Blood Sampling from Central Venous Lines: Vacutainer Method

Total Page:16

File Type:pdf, Size:1020Kb

Blood Sampling from Central Venous Lines: Vacutainer Method BLOOD SAMPLING FROM CENTRAL VENOUS LINES: VACUTAINER METHOD DOCUMENT TYPE: PROCEDURE Purpose Standards and procedure for blood sampling using the syringe method from central venous lines (CVL) including long term and short-term; cuffed/uncuffed external central venous catheters (CVCs), peripherally inserted central catheters and implanted ports. Standards Blood sampling requires a prescriber’s order indicating blood samples to be drawn. Blood may be sampled using the vacutainer method from: External Central Venous Catheters (CVC) Implanted Ports Short-term External Central Venous Catheters Hemodialysis/Apheresis Catheters The push-pull method is the preferred method of blood sampling from a Hemodialysis CVC but other methods can be used. Blood samplsing from a hemodialysis catheter is done only after consultation with a renal unit nurse or nephrologist. Although the vacutainer method is the preferred method for blood sampling from central venous lines for maintaining Blood and Body Fluid precautions, the syringe method is used: For all blood draws from PICC lines If vacutainer method is unsuccessful If small volumes are required for microtubes For drawing blood gas samples For drawing blood cultures Site Applicability Applicable in all BC Children’s Hospital areas where patients with central venous lines are cared for. Practice Level/Competencies Central line care, including blood sampling using syringe method from a CVL is considered a foundational nursing skill and is practiced once the nurse has: o Attended the Vascular Access Workshop, o Practiced the procedure in the lab setting, o Performs at least 3 blood sampling procedures on patients under supervision of a CVL competent RN, and o Has completed the CVL validation tool at the bedside with the appropriate clinical support person Equipment o Requisitions and computerized or addressograph labels for patient o Surface disinfectant wipe o Discard and sample syringes o Chlorhexidine 2% in 70% alcohol swabs x 3 per lumen o Vacutainer 1 per lumen o Appropriate blood collection tubes o Gloves, non-sterile o 10 mL syringe filled with normal saline 1 per lumen (x 2 if implanted port) o Sterile dead-end cap if interrupting infusion 1 per lumen CV.03.05 Published Date: 02-Nov-2018 Page 1 of 6 Review Date: 02-Nov-2021 This is a controlled document for BCCH& BCW internal use only – see Disclaimer at the end of the document. Refer to online version as the print copy may not be current. BLOOD SAMPLING FROM CENTRAL VENOUS LINES: VACUTAINER METHOD DOCUMENT TYPE: PROCEDURE If heparin locking, add: o 10 mL syringe filled with heparin 10units/mL (x2 if double lumen) o Swabcap™ (x 2 if double lumen) If drawing blood cultures, add: o Three more chlorhexidine 2% in 70% alcohol swabs o Blood culture bottles if required** **NOTE: If drawing blood cultures please refer to Pediatric Blood Culture Guide - note that syringe method is preferred for blood cultures to ensure adequate blood volume is placed into culture bottles. Procedure Steps Rationale 1. REFER to Bloodwork Test and Tubes quick Ensures correct amount of blood collected, reference guide or the Department of Pathology eLab sample placed in correct tube and handled Handbook to determine appropriate blood tubes and correctly. Reduces need to recollect samples. volumes and any special handling instructions. For blood culture instructions, REFER to Blood Culture Collection Protocol and recommended blood volumes for blood cultures chart to determine type of bottles and optimal volume of blood to add to each bottle. 2. IDENTIFY patient by comparing name on requisition Failure to correctly identify patients prior to and labels to patient ID band. If patient does not have procedures may result in errors. ID band (i.e. Ambulatory care patients), ask patient/caregiver for identification information (name, birthdate). Pease refer to Patient Identification Policy 3. EXPLAIN procedure. Evaluates and reinforces understanding of previously taught information and confirms consent for procedure. 4. CLEAN surface with disinfectant wipe. Routine infection control practices. Reduces 5. PERFORM hand hygiene for one minute. transmission of microorganisms. 