Screening Donated Blood for Transfusion- Transmissible Infections
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Transfusion Service Introduction Blood/Blood Products Requests and Turnaround Time Expectations
Transfusion Service Introduction All blood products and blood components are supplied to UnityPoint Health-Meriter Hospital by the American Red Cross Blood Services. Pathology consultation is available regarding blood and/or components and dosages. ABO and Rho(D)—specific type is used whenever possible for leuko-poor packed cell transfusions. ABO-compatible blood is used for all plasma and platelet components whenever possible. For any orders involving HLA-matched components, the patient must have been HLA typed (sent to the American Red Cross) a minimum of 48 hours prior to intended infusion of the component. HLA typing is only required once. Blood components that are thawed, pooled, washed, volume-reduced, or deglycerolized for a patient will be charged to the patient even if not transfused. The charge is done because these components may not be suitable for another patient. Examples include: Autologous or directed donations Pooled cryoprecipitate 4-hour expiration Thawed fresh frozen plasma 24-hour expiration Thawed cryoprecipitate 6-hour expiration Deglycerolized red cells 24-hour expiration Washed red cells 24-hour expiration All blood components must be completely infused within 4 hours of release from UnityPoint Health-Meriter Laboratories Blood Bank, or be infused within the expiration time. Refer to UnityPoint Health -Meriter’s Blood and Blood Products Transfusion Policy #123 for additional information located on MyMeriter. Blood/Blood Products Requests and Turnaround Time Expectations Requests from UnityPoint Health-Meriter Hospital are entered in the hospital computer system and print in the UnityPoint Health- Meriter Laboratories Blood Bank. For the comfort of the patient, it is important to coordinate collection for other tests with Blood Bank specimens. -
STI Screening Timetable
Patient Education Information from University Health Center’s STI Screening Clinic Page 1 of 1 STI Screening Timetable How long until STI (sexually transmitted infection) screening tests turn positive? How long until STI symptoms might show up? The time between infection and a positive test, or between infection and symptoms, is variable and depends on many factors, including the behavior of the infectious agent, how and where the body is infected, and the state of a person’s immune system and personal health. Many STIs don’t have any symptoms. The incubation period times listed in the chart below are averages only. If you have further questions or concerns, you can schedule an appointment with a clinician at 541-346-2770. STI screening test Window period (time from exposure until Incubation period (time between exposure and screening test turns positive) when symptoms appear) Chlamydia (urine specimen or swab of 1 week most of the time Often no symptoms vagina, rectum, throat) 2 weeks catches almost all 1-3 weeks on average Gonorrhea (urine specimen on swab of 1 week most of the time Often no symptoms, especially vaginal vagina, rectum, throat) 2 weeks catches almost all infections usually within 2-8 days but can be up to 2 weeks Syphilis (blood test, RPR) 1 month catches most Often symptoms too mild to notice 3 months catches almost all 10-90 days average 21 days HIV (oral cheek swab) 1 month catches most Sometimes mild body aches and fever within 1-2 3 months catches almost all weeks then can be months to years HIV (blood test, antigen/antibody -
Hepatitis B and C Testing: Why? Who? How? a Guidance Paper on Testing in Community and Harm Reduction Settings 1 Colophon
Hepatitis B and C testing: why? who? how? A guidance paper on testing in community and harm reduction settings 1 Colophon This paper is a product of the Correlation Hepatitis C Initiative. You can access the paper at www.hepatitis-c-initiative.eu Author: Danny Morris Review: M. Harris, A. Kautz, A. Leicht, H. Lochtenberg, E. Schatz Copyright © 2016 Copyrights remains with the publisher Correlation Network PO Box 10887 1001 EW Amsterdam The Netherlands Phone.: +31 20 5317600 Fax.: +31 20 4203528 [email protected] Correlation Network is a part of the international activities of the Regenboog Groep. For more information: www.deregenboog.org The production of this paper has been supported by an unrestricted grant from Gilead Sciences Europe Ltd 2 Acknowledgements We want to thank the author Danny Morris and all who helped to draft this paper and the Regenboog Group, Abbvie and GILEAD for their financial support of the Hepatitis C Initiative. Eberhard Schatz Correlation Hepatitis C Initiative Amsterdam, December 2016 “The Hepatitis C Initiative aims to enhance the momentum of current HCV treatment opportunities and strives for universal access to essential HCV prevention and treatment for the most affected and under-served communities: people who use drugs.” 