Guideline for the Prevention and Control of Norovirus Gastroenteritis Outbreaks in Healthcare Settings, 2011
VIII. Evidence Review
Question 3: What interventions best prevent or contain outbreaks of norovirus gastroenteritis in the healthcare setting?
To address this question, 69 studies [58,63,66,79,83-85,87,89,92,102,103,112,148-203] were critically reviewed for evidence of interventions that might prevent or attenuate an outbreak of norovirus. The available data dealt with viral shedding, recovery of norovirus, and components of an outbreak prevention or containment program, including the use of medications. The evidence consisted of 1 randomized controlled trial, 1 systematic review, 20 basic science studies, [112,162,163,185-201] 43 descriptive studies, [58,63,79,83-85,87,89,92,102,103,149-152,154-161,165-184] and 4 observational studies.[66,148,164,203] The findings from the evidence review and the grades of evidence for clinically relevant outcomes are shown in Evidence and Grade Table 3.
Q3.A Viral Shedding
This review did not identify studies demonstrating direct associations between viral shedding and infectivity. However, there was low-quality evidence to support an association between age and duration of viral shedding.[149,150] One observational study suggested that children under the age of six months may be at an increased risk of prolonged viral shedding (greater than two weeks), even after the resolution of symptoms. Other findings suggest that infants can shed higher titers of virus than levels reported in other age groups. High-quality evidence was available to demonstrate the presence of viral shedding in asymptomatic subjects, and low-quality evidence demonstrating that shedding can persist for up to 22 days following infection and 5 days after the resolution of symptoms.[150-152] The search strategy employed did not identify studies that correlated other clinical factors to duration of viral shedding.
Q3.B Recovery of Norovirus
There was low-quality evidence positively associating fomite contamination with norovirus infection.[153-159,161,163,194] Similarly, there was low-quality evidence demonstrating transfer of norovirus from fomites to hands. One basic science study demonstrated that norovirus on surfaces can be readily transferred to other fomites (telephones, taps, door handles) via fingertips in 30-50% of opportunities even when virus has been left to dry for 15 minutes. There was moderate quality evidence examining the norovirus contamination of the environment.[153-159,161,163] A single systematic review evaluated 5 outbreaks with environmental sampling data. Three of those outbreaks confirmed environmental contamination with norovirus. Of the over 200 swabs examined from the 5 outbreaks in this review, 36% identified norovirus contamination on various fomites such as curtains, carpets, cushions, commodes and toilets, furnishings and equipment within 3-4 feet of the patient, handrails, faucets, telephones, and door handles. However, in two outbreaks from which 47 environmental samples were collected, norovirus was not detected. Additional studies detected norovirus on kitchen surfaces, elevator buttons, and other patient equipment. [154-157, 194]
There was low-quality evidence regarding the duration of norovirus persistence. [154,155,157-159,161] Norovirus can persist in a dried state at room temperature for up to 21-28 days and, in a single observational study, was undetectable in areas of previously known contamination after 5 months had elapsed. Laboratory studies comparing FCV and MNV-1 also demonstrated persistence of virus in both dried and in fecal suspensions for a minimum of seven days on stainless steel preparations at 4°C and at room temperature.20 Within a systematic review, it was observed that norovirus may remain viable in carpets up to 12 days, despite regular vacuuming.153 Similarly, a cultivable surrogate for human strains of norovirus (FCV) was detected on computer keyboards and mice, as well as telephone components up to 72 hrs from its initial inoculation.156 This search strategy did not find studies in which the recovery of norovirus from fomites, food, and water sources was directly associated with transmission of infection in healthcare settings; however transmission from these sources has been well documented in other settings.
Q3.B.2 Foods and Food Preparation Surfaces
There was low-quality evidence suggesting that foods and food-preparation surfaces are significant sources of norovirus transmission in healthcare settings.112,162,163 There was moderate quality evidence among three basic science studies to suggest that norovirus can be recovered from foods such as meats and produce as well as from utensils and non-porous surfaces (e.g., stainless steel, laminate, ceramics) upon which foods are prepared.112,162,163 Two of these studies, comprised of low-quality evidence, suggested that the transfer of diluted aliquots of norovirus from stainless steel surfaces to wet and dry food, and through contaminated gloves was detectable using PCR methods. Norovirus transfer was statistically more efficient when it was inoculated onto moist surfaces compared to dry ones.[162,163]
There was low-quality evidence to suggest that norovirus persists for longer periods in meats compared to other foods and non-porous surfaces, both at 4°C and at room temperature. There was moderate quality evidence demonstrating that over a period of 7 days after application, both human norovirus genogroup I and a surrogate (FCV) could be detected among all surfaces tested.[112,162] Within the first hour, the log10 of FCV titers declined by 2-3, with an additional drop of 2-4 after 48 hours elapsed. Food and food-preparation areas can serve as a common source of contamination with norovirus in the absence of cleaning and disinfection.
