New Standards for an Old Disease:

Similar documents
TB Clinical Guidelines: Revision Highlights March 2014

Latent Tuberculosis Infections Controversies in Diagnosis and Management Update 2016

TUBERCULOSIS. Pathogenesis and Transmission

10/3/2017. Updates in Tuberculosis. Global Tuberculosis, WHO 2015 report. Objectives. Disclosures. I have nothing to disclose

2018 Tuberculosis Clinical Intensive: Infection Prevention & Control. > No disclosures

Mycobacterial Infections: What the Primary Provider Should Know about Tuberculosis

Ken Jost, BA, has the following disclosures to make:

New Tuberculosis Guidelines. Jason Stout, MD, MHS

TB Update: March 2012

Report on WHO Policy Statements

TUBERCULOSIS IN HEALTHCARE SETTINGS Diana M. Nilsen, MD, FCCP Director of Medical Affairs, Bureau of Tuberculosis Control New York City Department of

TB Contact Investigation

Case Management of the TB/HIV Infected Patient

TB In Detroit 2011* Early TB: Smudge Sign. Who is at risk for exposure to or infection with TB? Who is at risk for TB after exposure or infection?

Contact Investigation and Prevention in the USA

TB Laboratory for Nurses

New Approaches to the Diagnosis and Management of Tuberculosis Infection in Children and Adolescents

Diagnosis of tuberculosis in children

Tuberculosis Intensive

Pediatric Tuberculosis Lisa Y. Armitige, MD, PhD September 14, 2017

What the Primary Physician Should Know about Tuberculosis. Topics for Discussion. Global Impact of TB

Tuberculosis What you need to know. James Zoretic M.D., M.P.H. Regions 2 and 3 Director

TB: Management in an era of multiple drug resistance. Bob Belknap M.D. Denver Public Health November 2012

Let s Talk TB A Series on Tuberculosis, A Disease That Affects Over 2 Million Indians Every Year

TB CONTROL IN HEALTHCARE FACILITIES: A PRACTICAL GUIDE FOR PREVENTION

결핵노출접촉자감염관리 서울아산병원감염내과 김성한

TB BASICS: PRIORITIES AND CLASSIFICATIONS

5. HIV-positive individuals treated with INH should receive Pyridoxine (B6) 25 mg daily or 50 mg twice/thrice weekly on the same schedule as INH

Tuberculosis Populations at Risk

MEMORANDUM. Re: Guidance for follow-up of newly-arrived individual with Class B1 Tuberculosis Pulmonary Tuberculosis, no treatment

Understanding and Managing Latent TB Infection Arnold, Missouri October 5, 2010

Diagnosis of tuberculosis

TB Intensive Houston, Texas. Childhood Tuberculosis Kim Connelly Smith. November 12, 2009

Targeted Testing and the Diagnosis of. Latent Tuberculosis. Infection and Tuberculosis Disease

Using Xpert to discontinue airborne isolation The Consensus Statement

Diagnosis & Medical Case Management of TB Disease. Lisa Armitige, MD, PhD October 22, 2015

Pre-Treatment Evaluation. Treatment of Latent TB Infection (LTBI) Initiating Treatment: Patient Education. Before initiating treatment for LTBI:

CHAPTER 3: DEFINITION OF TERMS

Disclosures. Updates in TB for the PCP: Opportunities for Prevention. Objectives PART 1: WHY TEST? 4/14/2016. None

TB Intensive San Antonio, Texas November 11 14, 2014

Diagnosis and Medical Management of Latent TB Infection

Contact Investigation

Treatment of TB Infection Lisa Y. Armitige, MD, PhD April 7, 2015

TB: A Supplement to GP CLINICS

Tuberculosis Tools: A Clinical Update

Tuberculosis: A Provider s Guide to

CDC IMMIGRATION REQUIREMENTS:

What s New in TB Infection Control?

Tuberculosis: Where Are We Now?