3 Content Chapter 1: Introduction 6 1.1 Hepatitis B and C infect one in fifty adults in the European Region 9 1.2 Higher rates of hepatitis among vulnerable groups 9 1.3 A public health approach to hepatitis 9 1.4 Harm reduction as prevention 10 1.5 Diagnosing hepatitis B and C 10 1.6 Awareness raising - key recommendations 11 1.7 Testing and diagnosis - key recommendations 13 Chapter 2: Who should be tested 14 2.1 Barriers to testing 16 2.2 Barriers to testing and treatment may include 16 2.3 Overcoming barriers to testing 17 2.4 Testing as standard practice 18 2.5 Pre and post-test discussion 18 2.6 Serological testing for viral hepatitis 20 4 Chapter 3: Screening technologies and development of non-invasive techniques 22 3.1 Venapuncture 23 3.2 Dried blood spot testing 24 3.3. -
Fresh Frozen Plasma in General Practice
Practical guide to using frozen and fresh frozen plasma in general practice Why every practice should keep a bag in the freezer Kit Sturgess; MA; VetMB; PhD; CertVR; DSAM; CertVC; FRCVS RCVS Recognised Specialist in Small Animal Medicine Advanced Practitioner in Veterinary Cardiology Introduction Keeping stock at reasonable levels in a practice is vital to good business management balancing the need to have a product available against the costs of keeping stock that is not used and potentially may go out of date and need to be replaced (as well as subtle small costs of space, stock taking, disposal of out-of-date product etc.). Practices need, therefore, to make decisions about preparedness for ‘what if’ scenarios and have protocols in place. The difficult question for many practices is how bizarre/uncommon should these scenarios be to warrant keeping a drug or treatment in stock or buying a specialist piece of equipment. This can only really be answered on an individual practice basis as it will depend on the type of cases seen as well as the likely ability of clients to want to pay if the treatment/investigation is expensive and the relationship with other local practices in terms of borrowing treatments or using equipment. It is also important to try and understand the value that a particular drug or treatment will have on morbidity and mortality of a particular condition and whether the patient could be referred onwards if necessary so not having calcium available if presented with a seizuring hypocalcaemic patient would be a significant issue in that patient’s care. -
Donor Testing and Risk: Current Prevalence, Incidence, and Residual Risk of Transfusion-Transmissible Agents in US Allogeneic Donations
Donor Testing and Risk: Current Prevalence, Incidence, and Residual Risk of Transfusion-Transmissible Agents in US Allogeneic Donations Shimian Zou, Susan L. Stramer, and Roger Y. Dodd Over the past 20 years, there has been a major increase virus (HIV) and human T-cell lymphotropic virus did in the safety of the blood supply, as demonstrated by not. The incidence (/100 000 person-years) of HIV and declining rates of posttransfusion infection and reduc- HCV among repeat donors showed apparent increases tions in estimated residual risk for such infections. from 1.55 and 1.89 in 2000 through 2001 to 2.16 Reliable estimates of residual risk have been possible and 2.98 in 2007 through 2008. These observed within the American Red Cross system because of the fluctuations confirm the need for continuous monitor- availability of a large amount of reliable and consistent ing and evaluation. The residual risk of HIV, HCV, and data on donations and infectious disease testing human T-cell lymphotropic virus among all allogeneic results. Among allogeneic blood donations, the pre- donations is currently below 1 per 1 million donations, valence rates of infection markers for hepatitis C virus and that of hepatitis B surface antigen is close to 1 per (HCV) and hepatitis B virus have decreased over time, 300 000 donations. although rates for markers of human immunodeficiency © 2012 Elsevier Inc. All rights reserved. HE BLOOD SUPPLY in the United States DEMOGRAPHY OF DONOR POPULATIONS T and many other countries has become safer In 2008, a total of 3 830 094 volunteer blood than ever, thanks to continuing improvements in donors successfully made 6 638 877 blood dona- donor selection and testing, along with broad tions to ARC Blood Services, with whole blood and improvements in public health. -