This search strategy did not identify studies that measured the contribution of norovirus-contaminated water to outbreaks in the healthcare setting. However, there was moderate quality evidence to suggest that norovirus could be recovered from water. [155,158,160] Among three outbreaks that examined water as a source, one identified norovirus in 3 of 7 water samples. In outbreaks in the community, which were outside the scope of this review, contaminated surface water sources, well water, and recreational water venues have been associated with outbreaks of norovirus gastroenteritis.
Q3.C Components of an Outbreak Prevention/Containment Program
As with most infection-prevention and control activities, multiple strategies are instituted simultaneously during outbreaks in healthcare settings. Thus, it is difficult to single out particular interventions that may be more influential than others, as it is normally a combination of prudent interventions that reduce disease transmission. Numerous studies cite the early recognition of cases and the rapid implementation of infection control measures as key to controlling disease transmission. The following interventions represent a summary of key components in light of published primary literature and addressed in seminal guidelines on outbreaks of norovirus gastroenteritis.
Q3.C.1 Hand Hygiene
Q3.C.1.a Handwashing with soap and water
Very low-quality evidence was available to confirm that handwashing with soap and water prevents symptomatic norovirus infections. [63,66,79,85,89,102,103,165,166,168-171,173-177,183] Several descriptive studies emphasized hand hygiene as a primary prevention behavior and promoted it simultaneously with other practical interventions. Several outbreaks centered in healthcare augmented or reinforced hand hygiene behavior as an early intervention and considered it an effective measure aimed at outbreak control. [103,165,168,170,174,176,177,183] The protocols for hand hygiene that were reviewed included switching to the exclusive use of handwashing with soap and water, and a blend of handwashing with the adjunct use of alcohol-based hand sanitizers. Additional guidance is available in the 2002 HICPAC Guideline for Hand Hygiene in Health-Care Settings [PDF - 495 KB].
Q3.C.1.b Alcohol-based hand sanitizers
Very low-quality evidence was available to suggest that hand hygiene using alcohol-based hand sanitizers may reduce the likelihood of symptomatic norovirus infection. [66,87,169,171,205] Several studies used FDA-compliant alcohol-based hand antiseptics during periods of norovirus activity as an adjunct measure of hand hygiene. [66,87,168,169,171,205,206] Two studies used a commercially available 95% ethanol-based hand sanitizer along with handwashing with soap and water; but without a control group and with hand hygiene comprising one of several interventions, the relative contribution of hand hygiene to attenuating transmission was difficult to evaluate. [169,171] In the laboratory, even with 95% ethanol products, the maximum mean reduction in log10 titer reduction was 2.17. Evidence to evaluate the efficacy of alcohol-based hand disinfectants consisted of basic science studies using FCV as a surrogate for norovirus. Moderate quality evidence supported ethanol as a superior active ingredient in alcohol-based hand disinfectants compared to 1-propanol, particularly when simulated organic loads (e.g. fecal material) were used in conjunction with exposure to norovirus. [189,191,193,196] The use of hand sanitizers with mixtures of ethanol and propanol have shown effectiveness against FCV compared to products with single active ingredients (70% ethanol or propanol) under controlled conditions. There were no studies available to evaluate the effect of non-alcohol based hand sanitizers on norovirus persistence on skin surfaces.
Q3.C.1.c Role of artificial nails
Very low-quality evidence suggested that the magnitude in reduction of a norovirus surrogate (FCV) using a spectrum of soaps and hand disinfectants was significantly greater among volunteers with natural nails compared to those with artificial nails. A subanalysis showed that longer fingernails were associated with consistently greater hand contamination. Further evidence summarizing the impact of artificial and long fingernails in healthcare settings can be found in the HICPAC Guidelines for Hand Hygiene in Healthcare Settings.
