associated Laboratories (Pvt) Ltd FERUP SOFT GEL CAPSUL FERROUS FUMARATE 152MG +FOLIC ACID 1.5MG BP 12X10‚ 4X30 Cadila Healthcare Ltd Hemas Pharmaceuticals Pvt Ltd FERROVIT
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DIAGNOSTIC IMAGING ___________________________________________________ PATIENT NAME: Adela Torres PATIENT ID: 132463 DATE ADMITTED: 06/20/---- DATE DISCHARGE: 06/25/--- ADMITTING PHYSICIAN: Leon Medina‚ MD CONSULTATION: Sachi Kato‚ MD‚ Dermatology PROCEDURES Intravenous hydration. COMPLICATIONS None. ADMISSION DIAGNOSIS Stomatitis possibly methotrexate related. HOSPITAL COURSE This 57-year-old Cuban female was admitted from my office repeat severe stomatis
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Blood Film Staining – Normal & Malignant Cells Case Study 1 Male 72 yrs Hb 77g/l (NR 130-180) RBC 2.23 x 10¹²/l (NR 4.5-6.5) MCV 88fl (NR 76-96) WBC 98.2 x 10/l (NR 4-11) Platelets 28 x 10/l (NR 150-400) A) Calculation of PCV (packed cell volume or haematocrit) PCV = RBC (cells/l) x 10¯¹² x MCV (fl) RBC = 2.23 x 10¹²/l MCV = 88fl or 88 x 10/l PCV = 2.23 x 88 x10 PCV = 196.24/1000 PCV = 0.196 (NR 0.4-0.54) B) Calculation of MCH (mean cell volume) MCH = Hb
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Explain in details regarding the sideroblastic anemia. - The sideroblastic anemia is a heterogeneous group of blood disorders. This type of anemia will occur because an impaired ability of the bone marrow to produce normal red blood cells. The person who has these anemia can found sideroblasts (abnormal red blood cells) in the blood. Sideroblastic anemia can be categorized into three groups such as reversible‚ acquired and reversible hereditary. 2. Explain in details regarding the morphology of siderocytes
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Physiology Of Flight Term Paper DERYL OMATSEYE Everglades University Mr. Kirk Webster Sickle Cell Anemia Sickle cell anemia or also known as sickle cell disease is a hereditary genetic disease defined by the presence of odd shaped crescent-shaped red blood cells instead of the regular round disc like shape cells. Red blood cells transport oxygen from the lungs to various other organs and tissues with the help of a protein called hemoglobin. The main cause of sickle cell disease is
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Sickle cell anemia is a blood disorder that affects the 11th chromosome which is a hemoglobin gene. Hemoglobin is a protein located in red blood cells (RBCs) that carries oxygen through the body. This disorder is inherited from two parents with abnormal genes that are heterozygous (Rr). This means that both parents who have the trait may pass on the disorder to their offspring. The phenotype makeup is recessive. Those who inherit a normal copy of the chromosome 11 and a mutated chromosome will carry
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