Sexually Transmitted Infection Prevention and Treatment
Sexually Transmitted Infection Prevention and Treatment Kevin L. Ard, MD, MPH Massachusetts General Hospital, The Fenway Institute Disclosures I have no financial disclosures. Doxycycline PEP is not FDA-approved. Learning objectives 1. Describe the epidemiology of syphilis, chlamydia, gonorrhea, and other STIs among LGBTQ populations 2. Summarize optimal screening strategies for STIs. 3. Outline approaches to STI control that can be integrated into primary care. 3 Caveats ▪ Many (most?) LGBTQ people do not face a high risk of STIs. ▪ Clinical care must be individualized, not based on group risk. ▪ Data about STIs among cisgender WSW are limited. ▪ Terms that describe identity and behavior are imperfect and change over time. The rate of chlamydia diagnosis is increasing. Sexually Transmitted Disease Surveillance 2017, CDC Proportion of STI clinic patients testing positive for chlamydia Sexually Transmitted Disease Surveillance 2017, CDC The rate of gonorrhea diagnosis is increasing. Sexually Transmitted Disease Surveillance 2017, CDC MSM face an increasing disparity in the rate of gonorrhea. Sexually Transmitted Disease Surveillance 2017, CDC Antimicrobial resistance in gonorrhea is increasing. Resistanc e Elevated MICs Centers for Disease Control and Prevention. Sexually Transmitted Disease Surveillance 2017. Atlanta: U.S. Department of Health and Human Services; 2018. Neisseria gonorrhoeae — Percentage of Urethral Isolates with Elevated Azithromycin Minimum Inhibitory Concentrations (MICs) (≥2.0 µg/ml) and Elevated Ceftriaxone MICs (≥0.125 μg/ml) by Reported Sex of Sex Partners, Gonococcal Isolate Surveillance Project (GISP), 2011–2017 A. Azithromycin B. Ceftriaxone * No cases of elevated ceftriaxone MICs were reported among MSM in 2017. ACRONYMS: MSM = Gay, bisexual, and other men who have sex with men (collectively referred to as MSM); MSW = Men who have sex with women only. -
Blood Banking/Transfusion Medicine Fellowship Program
DEPARTMENT OF PATHOLOGY AND LABORATORY MEDICINE BLOOD BANKING/TRANSFUSION MEDICINE FELLOWSHIP PROGRAM THIS NEW ONE-YEAR ACGME-ACCREDITED FELLOWSHIP IN BLOOD BANKING/TRANSFUSION MEDICINE OFFERS STATE OF THE ART COMPREHENSIVE TRAINING IN BLOOD BANKING, COAGULATION, APHERESIS, AND HEMOTHERAPY AT THE MEMORIAL HERMANN HOSPITAL (MHH)-TEXAS MEDICAL CENTER (TMC) FOR PEDIATRICS AND ADULTS. This clinically-oriented fellowship is ideal for the candidate looking for exceptional experience in hemotherapy decision-making and coagulation consultation. We have a full spectrum of medical and surgical specialties, including a level 1 trauma center, as well as a busy solid organ transplant service (renal, liver, pancreas, cardiac, and lung). Fellows will rotate through: Our unique hemotherapy service: This innovative clinical consultative service for the Heart and Vascular Institute (HVI) allows fellows to serve as interventional blood banking consultants at the bed side as part of a multidisciplinary care team; our patients have complex bleeding and coagulopathy issues. Therapeutic apheresis service: This consultative service provide 24/7 direct patient care covering therapeutic plasmapheresis, red blood cell (RBC) exchanges, photopheresis, plateletpheresis, leukoreduction, therapeutic phlebotomies, and other related procedures on an inpatient and outpatient basis. We performed approximately over 1000 therapeutic plasma exchanges and RBC exchanges every year. Bloodbank: The MHH-TMC reference lab is one of the largest in Southeast Texas. This rotation provides extensive experience in interpreting antibody panel reports, working up transfusion reactions, investigating blood compatibility/incompatibility issues, and monitoring component usage. Gulf Coast Regional Blood Center: This rotation provides donor exposure in one of the largest community blood donation centers in the US as well as cellular therapy and immunohematology training. -