Latent Tuberculosis Infection (LTBI) Questions and Answers for Health Care Providers

Clinical and Public Health Impact of Nucleic Acid Amplification Tests (NAATs) for Tuberculosis

TB Prevention Who and How to Screen

DIAGNOSIS AND MEDICAL MANAGEMENT OF TB DISEASE

Preventing Tuberculosis (TB) Transmission in Ambulatory Surgery Centers. Heidi Behm, RN, MPH TB Controller HIV/STD/TB Program

Didactic Series. Latent TB Infection in HIV Infection

TB Nurse Case Management San Antonio, Texas July 18 20, 2012

Interferon Gamma Release Assay Testing for Latent Tuberculosis Infection: Physician Guidelines

Communicable Disease Control Manual Chapter 4: Tuberculosis

Peggy Leslie-Smith, RN

Original Article Evaluation of Xpert MTB/RIF in detection of pulmonary and extrapulmonary tuberculosis cases in China

Disclosures. Current Issues and Controversies in Child and Adolescent Tuberculosis 02/24/2016. NSTC 2016 Annual Meeting

Pediatric TB Lisa Armitige, MD, PhD September 28, 2011

Diagnosis and Treatment of Tuberculosis, 2011

Guidelines for. Tuberculosis (TB) Screening and. Treatment of Patients with. Chronic Kidney Disease(CKD), Patients Receiving Hemodialysis (HD),

Making the Diagnosis of Tuberculosis

TB in Corrections Phoenix, Arizona

Frances Morgan, PhD October 21, Comprehensive Care of Patients with Tuberculosis and Their Contacts October 19 22, 2015 Wichita, KS

Xpert MTB/RIF use for TB diagnosis in TB suspects with no significant risk of drug resistance or HIV infection. Results of Group Work

Management of Pediatric Tuberculosis in New Jersey

MEMORANDUM. Re: Guidance for follow-up of newly-arrived Individual with a Class B1 Tuberculosis Extrapulmonary Tuberculosis

Research Methods for TB Diagnostics. Kathy DeRiemer, PhD, MPH University of California, Davis Shanghai, China: May 8, 2012

Clinical Policy Title: Interferon-gamma release assays for tuberculosis screening

Tuberculosis and Diabetes Mellitus. Lana Kay Tyer, RN MSN WA State Department of Health TB Nurse Consultant

Contact Follow-Up and Treatment of LTBI in Households of Infectious Cases in Pakistan

Please distribute a copy of this information to each provider in your organization.

Northwestern Polytechnic University

Primary Care and TB Control Dr Helen Booth Consultant Thoracic Physician, UCLH Clinical Lead, Integrated TB NCL-Service

Didactic Series. Latent TB Infection in HIV Infection

Use of the Cepheid GeneXpert to Release Patients from Airborne Isolation

TB in Corrections Phoenix, Arizona

Tuberculosis Elimination: The Role of the Infection Preventionist

TB Intensive Tyler, Texas December 2-4, 2008

Tuberculosis (TB) Fundamentals for School Nurses

2017/2018 Annual Volunteer Tuberculosis Notice

Latent Tuberculosis Best Practices

What Is New in Combination TB Prevention? Lisa J. Nelson Treatment and Care (TAC) Team HIV Department WHO HQ

Childhood Tuberculosis Some Basic Issues. Jeffrey R. Starke, M.D. Baylor College of Medicine

LATENT TUBERCULOSIS. Robert F. Tyree, MD

A Clinician s Guide to the TB Laboratory

Epidemiology and diagnosis of MDR-TB in children H Simon Schaaf

A pilot study measuring the kinetic profile of IP-10 over the first 14 days of PTB chemotherapy

TB Intensive San Antonio, Texas August 7-10, 2012

Diagnosis and Medical Management of TB Disease. Quratulian Annie Kizilbash, MD, MPH March 17, 2015

has the following disclosures to make:

TB Infection Control in Healthcare Settings

Rebecca O. Sanchez, BSN., RN., MPH. has the following disclosures to make:

Clinical Policy Title: Interferon-gamma release assays for tuberculosis screening

Asking the Right Questions. A Visual Guide to Tuberculosis Case Management for Nurses. Reference Guide

Ongoing Research on LTBI and Research priorities in India

Diagnosis of TB: Laboratory Ken Jost Tuesday April 1, 2014

Transcription:

New Standards for an Old Disease: Practical Implications of the TB Standards TB Prevention and Control Saskatchewan September 16, 2015

Practical Implications of the TB Standards Learning Objectives At the end of this session you will be able to discuss and describe: 1. Diagnostic tools available in Saskatchewan including new technologies such as IGRA and Xpert assay. 2. Airborne precautions and home isolation new guidelines. 3. Contact investigations and treatment regimes changes.