6. PREPARE equipment using aseptic technique. To reduce risk of contaminating sample. If drawing blood cultures, SCRUB tops of blood culture tubes with chlorhexidine /alcohol wipes for 30 seconds. Allow to dry for 1 minute. 7. CLAMP catheter. If second lumen infusing, CLAMP Both lumens must be clamped to ensure no second lumen. contamination/dilution of blood samples. NOTE: Clamping before or after disconnecting IV infusion lines is appropriate as all neutron caps on CVLs are neutral displacement caps. 8. PAUSE infusion pumps or ACTIVATE the delay By clamping first, then stopping infusion, positive infusion feature if more than 2 minutes is required for pressure is established. blood sampling. 9. PERFORM hand hygiene. DON non-sterile gloves. Routine infection control practices. 10. REMOVE IV tubing and attach sterile dead-end cap to open end to keep covered. SCRUB the needleless connector for 30 seconds with a CV.03.05 Published Date: 02-Nov-2018 Page 2 of 6 Review Date: 02-Nov-2021 This is a controlled document for BCCH& BCW internal use only – see Disclaimer at the end of the document. Refer to online version as the print copy may not be current. BLOOD SAMPLING FROM CENTRAL VENOUS LINES: VACUTAINER METHOD DOCUMENT TYPE: PROCEDURE chlorhexidine/alcohol wipe. Allow to dry for 1 minute. OR REMOVE Swabcap™ and proceed to next 11. INSERT vacutainer into needleless connector. 12. UNCLAMP catheter and PRESS discard red-top Removes solution from catheter to ensure tube onto vacutainer needle. If experiencing difficulty uncontaminated blood specimen. with blood sampling from other central venous lines refer to Management of a Non-Functioning Central Venous Lines – Policy Ensure appropriate amount of blood for discard: TYPE OF CVL AMOUNT OF DISCARD Cuffed CVC < 10 kgs 1.5 mL Cuffed CVC > 10 kgs 3 mL Short-term CVC 1.5 mL Implanted Port 3 mL PICC and cuffed PICC <10 kg 1.5 mL PICC and cuffed PICC >10 kg 3 mL Hemodialysis/Apheresis 3 mL NOTE: Discard blood can be used in blood culture collection sample if CVL is not ethanol or antibiotic “locked”. May then place culture bottle directly on vacutainer to collect sample and omit discard. 13. CLAMP catheter. REMOVE discard blood tube and DISCARD. 14. PRESS sample blood tubes on to vacutainer To obtain total amount for transferring to needle in the following order: appropriate tubes. blood cultures Na Citrate blue top (coagulation studies) red top heparin green top (chemistries) EDTA tube lavender top (hematology, transfusion medicine) grey top other tubes as required… UNCLAMP catheter and allow each tube to fill up with adequate amount of blood required for lab test. Refer to online eLab handbook for required amounts of blood 15. MIX each tube immediately after drawing blood into Ensures blood cells are mixed with additives in it. GENTLY invert each tube 10 times. the tubes. Do not shake or will cause cell lysis. 16. CLAMP catheter and remove vacutainer. 17. ATTACH normal saline syringe onto needleless Creates positive pressure to maintain connector catheter patency. UNCLAMP catheter and with thumb on plunger of syringe and other hand on clamp, Two quick pushes creates turbulent flow to clear CV.03.05 Published Date: 02-Nov-2018 Page 3 of 6 Review Date: 02-Nov-2021 This is a controlled document for BCCH& BCW internal use only – see Disclaimer at the end of the document. Refer to online version as the print copy may not be current. BLOOD SAMPLING FROM CENTRAL VENOUS LINES: VACUTAINER METHOD DOCUMENT TYPE: PROCEDURE give two quick pushes, then with continuous catheter and help maintain patency. motion, FLUSH into cap and catheter with remaining normal saline: Type of CVL Saline Flush Cuffed CVC < 10 kgs 3 mL Cuffed CVC > 10 kgs 9 mL Short-term CVC 3 mL Implanted Port 18 mL (use 2 x 10 mL) PICC and cuffed PICC < 10 kgs 3 mL PICC and cuffed PICC > 10 kgs 9 mL Hemodialysis/Apheresis 9 mL 18. RECONNECT infusion set and commence infusion Resumes therapy as ordered. or heparin lock line as ordered. - If second lumen is in use, UNCLAMP second lumen and RECOMMENCE infusion. 19. LABEL specimen tubes at the patient's bedside. Safe blood sampling and transfusion practices. Label must include MRN, first and last name, date of Refer to Transfusion medicine manual. birth, date and time sample drawn and RN initials. May use computerized or addressograph labels if available, except for Group & Screen and Crossmatch.