specimen collection test quizlet

It is a method of collecting a urine sample for various tests, including urinalysis, cytology, and urine culture. Explain to the patient that this kind of urine collection involves first voiding approximately one half of the urine into the toilet, urinal, or bedpan, then collecting a portion of midstream urine in a sterile container, and allowing the rest to be pass into the toilet. The following could affect the hospital’s reimbursement under recent healthcare reform laws and regulations: TRIG : Patient Preparation: 1. The following is a brief description of each specimen type and instructions to process them properly. The sample is then taken to the laboratory for culture. Specimen Collection, Handling and Transport Page 6 of 6 All specimens transported via courier must be transported in sealed biohazard, leak-proof, puncture resistant container tightly closed before transportation. Record the ending date and time on the collection container and on the laboratory requisition. Instruct the patient to void a small amount of urine into the toilet to rinse out the urethra, void the midstream urine into the specimen cup, and the last of the stream into the toilet. His drive for educating people stemmed from working as a community health nurse. ... and compliance with applicable laws regarding specimen collection, confidentiality, chain of custody, and incident reporting. Quality & Professional Issues Test . If you don’t get an adequate sample on the first try, have him continue to cough until you’re able to collect a minimum of 15 ml. Expanded cost-per-Medicare beneficiary due to repeated specimen collections and unnecessary treatment. How to prevent common errors: Collect sufficient quantity. It is done to isolate and identify any pathogens, which may be medium. Collect ample amount of sample by using appropriate collection devices such as sterile, leak-proof specimen containers. With the use of a tongue blade, transfer a portion of the feces to the specimen container. Specimen Collection • Suspect or confirmed TB patients should be in a negative pressure room • Specimen collection is an aerosol generating procedure, anyone in the room during specimen collection must wear a particulate respirator type N-95 and be part of the respirator protection plan • All mycobacteria specimens are collected It is one way of knowing about the patient’s health status by identifying pathogens and analyzing urine, blood, sputum, and feces. Generally, the patient will be given one or more containers to collect and store urine over a 24-hour time period. If the specimen is not received within two hours of collection, specimen reception personnel must confirm that a tube containing an appropriate preservative has been used. This specimen shows the total amounts of wastes the kidneys are eliminating and the amount of each. Uncap the container but avoid touching the inside to ensure that it’s sterile. B. sufficient for a rapid test only. According to the FDA, 10 to 20 percent of pregnant women may not detect their pregnancy by testing on what they believe to be the first day of their first missed period. A sample of urine collected at any time of the day. However, it can be difficult to keep urine away from the stool sample. Proper collection of specimens is the most important step in the laboratory diagnosis of infectious diseases. Specimen processing instructions: Centrifuge the citrated blue-top tubes as soon as possible (within 60 minutes) at designated time and speed to obtain platelet-poor plasma ( 10,000/µL). The role of nurses in collecting, labeling, and ensuring the timely and proper delivery of specimens to the laboratory plays a very important thing in the hospital setting. Supplies and equipment