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SHEA NICU white paper series: Practical approaches for the prevention of viral respiratory infections

Published online by Cambridge University Press:  25 October 2023

Nisha Thampi*
Affiliation:
Children’s Hospital of Eastern Ontario, Ottawa, Ontario, Canada
Judith Guzman-Cottrill
Affiliation:
Oregon Health & Science University, Portland, Oregon, USA
Allison H. Bartlett
Affiliation:
University of Chicago and Comer Children’s Hospital, Chicago, Illinois, USA
Wendy Berg
Affiliation:
Children’s Minnesota, St. Paul, Minnesota, USA
Joseph B. Cantey
Affiliation:
The University of Texas Health Science Center, San Antonio, Texas, USA
Eimear Kitt
Affiliation:
Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, USA
Karen Ravin
Affiliation:
Nemours Children’s Health, Wilmington, Delaware, USA
Kenneth M. Zangwill
Affiliation:
Harbor-UCLA Medical Center, Torrance, California, USA
Alexis Elward
Affiliation:
Washington University School of Medicine, St. Louis, Missouri, USA
*
Corresponding author: Nisha Thampi; Email: nthampi@cheo.on.ca
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Abstract

This white paper provides clinicians and hospital leaders with practical guidance on the prevention and control of viral respiratory infections in the neonatal intensive care unit (NICU). This document serves as a companion to Centers for Disease Control and Prevention Healthcare Infection Control Practices Advisory Committee (HICPAC)’s “Prophylaxis and Screening for Prevention of Viral Respiratory Infections in Neonatal Intensive Care Unit Patients: A Systematic Review.” It provides practical, expert opinion and/or evidence-based answers to frequently asked questions about viral respiratory detection and prevention in the NICU. It was developed by a writing panel of pediatric and pathogen-specific experts who collaborated with members of the HICPAC systematic review writing panel and the SHEA Pediatric Leadership Council to identify questions that should be addressed. The document has been endorsed by SHEA, the American Hospital Association (AHA), The Joint Commission, the Pediatric Infectious Diseases Society (PIDS), the Association for Professionals in Infection Control and Epidemiology (APIC), the Infectious Diseases Society of America (IDSA), and the National Association of Neonatal Nurses (NANN).

Type
SHEA White Paper
Copyright
© The Author(s), 2023. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America

Viral respiratory infections (VRIs) are an important cause of morbidity and mortality among critically ill infants in the neonatal intensive care unit (NICU) (see Table 1 for abbreviations). The incidence of VRI varies across NICU settings, ranging from 1% to 8% in retrospective analyses of symptomatic patients. Reference Verboon-Maciolek, Krediet, Gerards, Fleer and van Loon1,Reference Ronchi, Michelow and Chapin2 This figure is likely underestimated; most NICUs do not routinely test for respiratory viruses among infants presenting with compatible symptoms. Prospective surveillance has revealed unrecognized VRI in >50% of infants at some point during their course of birth hospitalization, with evidence of seasonality. Reference Bennett, Tabarani and Bartholoma3

Table 1. Abbreviations

Infants may be infected with viral respiratory pathogens in the NICU setting from infected staff or visitors through the air or via contact with contaminated hands or shared patient equipment. Reference Marr and Tang4 Transmission of respiratory pathogens in the NICU is influenced by several factors, including the structural design of the unit and human behaviors. It is important for healthcare personnel (HCP) to consider healthcare-associated VRI (HA-VRI) for infants who develop signs of infection during their hospitalization and to investigate for a source and/or lapse in infection prevention practices.

Clinical manifestations of VRI can range from asymptomatic or mild upper-respiratory-tract illness to viral pneumonia, bronchiolitis, respiratory failure requiring mechanical ventilation, sepsis-like syndrome, and rarely, meningitis or encephalitis, with varying morbidity and mortality related to the infant’s gestational age and underlying medical fragility. Reference Poole, Camins, Prichard, Faye-Petersen and Hutto5,Reference Zinna, Lakshmanan and Tan6 Infants are relatively immunocompromised compared to older children and adults and are ineligible for vaccines against respiratory viruses. Thus, we must invest in infection prevention measures that offset transmission in the NICU setting.

This White Paper provides clinicians and hospital leaders with practical guidance on the prevention and control of VRI in the NICU. The term “infants” is used throughout instead of “neonates” because patients in the NICU may be beyond 28 days of age. The breadth of measures includes elimination strategies such as visitor restrictions and screening staff and caregivers for the presence of signs or symptoms; engineering controls including ventilation, masking for source control, distancing between patients, and controlled workflows to reduce foot traffic in the unit; administrative controls including policies and procedures for screening, sick leave, and isolation management; and availability of personal protective equipment (PPE) to care for patients under routine practices and additional precautions. Although many of the recommendations reflect standard principles of HA-VRI prevention, they are also relevant for infants with VRI admitted to an NICU from the community.

