Presentation is loading. Please wait.

Presentation is loading. Please wait.

WHAT’S FLU TO YOU? STOMACH “FLU” VERSUS INFLUENZA Jill Baber and Alicia Lepp North Dakota Department of Health Division of Disease Control 6/25/2015 Lunch.

Similar presentations


Presentation on theme: "WHAT’S FLU TO YOU? STOMACH “FLU” VERSUS INFLUENZA Jill Baber and Alicia Lepp North Dakota Department of Health Division of Disease Control 6/25/2015 Lunch."— Presentation transcript:

1 WHAT’S FLU TO YOU? STOMACH “FLU” VERSUS INFLUENZA Jill Baber and Alicia Lepp North Dakota Department of Health Division of Disease Control 6/25/2015 Lunch and Learn Presentation

2 “I HAD THE FLU…”

3

4 INFLUENZA = “FLU”

5 INFLUENZA STOMACH “FLU”

6  Stomach “flu” = “Winter Vomiting Disease”  Stomach “flu” = 24-hour bug  Stomach “flu” ≠ Influenza STOMACH “FLU” = NOROVIRUS

7  Influenza = “flu”  Seasonal flu  Pandemic Flu  Swine Flu  Avian Flu A “FLU” BY ANY OTHER NAME…

8 INFLUENZA

9  A common seasonal respiratory disease associated with high levels of morbidity and mortality each winter.  Common symptoms:  Fever  Cough  Sore throat  Headache  Body aches  Chills  Less common: vomiting (mostly in children) INFLUENZA

10  “Influenza-like illness” is a phrase used to describe respiratory illness fitting the case profile of influenza, but that may or may not be laboratory confirmed.  Important for tracking influenza because influenza may not always be confirmed with a laboratory test.  “Official” definition: fever (≥100°F) AND cough AND/OR sore throat “INFLUENZA-LIKE ILLNESS”

11  Abrupt onset of respiratory disease typically lasting 3-7 days, with related malaise and cough lasting up to two weeks.  Common complications include: pneumonia, bronchitis, sinus and ear infections and exacerbation of existing respiratory issues.  High risk groups: children, the elderly, pregnant woman and immunocompromised individuals.  Incubation period: 2 days. CLINICAL DISEASE

12  Infected persons can spread influenza about one day prior to symptom onset, and 5 to 7 days after symptom development. Children may be able to spread the virus for longer than 7 days.  Influenza is mainly transmitted via respiratory secretions in droplet form. Contact within contaminated surfaces is a secondary source of transmission.  General prevention efforts include:  Vaccination  Hand washing  Disinfection of surfaces  Not touching face with unwashed hands  Staying home when ill and avoiding others who are ill  Treatment with influenza antivirals has not been shown to shorten the transmission period. TRANSMISSION

13  Positive influenza lab tests are reportable to the North Dakota Department of Health.  Rapid  DFA  PCR  Negative rapid or DFA tests should not be used to rule out influenza.  Testing is also available through the Public Health Lab.  PCR (free!)  Respiratory Viral Panel (RVP)  In long term care settings, testing is recommended year round when two or more residents present with ILI within 72 hours.  Test kits can be provided during outbreak for influenza typing. LABORATORY CONFIRMATION

14  Laboratory-confirmed influenza is reportable in North Dakota.  Hospitalizations and adult deaths are not reportable in North Dakota but are still tracked. (And are appreciated!)  Hospitalizations obtained ad hoc from complete reports  Death information from individual reports and Vital Records data  Pediatric deaths are nationally notifiable  Sentinel site reporting.  Outpatient ILI reports  Laboratory reports  School absenteeism reports  Syndromic Surveillance (hospital ILI).  Long Term Care outbreaks (not just “Long Term Care”).  Information available weekly during the flu season at www.ndflu.com.www.ndflu.com INFLUENZA SURVEILLANCE

15  Influenza and other respiratory clusters are common in health care facilities.  Influenza is common wherever people congregate.  Communities with large numbers of elderly residents are especially susceptible to outbreaks.  Recommendations specific to health care facilities exist for:  vaccination  antiviral treatment  Infection prevention  infection control  Reporting  Special considerations for Long term care. CDC toolkit for long term care providers: http://www.cdc.gov/flu/toolkit/long-term- care/ INFLUENZA AND INFLUENZA-LIKE ILLNESS IN HEALTH CARE FACILITIES