* NOTE *Group & Screen and Crossmatch collection procedure: National Standards for safe transfusion practice require specimen labeling at the bedside Confirm patient identification - name, DOB, MRN on patient ID band matches with the requisition. Resolve any discrepancies prior to collection When possible, ask patient his/her name and DOB Specimen MUST be hand labeled at bedside only by the person who collected the specimen Computer generated labels are not to be used Label must contain patient name, DOB, MRN, date and time of collection and RN initials Sign requisition and record date and time of collection. Signing requisition confirms you have correctly identified the patient. 20. COMPLETE appropriate laboratory requisitions indicating the site where blood sample was obtained, RN initials, and date and time. On the transfusion medicine requisition: sign, date and time the CV.03.05 Published Date: 02-Nov-2018 Page 4 of 6 Review Date: 02-Nov-2021 This is a controlled document for BCCH& BCW internal use only – see Disclaimer at the end of the document. Refer to online version as the print copy may not be current. BLOOD SAMPLING FROM CENTRAL VENOUS LINES: VACUTAINER METHOD DOCUMENT TYPE: PROCEDURE requisition in the appropriate space. Your signature MUST include full last name, and first name or first initial.
Recommended publications
  • The Costs and Benefits of Moving to the ICD-10 Code Sets
    CHILDREN AND ADOLESCENTS This PDF document was made available from www.rand.org as a public CIVIL JUSTICE service of the RAND Corporation. EDUCATION ENERGY AND ENVIRONMENT Jump down to document HEALTH AND HEALTH CARE 6 INTERNATIONAL AFFAIRS POPULATION AND AGING The RAND Corporation is a nonprofit research PUBLIC SAFETY SCIENCE AND TECHNOLOGY organization providing objective analysis and effective SUBSTANCE ABUSE solutions that address the challenges facing the public TERRORISM AND HOMELAND SECURITY and private sectors around the world. TRANSPORTATION AND INFRASTRUCTURE U.S. NATIONAL SECURITY Support RAND Purchase this document Browse Books & Publications Make a charitable contribution For More Information Visit RAND at www.rand.org Explore RAND Science and Technology View document details Limited Electronic Distribution Rights This document and trademark(s) contained herein are protected by law as indicated in a notice appearing later in this work. This electronic representation of RAND intellectual property is provided for non-commercial use only. Permission is required from RAND to reproduce, or reuse in another form, any of our research documents for commercial use. This product is part of the RAND Corporation technical report series. Reports may include research findings on a specific topic that is limited in scope; present discus- sions of the methodology employed in research; provide literature reviews, survey instruments, modeling exercises, guidelines for practitioners and research profes- sionals, and supporting documentation;
    [Show full text]
  • Methods and Apparatus for Sampling and Analyzing Body Fluid
    Europäisches Patentamt *EP001579814A2* (19) European Patent Office Office européen des brevets (11) EP 1 579 814 A2 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.7: A61B 17/32 28.09.2005 Bulletin 2005/39 (21) Application number: 05005734.8 (22) Date of filing: 16.05.1997 (84) Designated Contracting States: (72) Inventors: AT BE CH DE DK ES FI FR GB GR IE IT LI LU MC • Douglas, Joel S. NL PT SE Los Altos Hills, CA 94022 (US) • Roe, Jeffrey N. (30) Priority: 17.05.1996 US 17133 P San Ramon, CA 94583 (US) 14.06.1996 US 19918 P • Radwanski, Ryszard 01.08.1996 US 23658 P Morgan Hill, CA 95037 (US) 03.09.1996 US 25340 P • Duchon, Brent G. 16.09.1996 US 714548 Garden Grove, CA 92845 (US) 17.09.1996 US 710456 08.10.1996 US 727074 (74) Representative: Vossius & Partner Siebertstrasse 4 (62) Document number(s) of the earlier application(s) in 81675 München (DE) accordance with Art. 76 EPC: 97929682.9 / 0 955 909 Remarks: This application was filed on 16 - 03 - 2005 as a (71) Applicant: Roche Diagnostics Operations, Inc. divisional application to the application mentioned Indianapolis, Indiana 46250 (US) under INID code 62. (54) Methods and apparatus for sampling and analyzing body fluid (57) A sampling device (10) for sampling body fluid includes a lancet (12) for making an incision, a capillary tube (18) for drawing up body fluid from the incision, and a test strip (30) affixed to an upper end of the capillary tube (18) for receiving the fluid.