Although the COVID-19 pandemic has significantly affected infection prevention and control practices in the NICU, pandemic-related measures are outside the scope of this document, which does not discuss prevention of infections due to SARS-CoV-2. In addition, this White Paper does not address topics already covered sufficiently in other references, such as infection-specific prevention and control guidance for neonatal populations available in the American Academy of Pediatrics Red Book: 2021 Report of the Committee on Infectious Diseases. Reference Kimberlin7

Intended use

The Society for Healthcare Epidemiology of America (SHEA) intends for this document to serve as a companion to the Centers for Disease Control and Prevention Healthcare Infection Control Practices Advisory Committee (HICPAC) “Prophylaxis and Screening for Prevention of Viral Respiratory Infections in Neonatal Intensive Care Unit Patients: A Systematic Review” 8 and to provide practical, expert opinion and/or evidence-based answers to frequently asked questions about viral respiratory detection and prevention in the NICU. The published literature does not contain sufficient high-quality studies to meet Grading of Recommendations Assessment, Development and Evaluation standards; therefore, they were not included in the HICPAC guideline. Reference Guyatt, Oxman and Vist9

No guideline, expert guidance, or policy paper can anticipate all situations. This document is meant to serve as an adjunct to individual judgment by qualified professionals. In general, these recommendations apply to nonoutbreak settings. HCP may implement additional measures during an outbreak or other special clinical scenarios. Further details and references are included in the HICPAC “Prophylaxis and Screening for Prevention of Viral Respiratory Infections in Neonatal Intensive Care Unit Patients: A Systematic Review.” 8

Methods

This document was developed by a writing panel of pediatric and pathogen-specific experts who collaborated with members of the HICPAC systematic review writing panel and the SHEA Pediatric Leadership Council to identify questions that should be addressed. Unlike the SHEA expert guidance format, this document is not based on a systematic literature search. Instead, for the selected topic, the authors provide practical approaches in question-and-answer format based on expert opinion and consensus within the context of the HICPAC systematic review.

The SHEA Guidelines Committee, the SHEA Publications Committee, the SHEA Board of Trustees, and the NICU Advisory Panel (see Authors section) reviewed this document. The document has been endorsed by the SHEA, the American Hospital Association (AHA), The Joint Commission, the Pediatric Infectious Diseases Society (PIDS), the Association for Professionals in Infection Control and Epidemiology (APIC), the Infectious Diseases Society of America (IDSA), and the National Association of Neonatal Nurses (NANN).

Authors

The authors are current and past members of the SHEA Guidelines Committee and the SHEA Pediatric Leadership Council, who serve as volunteers. Ms. Berg served as the representative from APIC. All authors have experience in the development of policies pertaining to pediatric infection prevention and either serve presently or served in the past at their respective institutions to develop policies.

The NICU Advisory Panel, which provided oversight and review of the document, is composed of representatives from SHEA, the American Academy of Pediatrics (AAP), AHA, APIC, IDSA, NANN, PIDS, The Joint Commission, and the Vermont Oxford Network.

Practical approaches: Questions and answers

(See Table 2 for a summary of questions and recommendations.)

Table 2. Questions and Recommendations

Question 1: How is a HA-VRI defined in the NICU?

Recommendation: A VRI may be designated as healthcare-associated when a patient has clinically significant signs (eg, apnea, rhinorrhea, pneumonia, sepsis-like syndrome, increased respiratory support), a positive viral respiratory test, and has been hospitalized for longer than the known incubation period for that organism.

Rationale: A practical definition of a HA-VRI takes into consideration the incubation period (the time from exposure to symptom onset) of the specific respiratory virus. Organizations should create a standardized approach for surveillance to track VRIs that may have been acquired in the healthcare setting. Among infants who have been hospitalized since birth, all VRIs should be considered healthcare acquired. In these cases, it may be useful to consider the incubation period of the specific virus to understand where the patient was most likely exposed, particularly if the infant has been transferred between facilities or units (Table 3).

Table 3. Incubation Periods and Minimum Duration for Viral Resporatory Infections

a Adapted from Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings Reference Siegel, Rhinehart, Jackson and Chiarello31 and AAP 2021 Red Book. Reference Kimberlin7,Reference Siegel, Rhinehart, Jackson and Chiarello31 NICUs may also implement additional precautions as per local protocols. Types of precautions for these infections are being reconsidered by various professional organizations at the time of writing. For all the respiratory viruses noted above, the minimum duration of isolation is the duration of illness. Young infants may shed viruses longer than older children and adults, and a more prolonged duration of isolation precautions may be indicated.

