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Approach to Lab Investigations By Mazen Badawi, MBBS Demonstrator, Department of Medicine KAAU
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General rules 1- order what you need 2- need is determined by : criteria of diagnosis, or monitoring, or excluding 3- follow up what you ordered 4- your patient deserves knowing all about him 5- special instructions to patient and nurses 6- order sheet problems
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MI CK, AST, LDH : not specific CK : MB heart, MM muscle, BB brain AST : heart, liver LDH : heart, liver, RBCs, other
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MI High AST Look for ALT Low ALTHigh ALT LIVERHEART
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MI Troponin I C A L CK = 6 hr to 3 days AST = 12 to 6 days LDH = 24 to 12 days Uses: Confirm Dx, Timing, Efficacy of treatment
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CSF Sugar = 0.4 – 0.8 Protein = 0.2 – 0.4 Cells = 0 – 5 lymphocytes Colorless
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CSF AFBGram stainProt.GlucoseCell countApperance Normal Bacterial meningitis TB aseptic
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CSF Protein- cell dissociation : Acute guillian barre syndrome Paraplegia Cerebellar tumor Disseminated sclerosis
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CBC report Platelet : 150 – 400 (x1000) RBC : 4.5 – 5.5 (million) WBC : 4 – 11 (x1000) Neutrophils 40-70% (2500-7500 absolute) Lymphocytes 20- 40% BT = in vivo, 2-4 min, punct dry stops, measures = CT = in vitro, 4- 8 min, in tube, measures =
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CBC What will happen if BM disease?
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CBC Normal retics 0.5 – 2 % Increase in hemorrhage, hemolysis, treated anemia Normoblasts is the same What does it mean if Retics are 0 ?
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CBC What is pokilocytosis? Anisocytosis? Both are seen in megaloblastic, hemolytic anemia
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CBC Number + size + shape of RBC : Polycythemia : check WBC, PLT. Why?
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CBC WBC : 1. Normal : check diff 2. High : Neut or Ly + Mono? 3. Low : Leucopenia *
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Anemia Normal PLT,WBC, Clotting and bleeding time Normochromic Retics 10-20% G6PD, SICKLE, SPHEROCYTOSIS Hypo Normal retics Eosinophils High in parasitic infection Normal in sidroblastic anemia +++ retics Thalassemia
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Anemia with Abnormal WBC, PLT, CT, BT All low = pancytopenia Normochromic = Aplastic a. Hypersplenism Aleukemic leuk. Hyperchromic =Megaloblastic High WBC <20000 + retics = acute blood loss Check BT, CT >30000 = Leukemia Blast +++ = acute - = chroic High BT + Purpura If low plt =TTP HIGH CT COAGULATION
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Urine report Volume = 800 – 1400 ml PH = 6 Protein = nil or trace Sugar = nil Bilirubin = nil or trace RBC = 0-5 WBC = 0-5 = Crystals = nil or + Casts = nil or hyaline Sp. Gravity = 1015 - 1025
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What to look for Nephrotic syndrome : proteinurea : 3 g/ 24hr Normal urinary protein = 0.150 gram Normal urinary albumin = 0.01 gram Pus cells : UTI Casts: coagulated proteins Hyaline casts = normal Granular = renal failure Epithelial cells = ATN White cell cast = pyelonephritis
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polyurea functionalDI >10101005Fixed 1010 DM Sugar +++ CRF Oligurea AGN RBC +++ cast Functional No RBC, hyaline cast >1010 Fixed 1010 ARF Ch. GN RBC+++ cast
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Kidney Function Tests Blood urea = dietary protein, tissue catabolism, liver funct, kidney funct Creatinine = kidney funct, muscle mass Creatinine clearance = calculated + measured Other indices
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Renal function Calculated Creatinine clearance: (140 – age ) x wt X 0.85 female s. Cr Or measure it in 24 hr!
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Stool Analysis Fat, RBC, pus, mucus Normal : Fat ++, RBC –ve, Pus +, Mucus +
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Stool Analysis Fat ++++ + RBC Steatorrhea 6 Grams DYSENTRY Bacillary Pus ++++ Mucus ++ Amoebic Pus ++ Mucus ++++ Malabsorption Maldigestion - Digested <75%
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LFT Bilirubin : direct, total Protein : total, albumin, globulin Enzymes: ALT, AST, ALP Prothrombin time
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LFT ALP is very high in : obstructive jaundice, bone lesions GGT increases in CLD esp. alcoholic Proteins : 70- 90 mg, A/G ratio 2/1, in CLD 1/1 Most specific:
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High bilirubin = Jaundic Indirect More Direct more Both Hemolytic All normal except: -High indirect -High LDH Obstructive High ALP hepatocellular A/G ratio -Normal = ALD - Decreased= CLD
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TB Acid fast bacilli stain Acid fast bacilli culture PPD PCR Radiology
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HBV HBsAg = 6 w 3 months, if persisted? HBsAb = recovery + immunity after 3 m HBc= in Bx only HBc Ab = all phases.IgM in replication HBeAg = infective + chronicity HBeAb = low infectivity PCR = best for replication
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Thank you…
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