    [Show full text]
  • Fluid Bodies: an Overview Evanjali Pradhan * *Department of Microbiology, Utkal University, India
    OPEN ACCESS Freely available online e a Journal of ISSN: 2168-9873 Applied Mechanical Engineering Editorial Fluid Bodies: An Overview Evanjali Pradhan * *Department of Microbiology, Utkal University, India EDITORIAL Arterial blood sampling, such as radial artery puncture Body fluids, also known as bodily fluids or biofluids, are the liquids Osmosis is a mechanism in which water travels from one that make up the human body. Total body water makes up about compartment of the body to another via semi-permeable cell 60% (60–67%) of the total body weight in lean, stable adult men; it membranes. Osmosis is the diffusion of water over a semi- is slightly lower in women. The amount of body fat is inversely permeable membrane from regions of higher concentration to proportional to the same percentage of fluid compared to body regions of lower concentration along an osmotic gradient. As a weight. For example, a lean 70 kg (160 pound) man has around 42 result, depending on the relative amounts of water and solutes (42-47) litres of water. present in cells and tissues, water can flow into and out of them. Health To ensure normal operation, a proper balance of solutes within and outside of cells must be maintained. Water makes up about The word "body fluid" is most widely used in medical and health 75 percent of the body mass in children, 50–60 percent in adult contexts. Body fluids are known as inherently unclean in current men and women, and as little as 45 percent in the elderly. Since medical, public health, and personal hygiene practises.
    [Show full text]
  • Labinvest201230.Pdf
    ANNUAL MEETING ABSTRACTS 81A found between the number of positive biopsies and mortality. Only 6 of 42 diffuse 329 Pathological Features of Adventitial infl ammatory Reaction in C4d+ cases evolved to show DSA and dysfunction. Thirty six of 42 diffuse C4d+ cases Acute Aortic Dissections showed no dysfunction, despite the presence of DSA in 6 of them. Thus interpreted LF Xu, C Miller, AP Burke. University of Maryland Medical Center, Baltimore, MD. as accommodation. Background: Histological reaction in the adventitia to aortic dissections has not been Conclusions: Serial staining of biopsies shows that: 1. Concomitant C4d and C3d well studied. We present histological fi ndings in a series of acute aortic dissections with positivity correlates highly with allograft dysfunction and DSA; 2. Diffuse C4d capillary emphasis regarding dating and infl ammatory reaction. staining alone should not be equated with AMR; 3. Most C4d+ episodes are single Design: We prospectively studied 43 surgically excised acute ascending aortic occurrences and asymptomatic; 4. The presence of C4d staining and DSA without dissections. We evaluated the histological reaction in the media and adventitia adjacent allograft dysfunction may indicate accommodation; 5. Only a small fraction of patients to the acute dissection plane in 4 or more sections of aorta oriented perpendicularly. with C4d staining alone may develop AMR on follow-up. Infl ammation (both degree and type) and stromal reaction were semiquantitated and correlated with duration of symptoms prior to surgical repair. 327 Carbonic Anhydrase IX – Hypoxia Marker in the Aortic Wall Results: Of the 43 cases, there were 31 men (ages 53 ± 14 years) and 13 women (ages Y Sheykin, S Rosen.