16 Treatment with influenza antivirals is recommended in a hospital setting for all confirmed and suspected cases of influenza when the patient is in a high-risk category. The CDC recommendation is to NOT WAIT for a positive test to begin antiviral treatment. INFLUENZA ANTIVIRALS Oseltamivir (Tamiflu) Zanamivir (Relenza)

17 In facilities with residents, treatment or prophylaxis with influenza antivirals are recommended for:  All confirmed and suspected cases of influenza when the patient is in a high risk category (treatment dose).  All resident contacts of confirmed and suspected cases of influenza when the contact is in a high-risk category (prophylactic dose):  Roommates  Activity partners  Residents on the same floor/wing/pod/etc.  All residents at a long term care facility during a confirmed outbreak.  NEW! All long term care staff contacts of confirmed and suspected cases during H3N2 seasons when the vaccine is poorly matched to the circulating strain (like 2014-15, prophylactic dose). INFLUENZA ANTIVIRALS

18 Yearly seasonal influenza vaccination is recommended for patients, residents, family members and health care workers.  Different kinds of seasonal influenza vaccines are available.  No current recommendations for particular vaccine types over others. INFECTION PREVENTION: VACCINATION

19  Daily active surveillance of residents, staff and visitors for ILI in a health care facility should be initiated during outbreaks.  Active surveillance should continue for one week after the most recent case is identified.  Active surveillance provides situational awareness and can guide other infection control measures. INFECTION CONTROL: ACTIVE SURVEILLANCE

20  In addition to following the standard precautions always recommended for health care settings, droplet precautions should be implemented for all residents with ILI. Examples:  Placing ill patients/residents in a private room. OR place residents suspected of having influenza together (cohorting).  Masking of staff and visitors when entering the room of an ILL patient/resident (dispose of mask upon exit).  Masking of the patient/resident during transport.  Share ILI status information with staff receiving patients/residents being transferred to another area.  Duration: 7 days after onset OR 24 hours after the resolution of fever and respiratory symptoms (or longer). INFECTION CONTROL: DROPLET PRECAUTIONS

21  Employees:  Track employee health  Have ill employees stay home  Visitors:  Discourage ill visitors from entering facility  Require masking of visitor  Restrict all visitors or young visitors during active outbreaks (facility discretion)  Post signs! INFECTION CONTROL: EMPLOYEE/VISITOR SCREENING Screen employees and visitors for respiratory illness:

22  Proper cleaning in infection are important to controlling influenza and other respiratory viruses that can live on surfaces for several hours.  Routine cleaning is typically sufficient:  Clean and disinfect surfaces and objects that are touched often  Use cleaning/disinfecting products approved by the EPA for effectiveness against influenza A viruses (alternative: solution of one tablespoon of bleach to 4 cups water)  For visibly dirty surfaces, clean with a general cleaner, rinse with water, and follow with an EPA-approved disinfectant.  Consider disinfecting wipes for often used electronic items, such as phones and computers  An outbreak of ILI presents a good opportunity to review cleaning procedures! INFECTION CONTROL: CLEANING AND DISINFECTION

23 Influenza-like illness “outbreaks” in health care institutional settings are reportable. ILI REPORTING

24  CDC definition of a long term care outbreak of influenza-like illness:  Two or more cases of ILI in residents (or residents and staff) that occur within 48 to 72 hours of each other, OR  One resident with a positive laboratory result for influenza  Laboratory confirmation is not necessary for an outbreak in a long term care facility to be reportable. ILI REPORTING: WHAT?

25  Required as part of reportable disease law for reporting nosocomial outbreaks.  Long term care outbreaks are tracked by CDC as an influenza indicator.  Reporting in aggregate  40 reported outbreaks in North Dakota for the 2014-15 season  Non-influenza ILI is important, as other respiratory diseases can cause outbreaks and even deaths.  Rhinovirus  Respiratory Syncytial Virus (RSV)  Human metapneumovirus ILI REPORTING: WHY?

26 Web-based reporting form: http://www.ndflu.com/Reporting/FluOutbreak.htm http://www.ndflu.com/Reporting/FluOutbreak.htm ILI REPORTING: WHERE?

27 ILI REPORTING WHERE?

28 Following the path of: www.NDFlu.comwww.NDFlu.com  Outbreak Reporting  Long Term Care Outbreaks this form will appear. ILI REPORTING: WHERE

29 NDDoH reporting form asks for:  Facility name, type, address and phone number  Reporter name and email  Total number of residents, staff, residents with illness and staff with illness  Date of onset for first case  Symptoms associated with the outbreak  If and where specimens were collected for laboratory confirmation  Vaccination status for ill residents  If antivirals have been given to residents affected or potentially affected by the outbreak  Any prevention measures taken by facility ILI REPORTING: WHAT?