Q3.C.2 Personal Protective Equipment
Very low-quality evidence among 1 observational and 13 descriptive studies[167-173,176-179,181,183] support the use of personal protective equipment (PPE) as a prevention measure against symptomatic norovirus infection. A single retrospective study failed to support the use of gowns as a significantly protective measure against norovirus infection during the outbreak among staff but did not consider the role of wearing gowns in avoiding patient-to-patient transmission. Mask or glove use was not evaluated in the self-administered questionnaire used in the study. Several observational and descriptive studies emphasized the use of gloves and isolation gowns for routine care of symptomatic patients, with the use of masks recommended when staff anticipated exposure to emesis or circumstances where virus may be aerosolized.[167-173,176-179,181,183[ The use of PPE was advocated for both staff and visitors in two outbreak studies.[169,179]
Q3.C.3 Leave Policies for Staff
There was very low-quality evidence among several studies to support the implementation of staff exclusion policies to prevent symptomatic norovirus infections in healthcare settings.[84,85,92,165,167-169,172,174,176,177,179-181,183,184] Fifteen descriptive studies emphasized granting staff sick time from the time of symptom onset to a minimum of 24 hours after symptom resolution.[84,85,92,167-169,172,176,177,179,180,183,184] The majority of studies opted for 48 hours after symptom resolution before staff could return to the workplace.[84,92,167,169,172,176,177,179,180,183,184] One study instituted a policy to exclude symptomatic staff from work until they had remained symptom-free for 72 hours. While selected studies have identified the ability of persons to shed virus for protracted periods post-infection, it is not well understood whether virus detection translates to norovirus infectivity. The literature search was unable to determine whether return to work policies were effective in reducing secondary transmission of norovirus in healthcare facilities.
Q3.C.4 Isolation/Cohorting of Symptomatic Patients
There was very low-quality evidence among several descriptive studies to support patient cohorting or placing patients on Contact Precautions as an intervention to prevent symptomatic norovirus infections in healthcare settings.[87,166-171,173,176,177,179-182,184] No evidence was available to encourage the use of Contact Precautions for sporadic cases, and the standard of care in these circumstances is to manage such cases with Standard Precautions. Fifteen descriptive studies used isolation precautions or cohorting practices as a primary means of outbreak management.[87,166-171,173,176,177,179-182,184] Patients were cared for in single occupancy (e.g., private) rooms, physically grouped into cohorts of symptomatic, exposed but asymptomatic, or unexposed within a ward, or alternatively, with entire wards placed under Contact Precautions. Exposure status typically was based on a person’s symptoms and/or physical and temporal proximity to norovirus activity. A few studies cited restricting patient movements within the ward, suspending group activities, and special considerations for therapy or other medical appointments during outbreak periods as adjunct measures to control the spread of norovirus.[63,169,182,183]
Q3.C.5 Staff Cohorting
Very low-quality evidence supported the implementation of staff cohorting and the exclusion of non-essential staff and volunteers to prevent symptomatic norovirus infections.[87,103,165,168-170,172,173,177,179,180,182,183] All studies addressing this topic were descriptive. Staff was designated to care for one cohort of patients (symptomatic, exposed but asymptomatic, or unexposed). Exposed staff was discouraged from working in unaffected clinical areas and from returning to care for unexposed patients before, at a minimum, allowing 48 hours from their last putative exposure to elapse. The search strategy did not identify healthcare personnel other than nursing, medical, environmental services, and paramedical staff who were assigned to staff cohorting. There were no identified studies that evaluated the infectious risk of assigning recovered staff as caregivers for asymptomatic patients.
Q3.C.6 Ward Closure
Low-quality evidence was available to support ward closure as an intervention to prevent symptomatic norovirus infections.[85,164-166,168,173,176-179,183,184] Ward closure focused on temporarily suspending transfers in or out of the ward, and discouraged or disallowed staff from working in clinical areas outside of the closed ward. One prospective controlled study evaluating 227 ward-level outbreaks between 2002 and 2003 demonstrated that outbreaks were significantly shorter (7.9 vs. 15.4 days, p<0.01) when wards were closed to new admissions. The mean duration of ward closure was 9.65 days, with a loss of 3.57 bed-days for each day the ward was closed. The duration of ward closure in the descriptive studies examined was dependent on facility resources and magnitude of the outbreaks. Allowing at least 48 hours from the resolution of the last case, followed by thorough environmental cleaning and disinfection was common before re-opening a ward. Other community-based studies have used closures as an opportunity to perform thorough environmental cleaning and disinfection before re-opening. Two studies moved all patients with symptoms of norovirus infection to a closed infectious disease ward and then performed thorough terminal cleaning of the vacated area.[170,172] In most instances, studies defended that it was preferable to minimize patient movements and transfers in an effort to contain environmental contamination.
Q3.C.7 Visitor Policies
There was very low-quality evidence demonstrating the impact of restriction and/or screening of visitors for symptoms consistent with norovirus infection.[168,170,173,182,183] In two studies, visitors were screened for symptoms of gastroenteritis using a standard questionnaire or evaluated by nursing staff prior to ward entry as part of multi-faceted outbreak control measures.[168,170] Other studies restricted visitors to immediate family, suspended all visitor privileges, or curtailed visitors from accessing multiple clinical areas.[182,183] The reviewed literature failed to identify research that considered the impact of different levels of visitor restrictions on outbreak containment.