    [Show full text]
  • High Five for Safe Arterial Blood Gas Sampling
    High Five for safe arterial blood gas sampling 1. Carraro P et al. Errors in a stat laboratory: Types and frequencies 10 years later. Clin Chem 2007; 53,7: 1338-42. Agenda . Introduction . Why the preanalytical phase is important . High Five for safe arterial blood gas sampling . Additional educational resources The preanalytical phase of arterial blood gas sampling Preanalytical errors are said “Several aspects of blood pH and to be the reason for up to gas analysis are unique among 62% of all errors in clinical and laboratory determinations, and, at the same laboratory medicine [1]. time, no other test results have more immediate impact on Error rate patient care” [2] Preanalytical phase 62% CLSI Analytical phase 15% Post-analytical phase 23% 1. Carraro P et al. Errors in a stat laboratory: Types and frequencies 10 years later. Clin Chem 2007; 53,7: 1338-42. 2. CLSI. Blood Gas and pH Analysis and Related Measurements; Approved Guideline – Second Edition. CLSI Document C46-A2. Wayne, PA: Clinical and Laboratory Standards Institute: 2009. 3. www.clsi.org. Safe arterial blood gas sampling: Path of workflow [1,2]: 1. Patient preparation – FOCUS ON: patient safety 2. Blood collection device FOCUS ON: sample integrity and operator safety 3. Sample collection FOCUS ON: safety for patient and operator 4. Sample handling FOCUS ON: sample integrity 5. Sample transport FOCUS ON: time to patient results 1. Clinical and Laboratory Standards Institute (CLSI). Procedures for the Collection of Arterial Blood Specimens; Approved Standard-Fourth Edition. H11-A4. Vol. 24 No. 28 [ISBN 1-56238-427-9]. Clinical and Laboratory Standards Institute, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 19087-1898, USA.
    [Show full text]
  • Phlebotomy Guidelines and Order of Draw
    165 Ashley Ave., Room 318 Charleston, SC 29425 Phone (843) 792-0707 Fax (843) 792-4896 Phlebotomy Guidelines and Order of Draw Specimen Collection Procedures The purpose of the document is to share the standard criteria for venous blood collection for medical laboratory testing. Proper specimen collection and handling is a critical part of obtaining a valid laboratory result. Specimens must be collected in the appropriate collection container, kit or device, correctly labeled and transported promptly to the laboratory. Staff responsible for sample collection should follow essential safeguards to ensure accurate testing and to provide quality patient care. 1. Always check patient identification band and compare to the name on the requisition and the specimen labels. Label specimens immediately following collection. Labels must be rechecked before sending to the lab. 2. Deliver specimens to the laboratory as soon after collection as possible. Certain analytes are unstable and testing should occur as soon after collection as possible to insure valid measurements. 3. Special Collection Procedures: o When obtaining a blood specimen from a catheter, the components of the blood collection system (catheter, luer lock, syringe, needle, and collection device) should be checked to ensure compatibility to avoid air leaks which may cause hemolysis and incorrect draw volumes. o Collection of the blood through lines that have been previously flushed with heparin should be avoided, if possible. o If the blood must be drawn through an indwelling catheter, possible heparin contamination and specimen dilution should be considered. The line should be flushed with 5 ml of saline and the first 5 ml of blood or six dead space volumes of the catheter discarded.
    [Show full text]
  • Methods Series Report #2016-02