required to collect a stool specimen are: Clean bedpan and cover (an extra bedpan or urinal if the patient must void), Plastic bag for transport of container with specimen to laboratory. Test results are a direct reflection of specimen integrity. Collect all urine voided during the next 24 hours. For many urine chemistry procedures the specimen of choice is 24-hour urine. Improperly labeled specimens will be rejected. These infections can include strep throat, pneumonia, tonsillitis, whooping cough, and meningitis. With regard to an infant patient, place the diaper in a leakproof bag, label it, and take the diaper and request form to the lab as soon as possible. Label both bottles with the patient’s identifying information and the type of culture that is, aerobic or anaerobic. A stool culture is the process of growing or culturing organisms existing in feces to see if any of them cause disease. Check expiration date before inoculating collection device. A blood culture is being done to determine which specific organism or bacteria is causing the problem and how best to combat it. A specimen will be rejected by the laboratory if it contains excessive numbers of epithelial cells from the mouth or throat or if it fails to show adequate numbers of neutrophils on gram staining. Tell him to flush the remaining stool down the toilet. However, nurses should not only possess the right knowledge, but as well as the skill and understanding in performing necessary procedures in accordance with the organization’s protocols, policies, and guidelines. Parainfluenza virus, Respiratory FilmArray) 1. Allow patient to wait one to two weeks after her first missed period to get the most accurate results. Specimen Preservation. Use one test requisition. Midstream “clean-catch” urine collection is the most common method of obtaining urine specimens from adults, particularly men. Example: Begin collecting the 24-hour urine specimen by voiding at 7:00 am and discarding the urine. 50 Flemington Road Parkville Victoria 3052 Australia, Site Map | Copyright | Terms and Conditions, A great children's hospital, leading the way, RCH Paediatric Blood Collection Volume Guide, 11p Methylation Studies (see >> Russell Silver Syndrome (11p15)), 16S PCR (see >> 16S rRNA Gene Nucleic Acid Detection), 17 Ketosteroids (see >> Urine Steroid Profile), 18s Panfungal Nucleic Acid Detection (see >> 18S rRNA Gene Nucleic Acid Detection), 18S PCR (see >> 18S rRNA Gene Nucleic Acid Detection), 2,3 Diphosphoglyceric Acid Mutase ( or 2,3DPGM), 25-OH Vitamin D (see >> Vitamin D (25 Hydroxy)), 5HIAA (see >> Urine Biogenic Amines (24hr)), 6-TGN ( 6- thioguaninenucleotides) (see >> Thiopurine (TPMT) Metabolites), ACE (see >> Angiotensin Converting Enzyme), Acid Base (without Lactate and Electrolytes) - Capillary (see >> Blood Gas), Acid Base including Lactate and Electrolytes - Capillary (see >> Blood Gas), ACR Urine (see >> Microalbumin (Includes Urine Creatinine), Urine), ACTH (see >> Adrenocorticotrophic Hormone (ACTH)), Activated T Cells and Double Negative T Cells, ADA/PNP (Adenosine Deaminase & Purine Nucleoside Phosphorylase), Adalimumab level (see >> Infliximab Level (and Anti TNFa Ab)), Adrenaline (see >> Urine Biogenic Amines (24hr)), AER Urine (see >> Microalbumin (Includes Urine Creatinine), Urine), AH100 (see >> Complement Function (Classical, Alternative, MBL)), AH50 (see >> Complement Function (Classical, Alternative, MBL)), Albumin Creatinine Ratio Urine (see >> Microalbumin (Includes Urine Creatinine), Urine), Albumin Excretion Rate Urine (see >> Microalbumin (Includes Urine Creatinine), Urine), Albumin Urine (see >> Microalbumin (Includes Urine Creatinine), Urine), Allergy (or Allergen Specific IgE) (see >> RAST), Alloimmune Thrombocytopenia (see >> Neonatal Alloimmune Thrombocytopenia Screen (NAIT, FMAIT)), alpha globin gene DNA analysis (see >> Thalassaemia/Haemoglobinopathy Genotype), Alpha Tryptase (TPSAB1) copy number gene testing, AMH (see >> Anti Mullerian Hormone (AMH)), AML-ETO t(8:21) (see >> RUNX1/RUNX1T1 Mutation), ANCA (Anti Neutrophil Cytoplasmic Antibody), Angiotensin II Type 1 Receptor (AT1R) antibodies – solid organ, Ankylosing Spondylitis Screen (see >> HLA Tissue Typing – HLA-B 27), Antenatal Screen (see >> Antenatal Micro Serology Screen), Antenatal Streptococcus agalactiae (GBS) Screen, Anti CD3 Proliferation - Separated (see >> Separated Lymphocyte Proliferation - anti-CD3), Anti Complement Factor H antibodies (see >> Complement Factor H Antibodies), Anti Endomysial IgA (see >> Coeliac Serology), Anti Factor H Antibodies (see >> Complement Factor H Antibodies), Anti Ganglioside Antibodies (see >> Anti GQ1b Antibodies), Anti Gliadin antibodies (IgA and IgG) (see >> Coeliac Serology), Anti Hu Antibodies (see >> Anti Neuronal Antibodies), Anti Interstitial Substance of Squamous Epithelium, Anti Intrinsic Factor Antibodies (see >> Intrinsic Factor Antibodies (IFA)), Anti JKA antibody titre (see >> Blood Group & Antibody Screen (Group & Hold) RWH Only), Anti JKA antibody titre (see >> Blood Group & Antibody Screen (Group & Hold) RCH Only), Anti MOG (Myelin Oligodendrocyte Glycoprotein), Anti Mullerian Inhibiting Substance (see >> Anti Mullerian Hormone (AMH)), Anti Parietal Cell Antibodies (see >> Parietal Cell Antibodies), Anti Phospholipase A2 Receptor Antibodies, Anti Platelet Antibodies (see >> Platelet Antibodies - Investigation of ITP), Anti Prothrombin (see >> Prothrombin Antibodies), Anti Ri Antibodies (see >> Anti Neuronal Antibodies), Anti Ro & Anti La (see >> Extractable Nuclear Antigens), Anti squamous epithelium antibody (see >> Anti Interstitial Substance of Squamous Epithelium), Anti Streptolysin O titre (see >> ASOT or ASO), Anti TNF Levels (see >> Infliximab Level (and Anti TNFa Ab)), Anti VGCC Antibodies (Anti Voltage Gated Calcium Antibodies), Anti VGKC Antibodies (Voltage Gated Potassium Channel Antibodies), Anti Yo Antibodies (see >> Anti Neuronal Antibodies), Anti ZnT8 (see >> Zinc Transporter Autoantibodies), Antibody Screen - RWH (see >> Blood Group & Antibody Screen (Group & Hold) RWH Only), Anti-Enterocyte Antibodies/Anti-Goblet Cell Antibodies, Antioxidants (see >> Total Antioxidant Status), Anti-PLA2R (see >> Anti Phospholipase A2 Receptor Antibodies), Antistreptolysin O Titre (see >> ASOT or ASO), AntiVGCC Antibodies (Anti Voltage Gated Calcium Antibodies), Aortopathy Next Generation Sequencing (NGS) Panel, APCR (Activated Protein C Resistance - Screening test for Factor V Leiden), APTT (Activated Partial Thromboplastin Time), Aquaporin-4 Antibodies (see >> NMO IgG - Neuromyelitis Optica IgG), Arrhythmia Next Generation Sequencing (NGS), Arrythmogenic Right Ventricular Cardiomyopathy (ARVC) Next Generation Sequencing(NGS), ASCA - Anti Saccharomyces cerevisiae antibodies, Aspergillus Serology (see >> Aspergillus Precipitins), AST (see >> Aspartate Aminotransferase (AST)), Atypical Mycobacteria Culture (see >> Mycobacterium genus or Atypical Mycobacteria or Pan Mycobacterial Culture), Autoantibodies for Immune Thrombocytopenia (see >> Platelet Antibodies - Investigation of ITP), Autoantibodies for Neutropenia (see >> Anti Neutrophil Antibody), B Cell Panel (including Memory B Cells, transitional B and plasmablasts), B Cells - High Sensitivity (see >> Lymphocyte Subsets - Immunology Includes CD3, CD4, CD8, CD19, NK, High Sens B Cells, HLADR & Naive T), B CELLS - Memory (see >> B Cell Panel (including Memory B Cells, transitional B and plasmablasts)), B. pertussis IgG & IgA (see >> Pertussis Serology), B27 (see >> HLA