For example, the incubation period for RSV is 2–8 days. If a patient develops RSV on day 10 of hospitalization, the infection should be considered healthcare acquired because the patient was exposed to RSV (through healthcare personnel, caregivers, or contaminated shared patient equipment) during that hospitalization. But if a patient develops RSV on day 5 of hospitalization, exposure may have occurred prior to or during admission and should be considered indeterminant. For patients not admitted since birth, RSV infection that develops on day 1 or 2 of admission can be considered community acquired because the exposure likely occurred prior to the patient’s admission.

Ill caregivers and visitors in the healthcare setting may be the source of infection in the infant. Recommendations to reduce transmission risk from caregivers and visitors are described in question 7.

Question 2: When should HCP test for VRIs?

In theory, early detection of HA-VRI would allow for prompt patient isolation and decrease risk of transmission in the NICU; however, weekly active surveillance with molecular testing for respiratory viruses does not appear to identify infants with HA-VRI sooner than testing either when signs develop Reference Poole, Camins, Prichard, Faye-Petersen and Hutto5,Reference Kidszun, Neurohr and Grondahl10 or as a standard component of sepsis work-ups. Reference Ronchi, Michelow and Chapin2,Reference Cerone, Santos and Tristram11

Individual patients based on clinical signs, index of suspicion

Recommendation: Test for VRI in infants who present with signs that could be consistent with infection, including apnea, bradycardia, fever, and poor feeding, Reference Dizdar, Aydemir and Erdeve12 and respiratory findings, including congestion, cough, tachypnea, and respiratory failure. Reference Rose, Washington and Wang13

Rationale: Rates of HA-VRI positivity in infants undergoing evaluation for suspected late-onset sepsis are up to 8%. Reference Ronchi, Michelow and Chapin2,Reference Cerone, Santos and Tristram11 Although there is no direct treatment for HA-VRIs other than influenza, identification of a viral cause of the clinical presentation may decrease unnecessary antibiotic treatment for the patient and protect other patients in the NICU by prompt isolation of the index case.

After exposure to caregiver or visitor

Recommendation: Isolating or testing asymptomatic infants exposed to respiratory viruses from caregivers or visitors is not routinely recommended, but oseltamivir prophylaxis for the infant could be considered after known influenza exposure. Reference Uyeki, Bernstein and Bradley14

Outbreak setting or possible in-hospital transmission (patient or HCP)

Recommendation: Active screening of asymptomatic infants may be considered to understand the extent of an outbreak and to monitor the impact of infection control interventions.

To document resolution of infection

Recommendation: In general, HCP should continue precautions for patients for at least the duration of illness. In patients without respiratory concerns and in the context of ongoing exposure concerns, HCP may consider a strategy of repeated molecular testing and continued isolation until testing is negative.

Rationale: Viral respiratory shedding in infants can be prolonged, and molecular tests can remain positive for weeks despite the absence of infectious virus. Reference Reid, Anderson, Cooley, Williamson and McGregor15Reference Hall17

Question 3: How can HA-VRIs in the NICU be prevented?

Recommendation: A bundled approach, including hand hygiene, visitor screening, staff illness and vaccination policies, proper isolation precautions and PPE, and environmental cleanliness, is recommended to prevent HA-VRIs in the NICU.

Rationale: As defined by the Institute for Healthcare Improvement, a bundle is a group of best practices that individually may improve care but, when applied together, clearly result in substantially greater improvement. 18 HCP should receive education on the rationale behind each individual bundle element, with consideration of an open display of bundle element compliance and healthcare-associated infection (HAI) rates available for review by unit. For the prevention of HA-VRIs in the NICU, implementation of the following bundle elements can be considered. Reference Hei, Bezpalko, Smathers, Coffin and Sammons19

Hand hygiene

Recommendation: The NICU actively should incorporate pre-existing hand hygiene programs. In addition to performing observations with in-the-moment feedback provided to staff, metrics on hand hygiene compliance should be available to the unit and hospital. Engagement and education of caregivers and families are important components of HAI prevention.

Rationale: Improvement in appropriate hand hygiene practices of visitors can significantly decrease HA-VRIs in the NICU. In one study, an increase in hand hygiene compliance from 27% to 85% resulted in a subsequent reduction in overall viral HAIs from 0.67 to 0.23 per 1,000 patient days. Reference Linam, Marrero, Honeycutt, Wisdom, Gaspar and Vijayan20 Such education can be considered on admission in addition to periods of vulnerability including unit clusters, outbreaks, and/or increased transmission of viral respiratory pathogens within the community. Practices that are essential for preventing HAIs in infants through hand hygiene have been reviewed elsewhere. Reference Glowicz, Landon and Sickbert Bennett21

Caregiver and visitor screening practices

Recommendation: Hospitals should implement caregiver and visitor screening practices that are sustainable for the resources available to their specific institution (see question 7). When a caregiver is sick, NICU leadership should clearly communicate the hospital’s infection prevention and control guidelines for when the caregiver can return to the unit.

