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Isolation Guidelines and Bloodborne Pathogen Exposures: HIV Post Exposure Prophylaxis with Rapid HIV Testing of Source; Mucous Membrane Exposures Gonzalo Bearman MD,MPH Assistant Professor of Medicine Associate Hospital Epidemiologist Outline • • • • • Isolation categories Bloodborne pathogens lists Exposure types Risk of transmission based on exposure VCUHS data of occupational bloodborne pathogen exposures • PPE: for mucous membrane exposures • PEP and Rapid HIV Testing- new protocol Goal of Isolation • Prevent transmission of microorganisms from infected or colonized patients to other patients, hospital visitors, and healthcare workers Types of Isolation Precautions Transmission-based Transmission-basedPrecautions Precautions -for -forpatients patientswith withdocumented documentedor orsuspected suspectedinfections infections -3 -3Types: Types: airborne, airborne,droplet dropletand andcontact contact Standard StandardPrecautions Precautions -Apply -Applyto toall allPatients Patients --Replace --ReplaceUniversal UniversalPrecautions Precautions Standard Precautions • Used for all patients • Must wear gloves when touching: – – – – Blood All body fluids Nonintact skin Mucous membranes • Wash hands immediately after glove removal and between patients Standard Precautions • Masks, eye protection, face shield: – Wear during activities likely to generate splashes or sprays • Gowns – Protect skin and soiling of clothing – Wear during activities likely to generate splashes or sprays • Sharps – Avoid recapping of needles – Avoid removing needles from syringes by hand – Place used sharps in puncture –resistant containers Airborne Precautions • Designed to prevent airborne transmission of droplet nuclei or dust particles containing infectious agents • For patient with documented or suspected: – – – – Measles Tuberculosis (primary or lanryngeal) Varicella (airborne + contact) Zoster (disseminated or immunocompromised patient; (airborne and contact) – SARS (Contact+airborne) Airborne Precautions • Room: – Negative pressure – Private – Door kept closed • Mask – Orange ‘duckbill’ mask required to enter room Empiric Use of Airborne Isolation • Vesicular rash (airborne+contact) • Maculopapular rash with coryza and fever • Cough + fever + upper lobe pulmonary infiltrate • Cough + fever + any infiltrate + HIV infection Droplet Precautions • Designed to prevent droplet (larger particle) transmission of infectious agents when the patient talks, coughs, or sneezes • For documented or suspected: – Adenovirus (droplet+contact) – Group A step pharyngitis, pneumonia, scarler fever (in infants, young children) – H. Influenza meningitis, epiglottitis – Infleunza, Mumps, Rubella – Meningococcal infections Empiric Use of Droplet Precautions • Meningitis • Petechial/ecchymotic rash and fever • Paroxysmal or severe persistent cough during periods of pertussis activity Contact Precautions • Used to prevent transmission of epidemiologically important organisms from an infected or colonized patient through direct (touching patient) or indirect (touching surfaces or objects in the patient’s environment) contact Contact Precautions • For suspected or documented: – – – – – – – – – Adenovirus (contact+droplet) Infectious diarrhea in diapered/incontinent patients Group A strep wound infections MDR bacteria (MRSA,VRE) Viral conjunctivitis Lice, scabies RSV infection Varicella (Contact+airborne) Zoster (disseminated or immunocompromised; contact+ airbrone – SARS (Contact+airborne) Blood and Body Fluid Exposures Potential Bloodborne Pathogens • • • Human Immunodeficiency Virus (HIV) Hepatitis Viruses As well as agents that cause... o o o o o o o o o o Babesiosis Brucellosis Leptospirosis Creutzfeldt -Jakob Disease HTLV-1 Infections Arboviral Infections Malaria Relapsing Fever Viral Hemorrhagic Fever Syphilis Transmission of these agents in the workplace can occur through the following routes: •Parenteral exposure - The pathogen is introduced directly into the body through a break in the skin, needlestick, or througha cut with a contaminated instrument or glass. •Mucous membrane exposure - Exposure through contact of a mucous membrane in the eye, nose or mouth. Risk of Infection after Contact with Infected Blood Percutaneous exposure: Prospective studies of several thousand HCWs indicate that the risk of seroconversion: HIV-infected blood is approximately 0.3%. Hepatitis B depends on the e antigen (e Ag) status of the patient. If the patient's blood is positive for the e Ag the risk of transmission -30% or about 