    HCUP Methods Series Contact Information: Healthcare Cost and Utilization Project (HCUP) Agency for Healthcare Research and Quality 5600 Fishers Lane Room 07W17B Mail Stop 7W25B Rockville, MD 20857 http://www.hcup-us.ahrq.gov For Technical Assistance with HCUP Products: Email: [email protected] or Phone: 1-866-290-HCUP Recommended Citation: Gibson T, Casto A, Young J, Karnell L, Coenen N. Impact of ICD-10- CM/PCS on Research Using Administrative Databases. HCUP Methods Series Report # 2016- 02 ONLINE. July 25, 2016. U.S. Agency for Healthcare Research and Quality. Available: http://www.hcup-us.ahrq.gov/reports/methods/methods.jsp. TABLE OF CONTENTS 1. EXECUTIVE SUMMARY ..................................................................................................... I 2. INTRODUCTION ................................................................................................................ 1 3. DIFFERENCES BETWEEN ICD-9-CM AND ICD-10-CM/PCS CODING SYSTEMS ........... 4 Diagnosis Coding Systems ............................................................................................. 4 Procedure Coding Systems ............................................................................................ 7 Focus Areas in the Medical and Surgical Section: Root Operations and Approaches ....10 4. LESSONS FROM DUALLY CODED DATA ........................................................................14 Differences in the ICD-9-CM and ICD-10-CM/PCS Coding Systems .............................14 Changes in Coding Rules ..............................................................................................15
    [Show full text]
  • Laboratory-General Specimen Collection and Handling Guidelines
    Laboratory-General Specimen Collection and Handling Guidelines Contents: Microbiology continued. Orders/Requests Stool Patient Preparation Throat or Pharynx Specimen Containers Tuberculosis (TB) Specimen Quality Urine Order of Draw Viral Specimen Transport VRE Surveillance (Vancomycin- Resistant entercoccus) Specimen Rejection Wound General Lab Sample/Source: Whole Blood Cytology (Cytopathology) Plasma Aspiration, Fine Needle Serum Aspiration, Cyst Fluids Urine Submission of slide Fecal (Stool) Tips on making smears Body Fluid Body Cavity Fluids Cerebrospinal Spinal Fluid Breast Nipple Secretions Synovial Fluid Brushing Specimens Microbiology Cerebrospinal Fluid (CSF) Sample/Source: Ectocervix, Endocervical canal, Vaginal pool Abscess (Deep aspirate) Pap Smear, Conventional Abscess (superficial swab) Pap Smear, Liquid Base Acid Fast Bacillus (AFB) Sputum Specimens Anaerobic Surface Scrape Specimen (Tzanck Smear) Aspirate, drainage, cyst fluid, or pustule Vaginal Wall (Maturation Index) Biopsy, Bone, Tissue Washing Specimens Blood (Adult) Histology (Anatomic Pathology) Blood )Pediatric Routine Submission Blood for Acid Fast Bacillus (AFB) Fresh Specimen Body Fluids Surgical Specimen and Microbiology test(s) Bronchial Washing Lavage Breast Tissue Catheter Tip Brushing Specimens C. difficile Toxin B Bronchial Washing and Brushings Chlamydia/Gonorrhea Amplified Detection Muscle Biopsy Crytococcal Antigen Renal Biopsy (Kidney) Cerebral Spinal Fluid (CSF) Renal calculi (Kidney/Bladder Stones) Ear (outer) Bone Marrow Ear (inner) Cytogenics Eye
    [Show full text]
  • Agenda ICD-9-CM Coordination and Maintenance Committee
    CMS WILL NO LONGER BE PROVIDING PAPER COPIES OF HANDOUTS FOR THE MEETING. ELECTRONIC COPIES OF ALL MEETING MATERIALS WILL BE POSTED ON THE CMS WEBSITE PRIOR TO THE MEETING AT HTTP://WWW.CMS.HHS.GOV/ICD9PROVIDERDIAGNOSTICCODES/03_MEETINGS.ASP DEPARTMENT OF HEALTH & HUMAN SERVICES Centers for Medicare & Medicaid Services 7500 Security Boulevard Baltimore, Maryland 21244-1850 Agenda ICD-9-CM Coordination and Maintenance Committee Department of Health and Human Services Centers for Medicare & Medicaid Services CMS Auditorium 7500 Security Boulevard Baltimore, MD 21244-1850 ICD-9-CM Volume 3, Procedures March 9 – March 10, 2011 Pat Brooks – Introductions and Committee overview Co-Chairperson March 9, 2011 9:00 AM – 5:30 PM ICD-9-CM Volume 3, Procedure presentations and public comments Phone lines are available for participants who are unable to attend in person and who want to listen to the proceedings. Participants on the phone lines will be in “listen only” mode and will not be able to ask questions or provide comments. Phone participants should send any procedure code comments in writing to [email protected] by April 1, 2011, the deadline for comments. We will not be posting an audio or written transcript of this meeting. 1 External participants dial: 1-877-267-1577 Meeting ID: 9141 ICD-9-CM Topics 1. Cardiac Valve Replacement: Transcatheter Aortic. Ann B. Fagan Transapical Aortic, and Pulmonary Craig R. Smith, MD Pages 9-12 NY-Presbyterian Hospital Doff B. McElhinney, MD Dept. of Cardiology; Children‟s Hospital, Boston, MA 2. PTCA/Atherectomy: Proposed revision of code 00.66 Ann B.