Rationale: Given the previously described risk of transmission, Reference Hanley, Odeniyi, Feemster, Coffin and Sammons22 sick and/or symptomatic visitors should be restricted from the NICU, and a process should exist for both requesting them to leave and ensuring reunification when safe to do so (as outlined in question 7). We recommend additional caregiver and visitor limitations during times of increased transmission risk in the unit, including but not limited to viral respiratory season or times of high viral respiratory activity within the community, and unit clusters and/or outbreaks.

Staff illness procedures

Recommendation: Robust and nonpunitive sick leave policies for staff are helpful in discouraging presenteeism (working despite personal illness). Refreshers on illness procedures should be considered annually and when increased transmission is noted in the unit and/or the community.

Rationale: NICU leadership should communicate to unit staff the hospital’s occupational health guidelines for when an ill HCP may return to work. Presenteeism (working despite personal illness) is a known contributor to respiratory viral transmission in healthcare settings, yet it is well described among HCP. Reference Szymczak, Smathers, Hoegg, Klieger, Coffin and Sammons23Reference Widera, Chang and Chen27 Presenteeism is caused by a combination of systems-based and complex sociocultural factors, including financial and/or job security, job discipline, social status within an organization, staffing levels, and access to or availability of sick-leave procedures. Reference Szymczak, Smathers, Hoegg, Klieger, Coffin and Sammons23,Reference Chow and Mermel24 Given well-described risks posed by presenteeism and its reduction noted by paid sick leave, such policies should be universally accessible to staff.

Vaccination and postexposure chemoprophylaxis

Recommendations:

  • Vaccination of HCP and caregivers against influenza and compliance with the facility’s seasonal vaccine policies are strongly recommended to prevent healthcare transmission of viral respiratory pathogens to infants, who are ineligible under age 6 months for the influenza vaccine and other vaccines to prevent VRI. 28

  • In the context of outbreak control, antiviral chemoprophylaxis against influenza with oseltamivir may be recommended for all asymptomatic patients on the unit and to immune-susceptible HCP following a risk assessment.

  • Palivizumab should not be used as part of RSV outbreak management to prevent further transmission within the unit. 29

Rationale: Individuals infected with influenza may shed the virus 1–2 days before symptom onset. HCP may therefore come into work with unrecognized infection and expose patients, caregivers, and colleagues who may be at higher risk for complications of influenza. Staff and caregiver vaccination against influenza can reduce introduction of influenza into the unit and further spread to susceptible HCP and patients in open bays or neighboring pods. Infants exposed to a known case of influenza in the unit (from caregiver, visitor, or HCP) can be offered oseltamivir as postexposure chemoprophylaxis according to clinical practice guidelines. Reference Kimberlin7 However, no data are available regarding appropriate dosing for infants under 14 days of life. Reference Kimberlin7 Moreover, no data are available regarding the effectiveness of preexposure chemoprophylaxis for HCP working on an outbreak unit. Reference Uyeki, Bernstein and Bradley14 In the context of an RSV outbreak in the NICU, we agree with the existing recommendation from the AAP Report of the Committee on Infectious Diseases that palivizumab not be used as part of RSV outbreak management to prevent further transmission within the unit, due to a paucity of data. 29

Isolation precautions and personal protective equipment (PPE)

Recommendation:

  • Patients should be placed on appropriate isolation precautions when first symptomatic, regardless of whether testing is sent.

  • Appropriate PPE should be worn for all patients on isolation precautions, donned and doffed in appropriate order.

  • There should be clear documentation of appropriate transmission-based precautions immediately placed in the patient’s chart, and clear signage should be placed at the entry to the patient’s room or bed space.

  • If resources allow, units may consider audits on donning and doffing of PPE and appropriate isolation procedures, with in-the-moment feedback and unit metrics on appropriate isolation precautions available for comparison.