Tissue Typing – HLA-B 27), B51 (see >> HLA Tissue Typing – HLA-B 51 (Behcet’s disease)), B58 (see >> HLA Tissue Typing – HLA-B 58:01 (Allopurinol hypersensitivity)), Bacterial screening - multiresistant organisms by culture, Bacterial Vaginosis (see >> Culture Genital Swab incl Microscopy), Beckwith Wiedemann Syndrome Gene Analysis (see >> Russell Silver Syndrome (11p15)), Bence Jones Protein (see >> Protein Electrophoresis, Urine), Beta 2 GP1 antibodies (see >> Anti Beta 2 Glycoprotein 1 (IgG)), Beta globin gene DNA analysis (see >> Thalassaemia/Haemoglobinopathy Genotype), Beta HCG Tumour Marker (see >> hCG (Human chorionic gonadotropin)), Bethesda Assay (see >> Factor VIII Inhibitor (Bethesda Assay)), Bil (see >> Serum Bilirubin - unconjugated & conjugated (SBR)), Bile Acids (Total) (see >> Total Bile Acids), Bile Salts (see >> Bile Acids (Non Fasting)), Biochemistry (Protein & Glucose) CSF (see >> Protein & Glucose, CSF), Biochemistry CSF (see >> Protein & Glucose, CSF), BioFire / Film Array (see >> Meningitis/Encephalitis Nucleic Acid Detection), Biopterin (see >> Pterins & Neurotransmitters - CSF), BK (see >> Polyomavirus (BK/JC) - Nucleic Acid Detection), Blood Film Examination - Referred from external source, Blood Glucose (BG) (see >> Glucose - Random), Blood Group & Antibody Screen (Group & Hold) RCH Only, Blood Group & Antibody Screen (Group & Hold) RWH Only, Blood Group and Antibody Screen Neonatal Extended Expiry (see >> ASBT), Blood Sugar Level (BSL) (see >> Glucose - Random), Bone Marrow - Cytogenetics (Adult) (see >> Cytogenetics - Adult), Bone Marrow - Cytogentics (Children) (see >> Cytogenetics - Children), Bone Marrow Examination - Referred from external source, Bone Marrow PCR (see >> BM PCR (Bone Marrow PCR)), Bone Marrow Transplant DNA Genotype Chimerism (see >> Post HSCT Chimerism), Bordetella Pertussis Nucleic Acid detection, Bordetella pertussis Serology (see >> Pertussis Serology), Borrelia burgdorfi serology (see >> Lyme Borreliosis Serology), brain (see >> Brain Natriuretic Peptide (BNP)), BrCa1 antigen (Breast Cancer 1 antigen Genetic Screen), BrCa2 antigen (Breast Cancer 2 antigen Genetic Screen), Breath Test (see >> Hydrogen Breath Test), C1Q Antibodies (see >> Complement C1Q Antibodies), C2 (see >> Complement Studies - other (free text)), C282Y and H63D Gene Mutation (see >> Haemochromotosis Gene Mutation / Haemochromotosis Screen), Calculus (see >> Renal Stone Analysis - Calculus), Candida auris screening (see >> Bacterial screening - multiresistant organisms by culture), carcinoembryonic antigen (see >> CEA (Carcinoembryonic antigen)), Cardiac Isoenzymes (see >> Creatine Kinase (CK)), Cardiolipin antibodies (see >> Anti Cardiolipin IgG (ACA)), Cardiomyopathy Next Generation Sequencing (NGS) Panel, CASA (see >> Cancer Associated Antigen (CASA)), Cat Scratch Disease Serology (see >> Bartonella Henselae Antibodies), Catecholamines (see >> Urinary Biogenic Amines - Random), Catecholamines Urine (see >> Urine Biogenic Amines (24hr)), CBA (see >> Von Willebrands Disease (VWD) Screen (includes vWF antigen, Collagen Binding Assay (CBA) & Ristocetin Cofactor (RiCoF))), CD11b (see >> Leucocyte Adhesion Deficiency Testing (CD11b/CD18)), CD18 (see >> Leucocyte Adhesion Deficiency Testing (CD11b/CD18)), CD45RA (see >> Lymphocyte Subsets - Immunology Includes CD3, CD4, CD8, CD19, NK, High Sens B Cells, HLADR & Naive T), CD59 (PNH investigation by flow cytometry) (see >> PNH investigation by flow cytometry), CEA (see >> CEA (Carcinoembryonic antigen)), Cell Surface markers (see >> Lymphocyte Subsets - Immunology Includes CD3, CD4, CD8, CD19, NK, High Sens B Cells, HLADR & Naive T), Cerebrospinal Fluid (CSF) (see >> Parechovirus Nucleic Acid Detection - CSF), CH50 or CH100 (see >> Complement