History Diagnosis of LTBI Tuberculin skin test (TST) Interferon gamma release assay (IGRA) Measures immune response to TB proteins in whole blood Available October 2015 at select sites Quantiferon TB Gold In-tube (QFT-GIT)

IGRA versus TST IGRA preferred: BCG Groups with poor rate of return for TST reads TST preferred: Repeat testing Serial testing TST and IGRA are acceptable but imperfect

Diagnosis of Active TB CXR, CT Smear microscopy, mycobacterial culture & DST sputum for AFB x 3 8 hours apart within a 24 hour period at least one early morning specimen History, signs and symptoms Nucleic Acid Amplification Tests GeneXpert MTB/RIF

GeneXpert MTB/RIF Fully automated rapid TB test simultaneously detects MTB & rifampin resistance Minimal biosafety requirements Does not replace culture 3 sputum still required only 1 processed with GeneXpert Results within 2-3 hours

TB Infection Prevention & Control The key: Rapid diagnosis Isolation Start of effective treatment Challenges: Delayed diagnosis Non-adherence with airborne precautions Non-adherence to treatment or inadequate treatment

Initiation of Airborne Precautions Required for all persons with suspected or confirmed respiratory (infectious) TB disease regardless of smear status. Some exceptions with pediatric and extrapulmonary TB.

Discontinuing Precautions in Facilities TB suspected discontinue upon TB physician, MRP or designate order if: Xpert MTB/RIF negative, OR 3 consecutive AFB-negative smears (if Xpert assay not available) Continue precautions if Xpert positive or at discretion of TB physician or MRP when TB still strongly suspected, no other dx, and Xpert &/or smears negative.

Discontinuing Precautions in Facilities Smear-positive TB confirmed discontinue upon TB physician order if: 1. 2 weeks (or 14 doses) of drug therapy, AND 2. Clinical improvement as assessed by the TB physician, MRP or designate, AND 3. 3 AFB negative smears following 2 weeks (14 doses) of drug therapy, OR if unable to produce sputum: i. 3 weeks (21 doses) of drug therapy, AND ii. Clinical improvement

Discontinuing Precautions in Facilities Smear-negative, culture-positive TB confirmed discontinue upon TB physician order if: 1. 5 consecutive doses of drug therapy taken and tolerated, AND 2. Clinical improvement as assessed by the TB physician, MRP or designate. Sputum collection not required.

Discontinuing Home Isolation TB suspected Same criteria as discontinuation in facility

Discontinuing Home Isolation Smear-positive TB confirmed discontinue upon TB physician order if: 1. 2 weeks of drug therapy (10 doses if M-F therapy or 14 if OD), AND 2. Clinical improvement.

Discontinuing Home Isolation Smear-negative, culture-positive TB confirmed discontinue upon TB physician order if: Drug therapy started and at least 1 dose taken AND tolerated.

Extrapulmonary TB In general, precautions and isolation not required - two exceptions: 1. Concurrent pulmonary TB (10-50% of cases) 2. AGMPs

Pediatrics In general, precautions and isolation not required for children < 10 years old. Exception: children with adult-type TB Consider accompanying adults as potential source of infection

Treatment Active TB Intensive: 2 months INH/RMP/PZA/EMB (EMB d/c if fully sensitive) OD or 5 times/week FLQ if drug resistance, intolerance to FLD or previously treated for active TB (d/c if fully sensitive) Continuation: 4 or 7 months INH/RMP thrice weekly

Treatment - LTBI Shorter alternative regimens available 4 months INH/RMP twice weekly 4 months daily RMP 6 and 9 months regimens also available 3 months once weekly INH/Rifapentine (Special Access Programme) Increase numbers being offered treatment SAT use in medically engaged

Contact Investigations Required for smear (+) and ( ) respiratory TB Smear-positive: Infectious period 3 months Evaluate high and medium priority contacts Smear-negative: Infectious period 4 weeks Evaluate high priority contacts

Prioritization of Contacts High Priority Medium Priority Low Priority 1. Household contacts 2. Close non-household or casual contacts AND immune vulnerable 3. Contacts exposed during AGMP without PPE Close non-household contacts NOT immune vulnerable Casual contacts NOT immune vulnerable

Summary of Practical Implications IGRA: Less over-diagnosis of LTBI r/t BCG, NTM Increased screening (and possible TLTBI) among groups with historical poor rates of return for TST Xpert assay: Rapid decisions on treatment and isolation Improved utilization of AIIR, patient flow

Summary of Practical Implications Airborne precautions: Targeted application based on case infectiousness and setting risk Enhanced adherence Improved utilization of AIIR Treatment: Individualized regimens duration, adherence, DOT burden Enhanced prevention through TLTBI

Summary of Practical Implications Contact investigations: Focus on those at greatest risk Targeted screening and follow-up Enhanced prevention with window prophylaxis and increasing TLTBI

Questions?