Rationale: Patient isolation and appropriate use of PPE are foundational infection prevention practices, both for standard and for transmission-based precautions, and have been shown to be effective in preventing transmission in the healthcare setting. By isolating the patient at the source, and by donning PPE targeting the predominant mode of transmission, the risk of healthcare-associated infection is reduced. Reference Picard, Edlund and Keddie30,Reference Siegel, Rhinehart, Jackson and Chiarello31 Guidelines on pathogen-specific recommendations for patient placement in negative pressure rooms have been published elsewhere. Reference Siegel, Rhinehart, Jackson and Chiarello31

Environmental cleanliness

Recommendations:

  • All shared equipment should be appropriately cleaned and disinfected after use and stored in designated clean utility areas. Reference Rutala and Weber32

  • At least once daily cleaning and disinfection of high-touch surfaces should be performed using an appropriate surface disinfectant registered by the country’s regulatory authority (eg, in the United States, the EPA) and consistent with hospital policy. Reference Kundrapu, Sunkesula, Jury, Sitzlar and Donskey33,34

  • Inpatient rooms should be kept clutter-free with support and education provided to families on the importance of their role in HAI prevention.

  • Ideally, families should keep bedside tables and windowsills clear. They should aim to keep personal items to a minimum, with no more than a 1-week supply of belongings, and place personal items in drawers where available.

  • Some NICUs have a set day-cleaning process (eg, every 14 days) to ensure ongoing decluttering and thorough disinfection.

Rationale: Optimal cleaning and disinfection of the patient environment should be a shared goal of unit staff, environmental services, and families. Although specific data may be limited, one modeling study showed significant success with this element of prevention, particularly when combined with additional high-yield bundle elements, predicting a decreased VRI risk by 21%–48%, with a 15% increase in hand hygiene and 2 surface cleanings. Reference Wilson, Reynolds and Canales35 Evidence surrounding the efficacy of UV-C light-based disinfection is evolving. If readily available, these may be considered adjunctive means of cleaning high-touch devices or equipment in patient-care areas such as phones, in addition to hand hygiene. Reference Demeersseman, Saegeman, Cossey, Devriese and Schuermans36Reference Rudhart, Gunther, Dapper, Stuck and Hoch38

Question 4. What is the optimal distance between patients for isolation when not in a private room?

Recommendation: Infants in the NICU who require respiratory isolation should be allocated as much space as is feasible, taking into consideration the physical layout of the NICU, patient census, and staffing level.

  • One meter (3 feet) between infants should be an absolute minimum.

  • The approach to distancing is not affected by the type of bed (crib, warmer, or isolette).

Rationale: The amount of physical space required by an infant in respiratory (droplet or airborne) precautions is usually measured either in linear distance from the next patient or in square footage dedicated to the care of the infant. At an absolute minimum, HICPAC recommends 1–2 m (3–6 feet) of linear distance for droplet isolation. Reference Siegel, Rhinehart, Jackson and Chiarello31 Ideally, however, infants should have as much space as possible to minimize the risk of horizontal transmission of their proven or suspected respiratory infection to another patient. Obviously, this can be quite challenging, as local circumstances will affect the space available.

The most immediate limitation, and the one that is the most challenging to change, is the physical layout of the NICU. Single-patient rooms (ie, private rooms) are preferred, as they maximize floor space while ensuring at least 1 physical wall between patients. Reference Siegel, Rhinehart, Jackson and Chiarello31,Reference Kilpatrick, Papile, Macones and Watterberg39 However, many NICUs utilize multibed rooms (bays or a large single room), where there is higher patient density in the space available for patient care. In addition, high patient census and low staffing levels can increase patient density, and HCP time demands have been associated with increased rates of horizontal infections in the NICU. Reference Haley and Bregman40,Reference Dahl and Solevag41 Finally, local practices such as cohorting (eg, moving an infant into a room or bay with other infants who share the same colonization or infection pattern) or parent requests to keep siblings close together despite different infection-related exposures can affect transmission risk.

Traditionally, infection prevention organizations used estimates of respiratory particle size as a guide for practice recommendations. Larger particles were assumed to fall to surfaces relatively quickly, and smaller particles were assumed to remain suspended in air for longer periods. Physical proximity of <1 meter (<3 feet) has been clearly associated with increased risk for respiratory transmission of infections such as Neisseria meningitidis and Streptococcus pyogenes. Reference Feigin, Baker, Herwaldt, Lampe, Mason and Whitney42,Reference Hamburger and Robertson43 Although respiratory particles historically were described as a dichotomy (large droplets versus small aerosols), the size of the particles is on a spectrum. Reference Leung44 Coughing, sneezing, and other aerosol-generating maneuvers can generate a variety of different-sized particles. Reference Javorka, Tomori and Zavarska45

Dispersion of respiratory secretions is also increased when babies require noninvasive ventilation support, such as high-flow nasal cannula or continuous positive airway pressure. Reference Sahih, Schultz and Wilson46 Finally, the potential for transmission also depends on the size of the room and available ventilation. Although isolettes may provide a physical barrier to viral respiratory pathogen exposure through air, the risks of transmission through direct and indirect contact are similar between bed types, so no recommendation is made on the minimum distance between specific bed types.