100 times that of HIV. HCV infection is 3% to 10% or about 10 times the risk following a single exposure to HIV-infected blood. Risk of Infection after Contact with Infected Blood • Mucous Membrane Exposure: – Risk of HIV Transmission • 0.09 % risk of transmission after a mucous membrane exposure to HIV infected blood. – Hepatitis B and C • Risk of transmission not well documented • Presumed to be less than in percutaneous injury – Although the risk of transmission associated with mucous membrane exposures is less, it is not negligible VCUHS Exposure Type Count % total BBF-Mucous Membrane (Splash) 103 29% BBFNeedlestick/Sharp 255 71% 358 100% Roughly Roughly1/3 1/3of ofall allemployee employeebloodborne bloodbornepathogen pathogenexposures exposuresat atVCUHS VCUHSare are Mucous Membrane Mucous Membrane Mucous Membrane Exposures Can be Prevented!!!!!! • PPE: Masks, faceshields / goggles – MUST BE WORN IN ANY PROCEDURE OR PATIENT CARE ACTIVITY THAT POSES A RISK OF BLOOD OR BODY FLUID SPLASH/SPLATTER/AEROSOLIZATION. – The include: • Phlebotomy and blood cultures • Suctioning of gastric or respiratory secretions • Removal of medical devices – CVC, ET tubes, Foley catheters, IV lines Personal Protective Equipment PPE PPEincludes includes masks, masks,masks masks with faceshields with faceshields and andgoggles goggles PPE PPEequipment equipment can canbe befound foundinin isolation isolationcarts, carts, and wall mounted and wall mounted PPE PPEstorage storageunits units Reveal:Rapid HIV Test MedMira Laboratories • Rapid HIV test performed on patient serum – HIV antibody test • SENSITIVITY: 99.8% – All positive tests are confirmed by western blot • Processing time for the test (upon receipt by the laboratory) is about 20-30 minutes. – It is critical that the the source blood be drawn immediately and delivered to the laboratory in an expeditious manner D id a p e rc u ta n e o u s o r M M e x p o s u re o c c u r th a t c a rrie s s ig n ific a n t ris k o f tra n s m is s io n o f H IV ? P E P n o t in d ic a te d ; n o fo llo w -u p n e e d e d N O Y es H a v e fe w e r th a n 3 6 h o u rs e la p s e d s in c e th e e x p o s u re o c c u rre d ? Y e s : P ro c e e d w ith R a p id H IV T e s tin g N O S a m p le m u s t b e o b ta in e d S T A T (s e r u m s e p a r a to r ) a n d s e n t v ia p n e u m a tic tu b e to Im m u n o lo g y L a b Is th e s o u rc e p a tie n t H IV in fe c te d a s d e te rm in e d b y ra p id te s tin g ? P E P T eam th e la b . P E P n o t o p tim a l b u t s h o u ld b e c o n s id e re d . If c o n s id e re d - p ro c e e d w ith ra p id H IV te s tin g o f s o u rc e a n d fo llo w a lg o rith m a c c o rd in g ly . P E P n o t in d ic a te d ; n o fo llo w -u p n e e d e d N O M e m b e r w ill b e n o tifie d o f b o th P O S I T I V E a n d N E G A T I V E r e s u lts b y I n itia te H A A R T (I F S O U R C E I S P O S I T I V E - 3 D R U G S A R E P R T H E S E A R E S T A N D IN G O R D E R S : • R e c o m m e n d e d re g im e n : z id o v u d in e 3 0 0 m g p o b id + la m iv u d in e 1 5 (o r C o m b iv ir 1 b id ) P L U S N e lfin a v ir 1 2 5 0 m g p o b id w ith fo o d • P e rfo rm b a s e lin e c o n fid e n tia l H IV te s tin g o f th e e x p o s e d h e a lth c a re h o u rs o f in itia tin g H A A R T • R e fe r to E m p lo y e e h e a lth fo r a d d itio n a l m a n a g e m e n t: H A A R T , H e p S o u rc e p a tie n t’s s e ro lo g ic te s t is c o n firm e d H IV n e g a tiv e a n d th e re is n o e v id e n c e o f a c u te re tro v ira l s y n d ro m e in th e s o u rc e p a tie n t. S to p P E P E F E R R E D ) 0 m g p o b id w o rk e r w ith in 7 2 a titis B a n d C S o u rc e p a tie n t’s s e ro lo g ic te s t is c o n firm e d H IV p o s itiv e o r in d e te rm in a te , o r s e ro lo g y is u n a b le to b e o b ta in e d . C o n tin u e P E P fo r 4 w e e k s Conclusion-1 • Mucous membrane blood and body fluid exposures are known risk factors for the transmission of HIV and Hepatitis B/C • Of all blood and body fluid exposures at VCUHS; mucous membrane exposure account for 30% nearly every year. • PPE (masks, faceshields or goggles) must be worn when a patient care activity poses a risk of BBF splash, spray or aerosolization. Conclusion-2 • New PEP protocol – Rapid HIV testing will now be employed • Processing time is about 20-30minutes upon receipt of the source patient’s blood • Blood must be obtained from the source in an expeditious manner • Rapid HIV test results will be reported back to the PEP member – Standing orders for Antiretrovirals; 3 regimen HAART