    [Show full text]
  • Cytology Sample Collection and Preparation for Veterinary Practitioners Dr Brett Stone and Dr George Reppas
    Cytology Sample Collection and Preparation for Veterinary Practitioners Dr Brett Stone and Dr George Reppas Since the mid 1960s, when the first reports of cytology appeared in the veterinary literature, cytology has become an extremely useful diagnostic aid in veterinary medicine. Cytology has many advantages over histopathology: • Cytology samples can be easily obtained pre-operatively, often without general anaesthesia and sometimes even without sedation, and can be used to screen patients for more comprehensive diagnosis. • Fine needle aspiration cytology is less costly than surgical biopsy in both sample collection and laboratory analysis. • The fine needle aspiration procedure is less likely to result in adverse effects when compared to tissue biopsy. • Because less sample processing is required, cytology results are available sooner than histopathology results. • ‘Quick’ checking for recurrence of local malignancies or regional lymph node metastases. • Pathologic micro-organisms involved in microbial infections of various organs (e.g., canine and feline leprosy, subcutaneous mycoses, bacterial prostatitis) diagnosed initially by cytology have a greater chance of being cultured successfully. • Techniques are being developed whereby the aspiration of neoplastic lymphoid cells from suspected malignant lymphomas can be immunocytochemically phenotyped into T & B cell populations either directly from FNA smears of lymph nodes or via flow cytometry - thereby avoiding costly and sometimes contraindicated general anaesthesia to perform an incisional/excisional surgical biopsy. • Cytology aspiration of particularly ‘hard to get to’ organs (e.g., pancreas, heart base), can be successfully sampled with the use of ultrasound guided techniques. However, cytology also has its limitations. As the cells/material being evaluated are ‘outside’ their normal environment, an assessment of cellular organisation, arrangement or architecture is often not possible by cytology.
    [Show full text]
  • A Percutaneous Needle Biopsy Technique for Sampling the Supraclavicular Brown Adipose Tissue Depot of Humans
    International Journal of Obesity (2015) 39, 1561–1564 © 2015 Macmillan Publishers Limited All rights reserved 0307-0565/15 www.nature.com/ijo SHORT COMMUNICATION A percutaneous needle biopsy technique for sampling the supraclavicular brown adipose tissue depot of humans M Chondronikola1,2,3,4,11, P Annamalai5,11, T Chao2,3, C Porter1,6, MK Saraf1,6, F Cesani7 and LS Sidossis1,3,4,6,8,9,10 Brown adipose tissue (BAT) has been proposed as a potential target tissue against obesity and its related metabolic complications. Although the molecular and functional characteristics of BAT have been intensively studied in rodents, only a few studies have used human BAT specimens due to the difficulty of sampling human BAT deposits. We established a novel positron emission tomography and computed tomography-guided Bergström needle biopsy technique to acquire human BAT specimens from the supraclavicular area in human subjects. Forty-three biopsies were performed on 23 participants. The procedure was tolerated well by the majority of participants. No major complications were noted. Numbness (9.6%) and hematoma (2.3%) were the two minor complications noted, which fully resolved. Thus, the proposed biopsy technique can be considered safe with only minimal risk of adverse events. Adoption of the proposed method is expected to increase the sampling of the supraclavicular BAT depot for research purposes so as to augment the scientific knowledge of the biology of human BAT. International Journal of Obesity (2015) 39, 1561–1564; doi:10.1038/ijo.2015.76 INTRODUCTION participants in accordance with the Declaration of Helsinki. The The recent re-discovery of human brown adipose tissue (BAT)1–4 Institutional Review Board and the Institute for Translational has triggered intense scientific interest in the potential of this Science Scientific Review Committee at the University of Texas tissue as a target against obesity and its metabolic abnormalities.
    [Show full text]
  • WHO Guidelines on Drawing Blood Best Practices in Phlebotomy (Eng)
    WHO guidelines on drawing blood: best practices in phlebotomy WHO Library Cataloguing-in-Publication Data WHO guidelines on drawing blood: best practices in phlebotomy. 1.Bloodletting – standards. 2.Phlebotomy – standards. 3.Needlestick injuries – prevention and control. 4.Guidelines. I.World Health Organization. ISBN 978 92 4 159922 1 (NLM classification: WB 381) © World Health Organization 2010 All rights reserved. Publications of the World Health Organization can be obtained from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected]). Requests for permission to reproduce or translate WHO publications – whether for sale or for noncommercial distribution – should be addressed to WHO Press, at the above address (fax: +41 22 791 4806; e-mail: [email protected]). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. All reasonable precautions have been taken by the World Health Organization to verify the information contained in this publication.
    [Show full text]