For neonatal care, the answer to the question, “How much space does this infant need?” is usually “How much space can you make?” A single-patient room is the optimal approach to preventing transmission in the unit. Barring that, physically moving the infant to a bed space where they have as much distance between themselves and other infants—particularly infants who are critically ill—is ideal. If possible, surrounding the isolated infant with a buffer of empty bed spaces is preferred. If NICU census or staffing levels do not allow creation of at least 1 meter (3 feet) of space, then it is important to collaborate promptly with administrative officials to open additional areas (eg, unused space that can be converted into NICU beds) or make additional staff available. These strategies have been used successfully in outbreak management, and failure to provide adequate separation may lead to ongoing transmission within the unit and declaration of an outbreak.

Question 5. How long should NICU patients with VRIs be isolated?

Recommendation: If respiratory signs were present at the time of VRI diagnosis, precautions should be continued for at least the duration of illness.

  • In the context of an ongoing exposure concern and in the absence of respiratory signs, HCP may consider repeat molecular testing and additional precautions until repeated testing is negative.

  • Precautions may be discontinued if clinical signs are attributable to a noninfectious etiology and respiratory viral testing is negative.

  • The duration of isolation following asymptomatic detection of respiratory viral pathogens is unclear. Testing of asymptomatic infants should be discouraged outside the outbreak setting (see question 2).

Rationale: Estimated rates of VRI are lower in the NICU than in other pediatric intensive care settings; however, the potential impacts on patient outcomes are significant. Reference Quach, Shah and Rubin47 VRIs in premature infants can result in the need for increased respiratory support, development of long-term morbidities such as bronchopulmonary dysplasia, longer duration of hospital stays, severe illness, and death. Reference Bennett, Tabarani and Bartholoma3,Reference Pichler, Assadian and Berger48,Reference Civardi, Tzialla, Baldanti, Strocchio, Manzoni and Stronati49 VRIs may present with nonspecific signs in infants, making detection of transmission chains and timely institution of isolation precautions challenging. The true scope and magnitude of these infections is not well understood. Reference Poole and Nyquist50

Although there are established guidelines for the duration of isolation precautions in pediatric and adult settings, NICU-specific guidance is not standardized. As a result, individual healthcare institutions may have varying practices. At the time of the writing of this document, the most recent HICPAC Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings from 2007 recommends the use of transmission-based precautions for suspected and confirmed VRIs. Reference Siegel, Rhinehart, Jackson and Chiarello31 For most respiratory viruses, including non–SARS-CoV-2 human coronaviruses, human metapneumovirus, parainfluenza, respiratory syncytial virus (RSV) and rhinovirus/enterovirus, continuation of isolation precautions for the duration of illness is recommended (Table 3). Reference Kimberlin7,Reference Siegel, Rhinehart, Jackson and Chiarello31 For influenza, isolation precautions are recommended for 7 days after illness onset or until 24 hours after the resolution of fever and respiratory symptoms, whichever is longer. 28 Premature infants may not present with typical respiratory signs and may have variable levels of immune compromise. As such, duration of isolation may be difficult to determine using current guidelines. Reference Poole and Nyquist50 In addition, infants may have prolonged illness and shed respiratory viruses longer than older children and adults, thus a more prolonged duration of isolation precautions may be indicated. Reference Hall, Douglas and Geiman16,Reference Takeyama, Hashimoto, Sato, Kawashima, Kawasaki and Hosoya51,Reference Rubin, Kohn, Nullet and Hill52

Question 6. In NICUs with “open bay” or “pod” layouts, what factors should be considered when determining a possible exposure to a patient with a VRI?

Recommendation:

  • From the infection prevention perspective, private rooms may create greater physical space between patients, visitors, and HCP, potentially decreasing pathogen exposure risk, and may decrease the use of multipatient equipment, further reducing risk.

  • In units with open bay or pod layouts, it is particularly important to review the standard operating procedures and policies (or instructions for use, IFUs) related to cleaning and disinfection of shared patient equipment. All units with concerns of intrafacility spread should, at a minimum, focus on systematically assessing and improving infection prevention practices among all staff.

Rationale: Identification and control of an infection source is foundational to prevent its spread to other patients and staff. This effort requires consideration of many factors, each of which will vary when applied to NICUs of differing size, design, and acuity level.