There was very low-quality evidence on the impact of staff and/or patient education on symptomatic norovirus infections.[166,168,169,172,173,182] Six studies simply described education promoted during outbreaks.[166,168,169,172,173,182] Content for education included recognizing symptoms of norovirus, understanding basic principles of disease transmission, understanding the components of transmission-based precautions, patient discharges and transfer policies, as well as cleaning and disinfection procedures. While many options are available, the studies that were reviewed used posters to emphasize hand hygiene and conducted one-on-one teaching with patients and visitors, as well as holding departmental seminars for staff. The literature reviewed failed to identify research that examined the impact of educational measures on the magnitude and duration of outbreaks of norovirus gastroenteritis, or what modes of education were most effective in promoting adherence to outbreak measures.
There was very low-quality evidence to suggest that surveillance for norovirus activity was an important measure in preventing symptomatic infection.[58,84,166,170] Four descriptive studies identified surveillance as a component of outbreak measurement and containment. Establishing a working case definition and performing active surveillance through contact tracing, admission screening, and patient chart review were suggested as actionable items during outbreaks. There was no available literature to determine whether active case-finding and tracking of new norovirus cases were directly associated with shorter outbreaks or more efficient outbreak containment.
Q3.C.10 Policy Development and Communication
Very low-quality evidence was available to support the benefits of having established written policies and a pre-arranged communication framework in facilitating the prevention and management of symptomatic norovirus infections. [63,84,172,182-184] Six descriptive studies outlined the need for mechanisms to disseminate outbreak information and updates to staff, laboratory liaisons, healthcare facility administration, and public health departments. [63,84,172,182-184] The search of the literature did not yield any studies to demonstrate that facilities with written norovirus policies already in place had fewer or shorter outbreaks of norovirus gastroenteritis.
Q3.C.11 Patient Transfers and Discharges
There was very low-quality evidence examining the benefit of delayed discharge or transfer for patients with symptomatic norovirus infection.[172,179,183,184] Transfer of patients after symptom resolution was supported in one study but discouraged unless medically necessary in three others. Discharge home was supported once a minimum of 48 hours had elapsed since the patient’s symptoms had resolved. For transfers to long-term care or assisted living, patients were held for five days after symptom resolution before transfer occurred. The literature search was unable to identify studies that compared the impact of conservative patient discharge policies for recovered, asymptomatic patients.
Q3.C.12 Environmental Disinfection
Q3.C.12.a Targeted surface disinfection
Very low-quality evidence was available to support cleaning and disinfection of frequently touched surfaces to prevent symptomatic norovirus infection.[79,153,168,183] One systematic review and three descriptive studies[79,168,183] highlighted the need to routinely clean and disinfect frequently touched surfaces (e.g., patient and staff bathrooms and clean and dirty utility rooms, tables, chairs, commodes, computer keyboards and mice, and items in close proximity to symptomatic patients). One systematic review and two descriptive studies[102,177,183,184] supported-steam cleaning carpets once an outbreak was declared over. Within the review, a single case report suggested that contaminated carpets may contain viable virus for a minimum of twelve days even after routine dry vacuuming. Routine cleaning and disinfection of non-porous flooring were supported by several studies, with particular attention to prompt cleaning of visible soiling from emesis or fecal material.[153,168] There were no studies directly addressing the impact of surface disinfection of frequently touched areas on outbreak prevention or containment.
Q3.C.12.b Process of environmental disinfection
There was very low-quality evidence supportive of enhanced cleaning during an outbreak of norovirus gastroenteritis.[168, 170, 177, 179] Several studies cited increasing the frequency of cleaning and disinfection during outbreaks of norovirus gastroenteritis.[168, 170, 177, 179] Ward-level cleaning was performed once to twice per day, with frequently touched surfaces and bathrooms cleaned and disinfected more frequently (e.g., hourly, once per shift, or three times daily). Studies also described enhancements to the process of environmental cleaning. Environmental services staff wore PPE while cleaning patient-care areas during outbreaks of norovirus gastroenteritis.[176,177, 179, 205] Personnel first cleaned the rooms of unaffected patients and then moved to the symptomatic patient areas . Adjunct measures to minimize environmental contamination from two descriptive studies included labeling patient commodes and expanding the cleaning radius for enhanced cleaning within the immediate patient area to include other proximal fixtures and equipment.[170,177] In another study, mop heads were changed at an interval of once every three rooms. This literature search was not able to identify whether there was an association with enhanced cleaning regimens during outbreaks of norovirus gastroenteritis and the attenuation in outbreak magnitude or duration.
