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Microsoft word - evaluation of anemia.doc

It is defined as "Reduction in either the red blood cell volume (HCT), or the concentration of
hemoglobin in the blood."
In general values more than 2SD below the mean warrant investigation.
HCT (2sd)
12 - 18 yrs M

However, relying strictly on a numerical definition of anemia may obscure significant
pathologic features, examples;
1. Female with C.O.P.D. Hb 13.5 may need detailed W/U if her baseline Hb has been 17.5

2. Patient with dehydration and normal Hct & Hb, may need further examination and his blood
values should be measured after hydration.
3. Patient with a significant CHF might appear Anemic from findings on his initial hemogram,
but values may return to normal after diuresis.
Anemia may be due to either to increase loss of red cells (hemorrhage or hemolytic) or decrease
production of red cells.
Increase loss of red cells or destruction is associated (at least in early stage) with effective
erythropoiesis and marrow hyperproliferation manifested by elevation of the reticulocyte count.
Corrected Reticulocytes % = Raw reticulocytes % X Pt's Hct/45
Reticulocyte Production Index (RPI) = corrected reticulocytes/maturation factor
Each differential diagnosis is guided by: 1. History and physical examination: * Family history; usually suggests an inherited Red cell disorder. * Chronic blood loss; ex. Women of reproductive age should be asked of menstrual flow. Occult bleeding is almost from G.I. tract, since patient will report pulmonary or urinary bleeding. *Drugs/toxin: A. Drugs causing marrow hypoplasia or aplasia; 1. Antimicrobial drugs; chloramphenicol, sulfas, streptomycin Anticonvulsant drugs: Dilantin, primidone, carbamazepine Anti-inflammatory drugs; phenylbutazone, tolbutamide Oral hypoglycemics; chlorpropamide, tolbutamide Tranquilizers; chlordiazepoxide, (Librium), meprobamate Major tranquilizers/ Antiemetics; Thorazine, /Compazine Miscellaneous; acetazolamide, potassium perchlorate B. Drugs causing hemolytic anemia: In G6PD; antimicrobial; sulfa, Nalidixic acid & others In immune hemolytic anemia; PCN, sulfa, quinine, methyldopa, levodopa C. Folate antagonists: D. Porphyrin/heme synthesis antagonists:
E. Drugs causing G.I. loss:
Nonsteroidal anti-inflammatory agents
F. Occupation & house hold customs and habits
Insecticide, cleansing fluids
* Chronic disease/Malignant disease; hepatic, thyroid dysfunction, collagen disease, R.A., etc .
Physical Exam: signs of chronic disease; joints disease, liver disease.
Pelvic/rectal exams are essential
Breast & Abdomen Exam
Signs of hemolytic anemia; Jaundice, splenomegaly
Neuro exam: vitamin B12 deficiency
Blood film:
As in the table;
(Next page)
1. Since the MCV represents an automated averaging of the size of all red cells in a blood sample, it is a reliable means of classifying anemias only when red cell population is fairly homogenous. The red cell distribution width; RDW is a calculated index, volumes above normal range (11.5% - 14.5%) correlate with anisocytosis. Thus when the RDW is significantly elevated the MCV is less reliable. 2. Mean Corpuscular Hemoglobin Concentration: MCHC: It's a red cell index values 32 - 36 gm/dl indicates normochromic and values below this range; hypochromia only is spherocytic disorders is the MCHC increased. Table 23 -3. Description and Significance of Various Forms of Red Corpuscles
Type of Cell
Physiologic Significance*
Clinical Disorders
Larger than normal (>8.5 µm diameter). Well early loss of nucleus) DNA synthesis-impaired megaloblastic maturation Diameter increased but MCV normal: often not it is: (a) well filled with hemoglobin (b) normal shape Exaggeration of normal central pallor; usually Hypochromic with central pigment; thin cell microcytic; surface to volume ratio decreased: no diseased vessels, and artificial surfaces in the circulation In various anemia especially megaloblast In shape of sickle; form assumed especially of Triangular or helmet-shaped, fragmented or greatly distorted RBC; smaller than normal physical agents Also in uremia malignant hypertension Shape of drop: usually microcytic, often also Less frequently in other forms of anemia; e.g., thalassemia RBC with spiny projections on surface Has 5 to 10 spicules of various lengths irregular in Has 20 to 30 spicules, evenly distributed over both , as result of changes in plasma or in RBC metabolism Uniconcave, as contrasted with normal biconcave RBC, slitlike instead of circular area of central Dense dehydrated, irregularly contracted may *RBC, red blood cell: MCV, mean cell volume, LCAT, lecithin cholesterol acytranslerase Table 24 - 10. Problems in Interpreting Serum Vitamin B12 Levels Falsely high values (concealing deficiency) Radioassay artifact Abnormal serum binding proteins (liver disease chronic myelocytic leukemia) Vitamin B12 injection preceding specimen collection Artifact due to radioactivity in serum (e.g., after gallium or technetium scans) In myeloma or aplastic anemia Normal pregnancy; oral contraceptives Transcobalamin I deficiency ? Severe iron deficiency Drugs interfering with microbiologic assays: antibiotics, chlorpromazine, antifolate drugs High -dose vitamin C TABLE 2: Ideal Diagnostic Approach to the Patient with a Low Serum Cobalamin Level of Uncertain Etiology 1. Recheck the serum cobalamin level 2. Careful review of the blood smear and, if possible, bone marrow aspirate smear. 3. Careful review of neurologic status. Include testing for mild neuropathy, memory impairment EEG and evoked potentials are often abnormal even in asymptomatic patients. Serum or urine methylmalonic acid Serum or urine homocysteine (also abnormal in folate deficiency) (Deoxyuridine suppression test of marrow, if available) (Holotranscobalmin II may be tested, if available; however, interpretation must be very cautious) 5. Schilling test or other test of free-cobalamin absorption. Avoid dual-isotope test, which sometimes gives falsely normal results. Note whether patient took antibiotics recently, which may inadvertently correct bacterial overgrowth in the gut. 6. If Schilling test result is normal, test food-cobalamin absorption if the test is available. If the latter is unavailable, gastric analysis for achlorhydria may be helpful sometimes. Is there folate deficiency? Is the patient positive for HIV? Is the patient taking drugs which intermittently affect cobalamin absorption? Does the patient have R binder deficiency?



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Microsoft word - augmentation par implants prothétiques_consignes_dr_binder.doc

« PLASTIE MAMMAIRE D’AUGMENTATION PAR IMPLANTS PROTHETIQUES» Traitements médicaux : • Un traitement antalgique de base (PARACETAMOL) vous a été prescrit, il doit être pris de façon systématique pendant 10 jours. Un traitement antalgique plus puissant (TRAMADOL) est nécessaire pendant 48 heures ou plus suivant l’intensité des douleurs. • Un myorelaxant (TETRAZEPAM) est

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