Neonatal unit design

The overall design of a neonatal unit can directly impact an infant’s exposure risk to respiratory pathogens. As the pediatric family-centered care model is followed in more NICU settings, many modern units are now designed with single-patient private rooms. In NICUs with open bays or pods, infants share ventilation airspace and often are near each other. In a study of 2 children’s hospitals, units with <50% single rooms had 1.33 (95% CI, 1.29–1.37) times higher HA-VRI rates than units with ≥50% single rooms; NICUs were not analyzed specifically. Reference Quach, Shah and Rubin47 This configuration may increase the risk of exposure to respiratory viruses that can also remain viable on shared patient equipment and other fomites for several hours to days. Reference Kramer, Schwebke and Kampf53 Although there is substantial contamination of “high touch” bedside privacy screens and curtains, Reference Cobrado, Silva-Dias, Azevedo and Rodrigues54 data suggesting a link to transmission are limited or inapplicable to the NICU setting.

Patient bed type

NICUs utilize a variety of infant beds, including open cribs, open radiant warmers, and isolettes. An open crib is similar to a warmer with regard to potential exposure to pathogens. Infant isolettes, in contrast, provide a physical barrier to most viral respiratory pathogen exposure through air, unless the source is someone who provides direct hands-on care to the patient (eg, the patient’s nurse or parent).

Patient equipment

In the NICU setting, contaminated equipment has been identified as a point source leading to indirect contact transmission of pathogens. Reference Kramer, Schwebke and Kampf53 For example, bacteria have been implicated in outbreaks related to rectal thermometers, breastmilk pump equipment, Reference Donowitz, Marsik, Fisher and Wenzel55 oxygen saturation probe covers, and even contaminated stethoscopes Reference Gastmeier, Groneberg, Weist and Ruden56,Reference Millan-Lou, Lopez and Bueno57 ; many of these involve noncritical surfaces. Appropriate disinfection in between each use may not occur for such devices in all NICUs. Reference Kalra, Amin and Albert58 Viral respiratory outbreaks in the NICU are not uncommon, but those linked directly to equipment are infrequently reported. Contaminated ophthalmologic equipment has been implicated in adenovirus NICU outbreaks during routine eye exams for retinopathy of prematurity. Reference Ersoy, Otlu, Turkcuoglu, Yetkin, Aker and Kuzucu59,Reference Sammons, Graf and Townsend60

HCP, caregivers, and visitors

In addition to patient-specific equipment, the point source for a single HAI or a cluster may be a staff member, a visitor, a shared fomite (eg, disposal sink), or other treatment or intervention that may or may not be centrally prepared (medication, tubing, misassigned breast milk, etc). All staff and visitors who may have interacted with an infected infant should be interviewed for the presence of symptoms. Notably, a point source is unlikely to be identified when considering a single infected infant. In up to 50% of outbreaks, no source was identified, which may contribute to underreporting of these NICU-based events. Reference Gastmeier, Loui and Stamm-Balderjahn61,Reference Johnson and Quach62 Also, many units do not have the resources to perform robust outbreak investigations. The rigor with which an individual NICU investigates a disease cluster and infection prevention practices among staff should result from input from all relevant stakeholders in the NICU and institution.

Many units assign individual staff to specific babies or create staff–patient cohorts when disease clusters occur. As a practical matter, this may be reasonable despite the inconsistency of the data on this intervention. Data also are inconsistent on the impact of patient-to-staff ratios during an outbreak as potential risks for ongoing disease spread. High ratios have frequently been linked to an increase in incidence, particularly for bacteria and device-related infection, but rarely as an independent risk factor. Reference Hensel, van den Bruck, Klare, Heldmann, Ghebremedhin and Jenke63,Reference Rogowski, Staiger, Patrick, Horbar, Kenny and Lake64 It may also be a proxy for patient census and other workflow adjustments.

Question 7. What are the best methods to screen for caregivers and visitors with respiratory illness, and are there reasonable age restrictions?

Caregiver and visitor screening practices

Recommendation:

  • A combination of procedures should be considered to minimize patients’ exposure to community-acquired pathogens.

  • At a minimum, these procedures should include symptom-based screening.

  • Additional measures, such as age-related visitor restriction, education of visitors on local prevention practices, and/or limitation of movement within the NICU, may be indicated during periods of high community transmission, as defined by public health authorities and as part of outbreak management.