30  Information from the report will be recorded by NDDoH influenza staff.  Follow-up often occurs in order to:  Provide CDC recommendations  Obtain any necessary additional information  Arrange for influenza test kits to be delivered  We are always happy to answer questions! ILI REPORTING

31 NOROVIRUS

32  Norovirus is very contagious.  Is the most common cause of acute gastroenteritis in the US.  Causes 19-21 million illnesses  Contributes to 56,000-71,000 hospitalizations  570-800 deaths  Can spread quickly in closed places, such as daycare centers, nursing homes, schools and cruise ships.  Causes acute but self-limited diarrhea, often with vomiting, abdominal cramping, fever and fatigue.  Most individuals recover from acute symptoms with 2-3 days, but can be more severe in vulnerable populations. NOROVIRUS

33  Norovirus was first identified as the cause of a gastroenteritis outbreak in Norwalk, Ohio, in 1968  Noroviruses are a group of nonenveloped, single-stranded RNA viruses classified into the genus Norovirus (previously referred to as Norwalk-like viruses or small round-structured viruses) of the family Caliciviridae.  Noroviruses can be divided into at least five genogroups, designated GI--GV, based on amino acid identity in the major structural protein. The strains that infect humans are found in GI, GII, and GIV, whereas the strains infecting cows and mice are found in GIII and GV, respectively NOROVIRUS

34  Since 2001, GII.4 viruses have been associated with the majority of viral gastroenteritis outbreaks worldwide. Recent studies have demonstrated that these viruses evolve over time through serial changes in the VP1 sequence, which allow evasion of immunity in the human population  Periodic increases in norovirus outbreaks tend to occur in association with the emergence of new GII.4 strains that evade population immunity. These emergent GII.4 strains rapidly replace existing strains predominating in circulation and can sometimes cause seasons with unusually high norovirus activity NOROVIRUS OUTBREAKS

35  Norovirus is a recognized cause of gastroenteritis outbreaks in healthcare facilities.  Healthcare facilities are the most commonly reported settings of norovirus gastroenteritis outbreaks in the US.  Outbreaks of gastroenteritis in healthcare settings pose a risk to patients, healthcare personnel, and to the efficient provision of healthcare services. NOROVIRUS IN HEALTHCARE FACILITIES

36

37  Infectious dose: 18-1000 viral particles  Incubation period: 12-48 hours  Acute-onset vomiting and/or diarrhea  Watery, non-bloody stools  Abdominal cramps, nausea, low-grade fever  30% infections asymptomatic  Most recover after 12-72 hours  Up to 10% seek medical attention; some require hospitalization and fluid therapy  More severe illness and death possible in elderly and those with other illnesses CLINICAL DISEASE

38  Primarily in stool, but can also be present in vomitus  Shedding peaks 4 days after exposure  In some individuals, shedding may occur for at least 2-3 weeks  May occur after resolution of symptoms VIRAL SHEDDING

39  Person to person  Direct fecal-oral  Ingestion of aerosolized vomitus  Indirect via fomites or contaminated environment  Food  Contamination by infected food handlers  Point of service or source (e.g., raspberries, oysters)  Recreational and Drinking Water  Well contamination from septic tank  Chlorination system breakdown  In healthcare, the most likely and common modes of transmission are through direct contact with infected persons or contaminated equipment TRANSMISSION OF DISEASE

40  Short-term immunity after infection  There is little cross protective immunity (against different genotypes)  No long-term immunity  Protection believed to last less than one year, and in some studies, protection may only last a few months  Genetic susceptibility  A portion of the population may be genetically resistant to norovirus infection  Currently no commercially available test to identify those who might carry genes conferring resistance to norovirus infection IMMUNITY TO NOROVIRUS

41  Reverse transcription polymerase chain reaction (RT-PCR) confirmation is the preferred diagnostic for norovirus  Differentiate genogroup I and genogroup II norovirus  Rapid commercial assays have recently been cleared by FDA for preliminary identification of norovirus when testing multiple specimens during outbreaks  Poor sensitivity (50%)  Samples that test negative should be confirmed by second technique LABORATORY CONFIRMATION OF NOROVIRUS

42  Consult with NDDoH prior to submitting samples for norovirus identification  Need multiple suspect cases before specimen testing can be performed  Stool specimens should be collected from individuals during acute phase of illness  Virus may be able to be detected in specimens taken later in the course of illness, but sensitivity is reduced  Submit stool specimens as early as possible during a potential outbreak or cluster  Both staff and patient cases can be tested SUBMITTING CLINICAL SAMPLES FOR NOROVIRUS TESTING

43  Key Infection Control Activities  Rapid identification and isolation of suspected cases of norovirus gastroenteritis  Communicating the presence of suspected cases to Infection Preventionists  Promoting increased adherence to hand hygiene, particularly the use of soap and water after contact with symptomatic patients  Enhanced environmental cleaning and disinfection  Promptly initiate investigations  Collection of clinical and epidemiological information  Obtain clinical samples WHAT SHOULD STAFF DO IF THEY SUSPECT NOROVIRUS?