Q3.C.12.c Patient-service items
There was very low-quality evidence to support the cleaning of patient equipment or service items to reduce symptomatic norovirus infections.[168,172,177] Three descriptive studies suggested that patient equipment/service items be cleaned and disinfected after use, with disposable patient care items discarded from patient rooms upon discharge.[168,172,177] A single descriptive study used disposable dishware and cutlery for symptomatic patients. There were no identified studies that directly examined the impact of disinfection of patient equipment on outbreaks of norovirus gastroenteritis.
Very low-quality evidence was available to examine the impact of fabric disinfection on norovirus infections.[153,168,177,183] One systematic review and three descriptive studies[168,177,183] suggested changing patient privacy curtains if they are visibly soiled or upon patient discharge. One descriptive study suggested that soiled, upholstered patient equipment should be steam cleaned[135, 159]. If this was not possible, those items were discarded. Two descriptive studies emphasized careful handling of soiled linens to minimize re-aerosolization of virus.[177,183] Wheeling hampers to the bedside or using hot soluble hamper bags (e.g., disposable) were suggested mechanisms to reduce self-contamination. This literature search did not identify studies that examined the direct impact of disinfection of fabrics on outbreaks of norovirus gastroenteritis or whether self- contamination with norovirus was associated with new infection.
Q.3.C.12.e Cleaning and disinfection agents
The overall quality of evidence on cleaning and disinfection agents was very low.[63,83,87,89,153,167,168,170,174,176-179,182,184] The outcomes examined were symptomatic norovirus infection, inactivation of human norovirus, and inactivation of FCV. Evidence for efficacy against norovirus was usually based on studies using FCV as a surrogate. However, FCV and norovirus exhibit different physiochemical properties and it is unclear whether inactivation of FCV reflects efficacy against human strains of norovirus. One systematic review and 14 descriptive studies[63,83,87,89,167,168,170,174,176-179,182,184] outlined strategies for containing environmental bioburden. The majority of outbreaks were managed with sodium hypochlorite in various concentrations as the primary disinfectant. The concentrations for environmental cleaning among these studies ranged from 0.1% to 6.15% sodium hypochlorite.
There was found moderate quality evidence to examine the impact of disinfection agents on human norovirus inactivation.[187,194,201] Three basic science studies evaluated the virucidal effects of select disinfectants against norovirus.[187,194,201] A decline of 3 in the log10 of human norovirus exposed to disinfectants in the presence of fecal material, a fetal bovine serum protein load, or both was achieved with 5% organic acid after 60 minutes of contact time, 6000 ppm free chlorine with 15 minutes of contact time, or a 1 or 2% peroxide solution for 60 minutes. This study also demonstrated that the range of disinfectants more readily inactivated FCV than human norovirus samples, suggesting that FCV may not have equivalent physical properties to those of human norovirus. One basic science study demonstrated a procedure to eliminate norovirus (genogroup II) from a melamine substrate using a two step process - a cleaning step to remove gross fecal material, followed by a 5000-ppm hypochlorite product with a one minute contact time. Cleaning with a detergent, or using a disinfectant alone failed to eliminate the virus.
Moderate quality evidence was available on the impact of disinfection agents on the human norovirus surrogate, FCV.[185,187,188,190-192,198-200] Nine basic science studies evaluated the activity of several disinfectants agents against FCV.[185,187,188,190-192,198-200] Only a single study showed equivalent efficacy between a quaternary ammonium compound and 1000 ppm hypochlorite on non-porous surfaces. In contrast, selected quaternary ammonium based-products, ethanol, and a 1% anionic detergent were all unable to inactivate FCV beyond a reduction of 1.25 in the log10 of virus, compared to 1000 ppm and 5000 ppm hypochlorite, 0.8% iodine, and 0.5% glutaraldehyde products.200 4% organic acid, 1% peroxide, and >2% aldehyde products showed inactivation of FCV but only with impractical contact times exceeding 1 hour.
Studies of disinfecting non-porous surfaces and hands evaluated the efficacy of varying dilutions of ethanol and isopropanol and determined that 70-90% ethanol was more efficacious at inactivating FCV compared to isopropanol, but unable to achieve a reduction of 3 in the log10 of the viral titer (99.9%), even after 10 minutes of contact. Other studies have shown that combinations of phenolic and quaternary ammonium compounds and peroxyacetic acid were only effective against FCV if they exceeded the manufacturers’ recommended concentrations by a factor of 2 to 4. The included basic science studies agents demonstrating complete inactivation of FCV were those containing hypochlorite, glutaraldehyde, hydrogen peroxide, iodine, or >5% sodium bicarbonate active ingredients. Not all of these products are feasible for use in healthcare settings.