Function (Classical, Alternative, MBL)), CH50 or CH100) (see >> Complement Function (Classical, Alternative, MBL)), Chicken Pox Serology (see >> Varicella Antibodies IgG & IgM), Chimerism Analysis - FISH sex (XY) (see >> Post HSCT Chimerism), Chitotriosidase (Gaucher Disease Monitoring), Cholesterol esterification (Niemann Pick type C) - Fibroblast, Chromosome breakage analysis (Ataxia Telangiectasia), Chromosome breakage analysis (Bloom syndrome), CK Isoenzymes (see >> Creatine Kinase (CK)), Clinical Exome (see >> Whole Exome Sequencing), Clotting (see >> Coagulation Screen (INR, APTT, Fibrinogen)), CMV PCR (see >> CMV Nucleic Acid detection), CMV Saliva (see >> CMV Nucleic Acid detection), CMV Urine (see >> CMV Nucleic Acid detection), CMV Viral Load (see >> CMV Nucleic Acid detection), Coag (see >> Coagulation Screen (INR, APTT, Fibrinogen)), Coagulation Screen (INR, APTT, Fibrinogen), Coeliac Genotype (see >> HLA Tissue Typing - HLA-DQ (Coeliac Genetic Susceptibility)), Collagen Binding Antigen (see >> Von Willebrands Disease (VWD) Screen (includes vWF antigen, Collagen Binding Assay (CBA) & Ristocetin Cofactor (RiCoF))), Collagen Binding Assay (CBA) (see >> Von Willebrands Disease (VWD) Screen (includes vWF antigen, Collagen Binding Assay (CBA) & Ristocetin Cofactor (RiCoF))), Colony Assay (see >> JMML Colony Culture), Colony Culture (see >> JMML Colony Culture), Complement - C1 esterase inhibitor studies, Complement Alternative Pathway (AP50 AH50 AH100) (see >> Complement Function (Classical, Alternative, MBL)), Complement Function (Classical, Alternative, MBL), Congenital Heart Disorders Next Generation Sequencing (NGS) Panel, Coombs Test (see >> Direct Antiglobulin Test), Corr Calcium (see >> Corrected Calcium (CCa)), COVID-19 (see >> SARS-CoV-2 (COVID-19) Nucleic Acid Detection), COVID-19 (see >> SARS-CoV-2 Nucleic Acid Detection (Rapid)), CPE (see >> Bacterial screening - multiresistant organisms by culture), CPE (Carbapenamase Producing Enterobacteriacaea) Screen (see >> Bacterial screening - multiresistant organisms by culture), Creatine Phosphokinase (see >> Creatine Kinase (CK)), CRIM- Cross reactive immunological material (Pompe Disease), Cross Linked Fibrinogen Degradation Products (see >> D Dimers), Crossmatch - RCH (see >> Blood Group & Antibody Screen (Group & Hold) RCH Only), Crossmatch - RWH Adult (see >> Blood Group & Antibody Screen (Group & Hold) RWH Only), CSA (Cyclosporin Levels) (see >> Cyclosporin), CSF Biochemistry (see >> Protein & Glucose, CSF), CSF Biochemistry (Protein & Glucose) (see >> Protein & Glucose, CSF), CSF Cytology (see >> Cytology (Non-haematological Tumour Cell Investigation), CSF), CSF Cytology (Tumour Cell Investigation) CSF (see >> Cytology (Non-haematological Tumour Cell Investigation), CSF), CSF Flow (Markers) (see >> Immunophenotyping), CSF hCG (see >> hCG (human chorionic gonadotropin), CSF), CSF Latex Agglutination (see >> Bacterial Antigens), CSF Leukaemia (see >> Cytology (Haematological Tumour Cell Investigation including cell count), CSF), CSF M/C/S (see >> Culture CSF including microscopy), CSF Neurotransmitters (see >> Neurotransmitters and Pterins-CSF), CSF Oligoclonal Bands (see >> Oligoclonal Bands, CSF), CSF Parechovirus Nucleic Acid Detection (see >> Parechovirus Nucleic Acid Detection - CSF), CSF Protein / Glucose (see >> Protein & Glucose, CSF), CSU (see >> Culture Urine including microscopy), CT (Chlamydia trachomatis) detection by Nucleic Acid detection (see >> Chlamydia trachomatis by PCR), Culture - Ear, Nose, Throat including microscopy, Culture Actinomyces Culture - Cervical Swab, Culture Eye (see >> Eye Swab Culture (Bacteriology)), Culture Fluids NON CSF including Microscopy, Culture Fungal - Skin/Hair/Nails including microscopy, Culture