44  In healthcare settings where risk of transmission is high, use of isolation precautions is often the most effective means of interrupting transmission  CONTACT PRECAUTIONS – single occupancy room with a dedicated bathroom, strict adherence to hand hygiene, wear gloves and gown upon room entry  Use Contact Precautions for a minimum of 48 hours after the resolution of symptoms  Symptomatic patients may be cohorted together  Exclude ill staff members and food handlers in healthcare facilities for a minimum of 48 hours following resolution of their symptoms  Exclude non-essential personnel and visitors INFECTION CONTROL: PATIENT ISOLATION OR COHORTING

45  Wash hands with soap and water after contact with symptomatic patients  Alcohol-based hand sanitizers  Currently available products appear to be relatively ineffective against norovirus  Consider using FDA-compliant alcohol-based hand sanitizers for other indications (e.g., before contact with norovirus patient) INFECTION CONTROL: HAND HYGIENE

46  The use of chemical cleaning and disinfecting agents are key in interrupting norovirus spread from contaminated environmental surfaces  Increase the frequency of cleaning and disinfection of patient care areas and frequently touched surfaces  e.g., increase ward/unit level cleaning to twice daily, with frequently touched surfaces cleaned and disinfected three times daily  Use commercial cleaning and disinfection products registered with the U.S. EPA [e.g., sodium hypochlorite (bleach) solution, hydrogen peroxide products, etc.).  http://www.epa.gov/pesticides/antimicrobials/list_g_norovirus.pdf http://www.epa.gov/pesticides/antimicrobials/list_g_norovirus.pdf  It is critical to follow manufacturer instructions for methods of application, amount, dilution and contact time. INFECTION CONTROL: ENVIRONMENTAL CLEANING AND DISINFECTION

47  To reduce transmission, and depending on the magnitude of the outbreak, cohort staff to care for patients who are  Asymptomatic unexposed  Asymptomatic, potentially exposed  Symptomatic  Remove communal or shared food items for staff or patients for the duration of the outbreak  Group activities for patients may need to be suspended; minimize patient movements within a patient care area to help control transmission INFECTION CONTROL: OTHER CONSIDERATIONS

48  Units can use a “line list” to track symptomatic staff and patients  During an outbreak, collect key information to assist with controlling the outbreak and to inform NDDoH on outbreak details  Suggested line list elements  Case (staff/patient) identifier  Case location  Symptoms  Outcome/Date of Resolution  Diagnostics submitted  http://www.epa.gov/pesticides/antimicrobials/list_g_norovirus.pdf http://www.epa.gov/pesticides/antimicrobials/list_g_norovirus.pdf SURVEILLANCE FOR NOROVIRUS CASES

49  Internal Communication  Report gastroenteritis outbreaks (e.g., 2 or more suspected or confirmed cases among staff or patients) to infection control units  Outbreaks should also be reported to clinical management  Important to include communications, laboratory, environmental services, admitting, occupational health departments http://www.cdc.gov/hai/pdfs/norovirus/216887-A- GICommFramewk508.pdf  External Communication  Report norovirus outbreaks to NDDoH  NDDoH enter norovirus outbreak data (among other pathogens) into CDC’s National Outbreak Reporting System (NORS) https://www.ndhealth.gov/disease/Gastroenteritis/Gastroenteritis.asp x REPORTING OUTBREAKS

50 Contact info: North Dakota Department of Health Division of Disease Control 701.328.2378 Jill Baber: jbaber@nd.gov (influenza, other respiratory)jbaber@nd.gov Laura Cronquist: lcronquist@nd.gov (norovirus, other enterics) lcronquist@nd.gov QUESTIONS?


Download ppt "WHAT’S FLU TO YOU? STOMACH “FLU” VERSUS INFLUENZA Jill Baber and Alicia Lepp North Dakota Department of Health Division of Disease Control 6/25/2015 Lunch."

Similar presentations


Ads by Google