In applications to various fabrics (100% cotton, 100% polyester, and cotton blends), FCV was inactivated completely by 2.6% glutaraldehyde, and showed >90% reductions of FCV titers when phenolics, 2.5% or 10% sodium bicarbonate, or 70% isopropanol were evaluated.190 In carpets consisting of olefin, polyester, nylon, or blends, 2.6% glutaraldehyde demonstrated >99.7% inactivation of FCV, with other disinfectants showing moderate to modest reductions in FCV titers. The experimental use of monochloramine as an alternative disinfectant to free chlorine in water treatment systems only demonstrated modest reductions in viral titer after 3 hours of contact time. The literature search did not evaluate publications using newer methods for environmental disinfection, such as ozone mist from a humidifying device, fumigation, UV irradiation, and fogging.
This search strategy was unable to find well-designed studies that compared virucidal efficacy of products on human norovirus, FCV, or other surrogate models among commonly used hospital disinfectants agents to establish practical standards, conditions, concentrations, and contact times. Ongoing laboratory studies are now exploring murine models as a surrogate that may exhibit greater similarity to human norovirus than FCV. Forthcoming research using this animal model may provide clearer direction regarding which disinfectants reduce norovirus environmental contamination from healthcare environments, while balancing occupational safety issues with the practicality of efficient and ready-to-use products.
There was very low-quality evidence suggesting that select medications may reduce the risk of illness or attenuate symptoms of norovirus.[202,203] Among elderly psychiatric patients, those on antipsychotic drugs plus trihexyphenidyl or benztropine were less likely to become symptomatic, as were those taking psyllium hydrophilic mucilloid. The pharmacodynamics to explain this outcome are unknown, and it is likely that these medications may either be a surrogate marker for another biologically plausible protective factor, or may impact norovirus through central or local effects on gastrointestinal motility. Those who received nitazoxanide, an anti-protozoal drug, were more likely to exhibit longer periods of norovirus illness than those patients who received placebo. The search strategy used in this review did not identify research that considered the effect of anti-peristaltics on the duration or outcomes of norovirus infection.
3.A.1 Consider extending the duration of isolation or cohorting precautions for outbreaks among infants and young children (e.g., under 2 years), even after resolution of symptoms, as there is a potential for prolonged viral shedding and environmental contamination. Among infants, there is evidence to consider extending contact precautions for up to 5 days after the resolution of symptoms.(Category II) (Key Question 3A)
3.A.2 Further research is needed to understand the correlation between prolonged shedding of norovirus and the risk of infection to susceptible patients (No recommendation/unresolved issue) (Key Question 3A)
3.B.1 Perform routine cleaning and disinfection of frequently touched environmental surfaces and equipment in isolation and cohorted areas, as well as high-traffic clinical areas. Frequently touched surfaces include, but are not limited to, commodes, toilets, faucets, hand/bedrailing, telephones, door handles, computer equipment, and kitchen preparation surfaces. (Category IB)(Key Question 3B)
3.B.2 Remove all shared or communal food items for patients or staff from clinical areas for the duration of the outbreak. (Category IB)(Key Question 3B)
3.C.1.a. Actively promote adherence to hand hygiene among healthcare personnel, patients, and visitors in patient care areas affected by outbreaks of norovirus gastroenteritis. (Category IB)(Key Question 3C)
3.C.1.b. During outbreaks, use soap and water for hand hygiene after providing care or having contact with patients suspected or confirmed with norovirus gastroenteritis. (Category IB)(Key Question 3C)
3.C.1.b.1. For all other hand hygiene indications (e.g., when hands are not visibly soiled and have not been in contact with diarrheal patients, contaminated surfaces, or other body fluids) refer to the 2002 HICPAC Guideline for Hand Hygiene in Health-Care Settings [PDF - 495 KB], which includes the indications for use of FDA-compliant alcohol based hand sanitizer. (Category IB)(Key Question 3C)
3.C.1.b.2. Consider ethanol-based hand sanitizers (60-95%) as the preferred active agent compared to other alcohol or non-alcohol based hand sanitizer products during outbreaks of norovirus gastroenteritis. (Category II) (Key Question 3C)
3.C.1.b.3. Further research is required to directly evaluate the efficacy of alcohol-based hand sanitizers against human strains of norovirus, or against a surrogate virus with properties convergent with human strains of norovirus. (No recommendation/unresolved issue) (Key Question 3C)