Rationale: Caregivers and visitors are a central part of the patient’s care team in the NICU, where family involvement is crucial and where additional visitors serve as necessary respite for families who are experiencing prolonged hospital stays with critically ill infants. Reference Murray and Swanson65 Yet, such benefits need to be weighed against the risk of neonatal exposure to sick caregivers, which is a known and potentially modifiable risk factor for pediatric HAIs and particularly HA-VRIs. Reference Hanley, Odeniyi, Feemster, Coffin and Sammons22,Reference Johnson, Akinboyo and Schaffzin66,Reference Paquette, Shephard, Bedard and Thampi67

Caregiver and visitor restriction policies and practices exist in most pediatric hospitals; however, approaches vary, including age-based, symptom-based policies and/or outbreak-specific policies existing either seasonally or year-round. Reference Pong, Beekmann, Faltamo, Polgreen and Shane68 Ideally, these would be symptom-based, maintained year-round, performed daily and in-person with accessible language and infographics. Given that this ideal is generally not feasible, units should consider a process that functions regularly within the extent of their available resources and, most importantly, with clear accountability for action.

Symptom-based screening of caregivers that focuses on infectious symptoms can limit the introduction of viral respiratory pathogens into the unit. NICUs should consider screening processes that function regularly within the extent of available resources and have a clear plan in place for who is accountable for sick caregivers or visitors at a unit level. Screening approaches may include face-to-face questioning and/or use of a smart phone or a paper-based method. Infographics depicting concerning symptoms are recommended to make the tool more accessible.

Family education is strongly recommended to enable caregivers to recognize and report potentially infectious symptoms. Moreover, ensuring a culture of safety in the NICU will empower staff to practice a gentle but direct approach if a caregiver is visibly ill. If they screen positive and symptoms are noted during their visit, they should be asked to leave and to identify an alternative caregiver. In situations where restriction of symptomatic caregivers and visitors from the unit is not possible, including times of critical illness or end of life, the NICU should ensure that appropriate mitigation measures are in place, in consultation with unit leadership and the infection prevention and control team.

Additional measures

During periods of routine visitation, we do not recommend a particular age restriction for visitors to the NICU. Each unit should consider their own specific needs and ability to support young children in an intensive care setting. For example, we consider it reasonable to have no more than 2 individuals be at the bedside at one time, and we recommend that families remain in their room, pod, or bedspace as much as feasibly possible. During periods of high VRI transmission in the community, as defined locally with public health partners, or in the context of a unit outbreak, the NICU may consider temporarily restricting visitation to essential caregivers. During periods of high VRI transmission or in the context of a unit outbreak, reliable masking among caregivers should be strongly considered as an additional source control measure. Access to shared eating spaces and lounges during these times may also be paused.

The NICU should consider engaging visitors and caregivers in the development of visitor/caregiver policies, with input from additional key working partners, where available, including family advisory and partner councils. Reference Linam, Marrero, Honeycutt, Wisdom, Gaspar and Vijayan20,Reference Johnson, Akinboyo and Schaffzin66,Reference Paquette, Shephard, Bedard and Thampi67

Acknowledgments

The authors wish to thank NICU Advisory Panel Chairs, Drs. Kristina Bryant and Deborah Yokoe. The authors thank Valerie Deloney, MBA, and Jennifer Rigatti for their organizational expertise in the development of this manuscript.

Financial support

The SHEA funded the development and publication of this document.

Competing interests

The following disclosures reflect what has been reported to SHEA. To provide transparency, SHEA requires full disclosure of all relationships, regardless of relevancy to the guideline topic. Evaluation of such relationships as potential conflicts of interest is determined by a review process. The assessment of disclosed relationships for possible conflicts of interest are based on the relative weight of the financial relationship (ie, monetary amount) and the relevance of the relationship (ie, the degree to which an association might reasonably be interpreted by an independent observer as related to the topic or recommendation of consideration). The reader of this guidance should be mindful of this when the list of disclosures is reviewed. N.T. is the primary investigator for a grant from the Canadian Institutes for Health Research on sampling surfaces in the community for SARS-CoV-2. K.Z. has a grant from the AHRQ to study antimicrobial stewardship in NICUs. All other authors report no conflicts of interest relevant to this article.

NICU Advisory Panel: Kenneth M. Zangwill, MD, American Academy of Pediatrics Section on Infectious Diseases (AAP/SOID); Kavita Bhat, MD, MPH, American Hospital Association (AHA); Jessica R. Rindels, MBA, BSN, RN, CIC, Association for Professionals in Infection Control and Epidemiology (APIC); Jill Jones, MS, APRN, NNP-BC, National Association of Neonatal Nurses (NANN); Pablo J. Sánchez, MD, Infectious Diseases Society of America (IDSA); Aaron M. Milstone, MD, Pediatric Infectious Diseases Society (PIDS); Margaret VanAmringe, MHS, The Joint Commission; and Judith Guzman-Cottrill, DO, The Vermont Oxford Network (VON).

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Figure 0

Table 1. Abbreviations

Figure 1

Table 2. Questions and Recommendations

Figure 2

Table 3. Incubation Periods and Minimum Duration for Viral Resporatory Infections