Transfusion Medicine/Blood Banking
Transfusion Medicine/Blood Banking REQUIRED rotation This is a onetime rotation and is not planned by PGY level. Objective: The objective of this rotation is to teach fellows the clinical and laboratory aspects of Transfusion Medicine and Blood Banking as it impacts hematology/oncology. Goals: The goal of this rotation is to teach fellows blood ordering practices, the difference of type and screen and type and cross matches and selection of appropriate products for transfusion. Fellows will also learn to perform, watch type and screen red cell antibodies and will learn the significance of ABO, Rh and other blood group antigen systems briefly so as to understand the significance of red cell antibodies in transfusion practices. Fellows will learn the different types of Blood components, their indications and contraindications and component modification. e.g. Irradiated and washed products, and special product request and transfusions e.g. granulocyte transfusion, CMV negative products etc. Fellows will learn and become proficient in the laboratory aspects of autoimmune hemolytic anemia, coagulopathies and bleeding disorders in relation to massive transfusions and the laboratory aspects and management of platelet refractoriness. Fellows will learn some aspects of coagulation factor replacement for factor deficiencies and inhibitors. Activities: Fellows will rotate in the Blood Bank at UMC and learn to perform, observe and interpret standard blood bank procedures such as ABO Rh typing, Antibody Screen, Antibody Identification and Direct Antiglobulin Test (DAT). Fellows will also watch platelet cross matching for platelet refractoriness. Fellows will attend and present a few didactic lectures of about 40 minutes on Blood Bank related topics as they apply to hematology/oncology like blood group antigens, Blood Component therapy, Transfusion reactions, Autoimmune hemolytic anemia, Platelet immunology and HLA as it applies to transfusion medicine. -
Current Practice in Transfusion Medicine April 2019
CURRENT PRACTICE IN TRANSFUSION MEDICINE APRIL 2019 Faculty/Speakers Luzmary Alverez Suzanne A. Arinsburg, DO Assistant Director, Blood Bank and Transfusion Services - Mount Sinai Hospital; Assistant Professor of Pathology - Icahn School of Medicine at Mount Sinai Scott Avecilla, MD, PhD Medical Director of Cellular Therapy and Assistant Medical Director of Transfusion Medicine, Department of Laboratory Medicine - Memorial Sloan Kettering Cancer Center Ian Bain, MD, PhD Ian received his medical training and PhD at the Albert Einstein College of Medicine in the Bronx, with his research work focusing on the transcriptional mechanisms underlying anergy in natural Regulatory T cells. He completed his training in Clinical Pathology, as well as subspecialty training in Molecular Genetic Pathology. Currently is a fellow in Transfusion Medicine and Apheresis at Yale-New Haven. He will be transitioning to a role as an Assistant Professor in the Department of Pathology at Mt Sinai Hospital/Icahn School of Medicine with a focus on transfusion medicine, apheresis and cell therapy. His academic interests center around mechanisms and sources of red cell alloimmunization, as well as the impact of novel immmunotherapies on autoantibody formation. Anna Burgos, MT(ASCP) SBB Senior Immunohematologist, Laboratory of Immunohematology and Genomics – New York Blood Center Carmelita Carrier, PhD Director, Fred H. Allen Laboratory of Immunogenetics, New York Blood Center Connie Cai Immunohematology, New York Blood Center Stephanie Dormesy Manager-Apheresis & -
FACTS ABOUT DONATING Blood WHY SHOULD I DONATE BLOOD? HOW MUCH BLOOD DO I HAVE? Blood Donors Save Lives
FACTS ABOUT DONATING BLOOD WHY SHOULD I DONATE BLOOD? HOW MUCH BLOOD DO I HAVE? Blood donors save lives. Volunteer blood donors provide An adult has about 10–11 pints. 