3.C.2.a Use a surgical or procedure mask and eye protection or a full face shield if there is an anticipated risk of splashes to the face during the care of patients, particularly among those who are vomiting. (Category IB)(Key Question 3C)
3.C.3 Develop and adhere to sick leave policies for healthcare personnel who have symptoms consistent with norovirus infection. (Category IB)(Key Question 3C)
3.C.3.a Exclude ill personnel from work for a minimum of 48 hours after the resolution of symptoms. Once personnel return to work, the importance of performing frequent hand hygiene should be reinforced, especially before and after each patient contact . (Category IB) (Key Question 3C)
3.C.4.a During outbreaks, place patients with norovirus gastroenteritis on Contact Precautions for a minimum of 48 hours after the resolution of symptoms to prevent further transmission. (Category IB)(Key Question 3C)
3.C.4.b When patients with norovirus gastroenteritis cannot be accommodated in single occupancy rooms, efforts should be made to separate them from asymptomatic patients. Dependent upon facility characteristics, approaches for cohorting patients during outbreaks may include placing patients in multi-occupancy rooms, or designating patient care areas or contiguous sections within a facility for patient cohorts. (Category IB) (Key Question 3C)
3.C.4.c Consider minimizing patient movements within a ward or unit during norovirus gastroenteritis outbreaks.(Category II) (Key Question 3C)
3.C.4.c.1 Consider restricting symptomatic and recovering patients from leaving the patient-care area unless it is for essential care or treatment to reduce the likelihood of environmental contamination and transmission of norovirus in unaffected clinical areas. (Category II) (Key Question 3C)
3.C.4.d Consider suspending group activities (e.g., dining events) for the duration of a norovirus outbreak. (Category II) (Key Question 3C)
3.C.5.a Establish protocols for staff cohorting in the event of an outbreak of norovirus gastroenteritis. Ensure staff care for one patient cohort on their ward and do not move between patient cohorts (e.g., patient cohorts may include symptomatic, asymptomatic exposed, or asymptomatic unexposed patient groups). (Category IB)(Key Question 3C)
3.C.5.b Staff who have recovered from recent suspected norovirus infection associated with this outbreak may be best suited to care for symptomatic patients until the outbreak resolves.(Category II) (Key Question 3C)
3.C.5.c Exclude non-essential staff, students, and volunteers from working in areas experiencing outbreaks of norovirus gastroenteritis. (Category IB)(Key Question 3C)
3.C.6 Consider the closure of wards to new admissions or transfers as a measure to attenuate the magnitude of an outbreak of norovirus gastroenteritis. The threshold for ward closure varies and depends on risk assessments by infection prevention personnel and facility leadership. (Category II) (Key Question 3C)
3.C.7.a Establish visitor policies for acute gastroenteritis (e.g., norovirus) outbreaks. (Category IB)(Key Question 3C)
3.C.7.b Restrict non-essential visitors from affected areas of the facility during outbreaks of norovirus gastroenteritis. (Category IB)(Key Question 3C)
3.C.7.b.1 For those affected areas where it is necessary to have continued visitor privileges during outbreaks, screen and exclude visitors with symptoms consistent with norovirus infection and ensure that they comply with hand hygiene and Contact Precautions. (Category IB)(Key Question 3C)
3.C.8.a Provide education to staff, patients, and visitors, including recognition of norovirus symptoms, preventing infection, and modes of transmission upon the recognition and throughout the duration of a norovirus gastroenteritis outbreak. (Category IB) (Key Question 3C)
3.C.8.b Consider providing educational sessions and making resources available on the prevention and management of norovirus before outbreaks occur, as part of annual trainings, and when sporadic cases are detected. (Category II) (Key Question 3C)
3.C.9.a Begin active case-finding when a cluster of acute gastroenteritis cases is detected in the healthcare facility. Use a specified case definition, and implement line lists to track both exposed and symptomatic patients and staff. Collect relevant epidemiological, clinical, and demographic data as well as information on patient location and outcomes. (Category IB)(Key Question 3C)
3.C.9.b As with all outbreaks, notify appropriate local and state health departments, as required by state and local public health regulations, if an outbreak of norovirus gastroenteritis is suspected. (Category IC) (Key Question 3C)
3.C.10 Develop written policies that specify the chains of communication needed to manage and report outbreaks of norovirus gastroenteritis. Key stakeholders such as clinical staff, environmental services, laboratory administration, healthcare facility administration and public affairs, as well as state or local public health authorities, should be included in the framework. (Category IB)(Key Question 3C)