Mycobacterium including Microscopy (see >> Mycobacterium tuberculosis Microscopy and Culture), Culture Pus/Wound/Aspirate including Microscopy (see >> Culture Superficial Swabs including Microscopy), Culture Pus/Wound/Aspirate including Microscopy (see >> Culture Urine including microscopy), Culture Superficial Swabs including Microscopy, Culture Urine including microscopy (see >> Culture Urine including microscopy), Cytology (Haematological Tumour Cell Investigation including cell count), CSF, Cytology (Non-haematological Tumour Cell Investigation), CSF, Cytology CSF (see >> Cytology (Non-haematological Tumour Cell Investigation), CSF), Cytomegalovirus Antibodies IgG & IgM (see >> CMV Antibodies IgG & IgM), Cytomegalovirus Nucleic Acid Detection (see >> CMV Nucleic Acid detection), Cytomegalovirus Resistance Testing (see >> CMV Resistance Testing), Cytospin (see >> Cytology (Non-haematological Tumour Cell Investigation), CSF), Cytospin (see >> Cytology (Haematological Tumour Cell Investigation including cell count), CSF), Cytotoxic Antibodies (see >> HLA Antibodies - Screen Only), DBS Testing for Pompe, Fabry, Gaucher - Genzyme Sanofi, Deamidated Gliadin Peptide Antibodies (DGP-IgG), DEB Stress test (see >> Fanconi Anaemia (FA)- chromosome studies/chromosome breakage studies), Dehydroepiandrosterone- Sulphate (see >> DHEA Sulphate), Delta 4 Androstenedione (see >> Androstenedione), Delta Antigen (see >> Hepatitis D Serology), Dentatorubral-Pallidoluysian Atrophy triplet repeat test (ATN1), Deoxypyridinoline (see >> Pyridinoline X links), DHR (see >> Neutrophil Oxidative Burst and Phagocytosis), Diamine Oxidase (see >> Histamine and 1-Methyl-Histamine - Whole Blood), Dilute Russell's Viper Venom Time (DRVVT) (see >> Lupus Anticoagulant / Lupus Inhibitor Screen - LA), Dipstick Urine (see >> Dipstick urinalysis), Direct Coombs Test (see >> Direct Antiglobulin Test), Disaccharidases, Maltase, Sucrase, Lactase and Isomaltase, DMD MLPA (see >> Duchenne/Becker Muscular Dystrophy Genetic Test (dystrophin)), DNA - PCR assays for Rhesus / Kell / Kidd & Duffy blood group system genes (see >> Red Cell Genotype (DNA analysis of blood group genes)), DNA analysis for Thalassaemia / Haemoglobinopathy (see >> Thalassaemia/Haemoglobinopathy Genotype), DNA microarray for HNF1 beta (see >> Microarray (Molecular Karyotype)), DNA Testing for Haemophilia A (see >> Factor VIII Genotype), DNA Testing for Haemophilia B (see >> Factor IX Gentoype), DNP Spot test for Keto Acids in MSUD - Urine, Donor Specific Antibodies (see >> HLA Antibodies – Specificity identification), Dopamine (see >> Urine Biogenic Amines (24hr)), DQ Genotyping (see >> HLA Tissue Typing - HLA-DQ (Coeliac Genetic Susceptibility)), Drug Screen (Quantitative/Confirmation), Urine, Duchenne/Becker Muscular Dystrophy Genetic Test (dystrophin), Duodenal Fluid Tryptic Activity (see >> Tryptic Activity, Duodenal Fluid), EBV (Epstein Barr Virus) viral load (see >> EBV (Epstein Barr Virus) PCR), EBV Serology (see >> Epstein Barr Virus Serology), Echinococcus granulosis (see >> Hydatid serology), ECP (see >> Eosinophilic Cationic Protein), eGFR - adult (see >> Estimated Glomerular Filtration Rate (eGFR) - adult), Elastase - Faeces (see >> Pancreatic Elastase 1), Electrolytes & Urea (EU) NOTE EU profile includes Creatinine, Electron Transport Chain (ETC) (see >> Respiratory Chain Enzymes), Emery-Dreifuss Genetic test (Lamin A/C, Emerin gene sequencing), ENA (see >> Extractable Nuclear Antigens), Enterovirus Nucleic Acid Detection (EV NAD), Epstein-Barr Virus Antibodies IgG & IgM (see >> Epstein Barr Virus Serology), Epstein-Barr Virus Nucleic Acid Detection (see >> EBV (Epstein Barr Virus) PCR), Erwinia L-Asparaginase (see >> L-Asparaginase), Erythrocyte Porphyrins (see >> Porphyrin, Red