100 percent of our community’s blood supply. Almost all of us will need blood products. HOW MUCH BLOOD WILL I donate? Whole blood donors give 500 milliliters, about one pint. WHO CAN DONATE BLOOD? Generally, you are eligible to donate if you are 16 years of WHAT HAPPENS TO BLOOD AFTER I donate? age or older, weigh at least 110 pounds and are in good Your blood is tested, separated into components, then health. Donors under 18 must have written permission distributed to local hospitals and trauma centers for from a parent or guardian prior to donation. patient transfusions. DOES IT HURT TO GIVE BLOOD? WHAT ARE THE MAIN BLOOD COMPONENTS? The sensation you feel is similar to a slight pinch on the Frequently transfused components include red blood arm. The process of drawing blood should take less than cells, which replace blood loss in patients during surgery ten minutes. or trauma; platelets, which are often used to control or prevent bleeding in surgery and trauma patients; and HOW DO I PREPARE FOR A BLOOD DONATION? plasma, which helps stop bleeding and can be used to We recommend that donors be well rested, eat a healthy treat severe burns. Both red blood cells and platelets meal, drink plenty of fluids and avoid caffeine and are often used to support patients undergoing cancer alcohol prior to donating. treatments. WHAT CAN I EXPECT WHEN I DONATE? WHEN CAN I DONATE AGAIN? At every donation, you will fill out a short health history You can donate whole blood every eight weeks, platelets questionaire. -
Summary of Blood Donor Deferral Following COVID-19 Vaccine And
Updated 04 14 2021 Updated Information from FDA on Donation of CCP, Blood Components and HCT/Ps, Including Information on COVID-19 Vaccines, Treatment with CCP or Monoclonals 1) HCT/P DONOR ELIGIBILITY: For the agency’s current thinking on HCT/P donation during the pandemic, including donor eligibility following vaccination to prevent COVID-19, refer to FDA’s January 4th Safety and Availability communication, Updated Information for Human Cell, Tissue, or Cellular or Tissue-based Product (HCT/P) Establishments Regarding the COVID-19 Pandemic. 2) CCP and ROUTINE BLOOD DONOR ELIGIBILITY: 2-1. Blood donor eligibility following COVID-19 vaccine Blood donor deferral following COVID-19 vaccines is not required. Consider the following information on FDA’s web page Updated Information for Blood Establishments Regarding the COVID-19 Pandemic and Blood Donation last updated 01/19/21” – see the full document on page 2 below. The blood establishment’s responsible physician must evaluate prospective donors and determine eligibility (21 CFR 630.5). The donor must be in good health and meet all donor eligibility criteria on the day of donation (21 CFR 630.10). The responsible physician may wish to consider the following: o individuals who received a nonreplicating, inactivated, or mRNA-based COVID-19 vaccine can donate blood without a waiting period, o individuals who received a live-attenuated viral COVID-19 vaccine, refrain from donating blood for a short waiting period (e.g., 14 days) after receipt of the vaccine, o individuals who are uncertain about which COVID-19 vaccine was administered, refrain from donating for a short waiting period (e.g., 14 days) if it is possible that the individual received a live-attenuated viral vaccine. -
Donor Sex, Age and Ethnicity Impact Stored Red Blood Cell Antioxidant Metabolism Through Mechanisms in Part Explained by Glucose
Blood Transfusion SUPPLEMENTARY APPENDIX Donor sex, age and ethnicity impact stored red blood cell antioxidant metabolism through mechanisms in part explained by glucose 6-phosphate dehydrogenase levels and activity Angelo D’Alessandro, 1,2,3 Xiaoyun Fu, 4 Tamir Kanias, 3,5 Julie A. Reisz, 1 Rachel Culp-Hill, 1 Yuelong Guo, 6 Mark T. Gladwin, 5 Grier Page, 6 Steve Kleinman, 7 Marion Lanteri, 8 Mars Stone, 8 Michael P. Busch, 8# and James C. Zimring 9# for the Recipi - ent Epidemiology and Donor Evaluation Study-III (REDS III) 1Department of Biochemistry and Molecular Genetics, University of Colorado Denver – Anschutz Medical Campus, Aurora, CO, USA; 2De - partment of Medicine – Division of Hematology, University of Colorado Denver – Anschutz Medical Campus, Aurora, CO, USA; 3Vitalant Re - search Institute (previously Blood Systems Research Institute), Denver, CO, USA; 4Bloodworks Northwest Research Institute, Seattle, WA, USA; 5University of Pittsburgh, Pittsburgh, PA, USA; 6RTI International, Atlanta, GA, USA; 7University of British Columbia, Victoria, Canada; 8Vi - talant Research Institute (previously Blood Systems Research Institute), San Francisco, CA, USA and 9University of Virginia, Charlotesville, VA, USA #MPB and JCZ contributed equally as co-senior authors ©2021 Ferrata Storti Foundation. This is an open-access paper. doi:10.3324/haematol. 2020.246603 Received: January 7, 2020. Accepted: March 27, 2020. Pre-published: April 2, 2020. Correspondence: ANGELO D’ALESSANDRO - [email protected] SUPPLEMENTARY MATERIAL