3.C.10.a Provide timely communication to personnel and visitors when an outbreak of norovirus gastroenteritis is identified and outline what policies and provisions need to be followed to prevent further transmission (Category IB) (Key Question 3C)
3.C.11 Consider limiting transfers to those for which the receiving facility is able to maintain Contact Precautions; otherwise, it may be prudent to postpone transfers until patients no longer require Contact Precautions. During outbreaks, medically suitable individuals recovering from norovirus gastroenteritis can be discharged to their place of residence.(Category II) (Key Question 3C)
3.C.12.a Clean and disinfect shared equipment between patients using EPA-registered products with label claims for use in healthcare. Follow the manufacturer’s recommendations for application and contact times. The EPA lists products with activity against norovirus on their website. (Category IC) (Key Question 3C)
3.C.12.b.1 Increase the frequency of cleaning and disinfection of patient care areas and frequently touched surfaces during outbreaks of norovirus gastroenteritis (e.g., consider increasing ward/unit level cleaning to twice daily to maintain cleanliness, with frequently touched surfaces cleaned and disinfected three times daily using EPA-approved products for healthcare settings). (Category IB)(Key Question 3C)
3.C.12.b.2 Clean and disinfect surfaces starting from the areas with a lower likelihood of norovirus contamination (e.g., tray tables, counter tops) to areas with highly contaminated surfaces (e.g., toilets, bathroom fixtures). Change mop heads when a new bucket of cleaning solution is prepared, or after cleaning large spills of emesis or fecal material. (Category IB)(Key Question 3C)
3.C.12.c.1 Consider discarding all disposable patient-care items and laundering unused linens from patient rooms after patients on isolation for norovirus gastroenteritis are discharged or transferred. Facilities can minimize waste by limiting the number of disposable items brought into rooms/areas on Contact Precautions.(Category II) (Key Question 3C)
3.C.12.c.2 No additional provisions for using disposable patient service items such as utensils or dishware are suggested for patients with symptoms of norovirus infection. Silverware and dishware may undergo normal processing and cleaning using standard procedures. (Category II) (Key Question 3C)
3.C.12.c.3 Use Standard Precautions for handling soiled patient-service items or linens, including the use of appropriate PPE. (Category IB)(Key Question 3C)
3.C.12.d.1 Consider avoiding the use of upholstered furniture and rugs or carpets in patient care areas, as these objects are difficult to clean and disinfect completely. If this option is not possible, immediately clean soilage, such as emesis or fecal material, from upholstery, using a manufacturer-approved cleaning agent or detergent. Opt for seating in patient-care areas that can withstand routine cleaning and disinfection. (Category II) (Key Question 3C)
3.C.12.d.2 Consider steam cleaning of upholstered furniture in patient rooms upon discharge. Consult with manufacturer's recommendations for cleaning and disinfection of these items. Consider discarding items that cannot be appropriately cleaned/disinfected. (Category II) (Key Question 3C)
3.C.12.d.3 During outbreaks, change privacy curtains when they are visibly soiled and upon patient discharge or transfer. (Category IB)(Key Question 3C)
3.C.12.d.4 Handle soiled linens carefully, without agitating them, to avoid dispersal of virus. Use Standard Precautions, including the use of appropriate PPE (e.g., gloves and gowns), to minimize the likelihood of cross-contamination. (Category IB)(Key Question 3C)
3.C.12.d.5 Double bagging, incineration, or modifications for laundering are not indicated for handling or processing soiled linen. (Category II) (Key Question 3C)
3.C.12.e.1 Clean surfaces and patient equipment prior to the application of a disinfectant. Follow the manufacturer’s recommendations for optimal disinfectant dilution, application, and surface contact time with an EPA-approved product with claims against norovirus. (Category IC) (Key Question 3C)
3.C.12.e.2 More research is required to clarify the effectiveness of cleaning and disinfecting agents against norovirus, either through the use of surrogate viruses or the development of human norovirus culture system. (No recommendation/unresolved issue) (Key Question 3C)
3.C.12.e.3 More research is required to clarify the effectiveness and reliability of fogging, UV irradiation, and ozone mists to reduce norovirus environmental contamination. (No recommendation/unresolved issue) (Key Question 3C)
3.C.12.e.4 More research is required to evaluate the virucidal capabilities of alcohol-based as well as non-alcohol based hand sanitizers against norovirus. (No recommendation/unresolved issue) (Key Question 3C)
3.D Further research is required to evaluate the utility of medications that may attenuate the duration and severity of norovirus illness. (No recommendation/unresolved issue)(Key Question 3D)