Cell), ESBL (see >> Bacterial screening - multiresistant organisms by culture), Estimated Glomerular Filtration Rate (eGFR) - adult, EU (see >> Electrolytes & Urea (EU) NOTE EU profile includes Creatinine), Exanthem subitum (see >> Human Herpes Virus 6 Nucleic Acid Detection - Blood), EXOME SEQUENCING (see >> Whole Exome Sequencing), Facioscapulohumeral Muscular Dystrophy type 1, Factor Assays (See individual Clotting Factors elsewhere), Factor B (see >> Complement Studies - other (free text)), Factor H (see >> Complement Studies - other (free text)), Factor H Antibodies (see >> Complement Factor H Antibodies), Factor I (see >> Complement Studies - other (free text)), Faecal Calprotectin (see >> Calprotectin, Faeces), Faecal Elastase (see >> Pancreatic Elastase 1), Faecal Parasites by Nucleic Acid Detection, Faecal Reducing Substances (see >> Reducing Substances, Faeces), Faeces Culture (Bacteriology) (see >> Culture -Faeces including microscopy), Familial Adenomatous Polyposis genetic test (APC gene sequencing), Fanconi Anaemia (FA)- chromosome studies/chromosome breakage studies, FBC (Full Blood Count, including differential), FBC (Full Blood Count, including differential) - FETUS, FBE (see >> FBC (Full Blood Count, including differential)), FDPs (Fibrin Degradation Products) (see >> D Dimers), Fetal DNA (for RHD gene) in maternal plasma (see >> Non-Invasive Prenatal Testing (NIPT/NIPA) for RhD), Fetal Hb (see >> Thalassaemia/Haemoglobinopathy Screen), Fetomaternal Alloimmune Neutropenia (see >> Neonatal Alloimmune Neutropenia Screen (NAIN; FMAIN)), Fetomaternal Alloimmune Thrombocytopenia (see >> Neonatal Alloimmune Thrombocytopenia Screen (NAIT, FMAIT)), Filipin Staining (Niemann Pick type C ) - Fibroblast, Flow Cytometry Erythrocyte Eosin-5-Maleimide Staining (see >> E5M (Eosin 5 maleimide) staining), Flow Cytometry for HS (Red Cell Membrane Disorders), Fluid for Microscopy & Culture (M/C/S) eg. The specimen vial must have the patient name or unique identifier that matches the test request form. And prepare himself when he feels the urge to have a bowel movement. Completed requisition is to be placed in the outside pocket. Instruct the patient to urinate, flush down the urine down the toilet when he gets up in the morning. Guaiac Fecal Occult Blood Test (gFOBT), 4.2. Tell the patient that he needs to collect a sample from his bowel by placing a sheet of plastic wrap or paper loosely across the toilet bowl to catch the stool or he can use a dry container to collect the stool. The certification test contains 145 questions that must be answered in 150 minutes with a passing score of 70%. Label the specimen properly and fill out test request form completely. An example of an optimum specimen/test match would be a first morning specimen for urinalysis and microscopic examination. Remove the syringe and needle while applying pressure to the venipuncture site with the cotton ball or gauze pad. Inject 5 cc of blood into the anaerobic bottle, not allowing air to enter the bottle. Submit all specimens within a series together in one specimen bag. Bring together all supplies and equipment needed to patient’s bedside. ), IgM (see >> Immunoglobulins (includes IgG,IgA & IgM)), IGRA (see >> Quantiferon Gold -QF Gold in tube), IL 2 Receptor - soluble (or sCD25) (see >> Soluble CD25 (Soluble IL-2 Receptor)), IL28B (see >> Hepatitis C Treatment IL28B Mutation), Immunoglobulin A (see >> Immunoglobulins (includes IgG,IgA & IgM)), Immunoglobulin G Subclasses (see >> IgG Subclasses - Requires Immunopathologist Approval. And check for presence of various substances in the laboratory best results, the. Time period accordance with Hospital Policy in 2008 with a bachelor of in... 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